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Search results 1 to 100 out of 121 for Chd7

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Category: Publication
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Type Details Score
Publication
24840056 | J:252089
First Author: Ogier JM
Year: 2014
Journal: PLoS One
Title: CHD7 deficiency in "Looper", a new mouse model of CHARGE syndrome, results in ossicle malformation, otosclerosis and hearing impairment.
Volume: 9
Issue: 5
Pages: e97559
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Publication
35418650 | J:336448
First Author: Liu C
Year: 2022
Journal: Nat Commun
Title: CHD7 regulates bone-fat balance by suppressing PPAR-γ signaling.
Volume: 13
Issue: 1
Pages: 1989
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Publication
35402599 | J:324165
First Author: Cheng J
Year: 2022
Journal: Ann Transl Med
Title: CHD7 in oocytes is essential for female fertility.
Volume: 10
Issue: 5
Pages: 260
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Publication
16207732 | J:104123
First Author: Bosman EA
Year: 2005
Journal: Hum Mol Genet
Title: Multiple mutations in mouse Chd7 provide models for CHARGE syndrome.
Volume: 14
Issue: 22
Pages: 3463-76
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Publication
29212025 | J:265988
First Author: Badodi S
Year: 2017
Journal: Cell Rep
Title: Convergence of BMI1 and CHD7 on ERK Signaling in Medulloblastoma.
Volume: 21
Issue: 10
Pages: 2772-2784
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Publication
36343670 | J:331474
 
First Author: Krueger LA
Year: 2022
Journal: Exp Eye Res
Title: Chromatin remodeler Chd7 regulates photoreceptor development and outer segment length.
Volume: 226
Pages: 109299
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Publication
27955690 | J:316976
First Author: Ohta S
Year: 2016
Journal: Mol Brain
Title: CHD7 promotes proliferation of neural stem cells mediated by MIF.
Volume: 9
Issue: 1
Pages: 96
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Publication
28317875 | J:243947
 
First Author: Feng W
Year: 2017
Journal: Nat Commun
Title: Chd7 is indispensable for mammalian brain development through activation of a neuronal differentiation programme.
Volume: 8
Pages: 14758
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Publication
33127760 | J:298597
First Author: Yan S
Year: 2020
Journal: Proc Natl Acad Sci U S A
Title: CHD7 regulates cardiovascular development through ATP-dependent and -independent activities.
Volume: 117
Issue: 46
Pages: 28847-28858
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Publication
29467333 | J:314662
 
First Author: Yao H
Year: 2018
Journal: JCI Insight
Title: CHD7 represses the retinoic acid synthesis enzyme ALDH1A3 during inner ear development.
Volume: 3
Issue: 4
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Publication
23827709 | J:199367
First Author: Feng W
Year: 2013
Journal: Cell Stem Cell
Title: The chromatin remodeler CHD7 regulates adult neurogenesis via activation of SoxC transcription factors.
Volume: 13
Issue: 1
Pages: 62-72
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Publication
24293546 | J:207089
First Author: Liu Y
Year: 2014
Journal: Hum Mol Genet
Title: CHD7 interacts with BMP R-SMADs to epigenetically regulate cardiogenesis in mice.
Volume: 23
Issue: 8
Pages: 2145-56
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Publication
34004180 | J:310063
 
