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Proceedings of the National Academy of Sciences of the United States of America

Volumn 98, Issue 9, 2001, Pages 5170-5174

Naturally variant autosomal and sex-linked loci determine the severity of iron overload in β2-microglobulin-deficient mice

(7) Sproule, Thomas J a Jazwinska, Elizabeth C b Britton, Robert S c Bacon, Bruce R c Fleming, Robert E c Sly, William S c Roopenian, Derry C a

a JACKSON LABORATORY (United States)

b QIMR BERGHOFER MEDICAL RESEARCH INSTITUTE (Australia)

c SAINT LOUIS UNIVERSITY SCHOOL OF MEDICINE (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BETA 2 MICROGLOBULIN; MAJOR HISTOCOMPATIBILITY ANTIGEN CLASS 1;

ALLELE; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CONTROLLED STUDY; DISEASE SEVERITY; GENE LOCUS; GENETIC LINKAGE; GENETIC VARIABILITY; HEMOCHROMATOSIS; HOMOZYGOSITY; IRON OVERLOAD; MOUSE; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; PROGENY; SEGREGATION ANALYSIS; STRAIN DIFFERENCE;

AGING; ANIMALS; BETA 2-MICROGLOBULIN; CROSSES, GENETIC; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HEME; HEMOCHROMATOSIS; HISTOCOMPATIBILITY ANTIGENS CLASS I; HLA ANTIGENS; IRON; IRON OVERLOAD; LINKAGE (GENETICS); LIVER; MALE; MEMBRANE PROTEINS; MICE; MICE, INBRED STRAINS; PHENOTYPE; SEX CHARACTERISTICS; SEX CHROMOSOMES; VARIATION (GENETICS);

ANIMALIA;

EID: 0035942201 PISSN: 00278424 EISSN: None Source Type: Journal
DOI: 10.1073/pnas.091088998 Document Type: Article

Times cited : (42)

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