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Search results 1 to 100 out of 172 for Snrpn

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Category: Publication
Type Details Score
Publication
First Author: Bressler J
Year: 2001
Journal: Nat Genet
Title: The SNRPN promoter is not required for genomic imprinting of the Prader-Willi/Angelman domain in mice.
Volume: 28
Issue: 3
Pages: 232-40
Publication
First Author: Blaydes SM
Year: 1999
Journal: Mamm Genome
Title: Analysis of murine Snrpn and human SNRPN gene imprinting in transgenic mice.
Volume: 10
Issue: 6
Pages: 549-55
Publication
First Author: Gray TA
Year: 1999
Journal: Proc Natl Acad Sci U S A
Title: An imprinted, mammalian bicistronic transcript encodes two independent proteins.
Volume: 96
Issue: 10
Pages: 5616-21
Publication
First Author: Gabriel JM
Year: 1998
Journal: Mamm Genome
Title: Structure and function correlations at the imprinted mouse Snrpn locus.
Volume: 9
Issue: 10
Pages: 788-93
Publication
First Author: Barr JA
Year: 1995
Journal: Mamm Genome
Title: Ubiquitous expression and imprinting of Snrpn in the mouse.
Volume: 6
Issue: 6
Pages: 405-7
Publication
First Author: Peery EG
Year: 2007
Journal: Mamm Genome
Title: A targeted deletion upstream of Snrpn does not result in an imprinting defect.
Volume: 18
Issue: 4
Pages: 255-62
Publication
First Author: Cattanach BM
Year: 1992
Journal: Nat Genet
Title: A candidate mouse model for Prader-Willi syndrome which shows an absence of Snrpn expression.
Volume: 2
Issue: 4
Pages: 270-4
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: Gray TA
Year: 1999
Journal: Nucleic Acids Res
Title: Concerted regulation and molecular evolution of the duplicated SNRPB'/B and SNRPN loci.
Volume: 27
Issue: 23
Pages: 4577-84
Publication
First Author: Shemer R
Year: 1997
Journal: Proc Natl Acad Sci U S A
Title: Structure of the imprinted mouse Snrpn gene and establishment of its parental-specific methylation pattern.
Volume: 94
Issue: 19
Pages: 10267-72
Publication
First Author: Leff SE
Year: 1992
Journal: Nat Genet
Title: Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader-Willi syndrome region.
Volume: 2
Issue: 4
Pages: 259-64
Publication
First Author: Gregory RI
Year: 2001
Journal: Mol Cell Biol
Title: DNA methylation is linked to deacetylation of histone H3, but not H4, on the imprinted genes Snrpn and U2af1-rs1.
Volume: 21
Issue: 16
Pages: 5426-36
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: Tsai TF
Year: 1999
Journal: Hum Mol Genet
Title: Paternal deletion from Snrpn to Ube3a in the mouse causes hypotonia, growth retardation and partial lethality and provides evidence for a gene contributing to Prader-Willi syndrome.
Volume: 8
Issue: 8
Pages: 1357-64
Publication
First Author: Huntriss JD
Year: 1994
Journal: Mol Biol Rep
Title: Mice lacking Snrpn expression show normal regulation of neuronal alternative splicing events.
Volume: 20
Issue: 1
Pages: 19-25
Publication
First Author: Szabó PE
Year: 1996
Journal: EMBO J
Title: Maternal and paternal genomes function independently in mouse ova in establishing expression of the imprinted genes Snrpn and Igf2r: no evidence for allelic trans-sensing and counting mechanisms.
Volume: 15
Issue: 22
Pages: 6018-25
Publication
First Author: Miyazaki K
Year: 2009
Journal: Gene
Title: Developmentally dynamic changes of DNA methylation in the mouse Snurf/Snrpn gene.
Volume: 432
Issue: 1-2
Pages: 97-101
Publication
First Author: Nicholls RD
Year: 1999
Journal: Acta Paediatr Suppl
Title: Genetic abnormalities in Prader-Willi syndrome and lessons from mouse models.