First Author: Balendran V
Year: 2021
Journal: Dev Biol
Title: Chromatin remodeler CHD7 is critical for cochlear morphogenesis and neurosensory patterning.
Volume: 477
Pages: 11-21
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Publication
20591827 | J:163172
First Author: Zentner GE
Year: 2010
Journal: Hum Mol Genet
Title: CHD7 functions in the nucleolus as a positive regulator of ribosomal RNA biogenesis.
Volume: 19
Issue: 18
Pages: 3491-501
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Publication
21532573 | J:187550
First Author: Engelen E
Year: 2011
Journal: Nat Genet
Title: Sox2 cooperates with Chd7 to regulate genes that are mutated in human syndromes.
Volume: 43
Issue: 6
Pages: 607-11
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Publication
23285124 | J:195755
First Author: Batsukh T
Year: 2012
Journal: PLoS One
Title: Identification and characterization of FAM124B as a novel component of a CHD7 and CHD8 containing complex.
Volume: 7
Issue: 12
Pages: e52640
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Publication
30108144 | J:264451
First Author: Marie C
Year: 2018
Journal: Proc Natl Acad Sci U S A
Title: Oligodendrocyte precursor survival and differentiation requires chromatin remodeling by Chd7 and Chd8.
Volume: 115
Issue: 35
Pages: E8246-E8255
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Publication
32883883 | J:296224
First Author: Hsu J
Year: 2020
Journal: Proc Natl Acad Sci U S A
Title: CHD7 and Runx1 interaction provides a braking mechanism for hematopoietic differentiation.
Volume: 117
Issue: 38
Pages: 23626-23635
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Publication
34732824 | J:314588
First Author: Ahmed M
Year: 2021
Journal: Commun Biol
Title: The chromatin remodelling factor Chd7 protects auditory neurons and sensory hair cells from stress-induced degeneration.
Volume: 4
Issue: 1
Pages: 1260
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Publication
25183173 | J:222062
First Author: Jones KM
Year: 2015
Journal: Stem Cells
Title: CHD7 maintains neural stem cell quiescence and prevents premature stem cell depletion in the adult hippocampus.
Volume: 33
Issue: 1
Pages: 196-210
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Publication
29168327 | J:262209
 
First Author: Whittaker DE
Year: 2017
Journal: Am J Med Genet C Semin Med Genet
Title: Distinct cerebellar foliation anomalies in a CHD7 haploinsufficient mouse model of CHARGE syndrome.
Volume: 175
Issue: 4
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Publication
28931573 | J:248928
First Author: Doi T
Year: 2017
Journal: J Neurosci
Title: Chd7 Collaborates with Sox2 to Regulate Activation of Oligodendrocyte Precursor Cells after Spinal Cord Injury.
Volume: 37
Issue: 43
Pages: 10290-10309
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Publication
26928066 | J:234565
First Author: He D
Year: 2016
Journal: Nat Neurosci
Title: Chd7 cooperates with Sox10 and regulates the onset of CNS myelination and remyelination.
Volume: 19
Issue: 5
Pages: 678-89
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Publication
- | J:207749
     
First Author: Liu Y
Year: 2014
Journal: MGI Direct Data Submission
Title: CHD7 interacts with BMP R-SMADs to epigenetically regulate cardiogenesis in mice
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Publication
22539951 | J:187200
First Author: Tian C
Year: 2012
Journal: PLoS One
Title: Otitis media in a new mouse model for CHARGE syndrome with a deletion in the Chd7 gene.
Volume: 7
Issue: 4
Pages: e34944
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Publication
17701983 | J:123608
First Author: Adams ME
Year: 2007
Journal: J Comp Neurol
Title: Defects in vestibular sensory epithelia and innervation in mice with loss of Chd7 function: implications for human CHARGE syndrome.
Volume: 504
Issue: 5
Pages: 519-32
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Publication
17334657 | J:119812
First Author: Hurd EA
Year: 2007
Journal: Mamm Genome
Title: Loss of Chd7 function in gene-trapped reporter mice is embryonic lethal and associated with severe defects in multiple developing tissues.
Volume: 18
Issue: 2
Pages: 94-104
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34588434 | J:336427
First Author: Reddy NC
Year: 2021
Journal: Nat Commun
Title: CHARGE syndrome protein CHD7 regulates epigenomic activation of enhancers in granule cell precursors and gyrification of the cerebellum.
Volume: 12
Issue: 1
Pages: 5702
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Publication
29615807 | J:262283
First Author: Ogier JM
Year: 2018
Journal: Sci Rep
Title: An intronic mutation in Chd7 creates a cryptic splice site, causing aberrant splicing in a mouse model of CHARGE syndrome.
Volume: 8
Issue: 1
Pages: 5482
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Publication
20736290 | J:164582
First Author: Hurd EA
Year: 2010
Journal: Development
Title: The ATP-dependent chromatin remodeling enzyme CHD7 regulates pro-neural gene expression and neurogenesis in the inner ear.
Volume: 137
Issue: 18
Pages: 3139-50
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Publication
28165338 | J:242933
First Author: Whittaker DE
Year: 2017
Journal: J Clin Invest
Title: The chromatin remodeling factor CHD7 controls cerebellar development by regulating reelin expression.
Volume: 127
Issue: 3
Pages: 874-887
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Publication
22658483 | J:187010
First Author: Jiang X
Year: 2012
Journal: Am J Pathol
Title: The mutation in Chd7 causes misexpression of Bmp4 and developmental defects in telencephalic midline.
Volume: 181
Issue: 2
Pages: 626-41
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Publication
22705977 | J:188806
First Author: Hurd EA
Year: 2012
Journal: Mech Dev
Title: Delayed fusion and altered gene expression contribute to semicircular canal defects in Chd7 deficient mice.
Volume: 129
Issue: 9-12
Pages: 308-23
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Publication
26102480 | J:225736
First Author: Payne S
Year: 2015
Journal: Dev Biol
Title: A critical role for the chromatin remodeller CHD7 in anterior mesoderm during cardiovascular development.
Volume: 405
Issue: 1
Pages: 82-95
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Publication
19855134 | J:154590
First Author: Randall V
Year: 2009
Journal: J Clin Invest
Title: Great vessel development requires biallelic expression of Chd7 and Tbx1 in pharyngeal ectoderm in mice.
Volume: 119
Issue: 11
Pages: 3301-10
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Publication
36288662 | J:332873
 
