372 results on '"Bartsch Jörg W"'
Search Results
2. Identification of ADAM proteinase substrates in neurodegeneration and neuroinflammation
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Guan Ziqiang, Mitterreiter Stefan, Lichtenthaler Stefan F, MInai Yuji, Wildeboer Dirk, Reipschläger Simone, Naus Silvia, Moss Marcia L, and Bartsch Jörg W
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Neurosciences. Biological psychiatry. Neuropsychiatry ,RC321-571 ,Neurophysiology and neuropsychology ,QP351-495 - Published
- 2007
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3. ADAM8 signaling drives neutrophil migration and ARDS severity
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Conrad, Catharina, Yildiz, Daniela, Cleary, Simon J, Margraf, Andreas, Cook, Lena, Schlomann, Uwe, Panaretou, Barry, Bowser, Jessica L, Karmouty-Quintana, Harry, Li, Jiwen, Berg, Nathaniel K, Martin, Samuel C, Aljohmani, Ahmad, Moussavi-Harami, S Farshid, Wang, Kristin M, Tian, Jennifer J, Magnen, Mélia, Valet, Colin, Qiu, Longhui, Singer, Jonathan P, Eltzschig, Holger K, Bertrams, Wilhelm, Herold, Susanne, Suttorp, Norbert, Schmeck, Bernd, Ball, Zachary T, Zarbock, Alexander, Looney, Mark R, and Bartsch, Jörg W
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Acute Respiratory Distress Syndrome ,Rare Diseases ,Pneumonia ,Lung ,2.1 Biological and endogenous factors ,Aetiology ,Respiratory ,ADAM Proteins ,Animals ,Antigens ,CD ,Cells ,Cultured ,Disease Models ,Animal ,Gene Expression Regulation ,Humans ,Male ,Membrane Proteins ,Mice ,Mice ,Inbred C57BL ,Microscopy ,Confocal ,RNA ,Respiratory Distress Syndrome ,CAPSys Study Group ,Inflammation ,Innate immunity ,Neutrophils ,Proteases ,Pulmonology - Abstract
Acute respiratory distress syndrome (ARDS) results in catastrophic lung failure and has an urgent, unmet need for improved early recognition and therapeutic development. Neutrophil influx is a hallmark of ARDS and is associated with the release of tissue-destructive immune effectors, such as matrix metalloproteinases (MMPs) and membrane-anchored metalloproteinase disintegrins (ADAMs). Here, we observed using intravital microscopy that Adam8-/- mice had impaired neutrophil transmigration. In mouse pneumonia models, both genetic deletion and pharmacologic inhibition of ADAM8 attenuated neutrophil infiltration and lung injury while improving bacterial containment. Unexpectedly, the alterations of neutrophil function were not attributable to impaired proteolysis but resulted from reduced intracellular interactions of ADAM8 with the actin-based motor molecule Myosin1f that suppressed neutrophil motility. In 2 ARDS cohorts, we analyzed lung fluid proteolytic signatures and identified that ADAM8 activity was positively correlated with disease severity. We propose that in acute inflammatory lung diseases such as pneumonia and ARDS, ADAM8 inhibition might allow fine-tuning of neutrophil responses for therapeutic gain.
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- 2022
4. Endosomal accumulation of APP in wobbler motor neurons reflects impaired vesicle trafficking: Implications for human motor neuron disease
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Troakes Claire, Shaw Christopher, Heimann Peter, Golfi Panagiota, Palmisano Ralf, Schmitt-John Thomas, and Bartsch Jörg W
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Neurosciences. Biological psychiatry. Neuropsychiatry ,RC321-571 ,Neurophysiology and neuropsychology ,QP351-495 - Abstract
Abstract Background The cause of sporadic amyotrophic lateral sclerosis (ALS) is largely unknown but hypotheses about disease mechanisms include oxidative stress, defective axonal transport, mitochondrial dysfunction and disrupted RNA processing. Whereas familial ALS is well represented by transgenic mutant SOD1 mouse models, the mouse mutant wobbler (WR) develops progressive motor neuron degeneration due to a point mutation in the Vps54 gene, and provides an animal model for sporadic ALS. VPS54 protein as a component of a protein complex is involved in vesicular Golgi trafficking; impaired vesicle trafficking might also be mechanistic in the pathogenesis of human ALS. Results In motor neurons of homozygous symptomatic WR mice, a massive number of endosomal vesicles significantly enlarged (up to 3 μm in diameter) were subjected to ultrastructural analysis and immunohistochemistry for the endosome-specific small GTPase protein Rab7 and for amyloid precursor protein (APP). Enlarged vesicles were neither detected in heterozygous WR nor in transgenic SOD1(G93A) mice; in WR motor neurons, numerous APP/Rab7-positive vesicles were observed which were mostly LC3-negative, suggesting they are not autophagosomes. Conclusions We conclude that endosomal APP/Rab7 staining reflects impaired vesicle trafficking in WR mouse motor neurons. Based on these findings human ALS tissues were analysed for APP in enlarged vesicles and were detected in spinal cord motor neurons in six out of fourteen sporadic ALS cases. These enlarged vesicles were not detected in any of the familial ALS cases. Thus our study provides the first evidence for wobbler-like aetiologies in human ALS and suggests that the genes encoding proteins involved in vesicle trafficking should be screened for pathogenic mutations.
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- 2011
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5. MicroRNA-149 Regulates Proliferation, Migration, and Invasion of Pituitary Adenoma Cells by Targeting ADAM12 and MMP14
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Zhang, Zhuo, Schäfer, Agnes, Voellger, Benjamin, Wang, Jun-wen, Lei, Ting, Nimsky, Christopher, and Bartsch, Jörg W.
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- 2022
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6. Proteolytically generated soluble Tweak Receptor Fn14 is a blood biomarker for γ‐secretase activity
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Güner, Gökhan, Aßfalg, Marlene, Zhao, Kai, Dreyer, Tobias, Lahiri, Shibojyoti, Lo, Yun, Slivinschi, Bianca Ionela, Imhof, Axel, Jocher, Georg, Strohm, Laura, Behrends, Christian, Langosch, Dieter, Bronger, Holger, Nimsky, Christopher, Bartsch, Jörg W, Riddell, Stanley R, Steiner, Harald, and Lichtenthaler, Stefan F
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- 2022
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7. Comparison of Whiskbroom and Pushbroom darkfield elastic light scattering spectroscopic imaging for head and neck cancer identification in a mouse model
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Bassler, Miriam C., Stefanakis, Mona, Sequeira, Inês, Ostertag, Edwin, Wagner, Alexandra, Bartsch, Jörg W., Roeßler, Marion, Mandic, Robert, Reddmann, Eike F., Lorenz, Anita, Rebner, Karsten, and Brecht, Marc
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- 2021
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8. Bach2 regulates autophagy to modulate UVA-induced photoaging in skin fibroblasts
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Wang, Mei, Lei, Mingxing, Chang, Li, Xing, Yang, Guo, Yingying, Pourzand, Charareh, Bartsch, Jörg W., Chen, Jingyi, Luo, Jiefu, Widya Karisma, Vega, Nisar, Muhammad Farrukh, Lei, Xia, and Zhong, Julia Li
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- 2021
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9. ADAM 8 as a novel target for doxorubicin delivery to TNBC cells using magnetic thermosensitive liposomes
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Alawak, Mohamad, Abu Dayyih, Alice, Mahmoud, Gihan, Tariq, Imran, Duse, Lili, Goergen, Nathalie, Engelhardt, Konrad, Reddy Pinnapireddy, Shashank, Jedelská, Jarmila, Awak, Muhannad, König, Alexander M., Brüßler, Jana, Bartsch, Jörg W., and Bakowsky, Udo
- Published
- 2021
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10. Elevated expression of the metalloproteinase ADAM8 associates with vascular diseases in mice and humans
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Schick, Daniel, Babendreyer, Aaron, Wozniak, Justyna, Awan, Tanzeela, Noels, Heidi, Liehn, Elisa, Bartsch, Jörg-W., Vlacil, Ann-Kathrin, Grote, Karsten, Zayat, Rashad, Goetzenich, Andreas, Ludwig, Andreas, and Dreymueller, Daniela
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- 2019
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11. Effects of anti-estrogens on cell invasion and survival in pituitary adenoma cells: A systematic study
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Hannen, Ricarda, Steffani, Marcella, Voellger, Benjamin, Carl, Barbara, Wang, Junwen, Bartsch, Jörg W., and Nimsky, Christopher
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- 2019
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12. A jack of all trades – ADAM8 as a signaling hub in inflammation and cancer.
