Results 1 to 10 of about 106 (74)
Hypertension is a dominating risk factor for cardiovascular disease. To characterize the genomic response to hypertension, we administered vehicle or angiotensin II to mice and performed gene expression analyses.
Catarina Rippe+7 more
doaj +3 more sources
OBJECTIVE: To investigate the associations of miRNA-132, miRNA-182, and miRNA-124 with long-term depression and elucidate their target genes and translational implications utilizing miRabel, a bioinformatics tool.
Shamaila Wadud+5 more
doaj +4 more sources
Complex control of GABA(A) receptor subunit mRNA expression: variation, covariation, and genetic regulation. [PDF]
GABA type-A receptors are essential for fast inhibitory neurotransmission and are critical in brain function. Surprisingly, expression of receptor subunits is highly variable among individuals, but the cause and impact of this fluctuation remains unknown.
Megan K Mulligan+5 more
doaj +4 more sources
Background Autism spectrum disorder (ASD) is a neurodevelopmental disorder that is difficult to diagnose. Inflammatory bowel disease (IBD) is a common chronic digestive disease. Previous studies have shown a potential correlation between ASD and IBD, but
Jinyi Zhu, Haoran Meng, Li Zhang, Yan Li
doaj +2 more sources
Background The tanshinones and phenolic acids in Salvia miltiorrhiza (also named Danshen) have been confirmed for the treatment of coronary heart disease (CHD), but the action mechanisms remain elusive.
Dongxue Wu+4 more
doaj +2 more sources
Analyzing and validating the prognostic value and mechanism of colon cancer immune microenvironment
Background Colon cancer is a disease with high malignancy and incidence in the world. Tumor immune microenvironment (TIM) and tumor mutational burden (TMB) have been proved to play crucial roles in predicting clinical outcomes and therapeutic efficacy ...
Xinyi Wang+4 more
doaj +2 more sources
The immunodeficiency, centromeric region instability, and facial anomalies syndrome (ICF) is the only disease known to result from a mutated DNA methyltransferase gene, namely, DNMT3B.
Melanie Ehrlich+2 more
exaly +2 more sources
PRDM16 expression and function in mammalian cochlear development
Abstract Background PR domain containing 16 (PRDM16) is a key transcriptional regulator in the development of craniofacial, adipose, and neural tissues. Our lab identified PRDM16 expression in the epithelial cells of the Kölliker's organ (KO) that starts at ~E13.5 and is maintained until KO disappearance.
Michael Ebeid+5 more
wiley +1 more source
Methylation refers to DNA markers responsible for gene‐activation. It is investigated if methylation changed in response to maternal folate intake during pregnancy. Eight genes have increased (hyper)methylation in fetal and adult mouse liver in response to maternal folate depletion.
Dieuwertje E. Kok+7 more
wiley +1 more source
Cultures of rat precision cut liver slices (PCLS) were used for ex vivo blood vessel function analysis via live recording. The sGC activator BI703704 differentiates from the sGC stimulator Riociguat in the prevention of serotonin induced blood vessel contraction of normal and fibrotic rat liver slices.
Anouk Oldenburger+6 more
wiley +1 more source