First Author: Ritter KE
Year: 2022
Journal: Hear Res
Title: Loss of the chromatin remodeler CHD7 impacts glial cells and myelination in the mouse cochlear spiral ganglion.
Volume: 426
Pages: 108633
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37052590 | J:338018
     
First Author: Stathopoulou A
Year: 2023
Journal: Cardiovasc Res
Title: CHARGE syndrome-associated CHD7 acts at ISL1-regulated enhancers to modulate second heart field gene expression.
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21875659 | J:220430
First Author: Hurd EA
Year: 2011
Journal: Hear Res
Title: Mature middle and inner ears express Chd7 and exhibit distinctive pathologies in a mouse model of CHARGE syndrome.
Volume: 282
Issue: 1-2
Pages: 184-95
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35129866 | J:329885
First Author: Bélanger C
Year: 2022
Journal: FASEB J
Title: CHARGE syndrome-associated proteins FAM172A and CHD7 influence male sex determination and differentiation through transcriptional and alternative splicing mechanisms.
Volume: 36
Issue: 3
Pages: e22176
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24026680 | J:204618
First Author: Micucci JA
Year: 2014
Journal: Hum Mol Genet
Title: CHD7 and retinoic acid signaling cooperate to regulate neural stem cell and inner ear development in mouse models of CHARGE syndrome.
Volume: 23
Issue: 2
Pages: 434-48
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Publication
19279158 | J:148116
First Author: Layman WS
Year: 2009
Journal: Hum Mol Genet
Title: Defects in neural stem cell proliferation and olfaction in Chd7 deficient mice indicate a mechanism for hyposmia in human CHARGE syndrome.
Volume: 18
Issue: 11
Pages: 1909-23
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26670829 | J:231044
First Author: Gage PJ
Year: 2015
Journal: Invest Ophthalmol Vis Sci
Title: Mouse Models for the Dissection of CHD7 Functions in Eye Development and the Molecular Basis for Ocular Defects in CHARGE Syndrome.
Volume: 56
Issue: 13
Pages: 7923-30
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Publication
29018080 | J:251954
First Author: Zhen T
Year: 2017
Journal: Blood
Title: Chd7 deficiency delays leukemogenesis in mice induced by Cbfb-MYH11.
Volume: 130
Issue: 22
Pages: 2431-2442
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30459807 | J:311089
 
First Author: Durruthy-Durruthy R
Year: 2018
Journal: Front Genet
Title: Single Cell Transcriptomics Reveal Abnormalities in Neurosensory Patterning of the Chd7 Mutant Mouse Ear.
Volume: 9
Pages: 473
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Publication
36232804 | J:330596
 