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Cook, Lena, Gharzia, Federico Guillermo, Bartsch, Jörg W., and Yildiz, Daniela
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CELL communication ,EXTRACELLULAR vesicles ,CELL motility ,DRUG target ,CELL survival - Abstract
As a member of the family of A Disintegrin And Metalloproteinases (ADAM) ADAM8 is preferentially expressed in lymphatic organs, immune cells, and tumor cells. The substrate spectrum for ADAM8 proteolytic activity is not exclusive but is related to effectors of inflammation and signaling in the tumor microenvironment. In addition, complexes of ADAM8 with extracellular binding partners such as integrin β‐1 cause an extensive intracellular signaling in tumor cells, thereby activating kinase pathways with STAT3, ERK1/2, and Akt signaling, which causes increased cell survival and enhanced motility. The cytoplasmic domain of ADAM8 harbors five SRC homology‐3 (SH3) domains that can potentially interact with several proteins involved in actin dynamics and cell motility, including Myosin 1F (MYO1F), which is essential for neutrophil motility. The concept of ADAM8 thus involves immune cell recruitment, in most cases leading to an enhancement of inflammatory (asthma, COPD) and tumor (including pancreatic and breast cancers) pathologies. In this review, we report on available studies that qualify ADAM8 as a therapeutic target in different pathologies. As a signaling hub, ADAM8 controls extracellular, intracellular, and intercellular communication, the latter one mainly mediated by the release of extracellular vesicles with ADAM8 as cargo. Here, we will dissect the contribution of different domains to these distinct ways of communication in several pathologies. We conclude that therapeutic targeting attempts for ADAM8 should consider blocking more than a single domain and that this requires a thorough evaluation of potent molecules targeting ADAM8 in an in vivo setting. [ABSTRACT FROM AUTHOR]
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- 2024
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13. Degradome of soluble ADAM10 and ADAM17 metalloproteases
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Scharfenberg, Franka, Helbig, Andreas, Sammel, Martin, Benzel, Julia, Schlomann, Uwe, Peters, Florian, Wichert, Rielana, Bettendorff, Maximilian, Schmidt-Arras, Dirk, Rose-John, Stefan, Moali, Catherine, Lichtenthaler, Stefan F., Pietrzik, Claus U., Bartsch, Jörg W., Tholey, Andreas, and Becker-Pauly, Christoph
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- 2020
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14. ADAM12 induces EMT and promotes cell migration, invasion and proliferation in pituitary adenomas via EGFR/ERK signaling pathway
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Wang, Junwen, Zhang, Zhuo, Li, Ran, Mao, Feng, Sun, Wei, Chen, Juan, Zhang, Huaqiu, Bartsch, Jörg-W., Shu, Kai, and Lei, Ting
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- 2018
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15. A jack of all trades – ADAM8 as a signaling hub in inflammation and cancer
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Cook, Lena, primary, Gharzia, Federico Guillermo, additional, Bartsch, Jörg W., additional, and Yildiz, Daniela, additional
- Published
- 2023
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16. Proteometabolomics of initial and recurrent glioblastoma highlights an increased immune cell signature with altered lipid metabolism
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Cosenza-Contreras, Miguel, primary, Schäfer, Agnes, additional, Sing, Justin, additional, Cook, Lena, additional, Stillger, Maren N, additional, Chen, Chia-Yi, additional, Hidalgo, Jose Villacorta, additional, Pinter, Niko, additional, Meyer, Larissa, additional, Werner, Tilman, additional, Bug, Darleen, additional, Haberl, Zeno, additional, Kübeck, Oliver, additional, Zhao, Kai, additional, Stei, Susanne, additional, Gafencu, Anca Violeta, additional, Ionita, Radu, additional, Brehar, Felix M, additional, Ferrer-Lozano, Jaime, additional, Ribas, Gloria, additional, Cerdá-Alberich, Leo, additional, Martí-Bonmatí, Luis, additional, Nimsky, Christopher, additional, Van Straaten, Alexis, additional, Biniossek, Martin L, additional, Föll, Melanie, additional, Cabezas-Wallscheid, Nina, additional, Büscher, Jörg, additional, Röst, Hannes, additional, Arnoux, Armelle, additional, Bartsch, Jörg W, additional, and Schilling, Oliver, additional
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- 2023
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17. Mucus Detachment by Host Metalloprotease Meprin β Requires Shedding of Its Inactive Pro-form, which Is Abrogated by the Pathogenic Protease RgpB
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Wichert, Rielana, Ermund, Anna, Schmidt, Stefanie, Schweinlin, Matthias, Ksiazek, Miroslaw, Arnold, Philipp, Knittler, Katharina, Wilkens, Frederike, Potempa, Barbara, Rabe, Björn, Stirnberg, Marit, Lucius, Ralph, Bartsch, Jörg W., Nikolaus, Susanna, Falk-Paulsen, Maren, Rosenstiel, Philip, Metzger, Marco, Rose-John, Stefan, Potempa, Jan, Hansson, Gunnar C., Dempsey, Peter J., and Becker-Pauly, Christoph
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- 2017
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18. A Novel Approach for Glioblastoma Treatment by Combining Apoptosis Inducers (TMZ, MTX, and Cytarabine) with E.V.A. (Eltanexor, Venetoclax, and A1210477) Inhibiting XPO1, Bcl-2, and Mcl-1.
