Genetics of the P2X7 receptor and human disease-Reference-Cited by-同舟云学术

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Genetics of the P2X7 receptor and human disease

Published:2009-03-25 Issue:2 Volume:5 Page:257-262
ISSN:1573-9538
Container-title:Purinergic Signalling
language:en
Short-container-title:Purinergic Signalling

Author:

Fuller Stephen J.,Stokes Leanne,Skarratt Kristen K.,Gu Ben J.,Wiley James S.

Publisher

Springer Science and Business Media LLC

Subject

Cell Biology,Cellular and Molecular Neuroscience,Molecular Biology

Link

http://link.springer.com/content/pdf/10.1007/s11302-009-9136-4.pdf

Reference28 articles.

1. International Human Genome Consortium (2004) Finishing the euchromatic sequence of the human genome. Nature 431(7011):931–45

2. The International HapMap Consortium (2005) A haplotype map of the human genome. Nature 437(7063):1299–1320

3. Ford D, Easton DF, Stratton M, Narod S, Goldgar D, Devilee P et al (1998) Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. The Breast Cancer Linkage Consortium. Am J Hum Genet 62(3):676–689

4. Burn J, Chapman P, Delhanty J, Wood C, Lalloo F, Cachon-Gonzalez MB et al (1991) The UK Northern region genetic register for familial adenomatous polyposis coli: use of age of onset, congenital hypertrophy of the retinal pigment epithelium, and DNA markers in risk calculations. J Med Genet 28(5):289–296

5. The Wellcome Trust Case Control Consortium (2007) Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature 447(7145):661–678

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