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Disease on EC 3.4.21.71 - Pancreatic elastase II

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DISEASE
TITLE OF PUBLICATION
LINK TO PUBMED
Aneurysm
Assessment of the role of pancreatic proteases in human abdominal aortic aneurysms and occlusive disease.
Aortic Aneurysm, Abdominal
Assessment of the role of pancreatic proteases in human abdominal aortic aneurysms and occlusive disease.
COVID-19
Inflammation Profiling of Critically Ill Coronavirus Disease 2019 Patients.
Genetic Diseases, Inborn
Comparative molecular docking analysis of essential oil constituents as elastase inhibitors.
Infections
Effects of a high-protein diet on host resistance to Paracoccidioides brasiliensis in mice.
What is the performance of novel synovial biomarkers for detecting periprosthetic joint infection in the presence of inflammatory joint disease?
Joint Diseases
What is the performance of novel synovial biomarkers for detecting periprosthetic joint infection in the presence of inflammatory joint disease?
Leukemia, Myelogenous, Chronic, BCR-ABL Positive
Association between BMI-1 expression, acute graft-versus-host disease, and outcome following allogeneic stem cell transplantation from HLA-identical siblings in chronic myeloid leukemia.
Expression of the leukemic prognostic marker CD7 is linked to epigenetic modifications in chronic myeloid leukemia.
Myocardial Infarction
Elastase-2, an angiotensin II-generating enzyme, contributes to increased angiotensin II in resistance arteries of mice with myocardial infarction.
Neoplasms
Inflammation Profiling of Critically Ill Coronavirus Disease 2019 Patients.
Neutrophil extracellular trap formation in supragingival biofilms.
The TLR4 Agonist Fibronectin Extra Domain A is Cryptic, Exposed by Elastase-2; use in a fibrin matrix cancer vaccine.
Netherton Syndrome
Elastase 2 is expressed in human and mouse epidermis and impairs skin barrier function in Netherton syndrome through filaggrin and lipid misprocessing.
[Elastase 2, a key player in the integrity of the epidermal barrier and in Netherton syndrome.]
Neutropenia
Heterozygous M1V variant of ELA-2 gene mutation associated with G-CSF refractory severe congenital neutropenia.
Homozygous HAX1 mutations in severe congenital neutropenia patients with sporadic disease: a novel mutation in two unrelated British kindreds.
Kostmann syndrome or infantile genetic agranulocytosis, part two: Understanding the underlying genetic defects in severe congenital neutropenia.
Low levels of serum elastase are not associated with mutations in ELA-2 elastase encoding gene in chronic idiopathic neutropenia.
Pancreatic Diseases
Human serum alpha 1-antichymotrypsin is an inhibitor of pancreatic elastases.
Pancreatitis
Isolation and characterization of a pancreatic elastase from plasma of patients with acute pancreatitis.
Studies on immunoreactive pancreatic elastase 2 in human serum.
Studies on the ascites fluid of acute pancreatitis in man.
Pulmonary Emphysema
Comparative molecular docking analysis of essential oil constituents as elastase inhibitors.
Retinal Vein Occlusion
Higher Aqueous Levels of Resistin and Lipocalin-2 Indicated Worse Visual Improvement following anti-VEGF Therapy in Patients with Retinal Vein Occlusion.
Wiskott-Aldrich Syndrome
Homozygous HAX1 mutations in severe congenital neutropenia patients with sporadic disease: a novel mutation in two unrelated British kindreds.