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Zhao, Kai, Braun, Madita, Meyer, Leonie, Otte, Katharina, Raifer, Hartmann, Helmprobst, Frederik, Möschl, Vincent, Pagenstecher, Axel, Urban, Hans, Ronellenfitsch, Michael W., Steinbach, Joachim P., Pesek, Jelena, Watzer, Bernhard, Nockher, Wolfgang A., Taudte, R. Verena, Neubauer, Andreas, Nimsky, Christopher, Bartsch, Jörg W., and Rusch, Tillmann
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VENETOCLAX ,CYTARABINE ,GLIOBLASTOMA multiforme ,DRUG efficacy ,APOPTOSIS ,CELL cycle ,BCL genes - Abstract
Adjuvant treatment for Glioblastoma Grade 4 with Temozolomide (TMZ) inevitably fails due to therapeutic resistance, necessitating new approaches. Apoptosis induction in GB cells is inefficient, due to an excess of anti-apoptotic XPO1/Bcl-2-family proteins. We assessed TMZ, Methotrexate (MTX), and Cytarabine (Ara-C) (apoptosis inducers) combined with XPO1/Bcl-2/Mcl-1-inhibitors (apoptosis rescue) in GB cell lines and primary GB stem-like cells (GSCs). Using CellTiter-Glo
® and Caspase-3 activity assays, we generated dose–response curves and analyzed the gene and protein regulation of anti-apoptotic proteins via PCR and Western blots. Optimal drug combinations were examined for their impact on the cell cycle and apoptosis induction via FACS analysis, paralleled by the assessment of potential toxicity in healthy mouse brain slices. Ara-C and MTX proved to be 150- to 10,000-fold more potent in inducing apoptosis than TMZ. In response to inhibitors Eltanexor (XPO1; E), Venetoclax (Bcl-2; V), and A1210477 (Mcl-1; A), genes encoding for the corresponding proteins were upregulated in a compensatory manner. TMZ, MTX, and Ara-C combined with E, V, and A evidenced highly lethal effects when combined. As no significant cell death induction in mouse brain slices was observed, we conclude that this drug combination is effective in vitro and expected to have low side effects in vivo. [ABSTRACT FROM AUTHOR]- Published
- 2024
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19. Synthesis and biological evaluation of analogues of the potent ADAM8 inhibitor cyclo(RLsKDK) for the treatment of inflammatory diseases and cancer metastasis
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Yim, Victor, Noisier, Anaïs F.M., Hung, Kuo-yuan, Bartsch, Jörg W., Schlomann, Uwe, and Brimble, Margaret A.
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- 2016
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20. Shedding of Endogenous Interleukin-6 Receptor (IL-6R) Is Governed by A Disintegrin and Metalloproteinase (ADAM) Proteases while a Full-length IL-6R Isoform Localizes to Circulating Microvesicles
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Schumacher, Neele, Meyer, Dörte, Mauermann, Andre, von der Heyde, Jan, Wolf, Janina, Schwarz, Jeanette, Knittler, Katharina, Murphy, Gillian, Michalek, Matthias, Garbers, Christoph, Bartsch, Jörg W., Guo, Songbo, Schacher, Beate, Eickholz, Peter, Chalaris, Athena, Rose-John, Stefan, and Rabe, Björn
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- 2015
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21. A colorimetric-based amplification system for proteinases including MMP2 and ADAM8
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Moss, Marcia L., Koller, Garrit, Bartsch, Jörg W., Rakow, Sinja, Schlomann, Uwe, and Rasmussen, Fred H.
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- 2015
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22. An MMP-inhibitor modified adhesive primer enhances bond durability to carious dentin
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Almahdy, Ahmed, Koller, Garrit, Festy, Frederic, Bartsch, Jörg W., Watson, Timothy F., and Banerjee, Avijit
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- 2015
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23. Roles of ADAM8 in elimination of injured muscle fibers prior to skeletal muscle regeneration
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Nishimura, Daigo, Sakai, Hiroshi, Sato, Takahiko, Sato, Fuminori, Nishimura, Satoshi, Toyama-Sorimachi, Noriko, Bartsch, Jörg W., and Sehara-Fujisawa, Atsuko
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- 2015
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24. Identification of Dysregulated microRNAs in Glioblastoma Stem-like Cells
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Evers, Lara, primary, Schäfer, Agnes, additional, Pini, Raffaella, additional, Zhao, Kai, additional, Stei, Susanne, additional, Nimsky, Christopher, additional, and Bartsch, Jörg W., additional
- Published
- 2023
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25. Basal cell adhesion molecule promotes metastasis‐associated processes in ovarian cancer
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Sivakumar, Suresh, primary, Lieber, Sonja, additional, Librizzi, Damiano, additional, Keber, Corinna, additional, Sommerfeld, Leah, additional, Finkernagel, Florian, additional, Roth, Katrin, additional, Reinartz, Silke, additional, Bartsch, Jörg W., additional, Graumann, Johannes, additional, Müller‐Brüsselbach, Sabine, additional, and Müller, Rolf, additional
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- 2023
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26. Correlation of MR-Based Metabolomics and Molecular Profiling in the Tumor Microenvironment of Temozolomide-Treated Orthotopic GL261 Glioblastoma in Mice.
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Zhao, Kai, Calero-Pérez, Pilar, Bopp, Miriam H. A., Möschl, Vincent, Pagenstecher, Axel, Mulero-Acevedo, Marta, Vázquez, Mario, Barcia, Carlos, Arús, Carles, Nimsky, Christopher, Rusch, Tillmann, Bartsch, Jörg W., and Candiota, Ana Paula
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PROGRAMMED cell death 1 receptors ,METABOLOMICS ,TUMOR microenvironment ,CYTOTOXIC T cells ,MEMBRANE proteins ,MATRIX metalloproteinases ,GLIOBLASTOMA multiforme - Abstract
The tumor microenvironment in glioblastoma (GB) is considered to be "cold", i.e., the fraction of cytotoxic T cells, for instance, is low. Instead, macrophages are the major immune cell population in GB, which stem either from tissue response (resident microglia) or recruitment of macrophages from the periphery, thereby undergoing tumor-dependent "imprinting" mechanisms by which macrophages can adapt a tumor-supportive phenotype. In this regard, it is important to describe the nature of macrophages associated with GB, in particular under therapy conditions using the gold standard chemotherapy drug temozolomide (TMZ). Here, we explored the suitability of combining information from in vivo magnetic resonance spectroscopic (MRS) approaches (metabolomics) with in vitro molecular analyses to assess therapy response and characterize macrophage populations in mouse GB using an isogenic GL261 model. For macrophage profiling, expression levels of matrix metalloproteinases (MMPs) and A disintegrin and metalloproteinases (ADAMs) were determined, since their gene products affect macrophage–tumor cell communication by extensive cleavage of immunomodulatory membrane proteins, such as PD-L1. In tumor mice with an overall therapy response, expression of genes encoding the proteases ADAM8, ADAM10, and ADAM17 was increased and might contribute to the immunosuppressive phenotype of GB and immune cells. In tumors responding to therapy, expression levels of ADAM8 were upregulated by TMZ, and higher levels of PD-L1 were correlated significantly. Using a CRISPR/Cas9 knockout of ADAM8 in GL261 cells, we demonstrated that soluble PD-L1 (sPD-L1) is only generated in the presence of ADAM8. Moreover, primary macrophages from WT and ADAM8-deficient mice showed ADAM8-dependent release of sPD-L1, independent of the macrophage polarization state. Since ADAM8 expression is induced in responding tumors and PD-L1 shedding is likely to decrease the anti-tumor activities of T-cells, we conclude that immunotherapy resistance is caused, at least in part, by the increased presence of proteases, such as ADAM8. [ABSTRACT FROM AUTHOR]
- Published
- 2023
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27. MicroRNA let-7b inhibits keratinocyte differentiation by targeting IL-6 mediated ERK signaling in psoriasis
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Wu, Yan, Liu, Liu, Bian, Chunxiang, Diao, Qingchun, Nisar, Muhammad Farrukh, Jiang, Xuemei, Bartsch, Jörg W., Zhong, Maojiao, Hu, Xiangyu, and Zhong, Julia Li
- Published
- 2018
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28. Expression of the zinc importer protein ZIP9/SLC39A9 in glioblastoma cells affects phosphorylation states of p53 and GSK-3β and causes increased cell migration
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Münnich, Nico, Wernhart, Simon, Hogstrand, Christer, Schlomann, Uwe, Nimsky, Christopher, and Bartsch, Jörg W.
