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Search results 1 to 88 out of 88 for Magel2

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Category: Publication
Type Details Score
Publication
First Author: Schaller F
Year: 2010
Journal: Hum Mol Genet
Title: A single postnatal injection of oxytocin rescues the lethal feeding behaviour in mouse newborns deficient for the imprinted Magel2 gene.
Volume: 19
Issue: 24
Pages: 4895-905
Publication  
First Author: Gigliucci V
Year: 2023
Journal: Front Neurosci
Title: Oxytocin receptors in the Magel2 mouse model of autism: Specific region, age, sex and oxytocin treatment effects.
Volume: 17
Pages: 1026939
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: Maillard J
Year: 2016
Journal: Hum Mol Genet
Title: Loss of Magel2 impairs the development of hypothalamic Anorexigenic circuits.
Volume: 25
Issue: 15
Pages: 3208-3215
Publication  
First Author: Ates T
Year: 2019
Journal: Neurobiol Dis
Title: Inactivation of Magel2 suppresses oxytocin neurons through synaptic excitation-inhibition imbalance.
Volume: 121
Pages: 58-64
Publication
First Author: Ieda D
Year: 2020
Journal: PLoS One
Title: Two mouse models carrying truncating mutations in Magel2 show distinct phenotypes.
Volume: 15
Issue: 8
Pages: e0237814
Publication
First Author: Bischof JM
Year: 2007
Journal: Hum Mol Genet
Title: Inactivation of the mouse Magel2 gene results in growth abnormalities similar to Prader-Willi syndrome.
Volume: 16
Issue: 22
Pages: 2713-9
Publication
First Author: Wijesuriya TM
Year: 2017
Journal: Hum Mol Genet
Title: The Prader-Willi syndrome proteins MAGEL2 and necdin regulate leptin receptor cell surface abundance through ubiquitination pathways.
Volume: 26
Issue: 21
Pages: 4215-4230
Publication  
First Author: Chen H
Year: 2020
Journal: JCI Insight
Title: Loss of MAGEL2 in Prader-Willi syndrome leads to decreased secretory granule and neuropeptide production.
Volume: 5
Issue: 17
Publication
First Author: Fountain MD
Year: 2017
Journal: Genes Brain Behav
Title: Magel2 knockout mice manifest altered social phenotypes and a deficit in preference for social novelty.
Volume: 16
Issue: 6
Pages: 592-600
Publication
First Author: Kamaludin AA
Year: 2016
Journal: Hum Mol Genet
Title: Muscle dysfunction caused by loss of Magel2 in a mouse model of Prader-Willi and Schaaf-Yang syndromes.
Volume: 25
Issue: 17
Pages: 3798-3809
Publication
First Author: Mercer RE
Year: 2013
Journal: PLoS Genet
Title: Magel2 is required for leptin-mediated depolarization of POMC neurons in the hypothalamic arcuate nucleus in mice.
Volume: 9
Issue: 1
Pages: e1003207
Publication
First Author: Meziane H
Year: 2015
Journal: Biol Psychiatry
Title: An Early Postnatal Oxytocin Treatment Prevents Social and Learning Deficits in Adult Mice Deficient for Magel2, a Gene Involved in Prader-Willi Syndrome and Autism.
Volume: 78
Issue: 2
Pages: 85-94
Publication
First Author: Boccaccio I
Year: 1999
Journal: Hum Mol Genet
Title: The human MAGEL2 gene and its mouse homologue are paternally expressed and mapped to the Prader-Willi region.
Volume: 8
Issue: 13
Pages: 2497-505
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: Vaidyanathan R
Year: 2020
Journal: Hum Mol Genet
Title: Colocalization of Oxtr with Prader-Willi syndrome transcripts in the trigeminal ganglion of neonatal mice.
Volume: 29
Issue: 12
Pages: 2065-2075
Publication  
First Author: Choi Y
Year: 2022
Journal: Life Sci Alliance
Title: Magel2 knockdown in hypothalamic POMC neurons innervating the medial amygdala reduces susceptibility to diet-induced obesity.
