Mice mutant for both Hoxa1 and Hoxb1 show extensive remodeling of the hindbrain and defects in craniofacial development

Development

Volumn 126, Issue 22, 1999, Pages 5027-5040

  Rossel, Mireille ^a,b   Capecchi, Mario R ^a  

^a UNIVERSITY OF UTAH SCHOOL OF MEDICINE   (United States)

^b UNIVERSITÉ LYON 1   (France)

Author keywords

Branchial arch; Craniofacial development; Hindbrain; Hoxa1; Hoxb1; Rhombomere

Indexed keywords

ANIMAL EXPERIMENT; ANIMAL TISSUE; APOPTOSIS; ARTICLE; BRAIN DEVELOPMENT; BRANCHIAL ARCH; CONTROLLED STUDY; CRANIOFACIAL DEVELOPMENT; EMBRYO; GENE EXPRESSION; GENE MUTATION; HOMOZYGOTE; MOUSE; NEUROMERE; NEWBORN; NONHUMAN; PRIORITY JOURNAL; RHOMBENCEPHALON;

ANIMALS; APOPTOSIS; AVIAN PROTEINS; BRANCHIAL REGION; CRANIOFACIAL ABNORMALITIES; DNA-BINDING PROTEINS; EARLY GROWTH RESPONSE PROTEIN 2; EMBRYONIC AND FETAL DEVELOPMENT; FETAL PROTEINS; GENOTYPE; HOMEODOMAIN PROTEINS; MAFB TRANSCRIPTION FACTOR; MICE; MICE, MUTANT STRAINS; MOTOR NEURONS; MUTATION; ONCOGENE PROTEINS; RECEPTOR PROTEIN-TYROSINE KINASES; RECEPTOR, EPHA4; RECEPTORS, RETINOIC ACID; RHOMBENCEPHALON; TRANSCRIPTION FACTOR AP-2; TRANSCRIPTION FACTORS;

ANIMALIA;

EID: 0033428617     PISSN: 09501991     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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