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UnknownSpecificity of problem-solving skills training in mothers of children newly diagnosed with cancer: results of a multisite randomized clinical trial.
Not available
S-EPMC3607672 | biostudies-literature
UnknownReproductive Risk Factor Patterns in Caribbean Women With Breast Cancer Across 4 Generations.
Not available
S-EPMC11581535 | biostudies-literature
UnknownIncorporation of Biomarkers Into Risk Assessment for Allocation of Antihypertensive Medication According to the 2017 ACC/AHA High Blood Pressure Guideline: A Pooled Cohort Analysis.
Not available
S-EPMC8330617 | biostudies-literature
UnknownInitial Vancomycin Taper for the Prevention of Recurrent Clostridioides difficile Infection: A Randomized Clinical Trial.
Not available
S-EPMC12949445 | biostudies-literature
UnknownLow-dose dopamine or low-dose nesiritide in acute heart failure with renal dysfunction: the ROSE acute heart failure randomized trial.
Not available
S-EPMC3934929 | biostudies-literature
UnknownElevated plasma complement factor H related 5 protein is associated with venous thromboembolism.
Not available
S-EPMC10247781 | biostudies-literature
GenomicsEGAD00000000055
COLO-829 is a publicly available immortal cancer cell line and COLO-829BL is a lymphoblastoid cell line derived from the same patient
EGAD00000000055 | EGA
GenomicsA Comprehensive Catalogue of Somatic Mutations from a Human Cancer Genome
We have carried out complete sequencing of the genome of the human male maligant melanoma cell line COLO-829 using the Illumina Genome Analyzer II. We generated a sequencing library with a median insert size of ~200 bp following random fragmentation and gel fractionation of the genomic DNA. We seque...
EGAS00000000052 | EGA
GenomicsICGC breast cancer sequencing project SNP6 data
Affymetrix SNP6.0 breast cancer genome sequencing data
EGAD00010000915 | EGA
GenomicsEGAS00001000195-sc-20150416 - samples
We propose to definitively characterise the somatic genetics of breast cancer through generation of comprehensive catalogues of somatic mutations in breast cancer cases by high coverage genome sequencing coupled with integrated transcriptomic and methylation analyses.
EGAD00001001337 | EGA
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