Alms1-disrupted mice recapitulate human Alström syndrome

Human Molecular Genetics

Volumn 14, Issue 16, 2005, Pages 2323-2333

  Collin, G B ^a   Cyr, E ^a   Bronson, R ^a,b   Marshall, J D ^a   Gifford, E J ^a   Hicks, W ^a   Murray, S A ^a   Zheng, Q Y ^a,c   Smith, R S ^a   Nishina, P M ^a   Naggert, J K ^a  

^a JACKSON LABORATORY   (United States)

^b HARVARD MEDICAL SCHOOL   (United States)

^c MEDICAL SCHOOL OF XI AN JIAOTONG UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

CELL PROTEIN; INSULIN; PROTEIN ALMS1; RHODOPSIN; UNCLASSIFIED DRUG;

ALSTROM SYNDROME; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; AUDITORY RESPONSE; B WAVE; BIOACCUMULATION; BRAIN STEM RESPONSE; CELL DEGENERATION; CELL LINE; CELL NUCLEUS; CELL TRANSPORT; CELL VACUOLE; CLINICAL FEATURE; CONTROLLED STUDY; ELECTRON MICROSCOPY; ELECTRORETINOGRAPHY; EMBRYO; EMBRYO CELL; FEMALE; GENE DISRUPTION; HEARING LOSS; HYPERGLYCEMIA; HYPERINSULINEMIA; HYPOGONADISM; IMMUNOHISTOCHEMISTRY; INSULIN RESISTANCE; MALE; MOUSE; NONHUMAN; OBESITY; PHOTORECEPTOR CELL; PRIORITY JOURNAL; PROTEIN FUNCTION; PROTEIN LOCALIZATION; RETINA CONE; RETINA DISEASE; STEM CELL; WEIGHT GAIN;

ANIMALS; DIABETES MELLITUS, TYPE 2; DISEASE MODELS, ANIMAL; ELECTRORETINOGRAPHY; FEMALE; HEARING LOSS; HUMANS; HYPERINSULINISM; INSULIN RESISTANCE; MALE; MICE; MICE, INBRED C57BL; MICE, KNOCKOUT; NERVE DEGENERATION; OBESITY; PROTEIN TRANSPORT; PROTEINS; RETINAL DEGENERATION; SEQUENCE HOMOLOGY, AMINO ACID; SYNDROME;

ANIMALIA;

EID: 26444443136     PISSN: 09646906     EISSN: 14602083     Source Type: Journal    
DOI: 10.1093/hmg/ddi235     Document Type: Article

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