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Search results 1 to 100 out of 111 for Asxl1

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Category: Publication
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Type Details Score
Publication
19880879 | J:183214
First Author: Lee SW
Year: 2010
Journal: J Biol Chem
Title: ASXL1 represses retinoic acid receptor-mediated transcription through associating with HP1 and LSD1.
Volume: 285
Issue: 1
Pages: 18-29
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Publication
35133065 | J:323194
First Author: Liu X
Year: 2022
Journal: Cancer Sci
Title: CHIP-associated mutant ASXL1 in blood cells promotes solid tumor progression.
Volume: 113
Issue: 4
Pages: 1182-1194
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Publication
29113963 | J:257690
First Author: Yang H
Year: 2018
Journal: Blood
Title: Gain of function of ASXL1 truncating protein in the pathogenesis of myeloid malignancies.
Volume: 131
Issue: 3
Pages: 328-341
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Publication
33758188 | J:303833
First Author: Fujino T
Year: 2021
Journal: Nat Commun
Title: Mutant ASXL1 induces age-related expansion of phenotypic hematopoietic stem cells through activation of Akt/mTOR pathway.
Volume: 12
Issue: 1
Pages: 1826
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Publication
21047783 | J:183204
First Author: Park UH
Year: 2011
Journal: J Biol Chem
Title: Additional sex comb-like (ASXL) proteins 1 and 2 play opposite roles in adipogenesis via reciprocal regulation of peroxisome proliferator-activated receptor {gamma}.
Volume: 286
Issue: 2
Pages: 1354-63
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Publication
29643185 | J:265682
First Author: Nagase R
Year: 2018
Journal: J Exp Med
Title: Expression of mutant Asxl1 perturbs hematopoiesis and promotes susceptibility to leukemic transformation.
Volume: 215
Issue: 6
Pages: 1729-1747
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Publication
24255920 | J:208085
First Author: Wang J
Year: 2014
Journal: Blood
Title: Loss of Asxl1 leads to myelodysplastic syndrome-like disease in mice.
Volume: 123
Issue: 4
Pages: 541-53
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Publication
30266822 | J:267079
First Author: Rohatgi N
Year: 2018
Journal: Blood Adv
Title: ASXL1 impairs osteoclast formation by epigenetic regulation of NFATc1.
Volume: 2
Issue: 19
Pages: 2467-2477
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Publication
24216483 | J:204177
First Author: Inoue D
Year: 2013
Journal: J Clin Invest
Title: Myelodysplastic syndromes are induced by histone methylation–altering ASXL1 mutations.
Volume: 123
Issue: 11
Pages: 4627-40
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Publication
30651633 | J:274256
First Author: Guo Y
Year: 2019
Journal: Leukemia
Title: ASXL1 alteration cooperates with JAK2V617F to accelerate myelofibrosis.
Volume: 33
Issue: 5
Pages: 1287-1291
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Publication
36526735 | J:344600
First Author: Braun TP
Year: 2023
Journal: Leukemia
Title: Asxl1 deletion disrupts MYC and RNA polymerase II function in granulocyte progenitors.
Volume: 37
Issue: 2
Pages: 478-487
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Publication
26095772 | J:223021
 
First Author: Balasubramani A
Year: 2015
Journal: Nat Commun
Title: Cancer-associated ASXL1 mutations may act as gain-of-function mutations of the ASXL1-BAP1 complex.
Volume: 6
Pages: 7307
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Publication
12657473 | -
 
