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Search results 1 to 67 out of 67 for Mkrn3

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Category: Publication
Type Details Score
Publication
First Author: Abreu AP
Year: 2020
Journal: J Clin Invest
Title: MKRN3 inhibits the reproductive axis through actions in kisspeptin-expressing neurons.
Volume: 130
Issue: 8
Pages: 4486-4500
Publication  
First Author: Pereira SA
Year: 2023
Journal: Endocrinology
Title: Mouse Testicular Mkrn3 Expression Is Primarily Interstitial, Increases Peripubertally, and Is Responsive to LH/hCG.
Volume: 164
Issue: 9
Publication  
First Author: Naulé L
Year: 2023
Journal: JCI Insight
Title: MKRN3 inhibits puberty onset via interaction with IGF2BP1 and regulation of hypothalamic plasticity.
Volume: 8
Issue: 8
Publication  
First Author: Li K
Year: 2021
Journal: J Exp Med
Title: E3 ligase MKRN3 is a tumor suppressor regulating PABPC1 ubiquitination in non-small cell lung cancer.
Volume: 218
Issue: 8
Publication
First Author: Li C
Year: 2020
Journal: Natl Sci Rev
Title: MKRN3 regulates the epigenetic switch of mammalian puberty via ubiquitination of MBD3.
Volume: 7
Issue: 3
Pages: 671-685
Publication
First Author: Li C
Year: 2021
Journal: Nucleic Acids Res
Title: MKRN3-mediated ubiquitination of Poly(A)-binding proteins modulates the stability and translation of GNRH1 mRNA in mammalian puberty.
Volume: 49
Issue: 7
Pages: 3796-3813
Publication
First Author: Stefan M
Year: 2011
Journal: Am J Physiol Endocrinol Metab
Title: Global deficits in development, function, and gene expression in the endocrine pancreas in a deletion mouse model of Prader-Willi syndrome.
Volume: 300
Issue: 5
Pages: E909-22
Publication
First Author: Lee S
Year: 2003
Journal: Gene Expr Patterns
Title: Prader-Willi syndrome transcripts are expressed in phenotypically significant regions of the developing mouse brain.
Volume: 3
Issue: 5
Pages: 599-609
Publication
First Author: Jong MT
Year: 1999
Journal: Hum Mol Genet
Title: Imprinting of a RING zinc-finger encoding gene in the mouse chromosome region homologous to the Prader-Willi syndrome genetic region.
Volume: 8
Issue: 5
Pages: 795-803
Publication
First Author: Kobayashi S
Year: 2002
Journal: Biochem Biophys Res Commun
Title: Paternal expression of a novel imprinted gene, Peg12/Frat3, in the mouse 7C region homologous to the Prader-Willi syndrome region.
Volume: 290
Issue: 1
Pages: 403-8
Publication
First Author: Lee S
Year: 2000
Journal: Hum Mol Genet
Title: Expression and imprinting of MAGEL2 suggest a role in Prader-willi syndrome and the homologous murine imprinting phenotype.
Volume: 9
Issue: 12
Pages: 1813-9
Publication
First Author: Gérard M
Year: 1999
Journal: Nat Genet
Title: Disruption of the mouse necdin gene results in early post-natal lethality.
Volume: 23
Issue: 2
Pages: 199-202
Publication
First Author: Watanabe T
Year: 2000
Journal: Hum Mol Genet
Title: Differential chromatin packaging of genomic imprinted regions between expressed and non-expressed alleles.
Volume: 9
Issue: 20
Pages: 3029-35
Publication
First Author: Toder R
Year: 1996
Journal: Chromosome Res
Title: The human/mouse imprinted genes IGF2, H19, SNRPN and ZNF127 map to two conserved autosomal clusters in a marsupial.
Volume: 4
Issue: 4
Pages: 295-300
Publication
First Author: Messerschmidt DM
Year: 2012
Journal: Science
Title: Trim28 is required for epigenetic stability during mouse oocyte to embryo transition.
