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Search results 1 to 100 out of 144 for Ndn

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Category: Publication
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Type Details Score
Publication
38732023 | J:348377
 
First Author: Vo NDN
Year: 2024
Journal: Int J Mol Sci
Title: The Role of Collagen VIII in the Aging Mouse Kidney.
Volume: 25
Issue: 9
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Publication
12629158 | J:82266
First Author: Ren J
Year: 2003
Journal: J Neurosci
Title: Absence of Ndn, encoding the Prader-Willi syndrome-deleted gene necdin, results in congenital deficiency of central respiratory drive in neonatal mice.
Volume: 23
Issue: 5
Pages: 1569-73
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Publication
34210967 | J:328507
First Author: Tamada K
Year: 2021
Journal: Nat Commun
Title: Genetic dissection identifies Necdin as a driver gene in a mouse model of paternal 15q duplications.
Volume: 12
Issue: 1
Pages: 4056
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Publication
19770359 | J:155490
First Author: Kubota Y
Year: 2009
Journal: Blood
Title: Necdin restricts proliferation of hematopoietic stem cells during hematopoietic regeneration.
Volume: 114
Issue: 20
Pages: 4383-92
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Publication
20665884 | J:164695
First Author: Bush JR
Year: 2010
Journal: Genesis
Title: Loss of Necdin impairs myosin activation and delays cell polarization.
Volume: 48
Issue: 9
Pages: 540-53
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Publication
24039599 | J:223046
First Author: Rieusset A
Year: 2013
Journal: PLoS Genet
Title: Stochastic loss of silencing of the imprinted Ndn/NDN allele, in a mouse model and humans with prader-willi syndrome, has functional consequences.
Volume: 9
Issue: 9
Pages: e1003752
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Publication
17826745 | J:125162
First Author: Friedman ER
Year: 2007
Journal: Biochem Biophys Res Commun
Title: Separate necdin domains bind ARNT2 and HIF1alpha and repress transcription.
Volume: 363
Issue: 1
Pages: 113-8
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Publication
10556298 | J:58785
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
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Publication
10915770 | J:63703
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
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Publication
18753379 | J:138789
First Author: Hasegawa K
Year: 2008
Journal: J Neurosci
Title: Necdin regulates p53 acetylation via Sirtuin1 to modulate DNA damage response in cortical neurons.
Volume: 28
Issue: 35
Pages: 8772-84
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Publication
10508517 | J:57890
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
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Publication
17108174 | J:115574
First Author: Kurita M
Year: 2006
Journal: J Neurosci
Title: Necdin downregulates CDC2 expression to attenuate neuronal apoptosis.
Volume: 26
Issue: 46
Pages: 12003-13
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Publication
12971993 | J:85656
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
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Publication
22514318 | J:184441
First Author: Hasegawa K
Year: 2012
Journal: J Neurosci
Title: Necdin controls Foxo1 acetylation in hypothalamic arcuate neurons to modulate the thyroid axis.
Volume: 32
Issue: 16
Pages: 5562-72
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Publication
9302265 | J:43448
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
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Publication
18930956 | J:143569
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
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Publication
15634360 | J:101829
 
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
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Publication
16707790 | J:108706
First Author: Kuwajima T
Year: 2006
Journal: J Neurosci
Title: Necdin promotes GABAergic neuron differentiation in cooperation with Dlx homeodomain proteins.
Volume: 26
Issue: 20
Pages: 5383-92
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Publication
2069569 | J:28227
First Author: Maruyama K
Year: 1991
Journal: Biochem Biophys Res Commun
Title: A novel brain-specific mRNA encoding nuclear protein (necdin) expressed in neurally differentiated embryonal carcinoma cells.
Volume: 178
Issue: 1
Pages: 291-6
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Publication
10319852 | J:55267
First Author: Tsai TF
Year: 1999
Journal: Nat Genet
Title: Necdin-deficient mice do not show lethality or the obesity and infertility of Prader-Willi syndrome.
Volume: 22
Issue: 1
Pages: 15-6
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Publication
11115855 | J:66557
First Author: Muscatelli F
Year: 2000
Journal: Hum Mol Genet
Title: Disruption of the mouse Necdin gene results in hypothalamic and behavioral alterations reminiscent of the human Prader-Willi syndrome.
Volume: 9
Issue: 20
Pages: 3101-10
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Publication
18557765 | J:140436
First Author: Bush JR
Year: 2008
Journal: Differentiation
Title: The Prader-Willi syndrome protein necdin interacts with the E1A-like inhibitor of differentiation EID-1 and promotes myoblast differentiation.
Volume: 76
Issue: 9
Pages: 994-1005
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Publication
22305984 | J:183684
First Author: Bush JR
Year: 2012
Journal: Gene
Title: Loss of the Prader-Willi obesity syndrome protein necdin promotes adipogenesis.
Volume: 497
Issue: 1
Pages: 45-51
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Publication
17954612 | J:135082
First Author: Deponti D
Year: 2007
Journal: J Cell Biol
Title: Necdin mediates skeletal muscle regeneration by promoting myoblast survival and differentiation.
Volume: 179
Issue: 2
Pages: 305-19
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Publication
7639751 | J:27985
First Author: Hayashi Y
Year: 1995
Journal: Biochem Biophys Res Commun
Title: Arrest of cell growth by necdin, a nuclear protein expressed in postmitotic neurons.
Volume: 213
Issue: 1
Pages: 317-24
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Publication
8615786 | J:32077
 