Volume: 5
Issue: 11
Publication
First Author: Stacher Hörndli CN
Year: 2019
Journal: Cell Rep
Title: Complex Economic Behavior Patterns Are Constructed from Finite, Genetically Controlled Modules of Behavior.
Volume: 28
Issue: 7
Pages: 1814-1829.e6
Publication
First Author: Mercer RE
Year: 2009
Journal: PLoS One
Title: Loss of magel2, a candidate gene for features of Prader-Willi syndrome, impairs reproductive function in mice.
Volume: 4
Issue: 1
Pages: e4291
Publication
First Author: Crutcher E
Year: 2019
Journal: Sci Rep
Title: mTOR and autophagy pathways are dysregulated in murine and human models of Schaaf-Yang syndrome.
Volume: 9
Issue: 1
Pages: 15935
Publication
First Author: Pravdivyi I
Year: 2015
Journal: Hum Mol Genet
Title: Progressive postnatal decline in leptin sensitivity of arcuate hypothalamic neurons in the Magel2-null mouse model of Prader-Willi syndrome.
Volume: 24
Issue: 15
Pages: 4276-83
Publication
First Author: Tennese AA
Year: 2011
Journal: Endocrinology
Title: Impaired hypothalamic regulation of endocrine function and delayed counterregulatory response to hypoglycemia in Magel2-null mice.
Volume: 152
Issue: 3
Pages: 967-78
Publication
First Author: Oncul M
Year: 2018
Journal: Hum Mol Genet
Title: Impaired melanocortin pathway function in Prader-Willi syndrome gene-Magel2 deficient mice.
Volume: 27
Issue: 18
Pages: 3129-3136
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: Carias KV
Year: 2020
Journal: PLoS One
Title: A MAGEL2-deubiquitinase complex modulates the ubiquitination of circadian rhythm protein CRY1.
Volume: 15
Issue: 4
Pages: e0230874
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: Kuwako K
Year: 2004
Journal: J Biol Chem
Title: Necdin-related MAGE proteins differentially interact with the E2F1 transcription factor and the p75 neurotrophin receptor.
Volume: 279
Issue: 3
Pages: 1703-12
Publication  
First Author: Watrin F
Year: 2005
Journal: BMC Genet
Title: The Prader-Willi syndrome murine imprinting center is not involved in the spatio-temporal transcriptional regulation of the Necdin gene.
Volume: 6
Pages: 1
Publication
First Author: Devos J
Year: 2011
Journal: J Circadian Rhythms
Title: Magel2, a Prader-Willi syndrome candidate gene, modulates the activities of circadian rhythm proteins in cultured cells.
Volume: 9
Issue: 1
Pages: 12
Publication
First Author: Lee S
Year: 2005
Journal: Hum Mol Genet
Title: Essential role for the Prader-Willi syndrome protein necdin in axonal outgrowth.
Volume: 14
Issue: 5
Pages: 627-37
Publication
First Author: Gur I
Year: 2014
Journal: PLoS One
Title: Necdin promotes ubiquitin-dependent degradation of PIAS1 SUMO E3 ligase.
Volume: 9
Issue: 6
Pages: e99503
Publication  
First Author: Ben-Cnaan E
Year: 2022
Journal: Int J Mol Sci
Title: The Metabolic Efficacy of a Cannabidiolic Acid (CBDA) Derivative in Treating Diet- and Genetic-Induced Obesity.
Volume: 23
Issue: 10
Publication
First Author: Hao YH
Year: 2013
Journal: Cell
Title: Regulation of WASH-dependent actin polymerization and protein trafficking by ubiquitination.
Volume: 152
Issue: 5
Pages: 1051-64
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: Miller NL
Year: 2009
Journal: Hum Mol Genet
Title: Necdin, a Prader-Willi syndrome candidate gene, regulates gonadotropin-releasing hormone neurons during development.
