Genomic medicine, gene polymorphisms, and human biological diversity

Seminars in Dialysis

Volumn 18, Issue 1, 2005, Pages 37-40

  Balakrishnan, Vaidyanathapuram S ^a   Rao, Madhumathi ^a   Jaber, Bertrand L ^b  

^a TUFTS MEDICAL CENTER   (United States)

^b ST ELIZABETH'S MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; MICROSATELLITE DNA;

ALLELE; BIODIVERSITY; BIOINFORMATICS; CELL FUNCTION; DIALYSIS; DNA SEQUENCE; ENVIRONMENTAL FACTOR; GENE DELETION; GENE EXPRESSION; GENE FREQUENCY; GENE FUNCTION; GENE INSERTION; GENE INTERACTION; GENE SEQUENCE; GENETIC ANALYSIS; GENETIC POLYMORPHISM; GENETIC VARIABILITY; GENOME ANALYSIS; GENOMICS; GENOTYPE; HEALTH; HEALTH CARE; HUMAN GENOME; HUMAN GENOME PROJECT; MEDICAL GENETICS; MEDICAL INFORMATION; MEDICINE; MOLECULAR EVOLUTION; PHENOTYPE; REGULATORY MECHANISM; REVIEW; SCIENCE; SEQUENCE ANALYSIS; SIGNAL TRANSDUCTION; SINGLE NUCLEOTIDE POLYMORPHISM; SOCIAL ASPECT; VARIABLE NUMBER OF TANDEM REPEAT;

BIODIVERSITY; GENETIC PREDISPOSITION TO DISEASE; GENOME, HUMAN; GENOTYPE; HUMANS; KIDNEY FAILURE, CHRONIC; POLYMORPHISM, GENETIC; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 14844309756     PISSN: 08940959     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1525-139X.2005.18102.x     Document Type: Review

References (17)

1. Lander E, Linton L, Birren B: Initial sequencing and analysis of the human genome. Nature 409:860-921, 2001
2. Venter J, Adams M, Myers E: The sequence of the human genome. Science 291:1304-1351, 2001
3. McKusik V, Ruddle F: A new discipline, a new name, a new journal. Genomics 1:1-2, 1987
4. Armstrong K, Eisen A, Weber B: Assessing the risk of breast cancer. N Engl J Med 342:564-571, 2000
5. Lynch H: Hereditary nonpolyposis colorectal cancer. Cytogenet Cell Genet 86:130-135, 1999
6. Michael N: Host genetic influences on HIV-1 pathogenesis. Curr Opin Immunol 11:466-474, 1999
7. Small P, Fujiwara P: Management of tuberculosis in the United States. N Engl J Med 345:189-200, 2001
8. Mouradian M: Recent advances in the genetics and pathogenesis of Parkinson disease. Neurology 58:179-185, 2002
9. St. George-Hyslop P: Molecular genetics of Alzheimer's disease. Semin Neurol 19:371-383, 1999
10. Anderson S, Bankier A, Barriel A: Sequence and organization of the human mitochondrial genome. Nature 290:457-474, 1981
11. Gravely B: Alternative splicing: increased diversity in the proteomic world. Trends Genet 17:100-107, 2001
12. Wang D, Fan J, Siao C: Large-scale identification, mapping and genotyping of single nucleotide polymorphisms in the human genome. Science 280:1077-1082, 1998
13. Saiki RK, Walsh PS, Levenson CH, Erlich HA: Genetic analysis of amplified DNA with immobilized sequence-specific oligonucleotide probes. Proc Natl Acad Sci 86:6230-6234, 1989
14. Chee M, Yang R, Hubbell E: Accessing genetic information with high density DNA arrays. Science 274:610-614, 1996
15. Syvanen A: From gels to chips: "minisequencing" primer extension for analysis of point mutations and single nucleotide polymorphisms. Hum Mutat 13:1-10, 1999
16. Day I, Humphries S: Electrophoresis for genotyping: microtitre array diagonal gel electrophoresis (MADGE) on horizontal polyacrylamide (H-PAGE) gels, Hydrolink, or agarose. Anal Biochem 222:389-395, 1994
17. Ronaghi M, Uhlen M, Nyren P: A sequencing method based on real-time pyrophosphate detection. Science 281:363-365, 1998