Volume: 335
Issue: 6075
Pages: 1499-502
Publication
First Author: Chai JH
Year: 2001
Journal: Mamm Genome
Title: Retrotransposed genes such as Frat3 in the mouse Chromosome 7C Prader-Willi syndrome region acquire the imprinted status of their insertion site.
Volume: 12
Issue: 11
Pages: 813-21
Publication
First Author: Cattanach BM
Year: 1997
Journal: Mamm Genome
Title: A candidate model for Angelman syndrome in the mouse.
Volume: 8
Issue: 7
Pages: 472-8
Publication
First Author: Bourc'his D
Year: 2001
Journal: Science
Title: Dnmt3L and the establishment of maternal genomic imprints.
Volume: 294
Issue: 5551
Pages: 2536-9
Publication
First Author: McBurney MW
Year: 2003
Journal: Mol Cell Biol
Title: The mammalian SIR2alpha protein has a role in embryogenesis and gametogenesis.
Volume: 23
Issue: 1
Pages: 38-54
Publication
First Author: Nicholls RD
Year: 1993
Journal: Proc Natl Acad Sci U S A
Title: Evaluation of potential models for imprinted and nonimprinted components of human chromosome 15q11-q13 syndromes by fine-structure homology mapping in the mouse.
Volume: 90
Issue: 5
Pages: 2050-4
Publication
First Author: Nakagaki A
Year: 2014
Journal: Gene
Title: Imprinting analysis of the mouse chromosome 7C region in DNMT1-null embryos.
Volume: 553
Issue: 1
Pages: 63-8
Publication
First Author: Skryabin BV
Year: 2007
Journal: PLoS Genet
Title: Deletion of the MBII-85 snoRNA gene cluster in mice results in postnatal growth retardation.
Volume: 3
Issue: 12
Pages: e235
Publication
First Author: Fukasawa M
Year: 2006
Journal: Cytogenet Genome Res
Title: Genomic imprinting in Dicer1-hypomorphic mice.
Volume: 113
Issue: 1-4
Pages: 138-43
Publication
First Author: Kozlov SV
Year: 2007
Journal: Nat Genet
Title: The imprinted gene Magel2 regulates normal circadian output.
Volume: 39
Issue: 10
Pages: 1266-72
Publication
First Author: Johnson DK
Year: 1995
Journal: Genetics
Title: Molecular analysis of 36 mutations at the mouse pink-eyed dilution (p) locus.
Volume: 141
Issue: 4
Pages: 1563-71
Publication
First Author: Choi JD
Year: 2001
Journal: Mamm Genome
Title: Microarray expression profiling of tissues from mice with uniparental duplications of chromosomes 7 and 11 to identify imprinted genes.
Volume: 12
Issue: 10
Pages: 758-64
Publication
First Author: Ogawa H
Year: 2006
Journal: FEBS Lett
Title: Disruption of parental-specific expression of imprinted genes in uniparental fetuses.
Volume: 580
Issue: 22
Pages: 5377-84
Publication
First Author: Tiklová K
Year: 2019
Journal: Nat Commun
Title: Single-cell RNA sequencing reveals midbrain dopamine neuron diversity emerging during mouse brain development.
Volume: 10
Issue: 1
Pages: 581
Publication
First Author: Gendrel AV
Year: 2013
Journal: Mol Cell Biol
Title: Epigenetic functions of smchd1 repress gene clusters on the inactive X chromosome and on autosomes.
Volume: 33
Issue: 16
Pages: 3150-65
Publication      
First Author: Toronto Centre for Phenogenomics
Year: 2013
Journal: MGI Direct Data Submission
Title: Strains and alleles submitted by Toronto Centre for Phenogenomics (NorCOMM2, funded by Genome Canada and Ontario Genomics Institute OGI-051).
