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Displaying 20 of 45 results for "CHD7"
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  1. RNA-seq of Chd7 wild type and mutant granule neuron progenitors BioProject

    ID: PRJNA293356

    Keywords: Transcriptome or Gene expression

    Access Type: download

  2. Genomic distribution of CHD7 on chromatin tracks H3K4 methylation patterns BioProject

    ID: PRJNA111453

    Keywords: Epigenomics

    Access Type: download

  3. CHD7 targets active gene enhancer elements to modulate ES cell-specific gene expression. BioProject

    ID: PRJNA127519

    Keywords: Other

    Access Type: download

  4. CHD7 controls cerebellar development via Reelin BioProject

    ID: PRJNA354712

    Keywords: Other

    Access Type: download

  5. Chromatin Remodeler CHD7 mutated in CHARGE Syndrome Interacts with Sox10 to Regulate Timing of CNS Myelination and Remyelination [RNA-seq] ArrayExpress

    ID: E-GEOD-72726

    Description: Mutations in CHD7, encoding ATP-dependent chromodomain-helicase-DNA-binding protein 7, in CHARGE syndrome leads to multiple congenital anomalies...

  6. Identification of Chd7 and Top2b regulated genes in cerebellar granule neurons BioProject

    ID: PRJNA309165

    Keywords: Transcriptome or Gene expression

    Access Type: download

  7. Chromatin Remodeler CHD7 mutated in CHARGE Syndrome Interacts with Sox10 to Regulate Timing of CNS Myelination and Remyelination [ChIP-seq] OmicsDI

    ID: E-GEOD-72725

    Date Released: 03-06-2016

    Description: Mutations in CHD7, encoding ATP-dependent chromodomain-helicase-DNA-binding protein 7, in CHARGE syndrome leads to multiple congenital anomalies...

  8. Genomic distribution of CHD7 on chromatin tracks H3K4 methylation patterns OmicsDI

    ID: E-GEOD-14460

    Date Released: 05-01-2014

    Description: CHD7 is a member of the chromodomain helicase DNA binding domain family of ATP-dependent chromatin remodeling enzymes. De novo mut...

  9. Chromatin Remodeler CHD7 mutated in CHARGE Syndrome Interacts with Sox10 to Regulate Timing of CNS Myelination and Remyelination [ChIP-seq] BioProject

    ID: PRJNA294770

    Keywords: Epigenomics

    Access Type: download

  10. ATAC-seq of Chd7 WT and mutant cerebellar granule neuron progenitors BioProject

    ID: PRJNA309175

    Keywords: Epigenomics

    Access Type: download

  11. CHD7 targets active gene enhancer elements to modulate ES cell-specific gene expression ArrayExpress

    ID: E-GEOD-22341

    Description: red between mouse ES cells of three genotypes: WT Chd7, Heterzygous Chd7 Null, Homozygous Chd7 Null. The hypothesis being tested was that CHD7, a chromatin r...

  12. Chromatin Remodeler CHD7 mutated in CHARGE Syndrome Interacts with Sox10 to Regulate Timing of CNS Myelination and Remyelination [RNA-seq] BioProject

    ID: PRJNA294769

    Keywords: Transcriptome or Gene expression

    Access Type: download

  13. CHD7 targets active gene enhancer elements to modulate ES cell-specific gene expression. OmicsDI

    ID: E-GEOD-22341

    Date Released: 05-02-2014

    Description: red between mouse ES cells of three genotypes: WT Chd7, Heterzygous Chd7 Null, Homozygous Chd7 Null. The hypothesis being tested was that CHD7, a chromatin r...

  14. BRK domain from human CHD7 PDB

    ID: PDB:2V0E

    Description: CHROMODOMAIN-HELICASE-DNA-BINDING PROTEIN 7 (E.C.3.6.1.-)

  15. BRK domain from human CHD7 PDB

    ID: PDB:2V0F

    Description: CHROMODOMAIN-HELICASE-DNA-BINDING PROTEIN 7 (E.C.3.6.1.-)

  16. Genomic distribution of CHD7 on chromatin tracks H3K4 methylation patterns ArrayExpress

    ID: E-GEOD-14460

    Description: CHD7 is a member of the chromodomain helicase DNA binding domain family of ATP-dependent chromatin remodeling enzymes. De novo mut...

  17. The Chromatin Remodeller CHD7 Lies Upstream of Semaphorin, Slit/Robo and Calcium Handling Pathways during Cardiovascular Development BioProject

    ID: PRJNA257189

    Keywords: Transcriptome or Gene expression

    Access Type: download

  18. Chromatin Remodeler CHD7 mutated in CHARGE Syndrome Interacts with Sox10 to Regulate Timing of CNS Myelination and Remyelination. BioProject

    ID: PRJNA294766

    Access Type: download

  19. CHD7 regulates gene networks involved in neural crest cell migration and axon guidance ArrayExpress

    ID: E-GEOD-46591

    Description: Heterozygous loss-of function mutations in CHD7 (chromodomain helicase DNA-binding protein 7) lead to CHARGE syndrome, a complex developmental disorder affecting craniofacial...

  20. CHD7 regulates gene networks involved in neural crest cell migration and axon guidance BioProject

    ID: PRJNA201065

    Keywords: Transcriptome or Gene expression

    Access Type: download


Displaying 20 of 45 results for "CHD7"