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1. Full Text PAR-1 contributes to the innate immune response during viral infection
by Antoniak, Silvio and Owens III, A. Phillip and Baunacke, Martin and Williams, Julie C and Lee, Rebecca D and Weithäuser, Alice and Sheridan, Patricia A and Malz, Ronny and Luyendyk, James P and Esserman, Denise A and Trejo, Jo Ann and Kirchhofer, Daniel and Blaxall, Burns C and Pawlinski, Rafal and Beck, Melinda A and Rauch, Ursula and Mackman, Nigel
Journal of Clinical Investigation, ISSN 0021-9738, 03/2013, Volume 123, Issue 3, pp. 1310 - 1322
Coagulation is a host defense system that limits the spread of pathogens. Coagulation proteases, such as thrombin, also activate cells by cleaving PARs. In... 
TOLL-LIKE RECEPTOR-3 | MEDICINE, RESEARCH & EXPERIMENTAL | NATURAL-KILLER-CELLS | ISCHEMIA/REPERFUSION INJURY | PROTEASE-ACTIVATED RECEPTORS | VIRUS-INFECTION | IN-VIVO | ENDOTHELIAL-CELLS | FACTOR MESSENGER-RNA | INTERFERON-BETA | TISSUE FACTOR EXPRESSION | Receptor, PAR-1 - metabolism | Humans | Male | Troponin I - blood | STAT1 Transcription Factor - metabolism | Myocardium - metabolism | HEK293 Cells | Interferon-beta - genetics | Influenza A virus - immunology | Myocarditis - immunology | Influenza A virus - physiology | Orthomyxoviridae Infections - metabolism | Coxsackievirus Infections - metabolism | Liver - metabolism | Mice, Inbred C57BL | Enterovirus - physiology | Myocarditis - blood | Immunity, Innate | STAT1 Transcription Factor - genetics | Toll-Like Receptor 3 - metabolism | Receptor, PAR-1 - genetics | Mice, Knockout | Myocarditis - virology | Animals | Interferon-beta - metabolism | Thromboplastin - genetics | Enterovirus - immunology | Mice | HeLa Cells | Thrombin - metabolism | Thromboplastin - metabolism | Fibrin - metabolism | Chemokine CXCL10 - metabolism | Coxsackievirus Infections - immunology | Orthomyxoviridae Infections - immunology | Receptor, PAR-1 - physiology | Virus diseases | Cell receptors | Immune response | Physiological aspects | Development and progression | Genetic aspects | Research | Index Medicus | Abridged Index Medicus
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2. Full Text Par-1 Regulates Tissue Growth by Influencing Hippo Phosphorylation Status and Hippo-Salvador Association
by Huang, Hong-Ling and Wang, Shimin and Yin, Meng-Xin and Dong, Liang and Wang, Chao and Wu, Wei and Lu, Yi and Feng, Miao and Dai, Chuanyang and Guo, Xiaocan and Li, Li and Zhao, Bin and Zhou, Zhaocai and Ji, Hongbin and Jiang, Jin and Zhao, Yun and Liu, Xin-Yuan and Zhang, Lei
PLoS Biology, ISSN 1544-9173, 08/2013, Volume 11, Issue 8, pp. e1001620 - e1001620
The evolutionarily conserved Hippo (Hpo) signaling pathway plays a pivotal role in organ size control by balancing cell proliferation and cell death. Here, we... 
ORGAN SIZE | DROSOPHILA HOMOLOG | GENE | SIGNALING PATHWAY | PROLIFERATION ARREST | BIOCHEMISTRY & MOLECULAR BIOLOGY | KINASE | BIOLOGY | TUMOR-SUPPRESSOR PROTEIN | CELL-CYCLE EXIT | TEAD/TEF FAMILY | PROMOTES APOPTOSIS | Phosphorylation | Signal Transduction | Receptor, PAR-1 - metabolism | Protein-Serine-Threonine Kinases - genetics | Intracellular Signaling Peptides and Proteins - metabolism | Drosophila Proteins - metabolism | Receptor, PAR-1 - genetics | Animals | Protein Binding | Drosophila Proteins - genetics | Drosophila melanogaster | Intracellular Signaling Peptides and Proteins - genetics | Protein-Serine-Threonine Kinases - metabolism | Index Medicus | Research & development | R&D | Cell growth | Insects | Plasmids | Cloning | Kinases | Gene expression | Experiments | Apoptosis
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3. Full Text Stabilization of Microtubule-Unbound Tau via Tau Phosphorylation at Ser262/356 by Par-1/MARK Contributes to Augmentation of AD-Related Phosphorylation and Aβ42-Induced Tau Toxicity
by Ando, Kanae and Maruko-Otake, Akiko and Ohtake, Yosuke and Hayashishita, Motoki and Sekiya, Michiko and Iijima, Koichi M
PLoS Genetics, ISSN 1553-7390, 03/2016, Volume 12, Issue 3, pp. e1005917 - e1005917
Abnormal accumulation of the microtubule-interacting protein tau is associated with neurodegenerative diseases including Alzheimer's disease (AD). β-amyloid... 
