Takeshima Y - Search Results

1

A prostaglandin D2 metabolite is elevated in the urine of Duchenne muscular dystrophy patients and increases further from 8 years old.

Nakagawa T, Takeuchi A, Kakiuchi R, Lee T, Yagi M, Awano H, Iijima K, Takeshima Y, Urade Y, Matsuo M. Nakagawa T, et al. Among authors: takeshima y. Clin Chim Acta. 2013 Aug 23;423:10-4. doi: 10.1016/j.cca.2013.03.031. Epub 2013 Apr 19. Clin Chim Acta. 2013. PMID: 23603101

2

C to T transition at the first nucleotide of codon 63 of the beta-globin gene corresponding to hemoglobin M-Saskatoon in an Indonesian boy.

Suryantoro P, Takeshima Y, Haryanto A, Matsuo M. Suryantoro P, et al. Among authors: takeshima y. Jpn J Hum Genet. 1995 Jun;40(2):195-201. doi: 10.1007/BF01883577. Jpn J Hum Genet. 1995. PMID: 7663000

3

Modulation of in vitro splicing of the upstream intron by modifying an intra-exon sequence which is deleted from the dystrophin gene in dystrophin Kobe.

Takeshima Y, Nishio H, Sakamoto H, Nakamura H, Matsuo M. Takeshima Y, et al. J Clin Invest. 1995 Feb;95(2):515-20. doi: 10.1172/JCI117693. J Clin Invest. 1995. PMID: 7860733 Free PMC article.

4

Amino-terminal deletion of 53% of dystrophin results in an intermediate Duchenne-Becker muscular dystrophy phenotype.

Takeshima Y, Nishio H, Narita N, Wada H, Ishikawa Y, Ishikawa Y, Minami R, Nakamura H, Matsuo M. Takeshima Y, et al. Neurology. 1994 Sep;44(9):1648-51. doi: 10.1212/wnl.44.9.1648. Neurology. 1994. PMID: 7936290

5

Twenty seven nucleotide deletion within exon 11 of the erythrocyte band 3 gene in Indonesian ovalocytosis.

Takeshima Y, Sofro AS, Suryantoro P, Narita N, Matsuo M. Takeshima Y, et al. Jpn J Hum Genet. 1994 Mar;39(1):181-5. doi: 10.1007/BF01915953. Jpn J Hum Genet. 1994. PMID: 8025294

6

Identification of a novel first exon in the human dystrophin gene and of a new promoter located more than 500 kb upstream of the nearest known promoter.

Nishio H, Takeshima Y, Narita N, Yanagawa H, Suzuki Y, Ishikawa Y, Ishikawa Y, Minami R, Nakamura H, Matsuo M. Nishio H, et al. Among authors: takeshima y. J Clin Invest. 1994 Sep;94(3):1037-42. doi: 10.1172/JCI117417. J Clin Invest. 1994. PMID: 8083345 Free PMC article.

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: takeshima y. Am J Hum Genet. 1994 Jan;54(1):53-61. Am J Hum Genet. 1994. PMID: 8279470 Free PMC article.

8

Induction of exon skipping of the dystrophin transcript in lymphoblastoid cells by transfecting an antisense oligodeoxynucleotide complementary to an exon recognition sequence.

Pramono ZA, Takeshima Y, Alimsardjono H, Ishii A, Takeda S, Matsuo M. Pramono ZA, et al. Among authors: takeshima y. Biochem Biophys Res Commun. 1996 Sep 13;226(2):445-9. doi: 10.1006/bbrc.1996.1375. Biochem Biophys Res Commun. 1996. PMID: 8806654

9

Japanese cases of type 1 thanatophoric dysplasia exclusively carry a C to T transition at nucleotide 742 of the fibroblast growth factor receptor 3 gene.

Pokharel RK, Alimsardjono H, Takeshima Y, Nakamura H, Naritomi K, Hirose S, Onishi S, Matsuo M. Pokharel RK, et al. Among authors: takeshima y. Biochem Biophys Res Commun. 1996 Oct 3;227(1):236-9. doi: 10.1006/bbrc.1996.1495. Biochem Biophys Res Commun. 1996. PMID: 8858131

10

A case of Becker muscular dystrophy resulting from the skipping of four contiguous exons (71-74) of the dystrophin gene during mRNA maturation.

Patria SY, Alimsardjono H, Nishio H, Takeshima Y, Nakamura H, Matsuo M. Patria SY, et al. Among authors: takeshima y. Proc Assoc Am Physicians. 1996 Jul;108(4):308-14. Proc Assoc Am Physicians. 1996. PMID: 8863344

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