Results 221 to 230 of about 38,229 (306)
Deciphering signaling mechanisms and developmental dynamics in extraembryonic mesoderm specification from hESCs. [PDF]
Niu B+14 more
europepmc +1 more source
Aox1 expression is negatively associated with the oxidative muscle fiber phenotype and is downregulated by endurance training. Aox1 deficiency enhances aerobic exercise capacity in mice, at least in part, through the upregulation of PGC‐1α, which promotes oxidative fiber‐type transition, boosts mitochondrial oxidative phosphorylation, and increases ...
Yan Liu+10 more
wiley +1 more source
Uncovering the circadian transcriptome of Nasonia vitripennis: insights into a non-canonical insect model. [PDF]
Tauber E.
europepmc +1 more source
hAMSC‐exo inhibited DPC damage by ameliorating DHT‐induced mitochondrial dysfunction in dependence on Wnt/β‐catenin signaling, and then potentially strengthened crosstalk between DPC and cycling HF cells, which was vital for appropriately regulating HFSC activity to initiate hair growth.
Xiao‐Yu Wang+7 more
wiley +1 more source
dbscATAC: a resource of single-cell super-enhancers/enhancers and gene markers derived from scATAC-seq data. [PDF]
Li Y+13 more
europepmc +1 more source
Obesity reduces in vitro fertilization pregnancy success, with significant decreases in the number of retrieved oocytes, mature oocytes, and cleavage embryos. Mevalonic acid rescues potential productive toxicity of the lipid‐lowering drug simvastatin in follicular development.
Fei Mao+8 more
wiley +1 more source
RECUR: Identifying recurrent amino acid substitutions from multiple sequence alignments
Robbins EH, Liu Y, Kelly S.
europepmc +1 more source
Global hinge sites of proteins as target sites for drug binding. [PDF]
Zhang H, Gur M, Bahar I.
europepmc +1 more source
Inversion techniques and combinatorial identities. Basic hypergeometric identities
Wenchang Chu
openalex +1 more source
Pathway Analyses of Inherited Neuropathies Identify Putative Common Mechanisms of Axon Degeneration
ABSTRACT Objective Inherited neuropathies (IN) are associated with over 100 different genetic mutations presenting with a variety of phenotypes. This complexity suggests multiple pathways may converge onto a limited number of downstream pathways to effect axonal injury.
Christopher R. Cashman+2 more
wiley +1 more source