Journal of Thrombosis and Haemostasis, ISSN 1538-7933, 05/2019, Volume 17, Issue 5, pp. 717 - 719
In recent years, the contact pathway of coagulation has received increased attention as it appears to be more relevant to pathologic thrombosis than to normal...
PLASMA | HUMAN HAGEMAN-FACTOR | FACTOR-XI | PERIPHERAL VASCULAR DISEASE | CONTACT ACTIVATION | HEMATOLOGY | BINDING | REVEALS
PLASMA | HUMAN HAGEMAN-FACTOR | FACTOR-XI | PERIPHERAL VASCULAR DISEASE | CONTACT ACTIVATION | HEMATOLOGY | BINDING | REVEALS
Journal Article
Advanced Drug Delivery Reviews, ISSN 0169-409X, 01/2013, Volume 65, Issue 1, pp. 71 - 79
The EPR effect results from the extravasation of macromolecules or nanoparticles through tumor blood vessels. We here provide a historical review of the EPR...
Tumor-selective drug delivery | Enhancement of the EPR effect | Fluorescent nanoprobes | Tumor blood vessel architecture | Inflammation | EPR effect mediators | Vascular effectors | Cancer | MOLECULAR-WEIGHT | SERRATIAL PROTEASE | ELEVATING BLOOD-PRESSURE | CANCER-CHEMOTHERAPY | KININ-GENERATING CASCADE | OILY CONTRAST-MEDIUM | ENHANCED VASCULAR-PERMEABILITY | NITRIC-OXIDE SCAVENGER | HAGEMAN-FACTOR | PHARMACOLOGY & PHARMACY | TARGETED DELIVERY | Neoplasms - metabolism | Nanoparticles - chemistry | Humans | Macromolecular Substances - administration & dosage | Capillary Permeability - drug effects | Neoplasms - blood supply | Antineoplastic Agents - administration & dosage | Antineoplastic Agents - chemistry | Antineoplastic Agents - toxicity | Neoplasms - drug therapy | Animals | Macromolecular Substances - chemistry | Antineoplastic Agents - pharmacokinetics | Nanoparticles - administration & dosage | Neoplasms - pathology | Drug Delivery Systems - methods | Hypertension | Drugs | Drug delivery systems | Care and treatment | Architecture | Albumin | Nitrogen compounds | Permeability | Endothelium | Vehicles | Nitric oxide | Angiotensin converting enzyme | Angiotensin | Physiological aspects | Vascular endothelial growth factor | Nanotechnology
Tumor-selective drug delivery | Enhancement of the EPR effect | Fluorescent nanoprobes | Tumor blood vessel architecture | Inflammation | EPR effect mediators | Vascular effectors | Cancer | MOLECULAR-WEIGHT | SERRATIAL PROTEASE | ELEVATING BLOOD-PRESSURE | CANCER-CHEMOTHERAPY | KININ-GENERATING CASCADE | OILY CONTRAST-MEDIUM | ENHANCED VASCULAR-PERMEABILITY | NITRIC-OXIDE SCAVENGER | HAGEMAN-FACTOR | PHARMACOLOGY & PHARMACY | TARGETED DELIVERY | Neoplasms - metabolism | Nanoparticles - chemistry | Humans | Macromolecular Substances - administration & dosage | Capillary Permeability - drug effects | Neoplasms - blood supply | Antineoplastic Agents - administration & dosage | Antineoplastic Agents - chemistry | Antineoplastic Agents - toxicity | Neoplasms - drug therapy | Animals | Macromolecular Substances - chemistry | Antineoplastic Agents - pharmacokinetics | Nanoparticles - administration & dosage | Neoplasms - pathology | Drug Delivery Systems - methods | Hypertension | Drugs | Drug delivery systems | Care and treatment | Architecture | Albumin | Nitrogen compounds | Permeability | Endothelium | Vehicles | Nitric oxide | Angiotensin converting enzyme | Angiotensin | Physiological aspects | Vascular endothelial growth factor | Nanotechnology
Journal Article
JOURNAL OF CLINICAL INVESTIGATION, ISSN 0021-9738, 09/2008, Volume 118, Issue 9, pp. 3208 - 3218
When blood is exposed to negatively charged surface materials such as glass, an enzymatic cascade known as the contact system becomes activated. This cascade...
