Long-range chromosomal engineering is more efficient in vitro than in vitro

Transgenic Research

Volumn 14, Issue 3, 2005, Pages 325-332

  Olson, Lisa E ^a,b   Tien, Jason ^a   South, Sarah ^a,c   Reeves, Roger H ^a  

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

^b UNIVERSITY OF REDLANDS   (United States)

^c UNIVERSITY OF UTAH   (United States)

Author keywords

Chromosome engineering; Cre LoxP; Down syndrome; TAMERE; Targeted meiotic recombination

Indexed keywords

CRE RECOMBINASE; INTEGRASE; LOX PROTEIN, MOUSE; NUCLEAR PROTEIN; PROTEIN LYSINE 6 OXIDASE; SCLEROPROTEIN; SYCP1 PROTEIN, MOUSE;

A J MOUSE; ANIMAL; ARTICLE; CELL LINE; CHROMOSOME; COMPARATIVE STUDY; CROSS BREEDING; CROSSING OVER; DISEASE MODEL; DOWN SYNDROME; GENE TRANSLOCATION; GENETIC ENGINEERING; GENETICS; HUMAN; IN VITRO STUDY; MALE; MOUSE; REPORTER GENE; STEM CELL;

ANIMALS; CELL LINE; CHROMOSOMES; CROSSES, GENETIC; CROSSING OVER, GENETIC; DISEASE MODELS, ANIMAL; DOWN SYNDROME; EXTRACELLULAR MATRIX PROTEINS; GENES, REPORTER; GENETIC ENGINEERING; HUMANS; INTEGRASES; MALE; MICE; MICE, INBRED A; NUCLEAR PROTEINS; PROTEIN-LYSINE 6-OXIDASE; STEM CELLS; TRANSLOCATION, GENETIC;

MUS MUSCULUS;

EID: 22144484182     PISSN: 09628819     EISSN: None     Source Type: Journal    
DOI: 10.1007/s11248-005-0389-6     Document Type: Article

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