First Author: Fisher CL
Year: 2003
Journal: Gene
Title: A human homolog of Additional sex combs, ADDITIONAL SEX COMBS-LIKE 1, maps to chromosome 20q11.
Volume: 306
Pages: 115-26
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Publication
29743720 | J:273079
First Author: Guo Y
Year: 2018
Journal: Leukemia
Title: Reduced BAP1 activity prevents ASXL1 truncation-driven myeloid malignancy in vivo.
Volume: 32
Issue: 8
Pages: 1834-1837
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Publication
28116354 | J:258185
First Author: Li Z
Year: 2017
Journal: Sci Adv
Title: ASXL1 interacts with the cohesin complex to maintain chromatid separation and gene expression for normal hematopoiesis.
Volume: 3
Issue: 1
Pages: e1601602
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Publication
29967380 | J:270023
First Author: Uni M
Year: 2019
Journal: Leukemia
Title: Modeling ASXL1 mutation revealed impaired hematopoiesis caused by derepression of p16Ink4a through aberrant PRC1-mediated histone modification.
Volume: 33
Issue: 1
Pages: 191-204
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Publication
30545639 | J:290952
First Author: An S
Year: 2019
Journal: Biochem Biophys Res Commun
Title: Asxl1 ablation in mouse embryonic stem cells impairs neural differentiation without affecting self-renewal.
Volume: 508
Issue: 3
Pages: 907-913
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Publication
27237378 | J:309947
First Author: Zhang P
Year: 2016
Journal: Stem Cell Reports
Title: Loss of Asxl1 Alters Self-Renewal and Cell Fate of Bone Marrow Stromal Cell, Leading to Bohring-Opitz-like Syndrome in Mice.
Volume: 6
Issue: 6
Pages: 914-925
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Publication
30226831 | J:270524
First Author: Zhang P
Year: 2018
Journal: J Clin Invest
Title: Chromatin regulator Asxl1 loss and Nf1 haploinsufficiency cooperate to accelerate myeloid malignancy.
Volume: 128
Issue: 12
Pages: 5383-5398
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Publication
24218140 | J:208092
First Author: Abdel-Wahab O
Year: 2013
Journal: J Exp Med
Title: Deletion of Asxl1 results in myelodysplasia and severe developmental defects in vivo.
Volume: 210
Issue: 12
Pages: 2641-59
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Publication
36005555 | J:337769
First Author: Shi Z
Year: 2023
Journal: Haematologica
Title: ASXL1 mutations accelerate bone marrow fibrosis via EGR1-TNFA axis-mediated neoplastic fibrocyte generation in myeloproliferative neoplasms.
Volume: 108
Issue: 5
Pages: 1359-1373
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Publication
26385183 | J:229413
First Author: Moon S
Year: 2015
Journal: Biochem Biophys Res Commun
Title: Role of Asxl1 in kidney podocyte development via its interaction with Wtip.
Volume: 466
Issue: 3
Pages: 560-6
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Publication
20436459 | -
First Author: Scheuermann JC
Year: 2010
Journal: Nature
Title: Histone H2A deubiquitinase activity of the Polycomb repressive complex PR-DUB.
Volume: 465
Issue: 7295
Pages: 243-7
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Publication
28697759 | J:274527
First Author: Hsu YC
Year: 2017
Journal: J Hematol Oncol
Title: The distinct biological implications of Asxl1 mutation and its roles in leukemogenesis revealed by a knock-in mouse model.
Volume: 10
Issue: 1
Pages: 139
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Publication
30389914 | J:267889
First Author: Moon S
Year: 2018
Journal: Cell Death Dis
Title: Asxl1 exerts an antiproliferative effect on mouse lung maturation via epigenetic repression of the E2f1-Nmyc axis.
Volume: 9
Issue: 11
Pages: 1118
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34699595 | J:322740
First Author: You X
Year: 2022
Journal: Blood
Title: Asxl1 loss cooperates with oncogenic Nras in mice to reprogram the immune microenvironment and drive leukemic transformation.
Volume: 139
Issue: 7
Pages: 1066-1079
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Publication
16606617 | J:114350
First Author: Cho YS
Year: 2006
Journal: J Biol Chem
Title: Additional sex comb-like 1 (ASXL1), in cooperation with SRC-1, acts as a ligand-dependent coactivator for retinoic acid receptor.
Volume: 281
Issue: 26
Pages: 17588-98
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Publication
28701722 | J:253719
First Author: Youn HS
Year: 2017
Journal: Sci Rep
Title: Asxl1 deficiency in embryonic fibroblasts leads to cellular senescence via impairment of the AKT-E2F pathway and Ezh2 inactivation.
Volume: 7
Issue: 1
Pages: 5198
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Publication
34433054 | J:316924
First Author: Yamamoto K
Year: 2021
Journal: Cell Rep
Title: A histone modifier, ASXL1, interacts with NONO and is involved in paraspeckle formation in hematopoietic cells.
Volume: 36
Issue: 8
Pages: 109576
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Publication
32381577 | J:324868
First Author: D'Altri T
Year: 2021
Journal: Haematologica
Title: The ASXL1-G643W variant accelerates the development of CEBPA mutant acute myeloid leukemia.
Volume: 106
Issue: 4
Pages: 1000-1007
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Publication
28516957 | J:249948
 
First Author: Micol JB
Year: 2017
Journal: Nat Commun
Title: ASXL2 is essential for haematopoiesis and acts as a haploinsufficient tumour suppressor in leukemia.
Volume: 8
Pages: 15429
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Publication
25750265 | -
 