Volume: 18
Issue: 2
Pages: 248-60
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: Gordeeva OF
Year: 2017
Journal: Russ J Dev Biol
Title: Expression of Cancer-Testis Antigens of the Mage Family in Mouse Oocytes and Early Embryos
Volume: 48
Issue: 4
Pages: 287-294
Publication      
First Author: Gordeeva O
Year: 2016
Journal: MGI Direct Data Submission
Title: Expression of the genes of the melanoma antigen (Mage) families in E7.5 mouse embryo
Publication      
First Author: Gordeeva O
Year: 2016
Journal: MGI Direct Data Submission
Title: Expression of the genes of the melanoma antigen (Mage) families in placenta
Publication      
First Author: Gordeeva O
Year: 2018
Journal: MGI Direct Data Submission
Title: Expression of the genes of the melanoma antigen (Mage) families in brain
Publication      
First Author: Gordeeva O
Year: 2018
Journal: MGI Direct Data Submission
Title: Expression of the genes of the melanoma antigen (Mage) families in heart
Publication      
First Author: Gordeeva O
Year: 2018
Journal: MGI Direct Data Submission
Title: Expression of the genes of the melanoma antigen (Mage) families in liver
Publication      
First Author: Gordeeva O
Year: 2018
Journal: MGI Direct Data Submission
Title: Expression Patterns of Cancer-Testis Antigens of Mage Families in Somatic and Reproductive Organs of Immunocompetent and Immunodeficient Mice
Publication      
First Author: Gordeeva O
Year: 2018
Journal: MGI Direct Data Submission
Title: Expression of the genes of the melanoma antigen (Mage) families in male and female gonad
Publication
First Author: Chomez P
Year: 2001
Journal: Cancer Res
Title: An overview of the MAGE gene family with the identification of all human members of the family.
Volume: 61
Issue: 14
Pages: 5544-51
Publication
First Author: Kumamoto T
Year: 2013
Journal: Cell Rep
Title: Foxg1 coordinates the switch from nonradially to radially migrating glutamatergic subtypes in the neocortex through spatiotemporal repression.
Volume: 3
Issue: 3
Pages: 931-45
Publication
First Author: Bischof JM
Year: 2005
Journal: Physiol Genomics
Title: Genome-wide analysis of gene transcription in the hypothalamus.
Volume: 22
Issue: 2
Pages: 191-6
Publication
First Author: Shaut CA
Year: 2008
Journal: PLoS Genet
Title: HOXA13 Is essential for placental vascular patterning and labyrinth endothelial specification.
Volume: 4
Issue: 5
Pages: e1000073
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: Colasante G
Year: 2009
Journal: Dev Biol
Title: Arx acts as a regional key selector gene in the ventral telencephalon mainly through its transcriptional repression activity.
Volume: 334
Issue: 1
Pages: 59-71
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: Gordeeva O
Year: 2019
Journal: Oncotarget
Title: Expression dynamics of Mage family genes during self-renewal and differentiation of mouse pluripotent stem and teratocarcinoma cells.
Volume: 10
Issue: 35
Pages: 3248-3266
Publication
First Author: Fulp CT
Year: 2008
Journal: Hum Mol Genet
Title: Identification of Arx transcriptional targets in the developing basal forebrain.
Volume: 17
Issue: 23
Pages: 3740-60
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: Boyle MP
Year: 2011
Journal: J Comp Neurol
Title: Cell-type-specific consequences of Reelin deficiency in the mouse neocortex, hippocampus, and amygdala.
Volume: 519
Issue: 11
Pages: 2061-89
Publication        
First Author: National Center for Biotechnology Information, National Library of Medicine, National Institutes of Health
Year: 2001
Title: GenBank Record Derived Information
Publication      
First Author: MouseBookTM
Year: 2005
Journal: Unpublished
Title: Information obtained from MouseBookTM, Medical Research Council Mammalian Genetics Unit, Harwell, UK.
