23 results on '"Rosenstein, C"'
Search Results
2. Compliant Wafer Level Package for Enhanced Reliability.
- Author
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Guilian Gao, Haba, B., Oganesian, V., Honer, K., Ovrutsky, D., Rosenstein, C., Axelrod, E., Hazanovich, F., and Aksenton, Y.
- Published
- 2007
- Full Text
- View/download PDF
3. Cellular localization of the molecular forms of acetylcholinesterase in rat diaphragm.
- Author
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Younkin, S G, Rosenstein, C, Collins, P L, and Rosenberry, T L
- Published
- 1982
- Full Text
- View/download PDF
4. Partial purification by vacuum distillation of a factor that increases the junctional acetylcholinesterase of organ cultured rat diaphragm
- Author
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Younkin, S.G., Younkin, L.H., Zoller, M., and Rosenstein, C.
- Published
- 1982
- Full Text
- View/download PDF
5. Characterization and Classification of Postoperative Cysts After Strabismus Surgery: Clinical, Histological, and Anterior Segment OCT Analysis in a Large German Cohort.
- Author
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Hufendiek K, Bredt M, Binter M, Rosenstein C, Greb O, Wiezorrek M, Framme C, Schittkowski M, and Hufendiek K
- Abstract
Introduction: In this work, we provide a detailed characterization of a rare complication-subconjunctival cyst formation after strabismus surgery-in a large German cohort., Methods: We conducted a retrospective analysis of 822 consecutive patients who underwent strabismus surgery between 2015 and 2022. The patients received comprehensive eye and orthoptic examinations preoperatively, at 1 day, and at 3 months postoperatively. Cysts were analyzed with slit-lamp examination, anterior segment optical coherence tomography (AS-OCT), and histopathological subsumption., Results: Nineteen cases of postoperative cysts were observed (2.3%), 12 of which underwent surgical revision. Clinical evaluation including slit-lamp and AS-OCT as well as histological analysis resulted in a classification of three types of cysts: type 1, which is a single hyporeflective cyst, type 2, which is a multilobular hyporeflective cyst, and type 3, a dense hyperreflective granulomatous-like cyst. Eta (η) correlation ratio analysis could show a correlation between time of clinical appearance and type of cyst (Eta = 0.63). Most cysts developed within 20 days after surgery. Not only did cysts more frequently affect the medial rectus muscle, which in most cases underwent a shortening procedure (11/19 tucks, 4/19 resections) for intermittent exotropia (X(T)), but the cyst also formed earlier than in the lateral rectus muscle (Eta = 0.45). No correlation could be shown between the type of surgical procedure and time of cyst occurrence (Eta = 0.1). Patient age and cyst type correlated strongly (Eta = 0.47). The underlying type of strabismus did not correlate with the type of cyst observed., Conclusions: Our cases showed a strong positive correlation to the type of strabismus (X(T)), age (young patients), and the procedure (tuck/resection). We introduce a grading system for postoperative cysts after strabismus surgery, complementing histopathology and slit-lamp aspects with AS-OCT information., (© 2023. The Author(s).)
- Published
- 2023
- Full Text
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6. Long-Term Multimodal Imaging Analysis of Selective Retina Therapy Laser Lesions.
- Author
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Binter M, Lindziute M, Rosenstein C, Framme C, and Tode J
- Abstract
This study evaluates the long-term effects of selective retina therapy (SRT) on the retinal pigment epithelium (RPE) and neuroretina in patients with central serous chorioretinopathy. SRT was performed on 36 patients using a Nd:YLF-Laser at 527 nm (R:GEN
® , Lutronic, Goyang-Si, Republic of Korea). A total of 994 titration spots were examined using up to three years' multimodal imaging. Leakage in fluorescein angiography (FA) was observed after SRT in 523 lesions and resolved after one month. SRT lesions were not visible clinically, but appeared as brightly reflective areas in infrared and multicolor images. Normal morphology was observed in optical coherence tomography (OCT) immediately after SRT. After one month, thickening of the RPE and interdigitation zone changes were seen and disappeared after 539 ± 308 days. No RPE atrophies occurred during the observation period. Decreased fundus autofluorescence (FAF) was mostly observed directly after SRT followed by increased FAF at one month, which faded over time. A significant decrease in the number of visible lesions in the FA and FAF was observed within the three-year follow-up. OCT findings are consistent with animal studies showing SRT-related defect closure by hypertrophy and migration of neighboring cells without RPE atrophy or photoreceptor damage. This suggests that SRT is a safe treatment option for macular diseases and does not lead to retinal atrophy.- Published
