1 - 25 of
102
results
for author:"Matsuo M."
in Literature Citations
| HnRNP C1/C2 may regulate exon 7 splicing in the spinal muscular atrophy gene SMN1. Irimura S., Kitamura K., Kato N., Saiki K., Takeuchi A., Gunadi, Matsuo M., Nishio H., Lee M.J. Kobe J Med Sci 54:E227-36(2009) · Mapped (13) |
| Autonomous regulation of osteosarcoma cell invasiveness by Wnt5a/Ror2 signaling. Enomoto M., Hayakawa S., Itsukushima S., Ren D.Y., Matsuo M., Tamada K., Oneyama C., Okada M., Takumi T., Nishita M. et al. Oncogene 28:3197-3208(2009) · Mapped (22) |
| Molecular mechanisms of subcellular localization of ABCG5 and ABCG8. Hirata T., Okabe M., Kobayashi A., Ueda K., Matsuo M. Biosci. Biotechnol. Biochem. 73:619-626(2009) · Mapped (10) |
| Muscle-specific overexpression of heparin-binding epidermal growth factor-like growth factor increases peripheral glucose disposal and insulin sensitivity. Fukatsu Y., Noguchi T., Hosooka T., Ogura T., Kotani K., Abe T., Shibakusa T., Inoue K., Sakai M., Tobimatsu K. et al. Endocrinology 150:2683-2691(2009) · Mapped (2) |
| Minimal change nephrotic syndrome associated with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome. Hashimura Y., Nozu K., Kanegane H., Miyawaki T., Hayakawa A., Yoshikawa N., Nakanishi K., Takemoto M., Iijima K., Matsuo M. Pediatr. Nephrol. 24:1181-1186(2009) · Mapped (5) |
| Two novel mutations in the ED1 gene in Japanese families with X-linked hypohidrotic ectodermal dysplasia. Gunadi, Miura K., Ohta M., Sugano A., Lee M.J., Sato Y., Matsunaga A., Hayashi K., Horikawa T., Miki K. et al. Pediatr. Res. 65:453-457(2009) · Mapped (1) |
| Ordered patterns of cell shape and orientational correlation during spontaneous cell migration. Maeda Y.T., Inose J., Matsuo M.Y., Iwaya S., Sano M. |
| Atypical phenotype of type I Bartter syndrome accompanied by focal segmental glomerulosclerosis. Yamazaki H., Nozu K., Narita I., Nagata M., Nozu Y., Fu X.J., Matsuo M., Iijima K., Gejyo F. Pediatr. Nephrol. 24:415-418(2009) · Mapped (8) |
| Direct interaction of nuclear liver X receptor-beta with ABCA1 modulates cholesterol efflux. Hozoji M., Munehira Y., Ikeda Y., Makishima M., Matsuo M., Kioka N., Ueda K. J. Biol. Chem. 283:30057-30063(2008) · Mapped (16) |
| Novel mutations in 21 patients with tuberous sclerosis complex and variation of tandem splice-acceptor sites in TSC1 exon 14. Sasongko T.H., Wataya-Kaneda M., Koterazawa K., Gunadi, Yusoff S., Harahap I.S., Lee M.J., Matsuo M., Nishio H. Kobe J Med Sci 54:E73-81(2008) · Mapped (10) |
| Dystrophin nonsense mutations can generate alternative rescue transcripts in lymphocytes. Nishiyama A., Takeshima Y., Zhang Z., Habara Y., Tran T.H., Yagi M., Matsuo M. Ann. Hum. Genet. 72:717-724(2008) · Mapped (71) |
| 2-Substituted-16-ene-22-thia-1alpha,25-dihydroxy-26,27-dimethyl-19-norvitamin D3 analogs: Synthesis, biological evaluation, and crystal structure. Shimizu M., Miyamoto Y., Takaku H., Matsuo M., Nakabayashi M., Masuno H., Udagawa N., DeLuca H.F., Ikura T., Ito N. Bioorg. Med. Chem. 16:6949-6964(2008) · Mapped (1) |
| SMN2 and NAIP gene dosages in Vietnamese patients with spinal muscular atrophy. Tran V.K., Sasongko T.H., Hong D.D., Hoan N.T., Dung V.C., Lee M.J., Gunadi, Takeshima Y., Matsuo M., Nishio H. Pediatr Int 50:346-351(2008) · Mapped (7) |
