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Search results 1 to 100 out of 150 for Hira

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Category: Publication
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Type Details Score
Publication
11408777 | J:71757
 
First Author: Hira K
Year: 2001
Journal: Int Arch Allergy Immunol
Title: Establishment and characterization of a murine mast cell line derived from NC/Nga mice.
Volume: 125 Suppl 1
Pages: 67-70
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Publication
35112132 | J:330257
 
First Author: Smith R
Year: 2022
Journal: Development
Title: The H3.3 chaperone Hira complex orchestrates oocyte developmental competence.
Volume: 149
Issue: 5
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Publication
9731536 | J:289456
First Author: Magnaghi P
Year: 1998
Journal: Nat Genet
Title: HIRA, a mammalian homologue of Saccharomyces cerevisiae transcriptional co-repressors, interacts with Pax3.
Volume: 20
Issue: 1
Pages: 74-7
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Publication
34242617 | J:310096
First Author: Murdaugh RL
Year: 2021
Journal: Stem Cell Reports
Title: The histone H3.3 chaperone HIRA restrains erythroid-biased differentiation of adult hematopoietic stem cells.
Volume: 16
Issue: 8
Pages: 2014-2028
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Publication
26549683 | J:309966
First Author: Nashun B
Year: 2015
Journal: Mol Cell
Title: Continuous Histone Replacement by Hira Is Essential for Normal Transcriptional Regulation and De Novo DNA Methylation during Mouse Oogenesis.
Volume: 60
Issue: 4
Pages: 611-25
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Publication
27518902 | J:236915
First Author: Dilg D
Year: 2016
Journal: PLoS One
Title: HIRA Is Required for Heart Development and Directly Regulates Tnni2 and Tnnt3.
Volume: 11
Issue: 8
Pages: e0161096
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Publication
33835048 | J:307815
First Author: Smith R
Year: 2021
Journal: Reproduction
Title: HIRA contributes to zygote formation in mice and is implicated in human 1PN zygote phenotype.
Volume: 161
Issue: 6
Pages: 697-707
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Publication
28600325 | J:249763
First Author: Valenzuela N
Year: 2017
Journal: J Cell Sci
Title: HIRA deficiency in muscle fibers causes hypertrophy and susceptibility to oxidative stress.
Volume: 130
Issue: 15
Pages: 2551-2563
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Publication
25512559 | J:217374
First Author: Rai TS
Year: 2014
Journal: Genes Dev
Title: HIRA orchestrates a dynamic chromatin landscape in senescence and is required for suppression of neoplasia.
Volume: 28
Issue: 24
Pages: 2712-25
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Publication
28515277 | J:246099
First Author: Li Y
Year: 2017
Journal: J Cell Biol
Title: Histone chaperone HIRA regulates neural progenitor cell proliferation and neurogenesis via β-catenin.
Volume: 216
Issue: 7
Pages: 1975-1992
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Publication
34140513 | J:307956
First Author: Blake GET
Year: 2021
Journal: Nat Commun
Title: Defective folate metabolism causes germline epigenetic instability and distinguishes Hira as a phenotype inheritance biomarker.
Volume: 12
Issue: 1
Pages: 3714
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Publication
26935106 | J:231593
First Author: Valenzuela N
Year: 2016
Journal: Dis Model Mech
Title: Cardiomyocyte-specific conditional knockout of the histone chaperone HIRA in mice results in hypertrophy, sarcolemmal damage and focal replacement fibrosis.
Volume: 9
Issue: 3
Pages: 335-45
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Publication
25197097 | J:216491
First Author: Soni S
Year: 2014
Journal: Proc Natl Acad Sci U S A
Title: Transcription factor EKLF (KLF1) recruitment of the histone chaperone HIRA is essential for β-globin gene expression.
Volume: 111
Issue: 37
Pages: 13337-42
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Publication
33417013 | J:316220
First Author: Jeanne M
Year: 2021
Journal: Hum Genet
Title: Haploinsufficiency of the HIRA gene located in the 22q11 deletion syndrome region is associated with abnormal neurodevelopment and impaired dendritic outgrowth.
Volume: 140
Issue: 6
Pages: 885-896
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Publication
8611624 | J:32513
First Author: Scamps C
Year: 1996
Journal: Biochim Biophys Acta
Title: The HIR protein family: isolation and characterization of a complete murine cDNA.
Volume: 1306
Issue: 1
Pages: 5-8
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Publication
11884616 | J:75491
First Author: Roberts C
Year: 2002
Journal: Mol Cell Biol
Title: Targeted mutagenesis of the Hira gene results in gastrulation defects and patterning abnormalities of mesoendodermal derivatives prior to early embryonic lethality.
Volume: 22
Issue: 7
Pages: 2318-28
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Publication
9063745 | J:38619
First Author: Wilming LG
Year: 1997
Journal: Hum Mol Genet
Title: The murine homologue of HIRA, a DiGeorge syndrome candidate gene, is expressed in embryonic structures affected in human CATCH22 patients.
Volume: 6
Issue: 2
Pages: 247-58
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Publication
15922569 | J:100803
First Author: van der Heijden GW
Year: 2005
Journal: Mech Dev
Title: Asymmetry in histone H3 variants and lysine methylation between paternal and maternal chromatin of the early mouse zygote.
Volume: 122
Issue: 9
Pages: 1008-22
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Publication
8111380 | J:32846
First Author: Halford S
Year: 1993
Journal: Hum Mol Genet
Title: Isolation of a putative transcriptional regulator from the region of 22q11 deleted in DiGeorge syndrome, Shprintzen syndrome and familial congenital heart disease.
Volume: 2
Issue: 12
Pages: 2099-107
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Publication
11342215 | J:67540
First Author: Lorain S
Year: 2001
Journal: Biochim Biophys Acta
Title: Identification of human and mouse HIRA-interacting protein-5 (HIRIP5), two mammalian representatives in a family of phylogenetically conserved proteins with a role in the biogenesis of Fe/S proteins.
Volume: 1517
Issue: 3
Pages: 376-83
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Publication
25087892 | J:212533
First Author: Lin CJ
Year: 2014
Journal: Dev Cell
Title: Hira-mediated H3.3 incorporation is required for DNA replication and ribosomal RNA transcription in the mouse zygote.
Volume: 30
Issue: 3
Pages: 268-79
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Publication
32075733 | J:286991
