90 results on '"Epstein, Charles J."'
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2. Enhanced expression of mitochondrial superoxide dismutase leads to prolonged in vivo cell cycle progression and up-regulation of mitochondrial thioredoxin
3. Prolonged ethanol administration depletes mitochondrial DNA in MnSOD-overexpressing transgenic mice, but not in their wild type littermates
4. DYRK1A-Dosage Imbalance Perturbs NRSF/REST Levels, Deregulating Pluripotency and Embryonic Stem Cell Fate in Down Syndrome
5. Increased App Expression in a Mouse Model of Down's Syndrome Disrupts NGF Transport and Causes Cholinergic Neuron Degeneration
6. Effect of the reduction of superoxide dismutase 1 and 2 or treatment with α-tocopherol on tumorigenesis in Atm-deficient mice
7. Absence of CuZn superoxide dismutase leads to elevated oxidative stress and acceleration of age-dependent skeletal muscle atrophy
8. Medical Genetics in the Genomic Medicine of the 21st Century
9. Medical geneticists in the 21st century
10. Selective neuronal vulnerability and inadequate stress response in superoxide dismutase mutant mice
11. Genetic testing: Hope or hype?
12. A biologically effective fullerene (C 60) derivative with superoxide dismutase mimetic properties
13. Multiple deficiencies in antioxidant enzymes in mice result in a compound increase in sensitivity to oxidative stress
14. Is modern genetics the new eugenics?
15. Effect of SOD1 overexpression on age- and noise-related hearing loss
16. Urea-selective Concentrating Defect in Transgenic Mice Lacking Urea Transporter UT-B
17. Slit1 and Slit2 Cooperate to Prevent Premature Midline Crossing of Retinal Axons in the Mouse Visual System
18. Increased sensitivity of homozygous Sod2 mutant mice to oxygen toxicity
19. From Down Syndrome to the “Human” in “Human Genetics”
20. Genetic modification of prenatal lethality and dilated cardiomyopathy in Mn superoxide dismutase mutant mice
21. Manganese Superoxide Dismutase Signals Matrix Metalloproteinase Expression via H2O2-dependent ERK1/2 Activation
22. Neonatal Mortality in an Aquaporin-2 Knock-in Mouse Model of Recessive Nephrogenic Diabetes Insipidus
23. Strain-dependent high-level expression of a transgene for manganese superoxide dismutase is associated with growth retardation and decreased fertility
24. Mice with a Partial Deficiency of Manganese Superoxide Dismutase Show Increased Vulnerability to the Mitochondrial Toxins Malonate, 3-Nitropropionic Acid, and MPTP
25. Nonmuscle Myosin Heavy Chain IIA Mutations Define a Spectrum of Autosomal Dominant Macrothrombocytopenias: May-Hegglin Anomaly and Fechtner, Sebastian, Epstein, and Alport-Like Syndromes
26. Autosomal-dominant giant platelet syndromes: a hint of the same genetic defect as in Fechtner syndrome owing to a similar genetic linkage to chromosome 22q11-13
27. Overexpression of CuZnSOD in coronary vascular cells attenuates myocardial ischemia/reperfusion injury
28. Defective Secretion of Saliva in Transgenic Mice Lacking Aquaporin-5 Water Channels
29. Characterization of the Antioxidant Status of the Heterozygous Manganese Superoxide Dismutase Knockout Mouse
30. CHAPTER 34 - Educational Strategies in Genomic Medicine
31. 2010 Victor A. McKusick Leadership Award Introduction and Address
32. Contributors
33. Meeting Announcement
34. College News
35. P2-101 Reduced LTP and enhanced inhibition in dentate gyrus of TS65DN mice, a model for down's syndrome
36. Some ethical implications of The Human Genome Project
37. Apoptosis as an anti-neoplastic mechanism in mice expressing a goblet cell-specific hybrid oncogene
38. Homozygosity Mapping of the Werner Syndrome Locus (WRN)
39. The long-range restriction map surrounding the mouse agouti locus reveals a disparity between physical and genetic distances
40. Oligosyndactyly: A lethal mutation in the mouse that results in mitotic arrest very early in development
41. Manipulation of myogenesis in vitro: Reversible inhibition by DMSO
42. Central Nervous System Expression of HIV-1 Gp120 Activates the Hypothalamic-Pituitary-Adrenal Axis: Evidence for Involvement of NMDA Receptors and Nitric Oxide Synthase
43. Increased Oxidative Damage Is Correlated to Altered Mitochondrial Function in Heterozygous Manganese Superoxide Dismutase Knockout Mice
44. Severely Impaired Urinary Concentrating Ability in Transgenic Mice Lacking Aquaporin-1 Water Channels
45. Mouse trisomy 16 as an animal model of human trisomy 21 (Down syndrome): Production of viable trisomy 16 ↔ diploid mouse chimeras
46. Protein synthetic patterns in teratocarcinoma stem cells and mouse embryos at early stages of development
47. Biochemical studies of growing mouse oocytes: Preparation of oocytes and analysis of glucose-6-phosphate dehydrogenase and lactate dehydrogenase activities
48. T-lymphocyte function and sensitivity to interferon in trisomy 21
49. Lack of relationship between blood and urine levels of glycosaminoglycans and lysomal enzymes
50. The mouse homolog of the human amyloid β protein (AD-AP) gene is located on the distal end of mouse chromosome 16: Further extension of the homology between human chromosome 21 and mouse chromosome 16
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