Homeobox family Hoxc localization during murine palate formation

Author:

Hirata Azumi1,Katayama Kentaro2,Tsuji Takehito3,Imura Hideto4,Natsume Nagato4,Sugahara Toshio4,Kunieda Tetsuo3,Nakamura Hiroaki5,Otsuki Yoshinori6

Affiliation:

1. Department of Anatomy and Cell Biology, Faculty of Medicine; Osaka Medical College; Takatsuki Osaka Japan

2. Division of Functional Morphology, Department of Basic Veterinary Medicine, School of Veterinary Medicine; Nippon Veterinary and Life Science University; Musashino Tokyo Japan

3. Department of Animal Science, Graduate School of Environmental and Life Science; Okayama University; Okayama Japan

4. Division of Research and Treatment for Oral and Maxillofacial Congenital Anomalies, School of Dentistry; Aichi-Gakuin University; Nagoya Aichi Japan

5. Department of Oral Histology, School of Dentistry; Matsumoto Dental University; Shiojiri Nagano Japan

6. Osaka Medical College; Takatsuki Osaka Japan

Publisher

Wiley

Subject

Developmental Biology,Embryology,General Medicine,Pediatrics, Perinatology and Child Health

Reference33 articles.

1. Msx homeobox gene family and craniofacial development;Alappat;Cell Res,2003

2. A mutation in HOXA2 is responsible for autosomal-recessive microtia in an Iranian family;Alasti;Am J Hum Genet,2008

3. The role of HOX genes in normal hematopoiesis and acute leukemia;Alharbi;Leukemia,2013

4. Hairy ears, Eh;Bangham;Mouse News Lett,1965

5. The mutant hairy ears, Eh, reported in MNL 33:68 is homozygous lethal;Bangham;Mouse News Lett,1968

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