Neurons - pathology | Phosphorylation | Receptor, PAR-1 - metabolism | Humans | tau Proteins - metabolism | Glycogen Synthase Kinase 3 beta | Tubulin - genetics | Alzheimer Disease - pathology | Microtubules - metabolism | Tubulin - metabolism | tau Proteins - genetics | Amyloid beta-Peptides - genetics | Amyloid beta-Peptides - metabolism | Neurons - metabolism | Disease Models, Animal | Drosophila - genetics | Animals, Genetically Modified | Hippocampus - pathology | Glycogen Synthase Kinase 3 - metabolism | Microtubules - pathology | Receptor, PAR-1 - genetics | Hippocampus - metabolism | Animals | Glycogen Synthase Kinase 3 - genetics | Alzheimer Disease - metabolism | Drosophila - metabolism | Alzheimer Disease - genetics | Index Medicus
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4. Full Text Inhibiting trophoblast PAR-1 overexpression suppresses sFlt-1-induced anti-angiogenesis and abnormal vascular remodeling: a possible therapeutic approach for preeclampsia
by Zhao, Yin and Zheng, YanFang and Liu, XiaoXia and Luo, QingQing and Wu, Di and Liu, XiaoPing and Zou, Li
MHR: Basic science of reproductive medicine, ISSN 1360-9947, 03/2018, Volume 24, Issue 3, pp. 158 - 169
Abstract STUDY QUESTION Is it possible to improve vascular remodeling by inhibiting the excessive expression of protease-activated receptor 1 (PAR-1) in... 
SFlt-1 | Angiogenesis | Trophoblast | PAR-1 | Preeclampsia | POSSIBLE INVOLVEMENT | THROMBIN | angiogenesis | PLACENTA | VEGF EXPRESSION | DEVELOPMENTAL BIOLOGY | preeclampsia | RELEASE | PROTEASE-ACTIVATED-RECEPTOR-1 | OBSTETRICS & GYNECOLOGY | PATHOGENESIS | REPRODUCTIVE BIOLOGY | KINASE 1 EXPRESSION | sFlt-1 | ENDOTHELIAL-CELLS | trophoblast | PROTEASE-ACTIVATED RECEPTOR-1 | Immunohistochemistry | Pre-Eclampsia - genetics | Cell Line | Enzyme-Linked Immunosorbent Assay | Receptor, PAR-1 - metabolism | Coculture Techniques | Rats | Male | Vascular Endothelial Growth Factor Receptor-1 - metabolism | Blotting, Western | Receptor, PAR-1 - genetics | Placenta - metabolism | Pregnancy | Animals | Vascular Remodeling - genetics | Female | Vascular Remodeling - physiology | Pre-Eclampsia - metabolism | Vascular Endothelial Growth Factor Receptor-1 - genetics | Index Medicus
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5. Full Text Galectin-3 facilitates cell motility in gastric cancer by Up-regulating protease-activated receptor-1(PAR-1) and matrix metalloproteinase-1(MMP-1)
by Kim, Seok-Jun and Shin, Ji-Young and Lee, Kang-Duck and Bae, Young-Ki and Choi, Il-Ju and Park, Seok Hee and Chun, Kyung-Hee
PLoS ONE, ISSN 1932-6203, 09/2011, Volume 6, Issue 9, pp. e25103 - e25103
Galectin-3 is known to regulate cancer metastasis. However, the underlying mechanism has not been defined. Through the DNA microarray studies after galectin-3... 