CROSS-BETA STRUCTURE | MEDICINE, RESEARCH & EXPERIMENTAL | CONTACT SYSTEM | INTRINSIC PATHWAY | BLOOD-COAGULATION | MOLECULAR-WEIGHT KININOGEN | AMYLOID FIBRIL | ADVERSE CLINICAL EVENTS | HAGEMAN-FACTOR | COMMON MECHANISM | BOVINE ALPHA-LACTALBUMIN
CROSS-BETA STRUCTURE | MEDICINE, RESEARCH & EXPERIMENTAL | CONTACT SYSTEM | INTRINSIC PATHWAY | BLOOD-COAGULATION | MOLECULAR-WEIGHT KININOGEN | AMYLOID FIBRIL | ADVERSE CLINICAL EVENTS | HAGEMAN-FACTOR | COMMON MECHANISM | BOVINE ALPHA-LACTALBUMIN
Journal Article
Bioconjugate Chemistry, ISSN 1043-1802, 05/2010, Volume 21, Issue 5, pp. 797 - 802
This paper briefly documents the history of the discovery of the EPR (enhanced permeability and retention) effect and elucidates an analogy between bacterial...
ELEVATING BLOOD-PRESSURE | CANCER-CHEMOTHERAPY | KININ-GENERATING CASCADE | BIOCHEMISTRY & MOLECULAR BIOLOGY | BIOCHEMICAL RESEARCH METHODS | CHEMISTRY, ORGANIC | CHEMISTRY, MULTIDISCIPLINARY | OILY CONTRAST-MEDIUM | ENHANCED VASCULAR-PERMEABILITY | IMAGE-ENHANCEMENT | NITRIC-OXIDE SCAVENGER | HAGEMAN-FACTOR | SOLID TUMOR | TARGETED DELIVERY | Animals | Capillary Permeability | Humans | Macromolecular Substances - administration & dosage | Macromolecular Substances - pharmacokinetics | Antineoplastic Agents - pharmacokinetics | Antineoplastic Agents - administration & dosage | Drug Delivery Systems - trends | Pharmaceutical Preparations - administration & dosage | Pharmacokinetics | Drug Delivery Systems - methods | Neoplasms - drug therapy
ELEVATING BLOOD-PRESSURE | CANCER-CHEMOTHERAPY | KININ-GENERATING CASCADE | BIOCHEMISTRY & MOLECULAR BIOLOGY | BIOCHEMICAL RESEARCH METHODS | CHEMISTRY, ORGANIC | CHEMISTRY, MULTIDISCIPLINARY | OILY CONTRAST-MEDIUM | ENHANCED VASCULAR-PERMEABILITY | IMAGE-ENHANCEMENT | NITRIC-OXIDE SCAVENGER | HAGEMAN-FACTOR | SOLID TUMOR | TARGETED DELIVERY | Animals | Capillary Permeability | Humans | Macromolecular Substances - administration & dosage | Macromolecular Substances - pharmacokinetics | Antineoplastic Agents - pharmacokinetics | Antineoplastic Agents - administration & dosage | Drug Delivery Systems - trends | Pharmaceutical Preparations - administration & dosage | Pharmacokinetics | Drug Delivery Systems - methods | Neoplasms - drug therapy
Journal Article
Blood, ISSN 0006-4971, 11/2012, Volume 120, Issue 22, pp. 4296 - 4303
Coagulation factor XII (FXII, Hageman factor, EC = 3.4.21.38) is the zymogen of the serine protease, factor XIIa (FXIIa). FXII is converted to FXIIa through...
