mouse WRN.Wu J., He J., Mountz J.D.Cited forNUCLEOTIDE SEQUENCECategorySequencesSourceUniProtKB unreviewed (TrEMBL)Submission Submitted to EMBL/GenBank/DDBJ databases (APR-1997)Cited in1
A deletion within the murine Werner syndrome helicase induces sensitivity to inhibitors of topoisomerase and loss of cellular proliferative capacity.Lebel M., Leder P.View abstractCategoriesFunction, SequencesSourceMGI: 109635PubMedEurope PMCProc Natl Acad Sci U S A 95:13097-13102 (1998)Mapped to9
Effect of age and apoptosis on the mouse homologue of the huWRN gene.Wu J., He J., Mountz J.D.View abstractCategorySequencesSourceMGI: 109635PubMedEurope PMCMech Ageing Dev 103:27-44 (1998)Mapped to7
Cloning of a mouse homologue of the human Werner syndrome gene and assignment to 8A4 by fluorescence in situ hybridization.Imamura O., Ichikawa K., Yamabe Y., Goto M., Sugawara M., Furuichi Y.CategorySequencesSourceMGI: 109635PubMedEurope PMCGenomics 41:298-300 (1997)Cited in1Mapped to6
Positional cloning of the Werner's syndrome gene.Yu C.-E., Oshima J., Fu Y.-H., Wijsman E.M., Hisama F., Alisch R., Matthews S., Nakura J., Miki T.[...], Schellenberg G.D.View abstractCategorySequencesSourceMGI: 109635PubMedEurope PMCScience 272:258-262 (1996)Cited in1Mapped to7
Global genetic analysis in mice unveils central role for cilia in congenital heart disease.Li Y., Klena N.T., Gabriel G.C., Liu X., Kim A.J., Lemke K., Chen Y., Chatterjee B., Devine W.[...], Lo C.W.View abstractCategoriesSequences, Phenotypes & VariantsSourceMGI: 109635PubMedEurope PMCNature 521:520-524 (2015)Mapped to99+
Large-scale gene trapping in C57BL/6N mouse embryonic stem cells.Hansen G.M., Markesich D.C., Burnett M.B., Zhu Q., Dionne K.M., Richter L.J., Finnell R.H., Sands A.T., Zambrowicz B.P., Abuin A.View abstractCategorySequencesSourceMGI: 109635PubMedEurope PMCGenome Res 18:1670-1679 (2008)Mapped to99+
Mapping genetic modulators of amyloid plaque deposition in TgCRND8 transgenic mice.Sebastiani G., Krzywkowski P., Dudal S., Yu M., Paquette J., Malo D., Gervais F., Tremblay P.View abstractCategoriesSequences, Phenotypes & VariantsSourceMGI: 109635PubMedEurope PMCHum Mol Genet 15:2313-2323 (2006)Mapped to46
Increased insulin, triglycerides, reactive oxygen species, and cardiac fibrosis in mice with a mutation in the helicase domain of the Werner syndrome gene homologue.Massip L., Garand C., Turaga R.V., Deschenes F., Thorin E., Lebel M.View abstractCategoriesSequences, Phenotypes & VariantsSourceMGI: 109635PubMedEurope PMCExp Gerontol 41:157-168 (2006)Mapped to7
The transcriptional landscape of the mammalian genome.Carninci P., Kasukawa T., Katayama S., Gough J., Frith M.C., Maeda N., Oyama R., Ravasi T., Lenhard B.[...], Hayashizaki Y.View abstractCategorySequencesSourceMGI: 109635PubMedEurope PMCScience 309:1559-1563 (2005)Cited in99+16Mapped to99+
Subtractive hybridisation screen identifies sexually dimorphic gene expression in the embryonic mouse gonad.McClive P.J., Hurley T.M., Sarraj M.A., van den Bergen J.A., Sinclair A.H.View abstractCategoriesSequences, ExpressionSourceMGI: 109635PubMedEurope PMCGenesis 37:84-90 (2003)Mapped to99+
Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs.Okazaki Y., Furuno M., Kasukawa T., Adachi J., Bono H., Kondo S., Nikaido I., Osato N., Saito R.[...], Hayashizaki Y.View abstractCategorySequencesSourceMGI: 109635PubMedEurope PMCNature 420:563-573 (2002)Cited in699+Mapped to99+
Mouse scrapie responsive gene 1 (Scrg1): genomic organization, physical linkage to sap30, genetic mapping on chromosome 8, and expression in neuronal primary cell cultures.Dron M., Tartare X., Guillo F., Haik S., Barbin G., Maury C., Tovey M., Dandoy-Dron F.View abstractCategorySequencesSourceMGI: 109635PubMedEurope PMCGenomics 70:140-149 (2000)Cited in1Mapped to23
Comparative aspects of the Werner syndrome gene.Oshima J.View abstractCategorySequencesSourceMGI: 109635PubMedEurope PMCIn Vivo 14:165-172 (2000)Mapped to7