Mendelian randomization study reveals the causal effect of sex hormone binding globulin on osteoporosis. [PDF]
Zuo GS, Huang Y, Wang Z, Wang H, Wu F.
europepmc +1 more source
Evaluating causal effect in time-to-event observarional data with propensity score matching
Danqi Zhu
openalex +1 more source
The cancer problem is increasing globally with projections up to the year 2050 showing unfavourable outcomes in terms of incidence and cancer‐related deaths. The main challenges are prevention, improved therapeutics resulting in increased cure rates and enhanced health‐related quality of life.
Ulrik Ringborg +43 more
wiley +1 more source
Neither VitD nor VitD binding protein or VitD receptor has causal effect on cancers: a Mendelian randomization study. [PDF]
Wang YZ, Liu HY, Liu J, Xu M, Yang YY.
europepmc +1 more source
Pharmacologic ascorbate (vitamin C) increases ROS, disrupts cellular metabolism, and induces DNA damage in CRPC cells. These effects sensitize tumors to PARP inhibition, producing synergistic growth suppression with olaparib in vitro and significantly delayed tumor progression in vivo. Pyruvate rescue confirms ROS‐dependent activity.
Nicolas Gordon +13 more
wiley +1 more source
Causal effect of potential risk factors on obstructive sleep apnea: a Mendelian randomization study. [PDF]
Chen J +6 more
europepmc +1 more source
LDAcoop: Integrating non‐linear population dynamics into the analysis of clonogenic growth in vitro
Limiting dilution assays (LDAs) quantify clonogenic growth by seeding serial dilutions of cells and scoring wells for colony formation. The fraction of negative wells is plotted against cells seeded and analyzed using the non‐linear modeling of LDAcoop.
Nikko Brix +13 more
wiley +1 more source
Estimating the causal effect of body mass index on gut microbiota variation
Hughes DA +5 more
europepmc +1 more source
Causal effect of coffee consumption on metabolic syndrome in Korean adults: a 2-sample Mendelian randomization study. [PDF]
Kim S, Shin D.
europepmc +1 more source
Therapeutic strategies for MMAE‐resistant bladder cancer through DPP4 inhibition
We established monomethyl auristatin E (MMAE)‐resistant bladder cancer (BC) cell lines by exposure to progressively increasing concentrations of MMAE in vitro. RNA sequencing showed DPP4 expression was increased in MMAE‐resistant BC cells. Both si‐DPP4 and the DPP4 inhibitor sitagliptin suppressed the viability of MMAE‐resistant BC cells.
Gang Li +10 more
wiley +1 more source

