The mouse acrodermatitis enteropathica gene Slc39a4 (Zip4) is essential for early development and heterozygosity causes hypersensitivity to zinc deficiency

Human Molecular Genetics

Volumn 16, Issue 12, 2007, Pages 1391-1399

  Dufner Beattie, Jodi ^a,d   Weaver, Benjamin P ^a   Geiser, Jim ^a   Bilgen, Mehmet ^a,b   Larson, Melissa ^a   Xu, Wenhao ^c   Andrews, Glen K ^a  

^a UNIVERSITY OF KANSAS SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF KANSAS MEDICAL CENTER   (United States)

^c UNIVERSITY OF VIRGINIA   (United States)

^d Apath LLC   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

PROTEIN ZIP4; UNCLASSIFIED DRUG; ZINC TRANSPORTER;

ACRODERMATITIS ENTEROPATHICA; ANIMAL CELL; ANIMAL TISSUE; ANOPHTHALMIA; ARTICLE; CONGENITAL HYDROCEPHALUS; CONTROLLED STUDY; EMBRYO; EXENCEPHALY; FEMALE; GENE EXPRESSION; GENE MUTATION; HETEROZYGOSITY; INTRAUTERINE GROWTH RETARDATION; KNOCKOUT MOUSE; MALE; MORPHOGENESIS; MOUSE; NONHUMAN; NUTRITIONAL DEFICIENCY; PRIORITY JOURNAL; PROGENY; PROTEIN FUNCTION; ZINC DEFICIENCY; ZINC METABOLISM;

ACRODERMATITIS; ALLELES; ANIMALS; CATION TRANSPORT PROTEINS; CELLS, CULTURED; EMBRYO; EMBRYONIC DEVELOPMENT; ENDODERM; FEMALE; HETEROZYGOTE; HOMOZYGOTE; MALE; MICE; MICE, INBRED C57BL; MICE, INBRED STRAINS; MICE, KNOCKOUT; MICROSCOPY, FLUORESCENCE; MODELS, GENETIC; ZINC;

EID: 34347352057     PISSN: 09646906     EISSN: 14602083     Source Type: Journal    
DOI: 10.1093/hmg/ddm088     Document Type: Article

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