Results 191 to 200 of about 4,753,986 (376)
Prevalence and genetic variants of G6PD deficiency among two Malagasy populations living in Plasmodium vivax-endemic areas [PDF]
Rosalind E. Howes +9 more
openalex +1 more source
Strategic validation of variants of uncertain significance inECHS1genetic testing [PDF]
Yoshihito Kishita +17 more
openalex +1 more source
This study characterizes the responses of primary acute myeloid leukemia (AML) patient samples to the MCL‐1 inhibitor MIK665. The results revealed that monocytic differentiation is associated with MIK665 sensitivity. Conversely, elevated ABCB1 expression is a potential biomarker of resistance to the treatment, which can be overcome by the combination ...
Joseph Saad +17 more
wiley +1 more source
Plasma‐based detection of actionable mutations is a promising approach in lung cancer management. Analysis of ctDNA with a multigene NGS panel identified TP53, KRAS, and EGFR as the most frequently altered, with TP53 and KRAS in treatment‐naïve patients and TP53 and EGFR in previously treated patients.
Giovanna Maria Stanfoca Casagrande +11 more
wiley +1 more source
Aggressive prostate cancer is associated with pericyte dysfunction
Tumor‐produced TGF‐β drives pericyte dysfunction in prostate cancer. This dysfunction is characterized by downregulation of some canonical pericyte markers (i.e., DES, CSPG4, and ACTA2) while maintaining the expression of others (i.e., PDGFRB, NOTCH3, and RGS5).
Anabel Martinez‐Romero +11 more
wiley +1 more source
Genetic testing in epithelial ovarian cancer includes both germline and tumor‐testing. This approach often duplicates resources. The current prospective study assessed the feasibility of tumor‐first multigene testing by comparing tumor tissue with germline testing of peripheral blood using an 18‐gene NGS panel in 106 patients.
Elisabeth Spenard +12 more
wiley +1 more source
Systemic lupus erythematosus: genetic variants in Xq28 region
Noha Doudar +3 more
doaj +1 more source
Detection of extrachromosomal circular DNA (eccDNA) in plasma samples from EGFR‐mutated non‐small cell lung cancer patients. Plasma was collected before and during treatment with the EGFR‐tyrosine kinase inhibitor osimertinib. Plasma eccDNA was detected in all cancer samples, and the presence of the EGFR gene on eccDNA serves as a potential biomarker ...
Simone Stensgaard +5 more
wiley +1 more source
Meta-analysis of TCF7L2 and SLC30A8 gene polymorphisms concerning type 2 diabetes risk
Background Diabetes, defined by high blood glucose readings, poses important worldwide health risks. T2DM is the most prevalent form, accounting for 90% of cases. Genetic variations in genes like SLC30 A8 (rs13266634) and TCF7L2 (rs7903146 and rs12255372)
Jethendra Kumar Muruganantham +1 more
doaj +1 more source
Genetic variants and the risk of gestational diabetes mellitus: a systematic review [PDF]
Cuilin Zhang +6 more
openalex +1 more source

