8 results on '"Paull, Daniel"'
Search Results
2. List of Contributors
- Author
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Alicea, Bradly, primary, Amano, Tomokazu, additional, Ambroggio, Jennifer, additional, Amarnath, Dasari, additional, Campbell, Keith H.S., additional, Surani, M. Azim, additional, Baeumer, Nicole, additional, Balbach, Sebastian T., additional, Bertolini, Marcelo, additional, Beyhan, Zeki, additional, Boiani, Michele, additional, Byrne, James A., additional, Callesen, Henrik, additional, Canovas, Sebastian, additional, Chavatte-Palmer, Pascale, additional, Chen, LiHow, additional, Choi, Inchul, additional, Cibelli, José B., additional, Colleoni, Silvia, additional, Crosetto, Nicola, additional, Dinnyes, Andras, additional, Drexler, Hannes C.A., additional, Duchi, Roberto, additional, Echelard, Yann, additional, Egli, Dieter, additional, Faber, David, additional, Fan, Jason, additional, First, Neal L., additional, Fissore, Rafael A., additional, Fuellen, Georg, additional, Fulka, Josef, additional, Galli, Cesare, additional, Gardner, David K., additional, Gavin, William, additional, Green, Ronald M., additional, Gurdon, J.B., additional, Hirano, Kunio, additional, Hoshino, Yoichiro, additional, Howard, Harlan, additional, Inoue, Kimiko, additional, Ishino, Fumitoshi, additional, Ito, Junya, additional, Jammes, Hélène, additional, Jones, Jeff, additional, Jones, Kathleen M., additional, Kent-First, Marijo, additional, Kato, Yoko, additional, Kishigami, Satoshi, additional, Ko, Minoru S.H., additional, Kohda, Takashi, additional, Lagutina, Irina, additional, Lane, Michelle, additional, Latham, Keith E., additional, Lazzari, Giovanna, additional, Lee, Byeong Chun, additional, Lee, Jiyoung, additional, Lee, Kiho, additional, Lee, Rita, additional, Loi, Pasqualino, additional, Malcuit, Christopher M., additional, Masiello, Nick, additional, Meade, Harry, additional, Meng, Qinggang, additional, Mitalipov, Shoukhrat, additional, Mizutani, Eiji, additional, Modlinski, Jacek, additional, Nguyen, Van Thuan, additional, Niemann, Heiner, additional, Ogura, Atsuo, additional, Page, Raymond L., additional, Paudel, Yogesh, additional, Paull, Daniel, additional, Pfeiffer, Martin J., additional, Piedrahita, Jorge A., additional, Pinmee, Boonya, additional, Polgar, Zsuzsanna, additional, Pommer, Jerry, additional, Prather, Randall S., additional, Pruett-Miller, Shondra M., additional, Ptak, Grazyna, additional, Rudenko, Larisa, additional, Saeki, Kazuhiro, additional, Schatten, Gerald, additional, Schmidt, Mette, additional, Schofield, Michael, additional, Seidel, George E., additional, Siatkowski, Marcin, additional, Simerly, Calvin, additional, Siripattarapravat, Kannika, additional, St. John, Justin C., additional, Stice, Steven L., additional, Sullivan, Eddie J., additional, Tachibana, Masahito, additional, Tada, Takashi, additional, Tancos, Zsuzsanna, additional, Taniguchi, Shunji, additional, Teperek-Tkacz, Marta, additional, Tian, Xiuchun (Cindy), additional, Trounson, Alan, additional, Tso Sun, Liang, additional, Tsunoda, Yukio, additional, Wakai, Takuya, additional, Wakamatsu, Yuko, additional, Wakayama, Sayaka, additional, Wakayama, Teruhiko, additional, Wang, Zhongde, additional, Zhang, Xia, additional, and Zhu, Jie, additional
- Published
- 2014
- Full Text
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3. Derivation and characterization of the NIH registry human stem cell line NYSCF101 under defined feeder-free conditions.
- Author
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Sevilla A, Forero E, Zimmer M, Martinez H, Reggio K, Paull D, Egli D, and Noggle S
- Subjects
- Cell Line, Female, Humans, United States, Antigens, Differentiation biosynthesis, Human Embryonic Stem Cells cytology, Human Embryonic Stem Cells metabolism, National Institutes of Health (U.S.), Registries
- Abstract
The human embryonic stem cell line NYSCFe002-A was derived from a day 6 blastocyst in feeder-free and antibiotic free conditions. The blastocyst was voluntarily donated for research as surplus after in vitro fertilization treatment following informed consent. The NYSCFe002-A line expresses all the pluripotency markers and has the potential to differentiate into all three germ layers in vitro. The line presents normal karyotype and is mycoplasma free. This line is registered as NYSCF101 on the NIH Registry., (Copyright © 2018 The Authors. Published by Elsevier B.V. All rights reserved.)
- Published
- 2018
- Full Text
- View/download PDF
4. Derivation and characterization of the NIH registry human stem cell line NYSCF100 line under defined feeder-free conditions.
- Author
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Sevilla A, Forero E, Zimmer M, Martinez H, Reggio K, Paull D, Egli D, and Noggle S
- Subjects
- Cell Line, Humans, National Institutes of Health (U.S.), Registries, United States, Human Embryonic Stem Cells metabolism
- Abstract
The human embryonic stem cell line NYSCFe001-A was derived from a day 6 blastocyst in feeder-free and antibiotic free conditions. The blastocyst was voluntarily donated for research as surplus after in vitro fertilization treatment following informed consent. The NYSCFe001-A line, registered as NYSCF100 on the NIH registry, presents normal karyotype, is mycoplasma free, expresses all the pluripotency markers and has the potential to differentiate into all three germ layers in vitro., (Copyright © 2018 The Authors. Published by Elsevier B.V. All rights reserved.)