First Author: Maruyama E
Year: 1996
Journal: Biochem J
Title: Biochemical characterization of mouse brain necdin.
Volume: 314 ( Pt 3)
Pages: 895-901
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Publication
9412790 | J:44959
First Author: Watrin F
Year: 1997
Journal: Eur J Hum Genet
Title: The mouse Necdin gene is expressed from the paternal allele only and lies in the 7C region of the mouse chromosome 7, a region of conserved synteny to the human Prader-Willi syndrome region.
Volume: 5
Issue: 5
Pages: 324-32
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Publication
9630521 | J:48345
First Author: Nakada Y
Year: 1998
Journal: Gene
Title: The human chromosomal gene for necdin, a neuronal growth suppressor, in the Prader-Willi syndrome deletion region.
Volume: 213
Issue: 1-2
Pages: 65-72
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Publication
10339753 | J:57203
 
First Author: Beechey CV
Year: 1999
Journal: Results Probl Cell Differ
Title: Appendix: imprinted genes and regions in mouse and human.
Volume: 25
Pages: 303-23
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Publication
19339547 | J:150505
First Author: Sciorati C
Year: 2009
Journal: J Cell Sci
Title: Necdin is expressed in cachectic skeletal muscle to protect fibers from tumor-induced wasting.
Volume: 122
Issue: Pt 8
Pages: 1119-25
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Publication
38832028 | J:353245
First Author: Dong Y
Year: 2024
Journal: iScience
Title: Deficiency in Prader-Willi syndrome gene necdin leads to attenuated cardiac contractility.
Volume: 27
Issue: 6
Pages: 109974
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39738217 | J:361386
First Author: Li X
Year: 2024
Journal: Sci Rep
Title: Prader-Willi syndrome protein necdin regulates the nucleocytoplasmic distribution and dopaminergic neuron development.
Volume: 14
Issue: 1
Pages: 31605
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Publication
10965153 | J:74072
First Author: Niinobe M
Year: 2000
Journal: Dev Neurosci
Title: Cellular and subcellular localization of necdin in fetal and adult mouse brain.
Volume: 22
Issue: 4
Pages: 310-9
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Publication
8557705 | J:30612
First Author: Uetsuki T
Year: 1996
Journal: J Biol Chem
Title: Structure and expression of the mouse necdin gene. Identification of a postmitotic neuron-restrictive core promoter.
Volume: 271
Issue: 2
Pages: 918-24
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Publication
9422723 | J:45609
First Author: Taniura H
Year: 1998
Journal: J Biol Chem
Title: Necdin, a postmitotic neuron-specific growth suppressor, interacts with viral transforming proteins and cellular transcription factor E2F1.
Volume: 273
Issue: 2
Pages: 720-8
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Publication
22776820 | J:189173
First Author: Asai T
Year: 2012
Journal: Blood
Title: Necdin, a p53 target gene, regulates the quiescence and response to genotoxic stress of hematopoietic stem/progenitor cells.
Volume: 120
Issue: 8
Pages: 1601-12
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Publication
22496793 | J:187108
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
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Publication
29087295 | J:258211
   