- 2023
- Full Text
- View/download PDF
7. Thiophene carboxamide inhibitors of JAK2 as potential treatments for myleoproliferative neoplasms.
- Author
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Haidle AM, Zabierek AA, Childers KK, Rosenstein C, Mathur A, Altman MD, Chan G, Xu L, Bachman E, Mo JR, Bouthillette M, Rush T, Tempest P, Marshall CG, and Young JR
- Subjects
- Aminoimidazole Carboxamide chemistry, Animals, Antineoplastic Agents chemical synthesis, Antineoplastic Agents chemistry, Antineoplastic Agents pharmacology, Disease Models, Animal, Enzyme Activation drug effects, Humans, Leukemia, Myeloid, Acute drug therapy, Microsomes drug effects, Microsomes enzymology, Models, Biological, Molecular Structure, Protein Kinase Inhibitors chemical synthesis, Protein Kinase Inhibitors chemistry, Protein Kinase Inhibitors pharmacology, Rats, Thiophenes chemistry, Aminoimidazole Carboxamide chemical synthesis, Aminoimidazole Carboxamide pharmacology, Janus Kinase 2 antagonists & inhibitors, Thiophenes chemical synthesis, Thiophenes pharmacology
- Abstract
A series of carboxamide-substituted thiophenes demonstrating inhibition of JAK2 is described. Development of this chemical series began with the bioisosteric replacement of a urea substituent by a pyridyl ring. Issues of chemical and metabolic stability were solved using the results of both in vitro and in vivo studies, ultimately delivering compounds such as 24 and 25 that performed well in an acute PK/PD model measuring p-STAT5 inhibition., (Copyright © 2014 Elsevier Ltd. All rights reserved.)
- Published
- 2014
- Full Text
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8. The discovery of reverse tricyclic pyridone JAK2 inhibitors. Part 2: lead optimization.
- Author
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Siu T, Kumarasinghe SE, Altman MD, Katcher M, Northrup A, White C, Rosenstein C, Mathur A, Xu L, Chan G, Bachman E, Bouthillette M, Dinsmore CJ, Marshall CG, and Young JR
- Subjects
- Adenosine Triphosphate chemistry, Adenosine Triphosphate metabolism, Animals, Binding Sites, Drug Evaluation, Preclinical, Half-Life, Janus Kinase 2 metabolism, Molecular Dynamics Simulation, Protein Kinase Inhibitors chemical synthesis, Protein Kinase Inhibitors pharmacokinetics, Protein Structure, Tertiary, Pyridones chemical synthesis, Pyridones pharmacokinetics, Rats, Structure-Activity Relationship, Sulfonamides chemical synthesis, Sulfonamides pharmacokinetics, Janus Kinase 2 antagonists & inhibitors, Protein Kinase Inhibitors chemistry, Pyridones chemistry, Sulfonamides chemistry
- Abstract
This communication discusses the discovery of novel reverse tricyclic pyridones as inhibitors of Janus kinase 2 (JAK2). By using a kinase cross screening approach coupled with molecular modeling, a unique inhibitor-water interaction was discovered to impart excellent broad kinase selectivity. Improvements in intrinsic potency were achieved by utilizing a rapid library approach, while targeted structural changes to lower lipophilicity led to improved rat pharmacokinetics. This multi-pronged approach led to the identification of 31, which demonstrated encouraging rat pharmacokinetics, in vivo potency, and excellent off-target kinase selectivity., (Copyright © 2014 Elsevier Ltd. All rights reserved.)
- Published
- 2014
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9. Identification of a selective inhibitor of murine intestinal alkaline phosphatase (ML260) by concurrent ultra-high throughput screening against human and mouse isozymes.
