Toda T - Search Results

1

Characterization of the complex 7q21.3 rearrangement in a patient with bilateral split-foot malformation and hearing loss.

Saitsu H, Kurosawa K, Kawara H, Eguchi M, Mizuguchi T, Harada N, Kaname T, Kano H, Miyake N, Toda T, Matsumoto N. Saitsu H, et al. Among authors: toda t. Am J Med Genet A. 2009 Jun;149A(6):1224-30. doi: 10.1002/ajmg.a.32877. Am J Med Genet A. 2009. PMID: 19449426

2

Haplotype-phenotype correlation in Fukuyama congenital muscular dystrophy.

Saito K, Osawa M, Wang ZP, Ikeya K, Fukuyama Y, Kondo-Iida E, Toda T, Ohashi H, Kurosawa K, Wakai S, Kaneko K. Saito K, et al. Among authors: toda t. Am J Med Genet. 2000 May 29;92(3):184-90. doi: 10.1002/(sici)1096-8628(20000529)92:3<184::aid-ajmg5>3.0.co;2-n. Am J Med Genet. 2000. PMID: 10817652

3

Muscular dystrophy and neuronal migration disorder caused by mutations in a glycosyltransferase, POMGnT1.

Yoshida A, Kobayashi K, Manya H, Taniguchi K, Kano H, Mizuno M, Inazu T, Mitsuhashi H, Takahashi S, Takeuchi M, Herrmann R, Straub V, Talim B, Voit T, Topaloglu H, Toda T, Endo T. Yoshida A, et al. Among authors: toda t. Dev Cell. 2001 Nov;1(5):717-24. doi: 10.1016/s1534-5807(01)00070-3. Dev Cell. 2001. PMID: 11709191 Free article.

4

[Identification of a gene for Fukuyama congenital muscular dystrophy and its pathomechanism].

Toda T, Kano H, Sasaki J, Tachikawa M, Kobayashi K. Toda T, et al. Tanpakushitsu Kakusan Koso. 2001 Dec;46(16 Suppl):2299-305. Tanpakushitsu Kakusan Koso. 2001. PMID: 11802383 Review. Japanese. No abstract available.

5

The constitutional t(17;22): another translocation mediated by palindromic AT-rich repeats.

Kurahashi H, Shaikh T, Takata M, Toda T, Emanuel BS. Kurahashi H, et al. Among authors: toda t. Am J Hum Genet. 2003 Mar;72(3):733-8. doi: 10.1086/368062. Epub 2003 Jan 29. Am J Hum Genet. 2003. PMID: 12557125 Free PMC article.

6

Fukuyama-type congenital muscular dystrophy (FCMD) and alpha-dystroglycanopathy.

Toda T, Kobayashi K, Takeda S, Sasaki J, Kurahashi H, Kano H, Tachikawa M, Wang F, Nagai Y, Taniguchi K, Taniguchi M, Sunada Y, Terashima T, Endo T, Matsumura K. Toda T, et al. Congenit Anom (Kyoto). 2003 Jun;43(2):97-104. doi: 10.1111/j.1741-4520.2003.tb01033.x. Congenit Anom (Kyoto). 2003. PMID: 12893968 Review.

7

Alternative splicing regulates the transcriptional activity of Drosophila heat shock transcription factor in response to heat/cold stress.

Fujikake N, Nagai Y, Popiel HA, Kano H, Yamaguchi M, Toda T. Fujikake N, et al. Among authors: toda t. FEBS Lett. 2005 Jul 4;579(17):3842-8. doi: 10.1016/j.febslet.2005.05.074. FEBS Lett. 2005. PMID: 15978579 Free 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

Partial tandem duplication of GRIA3 in a male with mental retardation.

Chiyonobu T, Hayashi S, Kobayashi K, Morimoto M, Miyanomae Y, Nishimura A, Nishimoto A, Ito C, Imoto I, Sugimoto T, Jia Z, Inazawa J, Toda T. Chiyonobu T, et al. Among authors: toda t. Am J Med Genet A. 2007 Jul 1;143A(13):1448-55. doi: 10.1002/ajmg.a.31798. Am J Med Genet A. 2007. PMID: 17568425

10

Genetically regulated epigenetic transcriptional activation of retrotransposon insertion confers mouse dactylaplasia phenotype.

Kano H, Kurahashi H, Toda T. Kano H, et al. Among authors: toda t. Proc Natl Acad Sci U S A. 2007 Nov 27;104(48):19034-9. doi: 10.1073/pnas.0705483104. Epub 2007 Nov 5. Proc Natl Acad Sci U S A. 2007. PMID: 17984064 Free PMC article.

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