Down syndrome mouse models Ts65Dn, Ts1Cje, and Ms1Cje/Ts65Dn exhibit variable severity of cerebellar phenotypes

Developmental Dynamics

Volumn 230, Issue 3, 2004, Pages 581-589

  Olson, L E ^a,c   Roper, R J ^a   Baxter, L L ^a,d   Carlson, E J ^b   Epstein, C J ^b   Reeves, Roger H ^a  

^a JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

^c UNIVERSITY OF REDLANDS   (United States)

^d NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

Author keywords

Cell density; Cerebellum; Down syndrome; Mouse model; Trisomy; Volume

Indexed keywords

ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BRAIN SIZE; CELL DENSITY; CEREBELLUM; CHROMOSOME 16; CHROMOSOME 21; CONTROLLED STUDY; DOWN SYNDROME; FEMALE; GENE ACTIVITY; GENE DOSAGE; GRANULE CELL; MALE; MOUSE; MOUSE STRAIN; MS1CJE MOUSE; NEUROPATHOLOGY; NONHUMAN; ORTHOLOGY; PHENOTYPE; PRIORITY JOURNAL; PURKINJE CELL; TRISOMY; TS1CJE MOUSE; TS65DN MOUSE;

ANIMALS; CEREBELLUM; CROSSES, GENETIC; DISEASE MODELS, ANIMAL; DOWN SYNDROME; FEMALE; GENETIC MARKERS; GRANULOCYTES; HUMANS; IMAGING, THREE-DIMENSIONAL; MALE; MICE; MICE, INBRED C3H; MICE, INBRED C57BL; ORGAN SIZE; PHENOTYPE; PROTEIN BIOSYNTHESIS; PURKINJE CELLS; SEQUENCE DELETION; TRISOMY;

EID: 3042612213     PISSN: 10588388     EISSN: None     Source Type: Journal    
DOI: 10.1002/dvdy.20079     Document Type: Article

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