HNRNPR | bioCADDIE Data Discovery Index
Mountain View
biomedical and healthCAre Data Discovery Index Ecosystem
help Advanced Search
Displaying 15 of 15 results for "HNRNPR"
i
  1. Solution structure of RRM domain in heterogeneous nuclear ribonucleoprotein R (hnRNP R) PDB

    ID: PDB:2DK2

    Description: Heterogeneous nuclear ribonucleoprotein R

  2. eukaryotic RNA recognition motif, RRM1, from the heterogeneous nuclear ribonucleoprotein H from Homo sapiens, Northeast Structural Genomics Consortium (NESG) Target HR8614... PDB

    ID: PDB:2LXU

    Description: Heterogeneous nuclear ribonucleoprotein H

  3. ROA1_MACMU UniProt:Swiss-Prot

    ID: Q28521

    Description: Heterogeneous nuclear ribonucleoprotein A1 Removed; alternate Heterogeneous

  4. RBMX_PANTR UniProt:Swiss-Prot

    ID: A5A6M3

    Description: the association to nascent RNAPII transcripts and nuclear localization Necessary for RNA-binding N-acetylmethionine; in Heterogeneous nuclear ribonucleoprotein G; alternate N-acetylvaline; in Heterogeneous nuclear

  5. HNRPQ_RAT UniProt:Swiss-Prot

    ID: Q7TP47

    Description: Removed Heterogeneous nuclear ribonucleoprotein Q RRM 1 RRM 2 RRM 3 1-1 1-2 2-1 2-2 1-3 2-3 1-4 1-5 1...

  6. Discovery of novel recurrent mutations and rearrangements in early T-cell precursor acute lymphoblastic leukaemia by whole genome sequencing ArrayExpress

    ID: E-GEOD-33315

    Description: ing GATA3, EP300, RUNX1, DNM2, ECT2L, HNRNPA1 and HNRNPR, as well as genes known to be mutated in T-ALL, including NOTCH1, PHF6, and WT1.. Five of 12 ETP ALL cases harboured novel chromosomal translocations, several of which accompanied complex multichromosomal rearrangements and resulted in the expression of chimeric in-frame fusion genes disrupting hematopoietic regulators, including ETV6-INO80D, NAP1L1-MLLT10 and RUNX1-EVX1. These results indicate that although ETP ALL is genetically heterogeneous, activation of Ras and cytokine receptor signalling distinguishes this disease from non-ETP ALL. These findings suggest that targeting this pathway may improve the currently dismal outcome of this disease. Gene expression profiling of an extended panel of childhood B-lineage and T-lineage acute lymphoblastic leukemia samples was performed us...

  7. Discovery of novel recurrent mutations and rearrangements in early T-cell precursor acute lymphoblastic leukaemia by whole genome sequencing ArrayExpress

    ID: E-GEOD-28497

    Description: ing GATA3, EP300, RUNX1, DNM2, ECT2L, HNRNPA1 and HNRNPR, as well as genes known to be mutated in T-ALL, including NOTCH1, PHF6, and WT1.. Five of 12 ETP ALL cases harboured novel chromosomal translocations, several of which accompanied complex multichromosomal rearrangements and resulted in the expression of chimeric in-frame fusion genes disrupting hematopoietic regulators, including ETV6-INO80D, NAP1L1-MLLT10 and RUNX1-EVX1. These results indicate that although ETP ALL is genetically heterogeneous, activation of Ras and cytokine receptor signalling distinguishes this disease from non-ETP ALL. These findings suggest that targeting this pathway may improve the currently dismal outcome of this disease. Gene expression profiling of an extended panel of childhood B-lineage and T-lineage acute lymphoblastic leukemia samples was performed us...

  8. HNRPK_RABIT UniProt:Swiss-Prot

    ID: O19049

    Description: Heterogeneous nuclear ribonucleoprotein K KH 1 1-1 3-1 KH 2 2-1 3-2 3-3 3-4 2-2 KH 3 1-2 3-5 ...