Volume: 88
Issue: 433
Pages: 99-104
Publication
First Author: Tsai TF
Year: 2002
Journal: Hum Mol Genet
Title: Evidence for translational regulation of the imprinted Snurf-Snrpn locus in mice.
Volume: 11
Issue: 14
Pages: 1659-68
Publication
First Author: Vitali P
Year: 2010
Journal: J Cell Sci
Title: Long nuclear-retained non-coding RNAs and allele-specific higher-order chromatin organization at imprinted snoRNA gene arrays.
Volume: 123
Issue: Pt 1
Pages: 70-83
Publication
First Author: Yang T
Year: 1998
Journal: Nat Genet
Title: A mouse model for Prader-Willi syndrome imprinting-centre mutations.
Volume: 19
Issue: 1
Pages: 25-31
Publication
First Author: Leung KN
Year: 2009
Journal: Hum Mol Genet
Title: Imprinting regulates mammalian snoRNA-encoding chromatin decondensation and neuronal nucleolar size.
Volume: 18
Issue: 22
Pages: 4227-38
Publication
First Author: Wu MY
Year: 2006
Journal: Genes Dev
Title: Deficiency of Rbbp1/Arid4a and Rbbp1l1/Arid4b alters epigenetic modifications and suppresses an imprinting defect in the PWS/AS domain.
Volume: 20
Issue: 20
Pages: 2859-70
Publication
First Author: Smith EY
Year: 2011
Journal: PLoS Genet
Title: Transcription is required to establish maternal imprinting at the Prader-Willi syndrome and Angelman syndrome locus.
Volume: 7
Issue: 12
Pages: e1002422
Publication
First Author: Wu MY
Year: 2006
Journal: Genesis
Title: Mouse imprinting defect mutations that model Angelman syndrome.
Volume: 44
Issue: 1
Pages: 12-22
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
Publication
First Author: Chamberlain SJ
Year: 2004
Journal: Hum Mol Genet
Title: Evidence for genetic modifiers of postnatal lethality in PWS-IC deletion mice.
Volume: 13
Issue: 23
Pages: 2971-7
Publication
First Author: Davies JR
Year: 2015
Journal: Eur J Neurosci
Title: Calorie seeking, but not hedonic response, contributes to hyperphagia in a mouse model for Prader-Willi syndrome.
Volume: 42
Issue: 4
Pages: 2105-13
Publication
First Author: Golding DM
Year: 2017
Journal: J Endocrinol
Title: Paradoxical leanness in the imprinting-centre deletion mouse model for Prader-Willi syndrome.
Volume: 232
Issue: 1
Pages: 123-135
Publication
First Author: Relkovic D
Year: 2010
Journal: Eur J Neurosci
Title: Behavioural and cognitive abnormalities in an imprinting centre deletion mouse model for Prader-Willi syndrome.
Volume: 31
Issue: 1
Pages: 156-64
Publication
First Author: Ozçelik T
Year: 1992
Journal: Nat Genet
Title: Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader-Willi syndrome critical region.
Volume: 2
Issue: 4
Pages: 265-9
Publication
First Author: Chamberlain SJ
Year: 2001
Journal: Genomics
Title: The Prader-Willi syndrome imprinting center activates the paternally expressed murine Ube3a antisense transcript but represses paternal Ube3a.
Volume: 73
Issue: 3
Pages: 316-22
Publication
First Author: Doe CM
Year: 2009
Journal: Hum Mol Genet
Title: Loss of the imprinted snoRNA mbii-52 leads to increased 5htr2c pre-RNA editing and altered 5HT2CR-mediated behaviour.
Volume: 18
Issue: 12
Pages: 2140-8
Publication  
First Author: Welden JR
Year: 2018
Journal: Neurosci Lett
Title: The posterior pituitary expresses the serotonin receptor 2C.
Volume: 684
Pages: 132-139
Publication
First Author: de los Santos T
Year: 2000
Journal: Am J Hum Genet
Title: Small evolutionarily conserved RNA, resembling C/D box small nucleolar RNA, is transcribed from PWCR1, a novel imprinted gene in the Prader-Willi deletion region, which Is highly expressed in brain.