Immunohistochemistry | Stomach Neoplasms - genetics | Immunoprecipitation | Oligonucleotide Array Sequence Analysis | Receptor, PAR-1 - metabolism | Humans | Galectin 3 - metabolism | Stomach Neoplasms - metabolism | Zebrafish | Galectin 3 - genetics | Reverse Transcriptase Polymerase Chain Reaction | Blotting, Western | Cell Movement - genetics | Cell Movement - physiology | Genetic Vectors - genetics | Receptor, PAR-1 - genetics | Animals | Chromatin Immunoprecipitation | Cell Line, Tumor | Lentivirus - genetics | In Vitro Techniques | Matrix Metalloproteinase 1 - metabolism | Matrix Metalloproteinase 1 - genetics | Proteins | DNA microarrays | Proteases | Analysis | Metastasis | Stomach cancer | Cancer | Transcription factors | Motility | Matrix metalloproteinases | Leukocyte migration | Laboratories | Proteinase-activated receptor 1 | Galectin-3 | Matrix metalloproteinase | Tissues | Cell surface | Metastases | Cell adhesion & migration | Angiogenesis | Epidermal growth factor | Protease | Metalloproteinase | Gastric cancer | Interstitial collagenase | Deoxyribonucleic acid--DNA | Enzymes | Activator protein 1 | Pharmacology | Gene expression | Bladder cancer | Overexpression | Lymphocytes B | Medical prognosis | In vivo methods and tests | Paxillin | Cell migration | Tumors | Index Medicus | Deoxyribonucleic acid | DNA
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6. Full Text Senescent Fibroblasts Enhance Early Skin Carcinogenic Events via a Paracrine MMP-PAR-1 Axis
by Malaquin, Nicolas and Vercamer, Chantal and Bouali, Fatima and Martien, Sébastien and Deruy, Emeric and Wernert, Nicolas and Chwastyniak, Maggy and Pinet, Florence and Abbadie, Corinne and Pourtier, Albin
PLoS ONE, ISSN 1932-6203, 05/2013, Volume 8, Issue 5, pp. e63607 - e63607
The incidence of carcinoma increases greatly with aging, but the cellular and molecular mechanisms underlying this correlation are only partly known. It is... 
EPITHELIAL-MESENCHYMAL TRANSITION | BREAST-CANCER | ACTIVATED RECEPTOR-1 | MATRIX METALLOPROTEINASES | TUMOR PROGRESSION | THROMBIN RECEPTOR PAR-1 | MULTIDISCIPLINARY SCIENCES | HEPATOCYTE GROWTH-FACTOR | MET TYROSINE KINASE | KERATINOCYTE MIGRATION | MELANOMA METASTASIS | Gene Expression | Matrix Metalloproteinases - genetics | Paracrine Communication | Receptor, PAR-1 - metabolism | Skin - metabolism | Humans | Cells, Cultured | Matrix Metalloproteinase 1 - biosynthesis | Epithelial-Mesenchymal Transition - genetics | Hepatocyte Growth Factor - pharmacology | Cell Transformation, Neoplastic - metabolism | Receptor, PAR-1 - genetics | Young Adult | Cell Movement - drug effects | Cell Transformation, Neoplastic - genetics | Cellular Senescence | Keratinocytes - metabolism | Adult | Female | Matrix Metalloproteinases - metabolism | Matrix Metalloproteinase 2 - biosynthesis | Skin - pathology | Transforming Growth Factor beta1 - pharmacology | Fibroblasts - metabolism | Analysis | Skin | Transformation | Senescence | Matrix metalloproteinases | Mesenchyme | Proteinase-activated receptor 1 | Blocking antibodies | Antibodies | Paracrine signalling | Metastasis | Matrix metalloproteinase | Carcinogenesis | Metastases | Carcinogens | Compartments | Transformed cells | Fibroblasts | Aging | Conditioning | Age | Interstitial collagenase | Secretion | Melanoma | Keratinocytes | Pharmacology | Breast cancer | Secretome | Inflammation | Gelatinase A | Molecular modelling | Skin carcinoma | Cell migration | Cancer | Tumors | Index Medicus
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7. Full Text Dust mite-derived Der f 3 activates a pro-inflammatory program in airway epithelial cells via PAR-1 and PAR-2
by Li, Bizhou and Zou, Zehong and Meng, Fanmei and Raz, Eyal and Huang, Yuye and Tao, Ailin and Ai, Yuncan
Molecular Immunology, ISSN 0161-5890, 05/2019, Volume 109, pp. 1 - 11
Protease activity of allergens has been suggested to be involved in the pathogenesis of allergic diseases. The major allergen Der f 3 from harbors serine... 
