Calcitriol ameliorates motor deficits and prolongs survival of Chrne-deficient mouse, a model for congenital myasthenic syndrome, by inducing Rspo2 Reviewed

Ohkawara B, Tomita H, Inoue T, Zhang S, Kanbara S, Koshimizu H, Miyasaka Y, Takeda JI, Nishiwaki H, Nakashima H, Ito M, Masuda A, Ishiguro N, Ogi T, Ohno T, Imagama S, Ohno K

Neurotherapeutics   Vol. 21 ( 2 ) page： e00318   2024.3

Splicing regulation of GFPT1 muscle-specific isoform and its roles in glucose metabolisms and neuromuscular junction Reviewed

Farshadyeganeh P, Nazim M, Zhang R, Ohkawara B, Nakajima K, Rahman MA, Nasrin F, Ito M, Takeda JI, Ohe K, Miyasaka Y, Ohno T, Masuda A, Ohno K

iScience   Vol. 26 ( 10 ) page： 107746   2023.10

C3H/HeNSlc mouse with low phospholipid transfer protein expression showed dyslipidemia Reviewed

Kobayashi M, Kanbe F, Ishii R, Tsubouchi H, Hirai K, Miyasaka Y, Ohno T, Oda H, Ikeda S, Katoh H, Ichiyanagi K, Ishikawa A, Murai A, Horio F

Sci Rep   Vol. 13 ( 1 ) page： 13813   2023.8

Neonatal lethality of mouse A/J-7SM consomic strain is caused by an insertion mutation in the Dchs1 gene Reviewed

Miyasaka Y, Kobayashi T, Gotoh N, Kuga M, Kobayashi M, Horio F, Hashimoto K, Kawabe T, Ohno T.

Mamm Genome   Vol. 34 ( 1 ) page： 32 - 43   2023.3

A novel ENU-induced Cpox mutation causes microcytic hypochromic anemia in mice Reviewed

Miyasaka Y, Okuda K, Miura I, Motegi H, Wakana S, Ohno T

Exp Anim   Vol. 71 ( 4 ) page： 433 - 441   2022.10

A novel model mouse for type 2 diabetes mellitus with early onset and persistent hyperglycemia Reviewed

Ohno T, Miyasaka Y, Yoshida K, Kobayashi M, Horio F, Yokoi N, Mizuno M, Ikegami H

Exp Anim   Vol. 71 ( 4 ) page： 510 - 518   2022.10

Two loci contribute to age-related hearing loss resistance in the Japanese wild-derived inbred MSM/Ms mice Reviewed

Yasuda SP, Miyasaka Y, Hou X, Obara Y, Shitara H, Seki Y, Matsuoka K, Takahashi A, Wakai E, Hibino H, Takada T, Shiroishi T, Kominami R, Kikkawa Y

Biomedicines   Vol. 10 ( 9 ) page： 2221   2022.9

E3 ubiquitin ligase RNF123-deficient mice exhibit reduced parasitemia and mortality in rodent malaria (Plasmodium yoelii 17XL) infection Reviewed

Miyasaka Y, Niwa S, Masuya T, Ishii R, Kobayashi M, Horio F, Ohno T

Parasitol Int   Vol. 88   page： 102542   2022.6

UVB-Induced skin autoinflammation due to Nlrp1b mutation and its inhibition by anti-IL-1β antibody Reviewed

Murase Y, Takeichi T, Koseki J, Miyasaka Y, Muro Y, Ohno T, Shimamura T, Akiyama M

Front Immunol   Vol. 13   page： 876390   2022.6

Autoinflammatory keratinization disease with hepatitis and autism reveals roles for JAK1 kinase hyperactivity in autoinflammation Reviewed

Takeichi T, Lee JYW, Okuno Y, Miyasaka Y, Murase Y, Yoshikawa T, Tanahashi K, Nishida E, Okamoto T, Ito K, Muro Y, Sugiura K, Ohno T, McGrath JA, Akiyama M

Front Immunol   Vol. 12   page： 737747   2022.1

Role of an Atypical Cadherin Gene, Cdh23 in Prepulse Inhibition, and Implication of CDH23 in Schizophrenia Reviewed

Balan S, Ohnishi T, Watanabe A, Ohba H, Iwayama Y, Toyoshima M, Hara T, Hisano Y, Miyasaka Y, Toyota T, Shimamoto-Mitsuyama C, Maekawa M, Numata S, Ohmori T, Shimogori T, Kikkawa Y, Hayashi T, Yoshikawa T.

Schizophr Bull   Vol. 47 ( 4 ) page： 1190 - 1200   2021.7

Ablation of Iah1, a candidate gene for diet-induced fatty liver, does not affect liver lipid accumulation in mice Reviewed

Masuya T, Suzuki M, Tsujimura J, Kanamori S, Miyasaka Y, Ohno T, Murai A, Horio F, Kobayashi M.

PLoS One   Vol. 15 ( 5 ) page： e0233087   2020.5

c.753A>G genome editing of a Cdh23 ahl allele delays age-related hearing loss and degeneration of cochlear hair cells in C57BL/6J mice Reviewed

Yasuda SP, Seki Y, Suzuki S, Ohshiba Y, Hou X, Matsuoka K, Wada K, Shitara H, Miyasaka Y, Kikkawa Y.

