Results 321 to 330 of about 1,019,575 (429)
Slowly Progressive Rhabdomyolysis Post COVID-19: Insights for Acute Kidney Injury Prediction With Discordant Creatine Kinase and Myoglobin Elevations. [PDF]
Okubo T+10 more
europepmc +1 more source
Abstract Background and Purpose The JAK–STAT signalling pathway has been extensively spotlighted as a therapeutic target for various diseases. This study assessed the inhibitory effects of a novel small molecule, IN‐115314, on JAK–STAT pathway. Experimental Approach The IC50 values of IN‐115314 for JAK1–pSTAT3 and JAK2–pSTAT5 were determined in canine ...
Jae‐Hun Ahn+16 more
wiley +1 more source
Maintaining energy provision in the heart: the creatine kinase system in ischaemia-reperfusion injury and chronic heart failure. [PDF]
Lygate CA.
europepmc +1 more source
CAR‐T Cell Therapy in Autoimmune Setting: A New Appealing Approach Extendable to Allergy?
Allergy, EarlyView.
Federico Rossi+2 more
wiley +1 more source
Significance of detecting cardiac troponin I and creatine kinase MB in critically Ill children without primary cardiac illness. [PDF]
Zhang Y, Cao Y, Xin Y, Liu Y.
europepmc +1 more source
ABSTRACT The DOCK3 gene (NM_004947.5) is located on chromosome 3p21.2 spanning 53 exons and encodes the dedicator of cytokinesis 3 protein. DOCK3 belongs to the family of guanine nucleotide exchange factors (GEFs) that activate GTPases. DOCK3 is expressed almost exclusively in the central nervous system and has been shown to promote axonal outgrowth ...
Khurram Liaqat+7 more
wiley +1 more source
Feasibility of aligning creatine kinase MB activity and mass data in multicentre trials using generalized additive modelling. [PDF]
Hoenicka M+4 more
europepmc +1 more source
Our Translational Loop integrates patient genetic data with Drosophila models to study disease mechanisms. We identified ACO2 variants in a patient linked to ICRD and show that our animal model mirrors key aspects of the disease. These insights help pinpoint therapeutic targets, advancing research toward treatments for rare genetic disorders.
Edgar Buhl+15 more
wiley +1 more source