High-efficiency full-length cDNA cloning.Carninci P., Hayashizaki Y.Cited forNUCLEOTIDE SEQUENCEStrainC57BL/6JTissueLiverCategoriesSequencesSourceUniProtKB unreviewed (TrEMBL)PubMedEurope PMCMethods Enzymol 303:19-44 (1999)Cited in99+Mapped to15
Normalization and subtraction of cap-trapper-selected cDNAs to prepare full-length cDNA libraries for rapid discovery of new genes.Carninci P., Shibata Y., Hayatsu N., Sugahara Y., Shibata K., Itoh M., Konno H., Okazaki Y., Muramatsu M., Hayashizaki Y.View abstractCited forNUCLEOTIDE SEQUENCEStrainC57BL/6JTissueLiverCategoriesSequencesSourceUniProtKB unreviewed (TrEMBL)PubMedEurope PMCGenome Res. 10:1617-1630 (2000)Cited in199+Mapped to10
RIKEN integrated sequence analysis (RISA) system--384-format sequencing pipeline with 384 multicapillary sequencer.Shibata K., Itoh M., Aizawa K., Nagaoka S., Sasaki N., Carninci P., Konno H., Akiyama J., Nishi K.[...], Togawa Y.View abstractCited forNUCLEOTIDE SEQUENCEStrainC57BL/6JTissueLiverCategoriesSequencesSourceUniProtKB unreviewed (TrEMBL)PubMedEurope PMCGenome Res 10:1757-1771 (2000)Cited in99+
Functional annotation of a full-length mouse cDNA collection.Kawai J., Shinagawa A., Shibata K., Yoshino M., Itoh M., Ishii Y., Arakawa T., Hara A., Fukunishi Y.[...], Hayashizaki Y.View abstractCited forNUCLEOTIDE SEQUENCEStrainC57BL/6JTissueLiverCategoriesSequencesSourceUniProtKB unreviewed (TrEMBL)PubMedEurope PMCNature 409:685-690 (2001)Cited in399+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 abstractCited forNUCLEOTIDE SEQUENCEStrainC57BL/6JTissueLiverCategoriesSequencesSourceUniProtKB unreviewed (TrEMBL)PubMedEurope PMCNature 420:563-573 (2002)Cited in699+Mapped to99+
No title available.Arakawa T., Carninci P., Fukuda S., Hashizume W., Hayashida K., Hori F., Iida J., Imamura K., Imotani K.[...], Hayashizaki Y.Cited forNUCLEOTIDE SEQUENCEStrainC57BL/6JTissueLiverCategoriesSequencesSourceUniProtKB unreviewed (TrEMBL)Submission Submitted to EMBL/GenBank/DDBJ databases (MAR-2004)Cited in99+
The Transcriptional Landscape of the Mammalian Genome.The FANTOM Consortium, Riken Genome Exploration Research Group and Genome Science Group (Genome Network Project Core Group)Cited forNUCLEOTIDE SEQUENCEStrainC57BL/6JTissueLiverCategoriesSequencesSourceUniProtKB unreviewed (TrEMBL)Science 309:1559-1563 (2005)Cited in199+
Antisense transcription in the mammalian transcriptome.FANTOM ConsortiumKatayama S., Tomaru Y., Kasukawa T., Waki K., Nakanishi M., Nakamura M., Nishida H., Yap C.C., Suzuki M.[...], Wahlestedt C.View abstractCited forNUCLEOTIDE SEQUENCEStrainC57BL/6JTissueLiverCategoriesSequencesSourceUniProtKB unreviewed (TrEMBL)PubMedEurope PMCScience 309:1564-1566 (2005)Cited in99+
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
Cloning, sequencing, and expression of a cDNA encoding beta-alanine synthase from rat liver.Kvalnes-Krick K.L., Traut T.W.View abstractAnnotationcloning and characterization of rat orthologCategoriesSequencesSourceGeneRif: 103149PubMedEurope PMCJ. Biol. Chem. 268:5686-5693 (1993)Cited in1Mapped to4
Studies of a mutation affecting pyrimidine degradation in inbred mice.Sanno Y., Holzer M., Schimke R.T.CategoriesFunctionSourceMGI: 2143535PubMedEurope PMCJ Biol Chem 245:5668-5676 (1970)Mapped to16
Genetic determinants of micronucleus formation in vivo.Adams D.J., Barlas B., McIntyre R.E., Salguero I., van der Weyden L., Barros A., Vicente J.R., Karimpour N., Haider A.[...], White J.K.View abstractSourceMGI: 2143535PubMedEurope PMCNature 627:130-136 (2024)Mapped to99+
