Results 21 to 30 of about 2,225 (187)

Biology of Cardiac Troponins: Emphasis on Metabolism

open access: yesBiology, 2022
Understanding of the biology of endo- and exogenous molecules, in particular their metabolism, is not only of great theoretical importance, but also of high practical significance, since many molecules serve as drug targets or markers for the laboratory ...
Aleksey M. Chaulin
doaj   +1 more source

Features of the Metabolisms of Cardiac Troponin Molecules—Part 1: The Main Stages of Metabolism, Release Stage

open access: yesCurrent Issues in Molecular Biology, 2022
Cardiac troponins (cTns) have long been the most valuable and specific biomarkers for detecting ischemic myocardial cells (MCs) injury, which is one of the key signs of myocardial infarction (MI).
Aleksey Michailovich Chaulin
doaj   +1 more source

A Leptin Receptor Antagonist Attenuates Adipose Tissue Browning and Muscle Wasting in Infantile Nephropathic Cystinosis-Associated Cachexia

open access: yesCells, 2021
Mice lacking the functional cystinosin gene (Ctns−/−), a model of infantile nephropathic cystinosis (INC), exhibit the cachexia phenotype with adipose tissue browning and muscle wasting.
Alex Gonzalez   +5 more
doaj   +1 more source

Activities critical to success and growth of clinical trials networks. What is needed and how are we doing? An Australian and New Zealand perspective

open access: yesTrials, 2023
Background Clinical trial evidence underpins evidence-based medicine and the improvement of healthcare worldwide. In Australasia, a significant proportion of clinical trials are conducted by geographically dispersed and multidisciplinary clinical ...
Megan Sanders   +4 more
doaj   +1 more source

Myocardial Injury Predicts Risk of Short-Term All-Cause Mortality in Patients With COVID-19: A Dose–Response Meta-Analysis

open access: yesFrontiers in Cardiovascular Medicine, 2022
ObjectivePredictive value of myocardial injury as defined by elevated cardiac tropnins (cTns) in patients with COVID-19 has not been fully investigated. We performed a meta-analysis to evaluate the dose–response relationship between myocardial injury and
Yuehua Li   +3 more
doaj   +1 more source

Targeting interleukin‐1 for reversing fat browning and muscle wasting in infantile nephropathic cystinosis

open access: yesJournal of Cachexia, Sarcopenia and Muscle, 2021
Background Ctns−/− mice, a mouse model of infantile nephropathic cystinosis, exhibit hypermetabolism with adipose tissue browning and profound muscle wasting.
Wai W. Cheung   +7 more
doaj   +1 more source

Evaluation of the efficacy of cystinosin supplementation through CTNS mRNA delivery in experimental models for cystinosis

open access: yesScientific Reports, 2023
Messenger RNA (mRNA) therapies are emerging in different disease areas, but have not yet reached the kidney field. Our aim was to study the feasibility to treat the genetic defect in cystinosis using synthetic mRNA in cell models and ctns −/− zebrafish ...
Tjessa Bondue   +15 more
doaj   +1 more source

Transcriptional and Posttranscriptional Regulation of the CTNS Gene [PDF]

open access: yesPediatric Research, 2011
Cell cysteine (Cys) levels and/or the [Cys/CySS] redox potential have been shown to regulate mRNA levels of the CTNS gene, which encodes for a lysosomal cystine (CySS) carrier that is defective in cystinosis. To investigate the mechanisms involved CTNS mRNA regulation, different portions of the CTNS promotor were cloned into a luciferase vector and ...
Corallini, Serena   +5 more
openaire   +2 more sources

Mutational spectrum of the CTNS gene in Italy [PDF]

open access: yesEuropean Journal of Human Genetics, 2003
Classic nephropathic or infantile cystinosis (NC) is an autosomal recessive disorder; the gene coding for the integral membrane protein cystinosin, which is responsible for membrane transport of cystine (CTNS), was cloned. Mutation analysis of the CTNS gene of Caucasian patients revealed a common 57-kb deletion, and several other mutations spread ...
S. Mason   +10 more
openaire   +5 more sources

Stem cell microvesicles transfer cystinosin to human cystinotic cells and reduce cystine accumulation in vitro. [PDF]

open access: yesPLoS ONE, 2012
Cystinosis is a rare disease caused by homozygous mutations of the CTNS gene, encoding a cystine efflux channel in the lysosomal membrane. In Ctns knockout mice, the pathologic intralysosomal accumulation of cystine that drives progressive organ damage ...
Diana M Iglesias   +13 more
doaj   +1 more source

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