Using mouse and zebrafish models to understand the etiology of developmental defects in Cornelia de Lange Syndrome

American Journal of Medical Genetics, Part C: Seminars in Medical Genetics

Volumn 172, Issue 2, 2016, Pages 138-145

  Kawauchi, Shimako ^a   Santos, Rosaysela ^a   Muto, Akihiko ^a   Lopez Burks, Martha E ^a   Schilling, Thomas F ^a   Lander, Arthur D ^a   Calof, Anne L ^a  

^a NONE

Author keywords

chromatin conformation; Hox genes; Nipped B like (NIPBL) gene; Protocadherin genes; Shh genes

Indexed keywords

NIPPED B LIKE PROTEIN; REGULATOR PROTEIN; UNCLASSIFIED DRUG; NIPBL PROTEIN, HUMAN; PROTEIN;

ARTICLE; CHROMATIN; CHROMOSOMAL LOCALIZATION; CONGENITAL HEART MALFORMATION; CONGENITAL MALFORMATION; CRANIOFACIAL MALFORMATION; DE LANGE SYNDROME; GENE EXPRESSION REGULATION; INTESTINE MALFORMATION; LIMB MALFORMATION; MOLECULAR PATHOLOGY; MOUSE MODEL; NEUROANATOMY; NONHUMAN; PRIORITY JOURNAL; PROTEIN FUNCTION; ZEBRA FISH; ANIMAL; CONGENITAL DISORDER; DEVELOPMENTAL DISORDER; DISEASE MODEL; GENE REGULATORY NETWORK; GENETICS; HUMAN; MOUSE;

ANIMALS; CONGENITAL ABNORMALITIES; DE LANGE SYNDROME; DEVELOPMENTAL DISABILITIES; DISEASE MODELS, ANIMAL; GENE EXPRESSION REGULATION; GENE REGULATORY NETWORKS; HUMANS; MICE; PROTEINS; ZEBRAFISH;

EID: 84968583526     PISSN: 15524868     EISSN: 15524876     Source Type: Journal    
DOI: 10.1002/ajmg.c.31484     Document Type: Article

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