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[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.
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.
Candidate genes for male factor infertility--validation.
Mori T, Kurahashi H, Shinka T, Nakahori Y, Taniguchi M, Toda T, Iwamoto T. Mori T, et al. Among authors: taniguchi m. Fertil Steril. 2006 Nov;86(5):1553-4; author reply 1554. doi: 10.1016/j.fertnstert.2006.05.011. Epub 2006 Aug 22. Fertil Steril. 2006. PMID: 16926002 Free article. No abstract available.
Residual laminin-binding activity and enhanced dystroglycan glycosylation by LARGE in novel model mice to dystroglycanopathy.
Kanagawa M, Nishimoto A, Chiyonobu T, Takeda S, Miyagoe-Suzuki Y, Wang F, Fujikake N, Taniguchi M, Lu Z, Tachikawa M, Nagai Y, Tashiro F, Miyazaki J, Tajima Y, Takeda S, Endo T, Kobayashi K, Campbell KP, Toda T. Kanagawa M, et al. Among authors: taniguchi m. Hum Mol Genet. 2009 Feb 15;18(4):621-31. doi: 10.1093/hmg/ddn387. Epub 2008 Nov 18. Hum Mol Genet. 2009. PMID: 19017726 Free PMC article.
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
3,177 results