133 related articles for article (PubMed ID: 10798356)
1. Identification of 187 single nucleotide polymorphisms (SNPs) among 41 candidate genes for ischemic heart disease in the Japanese population.
Ohnishi Y; Tanaka T; Yamada R; Suematsu K; Minami M; Fujii K; Hoki N; Kodama K; Nagata S; Hayashi T; Kinoshita N; Sato H; Sato H; Kuzuya T; Takeda H; Hori M; Nakamura Y
Hum Genet; 2000 Mar; 106(3):288-92. PubMed ID: 10798356
[TBL] [Abstract][Full Text] [Related]
2. Identification of 142 single nucleotide polymorphisms in 41 candidate genes for rheumatoid arthritis in the Japanese population.
Yamada R; Tanaka T; Ohnishi Y; Suematsu K; Minami M; Seki T; Yukioka M; Maeda A; Murata N; Saiki O; Teshima R; Kudo O; Ishikawa K; Ueyosi A; Tateishi H; Inaba M; Goto H; Nishizawa Y; Tohma S; Ochi T; Yamamoto K; Nakamura Y
Hum Genet; 2000 Mar; 106(3):293-7. PubMed ID: 10798357
[TBL] [Abstract][Full Text] [Related]
3. Catalog of 46 single-nucleotide polymorphisms (SNPs) in the microsomal glutathione S-transferase 1 (MGST1) gene.
Iida A; Saito S; Sekine A; Harigae S; Osawa S; Mishima C; Kondo K; Kitamura Y; Nakamura Y
J Hum Genet; 2001; 46(10):590-4. PubMed ID: 11587073
[TBL] [Abstract][Full Text] [Related]
4. Novel SNPs in cytochrome P450 oxidoreductase.
Hart SN; Li Y; Nakamoto K; Wesselman C; Zhong XB
Drug Metab Pharmacokinet; 2007 Aug; 22(4):322-6. PubMed ID: 17827787
[TBL] [Abstract][Full Text] [Related]
5. Catalog of 605 single-nucleotide polymorphisms (SNPs) among 13 genes encoding human ATP-binding cassette transporters: ABCA4, ABCA7, ABCA8, ABCD1, ABCD3, ABCD4, ABCE1, ABCF1, ABCG1, ABCG2, ABCG4, ABCG5, and ABCG8.
Iida A; Saito S; Sekine A; Mishima C; Kitamura Y; Kondo K; Harigae S; Osawa S; Nakamura Y
J Hum Genet; 2002; 47(6):285-310. PubMed ID: 12111378
[TBL] [Abstract][Full Text] [Related]
6. Patterns of single-nucleotide polymorphisms in candidate genes for blood-pressure homeostasis.
Halushka MK; Fan JB; Bentley K; Hsie L; Shen N; Weder A; Cooper R; Lipshutz R; Chakravarti A
Nat Genet; 1999 Jul; 22(3):239-47. PubMed ID: 10391210
[TBL] [Abstract][Full Text] [Related]
7. High-density single-nucleotide polymorphism (SNP) map in the 96-kb region containing the entire human DiGeorge syndrome critical region 2 (DGCR2) gene at 22q11.2.
Iida A; Ohnishi Y; Ozaki K; Ariji Y; Nakamura Y; Tanaka T
J Hum Genet; 2001; 46(10):604-8. PubMed ID: 11589220
[TBL] [Abstract][Full Text] [Related]
8. SNP and indel frequencies at transcription start sites and at canonical and alternative translation initiation sites in the human genome.
Neininger K; Marschall T; Helms V
PLoS One; 2019; 14(4):e0214816. PubMed ID: 30978217
[TBL] [Abstract][Full Text] [Related]
9. Genetic variations of VDR/NR1I1 encoding vitamin D receptor in a Japanese population.
Ukaji M; Saito Y; Fukushima-Uesaka H; Maekawa K; Katori N; Kaniwa N; Yoshida T; Nokihara H; Sekine I; Kunitoh H; Ohe Y; Yamamoto N; Tamura T; Saijo N; Sawada J
Drug Metab Pharmacokinet; 2007 Dec; 22(6):462-7. PubMed ID: 18159135
[TBL] [Abstract][Full Text] [Related]
10. Identification of 46 novel SNPs in the 130-kb region containing a myocardial infarction susceptibility gene on chromosomal band 6p21.