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- 2016
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29. ADAM8/MS2/CD156a : A metalloprotease-disintegrin involved in immune responses
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Bartsch, Jörg W., Naus, Silvia, Rittger, Andrea, Schlomann, Uwe, Wildeboer, Dirk, Hooper, Nigel M., editor, and Lendeckel, Uwe, editor
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- 2005
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30. The GBM Tumor Microenvironment as a Modulator of Therapy Response: ADAM8 Causes Tumor Infiltration of Tams through HB-EGF/EGFR-Mediated CCL2 Expression and Overcomes TMZ Chemosensitization in Glioblastoma
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Liu, Xiaojin, primary, Huang, Yimin, additional, Qi, Yiwei, additional, Wu, Shiqiang, additional, Hu, Feng, additional, Wang, Junwen, additional, Shu, Kai, additional, Zhang, Huaqiu, additional, Bartsch, Jörg W., additional, Nimsky, Christopher, additional, Dong, Fangyong, additional, and Lei, Ting, additional
- Published
- 2022
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31. ADAM8 expression in breast cancer derived brain metastases: Functional implications on MMP‐9 expression and transendothelial migration in breast cancer cells
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Conrad, Catharina, Götte, Malena, Schlomann, Uwe, Roessler, Marion, Pagenstecher, Axel, Anderson, Peter, Preston, Jane, Pruessmeyer, Jessica, Ludwig, Andreas, Li, Ran, Kamm, Roger D., Ritz, Rainer, Carl, Barbara, Nimsky, Christopher, and Bartsch, Jörg W.
- Published
- 2018
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32. Simultaneous Detection of Metalloprotease Activities in Complex Biological Samples Using the PrAMA (Proteolytic Activity Matrix Assay) Method
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Conrad, Catharina, primary, Miller, Miles A., additional, Bartsch, Jörg W., additional, Schlomann, Uwe, additional, and Lauffenburger, Douglas A., additional
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- 2017
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33. Eltanexor Effectively Reduces Viability of Glioblastoma and Glioblastoma Stem-Like Cells at Nano-Molar Concentrations and Sensitizes to Radiotherapy and Temozolomide
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Otte, Katharina, primary, Zhao, Kai, additional, Braun, Madita, additional, Neubauer, Andreas, additional, Raifer, Hartmann, additional, Helmprobst, Frederik, additional, Barrera, Felipe Ovalle, additional, Nimsky, Christopher, additional, Bartsch, Jörg W., additional, and Rusch, Tillmann, additional
- Published
- 2022
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34. ADAM9 Inhibition Increases Membrane Activity of ADAM10 and Controls α-Secretase Processing of Amyloid Precursor Protein
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Moss, Marcia L., Powell, Gary, Miller, Miles A., Edwards, Lori, Qi, Bin, Sang, Qing-Xiang Amy, De Strooper, Bart, Tesseur, Ina, Lichtenthaler, Stefan F., Taverna, Mara, Zhong, Julia Li, Dingwall, Colin, Ferdous, Taheera, Schlomann, Uwe, Zhou, Pei, Griffith, Linda G., Lauffenburger, Douglas A., Petrovich, Robert, and Bartsch, Jörg W.
- Published
- 2011
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35. The Metalloprotease-Disintegrin ADAM8 Alters the Tumor Suppressor miR-181a-5p Expression Profile in Glioblastoma Thereby Contributing to Its Aggressiveness
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Schäfer, Agnes, primary, Evers, Lara, additional, Meier, Lara, additional, Schlomann, Uwe, additional, Bopp, Miriam H. A., additional, Dreizner, Gian-Luca, additional, Lassmann, Olivia, additional, Ben Bacha, Aaron, additional, Benescu, Andreea-Cristina, additional, Pojskic, Mirza, additional, Preußer, Christian, additional, von Strandmann, Elke Pogge, additional, Carl, Barbara, additional, Nimsky, Christopher, additional, and Bartsch, Jörg W., additional
- Published
- 2022
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36. Radiogenomic Predictors of Recurrence in Glioblastoma—A Systematic Review
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Corr, Felix, primary, Grimm, Dustin, additional, Saß, Benjamin, additional, Pojskić, Mirza, additional, Bartsch, Jörg W., additional, Carl, Barbara, additional, Nimsky, Christopher, additional, and Bopp, Miriam H. A., additional
- Published
- 2022
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37. ADAM8-Dependent Extracellular Signaling in the Tumor Microenvironment Involves Regulated Release of Lipocalin 2 and MMP-9
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Cook, Lena, primary, Sengelmann, Marie, additional, Winkler, Birte, additional, Nagl, Constanze, additional, Koch, Sarah, additional, Schlomann, Uwe, additional, Slater, Emily P., additional, Miller, Miles A., additional, von Strandmann, Elke Pogge, additional, Dörsam, Bastian, additional, Preußer, Christian, additional, and Bartsch, Jörg W., additional
- Published
- 2022
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38. ADAM8 expression in invasive breast cancer promotes tumor dissemination and metastasis
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Romagnoli, Mathilde, Mineva, Nora D, Polmear, Michael, Conrad, Catharina, Srinivasan, Srimathi, Loussouarn, Delphine, Barillé‐Nion, Sophie, Georgakoudi, Irene, Dagg, Áine, McDermott, Enda W, Duffy, Michael J, McGowan, Patricia M., Schlomann, Uwe, Parsons, Maddy, Bartsch, Jörg W, and Sonenshein, Gail E
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- 2014
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39. Clinical Evaluation of Pathognomonic Salivary Protease Fingerprinting for Oral Disease Diagnosis
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Koller, Garrit, Schürholz, Eva, Ziebart, Thomas, Neff, Andreas, Frankenberger, Roland, and Bartsch, Jörg W.
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proteolysis ,FRET-peptides ,real-time protease activities ,Medicine ,extracellular matrix degradation ,Oral Biomarkers ,metalloproteases ,caries detection ,Article ,protease inhibition - Abstract
Dental decay (Caries) and periodontal disease are globally prevalent diseases with significant clinical need for improved diagnosis. As mediators of dental disease-specific extracellular matrix degradation, proteases are promising analytes. We hypothesized that dysregulation of active proteases can be functionally linked to oral disease status and may be used for diagnosis. To address this, we examined a total of 52 patients with varying oral disease states, including healthy controls. Whole mouth saliva samples and caries biopsies were collected and subjected to analysis. Overall proteolytic and substrate specific activities were assessed using five multiplexed, fluorogenic peptides. Peptide cleavage was further described by inhibitors targeting matrix metalloproteases (MMPs) and cysteine, serine, calpain proteases (CSC). Proteolytic fingerprints, supported by supervised machine-learning analysis, were delineated by total proteolytic activity (PepE) and substrate preference combined with inhibition profiles. Caries and peridontitis showed increased enzymatic activities of MMPs with common (PepA) and divergent substrate cleavage patterns (PepE), suggesting different MMP contribution in particular disease states. Overall, sensitivity and specificity values of 84.6% and 90.0%, respectively, were attained. Thus, a combined analysis of protease derived individual and arrayed substrate cleavage rates in conjunction with inhibitor profiles may represent a sensitive and specific tool for oral disease detection.
