196 results on '"Reddy, Sita"'
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2. Mbnl2 loss alters novel context processing and impairs object recognition memory
3. Reuse of Crushed Concrete in Granular Sub-Base in Pavements
4. Mbnl1 and Mbnl2 regulate brain structural integrity in mice
5. Muscleblind-like 3 deficit results in a spectrum of age-associated pathologies observed in myotonic dystrophy.
6. Muscleblind-Like 1 and Muscleblind-Like 3 Depletion Synergistically Enhances Myotonia by Altering Clc-1 RNA Translation.
7. Loss of muscleblind-like 1 results in cardiac pathology and persistence of embryonic splice isoforms.
8. Muscleblind1, but not Dmpk or Six5, contributes to a complex phenotype of muscular and motivational deficits in mouse models of myotonic dystrophy.
9. Asian Medicine in America: The Ayurvedic Case
10. Altered Phosphorylation and Intracellular Distribution of a (CUG)n Triplet Repeat RNA-Binding Protein in Patients with Myotonic Dystrophy and in Myotonin Protein Kinase Knockout Mice
11. Who owns yoga?
12. Myotonic Muscular Dystrophy Genetics and Cardiac Sequelae
13. Isolation of Cellular Promoters by Using a Retrovirus Promoter Trap
14. Fluorescence-Activated Sorting of Totipotent Embryonic Stem Cells Expressing Developmentally Regulated lacZ Fusion Genes
15. Downregulation of the Werner syndrome protein induces a metabolic shift that compromises redox homeostasis and limits proliferation of cancer cells
16. Characterization of Cardiac Conduction System Abnormalities in Mice with Targeted Disruption of Six5 Gene
17. Progressive Atrioventricular Conduction Block in a Mouse Myotonic Dystrophy Model
18. Lamin A, farnesylation and aging
19. Accumulation of distinct prelamin A variants in human diploid fibroblasts differentially affects cell homeostasis
20. Contributors
21. cis Effects of CTG Expansion in Myotonic Dystrophy Type 1
22. Perturbation of wild-type lamin A metabolism results in a progeroid phenotype
23. CK2-mediated stimulation of Pol I transcription by stabilization of UBF–SL1 interaction
24. Myotonia and muscle contractile properties in mice with SIX5 deficiency
25. Myotonic Muscular Dystrophy Genetics and Cardiac Sequelae
26. Six5 is required for spermatogenic cell survival and spermiogenesis
27. Temporarily insane: pathologising cultural difference in American criminal courts
28. DMPK dosage alterations result in atrioventricular conduction abnormalities in a mouse myotonic dystrophy model
29. The Werner Syndrome Helicase Coordinates Sequential Strand Displacement and FEN1-Mediated Flap Cleavage during Polymerase δ Elongation
30. Recent advances in understanding the role of lamins in health and disease
31. Overexpression of Smad2 Reveals Its Concerted Action with Smad4 in Regulating TGF-[Beta]-Mediated Epidermal Homeostasis
32. PROGRESSIVE ATRIOVENTRICULAR CONDUCTION BLOCK IN A MOUSE MYOTONIC DYSTROPHY MODEL
33. The Werner Syndrome Helicase Coordinates Sequential Strand Displacement and FEN1-Mediated Flap Cleavage during Polymerase δ Elongation.
34. Use of Animal Models to Understand Human Muscular Dystrophy
35. Downregulation of the W erner syndrome protein induces a metabolic shift that compromises redox homeostasis and limits proliferation of cancer cells
36. The Chloride Channelopathy in Knockout Mice of Muscleblind-Like Proteins
37. RNA Splicing Is Responsive to MBNL1 Dose
38. A filtering strategy identifies FOXQ1 as a potential effector of lamin A dysfunction
39. Transcriptome-wide Regulation of Pre-mRNA Splicing and mRNA Localization by Muscleblind Proteins
40. Expanded CUG Repeats Dysregulate RNA Splicing by Altering the Stoichiometry of the Muscleblind 1 Complex
41. Cell cycle-regulated association between the Werner syndrome protein and its molecular partners
42. RNA steady‐state defects in myotonic dystrophy are linked to nuclear exclusion of SHARP
43. Depletion of Ku70/80 reduces the levels of extrachromosomal telomeric circles and inhibits proliferation of ALT cells
44. Processing of human telomeres by the Werner syndrome protein
45. Muscleblind-like 1 (Mbnl1) Promotes Insulin Receptor Exon 11 Inclusion via Binding to a Downstream Evolutionarily Conserved Intronic Enhancer
46. Sacrilege and Cultural Heritage: Intangibles in Repatriation Case Law
47. Sequence-specific processing of telomeric 3' overhangs by the Werner syndrome protein exonuclease activity
48. Altered Nuclear Functions in Progeroid Syndromes: a Paradigm for Aging Research
49. Cytoplasmic CUG RNA Foci Are Insufficient to Elicit Key DM1 Features
50. WRN Controls Formation of Extrachromosomal Telomeric Circles and Is Required for TRF2 ΔB -Mediated Telomere Shortening
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