Airway epithelial cell | House dust mite (HDM) | Inflammation | Protease-activated receptor (PAR) | Protease | Der f 3 | IL-8 EXPRESSION | DENDRITIC CELLS | BIOCHEMISTRY & MOLECULAR BIOLOGY | CA2+ CHANNELS | DER-P-1 | KAPPA-B | IMMUNOLOGY | MAJOR ALLERGEN | TIGHT JUNCTIONS | PROTEOLYTIC ACTIVITY | CYTOKINE PRODUCTION | SERINE-PROTEASE | Inflammation - chemically induced | Inflammation - pathology | Humans | NF-kappa B - immunology | Serine Endopeptidases - pharmacology | Th2 Cells - immunology | Extracellular Signal-Regulated MAP Kinases - genetics | MAP Kinase Signaling System - immunology | Extracellular Signal-Regulated MAP Kinases - immunology | Gene Knockdown Techniques | Receptor, PAR-2 - immunology | MAP Kinase Signaling System - genetics | Allergens - immunology | Respiratory Mucosa - immunology | Serine Endopeptidases - immunology | Calcium Signaling - immunology | Cytokines - genetics | Th2 Cells - pathology | Cytokines - immunology | Receptor, PAR-2 - genetics | Th17 Cells - pathology | Inflammation Mediators - immunology | A549 Cells | Gene Expression Regulation - immunology | Epithelial Cells - pathology | Inflammation - immunology | Arthropod Proteins - immunology | Receptor, PAR-1 - genetics | Receptor, PAR-1 - immunology | Gene Expression Regulation - drug effects | Arthropod Proteins - pharmacology | Animals | MAP Kinase Signaling System - drug effects | NF-kappa B - genetics | Calcium Signaling - drug effects | Epithelial Cells - immunology | Inflammation - genetics | Th17 Cells - immunology | Allergens - pharmacology | Calcium Signaling - genetics | Pyroglyphidae - immunology | Allergens | Allergy | Medical colleges | RNA | Biological control | Thrombin | Respiratory tract diseases | Genetic engineering | Pests | B cells | Allergic reaction | Index Medicus
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8. Full Text Dendritic cell PAR1-S1P3 signalling couples coagulation and inflammation
by Andrade-Gordon, Patricia and Furlan-Freguia, Christian and Ruf, Wolfram and Bhattacharjee, Gourab and Derian, Claudia K and Schaffner, Florence and Niessen, Frank and Pawlinski, Rafal and Chun, Jerold and Rosen, Hugh
Nature, ISSN 0028-0836, 04/2008, Volume 452, Issue 7187, pp. 654 - 658
Defining critical points of modulation across heterogeneous clinical syndromes may provide insight into new therapeutic approaches. Coagulation initiated by... 
RESPONSES | POLYMICROBIAL SEPSIS | PROTEASE-ACTIVATED RECEPTORS | MICE DEFICIENT | P2X RECEPTOR | MULTIDISCIPLINARY SCIENCES | LYMPH-NODES | MOUSE MODEL | ENDOTOXEMIA | TISSUE FACTOR | SPHINGOSINE 1-PHOSPHATE | Sepsis - immunology | Receptor, PAR-1 - antagonists & inhibitors | Receptor, PAR-1 - metabolism | Receptors, Lysosphingolipid - deficiency | Dendritic Cells - immunology | Mice, Inbred C57BL | Phosphotransferases (Alcohol Group Acceptor) - deficiency | Phosphotransferases (Alcohol Group Acceptor) - genetics | Inflammation - immunology | Receptor, PAR-1 - deficiency | Receptor Cross-Talk - physiology | Receptor, PAR-1 - genetics | Phosphotransferases (Alcohol Group Acceptor) - metabolism | Inflammation - metabolism | Animals | Signal Transduction - drug effects | Sepsis - metabolism | Receptors, Lysosphingolipid - genetics | Dendritic Cells - drug effects | Lymphatic System - immunology | Mice | Blood Coagulation - physiology | Receptors, Lysosphingolipid - metabolism | Dendritic Cells - metabolism | Signal transduction | Biomedical research | Cellular biology | Inflammatory diseases | Blood clots | Index Medicus
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9. Full Text Common Signaling Pathways Link Activation of Murine PAR-1, LPA, and S1P Receptors to Proliferation of Astrocytes
by Scott D. Sorensen and Olivier Nicole and Richard D. Peavy and Lisa M. Montoya and C. Justin Lee and T. J. Murphy and Stephen F. Traynelis and John R. Hepler
Molecular Pharmacology, ISSN 0026-895X, 11/2003, Volume 64, Issue 5, pp. 1199 - 1209
Receptors for the serine protease thrombin and for lysophospholipids are coupled to G proteins and control a wide range of cellular functions, including... 
