Cdo Functions at Multiple Points in the Sonic Hedgehog Pathway, and Cdo-Deficient Mice Accurately Model Human Holoprosencephaly

Developmental Cell

Volumn 10, Issue 5, 2006, Pages 657-665

  Zhang, Wei ^a   Kang, Jong Sun ^a   Cole, Francesca ^a   Yi, Min Jeong ^a   Krauss, Robert S ^a  

^a MOUNT SINAI SCHOOL OF MEDICINE   (United States)

Author keywords

DEVBIO; SIGNALING

Indexed keywords

CDO PROTEIN; MEMBRANE PROTEIN; SONIC HEDGEHOG PROTEIN; TRANSCRIPTION FACTOR GLI1; UNCLASSIFIED DRUG;

ACCURACY; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; CONTROLLED STUDY; DISEASE SEVERITY; FEMALE; FOREBRAIN; GENE EXPRESSION PROFILING; GENETIC ASSOCIATION; GENETIC CODE; GENETIC TRANSFECTION; GENETIC VARIABILITY; HOLOPROSENCEPHALY; IN VITRO STUDY; LIMB DEFECT; MALE; MOUSE; MUSCLE DEVELOPMENT; NEWBORN; NONHUMAN; PRIORITY JOURNAL; PROTEIN DEFICIENCY; PROTEIN DETERMINATION; PROTEIN DOMAIN; PROTEIN FUNCTION; PROTEIN LOCALIZATION; PROTEIN TARGETING; REGULATORY MECHANISM; SIGNAL TRANSDUCTION;

ANIMALS; ANIMALS, NEWBORN; CELL ADHESION MOLECULES; DISEASE MODELS, ANIMAL; EMBRYO; GENE EXPRESSION REGULATION, DEVELOPMENTAL; HEDGEHOG PROTEINS; HOLOPROSENCEPHALY; HUMANS; MICE; MICE, INBRED C57BL; MUSCLE DEVELOPMENT; RNA, MESSENGER; SIGNAL TRANSDUCTION; TRANS-ACTIVATORS;

ANIMALIA; ERINACEIDAE;

EID: 33646120095     PISSN: 15345807     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.devcel.2006.04.005     Document Type: Article

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