1 - 25 of
66
results
for author:"Kawakami H."
in Literature Citations
| Screening for TARDBP mutations in Japanese familial amyotrophic lateral sclerosis. Kamada M., Maruyama H., Tanaka E., Morino H., Wate R., Ito H., Kusaka H., Kawano Y., Miki T., Nodera H. et al. J. Neurol. Sci. 284:69-71(2009) · Mapped (10) |
| Evidence for crucial role of hindgut expansion in directing proper migration of primordial germ cells in mouse early embryogenesis. Hara K., Kanai-Azuma M., Uemura M., Shitara H., Taya C., Yonekawa H., Kawakami H., Tsunekawa N., Kurohmaru M., Kanai Y. Dev. Biol. 330:427-439(2009) · Mapped (9) |
| LRRK2 mutations and risk variants in Japanese patients with Parkinson's disease. Zabetian C.P., Yamamoto M., Lopez A.N., Ujike H., Mata I.F., Izumi Y., Kaji R., Maruyama H., Morino H., Oda M. et al. Mov. Disord. 24:1034-1041(2009) · Mapped (4) |
| Human platelets express organic anion-transporting peptide 2B1, an uptake transporter for atorvastatin. Niessen J., Jedlitschky G., Grube M., Bien S., Schwertz H., Ohtsuki S., Kawakami H., Kamiie J., Oswald S., Starke K. et al. Drug Metab. Dispos. 37:1129-1137(2009) · Mapped (10) |
| Sall genes regulate region-specific morphogenesis in the mouse limb by modulating Hox activities. Kawakami Y., Uchiyama Y., Rodriguez Esteban C., Inenaga T., Koyano-Nakagawa N., Kawakami H., Marti M., Kmita M., Monaghan-Nichols P., Nishinakamura R. et al. Development 136:585-594(2009) · Mapped (67) |
| High mobility group box protein-1 in experimental autoimmune uveoretinitis. Watanabe T., Keino H., Sato Y., Kudo A., Kawakami H., Okada A.A. Invest. Ophthalmol. Vis. Sci. 50:2283-2290(2009) · Mapped (8) |
| Expression of galectin-1, a new component of slit diaphragm, is altered in minimal change nephrotic syndrome. Shimizu M., Khoshnoodi J., Akimoto Y., Kawakami H., Hirano H., Higashihara E., Hosoyamada M., Sekine Y., Kurayama R., Kurayama H. et al. Lab. Invest. 89:178-195(2009) · Mapped (1) |
| Establishment of testis-specific SOX9 activation requires high-glucose metabolism in mouse sex differentiation. Matoba S., Hiramatsu R., Kanai-Azuma M., Tsunekawa N., Harikae K., Kawakami H., Kurohmaru M., Kanai Y. Dev. Biol. 324:76-87(2008) · Mapped (23) |
| Exosome-like vesicles with dipeptidyl peptidase IV in human saliva. Ogawa Y., Kanai-Azuma M., Akimoto Y., Kawakami H., Yanoshita R. Biol. Pharm. Bull. 31:1059-1062(2008) · Mapped (2) |
| Pathogenic expansions of the SCA6 locus are associated with a common CACNA1A haplotype across the globe: founder effect or predisposing chromosome? Craig K., Takiyama Y., Soong B.W., Jardim L.B., Saraiva-Pereira M.L., Lythgow K., Morino H., Maruyama H., Kawakami H., Chinnery P.F. Eur. J. Hum. Genet. 16:841-847(2008) · Mapped (7) |
| A common mechanism for the ATP-DnaA-dependent formation of open complexes at the replication origin. Ozaki S., Kawakami H., Nakamura K., Fujikawa N., Kagawa W., Park S.Y., Yokoyama S., Kurumizaka H., Katayama T. J. Biol. Chem. 283:8351-8362(2008) · Mapped (1) |
| The GPCR modulator protein RAMP2 is essential for angiogenesis and vascular integrity. Ichikawa-Shindo Y., Sakurai T., Kamiyoshi A., Kawate H., Iinuma N., Yoshizawa T., Koyama T., Fukuchi J., Iimuro S., Moriyama N. et al. J. Clin. Invest. 118:29-39(2008) · Mapped (18) |
