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12,388 results
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Isolation and characterization of a novel serine threonine kinase gene on chromosome 3p22-21.3.
Tamari M, Daigo Y, Nakamura Y. Tamari M, et al. Among authors: nakamura y. J Hum Genet. 1999;44(2):116-20. doi: 10.1007/s100380050121. J Hum Genet. 1999. PMID: 10083736
Ataxin-7 associates with microtubules and stabilizes the cytoskeletal network.
Nakamura Y, Tagawa K, Oka T, Sasabe T, Ito H, Shiwaku H, La Spada AR, Okazawa H. Nakamura Y, et al. Hum Mol Genet. 2012 Mar 1;21(5):1099-110. doi: 10.1093/hmg/ddr539. Epub 2011 Nov 18. Hum Mol Genet. 2012. PMID: 22100762 Free PMC article.
Somatic mutations of a human mismatch repair gene, hMLH1, in tumors from patients with multiple primary cancers.
Sasaki S, Horii A, Shimada M, Han HJ, Yanagisawa A, Muto T, Nakamura Y. Sasaki S, et al. Among authors: nakamura y. Hum Mutat. 1996;7(3):275-8. doi: 10.1002/(SICI)1098-1004(1996)7:3<275::AID-HUMU15>3.0.CO;2-#. Hum Mutat. 1996. PMID: 8829664 No abstract available.
Isolation of novel mouse genes associated with ectopic ossification by differential display method using ttw, a mouse model for ectopic ossification.
Koshizuka Y, Ikegawa S, Sano M, Nakamura K, Nakamura Y. Koshizuka Y, et al. Among authors: nakamura k, nakamura y. Cytogenet Cell Genet. 2001;94(3-4):163-8. doi: 10.1159/000048809. Cytogenet Cell Genet. 2001. PMID: 11856874
Isolation of a novel human gene, MARKL1, homologous to MARK3 and its involvement in hepatocellular carcinogenesis.
Kato T, Satoh S, Okabe H, Kitahara O, Ono K, Kihara C, Tanaka T, Tsunoda T, Yamaoka Y, Nakamura Y, Furukawa Y. Kato T, et al. Among authors: nakamura y. Neoplasia. 2001 Jan-Feb;3(1):4-9. doi: 10.1038/sj.neo.7900132. Neoplasia. 2001. PMID: 11326310 Free PMC article.
Associations of distinct variants of the intestinal mucin gene MUC3A with ulcerative colitis and Crohn's disease.
Kyo K, Muto T, Nagawa H, Lathrop GM, Nakamura Y. Kyo K, et al. Among authors: nakamura y. J Hum Genet. 2001;46(1):5-20. doi: 10.1007/s100380170118. J Hum Genet. 2001. PMID: 11289722
Structural organization, complete genomic sequences and mutational analyses of the Fukuyama-type congenital muscular dystrophy gene, fukutin.
Kobayashi K, Sasaki J, Kondo-Iida E, Fukuda Y, Kinoshita M, Sunada Y, Nakamura Y, Toda T. Kobayashi K, et al. Among authors: nakamura y. FEBS Lett. 2001 Feb 2;489(2-3):192-6. doi: 10.1016/s0014-5793(01)02088-9. FEBS Lett. 2001. PMID: 11165248
Twenty single nucleotide polymorphisms (SNPs) and their allelic frequencies in four genes that are responsible for familial long QT syndrome in the Japanese population.
Iwasa H, Itoh T, Nagai R, Nakamura Y, Tanaka T. Iwasa H, et al. Among authors: nakamura y. J Hum Genet. 2000;45(3):182-3. doi: 10.1007/s100380050207. J Hum Genet. 2000. PMID: 10807545
The Fukuyama congenital muscular dystrophy story.
Toda T, Kobayashi K, Kondo-Iida E, Sasaki J, Nakamura Y. Toda T, et al. Among authors: nakamura y. Neuromuscul Disord. 2000 Mar;10(3):153-9. doi: 10.1016/s0960-8966(99)00109-1. Neuromuscul Disord. 2000. PMID: 10734260 Review.
[Impact of human genome analysis on the future medicine].
Nakamura Y. Nakamura Y. Nihon Yakurigaku Zasshi. 1999 Sep;114(3):126-30. doi: 10.1254/fpj.114.126. Nihon Yakurigaku Zasshi. 1999. PMID: 10553575 Review. Japanese.
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