First Author: Matarazzo V
Year: 2017
Journal: Elife
Title: Necdin shapes serotonergic development and SERT activity modulating breathing in a mouse model for Prader-Willi syndrome.
Volume: 6
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Publication
20220004 | J:158979
First Author: Kuwajima T
Year: 2010
Journal: J Neurosci
Title: Necdin promotes tangential migration of neocortical interneurons from basal forebrain.
Volume: 30
Issue: 10
Pages: 3709-14
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Publication
2571505 | J:10024
First Author: Prieto J
Year: 1989
Journal: Eur J Immunol
Title: MALA-2, mouse homologue of human adhesion molecule ICAM-1 (CD54).
Volume: 19
Issue: 9
Pages: 1551-7
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Publication
15978586 | J:99779
First Author: Moon HE
Year: 2005
Journal: FEBS Lett
Title: Negative regulation of hypoxia inducible factor-1alpha by necdin.
Volume: 579
Issue: 17
Pages: 3797-801
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15965783 | J:99883
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
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Publication
19386232 | J:154259
First Author: Liu X
Year: 2009
Journal: Mol Cell Neurosci
Title: Nogo-A inhibits necdin-accelerated neurite outgrowth by retaining necdin in the cytoplasm.
Volume: 41
Issue: 1
Pages: 51-61
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Publication
32667666 | J:294627
First Author: Lu R
Year: 2020
Journal: Nucleic Acids Res
Title: Necdin regulates BMAL1 stability and circadian clock through SGT1-HSP90 chaperone machinery.
Volume: 48
Issue: 14
Pages: 7944-7957
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Publication
25012566 | J:320702
 
First Author: Ju H
Year: 2014
Journal: Cell Commun Signal
Title: The alpha subunit of Go modulates cell proliferation and differentiation through interactions with Necdin.
Volume: 12
Pages: 39
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Publication
23785149 | J:199643
First Author: Huang Z
Year: 2013
Journal: J Neurosci
Title: Necdin controls proliferation and apoptosis of embryonic neural stem cells in an oxygen tension-dependent manner.
Volume: 33
Issue: 25
Pages: 10362-73
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Publication
12198120 | J:79877
First Author: Kobayashi M
Year: 2002
Journal: J Biol Chem
Title: Ectopic expression of necdin induces differentiation of mouse neuroblastoma cells.
Volume: 277
Issue: 44
Pages: 42128-35
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Publication
24349431 | J:211149
First Author: Wu M
Year: 2013
Journal: PLoS One
Title: The ciliary protein cystin forms a regulatory complex with necdin to modulate Myc expression.
Volume: 8
Issue: 12
Pages: e83062
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Publication
1394972 | J:2250
First Author: Aizawa T
Year: 1992
Journal: Brain Res Dev Brain Res
Title: Expression of necdin, an embryonal carcinoma-derived nuclear protein, in developing mouse brain.
Volume: 68
Issue: 2
Pages: 265-74
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Publication
14593116 | J:87556
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
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Publication
11959851 | J:77266
First Author: Sasaki A
Year: 2002
Journal: J Biol Chem
Title: A RING finger protein Praja1 regulates Dlx5-dependent transcription through its ubiquitin ligase activity for the Dlx/Msx-interacting MAGE/Necdin family protein, Dlxin-1.
Volume: 277
Issue: 25
Pages: 22541-6
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Publication
11168589 | J:74103
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
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Publication
11007541 | J:65556
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
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Publication
20876615 | J:166548
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
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Publication
18272695 | J:132276
First Author: Zanella S
Year: 2008
Journal: J Neurosci
Title: Necdin plays a role in the serotonergic modulation of the mouse respiratory network: implication for Prader-Willi syndrome.
Volume: 28
Issue: 7
Pages: 1745-55
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12828934 | J:84615
First Author: Krass KL
Year: 2003
Journal: Neurobiol Dis
Title: Genetic loci contributing to age-related hippocampal lesions in mice.
Volume: 13
Issue: 2
Pages: 102-8
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15272023 | J:143687
First Author: Kuwajima T
Year: 2004
Journal: J Biol Chem
Title: Necdin interacts with the Msx2 homeodomain protein via MAGE-D1 to promote myogenic differentiation of C2C12 cells.
Volume: 279
Issue: 39
Pages: 40484-93
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11845283 | J:72417
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
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11719692 | J:73452
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
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15470499 | J:93303
First Author: Krüger M
Year: 2004
Journal: EMBO J
Title: NSCL-1 and NSCL-2 synergistically determine the fate of GnRH-1 neurons and control necdin gene expression.
Volume: 23
Issue: 21
Pages: 4353-64
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12482959 | J:81010
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
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23819640 | J:355918
First Author: Mould AW
Year: 2013
Journal: Epigenetics Chromatin
Title: Smchd1 regulates a subset of autosomal genes subject to monoallelic expression in addition to being critical for X inactivation.
Volume: 6
Issue: 1
Pages: 19
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23609791 | J:198496
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
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Publication
18166085 | J:152022
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
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Publication
21912643 | J:177769
First Author: Aebischer J
Year: 2011
Journal: PLoS One
Title: Necdin protects embryonic motoneurons from programmed cell death.
Volume: 6
Issue: 9
Pages: e23764
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Publication
26971449 | J:236559
 