COAGULATION-FACTOR-XII | CONTACT SYSTEM | BLOOD-COAGULATION | HEREDITARY ANGIOEDEMA | MAST-CELLS | HAGEMAN-FACTOR | VASCULAR-PERMEABILITY | ARTERIAL THROMBUS FORMATION | HEMATOLOGY | TISSUE FACTOR | KININOGEN-BINDING-SITE | Factor XII - genetics | Hemostasis - physiology | Blood Vessels - metabolism | Humans | Hemostasis - genetics | Factor XII - physiology | Inflammation - etiology | Inflammation - blood | Mice, Knockout | Animals | Models, Biological | Thrombosis - etiology | Factor XII - metabolism | Inflammation - genetics | Blood Coagulation - genetics | Thrombosis - genetics | Mice | Blood Coagulation - physiology | Thrombosis - blood | Blood Vessels - physiology | Review
COAGULATION-FACTOR-XII | CONTACT SYSTEM | BLOOD-COAGULATION | HEREDITARY ANGIOEDEMA | MAST-CELLS | HAGEMAN-FACTOR | VASCULAR-PERMEABILITY | ARTERIAL THROMBUS FORMATION | HEMATOLOGY | TISSUE FACTOR | KININOGEN-BINDING-SITE | Factor XII - genetics | Hemostasis - physiology | Blood Vessels - metabolism | Humans | Hemostasis - genetics | Factor XII - physiology | Inflammation - etiology | Inflammation - blood | Mice, Knockout | Animals | Models, Biological | Thrombosis - etiology | Factor XII - metabolism | Inflammation - genetics | Blood Coagulation - genetics | Thrombosis - genetics | Mice | Blood Coagulation - physiology | Thrombosis - blood | Blood Vessels - physiology | Review
Journal Article
BLOOD, ISSN 0006-4971, 11/2019, Volume 134, Issue 19, pp. 1658 - 1669
The contact system produces the inflammatory peptide bradykinin and contributes to experimental thrombosis. C1 esterase-inhibitor (C1INH) deficiency or...
PLASMA KALLIKREIN | SUBSTRATE-SPECIFICITY | PROPROTEIN CONVERTASE | ACTIVATED PROTEIN-C | HEREDITARY ANGIOEDEMA | ADENOASSOCIATED VIRUS | FACTOR-XIA | ULCERATIVE-COLITIS | HAGEMAN-FACTOR | HEMATOLOGY | RECEPTOR ANTAGONIST
PLASMA KALLIKREIN | SUBSTRATE-SPECIFICITY | PROPROTEIN CONVERTASE | ACTIVATED PROTEIN-C | HEREDITARY ANGIOEDEMA | ADENOASSOCIATED VIRUS | FACTOR-XIA | ULCERATIVE-COLITIS | HAGEMAN-FACTOR | HEMATOLOGY | RECEPTOR ANTAGONIST
Journal Article
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, ISSN 0091-6749, 11/2016, Volume 138, Issue 5, pp. 1424 - 1425
Journal Article
Colloids and Surfaces B: Biointerfaces, ISSN 0927-7765, 12/2014, Volume 124, pp. 49 - 68
Blood coagulation and platelet adhesion remain major impediments to the use of biomaterials in implantable medical devices. There is still significant...
