1 - 25 of 41 results for author:"Azuma N." in Literature citations
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| Derivation of human differential photoreceptor-like cells from the iris by defined combinations of CRX, RX and NEUROD. Seko Y., Azuma N., Kaneda M., Nakatani K., Miyagawa Y., Noshiro Y., Kurokawa R., Okano H., Umezawa A. PLoS ONE 7:e35611-e35611(2012) · Mapped (6) |
| Mitochondrial and nuclear DNA analysis revealed a cryptic species and genetic introgression in Littorina sitkana (Mollusca, Gastropoda). Azuma N., Yamazaki T., Chiba S. Genetica 139:1399-1408(2011) · UniProtKB (2) |
| Two novel mutations in the EYS gene are possible major causes of autosomal recessive retinitis pigmentosa in the Japanese population. Hosono K., Ishigami C., Takahashi M., Park D.H., Hirami Y., Nakanishi H., Ueno S., Yokoi T., Hikoya A., Fujita T. et al. PLoS ONE 7:e31036-e31036(2012) · Mapped (4) |
| Sphingosine 1-phosphate (S1P)/S1P receptor 1 signaling regulates receptor activator of NF-kappaB ligand (RANKL) expression in rheumatoid arthritis. Takeshita H., Kitano M., Iwasaki T., Kitano S., Tsunemi S., Sato C., Sekiguchi M., Azuma N., Miyazawa K., Hla T. et al. Biochem. Biophys. Res. Commun. 419:154-159(2012) · Mapped (6) |
| Ophthalmic features of CHARGE syndrome with CHD7 mutations. Nishina S., Kosaki R., Yagihashi T., Azuma N., Okamoto N., Hatsukawa Y., Kurosawa K., Yamane T., Mizuno S., Tsuzuki K. et al. Am. J. Med. Genet. A 158A:514-518(2012) · Mapped (4) |
| Stress-activated protein kinase MKK7 regulates axon elongation in the developing cerebral cortex. Yamasaki T., Kawasaki H., Arakawa S., Shimizu K., Shimizu S., Reiner O., Okano H., Nishina S., Azuma N., Penninger J.M. et al. J. Neurosci. 31:16872-16883(2011) · Mapped (81) |
| Critical roles of cold shock domain protein A as an endogenous angiogenesis inhibitor in skeletal muscle. Saito Y., Nakagami H., Azuma N., Hirata S., Sanada F., Taniyama Y., Morishita R., Kaneda Y., Sasajima T. Antioxid. Redox Signal. 15:2109-2120(2011) · Mapped (7) |
| Molecular phylogeny of a red-snow-crab species complex using mitochondrial and nuclear DNA markers. Azuma N., Grant W.S., Templin W.D., Kunihiro Y., Mihara E., Yanagimoto T., Abe S. Zool. Sci. 28:286-292(2011) · UniProtKB (22) |
| A case of aniridia with unilateral Peters anomaly. Sawada M., Sato M., Hikoya A., Wang C., Minoshima S., Azuma N., Hotta Y. J AAPOS 15:104-106(2011) · Mapped (12) |
| Brain-specific Phgdh deletion reveals a pivotal role for L-serine biosynthesis in controlling the level of D-serine, an N-methyl-D-aspartate receptor co-agonist, in adult brain. Yang J.H., Wada A., Yoshida K., Miyoshi Y., Sayano T., Esaki K., Kinoshita M.O., Tomonaga S., Azuma N., Watanabe M. et al. J. Biol. Chem. 285:41380-41390(2010) · Mapped (2) |
| Population genetic structure and phylogeography of masu salmon (Oncorhynchus masou masou) inferred from mitochondrial and microsatellite DNA analyses. Yu J.N., Azuma N., Yoon M., Brykov V., Urawa S., Nagata M., Jin D.H., Abe S. Zool. Sci. 27:375-385(2010) · UniProtKB (3) |
| p38 Mitogen-activated protein kinase controls a switch between cardiomyocyte and neuronal commitment of murine embryonic stem cells by activating myocyte enhancer factor 2C-dependent bone morphogenetic protein 2 transcription. Wu J., Kubota J., Hirayama J., Nagai Y., Nishina S., Yokoi T., Asaoka Y., Seo J., Shimizu N., Kajiho H. et al. Stem Cells Dev. 19:1723-1734(2010) · Mapped (6) |
