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A-Z Articles Index by First Author's Last Name |
| Vakoc CR et al. Histone H3 lysine 9 methylation and HP1gamma are associated with transcription elongation through mammalian chromatin. Mol Cell. 2005 Aug 5;19(3):381-91. |
| Valente, L et al. Infantile Encephalopathy and Defective Mitochondrial DNA Translation in Patients with Mutations of Mitochondrial Elongation Factors EFG1 and EFTu. Am J Hum Genet. 2007 Jan;80(1):44-58. Epub 2006 Nov 15. |
| van der Zee J, et al. Clinical heterogeneity in 3 unrelated families linked to VCP p.Arg159His. 2009 Neurology 73:626-632 |
| Vang T et al. Autoimmune-associated lymphoid tyrosine phosphatase is a gain-of-function variant. Nat Genet. 2005 Dec;37(12):1317-9. Epub 2005 Nov 6. |
| vanHaelst MM, et al. Familial gigantism caused by an NSD1 mutation. Am J Med Genet A. 2005 Nov 15;139(1):40-4. |
| Vanneste E et al. Chromosome instability is common in human cleavage-stage embryos. Nat. Med. (2009) 15(5):577-583 |
| Vaz FM et al. Only one splice variant of the human TAZ gene encodes a functional protein with a role in cardiolipin metabolism. J Biol Chem. 2003 Oct 31;278(44):43089-94. Epub 2003 Aug 20. |
| Vega H et al, Roberts syndrome is caused by mutations in ESCO2, a human homolog of yeast ECO1 that is essential for the establishment of sister chromatid cohesion. Nat Genet. 2005 May;37(5):468-70. Epub 2005 Apr 10. |
| Verkarre V et al.Paternal mutation of the sulfonylurea receptor (SUR1) gene and maternal loss of 11p15 imprinted genes lead to persistent hyperinsulinism in focal adenomatous hyperplasia. J Clin Invest. 1998 Oct 1;102(7):1286-91. |
| Verlinsky et al. Preimplantation HLA Testing. JAMA 2004;291(17):2079-2085 |
| Vieira NM et al. Human multipotent adipose-derived stem cells restore dystrophin expression of Duchenne skeletal-muscle cells in vitro. Biol Cell. 2008 Apr;100(4):231-41. |
| Vieira NM et al. SJL dystrophic mice express a significant amount of human muscle proteins following systemic delivery of human adipose-derived stromal cells without immunosuppression. Stem Cells. 2008 Sep;26(9):2391-8. Epub 2008 Jun 26. |
| Vissers LE et al. Identification of disease genes by whole genome CGH arrays. Hum Mol Genet. 2005 Oct 15;14 Suppl 2:R215-23. |
| Vladutiu GD. Heterozygosity: an expanding role in proteomics. Mol Genet Metab. 2001 Sep-Oct;74(1-2):51-63. |
| Von Hoff D et al. (2009). Inhibition of the Hedgehog Pathway in Advanced Basal-Cell Carcinoma New England Journal of Medicine, 361 (12), 1164-1172 |
| Vrijenhoek T et al. Recurrent CNVs disrupt three candidate genes in schizophrenia patients. Am J Hum Genet. 2008 Oct;83(4):504-10. |
| Vulliamy T et al. The RNA component of telomerase is mutated in autosomal dominant dyskeratosis congenita. Nature. 2001;413:432-4. |