Kitoh Y - Search Results

1

Partial deletion of a dystrophin gene leads to exon skipping and to loss of an intra-exon hairpin structure from the predicted mRNA precursor.

Matsuo M, Nishio H, Kitoh Y, Francke U, Nakamura H. Matsuo M, et al. Among authors: kitoh y. Biochem Biophys Res Commun. 1992 Jan 31;182(2):495-500. doi: 10.1016/0006-291x(92)91759-j. Biochem Biophys Res Commun. 1992. PMID: 1734864

2

Amplification of ten deletion-rich exons of the dystrophin gene by polymerase chain reaction shows deletions in 36 of 90 Japanese families with Duchenne muscular dystrophy.

Kitoh Y, Matsuo M, Nishio H, Takumi T, Nakajima T, Masumura T, Koga J, Nakamura H. Kitoh Y, et al. Am J Med Genet. 1992 Feb 15;42(4):453-7. doi: 10.1002/ajmg.1320420408. Am J Med Genet. 1992. PMID: 1609827

3

Exon skipping during splicing of dystrophin mRNA precursor due to an intraexon deletion in the dystrophin gene of Duchenne muscular dystrophy kobe.

Matsuo M, Masumura T, Nishio H, Nakajima T, Kitoh Y, Takumi T, Koga J, Nakamura H. Matsuo M, et al. Among authors: kitoh y. J Clin Invest. 1991 Jun;87(6):2127-31. doi: 10.1172/JCI115244. J Clin Invest. 1991. PMID: 2040695 Free PMC article.

4

A very small frame-shifting deletion within exon 19 of the Duchenne muscular dystrophy gene.

Matsuo M, Masumura T, Nakajima T, Kitoh Y, Takumi T, Nishio H, Koga J, Nakamura H. Matsuo M, et al. Among authors: kitoh y. Biochem Biophys Res Commun. 1990 Jul 31;170(2):963-7. doi: 10.1016/0006-291x(90)92185-3. Biochem Biophys Res Commun. 1990. PMID: 2383276

5

Amplification of selected exons by polymerase chain reaction enables determination of the translational reading frame of dystrophin mRNA resulting from deletion mutations.

Kitoh Y, Matsuo M, Nishio H, Nakamura H. Kitoh Y, et al. Kobe J Med Sci. 1994 Apr;40(2):39-48. Kobe J Med Sci. 1994. PMID: 7823533

6

Brain- and muscle-type promoters of the dystrophin gene are selected in peripheral lymphocytes and Epstein Barr virus-transformed lymphoblastoid [correction of lymphoplastoid] cells.

Nishio H, Matsuo M, Kitoh Y, Narita N, Shimmoto M, Suzuki Y, Nakamura H. Nishio H, et al. Among authors: kitoh y. J Neurol. 1993 Dec;241(2):81-6. doi: 10.1007/BF00869768. J Neurol. 1993. PMID: 8138829

7

A novel point mutation (G-1 to T) in a 5' splice donor site of intron 13 of the dystrophin gene results in exon skipping and is responsible for Becker muscular dystrophy.

Hagiwara Y, Nishio H, Kitoh Y, Takeshima Y, Narita N, Wada H, Yokoyama M, Nakamura H, Matsuo M. Hagiwara Y, et al. Among authors: kitoh y. Am J Hum Genet. 1994 Jan;54(1):53-61. Am J Hum Genet. 1994. PMID: 8279470 Free PMC article.

8

Insertion of a 5' truncated L1 element into the 3' end of exon 44 of the dystrophin gene resulted in skipping of the exon during splicing in a case of Duchenne muscular dystrophy.

Narita N, Nishio H, Kitoh Y, Ishikawa Y, Ishikawa Y, Minami R, Nakamura H, Matsuo M. Narita N, et al. Among authors: kitoh y. J Clin Invest. 1993 May;91(5):1862-7. doi: 10.1172/JCI116402. J Clin Invest. 1993. PMID: 8387534 Free PMC article.

9

Screening of gene deletions by polymerase chain reaction in Japanese patients with Duchenne muscular dystrophy.

Nakajima T, Matsuo M, Kitoh Y, Takumi T, Nishio H, Masumura T, Koga J, Nakamura H. Nakajima T, et al. Among authors: kitoh y. J Neurol. 1991 Feb;238(1):6-8. doi: 10.1007/BF00319701. J Neurol. 1991. PMID: 2030378

10

Mechanisms of immunomodulation induced by blood transfusion: identification of humoral factors.

Uchida H, Tanaka H, Kitoh Y, Yanagisawa K, To H, Tago K, Mizuta K, Fujimura A, Tominaga S, Hashizume K, Kobayashi E. Uchida H, et al. Among authors: kitoh y. Transplant Proc. 2000 Mar;32(2):255-6. doi: 10.1016/s0041-1345(99)00948-3. Transplant Proc. 2000. PMID: 10715408 No abstract available.

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