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Search results 1 to 100 out of 172 for Atrx

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Category: Publication
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Type Details Score
Publication
24651726 | J:209584
First Author: Clynes D
Year: 2014
Journal: PLoS One
Title: ATRX dysfunction induces replication defects in primary mouse cells.
Volume: 9
Issue: 3
Pages: e92915
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Publication
20110566 | J:160497
First Author: Wong LH
Year: 2010
Journal: Genome Res
Title: ATRX interacts with H3.3 in maintaining telomere structural integrity in pluripotent embryonic stem cells.
Volume: 20
Issue: 3
Pages: 351-60
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Publication
20159591 | J:158584
First Author: Kernohan KD
Year: 2010
Journal: Dev Cell
Title: ATRX partners with cohesin and MeCP2 and contributes to developmental silencing of imprinted genes in the brain.
Volume: 18
Issue: 2
Pages: 191-202
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Publication
9545503 | J:47271
First Author: Picketts DJ
Year: 1998
Journal: Mamm Genome
Title: Comparison of the human and murine ATRX gene identifies highly conserved, functionally important domains.
Volume: 9
Issue: 5
Pages: 400-3
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Publication
17296936 | J:125897
First Author: Nan X
Year: 2007
Journal: Proc Natl Acad Sci U S A
Title: Interaction between chromatin proteins MECP2 and ATRX is disrupted by mutations that cause inherited mental retardation.
Volume: 104
Issue: 8
Pages: 2709-14
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Publication
28173139 | J:238641
First Author: Lagali PS
Year: 2016
Journal: Hum Mol Genet
Title: Retinal interneuron survival requires non-cell-autonomous Atrx activity.
Volume: 25
Issue: 21
Pages: 4787-4803
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Publication
24386478 | J:209836
First Author: Solomon LA
Year: 2013
Journal: PLoS One
Title: Loss of ATRX does not confer susceptibility to osteoarthritis.
Volume: 8
Issue: 12
Pages: e85526
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Publication
20211137 | J:167956
First Author: Goldberg AD
Year: 2010
Journal: Cell
Title: Distinct factors control histone variant H3.3 localization at specific genomic regions.
Volume: 140
Issue: 5
Pages: 678-91
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Publication
23114596 | J:193998
First Author: Huh MS
Year: 2012
Journal: J Clin Invest
Title: Compromised genomic integrity impedes muscle growth after Atrx inactivation.
Volume: 122
Issue: 12
Pages: 4412-23
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Publication
11823444 | J:74739
First Author: Bérubé NG
Year: 2002
Journal: Hum Mol Genet
Title: Neurodevelopmental defects resulting from ATRX overexpression in transgenic mice.
Volume: 11
Issue: 3
Pages: 253-61
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Publication
31671722 | J:293193
 
First Author: Marano D
Year: 2019
Journal: Int J Mol Sci
Title: ATRX Contributes to MeCP2-Mediated Pericentric Heterochromatin Organization during Neural Differentiation.
Volume: 20
Issue: 21
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Publication
29883366 | J:270882
First Author: Rowland ME
Year: 2018
Journal: Aging (Albany NY)
Title: Inactivation of hepatic ATRX in Atrx Foxg1cre mice prevents reversal of aging-like phenotypes by thyroxine.
Volume: 10
Issue: 6
Pages: 1223-1238
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Publication
36010860 | J:327867
 
First Author: Gaspar TB
Year: 2022
Journal: Cancers (Basel)
Title: Characterisation of an Atrx Conditional Knockout Mouse Model: Atrx Loss Causes Endocrine Dysfunction Rather Than Pancreatic Neuroendocrine Tumour.
Volume: 14
Issue: 16
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Publication
27171262 | J:316683
 
First Author: Huh MS
Year: 2016
Journal: Cell Death Dis
Title: Stalled replication forks within heterochromatin require ATRX for protection.
Volume: 7
Pages: e2220
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Publication
35976056 | J:330251
 