| The CNTN4 c.4256C>T mutation is rare in Japanese with inherited spinocerebellar ataxia. Tanaka E., Maruyama H., Morino H., Nakajima E., Kawakami H. J. Neurol. Sci. 266:180-181(2008) · Mapped (5) |
| Proteomics reveals N-linked glycoprotein diversity in Caenorhabditis elegans and suggests an atypical translocation mechanism for integral membrane proteins. Kaji H., Kamiie J., Kawakami H., Kido K., Yamauchi Y., Shinkawa T., Taoka M., Takahashi N., Isobe T. Mol. Cell. Proteomics 6:2100-2109(2007) · UniProtKB (759) |
| Imaging analysis reveals mechanistic differences between first- and second-phase insulin exocytosis. Ohara-Imaizumi M., Fujiwara T., Nakamichi Y., Okamura T., Akimoto Y., Kawai J., Matsushima S., Kawakami H., Watanabe T., Akagawa K. et al. J. Cell Biol. 177:695-705(2007) · Mapped (3) |
| A polymorphism of LOC387715 gene is associated with age-related macular degeneration in the Japanese population. Tanimoto S., Tamura H., Ue T., Yamane K., Maruyama H., Kawakami H., Kiuchi Y. Neurosci. Lett. 414:71-74(2007) · Mapped (2) |
| Potency of testicular somatic environment to support spermatogenesis in XX/Sry transgenic male mice. Ishii M., Tachiwana T., Hoshino A., Tsunekawa N., Hiramatsu R., Matoba S., Kanai-Azuma M., Kawakami H., Kurohmaru M., Kanai Y. Development 134:449-454(2007) · Mapped (3) |
| No association of complement factor H gene polymorphism and age-related macular degeneration in the Japanese population. Uka J., Tamura H., Kobayashi T., Yamane K., Kawakami H., Minamoto A., Mishima H.K. Retina (Philadelphia, Pa.) 26:985-987(2006) · Mapped (4) |
| Elevation of the post-translational modification of proteins by O-linked N-acetylglucosamine leads to deterioration of the glucose-stimulated insulin secretion in the pancreas of diabetic Goto-Kakizaki rats. Akimoto Y., Hart G.W., Wells L., Vosseller K., Yamamoto K., Munetomo E., Ohara-Imaizumi M., Nishiwaki C., Nagamatsu S., Hirano H. et al. Glycobiology 17:127-140(2007) · Mapped (1) |
| Collaborative analysis of alpha-synuclein gene promoter variability and Parkinson disease. Genetic Epidemiology of Parkinson's Disease (GEO-PD) Consortium JAMA 296:661-670(2006) · Mapped (3) |
| Redundant roles of Sox17 and Sox18 in postnatal angiogenesis in mice. Matsui T., Kanai-Azuma M., Hara K., Matoba S., Hiramatsu R., Kawakami H., Kurohmaru M., Koopman P., Kanai Y. J. Cell. Sci. 119:3513-3526(2006) · Mapped (42) |
| Identification and haplotype analysis of LRRK2 G2019S in Japanese patients with Parkinson disease. Zabetian C.P., Morino H., Ujike H., Yamamoto M., Oda M., Maruyama H., Izumi Y., Kaji R., Griffith A., Leis B.C. et al. Neurology 67:697-699(2006) · Mapped (4) |
| Mutant protein kinase Cgamma found in spinocerebellar ataxia type 14 is susceptible to aggregation and causes cell death. Seki T., Adachi N., Ono Y., Mochizuki H., Hiramoto K., Amano T., Matsubayashi H., Matsumoto M., Kawakami H., Saito N. et al. J. Biol. Chem. 280:29096-29106(2005) · Mapped (7) |
| Brain-derived neurotrophic factor gene polymorphisms in Japanese patients with sporadic Alzheimer's disease, Parkinson's disease, and multiple system atrophy. Nishimura M., Kuno S., Kaji R., Kawakami H. Mov. Disord. 20:1031-1033(2005) · Mapped (6) |
| Glutathione-S-transferase-1 and interleukin-1beta gene polymorphisms in Japanese patients with Parkinson's disease. Nishimura M., Kuno S., Kaji R., Yasuno K., Kawakami H. Mov. Disord. 20:901-902(2005) · Mapped (5) |
