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 abstractCited forNUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORMS 1; 2 AND 3)StrainC57BL/6J, DBA/2JTissueEmbryo, PlacentaCategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCScience 309:1559-1563 (2005)Cited in99+16Mapped to99+
The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).The MGC Project TeamView abstractCited forNUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 1)StrainFVB/NTissueSalivary glandCategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCGenome Res. 14:2121-2127 (2004)Cited in99+99+
Epigenetically modulated LRRC33 acts as a negative physiological regulator for multiple Toll-like receptors.Su X., Mei S., Liang X., Wang S., Liu J., Zhang Y., Bao Y., Chen Y., Che Y.[...], Yang R.View abstractCited forFUNCTION, DISRUPTION PHENOTYPECategoriesFunction, Phenotypes & VariantsSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCJ. Leukoc. Biol. 96:17-26 (2014)Cited in1Mapped to4
NRROS negatively regulates reactive oxygen species during host defence and autoimmunity.Noubade R., Wong K., Ota N., Rutz S., Eidenschenk C., Valdez P.A., Ding J., Peng I., Sebrell A.[...], Ouyang W.View abstractCited forSUBCELLULAR LOCATION, TISSUE SPECIFICITY, INDUCTION, INTERACTION WITH CYBB, DISRUPTION PHENOTYPECategoriesExpression, Interaction, Phenotypes & Variants, Subcellular LocationSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCNature 509:235-239 (2014)Cited in2Mapped to16
Mice deficient in NRROS show abnormal microglial development and neurological disorders.Wong K., Noubade R., Manzanillo P., Ota N., Foreman O., Hackney J.A., Friedman B.A., Pappu R., Scearce-Levie K., Ouyang W.View abstractCited forTISSUE SPECIFICITY, DISRUPTION PHENOTYPECategoriesExpression, Phenotypes & VariantsSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCNat. Immunol. 18:633-641 (2017)Cited in1Mapped to17
A milieu molecule for TGF-beta required for microglia function in the nervous system.Qin Y., Garrison B.S., Ma W., Wang R., Jiang A., Li J., Mistry M., Bronson R.T., Santoro D.[...], Springer T.A.View abstractCited forFUNCTION, SUBCELLULAR LOCATION, INTERACTION WITH TGFB1, DISRUPTION PHENOTYPE, TISSUE SPECIFICITY, DISULFIDE BONDS, GLYCOSYLATION, MUTAGENESIS OF CYS-219 AND CYS-363CategoriesFunction, PTM / Processing, Expression, Interaction, Phenotypes & Variants, Subcellular LocationSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCCell 174:156-171 (2018)Cited in4Mapped to7
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: 2445095PubMedEurope PMCNature 627:130-136 (2024)Mapped to99+
Cell-Type-Specific Gene Expression in Developing Mouse Neocortex: Intermediate Progenitors Implicated in Axon Development.Bedogni F., Hevner R.F.View abstractSourceMGI: 2445095PubMedEurope PMCFront Mol Neurosci 14:686034-686034 (2021)Mapped to99+
Biallelic mutations in NRROS cause an early onset lethal microgliopathy.Smith C., McColl B.W., Patir A., Barrington J., Armishaw J., Clarke A., Eaton J., Hobbs V., Mansour S.[...], Crow Y.J.AnnotationBiallelic mutations in NRROS cause an early onset lethal microgliopathy.CategoriesPhenotypes & VariantsSourceGeneRif: 224109PubMedEurope PMCActa Neuropathol. 139:947-951 (2020)Cited in1Mapped to1
Behavioral changes and growth deficits in a CRISPR engineered mouse model of the schizophrenia-associated 3q29 deletion.Rutkowski T.P., Purcell R.H., Pollak R.M., Grewenow S.M., Gafford G.M., Malone T., Khan U.A., Schroeder J.P., Epstein M.P.[...], Mulle J.G.View abstractCategoriesFunction, Phenotypes & VariantsSourceMGI: 2445095PubMedEurope PMCMol Psychiatry 26:772-783 (2021)Mapped to75
NRROS Negatively Regulates Osteoclast Differentiation by Inhibiting RANKL- Mediated NF-N:B and Reactive Oxygen Species Pathways.Kim J.H., Kim K., Kim I., Seong S., Kim N.View abstractAnnotationthis study presents NRROS as a novel negative regulator of RANKL-induced osteoclastogenesis.CategoriesFunctionSourceGeneRif: 224109PubMedEurope PMCMol Cells 38:904-910 (2015)Mapped to1
Genome-wide identification of endothelial cell-enriched genes in the mouse embryo.Takase H., Matsumoto K., Yamadera R., Kubota Y., Otsu A., Suzuki R., Ishitobi H., Mochizuki H., Kojima T.[...], Ema M.View abstractCategoriesExpressionSourceMGI: 2445095PubMedEurope PMCBlood 120:914-923 (2012)Mapped to77
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: 2445095PubMedEurope PMCNature 474:337-342 (2011)Mapped to99+
DLK1 is a novel regulator of bone mass that mediates estrogen deficiency- induced bone loss in mice.Abdallah B.M., Ditzel N., Mahmood A., Isa A., Traustadottir G.A., Schilling A.F., Ruiz-Hidalgo M.J., Laborda J., Amling M., Kassem M.View abstractCategoriesFunctionSourceMGI: 2445095PubMedEurope PMCJ Bone Miner Res 26:1457-1471 (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: 2445095PubMedEurope PMCPLoS Biol 9:e1000582-e1000582 (2011)Mapped to99+
A mouse knockout library for secreted and transmembrane proteins.Tang T., Li L., Tang J., Li Y., Lin W.Y., Martin F., Grant D., Solloway M., Parker L.[...], de Sauvage F.J.View abstractCategoriesFunction, SequencesSourceMGI: 2445095PubMedEurope PMCNat. Biotechnol. 28:749-755 (2010)Cited in2Mapped 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 abstractCategoriesSequencesSourceMGI: 2445095PubMedEurope PMCNature 420:563-573 (2002)Cited in699+Mapped to99+