Conditional knockout of the menkes disease copper transporter demonstrates its critical role in embryogenesis

PLoS ONE

Volumn 7, Issue 8, 2012, Pages

  Wang, Yanfang ^a,b   Zhu, Sha ^a,b   Weisman, Gary A ^a,b   Gitlin, Jonathan D ^c   Petris, Michael J ^a,b  

^a University of Missouri   (United States)

^b UNIVERSITY OF MISSOURI   (United States)

^c MARINE BIOLOGICAL LABORATORY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CRE RECOMBINASE; MENKES PROTEIN;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; ATP7A GENE; EMBRYO; EMBRYO DEVELOPMENT; EXON; EXON 11; FEMALE; GENE; GENE DELETION; GENE INACTIVATION; HETEROZYGOSITY; IN VIVO STUDY; LETHALITY; LIVE BIRTH; MALE; MENKES SYNDROME; MOUSE; NONHUMAN; NUCLEOTIDE SEQUENCE; PROTEIN DEPLETION; PROTEIN EXPRESSION;

ADENOSINE TRIPHOSPHATASES; ANIMALS; CATION TRANSPORT PROTEINS; DISEASE MODELS, ANIMAL; EMBRYO, MAMMALIAN; EMBRYONIC DEVELOPMENT; EXONS; FEMALE; FIBROBLASTS; GENE KNOCKOUT TECHNIQUES; GENE ORDER; GENE TARGETING; GENOTYPE; MALE; MENKES KINKY HAIR SYNDROME; MICE; MICE, KNOCKOUT; PHENOTYPE;

EID: 84865047664     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0043039     Document Type: Article

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