First Author: Sun C
Year: 2022
Journal: Dis Model Mech
Title: Context matters - Daxx and Atrx are not robust tumor suppressors in the murine endocrine pancreas.
Volume: 15
Issue: 8
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Publication
37296979 | J:336633
 
First Author: Gaspar TB
Year: 2023
Journal: Cancers (Basel)
Title: Generation of an Obese Diabetic Mouse Model upon Conditional Atrx Disruption.
Volume: 15
Issue: 11
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Publication
19774083 | J:153605
First Author: Solomon LA
Year: 2009
Journal: PLoS One
Title: Loss of ATRX in chondrocytes has minimal effects on skeletal development.
Volume: 4
Issue: 9
Pages: e7106
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Publication
27863708 | J:239322
First Author: Sailau ZK
Year: 2017
Journal: Acta Histochem
Title: Nuclear distribution of the chromatin-remodeling protein ATRX in mouse early embryogenesis.
Volume: 119
Issue: 1
Pages: 18-25
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Publication
26936505 | J:247300
First Author: Koschmann C
Year: 2016
Journal: Sci Transl Med
Title: ATRX loss promotes tumor growth and impairs nonhomologous end joining DNA repair in glioma.
Volume: 8
Issue: 328
Pages: 328ra28
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Publication
15668733 | J:95953
First Author: Bérubé NG
Year: 2005
Journal: J Clin Invest
Title: The chromatin-remodeling protein ATRX is critical for neuronal survival during corticogenesis.
Volume: 115
Issue: 2
Pages: 258-67
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Publication
21672208 | J:173600
 
First Author: Huyhn K
Year: 2011
Journal: BMC Dev Biol
Title: ATRX has a critical and conserved role in mammalian sexual differentiation.
Volume: 11
Pages: 39
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Publication
37925436 | J:342393
First Author: Rowland ME
Year: 2023
Journal: Nat Commun
Title: Systemic and intrinsic functions of ATRX in glial cell fate and CNS myelination in male mice.
Volume: 14
Issue: 1
Pages: 7090
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Publication
20865721 | J:168608
First Author: Nogami T
Year: 2011
Journal: Hippocampus
Title: Reduced expression of the ATRX gene, a chromatin-remodeling factor, causes hippocampal dysfunction in mice.
Volume: 21
Issue: 6
Pages: 678-87
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Publication
28093507 | J:238699
First Author: Tamming RJ
Year: 2017
Journal: Dis Model Mech
Title: Mosaic expression of Atrx in the mouse central nervous system causes memory deficits.
Volume: 10
Issue: 2
Pages: 119-126
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Publication
23284920 | J:195618
First Author: Conte D
Year: 2012
Journal: PLoS One
Title: Loss of Atrx sensitizes cells to DNA damaging agents through p53-mediated death pathways.
Volume: 7
Issue: 12
Pages: e52167
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Publication
18842153 | J:264378
 
First Author: Levy MA
Year: 2008
Journal: BMC Genomics
Title: The SWI/SNF protein ATRX co-regulates pseudoautosomal genes that have translocated to autosomes in the mouse genome.
Volume: 9
Pages: 468
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Publication
31895940 | J:283371
First Author: Lovejoy CA
Year: 2020
Journal: PLoS Biol
Title: ATRX affects the repair of telomeric DSBs by promoting cohesion and a DAXX-dependent activity.
Volume: 18
Issue: 1
Pages: e3000594
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Publication
29535300 | J:260738
First Author: Danussi C
Year: 2018
Journal: Nat Commun
Title: Atrx inactivation drives disease-defining phenotypes in glioma cells of origin through global epigenomic remodeling.
Volume: 9
Issue: 1
Pages: 1057
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Publication
36073547 | J:329449
 
