1 - 25 of
45
results
for author:"Kanai A."
in Literature Citations
| A novel mutation in the cornea-specific keratin 12 gene in Meesmann corneal dystrophy. Seto T., Fujiki K., Kishishita H., Fujimaki T., Murakami A., Kanai A. Jpn. J. Ophthalmol. 52:224-226(2008) · Mapped (1) |
| Association of soluble adhesion molecule and C-reactive protein levels with silent brain infarction in patients with and without type 2 diabetes. Umemura T., Kawamura T., Sakakibara T., Kanai A., Sano T., Hotta N., Sobue G. Curr Neurovasc Res 5:106-111(2008) · Mapped (9) |
| Identification of DOCK4 and its splicing variant as PIP3 binding proteins. Kanai A., Ihara S., Ohdaira T., Shinohara-Kanda A., Iwamatsu A., Fukui Y. IUBMB Life 60:467-472(2008) · Mapped (8) |
| A novel variant lattice corneal dystrophy caused by association of mutation (V625D) in TGFBI gene. Tian X., Fujiki K., Zhang Y., Murakami A., Li Q., Kanai A., Wang W., Hao Y., Ma Z. Am. J. Ophthalmol. 144:473-475(2007) · Mapped (5) |
| Stage-specific expression of Caenorhabditis elegans ribonuclease H1 enzymes with different substrate specificities and bivalent cation requirements. Kochiwa H., Itaya M., Tomita M., Kanai A. FEBS J. 273:420-429(2006) · Mapped (7) |
| Identification and expression analysis of putative mRNA-like non-coding RNA in Drosophila. Inagaki S., Numata K., Kondo T., Tomita M., Yasuda K., Kanai A., Kageyama Y. Genes Cells 10:1163-1173(2005) · Mapped (3) |
| Expression of functional nicotinic acetylcholine receptors in rat urinary bladder epithelial cells. Beckel J.M., Kanai A., Lee S.J., de Groat W.C., Birder L.A. Am. J. Physiol. Renal Physiol. 290:F103-10(2006) · Mapped (1) |
| Novel mutation (V505D) of the TGFBI gene found in a Chinese family with lattice corneal dystrophy, type I. Tian X., Fujiki K., Wang W., Murakami A., Xie P., Kanai A., Liu Z. Jpn. J. Ophthalmol. 49:84-88(2005) · UniProtKB (1) · Mapped (4) |
| Mutations in the membrane component, chromosome 1, surface marker 1 (M1S1) gene in gelatinous drop-like corneal dystrophy. Murakami A., Kimura S., Fujiki K., Fujimaki T., Kanai A. Jpn. J. Ophthalmol. 48:317-320(2004) · Mapped (2) |
| Analysis of COL8A2 gene mutation in Japanese patients with Fuchs' endothelial dystrophy and posterior polymorphous dystrophy. Kobayashi A., Fujiki K., Murakami A., Kato T., Chen L.-Z., Onoe H., Nakayasu K., Sakurai M., Takahashi M., Sugiyama K. et al. Jpn. J. Ophthalmol. 48:195-198(2004) · UniProtKB (1) · Mapped (3) |
| Bietti crystalline corneoretinal dystrophy is caused by mutations in the novel gene CYP4V2. Li A., Jiao X., Munier F.L., Schorderet D.F., Yao W., Iwata F., Hayakawa M., Kanai A., Shy Chen M., Alan Lewis R. et al. Am. J. Hum. Genet. 74:817-826(2004) · UniProtKB (1) · Mapped (2) |
| Compound heterozygous mutations of M1S1 gene in gelatinous droplike corneal dystrophy. Tian X., Fujiki K., Li Q., Murakami A., Xie P., Kanai A., Wang W., Liu Z. Am. J. Ophthalmol. 137:567-569(2004) · Mapped (2) |
| Mutation analysis of the TGFBI gene in Vietnamese with granular and Avellino corneal dystrophy. Cung l.e. X., Ha N.T., Chau H.M., Thanh T.K., Fujiki K., Murakami A., Hiratsuka Y., Kanai A. Jpn. J. Ophthalmol. 48:12-16(2004) · Mapped (14) |
