Inherited epimutation or a haplotypic basis for the propensity to silence? [3]

Nature Genetics

Volumn 39, Issue 5, 2007, Pages 573-

  Suter, Catherine M ^a   Martin, David I K ^b  

^a VICTOR CHANG CARDIAC RESEARCH INSTITUTE   (Australia)

^b CHILDREN S HOSPITAL OAKLAND RESEARCH INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

FRAGILE X MENTAL RETARDATION PROTEIN; PROTEIN MLH1; PROTEIN MSH2;

CHROMATIN STRUCTURE; COLORECTAL CANCER; DNA SEQUENCE; EPIGENETICS; GENE LOCUS; HAPLOTYPE; HUMAN; LETTER; MISMATCH REPAIR; PRIORITY JOURNAL; PROMOTER REGION; RECTUM MUCOSA; SPERMATOZOON; STATISTICAL SIGNIFICANCE;

ADAPTOR PROTEINS, SIGNAL TRANSDUCING; COLORECTAL NEOPLASMS, HEREDITARY NONPOLYPOSIS; DNA METHYLATION; EPIGENESIS, GENETIC; GENE SILENCING; GERM-LINE MUTATION; HUMANS; INHERITANCE PATTERNS; MOSAICISM; MUTS HOMOLOG 2 PROTEIN; NUCLEAR PROTEINS;

EID: 34247642769     PISSN: 10614036     EISSN: 15461718     Source Type: Journal    
DOI: 10.1038/ng0507-573a     Document Type: Letter

References (9)

1. Chan, T.L. et al. Nat. Genet. 38, 1178-1183 (2006).
2. Gazzoli, I., Loda, M., Garber, J., Syngal, S. & Kolodner, R.D. Cancer Res. 62, 3925-3928 (2002).
3. Suter, C.M., Martin, D.I. & Ward, R.L. Nat. Genet. 36, 497-501 (2004).
4. Miyakura, Y. et al. Clin. Gastroenterol. Hepatol. 2, 147-156 (2004).
5. Hitchins, M. et al. Gastroenterology 129, 1392-1399 (2005).
6. Hitchins, M.P. et al. N. Engl. J. Med. 356, 697-705 (2007).
7. Holliday, R. Science 238, 163-170 (1987).
8. van Overveld, P.G. et al. Nat. Genet. 35, 315-317 (2003).
9. Stöger, R., Kajimura, T.M., Brown, W.T. & Laird, C.D. Hum. Mol. Genet. 6, 1791-1801 (1997).