Volume: 67
Issue: 5
Pages: 1067-82
Publication
First Author: Johnstone KA
Year: 2006
Journal: Hum Mol Genet
Title: A human imprinting centre demonstrates conserved acquisition but diverged maintenance of imprinting in a mouse model for Angelman syndrome imprinting defects.
Volume: 15
Issue: 3
Pages: 393-404
Publication
First Author: DuBose AJ
Year: 2010
Journal: Neurogenetics
Title: Atp10a, a gene adjacent to the PWS/AS gene cluster, is not imprinted in mouse and is insensitive to the PWS-IC.
Volume: 11
Issue: 2
Pages: 145-51
Publication
First Author: Villar AJ
Year: 1994
Journal: Mol Reprod Dev
Title: Spatially restricted imprinting of mouse chromosome 7.
Volume: 37
Issue: 3
Pages: 247-54
Publication
First Author: Shemer R
Year: 2000
Journal: Nat Genet
Title: The imprinting box of the Prader-Willi/Angelman syndrome domain.
Volume: 26
Issue: 4
Pages: 440-3
Publication
First Author: Lopes FL
Year: 2009
Journal: Hum Mol Genet
Title: Reproductive and epigenetic outcomes associated with aging mouse oocytes.
Volume: 18
Issue: 11
Pages: 2032-44
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: 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: Meng L
Year: 2012
Journal: Hum Mol Genet
Title: Ube3a-ATS is an atypical RNA polymerase II transcript that represses the paternal expression of Ube3a.
Volume: 21
Issue: 13
Pages: 3001-12
Publication
First Author: Wu MY
Year: 2012
Journal: PLoS One
Title: An unexpected function of the Prader-Willi syndrome imprinting center in maternal imprinting in mice.
Volume: 7
Issue: 4
Pages: e34348
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: Kitsberg D
Year: 1993
Journal: Nature
Title: Allele-specific replication timing of imprinted gene regions.
Volume: 364
Issue: 6436
Pages: 459-63
Publication
First Author: Szabó PE
Year: 1995
Journal: Genes Dev
Title: Allele-specific expression and total expression levels of imprinted genes during early mouse development: implications for imprinting mechanisms.
Volume: 9
Issue: 24
Pages: 3097-108
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: 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: Szabó P
Year: 1994
Journal: Development
Title: Expression and methylation of imprinted genes during in vitro differentiation of mouse parthenogenetic and androgenetic embryonic stem cell lines.
Volume: 120
Issue: 6
Pages: 1651-60
Publication
First Author: Meng L
Year: 2013
Journal: PLoS Genet
Title: Truncation of Ube3a-ATS unsilences paternal Ube3a and ameliorates behavioral defects in the Angelman syndrome mouse model.
Volume: 9
Issue: 12
Pages: e1004039
Publication
First Author: Marjonen H
Year: 2018
Journal: PLoS One
Title: Early prenatal alcohol exposure alters imprinted gene expression in placenta and embryo in a mouse model.
Volume: 13
Issue: 5
Pages: e0197461
Publication
First Author: DuBose AJ
Year: 2012
Journal: Proc Natl Acad Sci U S A
Title: Temporal and developmental requirements for the Prader-Willi imprinting center.
Volume: 109
Issue: 9
Pages: 3446-50
Publication
First Author: Mann MR
Year: 2003
Journal: Biol Reprod
Title: Disruption of imprinted gene methylation and expression in cloned preimplantation stage mouse embryos.
Volume: 69
Issue: 3
Pages: 902-14
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: Nakao M
Year: 1996
Journal: Hum Mutat
Title: Advantages of RT-PCR and denaturing gradient gel electrophoresis for analysis of genomic imprinting: detection of new mouse and human expressed polymorphisms.
Volume: 7
Issue: 2
Pages: 144-8
Publication  
First Author: Cirio MC
Year: 2008
Journal: BMC Dev Biol
Title: Preimplantation expression of the somatic form of Dnmt1 suggests a role in the inheritance of genomic imprints.
Volume: 8
Pages: 9
Publication
First Author: Buettner VL
Year: 2005
Journal: Mamm Genome
Title: Novel paternally expressed intergenic transcripts at the mouse Prader-Willi/Angelman Syndrome locus.
