55 results on '"Vogt, Thomas F"'
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2. Contributors
3. Huntingtin loss in hepatocytes is associated with altered metabolism, adhesion, and liver zonation
4. Huntingtin loss in hepatocytes is associated with altered metabolism, adhesion, and liver zonation
5. Conformational dynamics and DNA recognition by human MutSbeta
6. Supplementary Figures 1-4 from PDK1 Attenuation Fails to Prevent Tumor Formation in PTEN-Deficient Transgenic Mouse Models
7. Supplementary Figures 1-4 from PDK1 Attenuation Fails to Prevent Tumor Formation in PTEN-Deficient Transgenic Mouse Models
8. Mapping brain gene coexpression in daytime transcriptomes unveils diurnal molecular networks and deciphers perturbation gene signatures
9. Developing HDAC4-Selective Protein Degraders To Investigate the Role of HDAC4 in Huntington’s Disease Pathology
10. HDinHD: A Rich Data Portal for Huntington’s Disease Research
11. Shape deformation analysis reveals the temporal dynamics of cell-type-specific homeostatic and pathogenic responses to mutant huntingtin
12. Author response: Shape deformation analysis reveals the temporal dynamics of cell-type-specific homeostatic and pathogenic responses to mutant huntingtin
13. In Vivo Analysis of Gene Knockdown in Tetracycline-Inducible shRNA Mice
14. DNA methylation study of Huntington’s disease and motor progression in patients and in animal models
15. Ultrasensitive quantitative measurement of huntingtin phosphorylation at residue S13
16. MicroRNA signatures of endogenous Huntingtin CAG repeat expansion in mice
17. Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease
18. Huntington's disease accelerates epigenetic aging of human brain and disrupts DNA methylation levels
19. Plasma Levels of Risk-Variant APOL1 Do Not Associate with Renal Disease in a Population-Based Cohort
20. Abstract 16204: Knock-down of 24-dehydrocholesterol Reductase Suppresses SREBP2: A Novel Approach to Reduce PCSK9 in vivo
21. Exome-wide association study identifies a TM6SF2 variant that confers susceptibility to nonalcoholic fatty liver disease
22. Demonstration of diet-induced decoupling of fatty acid and cholesterol synthesis by combining gene expression array and 2H2O quantification
23. Meiotic functions of RAD18
24. AAV8-Mediated Long-Term Expression of Human LCAT Significantly Improves Lipid Profiles in hCETP;Ldlr+/− Mice
25. PDK1 Attenuation Fails to Prevent Tumor Formation in PTEN-Deficient Transgenic Mouse Models
26. Manic fringe is not required for embryonic development, and fringe family members do not exhibit redundant functions in the axial skeleton, limb, or hindbrain
27. Dual role of Nr2e3 in photoreceptor development and maintenance
28. Pleiotrophin is an important regulator of the renin–angiotensin system in mouse aorta
29. Pleiotrophin is a major regulator of the catecholamine biosynthesis pathway in mouse aorta
30. P2-066 A genetically engineered mouse model with an enhanced beta-secretase substrate exhibits increased amyloid generation
31. P2-137 Secretase inhibitors reduce amyloid production in primary neurons from novel MWP HUAPP KI mice
32. Molecular genetic analysis of the glycosyltransferase Fringe in Drosophila
33. Mutations in Mcoln3 associated with deafness and pigmentation defects in varitint-waddler ( Va ) mice
34. Clock Regulatory Elements Control Cyclic Expression of Lunatic fringe during Somitogenesis
35. Large scale transgenic and cluster deletion analysis of the HoxD complex separate an ancestral regulatory module from evolutionary innovations
36. Identification, expression analysis, and mapping of B3galt6, a putative galactosyl transferase gene with similarity to Drosophila brainiac
37. Expression analysis and mapping of the mouse and human transcriptional regulator CA150
38. Fringe differentially modulates Jagged1 and Delta1 signalling through Notch1 and Notch2
39. Fringe is a glycosyltransferase that modifies Notch
40. Antagonists Go out on a Limb
41. Limbs move beyond the Radical fringe
42. Genomic structure, mapping, and expression analysis of the mammalian Lunatic, Manic, and Radical fringe genes
43. Evaluation of mouse Sfrp3/Frzb1 as a candidate for the lst, Ul, and Far mutants on Chromosome 2
44. Dorsal—ventral signaling in limb development
45. Genetic and Physical Mapping of the Mouse Ulnaless Locus
46. Genetic and Molecular Analysis of the Mouse Ulnaless Locus
47. Polydactyly in theStrong's luxoid mouse is suppressed bylimb deformity alleles
48. Mapping the midkine family of developmentally regulated signaling molecules
49. The same genomic region is disrupted in two transgene-induced limb deformity alleles
50. Parental-specific methylation of an imprinted transgene is established during gametogenesis and progressively changes during embryogenesis
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