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Genomics|April 21, 2009
A mutation of the WFDC1 gene is responsible for multiple ocular defects in cattleAbdol Rahim Abbasi, Maryam Khalaj, Takehito Tsuji, et al.
BMC Genetics|September 24, 2009
Characterization of the chromosomal inversion associated with the Koa mutation in the mouse revealed the cause of skeletal abnormalitiesKentaro Katayama, Sayaka Miyamoto, Aki Furuno, et al.
Experimental Animals|November 9, 2006
A deletion in the endothelin-B receptor gene is responsible for the Waardenburg syndrome-like phenotypes of WS4 miceShin Ohtani, Yusuke Shinkai, Akio Horibe, et al.
DNA Research : an International Journal for Rapid Publication of Reports on Genes and Genomes|May 6, 2005
A mutation in the serum and glucocorticoid-inducible kinase-like kinase (Sgkl) gene is associated with defective hair growth in miceKentaro Masujin, Taro Okada, Takehito Tsuji, et al.
The Journal of Reproduction and Development|April 4, 2008
Leydig cell hyperplasia in an ENU-induced mutant mouse with germ cell depletionMaryam Khalaj, Abdol Rahim Abbasi, Ryo Nishimura, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|August 18, 2005
An insertion mutation of the bovine Fii gene is responsible for factor XI deficiency in Japanese black cattleMasaki Kunieda, Takehito Tsuji, Abdol Rahim Abbasi, et al.
Congenital Anomalies|January 1, 2016
Homeobox family Hoxc localization during murine palate formationAzumi Hirata, Kentaro Katayama, Takehito Tsuji, et al.
Biomed Research International|March 20, 2013
Heparanase localization during palatogenesis in miceAzumi Hirata, Kentaro Katayama, Takehito Tsuji, et al.
Experimental Animals|February 8, 2008
Suppressed recombination on mouse chromosome 15 defined regions of chromosomal inversions associated with koala (koa) and hairy ears (eh) mutationsKentaro Katayama, Aki Furuno, Sayaka Miyamoto, et al.
Reproduction (Cambridge, England)|November 11, 2010
A missense mutation of the Dhh gene is associated with male pseudohermaphroditic rats showing impaired Leydig cell developmentYasuhiro Kawai, Junko Noguchi, Kouyou Akiyama, et al.
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