Year: 2015
Journal: J Biol Chem
Title: ASXL1 represses retinoic acid receptor-mediated transcription through associating with HP1 and LSD1.
Volume: 290
Issue: 10
Pages: 6008
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Publication
19861679 | J:155898
First Author: Fisher CL
Year: 2010
Journal: Blood
Title: Loss-of-function Additional sex combs like 1 mutations disrupt hematopoiesis but do not cause severe myelodysplasia or leukemia.
Volume: 115
Issue: 1
Pages: 38-46
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Publication
22542624 | J:183983
First Author: Kang M
Year: 2012
Journal: Biochem Biophys Res Commun
Title: Positive regulation of additional sex comb-like 1 gene expression by the pluripotency factor SOX2.
Volume: 421
Issue: 3
Pages: 621-6
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Publication
16412590 | J:106457
 
First Author: Fisher CL
Year: 2006
Journal: Gene
Title: Characterization of Asxl1, a murine homolog of Additional sex combs, and analysis of the Asx-like gene family.
Volume: 369
Pages: 109-18
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Publication
22878500 | J:187380
First Author: Dey A
Year: 2012
Journal: Science
Title: Loss of the tumor suppressor BAP1 causes myeloid transformation.
Volume: 337
Issue: 6101
Pages: 1541-6
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Publication
19833123 | J:157035
First Author: Fisher CL
Year: 2010
Journal: Dev Biol
Title: Additional sex combs-like 1 belongs to the enhancer of trithorax and polycomb group and genetically interacts with Cbx2 in mice.
Volume: 337
Issue: 1
Pages: 9-15
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34170818 | J:307674
   
First Author: Perez-Garcia V
Year: 2021
Journal: Elife
Title: BAP1/ASXL complex modulation regulates epithelial-mesenchymal transition during trophoblast differentiation and invasion.
Volume: 10
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Publication
34103328 | J:314445
First Author: Tirado-Gonzalez I
Year: 2021
Journal: Cancer Discov
Title: AXL Inhibition in Macrophages Stimulates Host-versus-Leukemia Immunity and Eradicates Naïve and Treatment-Resistant Leukemia.
Volume: 11
Issue: 11
Pages: 2924-2943
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12693553 | J:83413
First Author: Okazaki N
Year: 2003
Journal: DNA Res
Title: Prediction of the coding sequences of mouse homologues of KIAA gene: II. The complete nucleotide sequences of 400 mouse KIAA-homologous cDNAs identified by screening of terminal sequences of cDNA clones randomly sampled from size-fractionated libraries.
Volume: 10
Issue: 1
Pages: 35-48
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Publication
22876197 | J:188142
First Author: Bassett JH
Year: 2012
Journal: PLoS Genet
Title: Rapid-throughput skeletal phenotyping of 100 knockout mice identifies 9 new genes that determine bone strength.
Volume: 8
Issue: 8
Pages: e1002858
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24860998 | J:213577
First Author: McGinley AL
Year: 2014
Journal: Genesis
Title: Additional sex combs-like family genes are required for normal cardiovascular development.
Volume: 52
Issue: 7
Pages: 671-86
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Publication
23870131 | J:200082
First Author: White JK
Year: 2013
Journal: Cell
Title: Genome-wide generation and systematic phenotyping of knockout mice reveals new roles for many genes.
Volume: 154
Issue: 2
Pages: 452-64
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16869965 | J:119680
 
First Author: Millien G
Year: 2006
Journal: BMC Dev Biol
Title: Alterations in gene expression in T1 alpha null lung: a model of deficient alveolar sac development.
Volume: 6
Pages: 35
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25859222 | J:237754
 
First Author: Maga AM
Year: 2015
Journal: Front Physiol
Title: Quantitative trait loci affecting the 3D skull shape and size in mouse and prioritization of candidate genes in-silico.
Volume: 6
Pages: 92
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26398943 | J:225710
First Author: Tuck E
Year: 2015
Journal: Dis Model Mech
Title: A gene expression resource generated by genome-wide lacZ profiling in the mouse.
Volume: 8
Issue: 11
Pages: 1467-78
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15033168 | J:107647
First Author: Thuret S
Year: 2004
Journal: Mol Cell Neurosci
Title: Identification and developmental analysis of genes expressed by dopaminergic neurons of the substantia nigra pars compacta.
Volume: 25
Issue: 3
Pages: 394-405
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27480124 | J:237787
First Author: Liu X
Year: 2016
Journal: BMC Immunol
Title: Decreased expression levels of Ifi genes is associated to the increased resistance to spontaneous arthritis disease in mice deficiency of IL-1RA.
Volume: 17
Issue: 1
Pages: 25
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Publication
- | J:165965
     