- Author
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Ardecky RJ, Bobkova EV, Kiffer-Moreira T, Brown B, Ganji S, Zou J, Pass I, Narisawa S, Iano FG, Rosenstein C, Cheltsov A, Rascon J, Hedrick M, Gasior C, Forster A, Shi S, Dahl R, Vasile S, Su Y, Sergienko E, Chung TDY, Kaunitz J, Hoylaerts MF, Pinkerton AB, and Millán JL
- Subjects
- Acetanilides isolation & purification, Animals, Enzyme Activation drug effects, Enzyme Inhibitors chemistry, Enzyme Inhibitors isolation & purification, Enzyme Inhibitors pharmacology, Humans, Mice, Protein Isoforms chemistry, Sulfonamides isolation & purification, Acetanilides chemistry, Acetanilides pharmacology, Alkaline Phosphatase antagonists & inhibitors, Sulfonamides chemistry, Sulfonamides pharmacology
- Abstract
Alkaline phosphatase (AP) isozymes are present in a wide range of species from bacteria to man and are capable of dephosphorylation and transphosphorylation of a wide spectrum of substrates in vitro. In humans, four AP isozymes have been identified-one tissue-nonspecific (TNAP) and three tissue-specific-named according to the tissue of their predominant expression: intestinal (IAP), placental (PLAP) and germ cell (GCAP) APs. Modulation of activity of the different AP isozymes may have therapeutic implications in distinct diseases and cellular processes. For instance, changes in the level of IAP activity can affect gut mucosa tolerance to microbial invasion due to the ability of IAP to detoxify bacterial endotoxins, alter the absorption of fatty acids and affect ectopurinergic regulation of duodenal bicarbonate secretion. To identify isozyme selective modulators of the human and mouse IAPs, we developed a series of murine duodenal IAP (Akp3-encoded dIAP isozyme), human IAP (hIAP), PLAP, and TNAP assays. High throughput screening and subsequent SAR efforts generated a potent inhibitor of dIAP, ML260, with specificity for the Akp3-, compared to the Akp5- and Akp6-encoded mouse isozymes., (Copyright © 2013 Elsevier Ltd. All rights reserved.)
- Published
- 2014
- Full Text
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10. Discovery of 1-[3-(1-methyl-1H-pyrazol-4-yl)-5-oxo-5H-benzo[4,5]cyclohepta[1,2-b]pyridin-7-yl]-N-(pyridin-2-ylmethyl)methanesulfonamide (MK-8033): A Specific c-Met/Ron dual kinase inhibitor with preferential affinity for the activated state of c-Met.
- Author
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Northrup AB, Katcher MH, Altman MD, Chenard M, Daniels MH, Deshmukh SV, Falcone D, Guerin DJ, Hatch H, Li C, Lu W, Lutterbach B, Allison TJ, Patel SB, Reilly JF, Reutershan M, Rickert KW, Rosenstein C, Soisson SM, Szewczak AA, Walker D, Wilson K, Young JR, Pan BS, and Dinsmore CJ
- Subjects
- Animals, Benzocycloheptenes chemistry, Cell Line, Tumor, Dogs, Enzyme Activation drug effects, Female, Humans, Mice, Models, Molecular, Protein Conformation, Protein Kinase Inhibitors chemistry, Protein Kinase Inhibitors metabolism, Protein Kinase Inhibitors pharmacology, Proto-Oncogene Proteins c-met chemistry, Rats, Substrate Specificity, Sulfonamides chemistry, Xenograft Model Antitumor Assays, Benzocycloheptenes metabolism, Benzocycloheptenes pharmacology, Drug Discovery, Proto-Oncogene Proteins c-met antagonists & inhibitors, Proto-Oncogene Proteins c-met metabolism, Receptor Protein-Tyrosine Kinases antagonists & inhibitors, Sulfonamides metabolism, Sulfonamides pharmacology
- Abstract
This report documents the first example of a specific inhibitor of protein kinases with preferential binding to the activated kinase conformation: 5H-benzo[4,5]cyclohepta[1,2-b]pyridin-5-one 11r (MK-8033), a dual c-Met/Ron inhibitor under investigation as a treatment for cancer. The design of 11r was based on the desire to reduce time-dependent inhibition of CYP3A4 (TDI) by members of this structural class. A novel two-step protocol for the synthesis of benzylic sulfonamides was developed to access 11r and analogues. We provide a rationale for the observed selectivity based on X-ray crystallographic evidence and discuss selectivity trends with additional examples. Importantly, 11r provides full inhibition of tumor growth in a c-Met amplified (GTL-16) subcutaneous tumor xenograft model and may have an advantage over inactive form kinase inhibitors due to equal potency against a panel of oncogenic activating mutations of c-Met in contrast to c-Met inhibitors without preferential binding to the active kinase conformation.
- Published
- 2013
- Full Text
- View/download PDF
11. Discovery of 1-amino-5H-pyrido[4,3-b]indol-4-carboxamide inhibitors of Janus kinase 2 (JAK2) for the treatment of myeloproliferative disorders.
