CAPRIN1 | bioCADDIE Data Discovery Index
Mountain View
biomedical and healthCAre Data Discovery Index Ecosystem
help Advanced Search
Displaying 9 of 9 results for "CAPRIN1"
i
  1. Crystal structure of the HR-1 domain of human caprin-1 in the P3121 space group PDB

    ID: PDB:4WBP

    Description: Cytoplasmic activation/proliferation-associated protein-1 (caprin-1)

    gene.name: CAPRIN1, GPIAP1, GPIP137, M11S1, RNG105
  2. Crystal structure of the HR-1 domain of human caprin-1 in the C121 space group PDB

    ID: PDB:4WBE

    Description: Cytoplasmic activation/proliferation-associated protein-1 (caprin-1)

    gene.name: CAPRIN1, GPIAP1, GPIP137, M11S1, RNG105
  3. The mRNA-bound proteome and its global occupancy profile on protein-coding transcripts [PAR-CLIP] ArrayExpress

    ID: E-GEOD-38201

    Description: ng HIS/FLAG/HA-tagged ALKBH5, C17orf85, C22orf28, CAPRIN1, and ZC3H7B. We used 4-thiouridine (4SU) to enhance the crosslink and generated two PAR-CLIP cDNA libraries per protein....

  4. The mRNA-bound proteome and its global occupancy profile on protein-coding transcripts [PAR-CLIP] BioProject

    ID: PRJNA167443

    Keywords: Transcriptome or Gene expression

    Access Type: download

    dataset.description: ng HIS/FLAG/HA-tagged ALKBH5, C17orf85, C22orf28, CAPRIN1, and ZC3H7B. We used 4-thiouridine (4SU) to enhance the crosslink and generated two PAR-CLIP cDNA libraries per protein....
  5. Major Depressive Disorder blood gene expression ArrayExpress

    ID: E-GEOD-19738

    Description: n age 41.9 years)), we identified a set of genes (CAPRIN1, CLEC4A, KRT23, MLC1, PLSCR1, PROK2, ZBTB16) that serves as a molecular signature of MDD. These findings were validated for the primary cohort using an independent quantitative PCR method (P = 0.007). The difference between depressive patients and controls was confirmed (P = 0.019) in a replication cohort of 13 patients with MDD (mean age 42.8 years) and 14 controls (mean age 45.6 years). The MDD-signature score comprised of expression levels of 7 genes could discriminate depressive patients from controls with sensitivity of 76.9% and specificity of 71.8%. Conclusions: We show for the first time that molecular analysis of stimulated blood cells can be used as an endophenotype for MDD diagnosis, which is a milestone in establishing biomarkers for neuropsychiatric disorders with moderate heritability in general. Our results may provide a new entry point for following and predict...

  6. Detection of Clinically Relevant Genetic Variants in Autism Spectrum Disorder by Whole-Genome Sequencing OmicsDI

    ID: EGAS00001000850

    Date Released:

    Description: eight candidate ASD risk genes. Examples include CAPRIN1 and AFF2 (both linked to FMR1, which is involved in fragileX syndrome), VIP (involved in social-cognitive deficits), and other genes such as SCN2A and KCNQ2 (linked to epilepsy), NRXN1, andCHD7, which causes ASD-associated CHARGE syndrome. Taken together, these results suggest that WGS and thorough bioinformaticanalyses for de novo and rare inherited mutations will improve the detection of genetic variants likely to be associated with ASD orits accompanying clinical symptoms....

  7. The mRNA-bound proteome and its global occupancy profile on protein-coding transcripts [PAR-CLIP] OmicsDI

    ID: E-GEOD-38201

    Date Released: 05-03-2014

    Description: ng HIS/FLAG/HA-tagged ALKBH5, C17orf85, C22orf28, CAPRIN1, and ZC3H7B. We used 4-thiouridine (4SU) to enhance the crosslink and generated two PAR-CLIP cDNA libraries per protein....

  8. Major Depressive Disorder blood gene expression BioProject

    ID: PRJNA122201

    Keywords: Transcriptome or Gene expression

    Access Type: download

    dataset.description: n age 41.9 years)), we identified a set of genes (CAPRIN1, CLEC4A, KRT23, MLC1, PLSCR1, PROK2, ZBTB16) that serves as a molecular signature of MDD. These findings were validated for the primary cohort using an independent quantitative PCR method (P = 0.007). The difference between depressive patients and controls was confirmed (P = 0.019) in a replication cohort of 13 patients with MDD (mean age 42.8 years) and 14 controls (mean age 45.6 years). The MDD-signature score comprised of expression levels of 7 genes could discriminate depressive patients from controls with sensitivity of 76.9% and specificity of 71.8%. Conclusions: We show for the first time that molecular analysis of stimulated blood cells can be used as an endophenotype for MDD diagnosis, which is a milestone in establishing biomarkers for neuropsychiatric disorders with moderate heritability in general. Our results may provide a new entry point for following and predic...
  9. Major Depressive Disorder blood gene expression OmicsDI

    ID: E-GEOD-19738

    Date Released: 10-17-2011

    Description: n age 41.9 years)), we identified a set of genes (CAPRIN1, CLEC4A, KRT23, MLC1, PLSCR1, PROK2, ZBTB16) that serves as a molecular signature of MDD. These findings were validated for the primary cohort using an independent quantitative PCR method (P = 0.007). The difference between depressive patients and controls was confirmed (P = 0.019) in a replication cohort of 13 patients with MDD (mean age 42.8 years) and 14 controls (mean age 45.6 years). The MDD-signature score comprised of expression levels of 7 genes could discriminate depressive patients from controls with sensitivity of 76.9% and specificity of 71.8%. Conclusions: We show for the first time that molecular analysis of stimulated blood cells can be used as an endophenotype for MDD diagnosis, which is a milestone in establishing biomarkers for neuropsychiatric disorders with moderate heritability in general. Our results may provide a new entry point for following and predict...


Displaying 9 of 9 results for "CAPRIN1"