Publication      
First Author: MGI and IMPC
Year: 2017
Journal: MGI Direct Data Submission
Title: MGI Curation of Endonuclease-Mediated Alleles (CRISPR) from the International Mouse Phenotyping Consortium (IMPC)
Publication
First Author: Gray PA
Year: 2004
Journal: Science
Title: Mouse brain organization revealed through direct genome-scale TF expression analysis.
Volume: 306
Issue: 5705
Pages: 2255-7
Publication      
First Author: Velocigene
Year: 2008
Journal: MGI Direct Data Submission
Title: Alleles produced for the KOMP project by Velocigene (Regeneron Pharmaceuticals)
Publication        
First Author: DDB, FB, MGI, GOA, ZFIN curators
Year: 2001
Title: Gene Ontology annotation through association of InterPro records with GO terms
Publication      
First Author: Mouse Genome Informatics and the International Mouse Phenotyping Consortium (IMPC)
Year: 2014
Journal: Database Release
Title: Obtaining and Loading Phenotype Annotations from the International Mouse Phenotyping Consortium (IMPC) Database
Publication        
First Author: GOA curators
Year: 2016
Title: Automatic transfer of experimentally verified manual GO annotation data to orthologs using Ensembl Compara
Publication
First Author: Carninci P
Year: 2005
Journal: Science
Title: The transcriptional landscape of the mammalian genome.
Volume: 309
Issue: 5740
Pages: 1559-63
Publication        
First Author: MGD Nomenclature Committee
Year: 1995
Title: Nomenclature Committee Use
Publication
First Author: Adams DJ
Year: 2024
Journal: Nature
Title: Genetic determinants of micronucleus formation in vivo.
Volume: 627
Issue: 8002
Pages: 130-136
Publication        
First Author: UniProt-GOA
Year: 2012
Title: Gene Ontology annotation based on UniProtKB/Swiss-Prot keyword mapping
Publication      
First Author: The Jackson Laboratory Mouse Radiation Hybrid Database
Year: 2004
Journal: Database Release
Title: Mouse T31 Radiation Hybrid Data Load
Publication        
First Author: The Gene Ontology Consortium
Year: 2010
Title: Automated transfer of experimentally-verified manual GO annotation data to mouse-human orthologs
Publication
First Author: Diez-Roux G
Year: 2011
Journal: PLoS Biol
Title: A high-resolution anatomical atlas of the transcriptome in the mouse embryo.
Volume: 9
Issue: 1
Pages: e1000582
Publication      
First Author: MGI Genome Annotation Group and UniGene Staff
Year: 2015
Journal: Database Download
Title: MGI-UniGene Interconnection Effort
Publication      
First Author: Mouse Genome Informatics Scientific Curators
Year: 2010
Journal: Database Download
Title: Mouse Microarray Data Integration in Mouse Genome Informatics, the Affymetrix GeneChip Mouse Genome U74 Array Platform (A, B, C v2).
Publication        
First Author: Marc Feuermann, Huaiyu Mi, Pascale Gaudet, Dustin Ebert, Anushya Muruganujan, Paul Thomas
Year: 2010
Title: Annotation inferences using phylogenetic trees
Publication      
First Author: Mouse Genome Database and National Center for Biotechnology Information
Year: 2000
Journal: Database Release
Title: Entrez Gene Load
Publication      
First Author: Bairoch A
Year: 1999
Journal: Database Release
Title: SWISS-PROT Annotated protein sequence database
Publication        
First Author: Mouse Genome Informatics Scientific Curators
Year: 2005
Title: Obtaining and loading genome assembly coordinates from NCBI annotations
Publication      
First Author: Mouse Genome Informatics Group
Year: 2003
Journal: Database Procedure
Title: Automatic Encodes (AutoE) Reference
Publication      
First Author: Mouse Genome Informatics (MGI) and The National Center for Biotechnology Information (NCBI)
Year: 2010
Journal: Database Download
Title: Consensus CDS project
Publication      
First Author: Mouse Genome Informatics
Year: 2010
Journal: Database Release
Title: Protein Ontology Association Load.
