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Prevalence of the HOXB13 G84E prostate cancer risk allele in men treated with radical prostatectomy.
- Published in:
- BJU International, 2014, v. 113, n. 5, p. 830, doi. 10.1111/bju.12522
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- Article
Chromosomes 4 and 8 implicated in a genome wide SNP linkage scan of 762 prostate cancer families collected by the ICPCG.
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- Prostate, 2012, v. 72, n. 4, p. 410, doi. 10.1002/pros.21443
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- Publication type:
- Article
Human polymorphisms at long non-coding RNAs (lncRNAs) and association with prostate cancer risk.
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- Carcinogenesis, 2011, v. 32, n. 11, p. 1655, doi. 10.1093/carcin/bgr187
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- Publication type:
- Article
Individual and cumulative effect of prostate cancer risk-associated variants on clinicopathologic variables in 5,895 prostate cancer patients.
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- Prostate, 2009, v. 69, n. 11, p. 1195, doi. 10.1002/pros.20970
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- Publication type:
- Article
Fine mapping association study and functional analysis implicate a SNP in MSMB at 10q11 as a causal variant for prostate cancer risk.
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- Human Molecular Genetics, 2009, v. 18, n. 7, p. 1368, doi. 10.1093/hmg/ddp035
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- Article
Evidence for two independent prostate cancer risk–associated loci in the HNF1B gene at 17q12.
- Published in:
- Nature Genetics, 2008, v. 40, n. 10, p. 1153, doi. 10.1038/ng.214
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- Article
Cumulative effect of five genetic variants on prostate cancer risk in multiple study populations.
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- Prostate, 2008, v. 68, n. 12, p. 1257, doi. 10.1002/pros.20793
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- Publication type:
- Article
Association between sequence variants at 17q12 and 17q24.3 and prostate cancer risk in European and African Americans.
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- Prostate, 2008, v. 68, n. 7, p. 691, doi. 10.1002/pros.20754
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- Publication type:
- Article
Chromosome 8q24 risk variants in hereditary and non-hereditary prostate cancer patients.
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- Prostate, 2008, v. 68, n. 5, p. 489, doi. 10.1002/pros.20695
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- Publication type:
- Article
Two Genome-wide Association Studies of Aggressive Prostate Cancer Implicate Putative Prostate Tumor Suppressor Gene DAB2IP.
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- JNCI: Journal of the National Cancer Institute, 2007, v. 99, n. 24, p. 1836, doi. 10.1093/jnci/djm250
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- Publication type:
- Article
Association Between Two Unlinked Loci at 8q24 and Prostate Cancer Risk Among European Americans.
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- JNCI: Journal of the National Cancer Institute, 2007, v. 99, n. 20, p. 1525, doi. 10.1093/jnci/djm169
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- Article
Germline ATBF1 mutations and prostate cancer risk.
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- Prostate, 2006, v. 66, n. 10, p. 1082, doi. 10.1002/pros.20430
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- Publication type:
- Article
Two-locus genome-wide linkage scan for prostate cancer susceptibility genes with an interaction effect.
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- Human Genetics, 2006, v. 118, n. 6, p. 716, doi. 10.1007/s00439-005-0099-4
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- Publication type:
- Article
Genome-wide screen for prostate cancer susceptibility genes in men with clinically significant disease.
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- Prostate, 2005, v. 64, n. 4, p. 356, doi. 10.1002/pros.20249
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- Article
Mutational analysis of PINX1 in hereditary prostate cancer.
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- Prostate, 2004, v. 60, n. 4, p. 298, doi. 10.1002/pros.20075
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- Publication type:
- Article
Combined Genome-Wide Scan for Prostate Cancer Susceptibility Genes.
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- JNCI: Journal of the National Cancer Institute, 2004, v. 96, n. 16, p. 1240, doi. 10.1093/jnci/djh228
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- Article
Interaction effect of PTEN and CDKN1B chromosomal regions on prostate cancer linkage.
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- Human Genetics, 2004, v. 115, n. 3, p. 255
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- Publication type:
- Article
Genome-wide scan for prostate cancer susceptibility genes in the Johns Hopkins hereditary prostate cancer families(Jianfeng Xu and Elizabeth M. Gillanders contributed equally to this study.).
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- Prostate, 2003, v. 57, n. 4, p. 320, doi. 10.1002/pros.10306
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- Publication type:
- Article
Polymorphisms in the CYP1A1 gene are associated with prostate cancer risk.
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- International Journal of Cancer, 2003, v. 106, n. 3, p. 375, doi. 10.1002/ijc.11249
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- Article
Evaluation of SRD5A2 sequence variants in susceptibility to hereditary and sporadic prostate cancer.
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- Prostate, 2003, v. 56, n. 1, p. 37, doi. 10.1002/pros.10225
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- Publication type:
- Article
Sequence variants in the human 25-hydroxyvitamin D<sub>3</sub> 1-α-hydroxylase (CYP27B1) gene are not associated with prostate cancer risk.
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- Prostate, 2002, v. 53, n. 3, p. 175, doi. 10.1002/pros.10144
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- Article
Germline mutations and sequence variants of the macrophage scavenger receptor 1 gene are associated with prostate cancer risk.
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- Nature Genetics, 2002, v. 32, n. 2, p. 321, doi. 10.1038/ng994
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- Publication type:
- Article
Polymorphic GGC repeats in the androgen receptor gene are associated with hereditary and sporadic prostate cancer risk.
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- Human Genetics, 2002, v. 110, n. 2, p. 122, doi. 10.1007/s00439-001-0662-6
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- Publication type:
- Article
Linkage and association of CYP17 gene in hereditary and sporadic prostate cancer.
- Published in:
- International Journal of Cancer, 2001, v. 95, n. 6, p. 354, doi. 10.1002/1097-0215(20011120)95:6<354::AID-IJC1062>3.0.CO;2-3
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- Publication type:
- Article
Evidence for a prostate cancer linkage to chromosome 20 in 159 hereditary prostate cancer families.
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- Human Genetics, 2001, v. 108, n. 5, p. 430, doi. 10.1007/s004390100513
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- Publication type:
- Article
Linkage of prostate cancer susceptibility loci to chromosome 1.
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- Human Genetics, 2001, v. 108, n. 4, p. 335, doi. 10.1007/s004390100488
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- Article
No evidence for a role of BRCA1 or BRCA2 mutations in Ashkenazi Jewish families with hereditary prostate cancer.
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- Prostate, 1999, v. 39, n. 4, p. 280, doi. 10.1002/(SICI)1097-0045(19990601)39:4<280::AID-PROS8>3.0.CO;2-F
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- Publication type:
- Article
Characteristics of prostate cancer in families potentially linked to the hereditary prostate cancer
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- JAMA: Journal of the American Medical Association, 1997, v. 278, n. 15, p. 1251, doi. 10.1001/jama.1997.03550150055035
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- Article
Risk of cancer in relatives of prostate cancer probands.
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- JNCI: Journal of the National Cancer Institute, 1995, v. 87, n. 13, p. 991, doi. 10.1093/jnci/87.13.991
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- Article
Derivation and validation of a quantitative definition of specific reading disability for adults.
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- 1984
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- Publication type:
- journal article
Empirical Validation of Reading and Spelling Quotients.
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- Developmental Medicine & Child Neurology, 1982, v. 24, n. s45, p. 733, doi. 10.1111/j.1469-8749.1982.tb13695.x
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- Article