Surfaces | Blood compatibility | Biological response | Thrombosis | Coagulation | Biomaterials | MATERIALS SCIENCE, BIOMATERIALS | SELF-ASSEMBLED MONOLAYERS | DEPENDENT FUNCTIONAL-ACTIVITY | CHEMISTRY, PHYSICAL | CONTACT ACTIVATION | VON-WILLEBRAND-FACTOR | ATOMIC-FORCE MICROSCOPY | BIOPHYSICS | HUMAN HAGEMAN-FACTOR | MONOCLONAL-ANTIBODY BINDING | FIBRINOGEN ADSORPTION | ACTIVATED HUMAN PLATELETS | FACTOR FACTOR-XII | Blood Coagulation - drug effects | Humans | Surface Properties | Fibrinogen - chemistry | Blood Platelets - physiology | Proteins - chemistry | Biocompatible Materials - adverse effects | Biological products | Biomedical engineering | Blood coagulation | Surgical implants | Biomedical materials | Medical devices | Interrogation | Biological | Platelets
Surfaces | Blood compatibility | Biological response | Thrombosis | Coagulation | Biomaterials | MATERIALS SCIENCE, BIOMATERIALS | SELF-ASSEMBLED MONOLAYERS | DEPENDENT FUNCTIONAL-ACTIVITY | CHEMISTRY, PHYSICAL | CONTACT ACTIVATION | VON-WILLEBRAND-FACTOR | ATOMIC-FORCE MICROSCOPY | BIOPHYSICS | HUMAN HAGEMAN-FACTOR | MONOCLONAL-ANTIBODY BINDING | FIBRINOGEN ADSORPTION | ACTIVATED HUMAN PLATELETS | FACTOR FACTOR-XII | Blood Coagulation - drug effects | Humans | Surface Properties | Fibrinogen - chemistry | Blood Platelets - physiology | Proteins - chemistry | Biocompatible Materials - adverse effects | Biological products | Biomedical engineering | Blood coagulation | Surgical implants | Biomedical materials | Medical devices | Interrogation | Biological | Platelets
Journal Article
Journal of Thrombosis and Haemostasis, ISSN 1538-7933, 01/2016, Volume 14, Issue 1, pp. 28 - 39
Summary The contact activation system (CAS) and kallikrein/kinin system (KKS) are older recognized biochemical pathways that include several proteins that...
bradykinin | contact activation | kallikrein/kinin system | kininogen | prekallikrein | factor XII | Kininogen | Kallikrein/kinin system | Contact activation | Factor XII | Prekallikrein | Bradykinin | HEREDITARY ANGIOEDEMA | BLOOD-COAGULATION | MOLECULAR-WEIGHT KININOGEN | 4 TANDEM REPEATS | COAGULATION-FACTOR-XII | PLASMA PREKALLIKREIN | ENDOTHELIAL-CELLS | HAGEMAN-FACTOR | PERIPHERAL VASCULAR DISEASE | HEPARAN-SULFATE PROTEOGLYCANS | ANGIOEDEMA TYPE-III | HEMATOLOGY | Factor XIIa - metabolism | Plasma Kallikrein - metabolism | Thrombosis - physiopathology | Bradykinin - metabolism | Prekallikrein - immunology | Humans | Homeostasis | Inflammation | Kininogen, High-Molecular-Weight - metabolism | Prekallikrein - deficiency | Prekallikrein - metabolism | Animals | Kallikrein-Kinin System | Receptors, Bradykinin - metabolism | Blood Coagulation Disorders - immunology | Hemostasis | Factor XII - metabolism | Blood Coagulation | Mice | Proteins | Physiological aspects | Cells | Angiotensin
bradykinin | contact activation | kallikrein/kinin system | kininogen | prekallikrein | factor XII | Kininogen | Kallikrein/kinin system | Contact activation | Factor XII | Prekallikrein | Bradykinin | HEREDITARY ANGIOEDEMA | BLOOD-COAGULATION | MOLECULAR-WEIGHT KININOGEN | 4 TANDEM REPEATS | COAGULATION-FACTOR-XII | PLASMA PREKALLIKREIN | ENDOTHELIAL-CELLS | HAGEMAN-FACTOR | PERIPHERAL VASCULAR DISEASE | HEPARAN-SULFATE PROTEOGLYCANS | ANGIOEDEMA TYPE-III | HEMATOLOGY | Factor XIIa - metabolism | Plasma Kallikrein - metabolism | Thrombosis - physiopathology | Bradykinin - metabolism | Prekallikrein - immunology | Humans | Homeostasis | Inflammation | Kininogen, High-Molecular-Weight - metabolism | Prekallikrein - deficiency | Prekallikrein - metabolism | Animals | Kallikrein-Kinin System | Receptors, Bradykinin - metabolism | Blood Coagulation Disorders - immunology | Hemostasis | Factor XII - metabolism | Blood Coagulation | Mice | Proteins | Physiological aspects | Cells | Angiotensin
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 06/2008, Volume 358, Issue 23, pp. 2457 - 2467
Recently the heparin supply in 12 countries was found to be contaminated with a substance that caused hypotension and, in some cases, death. The contaminant...
