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UnknownComplete Surgical Excision Is Essential for the Management of Patients With Breast Implant-Associated Anaplastic Large-Cell Lymphoma.
Not available
S-EPMC4872006 | biostudies-literature
ProteomicsCovalent inhibitor design confers activity against both GDP- and GTP-bound forms of KRAS G12C
The discovery of KRAS G12C inactive state inhibitors represents a significant advancement in the field of precision oncology. While inactive state inhibition shows promise in patients, SWII-binding inhibitors targeting both inactive and active states remain an underdeveloped therapeutic modality. H...
ORGANISM(S): Homo sapiens (Human) 
2025-11-04 | PXD062227 | Pride
GenomicsPopulation whole-genome bisulfite sequencing across two tissues highlights environment as principal source of human methylome variation
The study includes whole-genome bisulfite sequencing (WGBS) on 34 adipose (7 MZ pairs, 6 DZ pairs and 8 singletons) and 27 blood (7 MZ pairs, 6 DZ pairs and 1 singleton) DNA samples derived from a total of 43 female twins belonging to the MuTHER/TwinsUK cohort. We generated 11.5 billion 100bp paired...
EGAS00001001569 | EGA
Genomicsena-DATASET-MCGILL-25-11-2015-16:17:41:115-10 - samples
Description not provided
EGAD00001001689 | EGA
Genomicsena-DATASET-MCGILL-25-11-2015-16:14:18:542-9 - samples
Description not provided
EGAD00001001688 | EGA
GenomicsMcGill-KCL WGBS
Data Access Committee EGAC00001000402
EGAC00001000402 | EGA
TranscriptomicsCharacterization of Functional Methylomes by Next-Generation RNA Sequencing
Comprehensive analysis of the human adipose epigenome by transcriptome, open chromatin and methylome sequencing studies.
ORGANISM(S): Homo sapiens 
2015-05-01 | E-MTAB-3182 | biostudies-arrayexpress
GenomicsCharacterization of Functional Methylomes by Next-Generation Methylation Capture Sequencing
Comprehensive analysis of the human adipose epigenome by transcriptome, open chromatin and methylome sequencing studies.
ORGANISM(S): Homo sapiens 
2015-05-01 | E-MTAB-3181 | biostudies-arrayexpress
GenomicsPD
WTCCC project samples from the Parkinson's disase cohort
EGAD00000000057 | EGA
GenomicsGenome wide association scan in Parkinson's disease
Genome-wide association scan was performed in 1,705 cases of parkinson's genotyped on the Illumina Human 660W SNP array, and 5,175 controls genotyped on the Illumina1.2M-Duo. Analysis was carried out on the overlaps set of SNPs.
EGAS00000000034 | EGA
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