Kano H - Search Results

1

Japanese founder duplications/triplications involving BHLHA9 are associated with split-hand/foot malformation with or without long bone deficiency and Gollop-Wolfgang complex.

Nagata E, Kano H, Kato F, Yamaguchi R, Nakashima S, Takayama S, Kosaki R, Tonoki H, Mizuno S, Watanabe S, Yoshiura K, Kosho T, Hasegawa T, Kimizuka M, Suzuki A, Shimizu K, Ohashi H, Haga N, Numabe H, Horii E, Nagai T, Yoshihashi H, Nishimura G, Toda T, Takada S, Yokoyama S, Asahara H, Sano S, Fukami M, Ikegawa S, Ogata T. Nagata E, et al. Among authors: kano h. Orphanet J Rare Dis. 2014 Oct 21;9:125. doi: 10.1186/s13023-014-0125-5. Orphanet J Rare Dis. 2014. PMID: 25351291 Free PMC article.

2

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. 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

3

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

Kano H, Kurahashi H, Toda T. Kano H, et al. 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.

4

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: kano h. 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

5

[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. Among authors: kano h. Tanpakushitsu Kakusan Koso. 2001 Dec;46(16 Suppl):2299-305. Tanpakushitsu Kakusan Koso. 2001. PMID: 11802383 Review. Japanese. No abstract available.

6

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: kano h. FEBS Lett. 2005 Jul 4;579(17):3842-8. doi: 10.1016/j.febslet.2005.05.074. FEBS Lett. 2005. PMID: 15978579 Free article.

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: kano h. 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 (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. Among authors: kano h. 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.

9

Deficiency of alpha-dystroglycan in muscle-eye-brain disease.

Kano H, Kobayashi K, Herrmann R, Tachikawa M, Manya H, Nishino I, Nonaka I, Straub V, Talim B, Voit T, Topaloglu H, Endo T, Yoshikawa H, Toda T. Kano H, et al. Biochem Biophys Res Commun. 2002 Mar 15;291(5):1283-6. doi: 10.1006/bbrc.2002.6608. Biochem Biophys Res Commun. 2002. PMID: 11883957

10

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: kano h. Dev Cell. 2001 Nov;1(5):717-24. doi: 10.1016/s1534-5807(01)00070-3. Dev Cell. 2001. PMID: 11709191 Free article.

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