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Displaying 20 of 71 results for "SMARCB1"
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  1. Transcriptional response to Smarcb1 re-expression in murine derived Smarcb1 deficient p53 null tumors OmicsDI

    ID: E-GEOD-46017

    Date Released: 01-13-2014

    Description: SMARCB1 (Snf5/Ini1/Baf47) is a potent tumor suppressor, the loss of which serves as the diagnostic feature in Malignant Rhabdoid Tu...

  2. Transcriptional response to Smarcb1 re-expression in murine derived Smarcb1 deficient p53 null tumors BioProject

    ID: PRJNA196906

    Keywords: Transcriptome or Gene expression

    Access Type: download

  3. Transcriptional response to Smarcb1 re-expression in murine derived Smarcb1 deficient p53 null tumors ArrayExpress

    ID: E-GEOD-46017

    Description: SMARCB1 (Snf5/Ini1/Baf47) is a potent tumor suppressor, the loss of which serves as the diagnostic feature in Malignant Rhabdoid Tu...

  4. SMARCB1-mediated SWI/SNF complex function is essential for enhancer regulation [primary tissue_ChIP-seq] BioProject

    ID: PRJNA291412

    Keywords: Epigenomics

    Access Type: download

  5. SMARCB1-mediated SWI/SNF complex function is essential for enhancer regulation BioProject

    ID: PRJNA291407

    Access Type: download

  6. Gene expression analysis of human haploid cells (HAP1) depleted of SMARCB1 and SMARCA4 ArrayExpress

    ID: E-GEOD-75515

    Description: wide expression levels in HAP1 cells upon loss of SMARCB1, SMARCA4 or both these genes together. The SMARCB1 and SMARCA4 genes were the hits from a genome wide screen involving genetrap mutagenesis to find new players ...

  7. Mouse Smarcb1-deficient models recapitulate subtypes of human rhabdoid tumors. BioProject

    ID: PRJNA269772

    Keywords: Transcriptome or Gene expression

    Access Type: download

  8. SMARCB1-mediated SWI/SNF complex function is essential for enhancer regulation [primary tissue_RNA-seq] BioProject

    ID: PRJNA291411

    Keywords: Transcriptome or Gene expression

    Access Type: download

  9. Gene expression analysis of human haploid cells (HAP1) depleted of SMARCB1 and SMARCA4 OmicsDI

    ID: E-GEOD-75515

    Date Released: 09-12-2016

    Description: wide expression levels in HAP1 cells upon loss of SMARCB1, SMARCA4 or both these genes together. The SMARCB1 and SMARCA4 genes were the hits from a genome wide screen involving genetrap mutagenesis to find new players ...

  10. SMARCB1-mediated SWI/SNF complex function is essential for enhancer regulation [cell line_ChIP-seq] BioProject

    ID: PRJNA291410

    Keywords: Epigenomics

    Access Type: download

  11. SMARCB1-mediated SWI/SNF complex function is essential for enhancer regulation [cell line_RNA-seq] BioProject

    ID: PRJNA291409

    Keywords: Transcriptome or Gene expression

    Access Type: download

  12. Gene expression analysis of human haploid cells (HAP1) depleted of SMARCB1 and SMARCA4 BioProject

    ID: PRJNA304449

    Keywords: Transcriptome or Gene expression

    Access Type: download

  13. SMARCB1-deficient rhaboid tumors of the kidney and renal medullary carcinomas. BioProject

    ID: PRJNA288603

    Keywords: Transcriptome or Gene expression

    Access Type: download

  14. SMARCB1-deficient rhaboid tumors of the kidney and renal medullary carcinomas ArrayExpress

    ID: E-GEOD-70421

    Description: We used microarrays to compared gene expression profilings in various tumors of the kidney. [human mRNA] 8 human RTK, 5 human RMC.

  15. Comprehensive analysis of a rare paediatric brain tumour; atypical teratoid rhabdoid tumour (ATRT) using genomic, epigenomic and transcriptomic techni... OmicsDI

    ID: EGAS00001000506

    Date Released:

    Description: it few other recurrently mutated loci except for SMARCB1/hSNF5. We integrated whole genome (n=15), exome, copy number, gene expression and methylation analyses to comprehensively interrogate 64 ATRTs and observed that structural events were relatively frequent in the ATRT genome (~3 tumour). In addition ...

  16. Transcription profiling of mouse SNF5 liver-specific inactivation in SNF5 flox/knockouts ArrayExpress

    ID: E-MEXP-241

    Description: Effect of liver-specific inactivation of SNF5 on liver transcriptome. Comparison of control and mutant livers.

  17. Genome variation profiling of A204 parental and acquired-resistance cells treated with Pazopanib, Dasatinib and Sunitinib BioProject

    ID: PRJNA343883

    Keywords: Variation

    Access Type: download

    dataset.description: racterised by a deficiency in the SWI/SNF subunit SMARCB1. Here we employ an integrated molecular profiling and chemical biology approach to demonstrate that the receptor tyrosine kinases (RTKs) PDGFRα and FGFR1 are coactivated in MRT cells and t...
  18. Solution structure of the human SNF5/INI1 domain PDB

    ID: PDB:5L7B

    Description: SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily B member 1

    gene.name: SMARCB1, BAF47, INI1, SNF5L1
  19. Gene expression data from ATRT tumor samples ArrayExpress

    ID: E-GEOD-70678

    Description: nces in demographics, tumor location, and type of SMARCB1 alterations, were identified. Whole-genome DNA and RNA sequencing found no recurrent mutations in addition to SMARCB1 that would explain the differences between subgroups. Whole-genome bisulfite sequencing and H3K27Ac chromatin-immunoprecipitation sequencing of primary tumors, however, revealed clear differences, leading to the identification of subgroup-specific regulatory networks and potential therapeutic targets. 49 ATRT samples were selected for RNA extraction and hybridization on Affymetrix Affymetrix Human...

  20. The genomic and epigenomic landscape of atypical teratoid rhabdoid tumors BioProject

    ID: PRJNA288790

    Keywords: Variation

    Access Type: download

    dataset.description: nces in demographics, tumor location, and type of SMARCB1 alterations, were identified. Whole-genome DNA and RNA sequencing found no recurrent mutations in addition to SMARCB1 that would explain the differences between subgroups. Whole-genome bisulfite sequencing and H3K27Ac chromatin-immunoprecipitation sequencing of primary tumors, however, revealed clear differences, leading to the identification of subgroup-specific regulatory networks and potential therapeutic targets. Overall design: 150 human ATRT tumor samples were profiled using the Illumina HumanMethylation450...

Displaying 20 of 71 results for "SMARCB1"