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The Journal of Heredity|August 31, 2007
Short-limbed dwarfism: slw is a new allele of Npr2 causing chondrodysplasiaChizuru Sogawa, Takehito Tsuji, Yusuke Shinkai, et al.
Reproduction (Cambridge, England)|June 15, 2012
NPPC/NPR2 signaling is essential for oocyte meiotic arrest and cumulus oophorus formation during follicular development in the mouse ovaryChiyo Kiyosu, Takehito Tsuji, Kaoru Yamada, et al.
The American Journal of Pathology|July 10, 2010
Gastrointestinal tract disorder in natriuretic peptide receptor B gene mutant miceChizuru Sogawa, Asaki Abe, Takehito Tsuji, et al.
Experimental Animals|November 10, 2009
Characterization and linkage mapping of an ENU-induced mutant mouse with defective spermatogenesisYuka Asano, Kouyou Akiyama, Takehito Tsuji, et al.
The Journal of Biological Chemistry|February 28, 2006
Reduced expression of the endothelin receptor type B gene in piebald mice caused by insertion of a retroposon-like element in intron 1Takahisa Yamada, Shin Ohtani, Takeshi Sakurai, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 1, 2023
A nonsense mutation in mouse Adamtsl2 causes uterine hypoplasia and an irregular estrous cycleYuka Iwanaga, Kaori Tsuji, Ayaka Nishimura, et al.
Animal Science Journal = Nihon Chikusan Gakkaiho|February 19, 2010
Exclusion of NEU1 and PPGB from candidate genes for a lysosomal storage disease in Japanese Black cattleAli Akbar Masoudi, Osamu Yamato, Kazuhiro Yoneda, et al.
Biochemical and Biophysical Research Communications|September 9, 2008
Hypomorphic mutation in mouse Nppc gene causes retarded bone growth due to impaired endochondral ossificationTakehito Tsuji, Eri Kondo, Akihiro Yasoda, et al.
Tropical Animal Health and Production|February 11, 2025
White coat color in Vietnamese native buffalo is attributed to the LINE1 insertion in ASIPThuy Thanh Nguyen, Quan Viet Le, Van Huu Nguyen, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|October 26, 2005
Linkage mapping of the locus responsible for congenital multiple ocular defects in cattle on bovine Chromosome 18Abdol Rahim Abbasi, Naoya Ihara, Toshio Watanabe, et al.
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