Lineage-specific biology revealed by a finished genome assembly of the mouse.Church D.M., Goodstadt L., Hillier L.W., Zody M.C., Goldstein S., She X., Bult C.J., Agarwala R., Cherry J.L.[...], Ponting C.P.View abstractCited forNUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]StrainC57BL/6JCategorySequencesSourceUniProtKB unreviewed (TrEMBL)PubMedEurope PMCPLoS Biol. 7:E1000112-E1000112 (2009)Cited in99+99+
Modernizing reference genome assemblies.Church D.M., Schneider V.A., Graves T., Auger K., Cunningham F., Bouk N., Chen H.C., Agarwala R., McLaren W.M.[...], Hubbard T.Cited forNUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]StrainC57BL/6JCategorySequencesSourceUniProtKB unreviewed (TrEMBL)PubMedEurope PMCPLoS Biol 9:e1001091-e1001091 (2011)Cited in99+
No title available.EnsemblCited forIDENTIFICATIONStrainC57BL/6JSourceUniProtKB unreviewed (TrEMBL)Submission Submitted to UniProtKB (AUG-2024)Cited in99+
Comparative FISH mapping of mouse and rat homologues of twenty-five human X-linked genes.Kuroiwa A., Watanabe T., Hishigaki H., Takahashi E., Namikawa T., Matsuda Y.View abstractCategorySequencesSourceMGI: 109626PubMedEurope PMCCytogenet Cell Genet 81:208-212 (1998)Mapped to99+
A comparative transcriptional map of a region of 250 kb on the human and mouse X chromosome between the G6PD and the FLN1 genes.Rivella S., Tamanini F., Bione S., Mancini M., Herman G., Chatterjee A., Maestrini E., Toniolo D.View abstractCategorySequencesSourceMGI: 109626PubMedEurope PMCGenomics 28:377-382 (1995)Mapped to64
Mice Deficient in TAZ (Wwtr1) Demonstrate Clinical Features of Late-Onset Fuchs' Endothelial Corneal Dystrophy.Leonard B.C., Park S., Kim S., Young L.J., Jalilian I., Cosert K., Zhang X., Skeie J.M., Shevalye H.[...], Thomasy S.M.View abstractCategorySubcellular LocationSourceMGI: 109626PubMedEurope PMCInvest Ophthalmol Vis Sci 64:22-22 (2023)Mapped to14
Genetic modifiers modulate phenotypic expression of tafazzin deficiency in a mouse model of Barth syndrome.Wang S., Yazawa E., Keating E.M., Mazumdar N., Hauschild A., Ma Q., Wu H., Xu Y., Shi X.[...], Pu W.T.View abstractCategoryFunctionSourceMGI: 109626PubMedEurope PMCHum Mol Genet 32:2055-2067 (2023)Mapped to13
DELE1 is protective for mitochondrial cardiomyopathy.Huynh H., Zhu S., Lee S., Bao Y., Pang J., Nguyen A., Gu Y., Chen C., Ouyang K.[...], Fang X.View abstractCategoryFunctionSourceMGI: 109626PubMedEurope PMCJ Mol Cell Cardiol 175:44-48 (2023)Mapped to73
Mitochondrial Stress Induces an HRI-eIF2alpha Pathway Protective for Cardiomyopathy.Zhu S., Nguyen A., Pang J., Zhao J., Chen Z., Liang Z., Gu Y., Huynh H., Bao Y.[...], Fang X.CategoryFunctionSourceMGI: 109626PubMedEurope PMCCirculation 146:1028-1031 (2022)Mapped to55
Tafazzin deficiency in mouse mesenchymal stem cells promote reprogramming of activated B lymphocytes toward immunosuppressive phenotypes.Zegallai H.M., Abu-El-Rub E., Olayinka-Adefemi F., Cole L.K., Sparagna G.C., Marshall A.J., Hatch G.M.View abstractCategoriesFunction, Phenotypes & VariantsSourceMGI: 109626PubMedEurope PMCFASEB J 36:e22443-e22443 (2022)Mapped to13
Myofibroblast YAP/TAZ activation is a key step in organ fibrogenesis.He X., Tolosa M.F., Zhang T., Goru S.K., Ulloa Severino L., Misra P.S., McEvoy C.M., Caldwell L., Szeto S.G.[...], Yuen D.A.View abstractCategoryFunctionSourceMGI: 109626PubMedEurope PMCJCI Insight 7:e146243-e146243 (2022)Mapped to30
A new murine model of Barth syndrome neutropenia links TAFAZZIN deficiency to increased ER stress-induced apoptosis.Sohn J., Milosevic J., Brouse T., Aziz N., Elkhoury J., Wang S., Hauschild A., van Gastel N., Cetinbas M.[...], Sykes D.B.View abstractCategoriesFunction, Phenotypes & VariantsSourceMGI: 109626PubMedEurope PMCBlood Adv 6:2557-2577 (2022)Mapped to13
Tafazzin deficiency impairs mitochondrial metabolism and function of lipopolysaccharide activated B lymphocytes in mice.Zegallai H.M., Abu-El-Rub E., Cole L.K., Field J., Mejia E.M., Gordon J.W., Marshall A.J., Hatch G.M.View abstractCategoryFunctionSourceMGI: 109626PubMedEurope PMCFASEB J 35:e22023-e22023 (2021)Mapped to13
