Expression of a novel aristaless related homeobox gene 'Arx' in the vertebrate telencephalon, diencephalon and floor plate.Miura H., Yanazawa M., Kato K., Kitamura K.View abstractCited forFUNCTION, NUCLEOTIDE SEQUENCE [MRNA]CategoriesFunction, SequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCMech. Dev. 65:99-109 (1997)Cited in2Mapped to6
No title available.Kitamura K.Cited forSEQUENCE REVISION TO 391 AND 442CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)Submission Submitted to EMBL/GenBank/DDBJ databases (AUG-2002)Cited in1
Homeobox genes and nervous development.Ohsaki K.Cited forNUCLEOTIDE SEQUENCE [GENOMIC DNA]StrainBALB/cJCategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)Thesis Japan(1999)Cited in1
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 reviewed (Swiss-Prot)PubMedEurope PMCPLoS Biol. 7:E1000112-E1000112 (2009)Cited in99+99+
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]StrainC57BL/6JTissueBrainCategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCGenome Res. 14:2121-2127 (2004)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]TissueBrain, TestisCategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCCell 143:1174-1189 (2010)Cited in99+99+Mapped to6
Mutation of ARX causes abnormal development of forebrain and testes in mice and X-linked lissencephaly with abnormal genitalia in humans.Kitamura K., Yanazawa M., Sugiyama N., Miura H., Iizuka-Kogo A., Kusaka M., Omichi K., Suzuki R., Kato-Fukui Y.[...], Morohashi K.View abstractCited forFUNCTION, DEVELOPMENTAL STAGE, DISRUPTION PHENOTYPECategoriesFunction, Expression, Phenotypes & VariantsSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCNat. Genet. 32:359-369 (2002)Cited in2Mapped to44
Histone demethylase KDM5C is a SAHA-sensitive central hub at the crossroads of transcriptional axes involved in multiple neurodevelopmental disorders.Poeta L., Padula A., Attianese B., Valentino M., Verrillo L., Filosa S., Shoubridge C., Barra A., Schwartz C.E.[...], Miano M.G.View abstractCited forFUNCTION, DISRUPTION PHENOTYPECategoriesFunction, Phenotypes & VariantsSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCHum. Mol. Genet. 28:4089-4102 (2019)Cited in5Mapped to42
Expression patterns of Brx1 (Rieg gene), Sonic hedgehog, Nkx2.2, Dlx1 and Arx during zona limitans intrathalamica and embryonic ventral lateral geniculate nuclear formation.Kitamura K., Miura H., Yanazawa M., Miyashita T., Kato K.View abstractCategoriesSequencesSourceMGI: 1097716PubMedEurope PMCMech. Dev. 67:83-96 (1997)Cited in2Mapped to23
Coordination between ECM and cell-cell adhesion regulates the development of islet aggregation, architecture, and functional maturation.Tixi W., Maldonado M., Chang Y.T., Chiu A., Yeung W., Parveen N., Nelson M.S., Hart R., Wang S.[...], Shih H.P.View abstractSourceMGI: 1097716PubMedEurope PMCElife 12:e90006-e90006 (2023)Mapped to99+
DOT1L deletion impairs the development of cortical parvalbumin-expressing interneurons.Cheffer A., Garcia-Miralles M., Maier E., Akol I., Franz H., Srinivasan V.S.V., Vogel T.View abstractSourceMGI: 1097716PubMedEurope PMCCereb Cortex 33:10272-10285 (2023)Mapped to99+
Major beta cell-specific functions of NKX2.2 are mediated via the NK2- specific domain.Abarinov V., Levine J.A., Churchill A.J., Hopwood B., Deiter C.S., Guney M.A., Wells K.L., Schrunk J.M., Guo Y.[...], Sussel L.View abstractSourceMGI: 1097716PubMedEurope PMCGenes Dev 37:490-504 (2023)Mapped to71
Distinct hyperactive RAS/MAPK alleles converge on common GABAergic interneuron core programs.Knowles S.J., Stafford A.M., Zaman T., Angara K., Williams M.R., Newbern J.M., Vogt D.View abstractCategoriesFunctionSourceMGI: 1097716PubMedEurope PMCDevelopment 150:dev201371-dev201371 (2023)Mapped to57