| Heterozygous orthodenticle homeobox 2 mutations are associated with variable pituitary phenotype. Dateki S., Kosaka K., Hasegawa K., Tanaka H., Azuma N., Yokoya S., Muroya K., Adachi M., Tajima T., Motomura K. et al. J. Clin. Endocrinol. Metab. 95:756-764(2010) · Mapped (4) |
| CrxOS maintains the self-renewal capacity of murine embryonic stem cells. Saito R., Yamasaki T., Nagai Y., Wu J., Kajiho H., Yokoi T., Noda E., Nishina S., Niwa H., Azuma N. et al. Biochem. Biophys. Res. Commun. 390:1129-1135(2009) · Mapped (4) |
| Impaired neurogenesis in embryonic spinal cord of Phgdh knockout mice, a serine deficiency disorder model. Kawakami Y., Yoshida K., Yang J.H., Suzuki T., Azuma N., Sakai K., Hashikawa T., Watanabe M., Yasuda K., Kuhara S. et al. Neurosci. Res. 63:184-193(2009) · UniProtKB (1) · Mapped (36) |
| SOX10 mutation in Waardenburg syndrome type II. Iso M., Fukami M., Horikawa R., Azuma N., Kawashiro N., Ogata T. Am. J. Med. Genet. A 146A:2162-2163(2008) · Mapped (5) |
| Inactivation of the 3-phosphoglycerate dehydrogenase gene in mice: changes in gene expression and associated regulatory networks resulting from serine deficiency. Furuya S., Yoshida K., Kawakami Y., Yang J.H., Sayano T., Azuma N., Tanaka H., Kuhara S., Hirabayashi Y. Funct. Integr. Genomics 8:235-249(2008) · Mapped (1) |
| Genetic variation and population structure of hair crab (Erimacrus isenbeckii ) in Japan inferred from mitochondrial DNA sequence analysis. Azuma N., Kunihiro Y., Sasaki J., Mihara E., Mihara Y., Yasunaga T., Jin D.H., Abe S. Mar. Biotechnol. 10:39-48(2008) · UniProtKB (9) |
| Cold shock domain protein A represses angiogenesis and lymphangiogenesis via inhibition of serum response element. Saito Y., Nakagami H., Kurooka M., Takami Y., Kikuchi Y., Hayashi H., Nishikawa T., Tamai K., Morishita R., Azuma N. et al. Oncogene 27:1821-1833(2008) · Mapped (4) |
| Three novel mutations of the PAX6 gene in Japanese aniridia patients. Kawano T., Wang C., Hotta Y., Sato M., Iwata-Amano E., Hikoya A., Fujita N., Koyama N., Shirai S., Azuma N. et al. J. Hum. Genet. 52:571-574(2007) · Mapped (12) |
| Phylogenetic relationships within parrots (Psittacidae) inferred from mitochondrial cytochrome-b gene sequences. Astuti D., Azuma N., Suzuki H., Higashi S. Zool. Sci. 23:191-198(2006) · UniProtKB (38) |
| Transdifferentiation of the retinal pigment epithelia to the neural retina by transfer of the Pax6 transcriptional factor. Azuma N., Tadokoro K., Asaka A., Yamada M., Yamaguchi Y., Handa H., Matsushima S., Watanabe T., Kida Y., Ogura T. et al. Hum. Mol. Genet. 14:1059-1068(2005) · Mapped (29) |
| The Pax6 isoform bearing an alternative spliced exon promotes the development of the neural retinal structure. Azuma N., Tadokoro K., Asaka A., Yamada M., Yamaguchi Y., Handa H., Matsushima S., Watanabe T., Kohsaka S., Kida Y. et al. Hum. Mol. Genet. 14:735-745(2005) · Mapped (12) |
| Mouse 3-phosphoglycerate dehydrogenase gene: genomic organization, chromosomal localization, and promoter analysis. Mitoma J., Furuya S., Shimizu M., Shinoda Y., Yoshida K., Azuma N., Tanaka H., Suzuki Y., Hirabayashi Y. Gene 334:15-22(2004) · Mapped (1) |
| Histological study of the hypertrophic placentas and open eyelids observed in cloned fetuses. Shimozawa N., Tajima S., Azuma N., Hioki K., Kono T., Ito M. J. Reprod. Dev. 49:221-226(2003) · Mapped (7) |