A mutation in Sec15l1 causes anemia in hemoglobin deficit (hbd) mice

Nature Genetics

Volumn 37, Issue 11, 2005, Pages 1270-1273

  Lim, Jackie E ^a,b   Jin, Ou ^a   Bennett, Carolyn ^a,b   Morgan, Kelly ^c   Wang, Fudi ^a,b   Trenor III, Cameron C ^a,b   Fleming, Mark D ^a,b   Andrews, Nancy C ^a,b,d  

^a BOSTON CHILDREN S HOSPITAL   (United States)

^b HARVARD MEDICAL SCHOOL   (United States)

^c BRIGHAM AND WOMEN S HOSPITAL   (United States)

^d HOWARD HUGHES MEDICAL INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EXOCYST; HEMOGLOBIN; PROTEIN RAB11; RAB PROTEIN; TRANSFERRIN; UNCLASSIFIED DRUG;

ANEMIA; ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; ENDOSOME; EXON; FEMALE; GENE DELETION; GENE INACTIVATION; GENE MUTATION; GENETIC ASSOCIATION; GENETIC DISORDER; GENOTYPE; HEMOGLOBIN DETERMINATION; IRON TRANSPORT; MALE; MOUSE; MOUSE STRAIN; NONHUMAN; NUCLEOTIDE SEQUENCE; PHENOTYPE; PRIORITY JOURNAL; PROTEIN FUNCTION; PROTEIN PROTEIN INTERACTION;

ANEMIA; ANIMALS; BONE MARROW TRANSPLANTATION; ENDOSOMES; GENETIC COMPLEMENTATION TEST; GTP-BINDING PROTEINS; HEMOGLOBINS; IRON; MEMBRANE PROTEINS; MICE; MICE, INBRED C57BL; MICE, MUTANT STRAINS; MOLECULAR SEQUENCE DATA; MUTAGENESIS, INSERTIONAL; MUTATION; RAB GTP-BINDING PROTEINS; RECEPTORS, TRANSFERRIN; RETROVIRIDAE; SEQUENCE DELETION; TRANSFERRIN;

ANIMALIA; MAMMALIA;

EID: 27644526967     PISSN: 10614036     EISSN: 15461718     Source Type: Journal    
DOI: 10.1038/ng1659     Document Type: Article

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