Yonekawa H - Search Results

1

Usher syndrome type I G (USH1G) is caused by mutations in the gene encoding SANS, a protein that associates with the USH1C protein, harmonin.

Weil D, El-Amraoui A, Masmoudi S, Mustapha M, Kikkawa Y, Lainé S, Delmaghani S, Adato A, Nadifi S, Zina ZB, Hamel C, Gal A, Ayadi H, Yonekawa H, Petit C. Weil D, et al. Among authors: yonekawa h. Hum Mol Genet. 2003 Mar 1;12(5):463-71. doi: 10.1093/hmg/ddg051. Hum Mol Genet. 2003. PMID: 12588794

2

Interactions in the network of Usher syndrome type 1 proteins.

Adato A, Michel V, Kikkawa Y, Reiners J, Alagramam KN, Weil D, Yonekawa H, Wolfrum U, El-Amraoui A, Petit C. Adato A, et al. Among authors: yonekawa h. Hum Mol Genet. 2005 Feb 1;14(3):347-56. doi: 10.1093/hmg/ddi031. Epub 2004 Dec 8. Hum Mol Genet. 2005. PMID: 15590703

3

Mutations in a new scaffold protein Sans cause deafness in Jackson shaker mice.

Kikkawa Y, Shitara H, Wakana S, Kohara Y, Takada T, Okamoto M, Taya C, Kamiya K, Yoshikawa Y, Tokano H, Kitamura K, Shimizu K, Wakabayashi Y, Shiroishi T, Kominami R, Yonekawa H. Kikkawa Y, et al. Among authors: yonekawa h. Hum Mol Genet. 2003 Mar 1;12(5):453-61. doi: 10.1093/hmg/ddg042. Hum Mol Genet. 2003. PMID: 12588793

4

Heterozygous mutation of Ush1g/Sans in mice causes early-onset progressive hearing loss, which is recovered by reconstituting the strain-specific mutation in Cdh23.

Miyasaka Y, Shitara H, Suzuki S, Yoshimoto S, Seki Y, Ohshiba Y, Okumura K, Taya C, Tokano H, Kitamura K, Takada T, Hibino H, Shiroishi T, Kominami R, Yonekawa H, Kikkawa Y. Miyasaka Y, et al. Among authors: yonekawa h. Hum Mol Genet. 2016 May 15;25(10):2045-2059. doi: 10.1093/hmg/ddw078. Epub 2016 Mar 2. Hum Mol Genet. 2016. PMID: 26936824

5

Alivin 1, a novel neuronal activity-dependent gene, inhibits apoptosis and promotes survival of cerebellar granule neurons.

Ono T, Sekino-Suzuki N, Kikkawa Y, Yonekawa H, Kawashima S. Ono T, et al. Among authors: yonekawa h. J Neurosci. 2003 Jul 2;23(13):5887-96. doi: 10.1523/JNEUROSCI.23-13-05887.2003. J Neurosci. 2003. PMID: 12843293 Free PMC article.

6

A small deletion hotspot in the type II keratin gene mK6irs1/Krt2-6g on mouse chromosome 15, a candidate for causing the wavy hair of the caracul (Ca) mutation.

Kikkawa Y, Oyama A, Ishii R, Miura I, Amano T, Ishii Y, Yoshikawa Y, Masuya H, Wakana S, Shiroishi T, Taya C, Yonekawa H. Kikkawa Y, et al. Among authors: yonekawa h. Genetics. 2003 Oct;165(2):721-33. doi: 10.1093/genetics/165.2.721. Genetics. 2003. PMID: 14573483 Free PMC article.

7

Whirlin complexes with p55 at the stereocilia tip during hair cell development.

Mburu P, Kikkawa Y, Townsend S, Romero R, Yonekawa H, Brown SD. Mburu P, et al. Among authors: yonekawa h. Proc Natl Acad Sci U S A. 2006 Jul 18;103(29):10973-8. doi: 10.1073/pnas.0600923103. Epub 2006 Jul 7. Proc Natl Acad Sci U S A. 2006. PMID: 16829577 Free PMC article.

8

Improved strain distribution patterns of SMXA recombinant inbred strains by microsatellite markers.

Ohno T, Katoh J, Kikkawa Y, Yonekawa H, Nishimura M. Ohno T, et al. Among authors: yonekawa h. Exp Anim. 2003 Oct;52(5):415-7. doi: 10.1538/expanim.52.415. Exp Anim. 2003. PMID: 14625408 Free article.

9

An atopic dermatitis-like skin disease with hyper-IgE-emia develops in mice carrying a spontaneous recessive point mutation in the Traf3ip2 (Act1/CIKS) gene.

Matsushima Y, Kikkawa Y, Takada T, Matsuoka K, Seki Y, Yoshida H, Minegishi Y, Karasuyama H, Yonekawa H. Matsushima Y, et al. Among authors: yonekawa h. J Immunol. 2010 Aug 15;185(4):2340-9. doi: 10.4049/jimmunol.0900694. Epub 2010 Jul 21. J Immunol. 2010. PMID: 20660351

10

Bezoar (Capra aegagrus) is a matriarchal candidate for ancestor of domestic goat (Capra hircus): evidence from the mitochondrial DNA diversity.

Takada T, Kikkawa Y, Yonekawa H, Kawakami S, Amano T. Takada T, et al. Among authors: yonekawa h. Biochem Genet. 1997 Oct;35(9-10):315-26. doi: 10.1023/a:1021869704889. Biochem Genet. 1997. PMID: 9475956

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