Wakana S - Search Results

1

Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament.

Tanaka S, Miura I, Yoshiki A, Kato Y, Yokoyama H, Shinogi A, Masuya H, Wakana S, Tamura M, Shiroishi T. Tanaka S, et al. Among authors: wakana s. Genomics. 2007 Dec;90(6):703-11. doi: 10.1016/j.ygeno.2007.07.013. Epub 2007 Oct 24. Genomics. 2007. PMID: 17920809 Free article.

2

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: wakana s. Genetics. 2003 Oct;165(2):721-33. doi: 10.1093/genetics/165.2.721. Genetics. 2003. PMID: 14573483 Free PMC article.

3

Phylogenetic conservation of a limb-specific, cis-acting regulator of Sonic hedgehog ( Shh).

Sagai T, Masuya H, Tamura M, Shimizu K, Yada Y, Wakana S, Gondo Y, Noda T, Shiroishi T. Sagai T, et al. Among authors: wakana s. Mamm Genome. 2004 Jan;15(1):23-34. doi: 10.1007/s00335-033-2317-5. Mamm Genome. 2004. PMID: 14727139

4

A series of ENU-induced single-base substitutions in a long-range cis-element altering Sonic hedgehog expression in the developing mouse limb bud.

Masuya H, Sezutsu H, Sakuraba Y, Sagai T, Hosoya M, Kaneda H, Miura I, Kobayashi K, Sumiyama K, Shimizu A, Nagano J, Yokoyama H, Kaneko S, Sakurai N, Okagaki Y, Noda T, Wakana S, Gondo Y, Shiroishi T. Masuya H, et al. Among authors: wakana s. Genomics. 2007 Feb;89(2):207-14. doi: 10.1016/j.ygeno.2006.09.005. Epub 2006 Oct 13. Genomics. 2007. PMID: 17049204 Free article.

5

A duplicated zone of polarizing activity in polydactylous mouse mutants.

Masuya H, Sagai T, Wakana S, Moriwaki K, Shiroishi T. Masuya H, et al. Among authors: wakana s. Genes Dev. 1995 Jul 1;9(13):1645-53. doi: 10.1101/gad.9.13.1645. Genes Dev. 1995. PMID: 7628698 Free article.

6

Genetic Dissection of Trabecular Bone Structure with Mouse Intersubspecific Consomic Strains.

Kataoka T, Tamura M, Maeno A, Wakana S, Shiroishi T. Kataoka T, et al. Among authors: wakana s. G3 (Bethesda). 2017 Oct 5;7(10):3449-3457. doi: 10.1534/g3.117.300213. G3 (Bethesda). 2017. PMID: 28855285 Free PMC article.

7

Enamelin (Enam) is essential for amelogenesis: ENU-induced mouse mutants as models for different clinical subtypes of human amelogenesis imperfecta (AI).

Masuya H, Shimizu K, Sezutsu H, Sakuraba Y, Nagano J, Shimizu A, Fujimoto N, Kawai A, Miura I, Kaneda H, Kobayashi K, Ishijima J, Maeda T, Gondo Y, Noda T, Wakana S, Shiroishi T. Masuya H, et al. Among authors: wakana s. Hum Mol Genet. 2005 Mar 1;14(5):575-83. doi: 10.1093/hmg/ddi054. Epub 2005 Jan 13. Hum Mol Genet. 2005. PMID: 15649948

8

A monogenic dominant mutation in Rom1 generated by N-ethyl-N-nitrosourea mutagenesis causes retinal degeneration in mice.

Sato H, Suzuki T, Ikeda K, Masuya H, Sezutsu H, Kaneda H, Kobayashi K, Miura I, Kurihara Y, Yokokura S, Nishida K, Tamai M, Gondo Y, Noda T, Wakana S. Sato H, et al. Among authors: wakana s. Mol Vis. 2010 Mar 10;16:378-91. Mol Vis. 2010. PMID: 20300562 Free PMC article.

9

A new mutation Rim3 resembling Re(den) is mapped close to retinoic acid receptor alpha (Rara) gene on mouse chromosome 11.

Sato H, Koide T, Masuya H, Wakana S, Sagai T, Umezawa A, Ishiguro S, Tamai M, Shiroishi T. Sato H, et al. Among authors: wakana s. Mamm Genome. 1998 Jan;9(1):20-5. doi: 10.1007/s003359900673. Mamm Genome. 1998. PMID: 9434940

10

Characterization of single nucleotide polymorphisms for a forward genetics approach using genetic crosses in C57BL/6 and BALB/c substrains of mice.

Miura I, Kikkawa Y, Yasuda SP, Shinogi A, Usuda D, Kumar V, Takahashi JS, Tamura M, Masuya H, Wakana S. Miura I, et al. Among authors: wakana s. Exp Anim. 2022 May 20;71(2):240-251. doi: 10.1538/expanim.21-0181. Epub 2021 Dec 28. Exp Anim. 2022. PMID: 34980769 Free PMC article.

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