Kobayashi K - Search Results

1

Linkage-disequilibrium mapping narrows the Fukuyama-type congenital muscular dystrophy (FCMD) candidate region to <100 kb.

Toda T, Miyake M, Kobayashi K, Mizuno K, Saito K, Osawa M, Nakamura Y, Kanazawa I, Nakagome Y, Tokunaga K, Nakahori Y. Toda T, et al. Among authors: kobayashi k. Am J Hum Genet. 1996 Dec;59(6):1313-20. Am J Hum Genet. 1996. PMID: 8940277 Free PMC article.

2

[Molecular genetics and merosin abnormality in Fukuyama-type congenital muscular dystrophy (FCMD)].

Toda T, Kobayashi K. Toda T, et al. Among authors: kobayashi k. Nihon Rinsho. 1997 Dec;55(12):3169-75. Nihon Rinsho. 1997. PMID: 9436430 Review. Japanese.

3

An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy.

Kobayashi K, Nakahori Y, Miyake M, Matsumura K, Kondo-Iida E, Nomura Y, Segawa M, Yoshioka M, Saito K, Osawa M, Hamano K, Sakakihara Y, Nonaka I, Nakagome Y, Kanazawa I, Nakamura Y, Tokunaga K, Toda T. Kobayashi K, et al. Nature. 1998 Jul 23;394(6691):388-92. doi: 10.1038/28653. Nature. 1998. PMID: 9690476

4

Founder-haplotype analysis in Fukuyama-type congenital muscular dystrophy (FCMD).

Kobayashi K, Nakahori Y, Mizuno K, Miyake M, Kumagai T, Honma A, Nonaka I, Nakamura Y, Tokunaga K, Toda T. Kobayashi K, et al. Hum Genet. 1998 Sep;103(3):323-7. doi: 10.1007/s004390050824. Hum Genet. 1998. PMID: 9799088

5

Novel mutations and genotype-phenotype relationships in 107 families with Fukuyama-type congenital muscular dystrophy (FCMD).

Kondo-Iida E, Kobayashi K, Watanabe M, Sasaki J, Kumagai T, Koide H, Saito K, Osawa M, Nakamura Y, Toda T. Kondo-Iida E, et al. Among authors: kobayashi k. Hum Mol Genet. 1999 Nov;8(12):2303-9. doi: 10.1093/hmg/8.12.2303. Hum Mol Genet. 1999. PMID: 10545611

6

Fukuyama-type congenital muscular dystrophy: the first human disease to be caused by an ancient retrotransposal integration.

Toda T, Kobayashi K. Toda T, et al. Among authors: kobayashi k. J Mol Med (Berl). 1999 Dec;77(12):816-23. doi: 10.1007/s001099900065. J Mol Med (Berl). 1999. PMID: 10682317 Review.

7

The Fukuyama congenital muscular dystrophy story.

Toda T, Kobayashi K, Kondo-Iida E, Sasaki J, Nakamura Y. Toda T, et al. Among authors: kobayashi k. Neuromuscul Disord. 2000 Mar;10(3):153-9. doi: 10.1016/s0960-8966(99)00109-1. Neuromuscul Disord. 2000. PMID: 10734260 Review.

8

Age and origin of the FCMD 3'-untranslated-region retrotransposal insertion mutation causing Fukuyama-type congenital muscular dystrophy in the Japanese population.

Colombo R, Bignamini AA, Carobene A, Sasaki J, Tachikawa M, Kobayashi K, Toda T. Colombo R, et al. Among authors: kobayashi k. Hum Genet. 2000 Dec;107(6):559-67. doi: 10.1007/s004390000421. Hum Genet. 2000. PMID: 11153909

9

YAC and cosmid contigs encompassing the Fukuyama-type congenital muscular dystrophy (FCMD) candidate region on 9q31.

Miyake M, Nakahori Y, Matsushita I, Kobayashi K, Mizuno K, Hirai M, Kanazawa I, Nakagome Y, Tokunaga K, Toda T. Miyake M, et al. Among authors: kobayashi k. Genomics. 1997 Mar 1;40(2):284-93. doi: 10.1006/geno.1996.4584. Genomics. 1997. PMID: 9119396

10

Prenatal diagnosis of Fukuyama-type congenital muscular dystrophy by microsatellite analysis.

Takai Y, Tsutsumi O, Harada I, Fujii T, Kashima T, Kobayashi K, Toda T, Taketani Y. Takai Y, et al. Among authors: kobayashi k. Hum Reprod. 1998 Feb;13(2):320-3. doi: 10.1093/humrep/13.2.320. Hum Reprod. 1998. PMID: 9557830

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