- Author
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Lim J, Taoka B, Otte RD, Spencer K, Dinsmore CJ, Altman MD, Chan G, Rosenstein C, Sharma S, Su HP, Szewczak AA, Xu L, Yin H, Zugay-Murphy J, Marshall CG, and Young JR
- Subjects
- Administration, Oral, Animals, Carbolines pharmacokinetics, Carbolines pharmacology, Crystallography, X-Ray, Dogs, Haplorhini, Hepatocytes metabolism, Indoles pharmacokinetics, Indoles pharmacology, Janus Kinase 2 metabolism, Mice, Mice, Inbred C57BL, Models, Molecular, Molecular Structure, Phosphorylation, Polycythemia Vera drug therapy, Pyridines pharmacokinetics, Pyridines pharmacology, Pyrimidines pharmacokinetics, Pyrimidines pharmacology, Rats, Stereoisomerism, Structure-Activity Relationship, Carbolines chemical synthesis, Indoles chemical synthesis, Janus Kinase 2 antagonists & inhibitors, Myeloproliferative Disorders drug therapy, Pyridines chemical synthesis, Pyrimidines chemical synthesis
- Abstract
The JAK-STAT pathway mediates signaling by cytokines, which control survival, proliferation, and differentiation of a variety of cells. In recent years, a single point mutation (V617F) in the tyrosine kinase JAK2 was found to be present with a high incidence in myeloproliferative disorders (MPDs). This mutation led to hyperactivation of JAK2, cytokine-independent signaling, and subsequent activation of downstream signaling networks. The genetic, biological, and physiological evidence suggests that JAK2 inhibitors could be effective in treating MPDs. De novo design efforts of new scaffolds identified 1-amino-5H-pyrido[4,3-b]indol-4-carboxamides as a new viable lead series. Subsequent optimization of cell potency, metabolic stability, and off-target activities of the leads led to the discovery of 7-(2-aminopyrimidin-5-yl)-1-{[(1R)-1-cyclopropyl-2,2,2-trifluoroethyl]amino}-5H-pyrido[4,3-b]indole-4-carboxamide (65). Compound 65 is a potent, orally active inhibitor of JAK2 with excellent selectivity, PK profile, and in vivo efficacy in animal models.
- Published
- 2011
- Full Text
- View/download PDF
12. Discovery of a 5H-benzo[4,5]cyclohepta[1,2-b]pyridin-5-one (MK-2461) inhibitor of c-Met kinase for the treatment of cancer.
- Author
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Katz JD, Jewell JP, Guerin DJ, Lim J, Dinsmore CJ, Deshmukh SV, Pan BS, Marshall CG, Lu W, Altman MD, Dahlberg WK, Davis L, Falcone D, Gabarda AE, Hang G, Hatch H, Holmes R, Kunii K, Lumb KJ, Lutterbach B, Mathvink R, Nazef N, Patel SB, Qu X, Reilly JF, Rickert KW, Rosenstein C, Soisson SM, Spencer KB, Szewczak AA, Walker D, Wang W, Young J, and Zeng Q
- Subjects
- Animals, Antineoplastic Agents pharmacokinetics, Antineoplastic Agents pharmacology, Benzocycloheptenes pharmacokinetics, Benzocycloheptenes pharmacology, Cell Line, Tumor, Crystallography, X-Ray, Dogs, Drug Screening Assays, Antitumor, Female, Haplorhini, Humans, Mice, Mice, Nude, Models, Molecular, Mutation, Neoplasm Transplantation, Phosphorylation, Protein Binding, Pyrazoles chemical synthesis, Pyrazoles pharmacokinetics, Pyrazoles pharmacology, Pyridines pharmacokinetics, Pyridines pharmacology, Rats, Receptor Protein-Tyrosine Kinases genetics, Structure-Activity Relationship, Sulfonamides chemical synthesis, Sulfonamides pharmacokinetics, Sulfonamides pharmacology, Transplantation, Heterologous, Antineoplastic Agents chemical synthesis, Benzocycloheptenes chemical synthesis, Pyridines chemical synthesis, Receptor Protein-Tyrosine Kinases antagonists & inhibitors
- Abstract
c-Met is a transmembrane tyrosine kinase that mediates activation of several signaling pathways implicated in aggressive cancer phenotypes. In recent years, research into this area has highlighted c-Met as an attractive cancer drug target, triggering a number of approaches to disrupt aberrant c-Met signaling. Screening efforts identified a unique class of 5H-benzo[4,5]cyclohepta[1,2-b]pyridin-5-one kinase inhibitors, exemplified by 1. Subsequent SAR studies led to the development of 81 (MK-2461), a potent inhibitor of c-Met that was efficacious in preclinical animal models of tumor suppression. In addition, biochemical studies and X-ray analysis have revealed that this unique class of kinase inhibitors binds preferentially to the activated (phosphorylated) form of the kinase. This report details the development of 81 and provides a description of its unique biochemical properties.