- Published
- 2021
40. Extracellular Vesicle-Based Detection of Pancreatic Cancer
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Verel-Yilmaz, Yesim, Fernández, Juan Pablo, Schäfer, Agnes, Nevermann, Sheila, Cook, Lena, Gercke, Norman, Helmprobst, Frederik, Jaworek, Christian, Pogge von Strandmann, Elke, Pagenstecher, Axel, Bartsch, Detlef K., Bartsch, Jörg W., and Slater, Emily P.
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Cell and Developmental Biology ,ADAM8 ,endocrine system diseases ,pancreatic cancer ,serum biomarkers ,Brief Research Report ,extracellular vesicles ,digestive system diseases ,miRNA - Abstract
Due to a grim prognosis, there is an urgent need to detect pancreatic ductal adenocarcinoma (PDAC) prior to metastasis. However, reliable diagnostic imaging methods or biomarkers for PDAC or its precursor lesions are still scarce. ADAM8, a metalloprotease-disintegrin, is highly expressed in PDAC tissue and negatively correlates with patient survival. The aim of our study was to determine the ability of ADAM8-positive extracellular vesicles (EVs) and cargo microRNAs (miRNAs) to discriminate precursor lesions or PDAC from healthy controls. In order to investigate enrichment of ADAM8 on EVs, these were isolated from serum of patients with PDAC (n = 52), precursor lesions (n = 7) and healthy individuals (n = 20). Nanoparticle Tracking Analysis and electron microscopy indicated successful preparation of EVs that were analyzed for ADAM8 by FACS. Additionally, EV cargo analyses of miRNAs from the same serum samples revealed the presence of miR-720 and miR-451 by qPCR and was validated in 20 additional PDAC samples. Statistical analyses included Wilcoxon rank test and ROC curves. FACS analysis detected significant enrichment of ADAM8 in EVs from patients with PDAC or precursor lesions compared to healthy individuals (p = 0.0005). ADAM8-dependent co-variates, miR-451 and miR-720 were also diagnostic, as patients with PDAC had significantly higher serum levels of miR-451 and lower serum levels of miR-720 than healthy controls and reached high sensitivity and specificity (AUC = 0.93 and 1.00, respectively) to discriminate PDAC from healthy control. Thus, detection of ADAM8-positive EVs and related cargo miR-720 and miR-451 may constitute a specific biomarker set for screening individuals at risk for PDAC.
- Published
- 2021
41. Inhibition of Carbonic Anhydrase 2 Overcomes Temozolomide Resistance in Glioblastoma Cells
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Zhao, Kai, primary, Schäfer, Agnes, additional, Zhang, Zhuo, additional, Elsässer, Katharina, additional, Culmsee, Carsten, additional, Zhong, Li, additional, Pagenstecher, Axel, additional, Nimsky, Christopher, additional, and Bartsch, Jörg W., additional
- Published
- 2021
- Full Text
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42. Discovery of Dimeric Arylsulfonamides as Potent ADAM8 Inhibitors
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Cuffaro, Doretta, primary, Camodeca, Caterina, additional, Tuccinardi, Tiziano, additional, Ciccone, Lidia, additional, Bartsch, Jörg W., additional, Kellermann, Tanja, additional, Cook, Lena, additional, Nuti, Elisa, additional, and Rossello, Armando, additional
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- 2021
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43. ADAM8 is a negative regulator of retinal neovascularization and of the growth of heterotopically injected tumor cells in mice
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Guaiquil, Victor H., Swendeman, Steven, Zhou, Wenhui, Guaiquil, Patricio, Weskamp, Gisela, Bartsch, Jörg W., and Blobel, Carl P.
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- 2010
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44. The Immune Microenvironment in Pancreatic Cancer
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Huber, Magdalena, Brehm, Corinna U., Gress, Thomas M., Buchholz, Malte, Alashkar Alhamwe, Bilal, Pogge von Strandmann, Elke, Slater, Emily P., Bartsch, Jörg W., Bauer, Christian, and Lauth, Matthias
- Subjects
natural killer cells ,T-cells ,pancreatic cancer ,tumor stroma ,Review ,Adenocarcinoma ,macrophages ,lcsh:Chemistry ,neutrophils ,lcsh:Biology (General) ,lcsh:QD1-999 ,Tumor Microenvironment ,Humans ,Immunotherapy ,cancer-associated fibroblasts ,lcsh:QH301-705.5 ,Carcinoma, Pancreatic Ductal - Abstract
The biology of solid tumors is strongly determined by the interactions of cancer cells with their surrounding microenvironment. In this regard, pancreatic cancer (pancreatic ductal adenocarcinoma, PDAC) represents a paradigmatic example for the multitude of possible tumor-stroma interactions. PDAC has proven particularly refractory to novel immunotherapies, which is a fact that is mediated by a unique assemblage of various immune cells creating a strongly immunosuppressive environment in which this cancer type thrives. In this review, we outline currently available knowledge on the cross-talk between tumor cells and the cellular immune microenvironment, highlighting the physiological and pathological cellular interactions, as well as the resulting therapeutic approaches derived thereof. Hopefully a better understanding of the complex tumor-stroma interactions will one day lead to a significant advancement in patient care.
- Published
- 2020
45. The ADAM10 Prodomain Is a Specific Inhibitor of ADAM10 Proteolytic Activity and Inhibits Cellular Shedding Events
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Moss, Marcia L., Bomar, Martha, Liu, Qian, Sage, Harvey, Dempsey, Peter, Lenhart, Patricia M., Gillispie, Patricia A., Stoeck, Alexander, Wildeboer, Dirk, Bartsch, Jörg W., Palmisano, Ralf, and Zhou, Pei
- Published
- 2007
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46. SH3P7/mAbp1 deficiency leads to tissue and behavioral abnormalities and impaired vesicle transport
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Connert, Sabine, Wienand, Simone, Thiel, Cora, Krikunova, Maria, Glyvuk, Nataliya, Tsytsyura, Yaroslav, Hilfiker‐Kleiner, Denise, Bartsch, Jörg W, Klingauf, Jürgen, and Wienands, Jürgen
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- 2006
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47. Formalin Fixation as Tissue Preprocessing for Multimodal Optical Spectroscopy Using the Example of Human Brain Tumour Cross Sections
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Stefanakis, Mona, primary, Lorenz, Anita, additional, Bartsch, Jörg W., additional, Bassler, Miriam C., additional, Wagner, Alexandra, additional, Brecht, Marc, additional, Pagenstecher, Axel, additional, Schittenhelm, Jens, additional, Boldrini, Barbara, additional, Hakelberg, Sabrina, additional, Noell, Susan, additional, Nimsky, Christopher, additional, Tatagiba, Marcos, additional, Ritz, Rainer, additional, Rebner, Karsten, additional, and Ostertag, Edwin, additional