First Author: Chen C
Year: 2020
Journal: Cell Rep
Title: HIRA, a DiGeorge Syndrome Candidate Gene, Confers Proper Chromatin Accessibility on HSCs and Supports All Stages of Hematopoiesis.
Volume: 30
Issue: 7
Pages: 2136-2149.e4
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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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23921552 | J:200067
First Author: Sarai N
Year: 2013
Journal: EMBO J
Title: WHSC1 links transcription elongation to HIRA-mediated histone H3.3 deposition.
Volume: 32
Issue: 17
Pages: 2392-406
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Publication
21414300 | J:171931
First Author: Yang JH
Year: 2011
Journal: Biochem Biophys Res Commun
Title: Histone chaperones cooperate to mediate Mef2-targeted transcriptional regulation during skeletal myogenesis.
Volume: 407
Issue: 3
Pages: 541-7
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Publication
22705305 | J:185969
First Author: Song TY
Year: 2012
Journal: Biochem Biophys Res Commun
Title: The role of histone chaperones in osteoblastic differentiation of C2C12 myoblasts.
Volume: 423
Issue: 4
Pages: 726-32
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Publication
27184122 | J:240212
First Author: Devaraju P
Year: 2017
Journal: Mol Psychiatry
Title: Haploinsufficiency of the 22q11.2 microdeletion gene Mrpl40 disrupts short-term synaptic plasticity and working memory through dysregulation of mitochondrial calcium.
Volume: 22
Issue: 9
Pages: 1313-1326
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Publication
18469815 | J:136969
First Author: Stark KL
Year: 2008
Journal: Nat Genet
Title: Altered brain microRNA biogenesis contributes to phenotypic deficits in a 22q11-deletion mouse model.
Volume: 40
Issue: 6
Pages: 751-60
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Publication
7851908 | J:21108
First Author: Mattei MG
Year: 1994
Journal: Genomics
Title: Mapping of the Tuple1 gene to mouse chromosome 16A-B1.
Volume: 23
Issue: 3
Pages: 717-8
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Publication
16684884 | J:110101
First Author: Paylor R
Year: 2006
Journal: Proc Natl Acad Sci U S A
Title: Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: implications for 22q11 deletion syndrome.
Volume: 103
Issue: 20
Pages: 7729-34
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Publication
9107688 | J:39611
First Author: Taylor C
Year: 1997
Journal: Mamm Genome
Title: Cloning and mapping of murine Dgcr2 and its homology to the Sez-12 seizure-related protein.
Volume: 8
Issue: 5
Pages: 371-5
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Publication
19884347 | J:156413
First Author: de Wit T
Year: 2010
Journal: Mol Cell Biol
Title: Tagged mutagenesis by efficient Minos-based germ line transposition.
Volume: 30
Issue: 1
Pages: 68-77
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Publication
25909911 | J:233815
First Author: Lai KM
Year: 2015
Journal: PLoS One
Title: Diverse Phenotypes and Specific Transcription Patterns in Twenty Mouse Lines with Ablated LincRNAs.
Volume: 10
Issue: 4
Pages: e0125522
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9284932 | J:42506
First Author: Botta A
Year: 1997
Journal: Cytogenet Cell Genet
Title: Assignment of the gene for a ubiquitin fusion degradation protein (Ufd1l) to mouse chromosome 16B1-B4, syntenic with the Tuple1 gene.
Volume: 77
Issue: 3-4
Pages: 264-5
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Publication
9192844 | J:41222
First Author: Sirotkin H
Year: 1997
Journal: Genomics
Title: Identification, characterization, and precise mapping of a human gene encoding a novel membrane-spanning protein from the 22q11 region deleted in velo-cardio-facial syndrome.
Volume: 42
Issue: 2
Pages: 245-51
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Publication
11239417 | J:67796
First Author: Merscher S
Year: 2001
Journal: Cell
Title: TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge syndrome.
Volume: 104
Issue: 4
Pages: 619-29
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11804793 | J:74505
First Author: Maynard TM
Year: 2002
Journal: Mech Dev
Title: RanBP1, a velocardiofacial/DiGeorge syndrome candidate gene, is expressed at sites of mesenchymal/epithelial induction.
Volume: 111
Issue: 1-2
Pages: 177-80
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Publication
9037598 | J:38193
First Author: Galili N
Year: 1997
Journal: Genome Res
Title: A region of mouse chromosome 16 is syntenic to the DiGeorge, velocardiofacial syndrome minimal critical region.
Volume: 7
Issue: 1
Pages: 17-26
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Publication
11242111 | J:67826
First Author: Guris DL
Year: 2001
Journal: Nat Genet
Title: Mice lacking the homologue of the human 22q11.2 gene CRKL phenocopy neurocristopathies of DiGeorge syndrome.
Volume: 27
Issue: 3
Pages: 293-8
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9383280 | J:44451
First Author: Botta A
Year: 1997
Journal: Mamm Genome
Title: Comparative mapping of the DiGeorge syndrome region in mouse shows inconsistent gene order and differential degree of gene conservation.
Volume: 8
Issue: 12
Pages: 890-5
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Publication
16595651 | J:113459
First Author: Nagamori I
Year: 2006
Journal: J Biol Chem
Title: Transcription factors, cAMP-responsive element modulator (CREM) and Tisp40, act in concert in postmeiotic transcriptional regulation.
Volume: 281
Issue: 22
Pages: 15073-81
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17097888 | J:116629
First Author: Meechan DW
Year: 2006
Journal: Mol Cell Neurosci
Title: Gene dosage in the developing and adult brain in a mouse model of 22q11 deletion syndrome.
Volume: 33
Issue: 4
Pages: 412-28
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9740669 | J:49844
First Author: Sutherland HF
Year: 1998
Journal: Genomics
Title: Cloning and comparative mapping of the DiGeorge syndrome critical region in the mouse.
Volume: 52
Issue: 1
Pages: 37-43
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12413905 | J:79898
First Author: Kochilas L
Year: 2002
Journal: Dev Biol
Title: The role of neural crest during cardiac development in a mouse model of DiGeorge syndrome.
Volume: 251
Issue: 1
Pages: 157-66
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19805316 | J:153232
First Author: Meechan DW
Year: 2009
Journal: Proc Natl Acad Sci U S A
Title: Diminished dosage of 22q11 genes disrupts neurogenesis and cortical development in a mouse model of 22q11 deletion/DiGeorge syndrome.
Volume: 106
Issue: 38
Pages: 16434-45
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Publication
- | J:238766
     
