Identification of the translocation breakpoints in the Ts65Dn and Ts1Cje mouse lines: Relevance for modeling down syndrome

Mammalian Genome

Volumn 22, Issue 11-12, 2011, Pages 674-684

  Duchon, Arnaud ^a   Raveau, Matthieu ^a   Chevalier, Claire ^a   Nalesso, Valérie ^a   Sharp, Andrew J ^b   Herault, Yann ^a,c,d  

^a UNIVERSITÉ DE STRASBOURG   (France)

^b MOUNT SINAI SCHOOL OF MEDICINE   (United States)

^c CNRS   (France)

^d INSTITUT CLINIQUE DE LA SOURIS   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ANEUPLOIDY; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CENTROMERE; CHROMOSOME 12; CHROMOSOME 17; CHROMOSOME BREAKAGE; CHROMOSOME TRANSLOCATION; CONTROLLED STUDY; DISEASE MODEL; DOWN SYNDROME; GENE OVEREXPRESSION; GENOTYPE; MONOSOMY; MOUSE; NONHUMAN; TELOMERE; TRISOMY;

ANIMALS; CELL LINE; COMPARATIVE GENOMIC HYBRIDIZATION; DISEASE MODELS, ANIMAL; DNA BREAKS; DOWN SYNDROME; GENE DUPLICATION; GENOTYPE; MICE; MICE, INBRED BALB C; MUTATION; MYOCARDIUM; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; TRANSLOCATION, GENETIC; TRISOMY;

MUS;

EID: 84655161322     PISSN: 09388990     EISSN: 14321777     Source Type: Journal    
DOI: 10.1007/s00335-011-9356-0     Document Type: Article

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