- Published
- 2021
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48. ADAM8/MS2/CD156a
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Bartsch, Jörg W., primary and Schlomann, Uwe, additional
- Published
- 2013
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49. Contributors
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Abbott, Catherine Anne, primary, Abraham, Carmela R., additional, Adachi, Hideki, additional, Adachi, Osao, additional, Adam, Zach, additional, Adams, Michael W.W., additional, Adang, Michael J., additional, Adham, Ibrahim M., additional, Aducci, Patrizia, additional, Agard, David A., additional, Agranovsky, Alexey A., additional, Akamatsu, Tetsuya, additional, Akiyama, Yoshinori, additional, Albrechtsen, Reidar, additional, Alejo, Alí, additional, Amberg, Sean M., additional, Amerik, Alexander Y., additional, Amparyup, Piti, additional, Andrade, Felipe, additional, Andrés, Germán, additional, Andrews, Daniel M., additional, Andrews, Robert K., additional, Antalis, Toni M., additional, Anthony, Colin S., additional, Aoki, Naoya, additional, Apte, Suneel S., additional, Arima, Kazunari, additional, Arlaud, Gérard, additional, Arni, Raghuvir Krishnaswamy, additional, Arnoux, Pascal, additional, Aronson, Nathan N., additional, Arthur, Michel, additional, Asano, Yasuhisa, additional, Ascenzi, Paolo, additional, Assakura, Marina T., additional, Auld, David S., additional, Ávila, Veridiana de Melo Rodrigues, additional, Avilés, Francesc X., additional, Awad, William M., additional, Bachhawat, Anand K., additional, Bai, Shan, additional, Baird, Teaster T., additional, Bajaj, S. Paul, additional, Baker, Susan C., additional, Banbula, Agnieszka, additional, Barrett, Alan J., additional, Barrowman, Jemima, additional, Bartlett, John D., additional, Bartsch, Jörg W., additional, Baschuk, Nikola, additional, Baskova, Isolda P., additional, Batra, Jyotsna, additional, Bauer, Karl, additional, Baumann, Ulrich, additional, Baumeister, Wolfgang, additional, Bauvois, Cédric, additional, Bayés, Alex, additional, Beauvais, Anne, additional, Becker-Pauly, Christoph, additional, Begley, Tadhg P., additional, Békés, Miklós, additional, Belas, Robert, additional, Beleford, Daniah, additional, Beppu, Teruhiko, additional, Bergmann, Ernst M., additional, Bernard, Bruno A., additional, Bernard, Dominique, additional, Berndt, Michael C., additional, Berruti, Giovanna, additional, Berry, Colin, additional, Bertenshaw, Greg P., additional, Betzel, Christian, additional, Bhaskarla, Chetana, additional, Bhosale, Manoj, additional, Bierbaum, Gabriele, additional, Bjarnason Jón, B., additional, Blaber, Michael, additional, Blackman, Michael J., additional, Blinkovsky, Alexander, additional, Boeke, Jef D., additional, Bogyo, Matthew, additional, Bohn, Stefan, additional, Boileau, Guy, additional, Boland, Mike, additional, Bolken, Tové C., additional, Bond, Judith S., additional, Bondeson, Jan, additional, Bordallo, Javier, additional, Borelli, Claudia, additional, Botelho, Tiago O., additional, Bott, Richard R., additional, Bourne, David G., additional, Bovenschen, Niels, additional, Bradshaw, Ralph A., additional, Breddam, Klaus, additional, Brew, Keith, additional, Brindley, Paul J., additional, Brinkman, Diane L., additional, Britton, Collette, additional, Broadbent, Jeff R., additional, Broadhurst, Anne, additional, Brómme, Dieter, additional, Broom, Murray, additional, Brown, Jeremy S., additional, Brown, Mark A., additional, Bruchhaus, Iris, additional, Burleigh, Barbara A., additional, Burns, Kristin E., additional, Burrows, James F., additional, Butler, Michael J., additional, Buttle, David J., additional, Byrd, Chelsea M., additional, Byun, Tony, additional, Cadel, Sandrine, additional, Caffrey, Conor R., additional, Cal, Santiago, additional, Caldentey, Javier, additional, Candela, Thomas, additional, Capasso, Clemente, additional, Capriogilio, Daniel R., additional, Carginale, Vincenzo, additional, Carmona, Adriana Karaoglanovic, additional, Carruthers, Vern B., additional, Castellino, Francis J., additional, Catanese, Joseph J., additional, Caterson, Bruce, additional, Caughey, George H., additional, Cawley, Naimh X., additional, Cawston, Tim E., additional, Cazzulo, Juan José, additional, Chai, Jijie, additional, Chai, Karl X., additional, Chaim, Olga Meiri, additional, Chang, L.S., additional, Chao, Julie, additional, Chapot-Chartier, Marie-Pierre, additional, Charli, Jean-Louis, additional, Charlier, Paulette, additional, Chave, Karen J., additional, Chen, Jian-Min, additional, Chen, Jinq-May, additional, Chen, Li-Mei, additional, Chen, Ya-Wen, additional, Chen, Yu-Yen, additional, Chevrier, Bernard, additional, Chich, Jean-François, additional, Chien, Jeremy, additional, Chimalapati, Suneeta, additional, Cho, Ki Joon, additional, Choi, Kwan Yong, additional, Chuang, Woei-Jer, additional, Chung, Chin Ha, additional, Chung, Ivy Yeuk Wah, additional, Clamagirand, Christine, additional, Clark, Ian M., additional, Clarke, Adrian K., additional, Clarke, Nicola E., additional, Clarke, Steven Gerard, additional, Clauziat, Philippe, additional, Clements, Judith A., additional, Coffinier, Catherine, additional, Cohen, Paul, additional, Colige, Alain, additional, Collignon, Anne, additional, Colloms, Sean D., additional, Conzelmann, Andreas, additional, Coombs, Graham H., additional, Cooney, Jakki C., additional, Cooper, Jonathan B., additional, Cooper, Max D., additional, Copeland, Nikki A., additional, Cottrell, Graeme S., additional, Coyle, Joseph T., additional, Craik, Charles S., additional, Creemers, John W.M., additional, Cretu, Daniela, additional, Croce, Jenifer, additional, Cross, Keith J., additional, Cueva, Rosario, additional, Cui, Sheng, additional, Cunha, Luis, additional, Cutting, Simon, additional, d’Enfert, Christophe, additional, D’Orchymont, Hugues, additional, Dahlbäck, Björn, additional, Dai, Shujia, additional, Dalbey, Ross E., additional, Dalton, John P., additional, Dando, Pam M., additional, Daniel, R.M., additional, Danilov, Sergei M., additional, Davies, Donna E., additional, De Araujo, Heloisa S., additional, De los Santos, Teresa, additional, de Luca, Viviana, additional, De Meester, Ingrid, additional, de Oliveira, Ana Karina, additional, de Oliveira, Eduardo Brandt, additional, De Oliveira, Pedro Lagerblad, additional, de Vos, Sarah, additional, Declercq, Jeroen, additional, Declercq, Wim, additional, Deghmane, Ala-Eddine, additional, Dekker, Niek, additional, Del Prete, Sonia, additional, Del Rosal, Marina, additional, Delmas, Bernard, additional, DeLotto, Robert, additional, Demidyuk, Ilya V., additional, Denison, Mark R., additional, Deussing, Jan M., additional, Devi, Lakshmi A., additional, Diamandis, Eleftherios P., additional, Diaz, Isabel, additional, Díaz-Perales, Araceli, additional, Dijkstra, Bauke