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/6JCategoriesSequencesSourceUniProtKB unreviewed (TrEMBL)PubMedEurope PMCPLoS Biol. 7:E1000112-E1000112 (2009)Cited in99+99+
A tissue-specific atlas of mouse protein phosphorylation and expression.Huttlin E.L., Jedrychowski M.P., Elias J.E., Goswami T., Rad R., Beausoleil S.A., Villen J., Haas W., Sowa M.E., Gygi S.P.View abstractCited forIDENTIFICATION BY MASS SPECTROMETRY [LARGE SCALE ANALYSIS]CategoriesSequencesSourceUniProtKB unreviewed (TrEMBL)PubMedEurope PMCCell 143:1174-1189 (2010)Cited in99+99+Mapped to6
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/6JCategoriesSequencesSourceUniProtKB 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+
Cotranscription of two RNA coding for the cell adhesion regulator and its variant in Reh leukemia cells.Molla A., Rouard-Talbot L., Block M.R.View abstractCategoriesSequencesSourceMGI: 2385906PubMedEurope PMCBiochim Biophys Acta 1315:6-8 (1996)Cited in1Mapped to9
Impaired flickering of the permeability transition pore causes SPG7 spastic paraplegia.Sambri I., Massa F., Gullo F., Meneghini S., Cassina L., Carraro M., Dina G., Quattrini A., Patanella L.[...], Casari G.View abstractCategoriesFunction, Phenotypes & VariantsSourceMGI: 2385906PubMedEurope PMCEBioMedicine 61:103050-103050 (2020)Mapped to13
CLUH regulates mitochondrial metabolism by controlling translation and decay of target mRNAs.Schatton D., Pla-Martin D., Marx M.C., Hansen H., Mourier A., Nemazanyy I., Pessia A., Zentis P., Corona T.[...], Rugarli E.I.View abstractCategoriesFunctionSourceMGI: 2385906PubMedEurope PMCJ Cell Biol 216:675-693 (2017)Mapped to99+
Alternative splicing of Spg7, a gene involved in hereditary spastic paraplegia, encodes a variant of paraplegin targeted to the endoplasmic reticulum.Mancuso G., Barth E., Crivello P., Rugarli E.I.View abstractCategoriesSubcellular LocationSourceMGI: 2385906PubMedEurope PMCPLoS ONE 7:E36337-E36337 (2012)Cited in2Mapped to12
A conditional knockout resource for the genome-wide study of mouse gene function.Skarnes W.C., Rosen B., West A.P., Koutsourakis M., Bushell W., Iyer V., Mujica A.O., Thomas M., Harrow J.[...], Bradley A.View abstractCategoriesFunction, Phenotypes & VariantsSourceMGI: 2385906PubMedEurope PMCNature 474:337-342 (2011)Mapped to99+
Autocatalytic processing of m-AAA protease subunits in mitochondria.Koppen M., Bonn F., Ehses S., Langer T.View abstractCategoriesFunctionSourceMGI: 2385906PubMedEurope PMCMol. Biol. Cell 20:4216-4224 (2009)Cited in3Mapped to21
Genetic interaction between the m-AAA protease isoenzymes reveals novel roles in cerebellar degeneration.Martinelli P., La Mattina V., Bernacchia A., Magnoni R., Cerri F., Cox G., Quattrini A., Casari G., Rugarli E.I.View abstractCategoriesFunctionSourceMGI: 2385906PubMedEurope PMCHum Mol Genet 18:2001-2013 (2009)Mapped to13
A mitochondrial protein compendium elucidates complex I disease biology.Pagliarini D.J., Calvo S.E., Chang B., Sheth S.A., Vafai S.B., Ong S.E., Walford G.A., Sugiana C., Boneh A.[...], Mootha V.K.View abstractCategoriesSubcellular LocationSourceMGI: 2385906PubMedEurope PMCCell 134:112-123 (2008)Cited in11Mapped to99+
Variable and tissue-specific subunit composition of mitochondrial m-AAA protease complexes linked to hereditary spastic paraplegia.Koppen M., Metodiev M.D., Casari G., Rugarli E.I., Langer T.View abstractCategoriesFunction, InteractionSourceMGI: 2385906PubMedEurope PMCMol. Cell. Biol. 27:758-767 (2007)Cited in4Mapped to19
Intramuscular viral delivery of paraplegin rescues peripheral axonopathy in a model of hereditary spastic paraplegia.Pirozzi M., Quattrini A., Andolfi G., Dina G., Malaguti M.C., Auricchio A., Rugarli E.I.View abstractCategoriesFunction, Phenotypes & VariantsSourceMGI: 2385906PubMedEurope PMCJ Clin Invest 116:202-208 (2006)Mapped to13
The m-AAA protease defective in hereditary spastic paraplegia controls ribosome assembly in mitochondria.Nolden M., Ehses S., Koppen M., Bernacchia A., Rugarli E.I., Langer T.View abstractCategoriesFunctionSourceMGI: 2385906PubMedEurope PMCCell 123:277-289 (2005)Cited in6Mapped to11
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 abstractCategoriesSequencesSourceMGI: 2385906PubMedEurope PMCScience 309:1559-1563 (2005)Cited in99+16Mapped to99+
Genomic analysis of mouse retinal development.Blackshaw S., Harpavat S., Trimarchi J., Cai L., Huang H., Kuo W.P., Weber G., Lee K., Fraioli R.E.[...], Cepko C.L.View abstractCategoriesSequences, ExpressionSourceMGI: 2385906PubMedEurope PMCPLoS Biol. 2:1411-1431 (2004)Cited in1Mapped to99+
Axonal degeneration in paraplegin-deficient mice is associated with abnormal mitochondria and impairment of axonal transport.Ferreirinha F., Quattrini A., Pirozzi M., Valsecchi V., Dina G., Broccoli V., Auricchio A., Piemonte F., Tozzi G.[...], Rugarli E.I.View abstractCategoriesFunction, Phenotypes & VariantsSourceMGI: 2385906PubMedEurope PMCJ. Clin. Invest. 113:231-242 (2004)Cited in1Mapped to7
Integrated analysis of protein composition, tissue diversity, and gene regulation in mouse mitochondria.Mootha V.K., Bunkenborg J., Olsen J.V., Hjerrild M., Wisniewski J.R., Stahl E., Bolouri M.S., Ray H.N., Sihag S.[...], Mann M.View abstractCategoriesExpression, Subcellular LocationSourceMGI: 2385906PubMedEurope PMCCell 115:629-640 (2003)Mapped to99+
Large-scale cDNA analysis reveals phased gene expression patterns during preimplantation mouse development.Ko M.S.H., Kitchen J.R., Wang X., Threat T.A., Wang X., Hasegawa A., Sun T., Grahovac M.J., Kargul G.J.[...], Doi H.View abstractCategoriesSequencesSourceMGI: 2385906PubMedEurope PMCDevelopment 127:1737-1749 (2000)Cited in1Mapped to99+