516 results on '"Pavan, William J."'
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2. Haplotype-based analysis resolves missing heritability in oculocutaneous albinism type 1B
3. Optimization of systemic AAV9 gene therapy in Niemann-Pick disease type C1 mice
4. Correlation of age of onset and clinical severity in Niemann–Pick disease type C1 with lysosomal abnormalities and gene expression
5. The RhoJ-BAD signaling network: An Achilles' heel for BRAF mutant melanomas.
6. Melanoma to Vitiligo: The Melanocyte in Biology & Medicine–Joint Montagna Symposium on the Biology of Skin/PanAmerican Society for Pigment Cell Research Annual Meeting
7. Strategic vision for improving human health at The Forefront of Genomics
8. Single‐cell profiling of MC1R‐inhibited melanocytes.
9. The MFSD12 p.Tyr182His common variant is sufficient to alter mouse agouti coat color.
10. The MFSD12 p.Tyr182His common variant is sufficient to alter mouse agouti coat color
11. Author Response: Transcriptomic profiling of tissue environments critical for post-embryonic patterning and morphogenesis of zebrafish skin
12. Transcriptomic profiling of tissue environments critical for post-embryonic patterning and morphogenesis of zebrafish skin
13. Transcriptomic profiling of tissue environments critical for post-embryonic patterning and morphogenesis of zebrafish skin
14. Author Response: Transcriptomic profiling of tissue environments critical for post-embryonic patterning and morphogenesis of zebrafish skin
15. Loci associated with skin pigmentation identified in African populations
16. SOX10 Ablation Arrests Cell Cycle, Induces Senescence, and Suppresses Melanomagenesis
17. Intrathecal 2-hydroxypropyl-β-cyclodextrin decreases neurological disease progression in Niemann-Pick disease, type C1: a non-randomised, open-label, phase 1–2 trial
18. Mutation of Melanosome Protein RAB38 in chocolate Mice
19. cDNA Microarrays Detect Activation of a Myogenic Transcription Program by the PAX3-FKHR Fusion Oncogene
20. Substantial Narrowing of the Niemann-Pick C Candidate Interval by Yeast Artificial Chromosome Complementation
21. Data from SOX10 Ablation Arrests Cell Cycle, Induces Senescence, and Suppresses Melanomagenesis
22. Supplementary Figure 4 from SOX10 Ablation Arrests Cell Cycle, Induces Senescence, and Suppresses Melanomagenesis
23. Loss of MC1R signaling implicates TBX3 in pheomelanogenesis and melanoma predisposition
24. MEK inhibition remodels the active chromatin landscape and induces SOX10 genomic recruitment in BRAF(V600E) mutant melanoma cells
25. Meta-analysis of GWA studies provides new insights on the genetic architecture of skin pigmentation in recently admixed populations
26. Glial-cell-derived neuroregulators control type 3 innate lymphoid cells and gut defence
27. Modeling Smith-Lemli-Opitz syndrome with induced pluripotent stem cells reveals a causal role for Wnt/β-catenin defects in neuronal cholesterol synthesis phenotypes
28. The Genetic Regulation of Pigment Cell Development
29. The Origin and Development of Neural Crest-Derived Melanocytes
30. Systemic AAV9 gene therapy improves the lifespan of mice with Niemann-Pick disease, type C1
31. Expanded Analysis of Pigmentation Genetics in UK Biobank
32. Interspecies Difference in the Regulation of Melanocyte Development by SOX10 and MITF
33. Improved systemic AAV gene therapy with a neurotrophic capsid in Niemann–Pick disease type C1 mice
34. Genomic analysis reveals distinct mechanisms and functional classes of SOX10-regulated genes in melanocytes
35. Ectopic differentiation of melanocyte stem cells is influenced by genetic background
36. Generation of Deletion Derivatives by Targeted Transformation of Human-Derived Yeast Artificial Chromosomes
37. Piebald Lethal (s l ) Acts Early to Disrupt the Development of Neural Crest-Derived Melanocytes
38. How a membrane transporter keeps melanocytes in the red
39. Transcriptomic profiling of tissue environments critical for post-embryonic patterning and morphogenesis of zebrafish skin
40. Distinct microRNA expression signatures are associated with melanoma subtypes and are regulated by HIF1A
41. Axing the cancer loop
42. A Unique Missense Allele of BAF155, a Core BAF Chromatin Remodeling Complex Protein, Causes Neural Tube Closure Defects in Mice
43. Mutations in TRIOBP, which encodes a putative cytoskeletal-organizing protein, are associated with nonsyndromic recessive deafness
44. The importance of having your SOX on: role of SOX10† in the development of neural crest-derived melanocytes and glia
45. Efficacy of N-acetylcysteine in phenotypic suppression of mouse models of Niemann–Pick disease, type C1
46. Postnatal lineage mapping of follicular melanocytes with the Tyr::CreERT2 transgene
47. Transcription factor hierarchy in Waardenburg syndrome: regulation of MITF expression by SOX10 and PAX3
48. Microarray expression analysis and identification of serum biomarkers for Niemann–Pick disease, type C1
49. Comparative analyses of the Dominant megacolon-SOX10 genomic interval in mouse and human
50. Isolation, genomic organization, and expression analysis of Men1, the murine homolog of the MEN1 gene
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