W., additional, Ding, Yan, additional, Dixon, Jack E., additional, Dodt, Johannes, additional, Dokland, Terje, additional, Dolenc, Iztok, additional, Dong, Ningzheng, additional, Dong, Tran Cat, additional, Dong, Ying, additional, Dongre, Mitesh, additional, Donovan, Mark, additional, Dore, Timothy M., additional, Dorstyn, Loretta, additional, Dou, Hong, additional, Dou, Zhicheng, additional, Dougall, Annette M., additional, Drag, Marcin, additional, Dudley, Edward G., additional, Dunn, Ben M., additional, Dupuy, Bruno, additional, Duque-Magalhāes, Maria Conceicāo, additional, Durá, M. Asunción, additional, Eeckhout, Yves, additional, Eijsink, Vincent, additional, Eisen, Arthur Z., additional, Eissa, Azza, additional, Eklund, Sandra, additional, Eletr, Ziad M., additional, Ellis, Vincent, additional, Engel, Wolfgang, additional, Erdös, Ervin G., additional, Escalante, Teresa, additional, Estell, David A., additional, Etscheid, Michael, additional, Evans, Herbert J., additional, Everett, Roger D., additional, Faesen, Alex C., additional, Fahrenholz, Falk, additional, Fanjul-Fernández, Miriam, additional, Farady, Christopher J., additional, Feller, Georges, additional, Feng, Hong, additional, Fenster, Kurt M., additional, Férec, Claude, additional, Ferrari, Silvia, additional, Fingleton, Barbara, additional, Fisher, Jed F., additional, Fives-Taylor, Paula M., additional, Fong, Loren G., additional, Forneris, F., additional, Forster, Brian M., additional, Forster, Friedrich, additional, Foster, Simon J., additional, Foulon, Thierry, additional, Foundling, Stephen I., additional, Fox, Jay William, additional, Franzetti, Bruno, additional, Frasch, Alejandra P., additional, Freeze, Hudson H., additional, Frère, Jean-Marie, additional, Frey, Teryl K., additional, Fricke, Beate, additional, Fricker, Lloyd D., additional, Fridman, Rafael, additional, Froelich, Christopher J., additional, Fröhlich, Camilla, additional, Fu, Hsueh-Liang, additional, Fuhrmann, Cynthia N., additional, Fujimura, Satoshi, additional, Fujiwara, Hiroshi, additional, Fukushima, Jun, additional, Fukuyama, Keiichi, additional, Fuller, Robert S., additional, Fusek, Martin, additional, Gaboriaud, Christine, additional, Gache, Christian, additional, Gakh, Oleksandr, additional, Gal, Peter, additional, Gao, Junjun, additional, García-Sastre, Adolfo, additional, Gardiner, Donald L., additional, Gatehouse, John A., additional, Gaucher, G.M., additional, Gauthier, Francis, additional, Ghuysen, Jean-Marie, additional, Gibson, Wade, additional, Gillies, Jennifer, additional, Glaser, Elzbieta, additional, Glaser, Fabian, additional, Glickman, Michael H., additional, Goettig, Peter, additional, Goffin, Colette, additional, Gohda, Eiichi, additional, Goldberg, Alfred L., additional, Goldberg, Daniel E., additional, Goldberg, Gregory I., additional, Goldfarb, Nathan E., additional, Gomis-Rüth, F. Xavier, additional, Gopal, B., additional, Gorbalenya, Alexander E., additional, Gordon, Stuart G., additional, Gorrell, Mark D., additional, Götz, Friedrich, additional, Goulas, Theodoros, additional, Gouzy-Darmon, Cécile, additional, Govind, K., additional, Gráf, Lászlo, additional, Granados, Robert R., additional, Gräwert, Melissa Ann, additional, Gray, Douglas A., additional, Graycar, Thomas P., additional, Green, Jonathan A., additional, Gremski, Luiza Helena, additional, Groll, Michael, additional, Gromova, Tania Yu, additional, Gros, P., additional, Grubman, Marvin J., additional, Grunden, Amy M., additional, Gudmundsdóttir, Ágústa, additional, Guinand, Micheline, additional, Gully, Djamel, additional, Gustchina, Alla, additional, Gutiérrez, José María, additional, Ha, Byung Hak, additional, Haeggström, Jesper Z., additional, Hageman, James H., additional, Haiko, Johanna, additional, Hailfinger, Stephan, additional, Haitchi, Hans Michael, additional, Han, Ji Seon, additional, Hanquez, Chantal, additional, Harada, Minoru, additional, Hara-Nishimura, Ikuko, additional, Harboe, Marianne, additional, Härd, Torleif, additional, Harris, David A., additional, Hassiepen, Ulrich, additional, Hata, Shoji, additional, Hattori, Akira, additional, He, Rong-Qiao, additional, Heck, Albert J.R., additional, Hendricks, Dirk F., additional, Henrich, Bernhard, additional, Henriet, Patrick, additional, Hernández-Arana, Andrés, additional, Herrera-Camacho, Irma, additional, Heussipp, Gerhard, additional, Hibino, Toshihiko, additional, Hicks, P.M., additional, Hillman, Bradley I., additional, Hiraoka, B. Yukihiro, additional, Hiratake, Jun, additional, Hizukuri, Yohei, additional, Ho, Heng-Chien, additional, Hoa, Ngo Thi, additional, Hochstrasser, Mark, additional, Hodge, Kathryn M., additional, Hofmann, Theo, additional, Hohn, Thomas, additional, Hoidal, John R., additional, Höltje, Joachim-Volker, additional, Homma, Koichi J., additional, Honek, John F., additional, Hook, Vivian Y.H., additional, Hooper, John D., additional, Hooper, Nigel M., additional, Hosoi, Kazuo, additional, Howe, Christopher J., additional, Hruby, Dennis E., additional, Hseih, James J.-D., additional, Hsu, Chun-Chieh, additional, Huang, Tony T., additional, Huang, Tur-Fu, additional, Huet, Yoann, additional, Hughes, Clare, additional, Hugonnet, Jean-Emmanuel, additional, Huston, Adrienne L., additional, Ibrahim-Granet, Oumaïma, additional, Ichishima, Eiji, additional, Ikehara, Yukio, additional, Inagami, Tadashi, additional, Ingram, Jessica, additional, Isaac, R.E., additional, Isaya, Grazia, additional, Isaza, Clara E., additional, Ishii, Shin-ichi, additional, Isnard, Amandine, additional, Ito, Kiyoshi, additional, Ito, Koreaki, additional, Itoh, Yoshifumi, additional, Iturrioz, Xavier, additional, Iwanaga, Sadaaki, additional, Jack, Ralph W., additional, Jackson, Mel C., additional, James, Michael N.G., additional, Janata, Jiří, additional, Janoir, Claire, additional, Janska, Hanna, additional, Jarrell, Ken F., additional, Jaskolski, Mariusz, additional, Jaswal, Sheila S., additional, Jean, Ying Y., additional, Jenne, Dieter E., additional, Jeon, Young Joo, additional, Jiang, Ping, additional, Johnson, John E., additional, Johnson, Michael D., additional, Johnston, James A., additional, Jones, Amanda, additional, Jones, Elizabeth W., additional, Joudiou, Carine, additional, Juliano, Luiz, additional, Jung, Hea-Jin, additional, Jupp, Ray, additional, Kagawa, Todd F., additional, Kalbacher, Hubert, additional, Kamata, Yayoi, additional, Kaminogawa, Shuichi, additional, Kamio, Yoshiyuki, additional, Kaneda, Makoto, additional, Kang, Sung Gyun, additional, Kang, Sung Hwan, additional, Kania, Mary, additional, Kantyka, Tomasz, additional, Kanzawa, Nobuyuki, additional, Karim, Abdulkarim Y., additional, Kasumi, Takafumi, additional, Kataoka, Hiroaki, additional, Kaur, Hardeep, additional, Kawabata, Shun-Ichiro, additional, Kawaguchi, Mari, additional, Kay, John, additional, Kaynar, Murat, additional, Keiler, Kenneth