Loss of Mitochondrial Ca<sup>2+</sup> Uniporter Limits Inotropic Reserve and Provides Trigger and Substrate for Arrhythmias in Barth Syndrome Cardiomyopathy.Bertero E., Nickel A., Kohlhaas M., Hohl M., Sequeira V., Brune C., Schwemmlein J., Abesser M., Schuh K.[...], Maack C.View abstractCategoriesFunction, Phenotypes & VariantsSourceMGI: 109626PubMedEurope PMCCirculation 144:1694-1713 (2021)Mapped to13
Cardiolipin Remodeling Defects Impair Mitochondrial Architecture and Function in a Murine Model of Barth Syndrome Cardiomyopathy.Zhu S., Chen Z., Zhu M., Shen Y., Leon L.J., Chi L., Spinozzi S., Tan C., Gu Y.[...], Fang X.View abstractCategoryFunctionSourceMGI: 109626PubMedEurope PMCCirc Heart Fail 14:e008289-e008289 (2021)Mapped to13
Tafazzin Deficiency Reduces Basal Insulin Secretion and Mitochondrial Function in Pancreatic Islets From Male Mice.Cole L.K., Agarwal P., Doucette C.A., Fonseca M., Xiang B., Sparagna G.C., Seshadri N., Vandel M., Dolinsky V.W., Hatch G.M.View abstractCategoriesFunction, Phenotypes & VariantsSourceMGI: 109626PubMedEurope PMCEndocrinology 162:bqab102-bqab102 (2021)Mapped to13
Expression pattern of transcriptional enhanced associate domain family member 1 (Tead1) in developing mouse molar tooth.Niki Y., Kobayashi Y., Moriyama K.View abstractCategorySequencesSourceMGI: 109626PubMedEurope PMCGene Expr Patterns 40:119182-119182 (2021)Mapped to80
Tafazzin Modulates Allergen-Induced Mast Cell Inflammatory Mediator Secretion.Maguire A.R.R., Crozier R.W.E., Hunter K.D., Claypool S.M., Fajardo V.A., LeBlanc P.J., MacNeil A.J.View abstractCategoryFunctionSourceMGI: 109626PubMedEurope PMCImmunohorizons 5:182-192 (2021)Mapped to13
Single-cell transcriptome landscape of ovarian cells during primordial follicle assembly in mice.Wang J.J., Ge W., Zhai Q.Y., Liu J.C., Sun X.W., Liu W.X., Li L., Lei C.Z., Dyce P.W.[...], Shen W.View abstractCategoryExpressionSourceMGI: 109626PubMedEurope PMCPLoS Biol 18:e3001025-e3001025 (2020)Mapped to45
Dynamic Cardiolipin Synthesis Is Required for CD8<sup>+</sup> T Cell Immunity.Corrado M., Edwards-Hicks J., Villa M., Flachsmann L.J., Sanin D.E., Jacobs M., Baixauli F., Stanczak M., Anderson E.[...], Pearce E.L.View abstractCategoryFunctionSourceMGI: 109626PubMedEurope PMCCell Metab 32:981-995.e7 (2020)Mapped to16
Cardiolipin deficiency in Barth syndrome is not associated with increased superoxide/H<sub>2</sub> O<sub>2</sub> production in heart and skeletal muscle mitochondria.Goncalves R.L.S., Schlame M., Bartelt A., Brand M.D., Hotamıslıgil G.S.View abstractCategoriesFunction, Phenotypes & VariantsSourceMGI: 109626PubMedEurope PMCFEBS Lett 595:415-432 (2021)Mapped to13
YAP and TAZ maintain PROX1 expression in the developing lymphatic and lymphovenous valves in response to VEGF-C signaling.Cha B., Ho Y.C., Geng X., Mahamud M.R., Chen L., Kim Y., Choi D., Kim T.H., Randolph G.J.[...], Srinivasan R.S.View abstractCategoryFunctionSourceMGI: 109626PubMedEurope PMCDevelopment 147:dev195453-dev195453 (2020)Mapped to46
Tafazzin deficiency impairs CoA-dependent oxidative metabolism in cardiac mitochondria.Le C.H., Benage L.G., Specht K.S., Li Puma L.C., Mulligan C.M., Heuberger A.L., Prenni J.E., Claypool S.M., Chatfield K.C.[...], Chicco A.J.View abstractCategoryFunctionSourceMGI: 109626PubMedEurope PMCJ Biol Chem 295:12485-12497 (2020)Mapped to13
Cardiolipin deficiency elevates susceptibility to a lipotoxic hypertrophic cardiomyopathy.Cole L.K., Mejia E.M., Sparagna G.C., Vandel M., Xiang B., Han X., Dedousis N., Kaufman B.A., Dolinsky V.W., Hatch G.M.View abstractCategoriesFunction, Phenotypes & VariantsSourceMGI: 109626PubMedEurope PMCJ Mol Cell Cardiol 144:24-34 (2020)Mapped to13
YAP1/TAZ drives ependymoma-like tumour formation in mice.Eder N., Roncaroli F., Domart M.C., Horswell S., Andreiuolo F., Flynn H.R., Lopes A.T., Claxton S., Kilday J.P.[...], Ultanir S.K.View abstractCategoryFunctionSourceMGI: 109626PubMedEurope PMCNat Commun 11:2380-2380 (2020)Mapped to33