Iida A; Ozaki K; Ohnishi Y; Tanaka T; Nakamura Y
J Hum Genet; 2003; 48(9):476-479. PubMed ID: 12920609
[TBL] [Abstract][Full Text] [Related]
11. Polymorphism of BMP4 gene in Indian goat breeds differing in prolificacy.
Sharma R; Ahlawat S; Maitra A; Roy M; Mandakmale S; Tantia MS
Gene; 2013 Dec; 532(1):140-5. PubMed ID: 24013084
[TBL] [Abstract][Full Text] [Related]
12. Identification of genetic variation in the 5' and 3' non-coding regions of the protamine genes in patients with protamine deregulation.
Hammoud S; Emery BR; Aoki VW; Carrell DT
Arch Androl; 2007; 53(5):267-74. PubMed ID: 18309899
[TBL] [Abstract][Full Text] [Related]
13. Highlight on DPYD gene polymorphisms and treatment by capecitabine (.).
Milano G
Scand J Clin Lab Invest Suppl; 2016; 245():S30-3. PubMed ID: 27454530
[TBL] [Abstract][Full Text] [Related]
14. Single nucleotide polymorphism analyses of the human proliferating cell nuclear antigen (pCNA) and flap endonuclease (FEN1) genes.
Ma X; Jin Q; Försti A; Hemminki K; Kumar R
Int J Cancer; 2000 Dec; 88(6):938-42. PubMed ID: 11093818
[TBL] [Abstract][Full Text] [Related]
15. High-density SNP map of human ITR, a gene associated with vascular remodeling.
Iida A; Tanaka T; Nakamura Y
J Hum Genet; 2003; 48(4):170-2. PubMed ID: 12730718
[TBL] [Abstract][Full Text] [Related]
16. Catalog of 86 single-nucleotide polymorphisms (SNPs) in three uridine diphosphate glycosyltransferase genes: UGT2A1, UGT2B15, and UGT8.
Iida A; Saito S; Sekine A; Mishima C; Kitamura Y; Kondo K; Harigae S; Osawa S; Nakamura Y
J Hum Genet; 2002; 47(10):505-10. PubMed ID: 12376738
[TBL] [Abstract][Full Text] [Related]
17. Identification of 197 genetic variations in six human methyltranferase genes in the Japanese population.
Saito S; Iida A; Sekine A; Miura Y; Sakamoto T; Ogawa C; Kawauchi S; Higuchi S; Nakamura Y
J Hum Genet; 2001; 46(9):529-37. PubMed ID: 11558902
[TBL] [Abstract][Full Text] [Related]
18. Human calcitonin receptor-like receptor for adrenomedullin: genomic structure, eight single-nucleotide polymorphisms, and haplotype analysis.
Nakazawa I; Nakajima T; Harada H; Ishigami T; Umemura S; Emi M
J Hum Genet; 2001; 46(3):132-6. PubMed ID: 11310580
[TBL] [Abstract][Full Text] [Related]
19. Catalog of 434 single-nucleotide polymorphisms (SNPs) in genes of the alcohol dehydrogenase, glutathione S-transferase, and nicotinamide adenine dinucleotide, reduced (NADH) ubiquinone oxidoreductase families.
Iida A; Saito S; Sekine A; Kitamoto T; Kitamura Y; Mishima C; Osawa S; Kondo K; Harigae S; Nakamura Y
J Hum Genet; 2001; 46(7):385-407. PubMed ID: 11450848
[TBL] [Abstract][Full Text] [Related]
20. Abundant sequence divergence in the native Japanese cattle Mishima-Ushi (Bos taurus) detected using whole-genome sequencing.
Tsuda K; Kawahara-Miki R; Sano S; Imai M; Noguchi T; Inayoshi Y; Kono T
Genomics; 2013 Oct; 102(4):372-8. PubMed ID: 23938316
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
