Piebald mutation on a C57BL/6J background
Author:
Affiliation:
1. Research Resources Center, RIKEN Brain Science Institute, Saitama 351-0198, Japan
Publisher
Japanese Society of Veterinary Science
Subject
General Veterinary
Reference23 articles.
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2. 2. Borrego, S., Ruiz-Ferrer, M., Fernández, R. M. and Antiñolo, G. 2013. Hirschsprung’s disease as a model of complex genetic etiology. Histol. Histopathol. 28: 1117–1136.
3. 3. Cheng, Z., Wang, X., Dhall, D., Zhao, L., Bresee, C., Doherty, T. M. and Frykman, P. K. 2011. Splenic lymphopenia in the endothelin receptor B-null mouse: implications for Hirschsprung associated enterocolitis. Pediatr. Surg. Int. 27: 145–150.
4. 4. Dang, R., Sasaki, N., Torigoe, D. and Agui, T. 2012. Anatomic modifications in the enteric nervous system of JF1 mice with the classic piebald mutation. J. Vet. Med. Sci. 74: 391–394.
5. 5. Dang, R., Sasaki, N., Nishino, T., Nakanishi, M., Torigoe, D. and Agui, T. 2012. Lymphopenia in Ednrb-deficient rat was strongly modified by genetic background. Biomed. Res. 33: 249–253.
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