First Author: Shanghai Model Organisms Center
Year: 2017
Journal: MGI Direct Data Submission
Title: Information obtained from the Shanghai Model Organisms Center (SMOC), Shanghai, China
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Publication
23077214 | J:191130
First Author: Maynard TM
Year: 2013
Journal: Hum Mol Genet
Title: 22q11 Gene dosage establishes an adaptive range for sonic hedgehog and retinoic acid signaling during early development.
Volume: 22
Issue: 2
Pages: 300-12
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10963672 | J:64380
First Author: Puech A
Year: 2000
Journal: Proc Natl Acad Sci U S A
Title: Normal cardiovascular development in mice deficient for 16 genes in 550 kb of the velocardiofacial/DiGeorge syndrome region.
Volume: 97
Issue: 18
Pages: 10090-5
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15778864 | J:98850
First Author: Prescott K
Year: 2005
Journal: Hum Genet
Title: Microarray analysis of the Df1 mouse model of the 22q11 deletion syndrome.
Volume: 116
Issue: 6
Pages: 486-96
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10704284 | J:60871
First Author: Lund J
Year: 2000
Journal: Genomics
Title: Comparative sequence analysis of 634 kb of the mouse chromosome 16 region of conserved synteny with the human velocardiofacial syndrome region on chromosome 22q11.2.
Volume: 63
Issue: 3
Pages: 374-83
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9405660 | J:45079
First Author: Puech A
Year: 1997
Journal: Proc Natl Acad Sci U S A
Title: Comparative mapping of the human 22q11 chromosomal region and the orthologous region in mice reveals complex changes in gene organization.
Volume: 94
Issue: 26
Pages: 14608-13
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10337614 | J:54501
First Author: Lund J
Year: 1999
Journal: Mamm Genome
Title: Sequence-ready physical map of the mouse chromosome 16 region with conserved synteny to the human velocardiofacial syndrome region on 22q11.2.
Volume: 10
Issue: 5
Pages: 438-43
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10725249 | J:60984
First Author: Ko MS
Year: 2000
Journal: Development
Title: Large-scale cDNA analysis reveals phased gene expression patterns during preimplantation mouse development.
Volume: 127
Issue: 8
Pages: 1737-49
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29078390 | J:249035
First Author: Kannan M
Year: 2017
Journal: Proc Natl Acad Sci U S A
Title: WD40-repeat 47, a microtubule-associated protein, is essential for brain development and autophagy.
Volume: 114
Issue: 44
Pages: E9308-E9317
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24721909 | J:209956
 
