- Home
- Publications
- Publication Search
- Publication Details
Title
Plasminflammation—An Emerging Pathway to Bradykinin Production
Authors
Keywords
-
Journal
Frontiers in Immunology
Volume 10, Issue -, Pages -
Publisher
Frontiers Media SA
Online
2019-08-27
DOI
10.3389/fimmu.2019.02046
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Identification of the recently described plasminogen gene mutation p.Lys330Glu in a family from Northern Germany with hereditary angioedema
- (2019) Andreas Recke et al. Clinical and Translational Allergy
- Knockdown of circulating C1 inhibitor induces neurovascular impairment, glial cell activation, neuroinflammation, and behavioral deficits
- (2019) Dorit Farfara et al. GLIA
- A missense mutation of the plasminogen gene in hereditary angioedema with normal C1 inhibitor in Japan
- (2018) Hiromasa Yakushiji et al. ALLERGY
- On the pathogenicity of the plasminogen K330E mutation for hereditary angioedema
- (2018) A. E. Germenis et al. ALLERGY
- Angioedema
- (2018) Samuel Luyasu et al. ANNALS OF ALLERGY ASTHMA & IMMUNOLOGY
- Coagulation factor XII in thrombosis and inflammation
- (2018) Coen Maas et al. BLOOD
- Cardiovascular diseases in congenital prekallikrein deficiency
- (2018) Antonio Girolami et al. BLOOD COAGULATION & FIBRINOLYSIS
- A transcriptomics study of hereditary angioedema attacks
- (2018) Giuseppe Castellano et al. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
- Hereditary angioedema with normal C1 inhibitor: Four types and counting
- (2018) Bruce L. Zuraw JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
- Hereditary angioedema: the plasma contact system out of control
- (2018) S. De Maat et al. JOURNAL OF THROMBOSIS AND HAEMOSTASIS
- Oral Plasma Kallikrein Inhibitor for Prophylaxis in Hereditary Angioedema
- (2018) Emel Aygören-Pürsün et al. NEW ENGLAND JOURNAL OF MEDICINE
- Blood-derived plasminogen drives brain inflammation and plaque deposition in a mouse model of Alzheimer’s disease
- (2018) Sarah K. Baker et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- A mechanism for hereditary angioedema with normal C1-inhibitor: an inhibitory regulatory role for the factor XII heavy chain
- (2018) Ivan Ivanov et al. BLOOD
- Dominant-negative SERPING1 variants cause intracellular retention of C1 inhibitor in hereditary angioedema
- (2018) Didde Haslund et al. JOURNAL OF CLINICAL INVESTIGATION
- Factor XII truncation accelerates activation in solution
- (2018) S. de Maat et al. JOURNAL OF THROMBOSIS AND HAEMOSTASIS
- Comparing Pathways of Bradykinin Formation in Whole Blood From Healthy Volunteers and Patients With Hereditary Angioedema Due to C1 Inhibitor Deficiency
- (2018) Xavier Charest-Morin et al. Frontiers in Immunology
- Cleaved kininogen as a biomarker for bradykinin release in hereditary angioedema
- (2017) Zonne L.M. Hofman et al. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
- Cytokine and estrogen stimulation of endothelial cells augments activation of the prekallikrein-high molecular weight kininogen complex: Implications for hereditary angioedema
- (2017) Kusumam Joseph et al. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
- Inhibiting Plasma Kallikrein for Hereditary Angioedema Prophylaxis
- (2017) Aleena Banerji et al. NEW ENGLAND JOURNAL OF MEDICINE
- Urticaria and Prodromal Symptoms Including Erythema Marginatum in Danish Patients with Hereditary Angioedema
- (2016) E Rasmussen et al. ACTA DERMATO-VENEREOLOGICA
- Treatment for hereditary angioedema with normal C1-INH and specific mutations in theF12gene (HAE-FXII)
- (2016) K. Bork et al. ALLERGY
- A Novel Approach to the Treatment of Orolingual Angioedema After Tissue Plasminogen Activator Administration
- (2016) Lesley Pahs et al. ANNALS OF EMERGENCY MEDICINE
- Polyphosphate colocalizes with factor XII on platelet-bound fibrin and augments its plasminogen activator activity
- (2016) J. L. Mitchell et al. BLOOD
- Hyperfibrinolysis increases blood-brain barrier permeability by a plasmin- and bradykinin-dependent mechanism
