Toda T - Search Results

1

Disease-associated marked hyperalphalipoproteinemia.

Hirano KI, Nagasaka H, Kobayashi K, Yamaguchi S, Suzuki A, Toda T, Doyu M. Hirano KI, et al. Among authors: toda t. Mol Genet Metab Rep. 2014 Jun 30;1:264-268. doi: 10.1016/j.ymgmr.2014.06.001. eCollection 2014. Mol Genet Metab Rep. 2014. PMID: 27896098 Free PMC article.

2

Effects of single ethanol administration on hepatic ornithine decarboxylase induction and polyamine metabolism.

Tanaka T, Nishiguchi S, Kuroki T, Kobayashi K, Matsui-Yuasa I, Otani S, Toda T, Monna T, Sukegawa Y. Tanaka T, et al. Among authors: toda t. Hepatology. 1991 Oct;14(4 Pt 1):696-700. doi: 10.1016/0270-9139(91)90060-9. Hepatology. 1991. PMID: 1916673

3

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

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

4

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

5

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. J Mol Med (Berl). 1999 Dec;77(12):816-23. doi: 10.1007/s001099900065. J Mol Med (Berl). 1999. PMID: 10682317 Review.

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

Fukutin is required for maintenance of muscle integrity, cortical histiogenesis and normal eye development.

Takeda S, Kondo M, Sasaki J, Kurahashi H, Kano H, Arai K, Misaki K, Fukui T, Kobayashi K, Tachikawa M, Imamura M, Nakamura Y, Shimizu T, Murakami T, Sunada Y, Fujikado T, Matsumura K, Terashima T, Toda T. Takeda S, et al. Among authors: toda t. Hum Mol Genet. 2003 Jun 15;12(12):1449-59. doi: 10.1093/hmg/ddg153. Hum Mol Genet. 2003. PMID: 12783852

8

[Fukuyama-type congenital muscular dystrophy and alpha-dystroglycanopathy].

Kobayashi K, Toda T. Kobayashi K, et al. Among authors: toda t. Tanpakushitsu Kakusan Koso. 2004 Nov;49(15 Suppl):2457-62. Tanpakushitsu Kakusan Koso. 2004. PMID: 15553001 Review. Japanese. No abstract available.

9

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.

10

Founder SVA retrotransposal insertion in Fukuyama-type congenital muscular dystrophy and its origin in Japanese and Northeast Asian populations.

Watanabe M, Kobayashi K, Jin F, Park KS, Yamada T, Tokunaga K, Toda T. Watanabe M, et al. Among authors: toda t. Am J Med Genet A. 2005 Nov 1;138(4):344-8. doi: 10.1002/ajmg.a.30978. Am J Med Genet A. 2005. PMID: 16222679

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

1,357 results

Search Page