Results 51 to 60 of about 1,033,501 (330)

The frequency of metabolic syndrome in patients with the subclinical hypothyroidism [PDF]

open access: yesVojnosanitetski Pregled, 2018
Background/Aim. An increased cardiovascular risk of thyroid dysfunction is associated with the impairment of lipid and lipoprotein metabolism, endothelial dysfunction, metabolic, hormonal, hemodynamic changes and coagulation disorders.
Mulić Mersudin   +4 more
doaj   +1 more source

Physiological conditions influencing regenerative potential of stem cells [PDF]

open access: yes, 2016
Stem cells are being used in the treatment of cardivovascular diseases. Here, we review the physiologic and pathologic conditions that impact the regenerative potential of stem cells in the treatment of cardiovascular diseases which include the influence
Avitabile, Daniele   +3 more
core   +1 more source

Structural biology of ferritin nanocages

open access: yesFEBS Letters, EarlyView.
Ferritin is a conserved iron‐storage protein that sequesters iron as a ferric mineral core within a nanocage, protecting cells from oxidative damage and maintaining iron homeostasis. This review discusses ferritin biology, structure, and function, and highlights recent cryo‐EM studies revealing mechanisms of ferritinophagy, cellular iron uptake, and ...
Eloise Mastrangelo, Flavio Di Pisa
wiley   +1 more source

Metabolic syndrome and restenosis of carotid artery [PDF]

open access: yesVojnosanitetski Pregled, 2014
[Projekat Ministarstva nauke Republike Srbije, br. III41002]
Maksimović Miloš   +2 more
doaj   +1 more source

Non-alcoholic fatty liver disease connections with fat-free tissues: A focus on bone and skeletal muscle [PDF]

open access: yes, 2017
The estimates of global incidence and prevalence of non-alcoholic fatty liver disease (NAFLD) are worrisome, due to the parallel burden of obesity and its metabolic complications. Indeed, excess adiposity and insulin resistance represent two of the major
Chiesa, Claudio   +4 more
core   +2 more sources

Molecular characterisation of human penile carcinoma and generation of paired epithelial primary cell lines

open access: yesMolecular Oncology, EarlyView.
Generation of two normal and tumour (cancerous) paired human cell lines using an established tissue culture technique and their characterisation is described. Cell lines were characterised at cellular, protein, chromosome and gene expression levels and for HPV status.
Simon Broad   +12 more
wiley   +1 more source

Prevalence of metabolic syndrome in mainland china: a meta-analysis of published studies

open access: yesBMC Public Health, 2016
Background Metabolic syndrome (MS) comprises a set of conditions that are risk factors for cardiovascular diseases and diabetes. Numerous epidemiological studies on MS have been conducted, but there has not been a systematic analysis of the prevalence of
Ri Li   +8 more
doaj   +1 more source

Comparison of the established definition criteria for diagnosing metabolic syndrome between overweight and obese children in Vojvodina [PDF]

open access: yesVojnosanitetski Pregled, 2011
Background/Aim. Metabolic syndrome is a clinical term which encompasses obesity, insulin resistance, dyslipidemia, hypertension, as well as an increased risk of the development of diabetes mellitus type 2 and cardiovascular disorders in early ...
Vorgučin Ivana   +3 more
doaj   +1 more source

Body composition in patients with early rheumatoid arthritis

open access: yesНаучно-практическая ревматология, 2021
Aim of the study was to clarify the body composition in patients with early rheumatoid arthritis before starting therapy with synthetic basic anti-inflammatory drugs, genetically engineered biological drugs and glucocorticoids using dual-energy X-ray ...
Yu. N. Gorbunova   +5 more
doaj   +1 more source

Rare diseases leading to childhood Glaucoma. epidemiology, pathophysiogenesis, and management [PDF]

open access: yes, 2015
Noteworthy heterogeneity exists in the rare diseases associated with childhood glaucoma. Primary congenital glaucoma is mostly sporadic; however, 10% to 40% of cases are familial. CYP1B1 gene mutations seem to account for 87% of familial cases and 27% of
Abdolrahimzadeh, Solmaz   +5 more
core   +3 more sources

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