MEDICINE, GENERAL & INTERNAL | PLASMA KALLIKREIN | COMPLEMENT | DEXTRAN SULFATE | INHIBITION | ALTERNATIVE PATHWAY | HAGEMAN-FACTOR | ANTITHROMBIN | COFACTOR | RABBIT | FACTOR-XII | Complement C3a - drug effects | United States | Humans | Middle Aged | Complement C5a - biosynthesis | Heparin - adverse effects | Complement C5a - drug effects | Chondroitin Sulfates - adverse effects | Anaphylaxis - chemically induced | China | Chondroitin Sulfates - analysis | Female | Complement Activation - drug effects | United States Food and Drug Administration | Complement C3a - biosynthesis | Drug Industry | Chondroitin Sulfates - pharmacology | Hypotension - chemically induced | Animals | Kallikreins - drug effects | Sus scrofa | Drug Contamination | Germany | Heparin - chemistry | Kallikreins - metabolism | Composition | Heparin | Health aspects | Chondroitin | Drug therapy | Hemodialysis | Family medical history | Index Medicus | Abridged Index Medicus
MEDICINE, GENERAL & INTERNAL | PLASMA KALLIKREIN | COMPLEMENT | DEXTRAN SULFATE | INHIBITION | ALTERNATIVE PATHWAY | HAGEMAN-FACTOR | ANTITHROMBIN | COFACTOR | RABBIT | FACTOR-XII | Complement C3a - drug effects | United States | Humans | Middle Aged | Complement C5a - biosynthesis | Heparin - adverse effects | Complement C5a - drug effects | Chondroitin Sulfates - adverse effects | Anaphylaxis - chemically induced | China | Chondroitin Sulfates - analysis | Female | Complement Activation - drug effects | United States Food and Drug Administration | Complement C3a - biosynthesis | Drug Industry | Chondroitin Sulfates - pharmacology | Hypotension - chemically induced | Animals | Kallikreins - drug effects | Sus scrofa | Drug Contamination | Germany | Heparin - chemistry | Kallikreins - metabolism | Composition | Heparin | Health aspects | Chondroitin | Drug therapy | Hemodialysis | Family medical history | Index Medicus | Abridged Index Medicus
Journal Article
BLOOD, ISSN 0006-4971, 12/2006, Volume 108, Issue 13, pp. 4045 - 4051
The role of the intrinsic coagulation system on the risk of myocardial infarction is unclear. In the Study of Myocardial Infarctions Leiden (SMILE) that...
FIBRINOLYSIS | ACTIVATION | MIDDLE-AGED MEN | MOLECULAR-WEIGHT KININOGEN | FACTOR-VIII | VENOUS THROMBOSIS | HAGEMAN-FACTOR | HEMOSTATIC FACTORS | CORONARY-HEART-DISEASE | HEMATOLOGY | DEFICIENCY
FIBRINOLYSIS | ACTIVATION | MIDDLE-AGED MEN | MOLECULAR-WEIGHT KININOGEN | FACTOR-VIII | VENOUS THROMBOSIS | HAGEMAN-FACTOR | HEMOSTATIC FACTORS | CORONARY-HEART-DISEASE | HEMATOLOGY | DEFICIENCY
Journal Article
PLoS ONE, ISSN 1932-6203, 02/2013, Volume 8, Issue 2, p. e53773
Background: Attacks of hereditary angioedema (HAE) are unpredictable and, if affecting the upper airway, can be lethal. Icatibant is used for physician- or...