First Author: Bartholf DeWitt S
Year: 2022
Journal: JCI Insight
Title: Loss of ATRX promotes aggressive features of osteosarcoma with increased NF-κB signaling and integrin binding.
Volume: 7
Issue: 17
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Publication
23563309 | J:201463
First Author: Watson LA
Year: 2013
Journal: J Clin Invest
Title: Atrx deficiency induces telomere dysfunction, endocrine defects, and reduced life span.
Volume: 123
Issue: 5
Pages: 2049-63
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Publication
32610139 | J:300792
First Author: Tamming RJ
Year: 2020
Journal: Cell Rep
Title: Atrx Deletion in Neurons Leads to Sexually Dimorphic Dysregulation of miR-137 and Spatial Learning and Memory Deficits.
Volume: 31
Issue: 13
Pages: 107838
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Publication
29095838 | J:252760
First Author: Huh MS
Year: 2017
Journal: PLoS One
Title: Recovery from impaired muscle growth arises from prolonged postnatal accretion of myonuclei in Atrx mutant mice.
Volume: 12
Issue: 11
Pages: e0186989
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Publication
25452430 | J:219406
First Author: Levy MA
Year: 2015
Journal: Hum Mol Genet
Title: ATRX promotes gene expression by facilitating transcriptional elongation through guanine-rich coding regions.
Volume: 24
Issue: 7
Pages: 1824-35
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Publication
16628246 | J:115836
First Author: Garrick D
Year: 2006
Journal: PLoS Genet
Title: Loss of Atrx affects trophoblast development and the pattern of X-inactivation in extraembryonic tissues.
Volume: 2
Issue: 4
Pages: e58
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Publication
20885787 | J:165659
First Author: Baumann C
Year: 2010
Journal: PLoS Genet
Title: Loss of maternal ATRX results in centromere instability and aneuploidy in the mammalian oocyte and pre-implantation embryo.
Volume: 6
Issue: 9
Pages: e1001137
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Publication
37200088 | J:337996
 
First Author: Floyd W
Year: 2023
Journal: J Clin Invest
Title: Atrx deletion impairs CGAS/STING signaling and increases sarcoma response to radiation and oncolytic herpesvirus.
Volume: 133
Issue: 13
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Publication
25395668 | J:217395
First Author: Ritchie K
Year: 2014
Journal: Biol Open
Title: ATRX is required for maintenance of the neuroprogenitor cell pool in the embryonic mouse brain.
Volume: 3
Issue: 12
Pages: 1158-63
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Publication
24990380 | J:323661
First Author: Kernohan KD
Year: 2014
Journal: Nucleic Acids Res
Title: Analysis of neonatal brain lacking ATRX or MeCP2 reveals changes in nucleosome density, CTCF binding and chromatin looping.
Volume: 42
Issue: 13
Pages: 8356-68
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19088125 | J:145002
First Author: Medina CF
Year: 2009
Journal: Hum Mol Genet
Title: Altered visual function and interneuron survival in Atrx knockout mice: inference for the human syndrome.
Volume: 18
Issue: 5
Pages: 966-77
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19020049 | J:142359
First Author: Seah C
Year: 2008
Journal: J Neurosci
Title: Neuronal death resulting from targeted disruption of the Snf2 protein ATRX is mediated by p53.
Volume: 28
Issue: 47
Pages: 12570-80
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Publication
30510993 | J:294540
First Author: Young CC
Year: 2019
Journal: Cell Mol Gastroenterol Hepatol
Title: The Loss of ATRX Increases Susceptibility to Pancreatic Injury and Oncogenic KRAS in Female But Not Male Mice.
Volume: 7
Issue: 1
Pages: 93-113
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21209221 | J:167847
First Author: Shioda N
Year: 2011
Journal: J Neurosci
Title: Aberrant calcium/calmodulin-dependent protein kinase II (CaMKII) activity is associated with abnormal dendritic spine morphology in the ATRX mutant mouse brain.
Volume: 31
Issue: 1
Pages: 346-58
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Publication
38609433 | J:347360
First Author: Fuentes ME
Year: 2024
Journal: Sci Rep
Title: Combined deletion of MEN1, ATRX and PTEN triggers development of high-grade pancreatic neuroendocrine tumors in mice.
Volume: 14
Issue: 1
Pages: 8510
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Publication
20651253 | J:209481
First Author: Lewis PW
Year: 2010
Journal: Proc Natl Acad Sci U S A
Title: Daxx is an H3.3-specific histone chaperone and cooperates with ATRX in replication-independent chromatin assembly at telomeres.
Volume: 107
Issue: 32
Pages: 14075-80
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Publication
21666677 | -
First Author: Eustermann S
Year: 2011
Journal: Nat Struct Mol Biol
Title: Combinatorial readout of histone H3 modifications specifies localization of ATRX to heterochromatin.
Volume: 18
Issue: 7
Pages: 777-82
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8978696 | J:37212
First Author: Le Douarin B
Year: 1996
Journal: EMBO J
Title: A possible involvement of TIF1 alpha and TIF1 beta in the epigenetic control of transcription by nuclear receptors.
Volume: 15
Issue: 23
Pages: 6701-15
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Publication
30231518 | J:303450
 