Publication
First Author: Shimogori T
Year: 2010
Journal: Nat Neurosci
Title: A genomic atlas of mouse hypothalamic development.
Volume: 13
Issue: 6
Pages: 767-75
Publication      
First Author: Lennon G
Year: 1999
Journal: Database Download
Title: WashU-HHMI Mouse EST Project
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: GemPharmatech
Year: 2020
Title: GemPharmatech Website.
Publication
First Author: Okazaki Y
Year: 2002
Journal: Nature
Title: Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs.
Volume: 420
Issue: 6915
Pages: 563-73
Publication        
First Author: Mouse Genome Informatics Scientific Curators
Year: 2000
Title: Gene Ontology Annotation by electronic association of SwissProt Keywords with GO terms
Publication        
First Author: Mouse Genome Informatics Scientific Curators
Year: 2010
Title: Human to Mouse ISO GO annotation transfer
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: 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: MGI Genome Annotation Group and UniGene Staff
Year: 2015
Journal: Database Download
Title: MGI-UniGene Interconnection Effort
Publication
First Author: Gaudet P
Year: 2011
Journal: Brief Bioinform
Title: Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium.
Volume: 12
Issue: 5
Pages: 449-62
Publication      
First Author: Mouse Genome Database and National Center for Biotechnology Information
Year: 2000
Journal: Database Release
Title: Entrez Gene Load
Publication        
First Author: Mouse Genome Informatics Scientific Curators
Year: 2005
Title: Obtaining and Loading Genome Assembly Coordinates from Ensembl Annotations
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: 2005
Title: Obtaining and loading genome assembly coordinates from NCBI annotations
Publication      
First Author: Bairoch A
Year: 1999
Journal: Database Release
Title: SWISS-PROT Annotated protein sequence database
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 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: 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: Mouse Genome Informatics
Year: 2010
Journal: Database Release
Title: Protein Ontology Association Load.
Publication
First Author: Kanber D
Year: 2009
Journal: Eur J Hum Genet
Title: A paternal deletion of MKRN3, MAGEL2 and NDN does not result in Prader-Willi syndrome.
Volume: 17
Issue: 5
Pages: 582-90
Publication  
First Author: Chibuk TK
Year: 2001
Journal: BMC Genet
Title: A necdin/MAGE-like gene in the chromosome 15 autism susceptibility region: expression, imprinting, and mapping of the human and mouse orthologues.
Volume: 2
Pages: 22
Publication
First Author: Dombret C
Year: 2012
Journal: Hum Mol Genet
Title: Loss of Maged1 results in obesity, deficits of social interactions, impaired sexual behavior and severe alteration of mature oxytocin production in the hypothalamus.
Volume: 21
Issue: 21
Pages: 4703-17
Publication  
First Author: Zapata RC
Year: 2023
Journal: Mol Metab
Title: Targeting Clic1 for the treatment of obesity: A novel therapeutic strategy to reduce food intake and body weight.
Volume: 76
Pages: 101794
Publication
First Author: Mahfouz A
Year: 2016
Journal: Proc Natl Acad Sci U S A
Title: Genome-wide coexpression of steroid receptors in the mouse brain: Identifying signaling pathways and functionally coordinated regions.
Volume: 113
Issue: 10
Pages: 2738-43
Publication
First Author: Tacer KF
Year: 2017
Journal: Biochem J
Title: Cellular and disease functions of the Prader-Willi Syndrome gene MAGEL2.
Volume: 474
Issue: 13
Pages: 2177-2190
Publication      
First Author: The Gene Expression Nervous System Atlas (GENSAT) Project, The Rockefeller University (New York, NY)
Year: 2005
Journal: Database Download
Title: MGI download of GENSAT transgene data
Publication
First Author: Gerhard DS
Year: 2004
Journal: Genome Res
Title: The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
Volume: 14
Issue: 10B
Pages: 2121-7