- Published
- 2018
- Full Text
- View/download PDF
5. Derivation and characterization of the NYSCFe003-A human embryonic stem cell line.
- Author
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Sevilla A, Forero E, Zimmer M, Martinez H, Reggio K, Paull D, Egli D, and Noggle S
- Subjects
- Blastocyst cytology, Cell Line, Cells, Cultured, Genotype, Human Embryonic Stem Cells metabolism, Humans, Karyotype, Male, Microscopy, Fluorescence, Human Embryonic Stem Cells cytology
- Abstract
The human embryonic stem cell line NYSCFe003-A was derived from a day 5 to day 6 blastocyst in feeder-free and antibiotic free conditions. The blastocyst was voluntarily donated for research as surplus after in vitro fertilization treatment following informed consent. The NYSCFe003-A line expresses all the pluripotency markers and has the potential to differentiate into all three germ layers in vitro. The line presents normal karyotype and is mycoplasma free., (Copyright © 2017 The Authors. Published by Elsevier B.V. All rights reserved.)
- Published
- 2017
- Full Text
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6. Induced pluripotent stem cells (iPSC) created from skin fibroblasts of patients with Prader-Willi syndrome (PWS) retain the molecular signature of PWS.
- Author
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Burnett LC, LeDuc CA, Sulsona CR, Paull D, Eddiry S, Levy B, Salles JP, Tauber M, Driscoll DJ, Egli D, and Leibel RL
- Subjects
- Animals, Cell Differentiation, Cell Line, Cellular Reprogramming, Comparative Genomic Hybridization, DNA Methylation, Fibroblasts cytology, Gene Dosage, Genotype, Humans, Induced Pluripotent Stem Cells metabolism, Induced Pluripotent Stem Cells transplantation, Mice, Mice, Inbred NOD, Neurons cytology, Neurons metabolism, Prader-Willi Syndrome genetics, Skin cytology, Teratoma pathology, Transcription Factors genetics, Transcription Factors metabolism, Tumor Suppressor Proteins genetics, snRNP Core Proteins genetics, Induced Pluripotent Stem Cells cytology, Prader-Willi Syndrome pathology
- Abstract
Prader-Willi syndrome (PWS) is a syndromic obesity caused by loss of paternal gene expression in an imprinted interval on 15q11.2-q13. Induced pluripotent stem cells were generated from skin cells of three large deletion PWS patients and one unique microdeletion PWS patient. We found that genes within the PWS region, including SNRPN and NDN, showed persistence of DNA methylation after iPSC reprogramming and differentiation to neurons. Genes within the PWS minimum critical deletion region remain silenced in both PWS large deletion and microdeletion iPSC following reprogramming. PWS iPSC and their relevant differentiated cell types could provide in vitro models of PWS., (Copyright © 2016 Michael Boutros, German Cancer Research Center, Heidelberg, Germany. Published by Elsevier B.V. All rights reserved.)
- Published
- 2016
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7. Differentiation of serum-free embryoid bodies from human induced pluripotent stem cells into networks.
- Author
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Nestor MW, Paull D, Jacob S, Sproul AA, Alsaffar A, Campos BA, and Noggle SA
- Subjects
- Adult, Calcium metabolism, Cell Culture Techniques, Cell Differentiation, Cells, Cultured, Electric Stimulation, Electrodes, Humans, Induced Pluripotent Stem Cells physiology, Male, Embryoid Bodies cytology, Induced Pluripotent Stem Cells cytology
- Abstract
Three-dimensional aggregation cultures allow for complex development of differentiated human induced pluripotent stem cells. However, this approach is not easily amenable to live-cell imaging and electrophysiological applications due to the thickness and the geometry of the tissue. Here, we present an improvement on the traditional aggregation method by combining the use of cell culture inserts with serum-free embryoid bodies (SFEBs). The use of this technique allows the structures to maintain their three-dimensional structure while thinning substantially. We demonstrate that this technique can be used for electrophysiological recodings as well as live-cell calcium imaging combined with electrical stimulation, akin to organotypic slice preparations. This provides an important experimental tool that can be used to bridge 3-D structures with traditional monolayer approaches used in stem cell applications., (Copyright © 2013 Elsevier B.V. All rights reserved.)
- Published
- 2013
- Full Text
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8. Altered vision near the hands.
- Author
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Abrams RA, Davoli CC, Du F, Knapp WH 3rd, and Paull D
- Subjects
- Attentional Blink, Humans, Movement, Attention, Hand, Reaction Time, Vision, Ocular, Visual Perception
- Abstract
The present study explored the manner in which hand position may affect visual processing. We studied three classic visual attention tasks (visual search, inhibition of return, and attentional blink) during which the participants held their hands either near the stimulus display, or far from the display. Remarkably, the hands altered visual processing: people shifted their attention between items more slowly when their hands were near the display. The same results were observed for both visible and invisible hands. This enhancement in vision for objects near the hands reveals a mechanism that could facilitate the detailed evaluation of objects for potential manipulation, or the assessment of potentially dangerous objects for a defensive response.
- Published
- 2008
- Full Text
- View/download PDF
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