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A-Z Articles Index by First Author's Last Name |
| Bacher CP et al. Transient colocalization of X-inactivation centres accompanies the initiation of X inactivation. Nat Cell Biol. 2006 Mar;8(3):293-299. Epub 2006 Jan 24. |
| Bacher U et al. Quantitative monitoring of NPM1 mutations provides a valid minimal residual disease parameter following allogeneic stem cell transplantation. Exp Hematol. 2009 Jan;37(1):135-42. |
Baker NL et al. Dominant collagen VI mutations are a common cause of Ullrich congenital muscular dystrophy. Hum Mol Genet. 2004 Nov 24; [Epub ahead of print] |
| Bakkaloglu B et al. Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders. Am J Hum Genet. 2008 Jan;82(1):165-73. |
| Barbour VM, et al. Alpha-thalassemia resulting from a negative chromosomal position effect. Blood. 2000 Aug 1;96(3):800-7. |
| Bard F. et al. Peripherally administered antibodies against amyloid beta-peptide enter the central nervous system and reduce pathology in a mouse model of Alzheimer disease. Nat Med.2000;6:916-9. |
| Battaglia A. Del 1p36 syndrome: a newly emerging clinical entity. Brain Dev. 2005 Aug;27(5):358-61. |
| Baudot A et al. From cancer genomes to cancer models: bridging the gaps. EMBO Rep. 2009 Apr;10(4):359-66. |
| Baur JA et al. Resveratrol improves health and survival of mice on a high-calorie diet. Nature. 2006 Nov 16;444(7117):337-342. Epub 2006 Nov 1. |
| Bautista DM et al. TRPA1 mediates the inflammatory actions of environmental irritants and proalgesic agents. Cell. 2006 Mar 24;124(6):1269-82. |
| Begley TJ et al. Molecular biology: A fix for RNA. Nature 2003 Feb 20;421(6925):795-6. |
| Benit P et al. Mutant NDUFS3 subunit of mitochondrial complex I causes Leigh syndrome. J Med Genet. 2004 Jan;41(1):14-7. |
| Berry-Kravis E et al. Neuropathic features in fragile X premutation carriers. Am J Med Genet A. 2007 Jan 1;143(1):19-26. |
| Bertram L and Tanzi RE. The genetic epidemiology of neurodegenerative disease. J Clin Invest. 2005 Jun;115(6):1449-57. |
| Bjorses P et al. Gene defect behind APECED: a new clue to autoimmunity. Hum Mol Genet 1998;7(10):1547-53. |
| Bluher M et al. Extended longevity in mice lacking the insulin receptor in adipose tissue. Science. 2003 Jan 24;299(5606):572-4. |
| Bolli N et al. A dose-dependent tug of war involving the NPM1 leukaemic mutant, nucleophosmin, and ARF. Leukemia. 2009 Mar;23(3):501-9. Epub 2008 Nov 13. |
| Bolnick DA et al. Genetics: The Science and Business of Genetic Ancestry Testing. Science. 2007 Oct 19;318 (5849): 399-400. |
| Bonnen et al. Haplotype and linkage disequilibrium architecture for human-cancer associated genes. Genome Res. 2002;12:1846-1853. |
| Boutin P et al. GAD2 on chromosome 10p12 is a candidate gene for human obesity. PLoS Biol. 2003 Dec;1(3):E68. Epub 2003 Nov 3. |
| Brambrink T, et al. Sequential expression of pluripotency markers during direct reprogramming of mouse somatic cells. Cell Stem Cell 2008, 2:151-159. |
| Braig M et al. Oncogene-induced senescence as an initial barrier in lymphoma development. Nature. 2005 Aug 4;436(7051):660-5. |
| Brems H et al. Germline loss-of-function mutations in SPRED1 cause a neurofibromatosis 1-like phenotype. Nat Genet. 2007 Sep;39(9):1120-6. Epub 2007 Aug 19. |
| Brennecke J et al. bantam encodes a developmentally regulated microRNA that controls cell proliferation and regulates the proapoptotic gene hid in Drosophila.Cell. 2003 Apr 4;113(1):25-36. |
| Bretherick KL et al. FMR1 repeat sizes in the fray zone and high end of the normal range are associated with premature ovarian failure. Hum Genet 2005 Aug; 117(4):376-82 |
| Brody LC et al. A Polymorphism, R653Q, in the Trifunctional Enzyme Methylenetetrahydrofolate Dehydrogenase/Methenyltetrahydrofolate Cyclohydrolase/Formyltetrahydrofolate Synthetase Is a Maternal Genetic Risk Factor for Neural Tube Defects: Report of the Birth Defects Research Group. Am J Hum Genet. 2002;71(5):1207-15. |
| Brown V et al. Microarray Identification of FMRP-Associated Brain mRNAs and Altered mRNA Translational Profiles in Fragile X Syndrome. Cell. 2001 Nov 16;107(4):477-87. |
| Bruder CE et al. Phenotypically concordant and discordant monozygotic twins display different DNA copy-number-variation profiles. Am J Hum Genet. 2008 Mar;82(3):763-71. Epub 2008 Feb 14. |
| Bruzzone R et al. Loss-of-function and residual channel activity of connexin26 mutations associated with non-syndromic deafness. FEBS Lett. 2003 Jan;533(1):79-88. |
| Buchner DA et al. SCNM1, a putative RNA splicing factor that modifies disease severity in mice. Science. 2003 Aug 15;301(5635):967-9. |
| Budde BS et al. tRNA splicing endonuclease mutations cause pontocerebellar hypoplasia. Nat Genet. 2008 Aug 17. [Epub ahead of print] |