- Published
- 2011
- Full Text
- View/download PDF
13. The discovery of tricyclic pyridone JAK2 inhibitors. Part 1: hit to lead.
- Author
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Siu T, Kozina ES, Jung J, Rosenstein C, Mathur A, Altman MD, Chan G, Xu L, Bachman E, Mo JR, Bouthillette M, Rush T, Dinsmore CJ, Marshall CG, and Young JR
- Subjects
- Animals, Binding Sites, Computer Simulation, Cyclization, Drug Evaluation, Preclinical, Heterocyclic Compounds, 3-Ring chemical synthesis, Heterocyclic Compounds, 3-Ring pharmacology, Janus Kinase 2 metabolism, Mice, Mice, Inbred C57BL, Pyridones chemical synthesis, Pyridones pharmacology, STAT5 Transcription Factor metabolism, Structure-Activity Relationship, Heterocyclic Compounds, 3-Ring chemistry, Janus Kinase 2 antagonists & inhibitors, Pyridones chemistry
- Abstract
This paper describes the discovery and design of a novel class of JAK2 inhibitors. Furthermore, we detail the optimization of a screening hit using ligand binding efficiency and log D. These efforts led to the identification of compound 41, which demonstrates in vivo activity in our study., (Copyright © 2010 Elsevier Ltd. All rights reserved.)
- Published
- 2010
- Full Text
- View/download PDF
14. Quality control procedures for dose-response curve generation using nanoliter dispense technologies.
- Author
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Quintero C, Rosenstein C, Hughes B, Middleton R, and Kariv I
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- Drug Evaluation, Preclinical methods, Hydrazines analysis, Hydrazines chemistry, Indicator Dilution Techniques, Inhibitory Concentration 50, Microfluidic Analytical Techniques, Quality Control, Sensitivity and Specificity, Dose-Response Relationship, Drug, Drug Evaluation, Preclinical standards, Microchemistry methods, Nanotechnology methods
- Abstract
With the advancement of high-throughput biomolecular screening techniques to the lead optimization stage, there is a critical need to quality control (QC) dose-response curves generated by robotic liquid handlers to ensure accurate affinity determinations. One challenge in evaluating the performance of liquid handlers is identifying and validating a robust method for testing dispense volumes across different instruments. Although traditional automated liquid handlers are still considered the standard platform in many laboratories, nanoliter dispensers are becoming more common and pose new challenges for routine quality control procedures. For example, standard gravimetric measurements are unreliable for testing the accuracy of nanoliter liquid dispenses. However, nanoliter dispensing technology allows for the conservation of compound, reduces compound carryover from well to well through discrete dispenses, and eliminates the need for intermediate compound dilution steps to achieve a low final DMSO assay concentration. Moreover, an intermediate dilution step in aqueous solution might result in compound precipitation at high concentrations. This study compared representative automation procedures done on a variety of liquid dispensers, including manual, traditional, and nanodispense volumes. The data confirmed the importance of establishing robust QC procedures for dose-response generation in addition to accuracy and precision determinations for each instrument, and they validated the use of nanoliter pipettors for dose-response testing. The results of this study also support the requirement for thorough mixing during serial compound dilutions prepared for high-throughput lead optimization strategies using traditional liquid handlers.