First Author: Mouse Genome Informatics and the Europhenome Mouse Phenotyping Resource
Year: 2010
Journal: Database Release
Title: Obtaining and Loading Phenotype Annotations from Europhenome
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Publication
- | J:175295
     
First Author: Mouse Genome Informatics and the Wellcome Trust Sanger Institute Mouse Genetics Project (MGP)
Year: 2011
Journal: Database Release
Title: Obtaining and Loading Phenotype Annotations from the Wellcome Trust Sanger Institute (WTSI) Mouse Resources Portal
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Publication
- | J:342607
       
First Author: Birgit Meldal and Sandra Orchard (1). (1) European Bioinformatics Institute (EBI), Hinxton, Cambridgeshire, United Kingdom
Year: 2023
Title: Manual transfer of experimentally-verified manual GO annotation data to homologous complexes by curator judgment of sequence, composition and function similarity
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Publication
30973865 | J:274872
First Author: Ingham NJ
Year: 2019
Journal: PLoS Biol
Title: Mouse screen reveals multiple new genes underlying mouse and human hearing loss.
Volume: 17
Issue: 4
Pages: e3000194
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17967808 | J:152068
First Author: Friedel RH
Year: 2007
Journal: Brief Funct Genomic Proteomic
Title: EUCOMM--the European conditional mouse mutagenesis program.
Volume: 6
Issue: 3
Pages: 180-5
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14681479 | J:122989
First Author: Visel A
Year: 2004
Journal: Nucleic Acids Res
Title: GenePaint.org: an atlas of gene expression patterns in the mouse embryo.
Volume: 32
Issue: Database issue
Pages: D552-6
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12520002 | J:91812
First Author: Stryke D
Year: 2003
Journal: Nucleic Acids Res
Title: BayGenomics: a resource of insertional mutations in mouse embryonic stem cells.
Volume: 31
Issue: 1
Pages: 278-81
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34321999 | J:313619
 
First Author: Bedogni F
Year: 2021
Journal: Front Mol Neurosci
Title: Cell-Type-Specific Gene Expression in Developing Mouse Neocortex: Intermediate Progenitors Implicated in Axon Development.
Volume: 14
Pages: 686034
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Publication
- | J:57656
     
First Author: Lennon G
Year: 1999
Journal: Database Download
Title: WashU-HHMI Mouse EST Project
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Publication
- | J:136110
     
First Author: Velocigene
Year: 2008
Journal: MGI Direct Data Submission
Title: Alleles produced for the KOMP project by Velocigene (Regeneron Pharmaceuticals)
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- | J:155845
     
First Author: Wellcome Trust Sanger Institute
Year: 2010
Journal: MGI Direct Data Submission
Title: Alleles produced for the EUCOMM and EUCOMMTools projects by the Wellcome Trust Sanger Institute
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Publication
- | J:72247
       
First Author: DDB, FB, MGI, GOA, ZFIN curators
Year: 2001
Title: Gene Ontology annotation through association of InterPro records with GO terms
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Publication
- | J:157065
     
First Author: Helmholtz Zentrum Muenchen GmbH
Year: 2010
Journal: MGI Direct Data Submission
Title: Alleles produced for the EUCOMM and EUCOMMTools projects by the Helmholtz Zentrum Muenchen GmbH (Hmgu)
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18799693 | J:142754
First Author: Hansen GM
Year: 2008
Journal: Genome Res
Title: Large-scale gene trapping in C57BL/6N mouse embryonic stem cells.
Volume: 18
Issue: 10
Pages: 1670-9
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Publication
- | J:155856
       
First Author: The Gene Ontology Consortium
Year: 2014
Title: Automated transfer of experimentally-verified manual GO annotation data to mouse-rat orthologs
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Publication
- | J:85000
       
First Author: Mouse Genome Informatics Scientific Curators
Year: 2003
Title: MGI Sequence Curation Reference
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Publication
- | J:78475
       
First Author: Mouse Genome Informatics Scientific Curators
Year: 2002
Title: Chromosome assignment of mouse genes using the Mouse Genome Sequencing Consortium (MGSC) assembly and the ENSEMBL Database
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16141072 | J:99680
First Author: Carninci P
Year: 2005
Journal: Science
Title: The transcriptional landscape of the mammalian genome.
Volume: 309
Issue: 5740
Pages: 1559-63
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Publication
- | J:141210
     
