Otx1 function overlaps with Otx2 in development of mouse forebrain and midbrain

Genes to Cells

Volumn 1, Issue 11, 1996, Pages 1031-1044

  Suda, Yoko ^a,b   Matsuo, Isao ^a   Kuratani, Shigeru ^a   Aizawa, Shinichi ^a  

^a KUMAMOTO UNIV SCHOOL OF MEDICINE   (Japan)

^b JAPAN IMMUNORESEARCH LABORATORIES   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

HOMEODOMAIN PROTEIN; NERVE PROTEIN; OTX1 PROTEIN, MOUSE; OTX2 PROTEIN, MOUSE; TRANSACTIVATOR PROTEIN; TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR OTX;

ANIMAL; ARTICLE; FOREBRAIN; GENETICS; HEAD; MORPHOGENESIS; MOUSE; MUTATION; NUCLEOTIDE SEQUENCE; PHENOTYPE; PHYSIOLOGY; PRENATAL DEVELOPMENT;

ANIMALS; BASE SEQUENCE; BODY PATTERNING; HEAD; HOMEODOMAIN PROTEINS; MICE; MUTATION; NERVE TISSUE PROTEINS; OTX TRANSCRIPTION FACTORS; PHENOTYPE; PROSENCEPHALON; TRANS-ACTIVATORS; TRANSCRIPTION FACTORS;

EID: 0030280509     PISSN: 13569597     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2443.1996.900288.x     Document Type: Article

References (1)

1. -/- mutants due to a defective anterior neuroectoderm specification during gastrulation. Development 121, 3279-3290.