- Published
- 2007
- Full Text
- View/download PDF
15. Candida osteomyelitis and diskitis after spinal surgery: an outbreak that implicates artificial nail use.
- Author
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Parry MF, Grant B, Yukna M, Adler-Klein D, McLeod GX, Taddonio R, and Rosenstein C
- Subjects
- Adult, Candida albicans isolation & purification, Candidiasis microbiology, Candidiasis transmission, Case-Control Studies, Cross Infection microbiology, Cross Infection transmission, Discitis microbiology, Diskectomy adverse effects, Electrophoresis, Gel, Pulsed-Field, Female, Health Personnel, Humans, Infectious Disease Transmission, Professional-to-Patient, Laminectomy adverse effects, Male, Middle Aged, Osteomyelitis microbiology, Prostheses and Implants adverse effects, Surgical Wound Infection microbiology, Time Factors, Candidiasis etiology, Cross Infection etiology, Discitis etiology, Nails microbiology, Osteomyelitis etiology, Surgical Wound Infection etiology
- Abstract
Postoperative wound infection after laminectomy is uncommon. In February 1997, 3 patients were confirmed to have postlaminectomy deep wound infections due to Candida albicans. No similar case had been seen during the previous 10 years. The infections were indolent, with a mean time from initial operation to diagnosis of 54 days (range, 26-83 days). All patients were successfully treated. Pulsed-field gel electrophoresis revealed the Candida isolates to be identical. A case-controlled study and medical record review revealed that a single operating room technician scrubbed on all 3 infected case patients but on only 32% of the uninfected controls. The technician had worn artificial nails for a 3-month period that included the dates of laminectomy site infections, and C. albicans was isolated from her throat. She was treated with fluconazole and removed from duty. No subsequent cases have occurred during the ensuing 3 years. Artificial nails are known to promote subungual growth of gram-negative bacilli and yeast. This may be clinically relevant, and hospitals should enforce policies to prevent operating room personnel from wearing artificial nails.
- Published
- 2001
- Full Text
- View/download PDF
16. Latex sensitization: on the rise in the NICU.
- Author
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Durkin D and Rich-Rosenstein C
- Subjects
- Adult, Humans, Infant, Newborn, Intensive Care Units, Neonatal, Latex Hypersensitivity epidemiology, Nursing Staff, Hospital, Occupational Diseases epidemiology, Latex Hypersensitivity etiology, Latex Hypersensitivity prevention & control, Occupational Diseases etiology, Occupational Diseases prevention & control
- Published
- 1998
17. Temporary vessel occlusion in spontaneously hypertensive and normotensive rats. Effect of single and multiple episodes on tissue metabolism and volume of infarction.
- Author
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Selman WR, Bhatti SU, Rosenstein CC, Lust WD, and Ratcheson RA
- Subjects
- Adenosine Triphosphate metabolism, Animals, Cerebral Infarction etiology, Cerebral Infarction pathology, Constriction, Glucose metabolism, Hypertension pathology, Ischemic Attack, Transient complications, Lactates metabolism, Male, Rats, Rats, Inbred SHR, Rats, Wistar, Brain metabolism, Cerebral Infarction metabolism, Hypertension metabolism, Temporal Arteries
- Abstract
Temporary occlusion of an intracranial artery is frequently necessary in the surgical management of intracranial aneurysms, arteriovenous malformations, and tumors. While the risks of vessel damage associated with clip application have been lessened by improved design, the threat of ischemic damage remains. It is unclear whether multiple, brief periods of clip application are more or less safe than a single period of occlusion, and whether the underlying cerebrovascular status influences the outcome from either method. The effect of each of these paradigms (single: 1-hour occlusion; multiple: three 20-minute episodes separated by 10 minutes of reperfusion) on histopathological outcome was assessed in a middle cerebral artery (MCA) occlusion model using both normotensive and spontaneously hypertensive rats. The mean volume of infarction (+/- standard error of the mean) was not different between the single-ischemic (49.4 +/- 17.3 cu mm) and the multiple-ischemic (42.9 +/- 12.9 cu mm) episode groups of normotensive rats, whereas in the spontaneously hypertensive rats a significant difference existed between the volume of infarction for the single-occlusion group (126.7 +/- 18.7 cu mm) and the multiple-occlusion group (162.4 +/- 15.5 cu mm) (p < 0.05). The metabolic data obtained from spontaneously hypertensive animals did not provide an explanation for the larger infarction in that there were no significant differences between the single- and multiple-occlusion groups with respect to tissue glucose, adenosine triphosphate, or lactate levels. The results suggest that intermittent reperfusion may have different effects depending not only on the degree and duration of ischemia and reperfusion, but also on the underlying cerebrovascular status.