Accelerating functional gene discovery in osteoarthritis.Butterfield N.C., Curry K.F., Steinberg J., Dewhurst H., Komla-Ebri D., Mannan N.S., Adoum A.T., Leitch V.D., Logan J.G.[...], Bassett J.H.D.View abstractSourceMGI: 2143535PubMedEurope PMCNat Commun 12:467-467 (2021)Mapped to99+
Mouse screen reveals multiple new genes underlying mouse and human hearing loss.Ingham N.J., Pearson S.A., Vancollie V.E., Rook V., Lewis M.A., Chen J., Buniello A., Martelletti E., Preite L.[...], Steel K.P.View abstractSourceMGI: 2143535PubMedEurope PMCPLoS Biol. 17:E3000194-E3000194 (2019)Cited in4Mapped to99+
The recently identified modifier of murine metastable epialleles, Rearranged L-Myc Fusion, is involved in maintaining epigenetic marks at CpG island shores and enhancers.Harten S.K., Oey H., Bourke L.M., Bharti V., Isbel L., Daxinger L., Faou P., Robertson N., Matthews J.M., Whitelaw E.View abstractCategoriesFunctionSourceMGI: 2143535PubMedEurope PMCBMC Biol 13:21-21 (2015)Mapped to44
Beta-ureidopropionase deficiency: phenotype, genotype and protein structural consequences in 16 patients.van Kuilenburg A.B., Dobritzsch D., Meijer J., Krumpel M., Selim L.A., Rashed M.S., Assmann B., Meinsma R., Lohkamp B.[...], Hennekam R.C.View abstractCategoriesSequences, Phenotypes & VariantsSourceMGI: 2143535PubMedEurope PMCBiochim. Biophys. Acta 1822:1096-1108 (2012)Cited in1Mapped to8
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: 2143535PubMedEurope PMCNature 474:337-342 (2011)Mapped to99+
A high-resolution anatomical atlas of the transcriptome in the mouse embryo.Diez-Roux G., Banfi S., Sultan M., Geffers L., Anand S., Rozado D., Magen A., Canidio E., Pagani M.[...], Ballabio A.View abstractCategoriesExpressionSourceMGI: 2143535PubMedEurope PMCPLoS Biol 9:e1000582-e1000582 (2011)Mapped to99+
A mutation in the pericentrin gene causes abnormal interneuron migration to the olfactory bulb in mice.Endoh-Yamagami S., Karkar K.M., May S.R., Cobos I., Thwin M.T., Long J.E., Ashique A.M., Zarbalis K., Rubenstein J.L., Peterson A.S.View abstractCategoriesFunctionSourceMGI: 2143535PubMedEurope PMCDev Biol 340:41-53 (2010)Mapped to99+
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: 2143535PubMedEurope PMCScience 309:1559-1563 (2005)Cited in99+16Mapped to99+
Beta-ureidopropionase deficiency: an inborn error of pyrimidine degradation associated with neurological abnormalities.van Kuilenburg A.B.P., Meinsma R., Beke E., Assmann B., Ribes A., Lorente I., Busch R., Mayatepek E., Abeling N.G.G.M.[...], van Gennip A.H.View abstractCategoriesSequences, Phenotypes & VariantsSourceMGI: 2143535PubMedEurope PMCHum. Mol. Genet. 13:2793-2801 (2004)Cited in1Mapped to8
GenePaint.org: an atlas of gene expression patterns in the mouse embryo.Visel A., Thaller C., Eichele G.View abstractCategoriesSequencesSourceMGI: 2143535PubMedEurope PMCNucleic Acids Res. 32:D552-D556 (2004)Cited in1Mapped to99+
Wnk1 kinase deficiency lowers blood pressure in mice: a gene-trap screen to identify potential targets for therapeutic intervention.Zambrowicz B.P., Abuin A., Ramirez-Solis R., Richter L.J., Piggott J., BeltrandelRio H., Buxton E.C., Edwards J., Finch R.A.[...], Sands A.T.View abstractCategoriesPhenotypes & VariantsSourceMGI: 2143535PubMedEurope PMCProc. Natl. Acad. Sci. U.S.A. 100:14109-14114 (2003)Cited in1Mapped to99+