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+
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 (JUN-2024)Cited in99+
DOCK3 regulates normal skeletal muscle regeneration and glucose metabolism.Samani A., Karuppasamy M., English K.G., Siler C.A., Wang Y., Widrick J.J., Alexander M.S.View abstractCategoriesFunctionSourceMGI: 2429763PubMedEurope PMCFASEB J 37:e23198-e23198 (2023)Mapped to25
DOCK3 is a dosage-sensitive regulator of skeletal muscle and Duchenne muscular dystrophy-associated pathologies.Reid A.L., Wang Y., Samani A., Hightower R.M., Lopez M.A., Gilbert S.R., Ianov L., Crossman D.K., Dell'Italia L.J.[...], Alexander M.S.View abstractCategoriesFunction, Phenotypes & VariantsSourceMGI: 2429763PubMedEurope PMCHum Mol Genet 29:2855-2871 (2020)Mapped to29
Dock3 overexpression and p38 MAPK inhibition synergistically stimulate neuroprotection and axon regeneration after optic nerve injury.Semba K., Namekata K., Kimura A., Harada C., Katome T., Yoshida H., Mitamura Y., Harada T.View abstractCategoriesFunctionSourceMGI: 2429763PubMedEurope PMCNeurosci Lett 581:89-93 (2014)Mapped to8
Dock3 protects myelin in the cuprizone model for demyelination.Namekata K., Kimura A., Harada C., Yoshida H., Matsumoto Y., Harada T.View abstractCategoriesFunction, ExpressionSourceMGI: 2429763PubMedEurope PMCCell Death Dis 5:e1395-e1395 (2014)Mapped to8
MicroRNA-486-dependent modulation of DOCK3/PTEN/AKT signaling pathways improves muscular dystrophy-associated symptoms.Alexander M.S., Casar J.C., Motohashi N., Vieira N.M., Eisenberg I., Marshall J.L., Gasperini M.J., Lek A., Myers J.A.[...], Kunkel L.M.View abstractCategoriesFunctionSourceMGI: 2429763PubMedEurope PMCJ Clin Invest 124:2651-2667 (2014)Mapped to43
Dock3 attenuates neural cell death due to NMDA neurotoxicity and oxidative stress in a mouse model of normal tension glaucoma.Namekata K., Kimura A., Kawamura K., Guo X., Harada C., Tanaka K., Harada T.View abstractCategoriesFunction, Phenotypes & VariantsSourceMGI: 2429763PubMedEurope PMCCell Death Differ 20:1250-1256 (2013)Mapped to14
Dock3 regulates BDNF-TrkB signaling for neurite outgrowth by forming a ternary complex with Elmo and RhoG.Namekata K., Watanabe H., Guo X., Kittaka D., Kawamura K., Kimura A., Harada C., Harada T.View abstractCategoriesFunctionSourceMGI: 2429763PubMedEurope PMCGenes Cells 17:688-697 (2012)Mapped to99+
Dock3 stimulates axonal outgrowth via GSK-3beta-mediated microtubule assembly.Namekata K., Harada C., Guo X., Kimura A., Kittaka D., Watanabe H., Harada T.View abstractCategoriesFunctionSourceMGI: 2429763PubMedEurope PMCJ Neurosci 32:264-274 (2012)Mapped to23
CHD5, a brain-specific paralog of Mi2 chromatin remodeling enzymes, regulates expression of neuronal genes.Potts R.C., Zhang P., Wurster A.L., Precht P., Mughal M.R., Wood W.H., Zhang Y., Becker K.G., Mattson M.P., Pazin M.J.View abstractCategoriesInteractionSourceMGI: 2429763PubMedEurope PMCPLoS ONE 6:E24515-E24515 (2011)Cited in3Mapped to44
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: 2429763PubMedEurope 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: 2429763PubMedEurope PMCPLoS Biol 9:e1000582-e1000582 (2011)Mapped to99+
Dock3 induces axonal outgrowth by stimulating membrane recruitment of the WAVE complex.Namekata K., Harada C., Taya C., Guo X., Kimura H., Parada L.F., Harada T.View abstractCategoriesFunctionSourceMGI: 2429763PubMedEurope PMCProc Natl Acad Sci U S A 107:7586-7591 (2010)Mapped to32
Loss of modifier of cell adhesion reveals a pathway leading to axonal degeneration.Chen Q., Peto C.A., Shelton G.D., Mizisin A., Sawchenko P.E., Schubert D.View abstractCategoriesFunctionSourceMGI: 2429763PubMedEurope PMCJ. Neurosci. 29:118-130 (2009)Cited in1Mapped to7
Rac activation and inactivation control plasticity of tumor cell movement.Sanz-Moreno V., Gadea G., Ahn J., Paterson H., Marra P., Pinner S., Sahai E., Marshall C.J.View abstractCategoriesFunctionSourceMGI: 2429763PubMedEurope PMCCell 135:510-523 (2008)Mapped to10
BGEM: an in situ hybridization database of gene expression in the embryonic and adult mouse nervous system.Magdaleno S., Jensen P., Brumwell C.L., Seal A., Lehman K., Asbury A., Cheung T., Cornelius T., Batten D.M.[...], Curran T.CategoriesSequencesSourceMGI: 2429763PubMedEurope PMCPLoS Biol 4:e86-e86 (2006)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: 2429763PubMedEurope PMCScience 309:1559-1563 (2005)Cited in99+16Mapped 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: 2429763PubMedEurope PMCProc. Natl. Acad. Sci. U.S.A. 100:14109-14114 (2003)Cited in1Mapped to99+
Disruption of a novel member of a sodium/hydrogen exchanger family and DOCK3 is associated with an attention deficit hyperactivity disorder-like phenotype.De Silva M.G., Elliott K., Dahl H.-H.M., Fitzpatrick E., Wilcox S., Delatycki M., Williamson R., Efron D., Lynch M., Forrest S.View abstractCategoriesSequencesSourceMGI: 2429763PubMedEurope PMCJ. Med. Genet. 40:733-740 (2003)Cited in2Mapped to15
Isolation and characterization of novel presenilin binding protein.Kashiwa A., Yoshida H., Lee S., Paladino T., Liu Y., Chen Q., Dargusch R., Schubert D., Kimura H.View abstractCategoriesSequencesSourceMGI: 2429763PubMedEurope PMCJ. Neurochem. 75:109-116 (2000)Cited in4Mapped to25