Developmental and growth defects in mice with combined deficiency of CK2 catalytic genes

Molecular and Cellular Biochemistry

Volumn 356, Issue 1-2, 2011, Pages 227-231

  Landesman Bollag, Esther ^a   Belkina, Anna ^a   Hovey, Beth ^a   Connors, Edward ^a   Cox, Charles ^a   Seldin, David C ^a  

^a BOSTON MEDICAL CENTER   (United States)

Author keywords

Casein kinase II; Homologous recombination; Mouse embryonic fibroblast; Protein kinase CK2

Indexed keywords

CASEIN KINASE II;

ALLELE; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; CELL CULTURE; CONTROLLED STUDY; DEVELOPMENTAL DISORDER; EMBRYO; EMBRYO DEATH; EMBRYO DEVELOPMENT; FEMALE; FIBROBLAST; GENE; GENE DELETION; GENE FUNCTION; GENE LOSS; GENE SILENCING; GENETIC ASSOCIATION; GROWTH DISORDER; HEART FUNCTION; INHERITANCE; LIFESPAN; MALE; MOUSE; NONHUMAN;

ANIMALS; BODY WEIGHT; CASEIN KINASE II; CATALYTIC DOMAIN; CELL PROLIFERATION; FIBROBLASTS; GROWTH AND DEVELOPMENT; HYDRONEPHROSIS; MALE; MICE; MICE, KNOCKOUT; PHENOTYPE; PROTEIN SUBUNITS; TIBIA; URINARY BLADDER;

MUS;

EID: 84855209107     PISSN: 03008177     EISSN: 15734919     Source Type: Journal    
DOI: 10.1007/s11010-011-0967-2     Document Type: Article

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