- (2016) O. A. Marcos-Contreras et al. BLOOD
- Plasmin is a natural trigger for bradykinin production in patients with hereditary angioedema with factor XII mutations
- (2016) Steven de Maat et al. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
- Angioedema attacks in patients with hereditary angioedema: Local manifestations of a systemic activation process
- (2016) Zonne L.M. Hofman et al. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
- Factor XII: form determines function
- (2016) S. de Maat et al. JOURNAL OF THROMBOSIS AND HAEMOSTASIS
- Erythema Marginatum as an Early Symptom of Hereditary Angioedema: Case Report of 2 Newborns
- (2016) I. Martinez-Saguer et al. PEDIATRICS
- Elevated D-dimers in attacks of hereditary angioedema are not associated with increased thrombotic risk
- (2015) A. Reshef et al. ALLERGY
- Defective glycosylation of coagulation factor XII underlies hereditary angioedema type III
- (2015) Jenny Björkqvist et al. JOURNAL OF CLINICAL INVESTIGATION
- Comprehensive study into the activation of the plasma enzyme systems during attacks of hereditary angioedema due to C1-inhibitor deficiency
- (2015) Dorottya Csuka et al. Orphanet Journal of Rare Diseases
- Activation of the factor XII-driven contact system in Alzheimer’s disease patient and mouse model plasma
- (2015) Daria Zamolodchikov et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Tranexamic acid as maintenance treatment for non-histaminergic angioedema: analysis of efficacy and safety in 37 patients
- (2014) C. Wintenberger et al. CLINICAL AND EXPERIMENTAL IMMUNOLOGY
- Plasmin deficiency leads to fibrin accumulation and a compromised inflammatory response in the mouse brain
- (2014) K. Hultman et al. JOURNAL OF THROMBOSIS AND HAEMOSTASIS
- The influence of trigger factors on hereditary angioedema due to C1-inhibitor deficiency
- (2014) Zsuzsanna Zotter et al. Orphanet Journal of Rare Diseases
- Contact System Activation on Endothelial Cells
- (2014) Steven de Maat et al. SEMINARS IN THROMBOSIS AND HEMOSTASIS
- Depression and anxiety in patients with hereditary angioedema
- (2013) Andrew S. Fouche et al. ANNALS OF ALLERGY ASTHMA & IMMUNOLOGY
- De novo homozygous mutation of the C1 inhibitor gene in a patient with hereditary angioedema
- (2013) Valeria Bafunno et al. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
- Ongoing Contact Activation in Patients with Hereditary Angioedema
- (2013) Joke Konings et al. PLoS One
- Hereditary angioedema with normal C1 inhibitor function: Consensus of an international expert panel
- (2012) Bruce L. Zuraw et al. ALLERGY AND ASTHMA PROCEEDINGS
- Recombinant C1-Inhibitor
- (2011) Anurag Relan et al. BIODRUGS
- Alterations of coagulation and fibrinolysis in patients with angioedema due to C1-inhibitor deficiency
- (2011) M. van Geffen et al. CLINICAL AND EXPERIMENTAL IMMUNOLOGY
- Landmark Publication from The American Journal of the Medical Sciences
- (2010) William Osler AMERICAN JOURNAL OF THE MEDICAL SCIENCES
- Human Plasminogen Kringle 3: Solution Structure, Functional Insights, Phylogenetic Landscape,
- (2010) Martin T. Christen et al. BIOCHEMISTRY
- Venous thrombosis risk associated with plasma hypofibrinolysis is explained by elevated plasma levels of TAFI and PAI-1
- (2010) M. E. Meltzer et al. BLOOD
- Icatibant, a New Bradykinin-Receptor Antagonist, in Hereditary Angioedema
- (2010) Marco Cicardi et al. NEW ENGLAND JOURNAL OF MEDICINE
- Regulation of cell signalling by uPAR
- (2009) Harvey W. Smith et al. NATURE REVIEWS MOLECULAR CELL BIOLOGY
- Misfolded proteins activate Factor XII in humans, leading to kallikrein formation without initiating coagulation
- (2008) Coen Maas et al. JOURNAL OF CLINICAL INVESTIGATION
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreAdd your recorded webinar
Do you already have a recorded webinar? Grow your audience and get more views by easily listing your recording on Peeref.
Upload Now