Murine models of VACTERL syndrome: Role of sonic hedgehog signaling pathway

Journal of Pediatric Surgery

Volumn 36, Issue 2, 2001, Pages 381-384

  Kim, Peter C W ^a   Mo, Rong ^a   Hui, Chi Chung ^a,b  

^a UNIVERSITY OF TORONTO   (Canada)

^b HOSPITAL FOR SICK CHILDREN   (Canada)

Author keywords

Sonic hedgehog signaling pathway; VACTERL syndrome

Indexed keywords

SONIC HEDGEHOG PROTEIN;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; CONFERENCE PAPER; CONGENITAL MALFORMATION; CONTROLLED STUDY; EMBRYO DEVELOPMENT; GENE TARGETING; GENETIC CODE; LIMB DEVELOPMENT; MIDGUT; MOUSE; NONHUMAN; OMPHALOCELE; PATHOGENESIS; PRIORITY JOURNAL; SIGNAL TRANSDUCTION; VERTEBRA MALFORMATION;

EID: 0035141226     PISSN: 00223468     EISSN: None     Source Type: Journal    
DOI: 10.1053/jpsu.2001.20722     Document Type: Conference Paper

References (14)

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3. Specific and redundant functions of Gli2 and Gli3 zinc finger genes in skeletal patterning and development
4. Essential functions of Gli2 and Gli3 in the formation of lung, trachea and esophagus
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6. Sonic hedgehog is essential to foregut development
7. New mouse models of congenital Anorectal Malformations (CAM)
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13. GLI3 frameshift mutations cause autosomal dominant Pallister-Hall syndrome
14. GLI3 mutations in human disorders mimic Drosophila Cubitus interruptus protein functions and localization