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Proteomicshuman nk cell line LC-MSMS - Recurrent GNAQ mutation encoding T96S in natural killer/T cell lymphoma
To identify protein binding partners of wild-type or Gαq T96S mutants using immunoprecipitation coupled to mass spectrometry.
ORGANISM(S): Homo sapiens (Human) 
2019-09-25 | PXD013285 | Pride
Lc-msms Nk cell line Human 
GenomicsUK_RCC_GWAS
Renal cell carcinoma (RCC) cases comprised adult patients with histologically proven RCC were collected through two sources within the UK. First, 856 cases from SORCE, a MRC collection of surgically treated RCC cases ascertained through UK clinical oncology centres. Second, 189 RCC cases collected t...
EGAD00010002310 | EGA
GenomicsUK renal cancer samples genotyped on Illumina OmniExpress BeadChip
Renal cell carcinoma (RCC) cases comprised adult patients with histologically proven RCC were collected through two sources within the UK. First, 856 cases from SORCE, a MRC collection of surgically treated RCC cases ascertained through UK clinical oncology centres. Second, 189 RCC cases collected t...
EGAS00001002336 | EGA
GenomicsUK RCC DAC
Data Access Committee EGAC00001002629
EGAC00001002629 | EGA
ProteomicsIntegrated Proteomics and Metabolomics Link Acne to the Action Mechanisms of Cryptotanshinone Intervention
The label-free methods of proteomic combined with metabolomics were applied to explore the mechanisms of Cryptotanshinone intervention in rats with acne. These results propose action mechanisms for the use of CPT in acne, as a safe and potential new drug.
ORGANISM(S): Rattus Rattus 
2021-07-12 | PXD027219 |
ProteomicsComputational Optimization of Spectral Library Size Improves DIA-MS Proteome Coverage and Applications to 15 Tumors
a computational strategy for the size optimization of DIA spectral library, which refines a comprehensive library by a prior analysis of DIA data of a particular tissue type
ORGANISM(S): Homo Sapiens 
2021-12-27 | PXD030648 |
GenomicsGenome wide association study for Bladder Cancer Risk

This study funded by the National Cancer Institute (NCI) involves conducting a genome-wide association study of common genetic variants to identify markers of susceptibility to bladder cancer.

This bladder GWAS has led to the discovery of three novel regions in the genome associated with...

phs000346.v1.p1 | EGA
GenomicsNational Cancer Institute Genome-Wide Association Study of Renal Cell Carcinoma

The National Cancer Institute (NCI) genome-wide association study (GWAS) of renal cell carcinoma (RCC) was conducted to investigate common genetic variants associated with RCC risk. The GWAS includes 1,453 RCC cases and 3,531 controls of European background from 4 studies (3 cohort, 1 case-con...

phs000351.v1.p1 | EGA
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