Itoh T - Search Results

1

Genomic organization and mutational analysis of HERG, a gene responsible for familial long QT syndrome.

Itoh T, Tanaka T, Nagai R, Kamiya T, Sawayama T, Nakayama T, Tomoike H, Sakurada H, Yazaki Y, Nakamura Y. Itoh T, et al. Hum Genet. 1998 Apr;102(4):435-9. doi: 10.1007/s004390050717. Hum Genet. 1998. PMID: 9600240

2

Voltage-shift of the current activation in HERG S4 mutation (R534C) in LQT2.

Nakajima T, Furukawa T, Hirano Y, Tanaka T, Sakurada H, Takahashi T, Nagai R, Itoh T, Katayama Y, Nakamura Y, Hiraoka M. Nakajima T, et al. Among authors: itoh t. Cardiovasc Res. 1999 Nov;44(2):283-93. doi: 10.1016/s0008-6363(99)00195-9. Cardiovasc Res. 1999. PMID: 10690305

3

Twenty single nucleotide polymorphisms (SNPs) and their allelic frequencies in four genes that are responsible for familial long QT syndrome in the Japanese population.

Iwasa H, Itoh T, Nagai R, Nakamura Y, Tanaka T. Iwasa H, et al. Among authors: itoh t. J Hum Genet. 2000;45(3):182-3. doi: 10.1007/s100380050207. J Hum Genet. 2000. PMID: 10807545

4

Correlation of genetic etiology with response to beta-adrenergic blockade among symptomatic patients with familial long-QT syndrome.

Itoh T, Kikuchi K, Odagawa Y, Takata S, Yano K, Okada S, Haneda N, Ogawa S, Nakano O, Kawahara Y, Kasai H, Nakayama T, Fukutomi T, Sakurada H, Shimizu A, Yazaki Y, Nagai R, Nakamura Y, Tanaka T. Itoh T, et al. J Hum Genet. 2001;46(1):38-40. doi: 10.1007/s100380170123. J Hum Genet. 2001. PMID: 11289718

5

Genomic organization and mutational analysis of KVLQT1, a gene responsible for familial long QT syndrome.

Itoh T, Tanaka T, Nagai R, Kikuchi K, Ogawa S, Okada S, Yamagata S, Yano K, Yazaki Y, Nakamura Y. Itoh T, et al. Hum Genet. 1998 Sep;103(3):290-4. doi: 10.1007/s004390050819. Hum Genet. 1998. PMID: 9799083

6

Characterization of S818L mutation in HERG C-terminus in LQT2. Modification of activation-deactivation gating properties.

Nakajima T, Kurabayashi M, Ohyama Y, Kaneko Y, Furukawa T, Itoh T, Taniguchi Y, Tanaka T, Nakamura Y, Hiraoka M, Nagai R. Nakajima T, et al. Among authors: itoh t. FEBS Lett. 2000 Sep 15;481(2):197-203. doi: 10.1016/s0014-5793(00)01988-8. FEBS Lett. 2000. PMID: 10996323 Free article.

7

Exon redefinition by a point mutation within exon 5 of the glucose-6-phosphatase gene is the major cause of glycogen storage disease type 1a in Japan.

Kajihara S, Matsuhashi S, Yamamoto K, Kido K, Tsuji K, Tanae A, Fujiyama S, Itoh T, Tanigawa K, Uchida M, et al. Kajihara S, et al. Among authors: itoh t. Am J Hum Genet. 1995 Sep;57(3):549-55. Am J Hum Genet. 1995. PMID: 7668282 Free PMC article.

8

Role of the epithelium in opposing H(2)O(2)-induced modulation of acetylcholine-induced contractions in rabbit intrapulmonary bronchiole.

Asano T, Hattori T, Tada T, Kajikuri J, Kamiya T, Saitoh M, Yamada Y, Itoh M, Itoh T. Asano T, et al. Among authors: itoh m, itoh t. Br J Pharmacol. 2001 Mar;132(6):1271-80. doi: 10.1038/sj.bjp.0703956. Br J Pharmacol. 2001. PMID: 11250878 Free PMC article.

9

Construction of a contiguous 874-kb sequence of the Escherichia coli -K12 genome corresponding to 50.0-68.8 min on the linkage map and analysis of its sequence features.

Yamamoto Y, Aiba H, Baba T, Hayashi K, Inada T, Isono K, Itoh T, Kimura S, Kitagawa M, Makino K, Miki T, Mitsuhashi N, Mizobuchi K, Mori H, Nakade S, Nakamura Y, Nashimoto H, Oshima T, Oyama S, Saito N, Sampei G, Satoh Y, Sivasundaram S, Tagami H, Horiuchi T, et al. Yamamoto Y, et al. Among authors: itoh t. DNA Res. 1997 Apr 28;4(2):91-113. doi: 10.1093/dnares/4.2.91. DNA Res. 1997. PMID: 9205837 Free article.

10

Erythematous papules in a patient with cardiac myxoma: a case report and review of the literature.

Misago N, Tanaka T, Hoshii T, Suda H, Itoh T. Misago N, et al. Among authors: itoh t. J Dermatol. 1995 Aug;22(8):600-5. doi: 10.1111/j.1346-8138.1995.tb03882.x. J Dermatol. 1995. PMID: 7560460 Review.

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