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Search results 601 to 638 out of 638 for Chd7

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Type Details Score
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:155221
     
First Author: Mouse Genome Informatics
Year: 2010
Journal: Database Release
Title: Protein Ontology Association Load.
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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: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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HT Experiment
GSE90466 | CHD7 controls cerebellar development via Reelin
 
Experiment Type: RNA-Seq
Study Type: WT vs. Mutant
Source: GEO
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Strain
MGI:3577179 | C3;COlaHsd-Chd7<Edy>/H
Attribute String: chemically induced mutation, mutant stock
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HT Experiment
GSE84127 | Expression analysis of Chd7 in mouse hematopoietic stem and progenitor cells [microarray]
 
Experiment Type: transcription profiling by array
Study Type: Baseline
Source: GEO
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Publication
39373572 | J:360933
First Author: LaFleur MW
Year: 2024
Journal: J Immunol
Title: In Vivo CRISPR Screening Reveals CHD7 as a Positive Regulator of Short-lived Effector Cells.
Volume: 213
Issue: 10
Pages: 1528-1541
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HT Experiment
E-GEOD-72726 | Chromatin Remodeler CHD7 mutated in CHARGE Syndrome Interacts with Sox10 to Regulate Timing of CNS Myelination and Remyelination [RNA-seq]
Series Id: GSE72726
Experiment Type: RNA-Seq
Study Type: WT vs. Mutant
Source: ArrayExpress
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HT Experiment
E-GEOD-46591 | CHD7 regulates gene networks involved in neural crest cell migration and axon guidance
Series Id: GSE46591
Experiment Type: transcription profiling by array
Study Type: WT vs. Mutant
Source: ArrayExpress
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HT Experiment
GSE103288 | CHD7 functions upstream of the retinoic acid synthetase ALDH1A3 to regulate inner ear development
 
Experiment Type: RNA-Seq
Study Type: WT vs. Mutant
Source: GEO
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Publication
36884301 | J:337552
First Author: Noda A
Year: 2023
Journal: Mol Biol Cell
Title: ATM-dependent phosphorylation of CHD7 regulates morphogenesis-coupled DSB stress response in fetal radiation exposure.
Volume: 34
Issue: 5
Pages: ar39
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Publication
32816902 | J:295727
 
First Author: Evsen L
Year: 2020
Journal: Development
Title: let-7 miRNAs inhibit CHD7 expression and control auditory-sensory progenitor cell behavior in the developing inner ear.
Volume: 147
Issue: 15
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HT Experiment
GSE59963 | The Chromatin Remodeller CHD7 Lies Upstream of Semaphorin, Slit/Robo and Calcium Handling Pathways during Cardiovascular Development
 
Experiment Type: transcription profiling by array
Study Type: WT vs. Mutant
Source: GEO
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Strain
MGI:3577088 | C3;C-Chd7<Todo>/H
Attribute String: chemically induced mutation, mutant stock
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HT Experiment
GSE229629 | Global gene expression changes in E9.5 cardiopharyngeal mesoderm (CPM) of Chd7 mutants versus controls
 
Experiment Type: RNA-Seq
Study Type: WT vs. Mutant
Source: GEO
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Protein
A2AJK6
Organism: Mus musculus/domesticus
Length: 2986  
Fragment?: false
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Protein
A2AJK6-3
Organism: Mus musculus/domesticus
Length: 2960  
Fragment?: false
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Protein
A2AJK6-2
Organism: Mus musculus/domesticus
Length: 558  
Fragment?: false
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Allele
Chd7<em1Smoc> | MGI:7288959
Name: chromodomain helicase DNA binding protein 7; endonuclease-mediated mutation 1, Shanghai Model Organisms Center
Allele Type: Endonuclease-mediated
Attribute String: Null/knockout
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Strain
MGI:6770654 | C57BL/6JSmoc-Chd7<em1Smoc>/Smoc
Attribute String: coisogenic, endonuclease-mediated mutation, mutant strain
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DO Term
DOID:0090084 | hypogonadotropic hypogonadism 5 with or without anosmia
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Allele
Chd7<Looper> | MGI:5505450
Name: chromodomain helicase DNA binding protein 7; looper
Allele Type: Chemically induced (ENU)
Attribute String: Null/knockout
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Publication
16400610 | -
First Author: Lalani SR
Year: 2006
Journal: Am J Hum Genet
Title: Spectrum of CHD7 mutations in 110 individuals with CHARGE syndrome and genotype-phenotype correlation.
Volume: 78
Issue: 2
Pages: 303-14
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Protein Coding Gene
MGI:1344395 | Chd3
Type: protein_coding_gene
Organism: mouse, laboratory
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HT Experiment
GSE84136 | Expression Profile of CHD7-Deficient Murine Long-term Hematopoietic Stem Cells
 
Experiment Type: transcription profiling by array
Study Type: WT vs. Mutant
Source: GEO
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Allele
Tg(Chd7-EGFP)IE59Gsat | MGI:4846936
Name: transgene insertion IE59, GENSAT Project at Rockefeller University
Allele Type: Transgenic
Attribute String: Reporter
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Strain
MGI:6281674 | BALB/c-Chd7<Looper>
Attribute String: coisogenic, mutant strain, chemically induced mutation
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Genotype
Genotype
Symbol: Chd7/Chd7<+>
Background: BALB/c-Chd7
Zygosity: ht
Has Mutant Allele: true
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Genotype
Genotype
Symbol: Chd7/Chd7<+>
Background: involves: BALB/c * C57BL/6
Zygosity: ht
Has Mutant Allele: true
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Strain
MGI:5003776 | STOCK Tg(Chd7-EGFP)IE59Gsat/Mmucd
Attribute String: mutant stock, transgenic
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HT Experiment
GSE163798 | Transcriptomes of control and Chd7-deficient spiral ganglia neurons and cochlear hair cells
 
Experiment Type: RNA-Seq
Study Type: WT vs. Mutant
Source: GEO
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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
37670778 | J:340466
First Author: Baxi AB
Year: 2023
Journal: iScience
Title: Time-resolved quantitative proteomic analysis of the developing Xenopus otic vesicle reveals putative congenital hearing loss candidates.
Volume: 26
Issue: 9
Pages: 107665
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Publication
37221016 | J:349229
 
First Author: Sallis S
Year: 2023
Journal: Life Sci Alliance
Title: The CHARGE syndrome-associated protein FAM172A controls AGO2 nuclear import.
Volume: 6
Issue: 8
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Publication
29907771 | J:267415
First Author: Su W
Year: 2018
Journal: Oncogene
Title: miR-30 disrupts senescence and promotes cancer by targeting both p16INK4A and DNA damage pathways.
Volume: 37
Issue: 42
Pages: 5618-5632
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Publication
30071041 | J:264351
First Author: Rivera-Reyes R
Year: 2018
Journal: PLoS One
Title: Proteomic analysis identifies transcriptional cofactors and homeobox transcription factors as TBX18 binding proteins.
Volume: 13
Issue: 8
Pages: e0200964
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Publication
- | J:100256
     
First Author: The Gene Expression Nervous System Atlas (GENSAT) Project, The Rockefeller University (New York, NY)
Year: 2005
Journal: Database Download
Title: MGI download of GENSAT transgene data
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