First Author: Mouse Genome Informatics (MGI) and National Center for Biotechnology Information (NCBI)
Year: 2008
Journal: Database Download
Title: Mouse Gene Trap Data Load from dbGSS
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14610273 | J:86696
First Author: Zambrowicz BP
Year: 2003
Journal: Proc Natl Acad Sci U S A
Title: Wnk1 kinase deficiency lowers blood pressure in mice: a gene-trap screen to identify potential targets for therapeutic intervention.
Volume: 100
Issue: 24
Pages: 14109-14
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21677750 | J:173534
First Author: Skarnes WC
Year: 2011
Journal: Nature
Title: A conditional knockout resource for the genome-wide study of mouse gene function.
Volume: 474
Issue: 7351
Pages: 337-42
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38355793 | J:345621
First Author: Adams DJ
Year: 2024
Journal: Nature
Title: Genetic determinants of micronucleus formation in vivo.
Volume: 627
Issue: 8002
Pages: 130-136
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Publication
- | J:23000
       
First Author: MGD Nomenclature Committee
Year: 1995
Title: Nomenclature Committee Use
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Publication
- | J:293217
       
First Author: GemPharmatech
Year: 2020
Title: GemPharmatech Website.
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Publication
- | J:60000
       
First Author: UniProt-GOA
Year: 2012
Title: Gene Ontology annotation based on UniProtKB/Swiss-Prot keyword mapping
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Publication
- | J:342587
       
First Author: AgBase, BHF-UCL, Parkinson's UK-UCL, dictyBase, HGNC, Roslin Institute, FlyBase and UniProtKB curators
Year: 2011
Title: Manual transfer of experimentally-verified manual GO annotation data to orthologs by curator judgment of sequence similarity
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Publication
- | J:68900
     
First Author: The Jackson Laboratory Mouse Radiation Hybrid Database
Year: 2004
Journal: Database Release
Title: Mouse T31 Radiation Hybrid Data Load
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Publication
- | J:164563
       
First Author: The Gene Ontology Consortium
Year: 2010
Title: Automated transfer of experimentally-verified manual GO annotation data to mouse-human orthologs
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21267068 | J:153498
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
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Publication
- | J:157972
     
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).
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Publication
- | J:75000
       
First Author: Mouse Genome Informatics Scientific Curators
Year: 2002
Title: Mouse Genome Informatics Computational Sequence to Gene Associations
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Publication
- | J:161428
       
First Author: Marc Feuermann, Huaiyu Mi, Pascale Gaudet, Dustin Ebert, Anushya Muruganujan, Paul Thomas
Year: 2010
Title: Annotation inferences using phylogenetic trees
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Publication
- | J:85324
     
First Author: Mouse Genome Informatics Group
Year: 2003
Journal: Database Procedure
Title: Automatic Encodes (AutoE) Reference
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Publication
- | J:144086
     
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
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Publication
- | J:144087
     
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
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Publication
- | J:53168
     
First Author: Bairoch A
Year: 1999
Journal: Database Release
Title: SWISS-PROT Annotated protein sequence database
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- | J:90438
       
First Author: Mouse Genome Informatics Scientific Curators
Year: 2005
Title: Obtaining and loading genome assembly coordinates from NCBI annotations
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Publication
- | J:63103
     
First Author: Mouse Genome Database and National Center for Biotechnology Information
Year: 2000
Journal: Database Release
Title: Entrez Gene Load
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Publication
- | J:155721
     
First Author: Mouse Genome Informatics (MGI) and The National Center for Biotechnology Information (NCBI)
Year: 2010
Journal: Database Download
Title: Consensus CDS project
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Publication
- | J:155221
     
First Author: Mouse Genome Informatics
Year: 2010
Journal: Database Release
Title: Protein Ontology Association Load.
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Publication
- | J:262123
     
First Author: Allen Institute for Brain Science
Year: 2004
Journal: Allen Institute
Title: Allen Brain Atlas: mouse riboprobes
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Publication
- | J:91388
       
First Author: Mouse Genome Informatics Scientific Curators
Year: 2005
Title: Obtaining and Loading Genome Assembly Coordinates from Ensembl Annotations
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Publication
38017104 | J:344860
First Author: Sui P
Year: 2024
Journal: Leukemia
Title: SRSF2 mutation cooperates with ASXL1 truncated alteration to accelerate leukemogenesis.
Volume: 38
Issue: 2
Pages: 408-411
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Publication
37917239 | J:344091
 
First Author: Ge G
Year: 2024
Journal: J Clin Invest
Title: Targeting lysine demethylase 6B ameliorates ASXL1 truncation-mediated myeloid malignancies in preclinical models.
Volume: 134
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