First Author: Collins SC
Year: 2022
Journal: Int J Mol Sci
Title: Characterization of Two Mouse Chd7 Heterozygous Loss-of-Function Models Shows Dysgenesis of the Corpus Callosum and Previously Unreported Features of CHARGE Syndrome.
Volume: 23
Issue: 19
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Publication
24975120 | J:214965
First Author: Sperry ED
Year: 2014
Journal: Dev Dyn
Title: The chromatin remodeling protein CHD7, mutated in CHARGE syndrome, is necessary for proper craniofacial and tracheal development.
Volume: 243
Issue: 9
Pages: 1055-66
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Publication
24368733 | J:207892
 
First Author: Yu T
Year: 2013
Journal: Elife
Title: Deregulated FGF and homeotic gene expression underlies cerebellar vermis hypoplasia in CHARGE syndrome.
Volume: 2
Pages: e01305
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19809474 | J:161880
First Author: Bergman JE
Year: 2010
Journal: Eur J Hum Genet
Title: Study of smell and reproductive organs in a mouse model for CHARGE syndrome.
Volume: 18
Issue: 2
Pages: 171-7
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30277262 | J:336450
First Author: Kasah S
Year: 2018
Journal: J Anat
Title: Autism-linked CHD gene expression patterns during development predict multi-organ disease phenotypes.
Volume: 233
Issue: 6
Pages: 755-769
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25119037 | J:217080
First Author: Van Nostrand JL
Year: 2014
Journal: Nature
Title: Inappropriate p53 activation during development induces features of CHARGE syndrome.
Volume: 514
Issue: 7521
Pages: 228-32
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29311329 | J:260599
First Author: Bélanger C
Year: 2018
Journal: Proc Natl Acad Sci U S A
Title: Dysregulation of cotranscriptional alternative splicing underlies CHARGE syndrome.
Volume: 115
Issue: 4
Pages: E620-E629
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Publication
21596839 | J:174086
First Author: Layman WS
Year: 2011
Journal: Hum Mol Genet
Title: Reproductive dysfunction and decreased GnRH neurogenesis in a mouse model of CHARGE syndrome.
Volume: 20
Issue: 16
Pages: 3138-50
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24728844 | J:270128
First Author: Schulz Y
Year: 2014
Journal: Hum Genet
Title: CHD7, the gene mutated in CHARGE syndrome, regulates genes involved in neural crest cell guidance.
Volume: 133
Issue: 8
Pages: 997-1009
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Publication
33846320 | J:335054
First Author: Badodi S
Year: 2021
Journal: Nat Commun
Title: Inositol treatment inhibits medulloblastoma through suppression of epigenetic-driven metabolic adaptation.
Volume: 12
Issue: 1
Pages: 2148
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11919684 | J:75619
First Author: Kiernan AE
Year: 2002
Journal: Mamm Genome
Title: ENU mutagenesis reveals a highly mutable locus on mouse Chromosome 4 that affects ear morphogenesis.
Volume: 13
Issue: 3
Pages: 142-8
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15916118 | J:99481
First Author: Hawker K
Year: 2005
Journal: Int J Audiol
Title: Two new mouse mutants with vestibular defects that map to the highly mutable locus on chromosome 4.
Volume: 44
Issue: 3
Pages: 171-7
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- | J:136796
First Author: He F
Year: 2003
Journal: Chinese Science Bulletin
Title: Large-scale screening of disease model through ENU mutagenesis in mice
Volume: 48
Issue: 24
Pages: 2665-2671
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15353999 | J:93173
First Author: Pau H
Year: 2004
Journal: Otol Neurotol
Title: Characterization of a new mouse mutant, flouncer, with a balance defect and inner ear malformation.
Volume: 25
Issue: 5
Pages: 707-13
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32610082 | J:308016
First Author: Markenscoff-Papadimitriou E
Year: 2020
Journal: Cell
Title: A Chromatin Accessibility Atlas of the Developing Human Telencephalon.
Volume: 182
Issue: 3
Pages: 754-769.e18
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16104381 | J:100636
First Author: Wang KS
Year: 2005
Journal: Mamm Genome
Title: Genetic and phenotypic analysis of Tcm, a mutation affecting early eye development.
Volume: 16
Issue: 5
Pages: 332-43
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25985275 | J:222928
First Author: Cariboni A
Year: 2015
Journal: J Clin Invest
Title: Dysfunctional SEMA3E signaling underlies gonadotropin-releasing hormone neuron deficiency in Kallmann syndrome.
Volume: 125
Issue: 6
Pages: 2413-28
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28373172 | J:242352
First Author: Ogawa R
Year: 2017
Journal: Biol Open
Title: Mouse embryonic dorsal root ganglia contain pluripotent stem cells that show features similar to embryonic stem cells and induced pluripotent stem cells.
Volume: 6
Issue: 5
Pages: 602-618
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35132236 | J:335585
First Author: Noack F
Year: 2022
Journal: Nat Neurosci
Title: Multimodal profiling of the transcriptional regulatory landscape of the developing mouse cortex identifies Neurog2 as a key epigenome remodeler.
Volume: 25
Issue: 2
Pages: 154-167
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27174565 | J:243974
 
