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Over-representation of PPARgamma sequence variants in sporadic cases of glioblastoma multiforme: preliminary evidence for common low penetrance modifiers for brain tumour risk in the general population.

Zhou XP, Smith WM, Gimm O, Mueller E, Gao X, Sarraf P, Prior TW, Plass C, von Deimling A, Black PM, Yates AJ, Eng C.

J Med Genet. 2000 Jun;37(6):410-4.


Opposite association of two PPARG variants with cancer: overrepresentation of H449H in endometrial carcinoma cases and underrepresentation of P12A in renal cell carcinoma cases.

Smith WM, Zhou XP, Kurose K, Gao X, Latif F, Kroll T, Sugano K, Cannistra SA, Clinton SK, Maher ER, Prior TW, Eng C.

Hum Genet. 2001 Aug;109(2):146-51.


The TGFBR1*6A allele is not associated with susceptibility to colorectal cancer in a Spanish population: a case-control study.

Castillejo A, Mata-Balaguer T, Montenegro P, Ochoa E, Lázaro R, Martínez-Cantó A, Castillejo MI, Guarinos C, Barberá VM, Guillén-Ponce C, Carrato A, Soto JL.

BMC Cancer. 2009 Jun 18;9:193. doi: 10.1186/1471-2407-9-193.


Large-scale evaluation of genetic variants in candidate genes for colorectal cancer risk in the Nurses' Health Study and the Health Professionals' Follow-up Study.

Hazra A, Chanock S, Giovannucci E, Cox DG, Niu T, Fuchs C, Willett WC, Hunter DJ.

Cancer Epidemiol Biomarkers Prev. 2008 Feb;17(2):311-9. doi: 10.1158/1055-9965.EPI-07-0195.


Genetic contribution to variable human CYP3A-mediated metabolism.

Lamba JK, Lin YS, Schuetz EG, Thummel KE.

Adv Drug Deliv Rev. 2002 Nov 18;54(10):1271-94. Review.


Expression and genetic analysis of tumor necrosis factor-alpha (TNF-alpha) G-308A polymorphism in sporadic Alzheimer's disease in a Southern China population.

Yang L, Lu R, Jiang L, Liu Z, Peng Y.

Brain Res. 2009 Jan 9;1247:178-81. doi: 10.1016/j.brainres.2008.10.019. Epub 2008 Nov 1.


Contribution of cyclin d1 (CCND1) and E-cadherin (CDH1) polymorphisms to familial and sporadic colorectal cancer.

Porter TR, Richards FM, Houlston RS, Evans DG, Jankowski JA, Macdonald F, Norbury G, Payne SJ, Fisher SA, Tomlinson I, Maher ER.

Oncogene. 2002 Mar 14;21(12):1928-33.


Overexpression of alpha4 chain-containing laminins in human glial tumors identified by gene microarray analysis.

Ljubimova JY, Lakhter AJ, Loksh A, Yong WH, Riedinger MS, Miner JH, Sorokin LM, Ljubimov AV, Black KL.

Cancer Res. 2001 Jul 15;61(14):5601-10.


Ancestral RET haplotype associated with Hirschsprung's disease shows linkage disequilibrium breakpoint at -1249.

Fernandez RM, Boru G, Peciña A, Jones K, López-Alonso M, Antiñolo G, Borrego S, Eng C.

J Med Genet. 2005 Apr;42(4):322-7. Erratum in: J Med Genet. 2005 Jun;42(6):502.


The ITGAV rs3738919-C allele is associated with rheumatoid arthritis in the European Caucasian population: a family-based study.

Jacq L, Garnier S, Dieudé P, Michou L, Pierlot C, Migliorini P, Balsa A, Westhovens R, Barrera P, Alves H, Vaz C, Fernandes M, Pascual-Salcedo D, Bombardieri S, Dequeker J, Radstake TR, Van Riel P, van de Putte L, Lopes-Vaz A, Glikmans E, Barbet S, Lasbleiz S, Lemaire I, Quillet P, Hilliquin P, Teixeira VH, Petit-Teixeira E, Mbarek H, Prum B, Bardin T, Cornélis F; European Consortium on Rheumatoid Arthritis Families.

Arthritis Res Ther. 2007;9(4):R63.


The molecular genetic basis and diagnosis of familial hypercholesterolemia in Denmark.

Jensen HK.

Dan Med Bull. 2002 Nov;49(4):318-45. Review.


[RET and GFRA1 germline polymorphisms in medullary thyroid cancer patients].

Severskaia NV, Saenko VA, Il'in AA, Chebotareva IV, Rumiantsev PO, Isaev PA, Medvedev VS, Iasmita S.

Mol Biol (Mosk). 2006 May-Jun;40(3):425-35. Russian.


CARD15 variants in patients with sporadic Parkinson's disease.

Bialecka M, Kurzawski M, Klodowska-Duda G, Opala G, Juzwiak S, Kurzawski G, Tan EK, Drozdzik M.

Neurosci Res. 2007 Mar;57(3):473-6. Epub 2006 Dec 14.


The PPAR{gamma} Pro12Ala polymorphism and risk for incident sporadic colorectal adenomas.

Gong Z, Xie D, Deng Z, Bostick RM, Muga SJ, Hurley TG, Hebert JR.

Carcinogenesis. 2005 Mar;26(3):579-85. Epub 2004 Nov 25.


Inheritance of the 194Trp and the 399Gln variant alleles of the DNA repair gene XRCC1 are associated with increased risk of early-onset colorectal carcinoma in Egypt.

Abdel-Rahman SZ, Soliman AS, Bondy ML, Omar S, El-Badawy SA, Khaled HM, Seifeldin IA, Levin B.

Cancer Lett. 2000 Oct 16;159(1):79-86.


TP53 codon 72 polymorphism is associated with age at onset of glioblastoma.

El Hallani S, Ducray F, Idbaih A, Marie Y, Boisselier B, Colin C, Laigle-Donadey F, Rodéro M, Chinot O, Thillet J, Hoang-Xuan K, Delattre JY, Sanson M.

Neurology. 2009 Jan 27;72(4):332-6. doi: 10.1212/


MC1R genotype modifies risk of melanoma in families segregating CDKN2A mutations.

Box NF, Duffy DL, Chen W, Stark M, Martin NG, Sturm RA, Hayward NK.

Am J Hum Genet. 2001 Oct;69(4):765-73. Epub 2001 Aug 8.


DNA sequence analysis of monoamine oxidase B gene coding and promoter regions in Parkinson's disease cases and unrelated controls.

Costa-Mallen P, Afsharinejad Z, Kelada SN, Costa LG, Franklin GM, Swanson PD, Longstreth WT Jr, Viernes HM, Farin FM, Smith-Weller T, Checkoway H.

Mov Disord. 2004 Jan;19(1):76-83.


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