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1 - 25 of 28 results for author:"Sugiyama N."Drop in Literature Citations

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Identification of DNA-dependent protein kinase as a cofactor for the forkhead transcription factor FoxA2.

Nock A., Ascano J.M., Jones T., Barrero M.J., Sugiyama N., Tomita M., Ishihama Y., Malik S.

J. Biol. Chem. 284:19915-19926(2009) · Mapped (1)

Secretion of active membrane type 1 matrix metalloproteinase (MMP-14) into extracellular space in microvesicular exosomes.

Hakulinen J., Sankkila L., Sugiyama N., Lehti K., Keski-Oja J.

J. Cell. Biochem. 105:1211-1218(2008) · Mapped (4)

Large-scale phosphorylation mapping reveals the extent of tyrosine phosphorylation in Arabidopsis.

Sugiyama N., Nakagami H., Mochida K., Daudi A., Tomita M., Shirasu K., Ishihama Y.

Mol. Syst. Biol. 4:193-193(2008) · Mapped (4)

Automated phosphoproteome analysis for cultured cancer cells by two-dimensional nanoLC-MS using a calcined titania/C18 biphasic column.

Imami K., Sugiyama N., Kyono Y., Tomita M., Ishihama Y.

Anal. Sci. 24:161-166(2008) · UniProtKB (450)

Regulation of the interaction of Disabled-1 with CIN85 by phosphorylation with Cyclin-dependent kinase 5.

Sato Y., Taoka M., Sugiyama N., Kubo K., Fuchigami T., Asada A., Saito T., Nakajima K., Isobe T., Hisanaga S.

Genes Cells 12:1315-1327(2007) · Mapped (12)

Involvement of cAMP response element-binding protein in the regulation of cell proliferation and the prolactin promoter of lactotrophs in primary culture.

Ishida M., Mitsui T., Yamakawa K., Sugiyama N., Takahashi W., Shimura H., Endo T., Kobayashi T., Arita J.

Am. J. Physiol. Endocrinol. Metab. 293:E1529-37(2007) · Mapped (1)

Isolation and characterization of okadaic acid binding proteins from the marine sponge Halichondria okadai.

Sugiyama N., Konoki K., Tachibana K.

Biochemistry 46:11410-11420(2007) · UniProtKB (3)

Complete nucleotide sequence of a Japanese isolate of Chrysanthemum virus B (genus Carlavirus).

Ohkawa A., Yamada M., Sayama H., Sugiyama N., Okuda S., Natsuaki T.

Arch. Virol. 152:2253-2258(2007) · UniProtKB (6)

Molecular cloning of grammistins, peptide toxins from the soapfish Pogonoperca punctata, by hemolytic screening of a cDNA library.

Kaji T., Sugiyama N., Ishizaki S., Nagashima Y., Shiomi K.

Peptides 27:3069-3076(2006) · UniProtKB (6)

Sustained cell proliferation of renal epithelial cells in mice with inv mutation.

Sugiyama N., Yokoyama T.

Genes Cells 11:1213-1224(2006) · Mapped (4)

Membranous glomerulonephritis development with Th2-type immune deviations in MRL/lpr mice deficient for IL-27 receptor (WSX-1).

Shimizu S., Sugiyama N., Masutani K., Sadanaga A., Miyazaki Y., Inoue Y., Akahoshi M., Katafuchi R., Hirakata H., Harada M. et al.

J. Immunol. 175:7185-7192(2005) · Mapped (6)

Further isolation and characterization of grammistins from the skin secretion of the soapfish Grammistes sexlineatus.

Sugiyama N., Araki M., Ishida M., Nagashima Y., Shiomi K.

Toxicon 45:595-601(2005) · UniProtKB (7)

Mesonephric FGF signaling is associated with the development of sexually indifferent gonadal primordium in chick embryos.

Yoshioka H., Ishimaru Y., Sugiyama N., Tsunekawa N., Noce T., Kasahara M., Morohashi K.

Dev. Biol. 280:150-161(2005) · UniProtKB (1)

Mutations of ARX are associated with striking pleiotropy and consistent genotype-phenotype correlation.

