A Gja1 missense mutation in a mouse model of oculodentodigital dysplasia

Development

Volumn 132, Issue 19, 2005, Pages 4375-4386

  Flenniken, Ann M ^a   Osborne, Lucy R ^a,b   Anderson, Nicole ^b   Ciliberti, Nadia ^c   Fleming, Craig ^a   Gittens, Joanne E I ^d   Gong, Xiang Qun ^d   Kelsey, Lois B ^a   Lounsbury, Crystal ^d   Moreno, Luisa ^a   Nieman, Brian J ^b,e   Peterson, Katie ^a   Qu, Dawei ^a   Roscoe, Wendi ^d   Shao, Qing ^d   Tong, Dan ^d   Veitch, Gregory I L ^d   Voronina, Irina ^a   Vukobradovic, Igor ^a   Wood, Geoffrey A ^a   Zhu, Yonghong ^e   Zirngibl, Ralph A ^b   Aubin, Jane E ^a,b   Bai, Donglin ^d   Bruneau, Benoit G ^b,e,f   Grynpas, Marc ^a,b   Henderson, Janet E ^g   Henkelman, R Mark ^b,e   McKerlie, Colin ^a,b,e   Sled, John G ^b,e   Stanford, William L ^a,b,c   Laird, Dale W ^d   Kidder, Gerald M ^d   Adamson, S Lee ^a,f   Rossant, Janet ^a,b   more..

^a MOUNT SINAI HOSPITAL   (Canada)

^b UNIVERSITY OF TORONTO   (Canada)

^c UNIVERSITY OF TORONTO   (Canada)

^d UNIVERSITY OF WESTERN ONTARIO   (Canada)

^e HOSPITAL FOR SICK CHILDREN   (Canada)

^f UNIVERSITY OF TORONTO   (Canada)

^g MCGILL UNIVERSITY   (Canada)

Author keywords

Connexin 43; Missense mutation; Mouse model; Oculodentodigital dysplasia

Indexed keywords

CONNEXIN 43; ETHYLNITROSOUREA; GAP JUNCTION PROTEIN; MUTANT PROTEIN;

AMINO ACID SUBSTITUTION; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; AUTOSOMAL DOMINANT DISORDER; BONE MASS; CELL JUNCTION; CELL POPULATION; CONTROLLED STUDY; CRANIOFACIAL MALFORMATION; ENAMEL HYPOPLASIA; GENE; GJA1 GENE; HEART DISEASE; HEMATOPOIETIC STEM CELL; MISSENSE MUTATION; MOLECULAR CLONING; MOUSE; MUSCLE STRENGTH; NONHUMAN; OCULODENTODIGITAL SYNDROME; POINT MUTATION; PRIORITY JOURNAL; SYMPTOMATOLOGY; SYNDACTYLY;

ABNORMALITIES, MULTIPLE; ANIMALS; BIOMECHANICS; BONE AND BONES; BONE DENSITY; CONNEXIN 43; CRANIOFACIAL ABNORMALITIES; DENTAL ENAMEL HYPOPLASIA; DISEASE MODELS, ANIMAL; ETHYLNITROSOUREA; EYE ABNORMALITIES; GAP JUNCTIONS; HEART DEFECTS, CONGENITAL; HUMANS; MICE; PENETRANCE; POINT MUTATION; STEM CELLS; SYNDACTYLY;

ANIMALIA;

EID: 27644536275     PISSN: 09501991     EISSN: None     Source Type: Journal    
DOI: 10.1242/dev.02011     Document Type: Article

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