|
|
|
|
A-Z Articles Index by First Author's Last Name |
| Calin GA et al. A MicroRNA signature associated with prognosis and progression in chronic lymphocytic leukemia. N Engl J Med. 2005 Oct 27;353(17):1793-801. |
| Callen E. et al. Breaks at telomeres and TRF2-independent end fusions in Fanconi anemia. Hum Mol Genet. 2002; 11:439-44. |
Cao YA et al. Shifting foci of hematopoiesis during reconstitution from single stem cells. Proc Natl Acad Sci U S A. 2004 Jan 6;101(1):221-6. Epub 2003 Dec 19. |
Carrel L and Willard HF. X-inactivation profile reveals extensive variability in X-linked gene expression in females. Nature. 2005 Mar 17;434(7031):400-4. |
| Cartegni L et al. Disruption of an SF2/ASF-dependent exonic splicing enhancer in SMN2 causes spinal muscular atrophy in the absence of SMN1. Nat Genet. 2002;30(4):377-84. |
| Caselli RJ et al. Longitudinal modeling of age-related memory decline and the APOE epsilon4 effect. NEJM 2009 July 16;361(3):255-263 |
Casper AM et al. Chromosomal instability at common fragile sites in seckel syndrome. J Hum Genet. 2004 Oct;75(4):654-60. Epub 2004 Aug 12. |
| Caspi A et al. Role of genotype in the cycle of violence in maltreated children. Science 2002 Aug 2;297(5582):851-4. |
| Castro AF et al. Rheb binds tuberous sclerosis complex 2 (TSC2) and promotes S6 kinase activation in a rapamycin- and farnesylation-dependent manner.J Biol Chem. 2003 Aug 29;278(35):32493-6. Epub 2003 Jul 03. |
| Cecconi M, et al. Mutation analysis of the NSD1 gene in a group of 59 patients with congenital overgrowth. Am J Med Genet A. 2005 Apr 30;134(3):247-53. |
| Chauhan NB & Siegel GJ Antisense inhibition at the beta-secretase-site of beta-amyloid precursor protein reduces cerebral amyloid and acetyl cholinesterase activity in Tg2576. Neuroscience. 2007 Apr 25;146(1):143-51. Epub 2007 Feb 14. |
| Cheadle JP, Sampson JR. Exposing the MYtH about base excision repair and human inherited disease. Hum Mol Genet. 2003 Oct 15;12 Spec No 2:R159-65. |
| Chen et al. Derepression of BDNF transcription involves calcium-dependent phosphorylation of MeCP2. Science. 2003 Oct 31;302(5646):885-9. |
| Chen H et al. Mitochondrial fusion protects against neurodegeneration in the cerebellum. Cell. 2007 Aug 10;130(3):548-62. |
| Chen, X et al. (2001). Variable deletion and duplication at recombination junction ends: implication for staggered double-strand cleavage in class-switch recombination. PNAS 98:13860-13865. |
| Chen Z et al. Crucial role of p53-dependent cellular senescence in suppression of Pten-deficient tumorigenesis. Nature. 2005 Aug 4;436(7051):725-30. |
| Chenevix-Trench G., et al. (2002) Dominant negative ATM mutations in breast cancer families. J Natl Cancer Inst 94(3):205-215. |
| Cho MK, and Sankar P. Forensic genetics and ethical, legal and social implications beyond the clinic. Nat Genet. 2004 Nov;36(11 Suppl):S8-12. |
| Chung Y et al. Embryonic and extraembryonic stem cell lines derived from single mouse blastomeres. Nature. 2005 Oct 16; [Epub ahead of print] |
| Citron M et al. Excessive production of amyloid beta-protein by peripheral cells of symptomatic and presymptomatic patients carrying the Swedish familial Alzheimer disease mutation. Proc Natl Acad Sci U S A. 1994 Dec 6;91(25):11993-7. |
| Coelho D et al. Gene identification for the cblD defect of vitamin B12 metabolism. N Engl J Med. 2008 Apr 3;358(14):1454-64. |
| Cohen MM et al. Teratogenesis of holoprosencephaly. Am J Med Genet 2002;109(1): 1-15. |
| Cohen-Cory S. The developing synapse: construction and modulation of synaptic structures and circuits. Science. 2002;298(5594):770-6.PMID:12399577 [PubMed-in process] |
| Cohn RD et al. Angiotensin II type 1 receptor blockade attenuates TGF-beta-induced failure of muscle regeneration in multiple myopathic states. Nat Med. 2007 Feb;13(2):204-10. Epub 2007 Jan 21. |
| Cole-Edwards, KK et al. c-Jun N-terminal kinase activation responses induced by hippocampal kindling are mediated by reactive astrocytes. J Neurosci. 2006 Aug 9;26(32):8295-304. |
| Conrad DF et al. A high-resolution survey of deletion polymorphism in the human genome. Nat Genet. 2006 Jan;38(1):75-81. |
| Corey DP et al. TRPA1 is a candidate for the mechanosensitive transduction channel of vertebrate hair cells. Nature. 2004 Dec 9;432(7018):723-30. Epub 2004 Oct 13. |
| Corydon MJ et al. Role of common gene variations in the molecular pathogenesis of short-chain acyl-CoA dehydrogenase deficiency. Pediatr Res. 2001 Jan;49(1):18-23. |
| Coyne JA Genetics and speciation.Nature. 1992 Feb 6;355(6360):511-5 |
| Cox GF et al. Intracytoplasmic sperm injection may increase the risk of imprinting defects. Am J Hum Genet. 2002 Jul;71(1):162-4. |
| Crisan M et al. A perivascular origin for mesenchymal stem cells in multiple human organs. Cell Stem Cell. 2008 Sep 11;3(3):301-13. |
| Crispino JD. GATA1 mutations in Down syndrome: implications for biology and diagnosis of children with transient myeloproliferative disorder and acute megakaryoblastic leukemia. Pediatr Blood Cancer. 2005 Jan;44(1):40-4. |
Cryns K et al. A genotype-phenotype correlation for GJB2 (connexin 26) deafness. J Med Genet. 2004 Mar;41(3):147-54. |
| Cui CY et al. EDA targets revealed by skin gene expression profiles of wild-type, Tabby and Tabby EDA-A1 transgenic mice. Hum Mol Genet. 2002;11:1763-73. |
| Cui H et al. Loss of IGF2 imprinting: A potential marker of colorectal cancer risk. Science 2003;299:1753-5. |
| Cui H et al. Loss of imprinting in colorectal cancer linked to hypomethylation of H19 and IGF2. Cancer Res 2002;62;6442-6. |
| Culbertson MR. Sense versus nonsense in DNA diagnostics. Nat Biotechnol. 2001; 19:413-414. |