Kato M., Das S., Petras K., Kitamura K., Morohashi K., Abuelo D.N., Barr M., Bonneau D., Brady A.F., Carpenter N.J. et al.

Hum. Mutat. 23:147-159(2004) · UniProtKB (1)

Changes in serum levels of hepatocyte growth factor in patients undergoing adult-to-adult living-donor liver transplantation.

Eguchi S., Yanaga K., Okudaira S., Sugiyama N., Miyamoto S., Furui J., Kanematsu T.

Transplantation 76:1769-1770(2003) · Mapped (3)

A Japanese family with familial Alzheimer's disease associated with presenilin 1 mutation: relationship between younger age of onset and ApoE gene polymorphism.

Marui W., Iseki E., Sugiyama N., Matsumura T., Suzuki K., Odawara T., Hino H., Kosaka K.

No To Shinkei 55:349-353(2003) · Mapped (5)

Lack of association in Japanese patients between neuroleptic malignant syndrome and the TaqI A polymorphism of the dopamine D2 receptor gene.

Kishida I., Kawanishi C., Furuno T., Matsumura T., Hasegawa H., Sugiyama N., Suzuki K., Yamada Y., Kosaka K.

Psychiatr. Genet. 13:55-57(2003) · Mapped (6)

Mutation of ARX causes abnormal development of forebrain and testes in mice and X-linked lissencephaly with abnormal genitalia in humans.

Kitamura K., Yanazawa M., Sugiyama N., Miura H., Iizuka-Kogo A., Kusaka M., Omichi K., Suzuki R., Kato-Fukui Y., Kamiirisa K. et al.

Nat. Genet. 32:359-369(2002) · UniProtKB (1) · Mapped (29)

Phytochrome mediates the external light signal to repress FT orthologs in photoperiodic flowering of rice.

Izawa T., Oikawa T., Sugiyama N., Tanisaka T., Yano M., Shimamoto K.

Genes Dev. 16:2006-2020(2002) · Mapped (2)

Familial frontotemporal dementia and parkinsonism with a novel N296H mutation in exon 10 of the tau gene and a widespread tau accumulation in the glial cells.

Iseki E., Matsumura T., Marui W., Hino H., Odawara T., Sugiyama N., Suzuki K., Sawada H., Arai T., Kosaka K.

Acta Neuropathol. 102:285-292(2001) · UniProtKB (1)

No evidence of an association between CYP2D6 polymorphisms among Japanese and dementia with Lewy bodies.

Furuno T., Kawanishi C., Iseki E., Onishi H., Sugiyama N., Suzuki K., Kosaka K.

Psychiatry Clin. Neurosci. 55:89-92(2001) · Mapped (18)

Lack of association in Japanese patients between neuroleptic malignant syndrome and a debrisoquine 4-hydroxylase genotype with low enzyme activity.

Kawanishi C., Furuno T., Onishi H., Sugiyama N., Suzuki K., Matsumura T., Ishigami T., Kosaka K.

Psychiatr. Genet. 10:145-147(2000) · Mapped (18)

A novel missense mutation (G209R) in exon 8 of the presenilin 1 gene in a Japanese family with presenile familial Alzheimer's disease.

Sugiyama N., Suzuki K., Matsumura T., Kawanishi C., Onishi H., Yamada Y., Iseki E., Kosaka K.

Hum. Mutat. 14:90-90(1999) · UniProtKB (1)

Pelizaeus-Merzbacher disease: three novel mutations and implication for locus heterogeneity.

Osaka H., Kawanishi C., Inoue K., Onishi H., Kobayashi T., Sugiyama N., Kosaka K., Nezu A., Fujii K., Sugita K. et al.

Ann. Neurol. 45:59-64(1999) · UniProtKB (1)

Lack of association between neuroleptic malignant syndrome and polymorphisms in the 5-HT1A and 5-HT2A receptor genes.

Kawanishi C., Hanihara T., Shimoda Y., Suzuki K., Sugiyama N., Onishi H., Miyakawa T., Yamada Y., Kosaka K.

Am J Psychiatry 155:1275-1277(1998) · Mapped (7)

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