206 related articles for article (PubMed ID: 15177551)
1. Many amino acid substitution variants identified in DNA repair genes during human population screenings are predicted to impact protein function.
Xi T; Jones IM; Mohrenweiser HW
Genomics; 2004 Jun; 83(6):970-9. PubMed ID: 15177551
[TBL] [Abstract][Full Text] [Related]
2. Identification of 127 amino acid substitution variants in screening 37 DNA repair genes in humans.
Mohrenweiser HW; Xi T; Vázquez-Matías J; Jones IM
Cancer Epidemiol Biomarkers Prev; 2002 Oct; 11(10 Pt 1):1054-64. PubMed ID: 12376507
[TBL] [Abstract][Full Text] [Related]
3. Computational prediction of the effects of non-synonymous single nucleotide polymorphisms in human DNA repair genes.
Nakken S; Alseth I; Rognes T
Neuroscience; 2007 Apr; 145(4):1273-9. PubMed ID: 17055652
[TBL] [Abstract][Full Text] [Related]
4. Bioinformatic processing to identify single nucleotide polymorphism that potentially affect Ape1 function.
Yu ET; Hadi MZ
Mutat Res; 2011 Jun; 722(2):140-6. PubMed ID: 20633698
[TBL] [Abstract][Full Text] [Related]
5. A bioinformatics approach for the phenotype prediction of nonsynonymous single nucleotide polymorphisms in human cytochromes P450.
Wang LL; Li Y; Zhou SF
Drug Metab Dispos; 2009 May; 37(5):977-91. PubMed ID: 19204079
[TBL] [Abstract][Full Text] [Related]
6. Survey of polymorphic sequence variation in the immediate 5' region of human DNA repair genes.
Mohrenweiser H
Mutat Res; 2007 Mar; 616(1-2):221-6. PubMed ID: 17161851
[TBL] [Abstract][Full Text] [Related]
7. Computational approaches for predicting the biological effect of p53 missense mutations: a comparison of three sequence analysis based methods.
Mathe E; Olivier M; Kato S; Ishioka C; Hainaut P; Tavtigian SV
Nucleic Acids Res; 2006; 34(5):1317-25. PubMed ID: 16522644
[TBL] [Abstract][Full Text] [Related]
8. Screening for deleterious nonsynonymous single-nucleotide polymorphisms in genes involved in steroid hormone metabolism and response.
Johnson MM; Houck J; Chen C
Cancer Epidemiol Biomarkers Prev; 2005 May; 14(5):1326-9. PubMed ID: 15894696
[TBL] [Abstract][Full Text] [Related]
9. Significance of amino acid substitution variants of DNA repair genes in radiosusceptibility of cervical cancer patients; a pilot study.
Farkasova T; Gurska S; Witkovsky V; Gabelova A
Neoplasma; 2008; 55(4):330-7. PubMed ID: 18505345
[TBL] [Abstract][Full Text] [Related]
10. Genetic diversity and function in the human cytosolic sulfotransferases.
Hildebrandt MA; Carrington DP; Thomae BA; Eckloff BW; Schaid DJ; Yee VC; Weinshilboum RM; Wieben ED
Pharmacogenomics J; 2007 Apr; 7(2):133-43. PubMed ID: 16801938
[TBL] [Abstract][Full Text] [Related]
11. In silico searching for disease-associated functional DNA variants.
Sethumadhavan R; Doss CG; Rajasekaran R
Methods Mol Biol; 2011; 760():239-50. PubMed ID: 21780001
[TBL] [Abstract][Full Text] [Related]
12. A Ser326Cys polymorphism in the DNA repair gene hOGG1 is not associated with sporadic Alzheimer's disease.
Coppedè F; Mancuso M; Lo Gerfo A; Manca ML; Petrozzi L; Migliore L; Siciliano G; Murri L
Neurosci Lett; 2007 Mar; 414(3):282-5. PubMed ID: 17240059
[TBL] [Abstract][Full Text] [Related]
13. Specific combinations of DNA repair gene variants and increased risk for non-small cell lung cancer.
Popanda O; Schattenberg T; Phong CT; Butkiewicz D; Risch A; Edler L; Kayser K; Dienemann H; Schulz V; Drings P; Bartsch H; Schmezer P
Carcinogenesis; 2004 Dec; 25(12):2433-41. PubMed ID: 15333465
[TBL] [Abstract][Full Text] [Related]
14. Distinguishing cancer-associated missense mutations from common polymorphisms.
Kaminker JS; Zhang Y; Waugh A; Haverty PM; Peters B; Sebisanovic D; Stinson J; Forrest WF; Bazan JF; Seshagiri S; Zhang Z
Cancer Res; 2007 Jan; 67(2):465-73. PubMed ID: 17234753
[TBL] [Abstract][Full Text] [Related]
15. Estimating the effect of human base excision repair protein variants on the repair of oxidative DNA base damage.
Sokhansanj BA; Wilson DM
Cancer Epidemiol Biomarkers Prev; 2006 May; 15(5):1000-8. PubMed ID: 16702383
[TBL] [Abstract][Full Text] [Related]
16. Statistical geometry based prediction of nonsynonymous SNP functional effects using random forest and neuro-fuzzy classifiers.
Barenboim M; Masso M; Vaisman II; Jamison DC
Proteins; 2008 Jun; 71(4):1930-9. PubMed ID: 18186470
[TBL] [Abstract][Full Text] [Related]
17. Prediction of deleterious functional effects of non-synonymous single nucleotide polymorphisms in human nuclear receptor genes using a bioinformatics approach.
Liu YH; Li CG; Zhou SF
Drug Metab Lett; 2009 Dec; 3(4):242-86. PubMed ID: 20050372
[TBL] [Abstract][Full Text] [Related]
18. Phenotype prediction of deleterious nonsynonymous single nucleotide polymorphisms in human alcohol metabolism-related genes: a bioinformatics study.
Wang LL; Yang AK; Li Y; Liu JP; Zhou SF
Alcohol; 2010 Aug; 44(5):425-38. PubMed ID: 20804942
[TBL] [Abstract][Full Text] [Related]
19. Familial adenomatous polyposis: aberrant splicing due to missense or silent mutations in the APC gene.
Aretz S; Uhlhaas S; Sun Y; Pagenstecher C; Mangold E; Caspari R; Möslein G; Schulmann K; Propping P; Friedl W
Hum Mutat; 2004 Nov; 24(5):370-80. PubMed ID: 15459959
[TBL] [Abstract][Full Text] [Related]
20. Functional effects of protein sequence polymorphisms in the organic cation/ergothioneine transporter OCTN1 (SLC22A4).
Urban TJ; Yang C; Lagpacan LL; Brown C; Castro RA; Taylor TR; Huang CC; Stryke D; Johns SJ; Kawamoto M; Carlson EJ; Ferrin TE; Burchard EG; Giacomini KM
Pharmacogenet Genomics; 2007 Sep; 17(9):773-82. PubMed ID: 17700366
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]