Publication        
First Author: Mouse Genome Informatics Scientific Curators
Year: 2005
Title: Obtaining and Loading Genome Assembly Coordinates from Ensembl Annotations
Publication      
First Author: Mouse Genome Informatics Scientific Curators
Year: 2009
Journal: Database Download
Title: Mouse Microarray Data Integration in Mouse Genome Informatics, the Affymetrix GeneChip Mouse Gene 1.0 ST Array Platform
Publication      
First Author: Allen Institute for Brain Science
Year: 2004
Journal: Allen Institute
Title: Allen Brain Atlas: mouse riboprobes
Publication      
First Author: Mouse Genome Informatics Scientific Curators
Year: 2009
Journal: Database Download
Title: Mouse Microarray Data Integration in Mouse Genome Informatics, the Affymetrix GeneChip Mouse Genome 430 2.0 Array Platform
Publication
First Author: Liu H
Year: 2017
Journal: Oncotarget
Title: Mkrn3 functions as a novel ubiquitin E3 ligase to inhibit Nptx1 during puberty initiation.
Volume: 8
Issue: 49
Pages: 85102-85109
Publication  
First Author: Stefan M
Year: 2005
Journal: BMC Genomics
Title: Genetic mapping of putative Chrna7 and Luzp2 neuronal transcriptional enhancers due to impact of a transgene-insertion and 6.8 Mb deletion in a mouse model of Prader-Willi and Angelman syndromes.
Volume: 6
Pages: 157
Publication
First Author: Gabriel JM
Year: 1999
Journal: Proc Natl Acad Sci U S A
Title: A transgene insertion creating a heritable chromosome deletion mouse model of Prader-Willi and angelman syndromes.
Volume: 96
Issue: 16
Pages: 9258-63
Publication
First Author: Stefan M
Year: 2005
Journal: Genomics
Title: A nonimprinted Prader-Willi Syndrome (PWS)-region gene regulates a different chromosomal domain in trans but the imprinted pws loci do not alter genome-wide mRNA levels.
Volume: 85
Issue: 5
Pages: 630-40
Publication
First Author: Ge Y
Year: 2002
Journal: Brain Res
Title: Anorexigenic melanocortin signaling in the hypothalamus is augmented in association with failure-to-thrive in a transgenic mouse model for Prader-Willi syndrome.
Volume: 957
Issue: 1
Pages: 42-5
Publication
First Author: Stefan M
Year: 2005
Journal: Endocrinology
Title: Hormonal and metabolic defects in a prader-willi syndrome mouse model with neonatal failure to thrive.
Volume: 146
Issue: 10
Pages: 4377-85
Publication
First Author: Nakagaki A
Year: 2018
Journal: Sci Rep
Title: Application of droplet digital PCR in the analysis of genome integration and organization of the transgene in BAC transgenic mice.
Volume: 8
Issue: 1
Pages: 6638
Publication
First Author: Dubose AJ
Year: 2011
Journal: Hum Mol Genet
Title: A new deletion refines the boundaries of the murine Prader-Willi syndrome imprinting center.
Volume: 20
Issue: 17
Pages: 3461-6
Publication
First Author: Bielinska B
Year: 2000
Journal: Nat Genet
Title: De novo deletions of SNRPN exon 1 in early human and mouse embryos result in a paternal to maternal imprint switch.
Volume: 25
Issue: 1
Pages: 74-8
Publication
First Author: Resnick JL
Year: 2013
Journal: Mamm Genome
Title: Recommendations for the investigation of animal models of Prader-Willi syndrome.
Volume: 24
Issue: 5-6
Pages: 165-78
Publication
First Author: Rodriguez-Jato S
Year: 2013
Journal: PLoS One
Title: Regulatory elements associated with paternally-expressed genes in the imprinted murine Angelman/Prader-Willi syndrome domain.
Volume: 8
Issue: 2
Pages: e52390