Analysis of the RNASEL gene in familial and sporadic prostate cancer

American Journal of Human Genetics

Volumn 71, Issue 1, 2002, Pages 116-123

  Wang, Liang ^a   McDonnell, Shannon K ^a   Elkins, David A ^a   Slager, Susan L ^a   Christensen, Eric ^a   Marks, Angela F ^a   Cunningham, Julie M ^a   Peterson, Brett J ^a   Jacobsen, Steven J ^a   Cerhan, James R ^a   Blute, Michael L ^b   Schaid, Daniel J ^a   Thibodeau, Stephen N ^a  

^a MAYO CLINIC   (United States)

^b DEPARTMENT OF UROLOGY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AGED; ARTICLE; CANCER GENETICS; CANCER RISK; CHROMOSOME 1Q; CONTROLLED STUDY; DNA POLYMORPHISM; EXON; FAMILIAL CANCER; GEL ELECTROPHORESIS; GENE; GENE MUTATION; GENETIC ASSOCIATION; GENETIC RISK; GENOTYPE; HUMAN; INTRON; MAJOR CLINICAL STUDY; MALE; MISSENSE MUTATION; POPULATION RESEARCH; PRIORITY JOURNAL; PROSTATE CANCER; RNASEL GENE;

EID: 18444374189     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/341281     Document Type: Article

References (34)

1. Evidence for a prostate cancer-susceptibility locus on chromosome 20
2. Predisposing gene for early-onset prostate cancer, localized on chromosome 1q42.2-43
3. Genetic epidemiology of prostate cancer in the Utah Mormon genealogy
4. Germline mutations in the RNASEL gene in HPC1 linked families
5. Mendelian inheritance of familial prostate cancer
6. BRCA2 germline mutations in male breast cancer cases and breast cancer families
7. Conformation-sensitive gel electrophoresis for rapid detection of single-base differences in double-stranded PCR products and DNA fragments: Evidence for solvent-induced bends in DNA heteroduplexes
8. Analysis of chromosome 1q42.2-43 in 152 families with high risk of prostate cancer
9. Systematic population-based assessment of cancer risk in first-degree relatives of cancer probands
10. 2 and C colorectal cancers
11. A dominant negative mutant of 2-5A-dependent RNase suppresses antiproliferative and antiviral effects of interferon
12. Conformation sensitive gel electrophoresis for simple and accurate detection of mutations: Comparison with denaturing gradient gel electrophoresis and nucleotide sequencing
13. Tumor-suppressor genes: News about the interferon connection
14. Familial prostatic cancer risk and low testosterone
15. History of the Rochester Epidemiology Project
16. Serum prostate-specific antigen in a community-based population of healthy men: Establishment of age-specific reference ranges
17. Multiplex CSGE: A universal mutation screening method
18. Association of HPC2/ELAC2 genotypes and prostate cancer
19. Longitudinal changes in peak urinary flow rates in a community-based cohort
20. ELAC2/HPC2 involvement in hereditary and sporadic prostate cancer
21. From genotypes to genes: Doubling the sample size
22. Evidence for autosomal dominant inheritance of prostate cancer
23. Evaluation of candidate genes in case-control studies: A statistical method to account for related subjects
24. Major susceptibility locus for prostate cancer on chromosome 1 suggested by a genome-wide search
25. Familial patterns of prostate cancer: A case-control analysis
26. Family history and the risk of prostate cancer
27. Polymorphisms in the prostate cancer susceptibility gene HPC2/ELAC2 in multiplex families and healthy controls
28. A candidate prostate cancer susceptibility gene at chromosome 17p
29. Microsatellite instability in colorectal cancer: Different mutator phenotypes and the principal involvement of hMLH1
30. Role of HPC2/ELAC2 in hereditary prostate cancer
31. Family history and prostate cancer risk in black, white, and Asian men in the United States and Canada
32. Evidence for a prostate cancer susceptibility locus on the X chromosome
33. Evaluation of linkage and association of HPC2/ELAC2 in patients with familial or sporadic prostate cancer
34. Longitudinal data analysis for discrete and continuous outcomes