Results 141 to 150 of about 6,585 (184)

Genetic Basis of Brugada Syndrome. [PDF]

Biomedicines
Xie X, Chen Y, Li Z, Sun Y, Chen G.
europepmc   +1 more source

lncRNA LINC02323 predicts adverse neoadjuvant chemotherapy outcomes of gastric cancer patients and regulates cell sensitivity to 5-fluorouracil by negatively modulating miR-139-3p. [PDF]

Ann Med
Chen Z, Zhang X, Li Z, Zhang H, Wang Z.
europepmc   +1 more source

Genetic Evidence for the Benefits and Risks of Glucose-Lowering Drugs on Cardiovascular-Kidney-Metabolic Syndrome: A Drug-Target Mendelian Randomization Study. [PDF]

Int J Med Sci
Lu J, Sun S, Shang X, Jiang S, Deng Z, Wang S, Wei C, Hu J, Li W.   +8 more
europepmc   +1 more source

A novel ABCC9 variant in a Greek family with Cantu syndrome affecting multiple generations highlights the functional role of the SUR2B NBD1. [PDF]

Am J Med Genet A
Gao J, Ververi A, Thompson E, Tryon R, Sotiriadis A, Rouvalis F, Grange DK, Giannios C, Nichols CG.   +8 more
europepmc   +1 more source

Endothelial-Enriched lncRNA Gm39822 Modulates Inflammation and Dysfunction in Non-Diabetic Endothelial Cells. [PDF]

Int J Mol Sci
Chandra A, Bektik E, Randhawa V, Feinberg MW.   +3 more
europepmc   +1 more source

Combining Apatinib and Oxaliplatin Remodels the Immunosuppressive Tumor Microenvironment and Sensitizes Desert-Type Gastric Cancer to Immunotherapy. [PDF]

Cancer Res
Lin GT, Yan C, Li LJ, Qiu XW, Zhao YX, Lin JL, Chen YJ, Feng C, Chen SQ, Xie JW, Zheng CH, Nomura S, Huang CM, Li P, Cao LL.   +14 more
europepmc   +1 more source

Gain-of-function mutations in KATP channel subunits compromise colonic tight junction integrity and epithelial homeostasis in murine models of Cantú syndrome. [PDF]

Front Med (Lausanne)
Maqoud F, Mallardi D, Orlando A, Tricarico D, Nichols CG, Antonacci M, Bianco G, Armentano R, Grassi I, Valentini AM, Russo F.   +10 more
europepmc   +1 more source

A Chromosome-level Assembly and Functional Genomic Resources for the Model Annelid Capitella teleta. [PDF]

Genome Biol Evol
Davies BE, Gonzalez P, Sur A, Wei J, Frankish T, Montagne J, Carrillo-Baltodano AM, Guynes K, Liang Y, Donnellan RD, Travis Moreland R, Singh S, Zhang S, Yu R, Wolfsberg TG, Meyer NP, Seaver EC, Baxevanis AD, Martín-Durán JM.   +18 more
europepmc   +1 more source

A <i>de novo</i> variant of the <i>COL3A1</i> gene: causality of vascular Ehlers-Danlos syndrome. [PDF]

Adv Lab Med
Gutiérrez Romero E, Padilla Apuntate N, Izquierdo Álvarez S.   +2 more
europepmc   +1 more source