Researchers have developed the first comprehensive atlas of allele-specific DNA methylation across 39 human cell types, revealing a complex landscape of epigenetic regulation. The study identified ...
The presence of the single nucleotide variation HLA-DRB1*01:03 was associated with severe ulcerative colitis, according to a Danish genome-wide association study. The association between the ...
In a recent study published in the Scientific Reports Journal, researchers used next-generation exome-wide sequencing to identify any association between treatment-resistant depression and uncommon ...
Cystic fibrosis is caused by mutations in the gene encoding the cystic fibrosis transmembrane conductance regulator (CFTR) protein, and nearly 90% of patients have at least one copy of the Phe508del ...
Previous research has revealed that the Apolipoprotein-ε4 (APOE-ε4) allele increases the risk for a variety of diseases in aging populations, specifically Alzheimer's and cardiovascular disease. And ...
In recent years, the DRD4 gene has remained the target of attention for its association with a number of the key staples of common behavioral disorders and illnesses – ADHD 1, Schizophrenia 2, and ...
PTPN11variants in chronic myelomonocytic leukemia: Phenotypic and prognostic correlates. Safety and efficacy of CD7-CAR-T cell in patients with relapsed/refractory T ...
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