First Author: Yamaguchi K
Year: 2018
Journal: Int J Mol Sci
Title: SA4503, A Potent Sigma-1 Receptor Ligand, Ameliorates Synaptic Abnormalities and Cognitive Dysfunction in a Mouse Model of ATR-X Syndrome.
Volume: 19
Issue: 9
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29785027 | J:271579
First Author: Shioda N
Year: 2018
Journal: Nat Med
Title: Targeting G-quadruplex DNA as cognitive function therapy for ATR-X syndrome.
Volume: 24
Issue: 6
Pages: 802-813
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17503331 | J:128058
First Author: Muers MR
Year: 2007
Journal: Am J Hum Genet
Title: Defining the cause of skewed X-chromosome inactivation in X-linked mental retardation by use of a mouse model.
Volume: 80
Issue: 6
Pages: 1138-49
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28186538 | J:241019
First Author: Kugler J
Year: 2017
Journal: Carcinogenesis
Title: Elevated HMGN4 expression potentiates thyroid tumorigenesis.
Volume: 38
Issue: 4
Pages: 391-401
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33197500 | J:299962
 
First Author: Lagali PS
Year: 2021
Journal: Neuroscience
Title: Sensory Experience Modulates Atrx-mediated Neuronal Integrity in the Mouse Retina.
Volume: 452
Pages: 169-180
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31029404 | J:301026
First Author: Bogolyubova IO
Year: 2019
Journal: Acta Histochem
Title: The dynamics of DAXX protein distribution in the nucleus of mouse early embryos.
Volume: 121
Issue: 4
Pages: 522-529
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38616920 | J:347585
First Author: León NY
Year: 2024
Journal: iScience
Title: Y chromosome damage underlies testicular abnormalities in ATR-X syndrome.
Volume: 27
Issue: 5
Pages: 109629
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15252119 | J:91881
First Author: Ishov AM
Year: 2004
Journal: J Cell Sci
Title: Heterochromatin and ND10 are cell-cycle regulated and phosphorylation-dependent alternate nuclear sites of the transcription repressor Daxx and SWI/SNF protein ATRX.
Volume: 117
Issue: Pt 17
Pages: 3807-20
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Publication
23444137 | J:228107
First Author: Chang FT
Year: 2013
Journal: Nucleic Acids Res
Title: PML bodies provide an important platform for the maintenance of telomeric chromatin integrity in embryonic stem cells.
Volume: 41
Issue: 8
Pages: 4447-58
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Publication
15242786 | J:92329
First Author: De La Fuente R
Year: 2004
Journal: Dev Biol
Title: ATRX, a member of the SNF2 family of helicase/ATPases, is required for chromosome alignment and meiotic spindle organization in metaphase II stage mouse oocytes.
Volume: 272
Issue: 1
Pages: 1-14
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23892236 | J:203136
First Author: Solomon LA
Year: 2013
Journal: Hum Mol Genet
Title: Targeted loss of the ATR-X syndrome protein in the limb mesenchyme of mice causes brachydactyly.
Volume: 22
Issue: 24
Pages: 5015-25
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21427128 | J:171630
First Author: Bagheri-Fam S
Year: 2011
Journal: Hum Mol Genet
Title: Defective survival of proliferating Sertoli cells and androgen receptor function in a mouse model of the ATR-X syndrome.
Volume: 20
Issue: 11
Pages: 2213-24
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26477563 | J:227628
 