  9. N6-methyladenosine Recruits HNRNPG for Alternative Splicing Regulation BioProject

    ID: PRJNA298926

    Keywords: Other

    Access Type: download

    dataset.description: nism remains unclear. We find the splicing factor heterogeneous nuclear ribonucleoprotein G (HNRNPG) selectively binds m6A-modified RNA in vitro and in vivo. Transcriptome-wide identification of HNRNPG binding sites reveals the binding sequence specificity of HNRNPG (AGRAC, R=A/G), which embeds the m6A consensus motif. The m6A methylation makes the binding sequence more accessible to facilitate HNRNPG binding. In total, we id...
  10. Analysis of pre-mRNA splicing trans-regulation in human lymphoblastoid cell lines BioProject

    ID: PRJNA230267

    Keywords: Transcriptome or Gene expression

    Access Type: download

  11. Discovery of novel recurrent mutations and rearrangements in early T-cell precursor acute lymphoblastic leukaemia by whole genome sequencing BioProject

    ID: PRJNA149299

    Keywords: Transcriptome or Gene expression

    Access Type: download

    dataset.description: ing GATA3, EP300, RUNX1, DNM2, ECT2L, HNRNPA1 and HNRNPR, as well as genes known to be mutated in T-ALL, including NOTCH1, PHF6, and WT1.. Five of 12 ETP ALL cases harboured novel chromosomal translocations, several of which accompanied complex multichromosomal rearrangements and resulted in the expression of chimeric in-frame fusion genes disrupting hematopoietic regulators, including ETV6-INO80D, NAP1L1-MLLT10 and RUNX1-EVX1. These results indicate that although ETP ALL is genetically heterogeneous, activation of Ras and cytokine receptor signalling distinguishes this disease from non-ETP ALL. These findings suggest that targeting this pathway may improve the currently dismal outcome of this disease. Overall design: Gene expression profiling of an extended panel of childhood B-lineage and T-lineage acute lymphoblastic leukemia samples ...
  12. Discovery of novel recurrent mutations and rearrangements in early T-cell precursor acute lymphoblastic leukaemia by whole genome sequencing OmicsDI

    ID: E-GEOD-33315

    Date Released: 01-16-2012

    Description: ing GATA3, EP300, RUNX1, DNM2, ECT2L, HNRNPA1 and HNRNPR, as well as genes known to be mutated in T-ALL, including NOTCH1, PHF6, and WT1.. Five of 12 ETP ALL cases harboured novel chromosomal translocations, several of which accompanied complex multichromosomal rearrangements and resulted in the expression of chimeric in-frame fusion genes disrupting hematopoietic regulators, including ETV6-INO80D, NAP1L1-MLLT10 and RUNX1-EVX1. These results indicate that although ETP ALL is genetically heterogeneous, activation of Ras and cytokine receptor signalling distinguishes this disease from non-ETP ALL. These findings suggest that targeting this pathway may improve the currently dismal outcome of this disease. Gene expression profiling of an extended panel of childhood B-lineage and T-lineage acute lymphoblastic leukemia samples was performed us...

  13. Discovery of novel recurrent mutations and rearrangements in early T-cell precursor acute lymphoblastic leukaemia by whole genome sequencing OmicsDI

    ID: E-GEOD-28497

    Date Released: 05-20-2011

    Description: ing GATA3, EP300, RUNX1, DNM2, ECT2L, HNRNPA1 and HNRNPR, as well as genes known to be mutated in T-ALL, including NOTCH1, PHF6, and WT1.. Five of 12 ETP ALL cases harboured novel chromosomal translocations, several of which accompanied complex multichromosomal rearrangements and resulted in the expression of chimeric in-frame fusion genes disrupting hematopoietic regulators, including ETV6-INO80D, NAP1L1-MLLT10 and RUNX1-EVX1. These results indicate that although ETP ALL is genetically heterogeneous, activation of Ras and cytokine receptor signalling distinguishes this disease from non-ETP ALL. These findings suggest that targeting this pathway may improve the currently dismal outcome of this disease. Gene expression profiling of an extended panel of childhood B-lineage and T-lineage acute lymphoblastic leukemia samples was performed us...

  14. HNRC4_HUMAN UniProt:Swiss-Prot

    ID: P0DMR1

    Description: Heterogeneous nuclear ribonucleoprotein C-like 4 RRM

  15. Naa50p amino-terminal acetyltransferase bound to substrate peptide fragment and CoA PDB

    ID: PDB:3TFY

    Description: N-alpha-acetyltransferase 50, NatE catalytic subunit (E.C.2.3.1.-), hnRNP F


Displaying 15 of 15 results for "HNRNPR"