- Published
- 1994
- Full Text
- View/download PDF
18. Dual chain migration: post-1965 Filipino immigration to the United States.
- Author
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Liu JM, Ong PM, and Rosenstein C
- Subjects
- Americas, Asia, Asia, Southeastern, Demography, Developed Countries, Developing Countries, Economics, North America, Philippines, Population, Population Characteristics, Population Dynamics, Research, Social Class, Socioeconomic Factors, United States, Censuses, Educational Status, Emigration and Immigration, Social Change
- Abstract
In analyzing Filipino migration to the United States since 1965, the authors identify two distinct chains of immigrants. One derives from the Filipinos who entered the country prior to 1965; the other comes from the flow of highly trained professionals who immigrated during the late 1960s and early 1970s. "To establish the historical basis for the two patterns of immigration that unfolded in the post-1965 period, the article begins with a brief examination of Filipino immigration to the United States. An analysis of the modes of entry used in both chains follows this overview. The study concludes with a discussion of the degree of convergence in these two chains and the consequences of each for contemporary Filipino-American community development." Data are from published U.S. census material and from Immigration and Naturalization Service reports and tapes dating from 1972 to 1985., (excerpt)
- Published
- 1991
19. THE CHLORINE TREATMENT OF CONTAMINATED OYSTERS.
- Author
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Krumweide C, Park WH, Cooper G, Grund M, Tyler C, and Rosenstein C
- Published
- 1926
- Full Text
- View/download PDF
20. EFFECT OF STORAGE AND CHANGING SEA WATER ON CONTAMINATED OYSTERS.
- Author
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Krumwiede C, Park WH, Cooper G, Grund M, Tyler CH, and Rosenstein C
- Published
- 1926
- Full Text
- View/download PDF
21. THE SEPARATION OF TYPES AMONG THE PNEUMOCOCCI HITHERTO CALLED GROUP IV AND THE DEVELOPMENT OF THERAPEUTIC ANTISERUMS FOR THESE TYPES.
- Author
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Cooper G, Edwards M, and Rosenstein C
- Abstract
The pneumococci hitherto known as Group IV have been separated into ten types which have been designated by Roman numerals from IV to XIII. These have been correlated as far as possible with the types described by others. The prevalence and mortality of cases due to each type have been estimated in the limited number of cases studied. Laboratory tests indicated that therapeutic antiserums for Types I, II and III have very little protective power against the recently separated types. Monovalent antiserums of high agglutinative and protective power were prepared in rabbits for each type. Several monovalent antiserums each specific for a type, which are suitable for agglutination and experimental therapeutic use, have been obtained by immunizing horses. An antiserum prepared for one type had very little cross-protective power against other types.
- Published
- 1929
- Full Text
- View/download PDF
22. THE FURTHER SEPARATION OF TYPES AMONG THE PNEUMOCOCCI HITHERTO INCLUDED IN GROUP IV AND THE DEVELOPMENT OF THERAPEUTIC ANTISERA FOR THESE TYPES.
- Author
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Cooper G, Rosenstein C, Walter A, and Peizer L
- Abstract
The unclassified strains known as Group IV have been separated into twenty-nine types which are designated by the Roman numerals IV and XXXII. Only a small percentage of the pneumococcus strains isolated in New York City for this study were left unclassified. The majority of the types gave very slight cross-reactions, the exceptions being Types II and V, III and VIII, VII and XVIII and XV and XXX. In the series of cases studied, Types IV, V, VII and VIII were found more prevalent in the lobar pneumonia of adults and Types V, VI a and XIV in children. The majority of the types were also found in normal individuals and in persons having respiratory infections other than pneumonia. Types VI a and XIX were most prevalent in the limited number of strains studied by us. Fourteen of the types were found in pneumococcus meningitis; Type XVIII was found most often. Antisera suitable for clinical trial have been prepared for fourteen types. From the majority of the horses inoculated for more than a year, antisera having 500 to 1000 units per cc. were obtained. Antisera of lower potency were concentrated and preparations obtained equal to or stronger than high grade unconcentrated serum. Potent bivalent antisera have been prepared for types which were found to give marked cross-agglutination reactions. The results with each type as to prevalence, severity of cases, presence in normal individuals, and in spinal meningitis, potency of antisera produced for therapeutic trial and virulence of strains for mice have been considered under the different type headings.
- Published
- 1932
- Full Text
- View/download PDF
23. The Purification of Contaminated Oysters in Natural Waters.
- Author
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Krumwiede C, Park WH, Cooper G, Grund M, Tyler C, and Rosenstein C
- Published
- 1928
- Full Text
- View/download PDF
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