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A-Z Articles Index by First Author's Last Name |
| Tallini G. Oncocytic tumours. Virchows Arch. 1998 Jul;433(1):5-12. |
| Tang X et al. Very low penetrance of hearing loss in seven Han Chinese pedigrees carrying the deafness-associated 12S rRNA A1555G mutation. Gene. 2007 Jan 24; [Epub ahead of print] |
| Taniguchi T et al. S-phase-specific interaction of the Fanconi anemia protein, FANCD2, with BRCA1 and RAD51. Blood. 2002 Oct 1;100(7):2414-20. |
| Taniguchi T et al. Convergence of the fanconi anemia and ataxia telangiectasia signaling pathways. Cell. 2002 May 17;109(4):459-72. |
Tao J et al. Mutations in the X-Linked Cyclin-Dependent KinaseLike 5 (CDKL5/STK9) Gene Are Associated with Severe Neurodevelopmental Retardation. Am. J. Hum. Genet., 75: 000, 2004 |
| Tartaglia M et al. SHP-2 and myeloid malignancies. Curr Opin Hematol. 2004 Jan;11(1):44-50. |
| Tartaglia M et al. Somatic mutations in PTPN11 in juvenile myelomonocytic leukemia, myelodysplastic syndromes and acute myeloid leukemia. Nat Genet. 2003 Jun;34(2):148-50. |
| Tartaglia M et al. PTPN11 Mutations in Noonan Syndrome: Molecular spectrum, genotype-phenotype correlation, and phenotypic heterogeneity. Am J Hum Genet. 2002; 70:1555-1563. |
| Tartaglia M et al. Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome. Nat Genet. 2001; 29:465-468. |
| Tatton-Brown K, et al. Childhood Overgrowth Collaboration. Multiple mechanisms are implicated in the generation of 5q35 microdeletions in Sotos syndrome. J Med Genet. 2005 Apr;42(4):307-13. |
| Tatton-Brown K, et al. Childhood Overgrowth Collaboration. Genotype-phenotype associations in Sotos syndrome: an analysis of 266 individuals with NSD1 aberrations. Am J Hum Genet. 2005 Aug;77(2):193-204. |
| Taverna SD et al. Methylation of histone h3 at lysine 9 targets programmed DNA elimination in tetrahymena. Cell. 2002 Sep 20;110(6):701-11. |
| Tee AR et al. Tuberous sclerosis complex gene products, Tuberin and Hamartin, control mTOR signaling by acting as a GTPase-activating protein complex toward Rheb. Curr Biol. 2003 Aug 5;13(15):1259-68. |
| Thomas G et al. Multiple loci identified in a genome-wide association study of prostate cancer. Nat Genet. 2008 Mar;40(3):310-5. Epub 2008 Feb 10. |
| Thomas M et al. Targeting MLL-AF4 with short interfering RNAs inhibits clonogenicity and engraftment of t(4;11)-positive human leukemic cells. Blood. 2005 Nov 15;106(10):3559-66. Epub 2005 Jul 26. |
| Thorn CF, et al. PharmGKB: the pharmacogenetics and pharmacogenomics knowledge base. Methods Mol Biol. 2005;311:179-91. |
| Tian C et al. Analysis and application of European genetic substructure using 300 K SNP information. PLoS Genet. 2008 Jan;4(1):e4. |
| Tiedt R et al. Ratio of mutant JAK2-V617F to wild-type Jak2 determines the MPD phenotypes in transgenic mice. Blood. 2008 Apr 15;111(8):3931-40. Epub 2007 Dec 26. |
| Tiemann-Boege I et al. The observed human sperm mutation frequency cannot explain the achondroplasia paternal age effect. Proc Natl Acad Sci U S A. 2002 Nov 12;99(23):14952-7. |
| Tischkowitz M et al. Analysis of PALB2/FANCN-associated breast cancer families. Proc Natl Acad Sci U S A. 2007 Apr 9; [Epub ahead of print] |
Tonkin ET et al., NIPBL, encoding a homolog of fungal Scc2-type sister chromatid cohesion proteins and fly Nipped-B, is mutated in Cornelia de Lange syndrome. Nat Genet. 2004 Jun;36(6):636-41. Epub 2004 May 16. |
| Toro JR et al. Mutations in the fumarate hydratase gene cause hereditary leiomyomatosis and renal cell cancer in families in North America. Am J Hum Genet. 2003 Jul;73(1):95-106. Epub 2003 May 22. |
| Tucker T et al. Massively parallel sequencing: the next big thing in genetic medicine. Am J Hum Genet. 2009;85:142-54. |
| Tufarelli C, et al. Transcription of antisense RNA leading to gene silencing and methylation as a novel cause of human genetic disease. Nat Genet. 2003 Jun;34(2):157-65. |
| Turner DJ et al. Germline rates of de novo meiotic deletions and duplications causing several genomic disorders. Nat Genet 2007 Dec 2; [Epub ahead of print] |
| Tuzun E et al. Fine-scale structural variation of the human genome. Nat Genet. 2005 Jul;37(7):727-32. |