Volume: 16
Issue: 4
Pages: 219-27
Publication
First Author: Landers M
Year: 2004
Journal: Nucleic Acids Res
Title: Regulation of the large (approximately 1000 kb) imprinted murine Ube3a antisense transcript by alternative exons upstream of Snurf/Snrpn.
Volume: 32
Issue: 11
Pages: 3480-92
Publication
First Author: Peters J
Year: 2004
Journal: Brief Funct Genomic Proteomic
Title: Identification and characterisation of imprinted genes in the mouse.
Volume: 2
Issue: 4
Pages: 320-33
Publication
First Author: Gerrelli D
Year: 1991
Journal: Nucleic Acids Res
Title: Cloning and sequencing of a mouse embryonal carcinoma cell mRNA encoding the tissue specific RNA splicing protein SmN.
Volume: 19
Issue: 23
Pages: 6642
Publication
First Author: Szabó PE
Year: 2002
Journal: Mech Dev
Title: Allele-specific expression of imprinted genes in mouse migratory primordial germ cells.
Volume: 115
Issue: 1-2
Pages: 157-60
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: 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: Ariel M
Year: 1993
Journal: Cold Spring Harb Symp Quant Biol
Title: Allele-specific structures in the mouse Igf2-H19 domain.
Volume: 58
Pages: 307-13
Publication
First Author: Séraphin B
Year: 1995
Journal: EMBO J
Title: Sm and Sm-like proteins belong to a large family: identification of proteins of the U6 as well as the U1, U2, U4 and U5 snRNPs.
Volume: 14
Issue: 9
Pages: 2089-98
Publication
First Author: Szabó PE
Year: 1995
Journal: Genes Dev
Title: Biallelic expression of imprinted genes in the mouse germ line: implications for erasure, establishment, and mechanisms of genomic imprinting.
Volume: 9
Issue: 15
Pages: 1857-68
Publication
First Author: Howell CY
Year: 2001
Journal: Cell
Title: Genomic imprinting disrupted by a maternal effect mutation in the Dnmt1 gene.
Volume: 104
Issue: 6
Pages: 829-38
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: Kaneko-Ishino T
Year: 1995
Journal: Nat Genet
Title: Peg1/Mest imprinted gene on chromosome 6 identified by cDNA subtraction hybridization.
Volume: 11
Issue: 1
Pages: 52-9
Publication
First Author: Kobayashi S
Year: 2000
Journal: Genes Cells
Title: Mouse Peg9/Dlk1 and human PEG9/DLK1 are paternally expressed imprinted genes closely located to the maternally expressed imprinted genes: mouse Meg3/Gtl2 and human MEG3.
Volume: 5
Issue: 12
Pages: 1029-37
Publication
First Author: Arnaud P
Year: 2006
Journal: Hum Mol Genet
Title: Stochastic imprinting in the progeny of Dnmt3L-/- females.
Volume: 15
Issue: 4
Pages: 589-98
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: McLaughlin KJ
Year: 1996
Journal: Development
Title: Mouse embryos with paternal duplication of an imprinted chromosome 7 region die at midgestation and lack placental spongiotrophoblast.
Volume: 122
Issue: 1
Pages: 265-70
Publication
First Author: Obata Y
Year: 1998
Journal: Development
Title: Disruption of primary imprinting during oocyte growth leads to the modified expression of imprinted genes during embryogenesis.
Volume: 125
Issue: 8
Pages: 1553-60
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: MacDonald HR
Year: 1997
Journal: Hum Mol Genet
Title: The necdin gene is deleted in Prader-Willi syndrome and is imprinted in human and mouse.
Volume: 6
Issue: 11
Pages: 1873-8
Publication
First Author: de Waal E
Year: 2014
Journal: Biol Reprod
Title: In vitro culture increases the frequency of stochastic epigenetic errors at imprinted genes in placental tissues from mouse concepti produced through assisted reproductive technologies.
Volume: 90
Issue: 2
Pages: 22
Publication        
First Author: MGD Nomenclature Committee
Year: 1995
Title: Nomenclature Committee Use
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: Ciccone DN
Year: 2009
Journal: Nature
Title: KDM1B is a histone H3K4 demethylase required to establish maternal genomic imprints.