| Differing roles of mitochondrial nitric oxide synthase in cardiomyocytes and urothelial cells. Kanai A., Epperly M., Pearce L., Birder L., Zeidel M., Meyers S., Greenberger J., de Groat W., Apodaca G., Peterson J. Am. J. Physiol. Heart Circ. Physiol. 286:H13-21(2004) · Mapped (17) |
| Identification of novel mutations of the CHST6 gene in Vietnamese families affected with macular corneal dystrophy in two generations. Ha N.T., Chau H.M., Cung le X., Thanh T.K., Fujiki K., Murakami A., Hiratsuka Y., Hasegawa N., Kanai A. Cornea 22:508-511(2003) · UniProtKB (1) |
| Mutation analysis of the carbohydrate sulfotransferase gene in Vietnamese with macular corneal dystrophy. Ha N.T., Chau H.M., Cung le X., Thanh T.K., Fujiki K., Murakami A., Hiratsuka Y., Kanai A. Invest. Ophthalmol. Vis. Sci. 44:3310-3316(2003) · UniProtKB (1) |
| Mutations in the CHST6 gene in patients with macular corneal dystrophy: immunohistochemical evidence of heterogeneity. Iida-Hasegawa N., Furuhata A., Hayatsu H., Murakami A., Fujiki K., Nakayasu K., Kanai A. Invest. Ophthalmol. Vis. Sci. 44:3272-3277(2003) · UniProtKB (1) |
| OPA1 gene mutations in Japanese patients with bilateral optic atrophy unassociated with mitochondrial DNA mutations at nt 11778, 3460, and 14484. Yamada T., Hayasaka S., Matsumoto M., Budu, Esa T., Hayasaka Y., Endo M., Nagaki Y., Fujiki K., Murakami A. et al. Jpn. J. Ophthalmol. 47:409-411(2003) · Mapped (2) |
| Molecular cloning of ELOVL4 gene from cynomolgus monkey (Macaca fascicularis). Umeda S., Ayyagari R., Suzuki M.T., Ono F., Iwata F., Fujiki K., Kanai A., Takada Y., Yoshikawa Y., Tanaka Y. et al. Exp. Anim. 52:129-135(2003) · UniProtKB (1) |
| A novel mutation of the TGFBI gene found in a Vietnamese family with atypical granular corneal dystrophy. Ha N.T., Cung le X., Chau H.M., Thanh T.K., Fujiki K., Murakami A., Kanai A. Jpn. J. Ophthalmol. 47:246-248(2003) · UniProtKB (1) |
| A novel mutation of M1S1 gene found in a Vietnamese patient with gelatinous droplike corneal dystrophy. Ha N.T., Chau H.M., Cung l.e. X., Thanh T.K., Fujiki K., Murakami A., Kanai A. Am. J. Ophthalmol. 135:390-393(2003) · Mapped (2) |
| Expression cloning and characterization of a novel gene that encodes the RNA-binding protein FAU-1 from Pyrococcus furiosus. Kanai A., Oida H., Matsuura N., Doi H. Biochem. J. 372:253-261(2003) · UniProtKB (1) |
| Heterozygous Ala137Pro mutation in keratin 12 gene found in Japanese with Meesmann's corneal dystrophy. Takahashi K., Takahashi K., Murakami A., Okisaka S., Kimura T., Kanai A. Jpn. J. Ophthalmol. 46:673-674(2002) · UniProtKB (1) |
| Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs. Okazaki Y., Furuno M., Kasukawa T., Adachi J., Bono H., Kondo S., Nikaido I., Osato N., Saito R., Suzuki H. et al. Nature 420:563-573(2002) · UniProtKB (17,872) · Mapped (20,305) |
| Altered urinary bladder function in mice lacking the vanilloid receptor TRPV1. Birder L.A., Nakamura Y., Kiss S., Nealen M.L., Barrick S., Kanai A.J., Wang E., Ruiz G., De Groat W.C., Apodaca G. et al. Nat. Neurosci. 5:856-860(2002) · Mapped (2) |