Testicular macrophages are recruited during a narrow fetal time window and promote organ-specific developmental functions.Gu X., Heinrich A., Li S.Y., DeFalco T.View abstractCategoriesExpressionSourceMGI: 1097716PubMedEurope PMCNat Commun 14:1439-1439 (2023)Mapped to99+
ISL1 controls pancreatic alpha cell fate and beta cell maturation.Bohuslavova R., Fabriciova V., Lebron-Mora L., Malfatti J., Smolik O., Valihrach L., Benesova S., Zucha D., Berkova Z.[...], Pavlinkova G.View abstractCategoriesFunctionSourceMGI: 1097716PubMedEurope PMCCell Biosci 13:53-53 (2023)Mapped to60
Large-Scale Functional Assessment of Genes Involved in Rare Diseases with Intellectual Disabilities Unravels Unique Developmental and Behaviour Profiles in Mouse Models.Meziane H., Birling M.C., Wendling O., Leblanc S., Dubos A., Selloum M., Pavlovic G., Sorg T., Kalscheuer V.M.[...], Herault Y.View abstractSourceMGI: 1097716PubMedEurope PMCBiomedicines 10:3148-3148 (2022)Mapped to99
Bmi1 suppresses protein synthesis and promotes proteostasis in hematopoietic stem cells.Burgess R.J., Zhao Z., Nakada D., Morrison S.J.View abstractCategoriesFunction, Phenotypes & VariantsSourceMGI: 1097716PubMedEurope PMCGenes Dev 36:887-900 (2022)Mapped to12
Generation of FLAG-tagged Arx knock-in mouse model.Lim Y., Cho I.T., Golden J.A., Cho G.View abstractCategoriesFunction, Subcellular LocationSourceMGI: 1097716PubMedEurope PMCGenesis 60:e23479-e23479 (2022)Mapped to1
Origin, specification and differentiation of a rare supporting-like lineage in the developing mouse gonad.Mayere C., Regard V., Perea-Gomez A., Bunce C., Neirijnck Y., Djari C., Bellido-Carreras N., Sararols P., Reeves R.[...], Nef S.View abstractCategoriesFunction, ExpressionSourceMGI: 1097716PubMedEurope PMCSci Adv 8:eabm0972-eabm0972 (2022)Mapped to66
Deregulation of microtubule organization and RNA metabolism in Arx models for lissencephaly and developmental epileptic encephalopathy.Drongitis D., Caterino M., Verrillo L., Santonicola P., Costanzo M., Poeta L., Attianese B., Barra A., Terrone G.[...], Miano M.G.View abstractCategoriesFunction, Phenotypes & VariantsSourceMGI: 1097716PubMedEurope PMCHum Mol Genet 31:1884-1908 (2022)Mapped to1
An essential role for Polycomb Repressive Complex 2 in the mouse ovary.Prokopuk L., Jarred E.G., Blucher R.O., McLaughlin E.A., Stringer J.M., Western P.S.View abstractCategoriesFunctionSourceMGI: 1097716PubMedEurope PMCReproduction 163:167-182 (2022)Mapped to99+
Cell-Type-Specific Gene Expression in Developing Mouse Neocortex: Intermediate Progenitors Implicated in Axon Development.Bedogni F., Hevner R.F.View abstractSourceMGI: 1097716PubMedEurope PMCFront Mol Neurosci 14:686034-686034 (2021)Mapped to99+
The Type 3 Deiodinase Is a Critical Modulator of Thyroid Hormone Sensitivity in the Fetal Brain.Martinez M.E., Hernandez A.View abstractCategoriesExpressionSourceMGI: 1097716PubMedEurope PMCFront Neurosci 15:703730-703730 (2021)Mapped to99+
NEUROD1 Is Required for the Early alpha and beta Endocrine Differentiation in the Pancreas.Bohuslavova R., Smolik O., Malfatti J., Berkova Z., Novakova Z., Saudek F., Pavlinkova G.View abstractCategoriesFunctionSourceMGI: 1097716PubMedEurope PMCInt J Mol Sci 22:6713-6713 (2021)Mapped to62
Cascade diversification directs generation of neuronal diversity in the hypothalamus.Zhang Y.H., Xu M., Shi X., Sun X.L., Mu W., Wu H., Wang J., Li S., Su P.[...], Wu Q.F.View abstractCategoriesFunction, ExpressionSourceMGI: 1097716PubMedEurope PMCCell Stem Cell 28:1483-1499.e8 (2021)Mapped to75