| Early diagnosis of maple syrup urine disease using polymerase chain reaction-based mutation detection. Silao C.L., Padilla C.D., Matsuo M. Pediatr Int 50:312-314(2008) · Mapped (3) |
| Heregulin-induced activation of ErbB3 by EGFR tyrosine kinase activity promotes tumor growth and metastasis in melanoma cells. Ueno Y., Sakurai H., Tsunoda S., Choo M.K., Matsuo M., Koizumi K., Saiki I. Int. J. Cancer 123:340-347(2008) · Mapped (23) |
| Germ-line mutation of KCNQ2, p.R213W, in a Japanese family with benign familial neonatal convulsion. Sadewa A.H., Sasongko T.H., Lee M.J., Daikoku K., Yamamoto A., Yamasaki T., Tanaka S., Matsuo M., Nishio H. Pediatr Int 50:167-171(2008) · Mapped (9) |
| Wide ranges of serum myostatin concentrations in Duchenne muscular dystrophy patients. Awano H., Takeshima Y., Okizuka Y., Saiki K., Yagi M., Matsuo M. Clin. Chim. Acta 391:115-117(2008) · Mapped (2) |
| Hypomutability at the polyadenine tract in SMN intron 3 shows the invariability of the a-SMN protein structure. Sasongko T.H., Yusoff S., Lee M.J., Nishioka E., Matsuo M., Nishio H. Ann. Hum. Genet. 72:288-291(2008) · Mapped (3) |
| Mutation analysis of the ornithine transcarbamylase (OTC) gene in five Japanese OTC deficiency patients revealed two known and three novel mutations including a deep intronic mutation. Ogino W., Takeshima Y., Nishiyama A., Okizuka Y., Yagi M., Tsuneishi S., Saiki K., Kugo M., Matsuo M. Kobe J Med Sci 53:229-240(2007) · Mapped (1) |
| Tandem duplications of two separate fragments of the dystrophin gene in a patient with Duchenne muscular dystrophy. Zhang Z., Takeshima Y., Awano H., Nishiyama A., Okizuka Y., Yagi M., Matsuo M. J. Hum. Genet. 53:215-219(2008) · Mapped (71) |
| Comparative study on nobiletin metabolism with liver microsomes from rats, Guinea pigs and hamsters and rat cytochrome p450. Koga N., Matsuo M., Ohta C., Haraguchi K., Matsuoka M., Kato Y., Ishii T., Yano M., Ohta H. Biol. Pharm. Bull. 30:2317-2323(2007) · Mapped (2) |
| A strong exonic splicing enhancer in dystrophin exon 19 achieve proper splicing without an upstream polypyrimidine tract. Habara Y., Doshita M., Hirozawa S., Yokono Y., Yagi M., Takeshima Y., Matsuo M. J. Biochem. 143:303-310(2008) · Mapped (71) |
| Mutated response regulator graR is responsible for phenotypic conversion of Staphylococcus aureus from heterogeneous vancomycin-intermediate resistance to vancomycin-intermediate resistance. Neoh H.-M., Cui L., Yuzawa H., Takeuchi F., Matsuo M., Hiramatsu K. Antimicrob. Agents Chemother. 52:45-53(2008) · UniProtKB (2,684) |
| DnaB and DnaI temperature-sensitive mutants of Staphylococcus aureus: evidence for involvement of DnaB and DnaI in synchrony regulation of chromosome replication. Li Y., Kurokawa K., Reutimann L., Mizumura H., Matsuo M., Sekimizu K. Microbiology (Reading, Engl.) 153:3370-3379(2007) · Mapped (1) |
| Sphingomyelin-dependence of cholesterol efflux mediated by ABCG1. Sano O., Kobayashi A., Nagao K., Kumagai K., Kioka N., Hanada K., Ueda K., Matsuo M. J. Lipid Res. 48:2377-2384(2007) · Mapped (4) |