First Author: Sarkar MK
Year: 2015
Journal: Nat Commun
Title: An Xist-activating antisense RNA required for X-chromosome inactivation.
Volume: 6
Pages: 8564
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34722536 | J:312431
 
First Author: Matsuura R
Year: 2021
Journal: Front Cell Dev Biol
Title: Ectopic Splicing Disturbs the Function of Xist RNA to Establish the Stable Heterochromatin State.
Volume: 9
Pages: 751154
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8162050 | J:16603
First Author: Gecz J
Year: 1994
Journal: Hum Mol Genet
Title: Cloning and expression of the murine homologue of a putative human X-linked nuclear protein gene closely linked to PGK1 in Xq13.3.
Volume: 3
Issue: 1
Pages: 39-44
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16935872 | J:116972
First Author: Heyer WD
Year: 2006
Journal: Nucleic Acids Res
Title: Rad54: the Swiss Army knife of homologous recombination?
Volume: 34
Issue: 15
Pages: 4115-25
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21317870 | J:170334
First Author: Shibata A
Year: 2011
Journal: EMBO J
Title: Factors determining DNA double-strand break repair pathway choice in G2 phase.
Volume: 30
Issue: 6
Pages: 1079-92
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21357745 | J:170686
First Author: Agarwal S
Year: 2011
Journal: J Cell Biol
Title: ATP-dependent and independent functions of Rad54 in genome maintenance.
Volume: 192
Issue: 5
Pages: 735-50
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37072228 | J:341518
First Author: Guthmann M
Year: 2023
Journal: Genes Dev
Title: A change in biophysical properties accompanies heterochromatin formation in mouse embryos.
Volume: 37
Issue: 7-8
Pages: 336-350
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- | J:160967
     
First Author: Cox BJ
Year: 2010
Journal: MGI Direct Data Submission
Title: Phenotypic annotation of the mouse X chromosome
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20548051 | J:163340
First Author: Cox BJ
Year: 2010
Journal: Genome Res
Title: Phenotypic annotation of the mouse X chromosome.
Volume: 20
Issue: 8
Pages: 1154-64
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10757799 | J:61569
First Author: Dronkert ML
Year: 2000
Journal: Mol Cell Biol
Title: Mouse RAD54 affects DNA double-strand break repair and sister chromatid exchange.
Volume: 20
Issue: 9
Pages: 3147-56
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30126901 | J:266555
 