CELLS | THROMBIN RECEPTORS | LYSOPHOSPHATIDIC ACID | P115 RHOGEF | RAT ASTROCYTES | PROTEIN-COUPLED RECEPTORS | PHARMACOLOGY & PHARMACY | CENTRAL-NERVOUS-SYSTEM | PROTHROMBIN MESSENGER-RNA | BRAIN | SPHINGOSINE 1-PHOSPHATE | Astrocytes - cytology | Transcription, Genetic - drug effects | Receptors, G-Protein-Coupled - metabolism | Receptor, PAR-1 - metabolism | Receptors, Lysophospholipid | RNA, Messenger - metabolism | Receptor, PAR-1 - genetics | Cell Division - physiology | Lysophospholipids | Astrocytes - physiology | Sphingosine - analogs & derivatives | Animals | Signal Transduction - physiology | Mice | Receptors, G-Protein-Coupled - genetics | Sphingosine - metabolism | Thrombin - metabolism | Oligopeptides - pharmacology | Receptors, Lysophosphatidic Acid | Index Medicus
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10. Full Text Matrix Metalloproteinase-1 and Thrombin Differentially Activate Gene Expression in Endothelial Cells via PAR-1 and Promote Angiogenesis
by Blackburn, Jessica S and Brinckerhoff, Constance E
American Journal of Pathology, The, ISSN 0002-9440, 2008, Volume 173, Issue 6, pp. 1736 - 1746
Many tumor types express matrix metalloproteinase-1 (MMP-1); its collagenase activity facilitates both tumor cell invasion and metastasis. MMP-1 expression is... 
Pathology | IN-VITRO | INVASION | METASTASIS | MELANOMA | INHIBITION | TUMOR PROGRESSION | CANCER CELLS | GROWTH | PATHOLOGY | RECEPTORS | HUMAN FIBROBLAST COLLAGENASE | Biocompatible Materials - metabolism | Cell Line | Gene Expression | MAP Kinase Signaling System - physiology | Receptor, PAR-1 - metabolism | Humans | Molecular Sequence Data | Proteoglycans - metabolism | Receptor, PAR-1 - genetics | Thrombin - genetics | Collagen - metabolism | Neovascularization, Physiologic - physiology | Endothelial Cells - cytology | Platelet Endothelial Cell Adhesion Molecule-1 - metabolism | Enzyme Activation | Laminin - metabolism | Thrombin - metabolism | Matrix Metalloproteinase 1 - metabolism | Drug Combinations | Endothelial Cells - physiology | Matrix Metalloproteinase 1 - genetics | Index Medicus | Abridged Index Medicus | Regular
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11. Full Text Impact of a functional polymorphism in the PAR-1 gene promoter in COPD and COPD exacerbations
by Platé, Manuela and Lawson, Phillippa J and Hill, Michael R and Quint, Jennifer K and Kumari, Meena and Laurent, Geoffrey J and Wedzicha, Jadwiga A and Chambers, Rachel C and Hurst, John R
American Journal of Physiology - Lung Cellular and Molecular Physiology, ISSN 1040-0605, 08/2014, Volume 307, Issue 4, pp. L311 - L316
Proteinase-activated receptor-1 (PAR-1) plays a key role in mediating the interplay between coagulation and inflammation in response to injury. The aim of this... 
PAR-1 | COPD exacerbation | SNP | F2R | COPD | COHORT PROFILE | FIBROSIS | PHYSIOLOGY | MARKERS | INJURY | RECEPTOR | OBSTRUCTIVE PULMONARY-DISEASE | PROCOAGULANT | THERAPY | RESPIRATORY SYSTEM | FREQUENCY | COAGULATION | Genetic Predisposition to Disease | Humans | Polymorphism, Single Nucleotide | Pulmonary Disease, Chronic Obstructive - physiopathology | Longitudinal Studies | Promoter Regions, Genetic - genetics | Receptor, PAR-1 - genetics | Polymorphism, Genetic | Pulmonary Disease, Chronic Obstructive - genetics | Receptor, PAR-1 - physiology | Physiological aspects | Genetic research | Lung diseases, Obstructive | Genetic aspects | Single nucleotide polymorphisms | Genotype & phenotype | Chronic obstructive pulmonary disease | Gene expression | Polymorphism | Index Medicus
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