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4 results for uniprot:Q9R1A9Drop in citationmapping

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TREX2 exonuclease defective cells exhibit double-strand breaks and chromosomal fragments but not Robertsonian translocations.

Dumitrache L.C., Hu L., Hasty P.

Mutat. Res. 662:84-87(2009) GeneRIF 24102 · Mapped (6)
Trex2 deletion caused high levels of Robertsonian translocations (RbTs) showing Trex2 is important for chromosomal maintenance. GeneRIF 24102

ORFless, intronless, and mutant transcription units in the mouse t complex responder (Tcr) locus.

Schimenti J.C.

Mamm. Genome 10:969-976(1999) MGI 1346343 · UniProtKB (2) · Mapped (10)

Xlr3b is a new imprinted candidate for X-linked parent-of-origin effects on cognitive function in mice.

Davies W., Isles A., Smith R., Karunadasa D., Burrmann D., Humby T., Ojarikre O., Biggin C., Skuse D., Burgoyne P. et al.

Nat. Genet. 37:625-629(2005) MGI 1346343 · Mapped (28)

Increased Susceptibility to Skin Carcinogenesis in TREX2 Knockout Mice.

Parra D., Manils J., Castellana B., Vina-Vilaseca A., Moran-Salvador E., Vazquez-Villoldo N., Tarancon G., Borras M., Sancho S., Benito C. et al.

Cancer Res. 69:6676-6684(2009) MGI 1346343 GeneRIF 24102 · Mapped (2)
A tumor suppressor role for TREX2 in skin carcinogenesis through which it contributes to keratinocyte apoptosis under conditions of genotoxic stress. GeneRIF 24102

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