Volume: 461
Issue: 7262
Pages: 415-8
Publication
First Author: Brilliant MH
Year: 1994
Journal: Genetics
Title: The original pink-eyed dilution mutation (p) arose in Asiatic mice: implications for the H4 minor histocompatibility antigen, Myod1 regulation and the origin of inbred strains.
Volume: 138
Issue: 1
Pages: 203-11
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: Hata K
Year: 2002
Journal: Development
Title: Dnmt3L cooperates with the Dnmt3 family of de novo DNA methyltransferases to establish maternal imprints in mice.
Volume: 129
Issue: 8
Pages: 1983-93
Publication
First Author: Arima T
Year: 2006
Journal: Dev Biol
Title: Loss of the maternal imprint in Dnmt3Lmat-/- mice leads to a differentiation defect in the extraembryonic tissue.
Volume: 297
Issue: 2
Pages: 361-73
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: Morita S
Year: 2007
Journal: Genomics
Title: One Argonaute family member, Eif2c2 (Ago2), is essential for development and appears not to be involved in DNA methylation.
Volume: 89
Issue: 6
Pages: 687-96
Publication
First Author: Kantor B
Year: 2003
Journal: Gene Expr Patterns
Title: Expression and localization of components of the histone deacetylases multiprotein repressory complexes in the mouse preimplantation embryo.
Volume: 3
Issue: 6
Pages: 697-702
Publication
First Author: Bartolomei MS
Year: 1994
Journal: Nat Genet
Title: The search for imprinted genes.
Volume: 6
Issue: 3
Pages: 220-1
Publication
First Author: Tilghman SM
Year: 1999
Journal: Cell
Title: The sins of the fathers and mothers: genomic imprinting in mammalian development.
Volume: 96
Issue: 2
Pages: 185-93
Publication
First Author: Kaneda M
Year: 2004
Journal: Nature
Title: Essential role for de novo DNA methyltransferase Dnmt3a in paternal and maternal imprinting.
Volume: 429
Issue: 6994
Pages: 900-3
Publication
First Author: Dhar MS
Year: 1997
Journal: Mamm Genome
Title: A microsatellite map of the pink-eyed dilution (p) deletion complex in mouse chromosome 7.
Volume: 8
Issue: 2
Pages: 143-5
Publication
First Author: Warden CH
Year: 1995
Journal: J Clin Invest
Title: Identification of four chromosomal loci determining obesity in a multifactorial mouse model.
Volume: 95
Issue: 4
Pages: 1545-52
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: Mann M
Year: 1995
Journal: Dev Genet
Title: Identification of genes showing altered expression in preimplantation and early postimplantation parthenogenetic embryos.
Volume: 17
Issue: 3
Pages: 223-32
Publication
First Author: Wymore RS
Year: 1994
Journal: Genomics
Title: Genomic organization, nucleotide sequence, biophysical properties, and localization of the voltage-gated K+ channel gene KCNA4/Kv1.4 to mouse chromosome 2/human 11p14 and mapping of KCNC1/Kv3.1 to mouse 7/human 11p14.3-p15.2 and KCNA1/Kv1.1 to human 12p13.
Volume: 20
Issue: 2
Pages: 191-202
Publication
First Author: Ferrón SR
Year: 2011
Journal: Nature
Title: Postnatal loss of Dlk1 imprinting in stem cells and niche astrocytes regulates neurogenesis.
Volume: 475
Issue: 7356
Pages: 381-5
Publication        
First Author: Mouse Genome Informatics Scientific Curators
Year: 2002
Title: MGC Data curation in Mouse Genome Informatics
Publication
First Author: Martin JF
Year: 1994
Journal: Mol Cell Biol
Title: A Mef2 gene that generates a muscle-specific isoform via alternative mRNA splicing.
Volume: 14
Issue: 3
Pages: 1647-56
Publication
First Author: Mager J
Year: 2003
Journal: Nat Genet
Title: Genome imprinting regulated by the mouse Polycomb group protein Eed.
Volume: 33
Issue: 4
Pages: 502-7