Results 41 to 50 of about 806 (131)
Treatment of severe stable COPD:the multidimensional approach of treatable traits [PDF]
Now that additional treatment options for severe chronic obstructive pulmonary disease (COPD) have emerged in recent years, patients with severe COPD should not be left in the rather hopeless situation of "there is nothing to improve" any more.
Duiverman, Marieke L +7 more
core +1 more source
Abstract Aims Most proteomic analyses in patients with heart failure (HF) focus on the stable ambulatory setting; pathways that drive acute decompensated heart failure (ADHF) are largely uncharacterized. We aimed to examine the associations of cardiometabolic proteins with HF rehospitalization, mortality and diuretic response in patients with ADHF ...
Kenneth T. Hubbell +8 more
wiley +1 more source
Pre‐Existing Diabetes Alters Pulmonary Inflammatory Gene Expression Priming for Injury
Diabetes mellitus (DM) is linked to cardiovascular complications, but its effects on lung health are less understood. Using a streptozotocin‐induced DM mouse model, we found that DM alone upregulated inflammatory pathways, disrupted endothelial integrity, and increased cytokine expression and lung fluid accumulation.
Abdulaziz H. Alanazi +5 more
wiley +1 more source
Relevance of obesity and overweight to salivary and plasma proteomes of human young adults from Brazil / Relevância da obesidade e sobrepeso para os proteomas salivares e plasmáticos de adultos jovens humanos do Brasil [PDF]
Obesity is a chronic condition related to multiple comorbidities such as hypertension, type 2 diabetes, periodontal and cardiovascular diseases. Obesity can lead to a metabolic change, creating a prolonged and low-intensity inflammatory process.
da Silva, Carlos Vinicius Ferreira +5 more
core
Abstract While members of large paralogous protein families share structural features, their functional niches often diverge significantly. Serine protease inhibitors (SERPINs), whose members typically function as covalent inhibitors of serine proteases, are one such family.
Laura M. Haynes +4 more
wiley +1 more source
Most gene therapies function via manipulating hepatocytes, while it remains difficult to modulate macrophages and other non‐parenchymal cells. Fundamental cell biology is demonstrated, but not a lack of uptake accounts for the lack of translation: hepatocytes are polyploid cells and their polyploidy enables them to contain significantly higher amounts ...
Cheng Lin +22 more
wiley +1 more source
Introduction. Panniculitis is one of the rarest manifestations of α1-antitrypsin (AAT) deficiency. The disease is characterised by a typicalclinical picture with inflammatory tumours, necrosis, ulcerations, fistulasand oily liquid.
Michał Skroński +3 more
doaj
Alpha‐1 Antitrypsin Inclusions Sequester GRP78 in a Bile Acid–Inducible Manner
ABSTRACT Background and Aims The homozygous PiZ mutation (PIZZ genotype) constitutes the predominant cause of severe alpha‐1 antitrypsin (AAT) deficiency and leads to liver disease via hepatocellular AAT aggregation. We systematically analysed the composition of AAT aggregates and studied the impact of bile acids.
Igor Spivak +13 more
wiley +1 more source
CREG1: Its Role as a Master Regulator of Liver Function [PDF]
Mammalian development involves a complex system of regulatory signals and reactions resulting in highly differentiated cell types with specific structure and function.
Jahan, Iffat
core +1 more source
Malaria is a parasitic infectious disease considered a public health problem. Acute respiratory distress syndrome (ARDS) is a complication in malaria‐infected individuals with a high mortality rate (80% to 100%) and can occur before, during, or after antimalarial drug treatment. Although inflammation and epithelial/endothelial injury pathways have been
Lívia Rosa-Fernandes +9 more
wiley +1 more source