First Author: Cai X
Year: 2016
Journal: Sci Rep
Title: Homozygous mutation of VPS16 gene is responsible for an autosomal recessive adolescent-onset primary dystonia.
Volume: 6
Pages: 25834
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31444215 | J:284143
 
First Author: Phillips HM
Year: 2019
Journal: Development
Title: Pax9 is required for cardiovascular development and interacts with Tbx1 in the pharyngeal endoderm to control 4th pharyngeal arch artery morphogenesis.
Volume: 146
Issue: 18
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23319608 | J:193698
First Author: Li W
Year: 2013
Journal: Proc Natl Acad Sci U S A
Title: Brg1 governs distinct pathways to direct multiple aspects of mammalian neural crest cell development.
Volume: 110
Issue: 5
Pages: 1738-43
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10932191 | J:63816
First Author: Nolan PM
Year: 2000
Journal: Nat Genet
Title: A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse.
Volume: 25
Issue: 4
Pages: 440-3
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34124068 | J:308709
 
First Author: Durán Alonso MB
Year: 2021
Journal: Front Cell Dev Biol
Title: Meis2 Is Required for Inner Ear Formation and Proper Morphogenesis of the Cochlea.
Volume: 9
Pages: 679325
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22921202 | J:188772
First Author: Voss AK
Year: 2012
Journal: Dev Cell
Title: MOZ regulates the Tbx1 locus, and Moz mutation partially phenocopies DiGeorge syndrome.
Volume: 23
Issue: 3
Pages: 652-63
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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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23012479 | J:190322
First Author: Archambaud C
Year: 2012
Journal: Proc Natl Acad Sci U S A
Title: Impact of lactobacilli on orally acquired listeriosis.
Volume: 109
Issue: 41
Pages: 16684-9
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- | 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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- | 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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18973680 | J:141291
 
First Author: Tamplin OJ
Year: 2008
Journal: BMC Genomics
Title: Microarray analysis of Foxa2 mutant mouse embryos reveals novel gene expression and inductive roles for the gastrula organizer and its derivatives.
Volume: 9
Pages: 511
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10512203 | J:93290
First Author: Araki K
Year: 1999
Journal: Cell Mol Biol (Noisy-le-grand)
Title: Exchangeable gene trap using the Cre/mutated lox system.
Volume: 45
Issue: 5
Pages: 737-50
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15840001 | J:110088
First Author: Taniwaki T
Year: 2005
Journal: Dev Growth Differ
Title: Characterization of an exchangeable gene trap using pU-17 carrying a stop codon-beta geo cassette.
Volume: 47
Issue: 3
Pages: 163-72
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- | 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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18554416 | J:139177
First Author: Hoffman BG
Year: 2008
Journal: Genome Biol
Title: Identification of transcripts with enriched expression in the developing and adult pancreas.
Volume: 9
Issue: 6
Pages: R99
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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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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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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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- | J:204812
     
First Author: International Mouse Strain Resource
Year: 2014
Journal: Database Download
Title: MGI download of germline transmission data for alleles from IMSR strain data
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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:326541
       
First Author: Cyagen Biosciences Inc.
Year: 2022
Title: Cyagen Biosciences Website.
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Publication
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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- | 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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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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Publication
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