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19 results
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A novel family of bromodomain genes.
Jones MH, Hamana N, Nezu Ji, Shimane M. Jones MH, et al. Among authors: nezu ji. Genomics. 2000 Jan 1;63(1):40-5. doi: 10.1006/geno.1999.6071. Genomics. 2000. PMID: 10662543
Molecular identification and characterization of novel members of the human organic anion transporter (OATP) family.
Tamai I, Nezu J, Uchino H, Sai Y, Oku A, Shimane M, Tsuji A. Tamai I, et al. Biochem Biophys Res Commun. 2000 Jun 24;273(1):251-60. doi: 10.1006/bbrc.2000.2922. Biochem Biophys Res Commun. 2000. PMID: 10873595
Loss of cytoplasmic retention ability of mutant LKB1 found in Peutz-Jeghers syndrome patients.
Nezu J, Oku A, Shimane M. Nezu J, et al. Biochem Biophys Res Commun. 1999 Aug 11;261(3):750-5. doi: 10.1006/bbrc.1999.1047. Biochem Biophys Res Commun. 1999. PMID: 10441497
Primary systemic carnitine deficiency is caused by mutations in a gene encoding sodium ion-dependent carnitine transporter.
Nezu J, Tamai I, Oku A, Ohashi R, Yabuuchi H, Hashimoto N, Nikaido H, Sai Y, Koizumi A, Shoji Y, Takada G, Matsuishi T, Yoshino M, Kato H, Ohura T, Tsujimoto G, Hayakawa J, Shimane M, Tsuji A. Nezu J, et al. Nat Genet. 1999 Jan;21(1):91-4. doi: 10.1038/5030. Nat Genet. 1999. PMID: 9916797
Molecular cloning of a novel vascular endothelial growth factor, VEGF-D.
Yamada Y, Nezu J, Shimane M, Hirata Y. Yamada Y, et al. Genomics. 1997 Jun 15;42(3):483-8. doi: 10.1006/geno.1997.4774. Genomics. 1997. PMID: 9205122
Identification of two novel human putative serine/threonine kinases, VRK1 and VRK2, with structural similarity to vaccinia virus B1R kinase.
Nezu J, Oku A, Jones MH, Shimane M. Nezu J, et al. Genomics. 1997 Oct 15;45(2):327-31. doi: 10.1006/geno.1997.4938. Genomics. 1997. PMID: 9344656
No evidence of Peutz-Jeghers syndrome gene LKB1 involvement in left-sided colorectal carcinomas.
Launonen V, Avizienyte E, Loukola A, Laiho P, Salovaara R, Järvinen H, Mecklin JP, Oku A, Shimane M, Kim HC, Kim JC, Nezu J, Aaltonen LA. Launonen V, et al. Cancer Res. 2000 Feb 1;60(3):546-8. Cancer Res. 2000. PMID: 10676634
Peutz-Jeghers syndrome is caused by mutations in a novel serine threonine kinase.
Jenne DE, Reimann H, Nezu J, Friedel W, Loff S, Jeschke R, Müller O, Back W, Zimmer M. Jenne DE, et al. Nat Genet. 1998 Jan;18(1):38-43. doi: 10.1038/ng0198-38. Nat Genet. 1998. PMID: 9425897
Loss of LKB1 kinase activity in Peutz-Jeghers syndrome, and evidence for allelic and locus heterogeneity.
Mehenni H, Gehrig C, Nezu J, Oku A, Shimane M, Rossier C, Guex N, Blouin JL, Scott HS, Antonarakis SE. Mehenni H, et al. Am J Hum Genet. 1998 Dec;63(6):1641-50. doi: 10.1086/302159. Am J Hum Genet. 1998. PMID: 9837816 Free PMC article.
Controlled conductivity at low pH in Protein L chromatography enables separation of bispecific and other antibody formats by their binding valency.
Chen C, Wakabayashi T, Muraoka M, Shu F, Wei Shan C, Chor Kun C, Tim Jang C, Soehano I, Shimizu Y, Igawa T, Nezu JI. Chen C, et al. Among authors: nezu ji. MAbs. 2019 May/Jun;11(4):632-638. doi: 10.1080/19420862.2019.1583996. Epub 2019 Mar 21. MAbs. 2019. PMID: 30898021 Free PMC article.
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