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Items: 1 to 20 of 65

1.

Reduced purifying selection prevails over positive selection in human copy number variant evolution.

Nguyen DQ, Webber C, Hehir-Kwa J, Pfundt R, Veltman J, Ponting CP.

Genome Res. 2008 Nov;18(11):1711-23. doi: 10.1101/gr.077289.108. Epub 2008 Aug 7.

2.

Extensive copy-number variation of the human olfactory receptor gene family.

Young JM, Endicott RM, Parghi SS, Walker M, Kidd JM, Trask BJ.

Am J Hum Genet. 2008 Aug;83(2):228-42. doi: 10.1016/j.ajhg.2008.07.005.

3.

Distribution and functional impact of DNA copy number variation in the rat.

Guryev V, Saar K, Adamovic T, Verheul M, van Heesch SA, Cook S, Pravenec M, Aitman T, Jacob H, Shull JD, Hubner N, Cuppen E.

Nat Genet. 2008 May;40(5):538-45. doi: 10.1038/ng.141.

PMID:
18443591
4.

The hominoid-specific oncogene TBC1D3 activates Ras and modulates epidermal growth factor receptor signaling and trafficking.

Wainszelbaum MJ, Charron AJ, Kong C, Kirkpatrick DS, Srikanth P, Barbieri MA, Gygi SP, Stahl PD.

J Biol Chem. 2008 May 9;283(19):13233-42. doi: 10.1074/jbc.M800234200. Epub 2008 Mar 4.

5.

The fine-scale and complex architecture of human copy-number variation.

Perry GH, Ben-Dor A, Tsalenko A, Sampas N, Rodriguez-Revenga L, Tran CW, Scheffer A, Steinfeld I, Tsang P, Yamada NA, Park HS, Kim JI, Seo JS, Yakhini Z, Laderman S, Bruhn L, Lee C.

Am J Hum Genet. 2008 Mar;82(3):685-95. doi: 10.1016/j.ajhg.2007.12.010. Epub 2008 Jan 24.

6.

Analysis of copy number variation in the rhesus macaque genome identifies candidate loci for evolutionary and human disease studies.

Lee AS, Gutiérrez-Arcelus M, Perry GH, Vallender EJ, Johnson WE, Miller GM, Korbel JO, Lee C.

Hum Mol Genet. 2008 Apr 15;17(8):1127-36. doi: 10.1093/hmg/ddn002. Epub 2008 Jan 7.

PMID:
18180252
7.

The drifting human genome.

Zhang J.

Proc Natl Acad Sci U S A. 2007 Dec 18;104(51):20147-8. No abstract available. Erratum in: Proc Natl Acad Sci U S A. 2008 Jul 1;105(26):9129.

8.

Genomic drift and copy number variation of sensory receptor genes in humans.

Nozawa M, Kawahara Y, Nei M.

Proc Natl Acad Sci U S A. 2007 Dec 18;104(51):20421-6. Epub 2007 Dec 5.

9.

A portrait of copy-number polymorphism in Drosophila melanogaster.

Dopman EB, Hartl DL.

Proc Natl Acad Sci U S A. 2007 Dec 11;104(50):19920-5. Epub 2007 Dec 4.

10.

A phylogenetic and functional overview of inflammatory caspases and caspase-1-related CARD-only proteins.

Kersse K, Vanden Berghe T, Lamkanfi M, Vandenabeele P.

Biochem Soc Trans. 2007 Dec;35(Pt 6):1508-11. Review.

PMID:
18031255
11.

Recurrent DNA copy number variation in the laboratory mouse.

Egan CM, Sridhar S, Wigler M, Hall IM.

Nat Genet. 2007 Nov;39(11):1384-9. Epub 2007 Oct 28.

PMID:
17965714
12.

Accelerated rate of gene gain and loss in primates.

Hahn MW, Demuth JP, Han SG.

Genetics. 2007 Nov;177(3):1941-9. Epub 2007 Oct 18.

13.

Ancestral reconstruction of segmental duplications reveals punctuated cores of human genome evolution.

Jiang Z, Tang H, Ventura M, Cardone MF, Marques-Bonet T, She X, Pevzner PA, Eichler EE.

Nat Genet. 2007 Nov;39(11):1361-8. Epub 2007 Oct 7.

PMID:
17922013
14.

Paired-end mapping reveals extensive structural variation in the human genome.

Korbel JO, Urban AE, Affourtit JP, Godwin B, Grubert F, Simons JF, Kim PM, Palejev D, Carriero NJ, Du L, Taillon BE, Chen Z, Tanzer A, Saunders AC, Chi J, Yang F, Carter NP, Hurles ME, Weissman SM, Harkins TT, Gerstein MB, Egholm M, Snyder M.

Science. 2007 Oct 19;318(5849):420-6. Epub 2007 Sep 27.

15.

Gene conversion: mechanisms, evolution and human disease.

Chen JM, Cooper DN, Chuzhanova N, Férec C, Patrinos GP.

Nat Rev Genet. 2007 Oct;8(10):762-75. Epub 2007 Sep 11. Review.

PMID:
17846636
16.

Hominoid lineage specific amplification of low-copy repeats on 22q11.2 (LCR22s) associated with velo-cardio-facial/digeorge syndrome.

Babcock M, Yatsenko S, Hopkins J, Brenton M, Cao Q, de Jong P, Stankiewicz P, Lupski JR, Sikela JM, Morrow BE.

Hum Mol Genet. 2007 Nov 1;16(21):2560-71. Epub 2007 Aug 3.

PMID:
17675367
17.

Gene copy number variation spanning 60 million years of human and primate evolution.

Dumas L, Kim YH, Karimpour-Fard A, Cox M, Hopkins J, Pollack JR, Sikela JM.

Genome Res. 2007 Sep;17(9):1266-77. Epub 2007 Jul 31.

18.

The population genetics of structural variation.

Conrad DF, Hurles ME.

Nat Genet. 2007 Jul;39(7 Suppl):S30-6. Review.

19.

Mutational and selective effects on copy-number variants in the human genome.

Cooper GM, Nickerson DA, Eichler EE.

Nat Genet. 2007 Jul;39(7 Suppl):S22-9. Review.

PMID:
17597777
20.

FCGR3B copy number variation is associated with susceptibility to systemic, but not organ-specific, autoimmunity.

Fanciulli M, Norsworthy PJ, Petretto E, Dong R, Harper L, Kamesh L, Heward JM, Gough SC, de Smith A, Blakemore AI, Froguel P, Owen CJ, Pearce SH, Teixeira L, Guillevin L, Graham DS, Pusey CD, Cook HT, Vyse TJ, Aitman TJ.

Nat Genet. 2007 Jun;39(6):721-3. Epub 2007 May 21.

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