Conditional inactivation of the peroxisome biogenesis Pex13 gene by Cre-loxP excision

Genesis

Volumn 32, Issue 2, 2002, Pages 179-180

  Bjorkman, Jonas ^a   Tonks, Ian ^b   Maxwell, Megan A ^a   Paterson, Carol ^b   Kay, Graham F ^b,c   Crane, Denis I ^a  

^a GRIFFITH UNIVERSITY   (Australia)

^b UNIVERSITY OF QUEENSLAND   (Australia)

^c Sylvia and Charles Viertel Charitable Foundation   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; NEOMYCIN; RECOMBINASE;

ALLELE; ANIMAL CELL; ARTICLE; BIOGENESIS; CELL CLONE; EMBRYO; EMBRYO CELL; GENE INACTIVATION; MOUSE; NONHUMAN; PEROXISOME; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SOUTHERN BLOTTING; STEM CELL; TRANSGENE;

ANIMALS; FEMALE; GENE SILENCING; INTEGRASES; MALE; MEMBRANE PROTEINS; MICE; MICE, TRANSGENIC; PEROXISOMES; VIRAL PROTEINS;

ANIMALIA;

EID: 0036198223     PISSN: 1526954X     EISSN: None     Source Type: Journal    
DOI: 10.1002/gene.10044     Document Type: Article

References (5)

1. Pex13, the mouse ortholog of the human peroxisome biogenesis disorder PEX13 gene: Gene structure, tissue expression and localization of the protein to peroxisomes
2. PEX13 is mutated in complementation group 13 of the peroxisome-biogenesis disorders
3. High-efficiency deleter mice show that FLPe is an alternative to Cre-loxP
4. A Cre-transgenic mouse strain for the ubiquitous deletion of loxP-flanked gene segments including deletion in germ cells
5. Nonsense and temperature-sensitive mutations in PEX13 are the cause of complementation group H of peroxisome biogenesis disorders