ANTAGONIST ICATIBANT | ACTIVATION | C1-INHIBITOR CONCENTRATE | PLASMA | EDEMA | MULTIDISCIPLINARY SCIENCES | HAGEMAN-FACTOR | RECEPTOR ANTAGONIST | BRADYKININ | PREKALLIKREIN | DEFICIENCY | Angioneurotic edema | Care and treatment | Bradykinin | Physiological aspects | Genetic aspects | Research | Diagnosis | Health care | Edema | Dermatology | Angioedema | Patients | Asthma | Mode of action | Studies | Respiratory tract | Hospitals | Early experience | Adults
ANTAGONIST ICATIBANT | ACTIVATION | C1-INHIBITOR CONCENTRATE | PLASMA | EDEMA | MULTIDISCIPLINARY SCIENCES | HAGEMAN-FACTOR | RECEPTOR ANTAGONIST | BRADYKININ | PREKALLIKREIN | DEFICIENCY | Angioneurotic edema | Care and treatment | Bradykinin | Physiological aspects | Genetic aspects | Research | Diagnosis | Health care | Edema | Dermatology | Angioedema | Patients | Asthma | Mode of action | Studies | Respiratory tract | Hospitals | Early experience | Adults
Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2016, Volume 138, Issue 5, pp. 1414 - 1423.e9
Background Patients with angioedema experience unpredictable attacks of tissue swelling in which bradykinin is implicated. Several distinct mutations in Factor...
Allergy and Immunology | kininogen | Angioedema | plasmin | bradykinin | plasma kallikrein | Factor XII | C1 esterase inhibitor | Kininogen | Immunology | Bradykinin | Plasma kallikrein | Immunology and Allergy | Plasmin | Journal Article | KALLIKREIN CLEAVAGE | CONTACT SYSTEM ACTIVATION | IMMUNOLOGY | FIBRINOLYTIC SYSTEM | NORMAL C1-INHIBITOR | DEFICIENCY | C1 INHIBITOR | F12 GENE | ALLERGY | HAGEMAN-FACTOR | COAGULATION | ALTEPLASE TREATMENT | Pregnancy | Bradykinin - metabolism | Factor XII - genetics | Angioedemas, Hereditary - metabolism | Factor XII - metabolism | Humans | Antifibrinolytic Agents - pharmacology | Female | Complement C1 Inhibitor Protein - metabolism | Mutation | Fibrinolysin - metabolism | Aminocaproic Acid - pharmacology | Angioneurotic edema | Care and treatment | Genetic aspects | Medical research | Medicine, Experimental | Kallikrein | Proteins | Plasma | Life sciences | Patients
Allergy and Immunology | kininogen | Angioedema | plasmin | bradykinin | plasma kallikrein | Factor XII | C1 esterase inhibitor | Kininogen | Immunology | Bradykinin | Plasma kallikrein | Immunology and Allergy | Plasmin | Journal Article | KALLIKREIN CLEAVAGE | CONTACT SYSTEM ACTIVATION | IMMUNOLOGY | FIBRINOLYTIC SYSTEM | NORMAL C1-INHIBITOR | DEFICIENCY | C1 INHIBITOR | F12 GENE | ALLERGY | HAGEMAN-FACTOR | COAGULATION | ALTEPLASE TREATMENT | Pregnancy | Bradykinin - metabolism | Factor XII - genetics | Angioedemas, Hereditary - metabolism | Factor XII - metabolism | Humans | Antifibrinolytic Agents - pharmacology | Female | Complement C1 Inhibitor Protein - metabolism | Mutation | Fibrinolysin - metabolism | Aminocaproic Acid - pharmacology | Angioneurotic edema | Care and treatment | Genetic aspects | Medical research | Medicine, Experimental | Kallikrein | Proteins | Plasma | Life sciences | Patients
Journal Article