Taniguchi M - Search Results

1

Genetic variation affects de novo translocation frequency.

Kato T, Inagaki H, Yamada K, Kogo H, Ohye T, Kowa H, Nagaoka K, Taniguchi M, Emanuel BS, Kurahashi H. Kato T, et al. Among authors: taniguchi m. Science. 2006 Feb 17;311(5763):971. doi: 10.1126/science.1121452. Science. 2006. PMID: 16484486 Free PMC article.

2

Chromosomal instability mediated by non-B DNA: cruciform conformation and not DNA sequence is responsible for recurrent translocation in humans.

Inagaki H, Ohye T, Kogo H, Kato T, Bolor H, Taniguchi M, Shaikh TH, Emanuel BS, Kurahashi H. Inagaki H, et al. Among authors: taniguchi m. Genome Res. 2009 Feb;19(2):191-8. doi: 10.1101/gr.079244.108. Epub 2008 Nov 7. Genome Res. 2009. PMID: 18997000 Free PMC article.

3

Cruciform DNA structure underlies the etiology for palindrome-mediated human chromosomal translocations.

Kurahashi H, Inagaki H, Yamada K, Ohye T, Taniguchi M, Emanuel BS, Toda T. Kurahashi H, et al. Among authors: taniguchi m. J Biol Chem. 2004 Aug 20;279(34):35377-83. doi: 10.1074/jbc.M400354200. Epub 2004 Jun 20. J Biol Chem. 2004. PMID: 15208332 Free PMC article.

4

[Single gene disorder].

Taniguchi M, Kurahashi H. Taniguchi M, et al. Nihon Rinsho. 2005 Dec;63 Suppl 12:57-63. Nihon Rinsho. 2005. PMID: 16416771 Review. Japanese. No abstract available.

5

Screening of genes involved in chromosome segregation during meiosis I: toward the identification of genes responsible for infertility in humans.

Kogo H, Kowa-Sugiyama H, Yamada K, Bolor H, Tsutsumi M, Ohye T, Inagaki H, Taniguchi M, Toda T, Kurahashi H. Kogo H, et al. Among authors: taniguchi m. J Hum Genet. 2010 May;55(5):293-9. doi: 10.1038/jhg.2010.26. Epub 2010 Mar 26. J Hum Genet. 2010. PMID: 20339383

6

Analysis of gene-expression profiles by oligonucleotide microarray in children with influenza.

Kawada JI, Kimura H, Kamachi Y, Nishikawa K, Taniguchi M, Nagaoka K, Kurahashi H, Kojima S, Morishima T. Kawada JI, et al. Among authors: taniguchi m. J Gen Virol. 2006 Jun;87(Pt 6):1677-1683. doi: 10.1099/vir.0.81670-0. J Gen Virol. 2006. PMID: 16690933

7

Expression profiling of muscles from Fukuyama-type congenital muscular dystrophy and laminin-alpha 2 deficient congenital muscular dystrophy; is congenital muscular dystrophy a primary fibrotic disease?

Taniguchi M, Kurahashi H, Noguchi S, Sese J, Okinaga T, Tsukahara T, Guicheney P, Ozono K, Nishino I, Morishita S, Toda T. Taniguchi M, et al. Biochem Biophys Res Commun. 2006 Apr 7;342(2):489-502. doi: 10.1016/j.bbrc.2005.12.224. Epub 2006 Feb 3. Biochem Biophys Res Commun. 2006. PMID: 16487936

8

Aberrant neuromuscular junctions and delayed terminal muscle fiber maturation in alpha-dystroglycanopathies.

Taniguchi M, Kurahashi H, Noguchi S, Fukudome T, Okinaga T, Tsukahara T, Tajima Y, Ozono K, Nishino I, Nonaka I, Toda T. Taniguchi M, et al. Hum Mol Genet. 2006 Apr 15;15(8):1279-89. doi: 10.1093/hmg/ddl045. Epub 2006 Mar 10. Hum Mol Genet. 2006. PMID: 16531417

9

Basement membrane fragility underlies embryonic lethality in fukutin-null mice.

Kurahashi H, Taniguchi M, Meno C, Taniguchi Y, Takeda S, Horie M, Otani H, Toda T. Kurahashi H, et al. Among authors: taniguchi y, taniguchi m. Neurobiol Dis. 2005 Jun-Jul;19(1-2):208-17. doi: 10.1016/j.nbd.2004.12.018. Neurobiol Dis. 2005. PMID: 15837576

10

Fukutin and alpha-dystroglycanopathies.

Toda T, Chiyonobu T, Xiong H, Tachikawa M, Kobayashi K, Manya H, Takeda S, Taniguchi M, Kurahashi H, Endo T. Toda T, et al. Among authors: taniguchi m. Acta Myol. 2005 Oct;24(2):60-3. Acta Myol. 2005. PMID: 16550916 Review.

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