First Author: Sakakibara Y
Year: 2018
Journal: Development
Title: Role of SmcHD1 in establishment of epigenetic states required for the maintenance of the X-inactivated state in mice.
Volume: 145
Issue: 18
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9736627 | J:50055
First Author: Takata M
Year: 1998
Journal: EMBO J
Title: Homologous recombination and non-homologous end-joining pathways of DNA double-strand break repair have overlapping roles in the maintenance of chromosomal integrity in vertebrate cells.
Volume: 17
Issue: 18
Pages: 5497-508
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30335163 | J:269314
First Author: Park J
Year: 2018
Journal: Nucleic Acids Res
Title: Long non-coding RNA ChRO1 facilitates ATRX/DAXX-dependent H3.3 deposition for transcription-associated heterochromatin reorganization.
Volume: 46
Issue: 22
Pages: 11759-11775
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28684628 | J:243417
First Author: Sakata Y
Year: 2017
Journal: Development
Title: Defects in dosage compensation impact global gene regulation in the mouse trophoblast.
Volume: 144
Issue: 15
Pages: 2784-2797
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30204892 | J:330465
First Author: Russo A
Year: 2018
Journal: Mutagenesis
Title: Rad54/Rad54B deficiency is associated to increased chromosome breakage in mouse spermatocytes.
Volume: 33
Issue: 4
Pages: 323-332
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21057507 | J:166895
First Author: Li S
Year: 2010
Journal: Nat Neurosci
Title: An age-related sprouting transcriptome provides molecular control of axonal sprouting after stroke.
Volume: 13
Issue: 12
Pages: 1496-504
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22500635 | J:188393
First Author: Michod D
Year: 2012
Journal: Neuron
Title: Calcium-dependent dephosphorylation of the histone chaperone DAXX regulates H3.3 loading and transcription upon neuronal activation.
Volume: 74
Issue: 1
Pages: 122-35
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14654002 | J:86824
First Author: Payer B
Year: 2003
Journal: Curr Biol
Title: Stella is a maternal effect gene required for normal early development in mice.
Volume: 13
Issue: 23
Pages: 2110-7
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32821827 | J:312564
First Author: Wasylishen AR
Year: 2020
Journal: Sci Adv
Title: Daxx maintains endogenous retroviral silencing and restricts cellular plasticity in vivo.
Volume: 6
Issue: 32
Pages: eaba8415
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20150414 | J:173439
First Author: Wang H
Year: 2010
Journal: Nucleic Acids Res
Title: Characteristics of DNA-binding proteins determine the biological sensitivity to high-linear energy transfer radiation.
Volume: 38
Issue: 10
Pages: 3245-51
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24270455 | J:304578
First Author: Maxwell SS
Year: 2013
Journal: RNA Biol
Title: Chromatin context and ncRNA highlight targets of MeCP2 in brain.
Volume: 10
Issue: 11
Pages: 1741-57
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8921375 | J:35799
First Author: Cecchi C
Year: 1996
Journal: Genomics
Title: Genomic organization of the mottled gene, the mouse homologue of the human Menkes disease gene.
Volume: 37
Issue: 1
Pages: 96-104
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19615340 | J:152540
First Author: Kondo N
Year: 2009
Journal: Biochem Biophys Res Commun
Title: DNA ligase IV as a new molecular target for temozolomide.
Volume: 387
Issue: 4
Pages: 656-60
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29719265 | J:270804
First Author: Philip B
Year: 2018
Journal: Cell Rep
Title: Mutant IDH1 Promotes Glioma Formation In Vivo.
Volume: 23
Issue: 5
Pages: 1553-1564
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26836306 | J:269736
   
First Author: Ancelin K
Year: 2016
Journal: Elife
Title: Maternal LSD1/KDM1A is an essential regulator of chromatin and transcription landscapes during zygotic genome activation.
Volume: 5
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15522233 | J:93510
First Author: Wang L
Year: 2004
Journal: Biochem Biophys Res Commun
Title: Identification of potential nuclear reprogramming and differentiation factors by a novel selection method for cloning chromatin-binding proteins.
Volume: 325
Issue: 1
Pages: 302-7
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7874112 | J:21528
First Author: Stayton CL
Year: 1994
Journal: Hum Mol Genet
Title: Cloning and characterization of a new human Xq13 gene, encoding a putative helicase.
Volume: 3
Issue: 11
Pages: 1957-64
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23362347 | J:194052
First Author: Corbel C
Year: 2013
Journal: Development
Title: Unusual chromatin status and organization of the inactive X chromosome in murine trophoblast giant cells.
Volume: 140
Issue: 4
Pages: 861-72
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36635505 | J:339367
First Author: Masui O
Year: 2023
Journal: Nat Cell Biol
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MouseMine is a collaboration between MGI at The Jackson Laboratory and the InterMine project at the Cambridge Systems Biology Centre. MouseMine is funded through a grant from the NIH/NHGRI.The Jackson Laboratory makes no representation about the suitability or accuracy of this software or data for any purpose, and makes no warranties, either express or implied, including merchantability and fitness for a particular purpose or that the use of this software or data will not infringe any third party patents, copyrights, trademarks, or other rights. the software and data are provided "as is". This software and data are provided to enhance knowledge and encourage progress in the scientific community and are to be used only for research and educational purposes. Any reproduction or use for commercial purpose is prohibited without the prior express written permission of the Jackson Laboratory.

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