Hear Res   Vol. 389   page： 107926   2020.4

SDR9C7 catalyzes critical dehydrogenation of acylceramides for skin barrier formation Reviewed

Takeichi T, Hirabayashi T, Miyasaka Y, Kawamoto A, Okuno Y, Taguchi S, Tanahashi K, Murase C, Takama H, Tanaka K, Boeglin WE, Calcutt MW, Watanabe D, Kono M, Muro Y, Ishikawa J, Ohno T, Brash AR, Akiyama M.

J Clin Invest   Vol. 130 ( 2 ) page： 890 - 903   2020.2

Mouse NC/Jic strain provides novel insights into host genetic factors for malaria research Reviewed

Ohno T, Miyasaka Y, Kuga M, Ushida K, Matsushima M, Kawabe T, Kikkawa Y, Mizuno M, Takahashi M

Exp Anim   Vol. 68 ( 3 ) page： 243 - 255   2019.3

OHC-TRECK: A Novel System Using a Mouse Model for Investigation of the Molecular Mechanisms Associated with Outer Hair Cell Death in the Inner Ear Reviewed

Matsuoka K, Wada K, Miyasaka Y, Yasuda SP, Seki Y, Nishito Y, Yonekawa H, Taya C, Shitara H, Kikkawa Y.

Sci Rep   Vol. 9 ( 1 ) page： 5285   2019.3

Intestinal immunity suppresses carrying capacity of rats for the model tapeworm, Hymenolepis diminuta Reviewed

Ohno T, Kai T, Miyasaka Y, Maruyama H, Ishih A, Kino H.

Parasitol Int   Vol. 67 ( 4 ) page： 357 - 361   2018.8

Congenic mapping and candidate gene analysis for streptozotocin-induced diabetes susceptibility locus on mouse chromosome 11 Reviewed

Maegawa T, Miyasaka Y, Kobayashi M, Babaya N, Ikegami H, Horio F, Takahashi M, Ohno T.

Mamm Genome   Vol. 29 ( 3-4 ) page： 273 - 280   2018.4

A novel splice site mutation of myosin VI in mice leads to stereociliary fusion caused by disruption of actin networks in the apical region of inner ear hair cells Reviewed

Seki Y, Miyasaka Y, Suzuki S, Wada K, Yasuda SP, Matsuoka K, Ohshiba Y, Endo K, Ishii R, Shitara H, Kitajiri SI, Nakagata N, Takebayashi H, Kikkawa Y.

PLoS One   Vol. 12 ( 8 ) page： e0183477   2017.8

A new missense mutation in the paired domain of the mouse Pax3 gene Reviewed

Ohno T, Maegawa T, Katoh H, Miyasaka Y, Suzuki M, Kobayashi M, Horio F.

Exp Anim   Vol. 66 ( 3 ) page： 245 - 250   2017.4

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

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, Hiromichi Y, Kikkawa Y.

Hum Mol Genet   Vol. 25 ( 10 ) page： 2045 - 2059   2016.3

Quantitative trait loci on chromosome 5 for susceptibility to frequency-specific effects on hearing in DBA/2J mice Reviewed

Suzuki S, Ishikawa M, Ueda T, Ohshiba Y, Miyasaka Y, Okumura K, Yokohama M, Taya C, Matsuoka K, Kikkawa Y.

Exp Anim   Vol. 64 ( 3 ) page： 241 - 251   2015.3

Dilation of the inferior colliculus and hypersensitivity to sound in Wnt1-cre and Wnt1-GAL4 double-transgenic mice Reviewed

Nakajima M, Nishikawa C, Miyasaka Y, Kikkawa Y, Mori H, Tsuruta M, Okuyama S, Furukawa Y.

  Vol. 566   page： 236 - 240   2014.4

Compound Heterozygosity of the Functionally Null Cdh23v-ngt and Hypomorphic Cdh23ahl Alleles Leads to Early-onset Progressive Hearing Loss in Mice Reviewed

Miyasaka Y, Suzuki S, Ohshiba Y, Watanabe K, Sagara Y, Yasuda SP, Matsuoka K, Shitara H, Yonekawa H, Kominami R, Kikkawa Y.

Exp Anim   Vol. 62 ( 4 ) page： 333 - 346   2013.10

Independent genetic control of early and late stages of chemically induced skin tumors in a cross of a Japanese wild-derived inbred mouse strain, MSM/Ms Reviewed

Okumura K, Sato M, Saito M, Miura I, Wakana S, Mao JH, Miyasaka Y, Kominami R, Wakabayashi Y.

Carcinogenesis   Vol. 33   page： 2260 - 2268   2012.11

Advantages of a mouse model for human hearing impairment Reviewed

Kikkawa Y, Seki Y, Okumura K, Ohshiba Y, Miyasaka Y, Suzuki S, Ozaki M, Matsuoka K, Noguchi Y, Yonekawa H.

Exp Anim   Vol. 61 ( 2 ) page： 85 - 98   2012.4

Bcl11b heterozygosity leads to age-related hearing loss and degeneration of outer hair cells of the mouse cochlea Reviewed

Okumura H, Miyasaka Y, Morita Y, Nomura T, Mishima Y, Takahashi S, Kominami R.

Exp Anim   Vol. 60 ( 4 ) page： 355 - 361   2011.7

大学院基盤医科学実習（マウスの基本的な取り扱いと実験手法）

2019