First Author: Liakath-Ali K
Year: 2014
Journal: Nat Commun
Title: Novel skin phenotypes revealed by a genome-wide mouse reverse genetic screen.
Volume: 5
Pages: 3540
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25452572 | J:235630
First Author: Paronett EM
Year: 2015
Journal: Cereb Cortex
Title: Ranbp1, Deleted in DiGeorge/22q11.2 Deletion Syndrome, is a Microcephaly Gene That Selectively Disrupts Layer 2/3 Cortical Projection Neuron Generation.
Volume: 25
Issue: 10
Pages: 3977-93
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14614146 | J:86704
First Author: Maynard TM
Year: 2003
Journal: Proc Natl Acad Sci U S A
Title: A comprehensive analysis of 22q11 gene expression in the developing and adult brain.
Volume: 100
Issue: 24
Pages: 14433-8
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24357327 | J:213451
First Author: Karpinski BA
Year: 2014
Journal: Dis Model Mech
Title: Dysphagia and disrupted cranial nerve development in a mouse model of DiGeorge (22q11) deletion syndrome.
Volume: 7
Issue: 2
Pages: 245-57
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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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16602821 | J:162220
First Author: Magdaleno S
Year: 2006
Journal: PLoS Biol
Title: BGEM: an in situ hybridization database of gene expression in the embryonic and adult mouse nervous system.
Volume: 4
Issue: 4
Pages: e86
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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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Publication
- | J:342605
       
First Author: GOA curators
Year: 2016
Title: Automatic transfer of experimentally verified manual GO annotation data to orthologs using Ensembl Compara
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Publication
- | J:109762
     
First Author: Mouse Genome Informatics and VEGA Genome Database Project
Year: 2006
Journal: Database Release
Title: Collaboration to Associate VEGA (Vertebrate Genome Annotation) Mouse Gene Models with MGI Markers
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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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Publication
- | J:23000
       
First Author: MGD Nomenclature Committee
Year: 1995
Title: Nomenclature Committee Use
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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: Mouse Genome Informatics Scientific Curators
Year: 2010
Title: Human to Mouse ISO GO annotation transfer
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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: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:155221
     
First Author: Mouse Genome Informatics
Year: 2010
Journal: Database Release
Title: Protein Ontology Association Load.
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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: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:85324
     
First Author: Mouse Genome Informatics Group
Year: 2003
Journal: Database Procedure
Title: Automatic Encodes (AutoE) Reference
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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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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
- | 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: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: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: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:94338
     
First Author: NIH Mouse Knockout Inventory
Year: 2004
Journal: MGI Direct Data Submission
Title: Information obtained from the NIH Mouse Knockout Inventory
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Publication
- | J:24194
     
First Author: The Jackson Laboratory Backcross DNA Panel Mapping Resource
Year: 1999
Journal: Database Release
Title: JAX BSS Panel Mapping Data
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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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Publication
- | J:81858
       
First Author: Mouse Genome Informatics Scientific Curators
Year: 2003
Title: Data Curation Using Mouse Genome Assembly
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Publication
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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Publication
- | J:57656
     
First Author: Lennon G
Year: 1999
Journal: Database Download
Title: WashU-HHMI Mouse EST Project
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Publication
- | 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: Mouse Genome Informatics Scientific Curators
Year: 2001
Title: Gene Ontology Annotation by the MGI Curatorial Staff
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Publication
- | J:342604
       
First Author: UniProt-GOA
Year: 2012
Title: Gene Ontology annotation based on UniProtKB/Swiss-Prot Subcellular Location vocabulary mapping, accompanied by conservative changes to GO terms applied by UniProt
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