1 - 25 of 61 results for author:"Fujiki K." in Literature citations
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| CFTR polymorphisms of healthy individuals in two Chinese cities--Changchun and Nanjing. Jin C.X., Fujiki K., Song Y., Ping Z., Nakakuki M., Wei M.X., Zhang S.M., Ishiguro H., Naruse S. Nagoya J Med Sci 74:293-301(2012) · Mapped (45) |
| Endocannabinoid-Goalpha signalling inhibits axon regeneration in Caenorhabditis elegans by antagonizing Gqalpha-PKC-JNK signalling. Pastuhov S.I., Fujiki K., Nix P., Kanao S., Bastiani M., Matsumoto K., Hisamoto N. Nat Commun 3:1136-1136(2012) · Mapped (1) |
| OPA1 mutations in Japanese patients suspected to have autosomal dominant optic atrophy. Hamahata T., Fujimaki T., Fujiki K., Miyazaki A., Mizota A., Murakami A. Jpn. J. Ophthalmol. 56:91-97(2012) · Mapped (10) |
| A novel nonsense mutation in rhodopsin gene in two Indonesian families with autosomal recessive retinitis pigmentosa. Kartasasmita A., Fujiki K., Iskandar E., Sovani I., Fujimaki T., Murakami A. Ophthalmic Genet. 32:57-63(2011) · Mapped (1) |
| Mutation analysis of CHST6 gene in Chinese patients with macular corneal dystrophy. Liu Z., Tian X., Iida N., Fujiki K., Xie P., Wang W., Ma Z., Kanai A., Murakami A. Cornea 29:883-888(2010) · Mapped (1) |
| The Caenorhabditis elegans Ste20-related kinase and Rac-type small GTPase regulate the c-Jun N-terminal kinase signaling pathway mediating the stress response. Fujiki K., Mizuno T., Hisamoto N., Matsumoto K. Mol. Cell. Biol. 30:995-1003(2010) · Mapped (16) |
| A case of oculodentodigital dysplasia syndrome with novel GJA1 gene mutation. Himi M., Fujimaki T., Yokoyama T., Fujiki K., Takizawa T., Murakami A. Jpn. J. Ophthalmol. 53:541-545(2009) · Mapped (6) |
| In vivo laser confocal microscopy findings and mutational analysis for Schnyder's crystalline corneal dystrophy. Kobayashi A., Fujiki K., Murakami A., Sugiyama K. Ophthalmology 116:1029-37.e1(2009) · Mapped (1) |
| Characterization of rainbow trout CHK2 and its potential as a genotoxicity biomarker. Steinmoeller J.D., Fujiki K., Arya A., Muller K.M., Bols N.C., Dixon B., Duncker B.P. Comp. Biochem. Physiol. C Toxicol. Pharmacol. 149:491-499(2009) · UniProtKB (1) |
| Role of the Caenorhabditis elegans Shc adaptor protein in the c-Jun N-terminal kinase signaling pathway. Mizuno T., Fujiki K., Sasakawa A., Hisamoto N., Matsumoto K. Mol. Cell. Biol. 28:7041-7049(2008) · Mapped (11) |
| 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) |
| In vivo laser confocal microscopic findings of corneal stromal dystrophies. Kobayashi A., Fujiki K., Fujimaki T., Murakami A., Sugiyama K. Arch. Ophthalmol. 125:1168-1173(2007) · Mapped (4) |
| 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 (3) |
| Cloning and characterization of a cDNA encoding walleye (Sander vitreum) beta-2 microglobulin. Christie D., Wei G., Fujiki K., Dixon B. Fish Shellfish Immunol. 22:727-733(2007) · UniProtKB (1) |
| Hypoxic regulation of vascular endothelial growth factor through the induction of phosphatidylinositol 3-kinase/Rho/ROCK and c-Myc. Mizukami Y., Fujiki K., Duerr E.M., Gala M., Jo W.S., Zhang X., Chung D.C. J. Biol. Chem. 281:13957-13963(2006) · Mapped (24) |
| 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 (2) |
| 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 (3) |
| 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) |
| A finger sweat chloride test for the detection of a high-risk group of chronic pancreatitis. Naruse S., Ishiguro H., Suzuki Y., Fujiki K., Ko S.B., Mizuno N., Takemura T., Yamamoto A., Yoshikawa T., Jin C. et al. Pancreas 28:e80-5(2004) · Mapped (45) |
| 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 (3) |
| 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 (12) |
| Analysis of genomic and expressed major histocompatibility class Ia and class II genes in a hexaploid Lake Tana African 'large' barb individual (Barbus intermedius). Kruiswijk C.P., Hermsen T., Fujiki K., Dixon B., Savelkoul H.F., Stet R.J. Immunogenetics 55:770-781(2004) · UniProtKB (16) |
| Molecular cloning and characterization of calreticulin from rainbow trout ( Oncorhynchus mykiss). Kales S., Fujiki K., Dixon B. Immunogenetics 55:717-723(2004) · UniProtKB (2) |
| Molecular cloning and characterization of rainbow trout (Oncorhynchus mykiss) C5a anaphylatoxin receptor. Fujiki K., Liu L., Sundick R.S., Dixon B. Immunogenetics 55:640-646(2003) · UniProtKB (1) |
| 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) |