First Author: Hasegawa K
Year: 2016
Journal: Nat Commun
Title: Promotion of mitochondrial biogenesis by necdin protects neurons against mitochondrial insults.
Volume: 7
Pages: 10943
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Publication
25300248 | J:217174
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
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26780092 | J:356775
First Author: Fan J
Year: 2016
Journal: Nat Methods
Title: Characterizing transcriptional heterogeneity through pathway and gene set overdispersion analysis.
Volume: 13
Issue: 3
Pages: 241-4
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39738558 | J:360634
First Author: Ziętek MM
Year: 2024
Journal: Sci Rep
Title: Prenatal gene-environment interactions mediate the impact of advanced maternal age on mouse offspring behavior.
Volume: 14
Issue: 1
Pages: 31733
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Publication
16049186 | J:100024
First Author: Kuwako K
Year: 2005
Journal: J Neurosci
Title: Disruption of the paternal necdin gene diminishes TrkA signaling for sensory neuron survival.
Volume: 25
Issue: 30
Pages: 7090-9
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Publication
15649943 | J:96395
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
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Publication
18570257 | J:137167
First Author: Tennese AA
Year: 2008
Journal: Dev Dyn
Title: Loss of the Prader-Willi syndrome protein necdin causes defective migration, axonal outgrowth, and survival of embryonic sympathetic neurons.
Volume: 237
Issue: 7
Pages: 1935-43
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Publication
14643685 | J:86964
First Author: Andrieu D
Year: 2003
Journal: Gene Expr Patterns
Title: Expression of the Prader-Willi gene Necdin during mouse nervous system development correlates with neuronal differentiation and p75NTR expression.
Volume: 3
Issue: 6
Pages: 761-5
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Publication
17893678 | J:125637
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
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18448610 | J:137668
First Author: Lui JC
Year: 2008
Journal: Am J Physiol Regul Integr Comp Physiol
Title: An imprinted gene network that controls mammalian somatic growth is down-regulated during postnatal growth deceleration in multiple organs.
Volume: 295
Issue: 1
Pages: R189-96
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Publication
24911587 | J:284695
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
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Publication
11454705 | J:70396
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
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19762426 | J:153616
First Author: Gabory A
Year: 2009
Journal: Development
Title: H19 acts as a trans regulator of the imprinted gene network controlling growth in mice.
Volume: 136
Issue: 20
Pages: 3413-21
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16600913 | J:107294
First Author: Chang Y
Year: 2006
Journal: Genes Dev
Title: Role of heat-shock factor 2 in cerebral cortex formation and as a regulator of p35 expression.
Volume: 20
Issue: 7
Pages: 836-47
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15972963 | J:99506
First Author: Pagliardini S
Year: 2005
Journal: Am J Pathol
Title: Developmental abnormalities of neuronal structure and function in prenatal mice lacking the prader-willi syndrome gene necdin.
Volume: 167
Issue: 1
Pages: 175-91
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24392139 | J:212574
First Author: Minamide R
Year: 2014
Journal: PLoS One
Title: Antagonistic interplay between necdin and Bmi1 controls proliferation of neural precursor cells in the embryonic mouse neocortex.
Volume: 9
Issue: 1
Pages: e84460
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Publication
22154806 | J:197015
First Author: Thompson PJ
Year: 2012
Journal: J Mol Biol
Title: CECR2 is involved in spermatogenesis and forms a complex with SNF2H in the testis.
Volume: 415
Issue: 5
Pages: 793-806
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Publication
23139813 | J:195360
First Author: Seibt J
Year: 2012
Journal: PLoS One
Title: Expression at the imprinted dlk1-gtl2 locus is regulated by proneural genes in the developing telencephalon.
Volume: 7
Issue: 11
Pages: e48675
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Publication
18483557 | J:136953
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
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Publication
17116257 | J:119656
 
First Author: Andrieu D
Year: 2006
Journal: BMC Dev Biol
Title: Sensory defects in Necdin deficient mice result from a loss of sensory neurons correlated within an increase of developmental programmed cell death.
Volume: 6
Pages: 56
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Publication
21343540 | J:172308
First Author: Stefan M
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