The mineralization phenotype in Abcc6 -/- mice is affected by Ggcx gene deficiency and genetic background-a model for pseudoxanthoma elasticum

Journal of Molecular Medicine

Volumn 88, Issue 2, 2010, Pages 173-181

  Li, Qiaoli ^a   Uitto, Jouni ^a  

^a THOMAS JEFFERSON UNIVERSITY   (United States)

Author keywords

ABC transporters; Ectopic mineralization; Heritable skin diseases; Pseudoxanthoma elasticum

Indexed keywords

ATP BINDING CASSETTE FAMILY C MEMBER 6; MEMBRANE PROTEIN; MULTIDRUG RESISTANCE PROTEIN 6; PROTEIN GGCX; UNCLASSIFIED DRUG;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; DISEASE SEVERITY; EXON; GENE DELETION; GENE FUNCTION; GENE MUTATION; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC VARIABILITY; GENOTYPE PHENOTYPE CORRELATION; HETEROZYGOSITY; HISTOPATHOLOGY; LOSS OF FUNCTION MUTATION; MINERALIZATION; MORPHOMETRICS; NONHUMAN; PHENOTYPE; PSEUDOXANTHOMA ELASTICUM;

ANIMALS; ATP-BINDING CASSETTE TRANSPORTERS; CARBON-CARBON LIGASES; DIET; DISEASE MODELS, ANIMAL; MAGNESIUM; MICE; MICE, INBRED C57BL; MICE, KNOCKOUT; MINERALS; MUTATION; PHENOTYPE; PSEUDOXANTHOMA ELASTICUM;

EID: 76649116557     PISSN: 09462716     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00109-009-0522-8     Document Type: Article

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