Kanazawa I - Search Results

1

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. Among authors: kanazawa i. Nature. 1998 Jul 23;394(6691):388-92. doi: 10.1038/28653. Nature. 1998. PMID: 9690476

2

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: kanazawa i. Am J Hum Genet. 1996 Dec;59(6):1313-20. Am J Hum Genet. 1996. PMID: 8940277 Free PMC article.

3

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: kanazawa i. Genomics. 1997 Mar 1;40(2):284-93. doi: 10.1006/geno.1996.4584. Genomics. 1997. PMID: 9119396

4

Genetic identity of Fukuyama-type congenital muscular dystrophy and Walker-Warburg syndrome.

Toda T, Yoshioka M, Nakahori Y, Kanazawa I, Nakamura Y, Nakagome Y. Toda T, et al. Among authors: kanazawa i. Ann Neurol. 1995 Jan;37(1):99-101. doi: 10.1002/ana.410370118. Ann Neurol. 1995. PMID: 7818265

5

Refined mapping of a gene responsible for Fukuyama-type congenital muscular dystrophy: evidence for strong linkage disequilibrium.

Toda T, Ikegawa S, Okui K, Kondo E, Saito K, Fukuyama Y, Yoshioka M, Kumagai T, Suzumori K, Kanazawa I, et al. Toda T, et al. Among authors: kanazawa i. Am J Hum Genet. 1994 Nov;55(5):946-50. Am J Hum Genet. 1994. PMID: 7977357 Free PMC article.

6

Three-dimensional MR imaging of brain surface anomalies in Fukuyama-type congenital muscular dystrophy.

Toda T, Watanabe T, Matsumura K, Sunada Y, Yamada H, Nakano I, Mannen T, Kanazawa I, Shimizu T. Toda T, et al. Among authors: kanazawa i. Muscle Nerve. 1995 May;18(5):508-17. doi: 10.1002/mus.880180506. Muscle Nerve. 1995. PMID: 7739638

7

A unique origin and multistep process for the generation of expanded DRPLA triplet repeats.

Yanagisawa H, Fujii K, Nagafuchi S, Nakahori Y, Nakagome Y, Akane A, Nakamura M, Sano A, Komure O, Kondo I, Jin DK, Sørensen SA, Potter NT, Young SR, Nakamura K, Nukina N, Nagao Y, Tadokoro K, Okuyama T, Miyashita T, Inoue T, Kanazawa I, Yamada M. Yanagisawa H, et al. Among authors: kanazawa i. Hum Mol Genet. 1996 Mar;5(3):373-9. doi: 10.1093/hmg/5.3.373. Hum Mol Genet. 1996. PMID: 8852663

8

Identification of CAG repeat-containing genes expressed in human brain as candidate genes for autosomal dominant spinocerebellar ataxias and other neurodegenerative diseases.

Tachikawa M, Nagai Y, Nakamura K, Kobayashi K, Fujiwara T, Han HJ, Nakabayashi Y, Ichikawa Y, Goto J, Kanazawa I, Nakamura Y, Toda T. Tachikawa M, et al. Among authors: kanazawa i. J Hum Genet. 2002;47(6):275-8. doi: 10.1007/s100380200039. J Hum Genet. 2002. PMID: 12111376

9

A linkage study with DNA markers (D4S95, D4S115, and D4S111) in Japanese Huntington disease families.

Watanabe M, Kondo I, Nissato S, Wakisaka A, Toda T, Ikeda J, Wasmuth JJ, Gusella JF, Kanazawa I. Watanabe M, et al. Among authors: kanazawa i. Jpn J Hum Genet. 1993 Jun;38(2):193-201. doi: 10.1007/BF01883710. Jpn J Hum Genet. 1993. PMID: 8102909

10

Regional and cellular expression of the Machado-Joseph disease gene in brains of normal and affected individuals.

Nishiyama K, Murayama S, Goto J, Watanabe M, Hashida H, Katayama S, Nomura Y, Nakamura S, Kanazawa I. Nishiyama K, et al. Among authors: kanazawa i. Ann Neurol. 1996 Nov;40(5):776-81. doi: 10.1002/ana.410400514. Ann Neurol. 1996. PMID: 8957019

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