Toda T - Search Results

1

Calbindin 1, fibroblast growth factor 20, and alpha-synuclein in sporadic Parkinson's disease.

Mizuta I, Tsunoda T, Satake W, Nakabayashi Y, Watanabe M, Takeda A, Hasegawa K, Nakashima K, Yamamoto M, Hattori N, Murata M, Toda T. Mizuta I, et al. Among authors: toda t. Hum Genet. 2008 Aug;124(1):89-94. doi: 10.1007/s00439-008-0525-5. Epub 2008 Jun 22. Hum Genet. 2008. PMID: 18568448

2

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. Am J Hum Genet. 1994 Nov;55(5):946-50. Am J Hum Genet. 1994. PMID: 7977357 Free PMC article.

3

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: toda t. Jpn J Hum Genet. 1993 Jun;38(2):193-201. doi: 10.1007/BF01883710. Jpn J Hum Genet. 1993. PMID: 8102909

4

Spermatogenic ability is different among males in different Y chromosome lineage.

Kuroki Y, Iwamoto T, Lee J, Yoshiike M, Nozawa S, Nishida T, Ewis AA, Nakamura H, Toda T, Tokunaga K, Kotliarova SE, Kondoh N, Koh E, Namiki M, Shinka T, Nakahori Y. Kuroki Y, et al. Among authors: toda t. J Hum Genet. 1999;44(5):289-92. doi: 10.1007/s100380050162. J Hum Genet. 1999. PMID: 10496069

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: toda t. Hum Mol Genet. 1999 Nov;8(12):2303-9. doi: 10.1093/hmg/8.12.2303. Hum Mol Genet. 1999. PMID: 10545611

6

Neuronal expression of the fukutin gene.

Sasaki J, Ishikawa K, Kobayashi K, Kondo-Iida E, Fukayama M, Mizusawa H, Takashima S, Sakakihara Y, Nakamura Y, Toda T. Sasaki J, et al. Among authors: toda t. Hum Mol Genet. 2000 Dec 12;9(20):3083-90. doi: 10.1093/hmg/9.20.3083. Hum Mol Genet. 2000. PMID: 11115853

7

An autosomal dominant cerebellar ataxia linked to chromosome 16q22.1 is associated with a single-nucleotide substitution in the 5' untranslated region of the gene encoding a protein with spectrin repeat and Rho guanine-nucleotide exchange-factor domains.

Ishikawa K, Toru S, Tsunemi T, Li M, Kobayashi K, Yokota T, Amino T, Owada K, Fujigasaki H, Sakamoto M, Tomimitsu H, Takashima M, Kumagai J, Noguchi Y, Kawashima Y, Ohkoshi N, Ishida G, Gomyoda M, Yoshida M, Hashizume Y, Saito Y, Murayama S, Yamanouchi H, Mizutani T, Kondo I, Toda T, Mizusawa H. Ishikawa K, et al. Among authors: toda t. Am J Hum Genet. 2005 Aug;77(2):280-96. doi: 10.1086/432518. Epub 2005 Jul 6. Am J Hum Genet. 2005. PMID: 16001362 Free PMC article.

8

Genomic rearrangement at 10q24 in non-syndromic split-hand/split-foot malformation.

Kano H, Kurosawa K, Horii E, Ikegawa S, Yoshikawa H, Kurahashi H, Toda T. Kano H, et al. Among authors: toda t. Hum Genet. 2005 Dec;118(3-4):477-83. doi: 10.1007/s00439-005-0074-0. Epub 2005 Oct 19. Hum Genet. 2005. PMID: 16235095

9

Multiple candidate gene analysis identifies alpha-synuclein as a susceptibility gene for sporadic Parkinson's disease.

Mizuta I, Satake W, Nakabayashi Y, Ito C, Suzuki S, Momose Y, Nagai Y, Oka A, Inoko H, Fukae J, Saito Y, Sawabe M, Murayama S, Yamamoto M, Hattori N, Murata M, Toda T. Mizuta I, et al. Among authors: toda t. Hum Mol Genet. 2006 Apr 1;15(7):1151-8. doi: 10.1093/hmg/ddl030. Epub 2006 Feb 24. Hum Mol Genet. 2006. PMID: 16500997

10

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. Among authors: toda t. 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

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