C., additional, Kelly, R.M., additional, Kenton, Nathaniel T., additional, Kerr, Michael A., additional, Kersse, Kristof, additional, Kervinen, Jukka, additional, Kessler, Benedikt M., additional, Kessler, Efrat, additional, Khoronen, Timo K., additional, Kidd, Simon, additional, Kikkert, Marjolein, additional, Kilian, Mogens, additional, Kim, Do-Hyung, additional, Kim, Doyoun, additional, Kim, Eunice EunKyeong, additional, Kim, In Seop, additional, Kim, Jung-Gun, additional, Kim, Kyeong Kyu, additional, Kim, Kyung Hyun, additional, Kimber, Matthew S., additional, Kimura, Yukio, additional, Kirschke, Heidrun, additional, Kiso, Yoshiaki, additional, Kleanthous, Colin, additional, Klein, Jürgen R., additional, Klemba, Michael, additional, Kmiec, Beata, additional, Kobayashi, Hideyuki, additional, Kodama, Hiroyuki, additional, Koelsch, Gerald, additional, Kok, Jan, additional, Kolattukody, P.E., additional, Kolb, Fabrice A., additional, Kolmar, Harald, additional, Komori, Yumiko, additional, Konvalinka, Jan, additional, Korkmaz, Brice, additional, Kostrov, Sergey V., additional, Kräusslich, Hans-Georg, additional, Krczal, Gabi, additional, Kress, Lawrence F., additional, Kristjánsson, Magnüs Már, additional, Kučera, Tomáš, additional, Kukday, Sayali S., additional, Kumagai, Hidehiko, additional, Kumar, Sharad, additional, Kumarasiri, Malika, additional, Kumazaki, Takashi, additional, Kümmerer, Beate M., additional, Kuno, Kouji, additional, Kurkinen, Markku, additional, Kutejová, Eva, additional, Kveiborg, Marie, additional, Kwarciak, Agnieszka, additional, Laakkonen, Liisa, additional, Labrou, Nikolaos E., additional, Laing, Gavin D., additional, Lamppa, Gayle, additional, Langer, Thomas, additional, Laursen, Richard A., additional, Lawrenson, Richard A., additional, Layne, Matthew D., additional, Le Bonniec, Bernard F., additional, Leal, María C., additional, Lechan, Ronald M., additional, Lee, David H., additional, Lee, Irene, additional, Lee, Jae, additional, Lee, Kye Joon, additional, Lee, Soohee, additional, Lei, Xiaobo, additional, Leis, Jonathan, additional, LeMosy, Ellen K., additional, Lepage, Thierry, additional, Leppla, Stephen H., additional, Lesner, Adam, additional, Lessard, Ivan A.D., additional, Lhomond, Guy, additional, Li, Huilin, additional, Li, Shu-Ming, additional, Li, Weiguo, additional, Liao, Ta-Hsiu, additional, Liddington, Robert C., additional, Lieber, Toby, additional, Lijnen, H.R., additional, Lima, Christopher D., additional, Lin, Chen-Yong, additional, Lin, Gang, additional, Lin, Ming T., additional, Lin, Xinli, additional, Lin, Yee-Shin, additional, Lindsay, L.L., additional, Lipscomb, William N., additional, Little, John W., additional, Liu, Ching-Chuan, additional, Liu, Chuan-ju, additional, Lively, Mark O., additional, Livnat-Levanon, Nurit, additional, Ljungdahl, Per O., additional, Llorens-Cortes, Catherine, additional, Lobel, Peter, additional, Loh, Y. Peng, additional, Lohi, Jouko, additional, Lomonossoff, G.P., additional, Looze, Yvan, additional, López-Otin, Carlos, additional, Lopez-Quezada, Landys, additional, Loukas, Alex, additional, Lu, Long-Sheng, additional, Lundwall, Áke, additional, Luo, Liu-Ying, additional, Lupas, Andrei, additional, Luthe, Dawn S., additional, Lynch, Nicholas J., additional, Lyons, Peter J., additional, MacKay, Vivian L., additional, Macleod, Jesica M. Levingston, additional, Magdolen, Viktor, additional, Mainardi, Jean-Luc, additional, Mäkinen, Kauko K., additional, Mallari, Jeremy P., additional, Manandhar, Surya P., additional, Mandelbaum, Fajga R., additional, Manicone, Anne M., additional, Mansfeld, Johanna, additional, Marcotrigiano, Joseph, additional, Mares, Michael, additional, Marfany, Gemma, additional, Markland, Francis S., additional, Marokházi, Judith, additional, Marquis, Hélène, additional, Marr, Robert A., additional, Martegani, Enzo, additional, Martin, Erik W., additional, Martinez, Manuel, additional, Martins, L. Miguel, additional, Maruyama, Masato, additional, Maruyama, Masugi, additional, Maruyama, Sususmu, additional, Masaki, Takeharu, additional, Massoumi, Ramin, additional, Mathew, Rency T., additional, Matrisian, Lynn M., additional, Matsuda, Yoshihiro, additional, Matsushita, Osamu, additional, Matuschek, Marco, additional, Matušková, Anna, additional, Matúz, Krisztina, additional, Mauch, Cornelia, additional, Maurizi, Michael R., additional, Mayr, Lorenz M., additional, McCafferty, Dewey G., additional, McDonald, J. Ken, additional, McKerrow, James H., additional, McMillan, David, additional, Mecham, Robert P., additional, Mehta, Darshini P., additional, Meisinger, Chris, additional, Mellors, Alan, additional, Melton, Roger G., additional, Melvin, Jeffrey A., additional, Ménard, Robert, additional, Menéndez-Arias, Luis, additional, Menezes, Milene C., additional, Mesecar, Andrew, additional, Mesnage, Stéphane, additional, Meyer, Diane H., additional, Meyers, Gregor, additional, Michaelis, Susan, additional, Michalska, Karolina, additional, Mielicki, Wojciech P., additional, Mierau, Igor, additional, Mikoulinskaia, Galina V., additional, Miller, Charles G., additional, Miller, Lydia K., additional, Mills, John, additional, Mills, Kenneth V., additional, Min, Jinrong, additional, Mistou, Michel-Yves, additional, Misumi, Yoshio, additional, Miyoshi, Shin-ichi, additional, Mizutani, Shigehiko, additional, Mobashery, Shahriar, additional, Mochizuki, Satsuki, additional, Mock, William L., additional, Möhrlen, Frank, additional, Moiré, Nathalie, additional, Monahan, Paul E., additional, Moncada-Pazos, Angela, additional, Monnet, Véronique, additional, Monod, Michel, additional, Montecucco, Cesare, additional, Morelli, Laura, additional, Mori, Sumiko, additional, Morita, Takashi, additional, Morrissey, James H., additional, Morse, Richard J., additional, Mort, John S., additional, Mortensen, Uffe H., additional, Morty, Rory E., additional, Moss, Joel, additional, Motoshima, Hidemasa, additional, Mottram, Jeremy C., additional, Moura-da-Silva, Ana M., additional, Mudgett, Mary Beth, additional, Mundt, Egbert, additional, Murakami, Kazuo, additional, Murakami, Mario Tyago, additional, MurakamiMurofoshi, Kimiko, additional, Murao, Sawao, additional, Murphy, Gillian, additional, Murthy, M.R.N., additional, Muta, Tatsushi, additional, Myburgh, Elmarie, additional, Mzhavia, Nino, additional, Nabi, A.H.M. 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- 2013
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50. ADAM8 in Asthma. Friend or Foe to Airway Inflammation?
- Author
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Chen, Jun, Jiang, Xuemei, Duan, Yiyuan, Long, Jiaoyue, Bartsch, Jörg W., and Deng, Linhong
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- 2013
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