Characterization of the Skeletal Fusion with Sterility (sks) Mouse Showing Axial Skeleton Abnormalities Caused by Defects of Embryonic Skeletal Development

Por Akiyama, Kouyou, Katayama, Kentaro, Tsuji, Takehito, Kunieda, Tetsuo
Publicado em 2014

Gastrointestinal Tract Disorder in Natriuretic Peptide Receptor B Gene Mutant Mice

Por Sogawa, Chizuru, Abe, Asaki, Tsuji, Takehito, Koizumi, Mitsuru, Saga, Tsuneo, Kunieda, Tetsuo
Publicado em 2010

An ENU-induced mutation in the mouse Rnf212 gene is associated with male meiotic failure and infertility

Por Fujiwara, Yasuhiro, Matsumoto, Hirokazu, Akiyama, Kouyou, Srivastava, Anuj, Chikushi, Mizuho, Handel, Mary Ann, Kunieda, Tetsuo
Publicado no Reproduction (2014)

Characterization of the chromosomal inversion associated with the Koa mutation in the mouse revealed the cause of skeletal abnormalities

Por Katayama, Kentaro, Miyamoto, Sayaka, Furuno, Aki, Akiyama, Kouyou, Takahashi, Sakino, Suzuki, Hiroetsu, Tsuji, Takehito, Kunieda, Tetsuo
Publicado em 2009

Mutant phenotype analysis suggests potential roles for C-type natriuretic peptide receptor (NPR-B) in male mouse fertility

Por Sogawa, Chizuru, Fujiwara, Yasuhiro, Tsukamoto, Satoshi, Ishida, Yuka, Yoshii, Yukie, Furukawa, Takako, Kunieda, Tetsuo, Saga, Tsuneo
Publicado em 2014

The Critical Roles of Serum/Glucocorticoid-Regulated Kinase 3 (SGK3) in the Hair Follicle Morphogenesis and Homeostasis : The Allelic Difference Provides Novel Insights into Hair F...

Por Okada, Taro, Ishii, Yoshiyuki, Masujin, Kentaro, Yasoshima, Akira, Matsuda, Junichiro, Ogura, Atsuo, Nakayama, Hiroyuki, Kunieda, Tetsuo, Doi, Kunio
Publicado em 2006

A Mutation in the Nuclear Pore Complex Gene Tmem48 Causes Gametogenesis Defects in Skeletal Fusions with Sterility (sks) Mice

Por Akiyama, Kouyou, Noguchi, Junko, Hirose, Michiko, Kajita, Shimpei, Katayama, Kentaro, Khalaj, Maryam, Tsuji, Takehito, Fairfield, Heather, Byers, Candice, Reinholdt, Laura, Ogura, Atsuo, Kunieda, Tetsuo
Publicado em 2013

Tudor domain containing 12 (TDRD12) is essential for secondary PIWI interacting RNA biogenesis in mice

Por Pandey, Radha Raman, Tokuzawa, Yoshimi, Yang, Zhaolin, Hayashi, Eri, Ichisaka, Tomoko, Kajita, Shimpei, Asano, Yuka, Kunieda, Tetsuo, Sachidanandam, Ravi, Chuma, Shinichiro, Yamanaka, Shinya, Pillai, Ramesh S.
Publicado em 2013

Ellis van Creveld2 is required for postnatal craniofacial bone development

Por Badri, Mohammed K., Zhang, Honghao, Ohyama, Yoshio, Venkitapathi, Sundharamani, Kamiya, Nobuhiro, Takeda, Haruko, Ray, Manas, Scott, Greg, Tsuji, Takehito, Kunieda, Tetsuo, Mishina, Yuji, Mochida, Yoshiyuki
Publicado no Anat Rec (Hoboken) (2016)

Generation of Evc2/Limbin global and conditional KO mice and its roles during mineralized tissue formation

Por Zhang, Honghao, Takeda, Haruko, Tsuji, Takehito, Kamiya, Nobuhiro, Rajderkar, Sudha, Louie, Ke’ Ale, Collier, Crystal, Scott, Greg, Ray, Manas, Mochida, Yoshiyuki, Kaartinen, Vesa, Kunieda, Tetsuo, Mishina, Yuji
Publicado no Genesis (2015)

Expression of Evc2 in craniofacial tissues and craniofacial bone defects in Evc2 knockout mouse

Por Badri, Mohammed K., Zhang, Honghao, Ohyama, Yoshio, Venkitapathi, Sundharamani, Alamoudi, Ahmed, Kamiya, Nobuhiro, Takeda, Haruko, Ray, Manas, Scott, Greg, Tsuji, Takehito, Kunieda, Tetsuo, Mishina, Yuji, Mochida, Yoshiyuki
Publicado no Arch Oral Biol (2016)

Dmp1-deficient Mice Display Severe Defects in Cartilage Formation Responsible for a Chondrodysplasia-like Phenotype

Por Ye, Ling, Mishina, Yuji, Chen, Di, Huang, Haiyang, Dallas, Sarah L., Dallas, Mark R., Sivakumar, Pitchumani, Kunieda, Tetsuo, Tsutsui, Takeo W., Boskey, Adele, Bonewald, Lynda F., Feng, Jian Q.
Publicado em 2004

A Missense Mutation in Rev7 Disrupts Formation of Polζ, Impairing Mouse Development and Repair of Genotoxic Agent-induced DNA Lesions

Por Khalaj, Maryam, Abbasi, Abdolrahim, Yamanishi, Hiroshi, Akiyama, Kouyou, Wakitani, Shuso, Kikuchi, Sotaro, Hirose, Michiko, Yuzuriha, Misako, Magari, Masaki, Degheidy, Heba A., Abe, Kuniya, Ogura, Atsuo, Hashimoto, Hiroshi, Kunieda, Tetsuo
Publicado em 2014

Positional cloning of the gene LIMBIN responsible for bovine chondrodysplastic dwarfism

Por Takeda, Haruko, Takami, Marika, Oguni, Tomoko, Tsuji, Takehito, Yoneda, Kazuhiro, Sato, Hiroaki, Ihara, Naoya, Itoh, Tomohito, Kata, Srinivas R., Mishina, Yuji, Womack, James E., Moritomo, Yasuo, Sugimoto, Yoshikazu, Kunieda, Tetsuo
Publicado em 2002

Elevated Fibroblast Growth Factor Signaling Is Critical for the Pathogenesis of the Dwarfism in Evc2/Limbin Mutant Mice

Por Zhang, Honghao, Kamiya, Nobuhiro, Tsuji, Takehito, Takeda, Haruko, Scott, Greg, Rajderkar, Sudha, Ray, Manas K., Mochida, Yoshiyuki, Allen, Benjamin, Lefebvre, Veronique, Hung, Irene H., Ornitz, David M., Kunieda, Tetsuo, Mishina, Yuji
Publicado no PLoS Genet (2016)

Essential Role of Fkbp6 in Male Fertility and Homologous Chromosome Pairing in Meiosis

Por Crackower, Michael A., Kolas, Nadine K., Noguchi, Junko, Sarao, Renu, Kikuchi, Kazuhiro, Kaneko, Hiroyuki, Kobayashi, Eiji, Kawai, Yasuhiro, Kozieradzki, Ivona, Landers, Rushin, Mo, Rong, Hui, Chi-Chung, Nieves, Edward, Cohen, Paula E., Osborne, Lucy R., Wada, Teiji, Kunieda, Tetsuo, Moens, Peter B., Penninger, Josef M.
Publicado em 2003