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1. Full Text Universal vaccine based on ectodomain of matrix protein 2 of influenza A: Fc receptors and alveolar macrophages mediate protection
by El Bakkouri, Karim and Descamps, Francis and De Filette, Marina and Smet, Anouk and Festjens, Els and Birkett, Ashley and Van Rooijen, Nico and Verbeek, Sjef and Fiers, Walter and Saelens, Xavier
Journal of Immunology, ISSN 0022-1767, 01/2011, Volume 186, Issue 2, pp. 1022 - 1031
The ectodomain of matrix protein 2 (M2e) of influenza A virus is an attractive target for a universal influenza A vaccine: the M2e sequence is highly conserved... 
GAMMA-RIII CD16 | M2 PROTEIN | PHAGOCYTOSIS | MICRODOMAINS | VIRUS-REPLICATION | EXTRACELLULAR DOMAIN | MONOCLONAL-ANTIBODY | MICE | INFECTION | IMMUNOLOGY | SUBCLASS | Orthomyxoviridae Infections - prevention & control | Protein Interaction Domains and Motifs - immunology | Viral Matrix Proteins - genetics | Macrophages, Alveolar - pathology | Viral Matrix Proteins - therapeutic use | Influenza A virus - genetics | Cell Death - immunology | Immunoglobulin G - toxicity | Receptors, IgG - deficiency | Receptors, IgG - metabolism | Receptors, Fc - deficiency | Receptors, Fc - therapeutic use | Cell Death - genetics | Protein Interaction Domains and Motifs - genetics | Influenza Vaccines - therapeutic use | Female | Influenza A virus - immunology | Receptors, Fc - physiology | Macrophages, Alveolar - immunology | Disease Models, Animal | Macrophages, Alveolar - virology | Receptors, IgG - physiology | Mice, Inbred C57BL | Orthomyxoviridae Infections - pathology | Mice, Knockout | Animals | Influenza Vaccines - immunology | Influenza Vaccines - genetics | Immunization, Passive | Mice | Mice, Inbred BALB C | Viral Matrix Proteins - immunology | Lymphocyte Depletion - methods | Orthomyxoviridae Infections - immunology | Cytotoxicity, Immunologic | Immunoglobulin G - metabolism | Index Medicus | Abridged Index Medicus
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2. Full Text Robust therapeutic efficacy of matrix metalloproteinase-2-cleavable fas-1-RGD peptide complex in chronic inflammatory arthritis
by Nam, Eon Jeong and Kang, Jin Hee and Sa, Keum Hee and Sung, Shijin and Park, Jae Yong and Jo, Dong-Gyu and Park, Jae Hyung and Kim, In San and Kang, Young Mo
PLoS ONE, ISSN 1932-6203, 10/2016, Volume 11, Issue 10, pp. e0164102 - e0164102
Objective Therapeutic agents that are transformable via introducing cleavable linkage by locally enriched MMP-2 within inflamed synovium would enhance... 
RHEUMATOID-ARTHRITIS | COLLAGEN-INDUCED ARTHRITIS | CELLS | ACTIVATION | ANGIOGENESIS | MULTIDISCIPLINARY SCIENCES | ALPHA-V-BETA-3 INTEGRIN | DISEASE | INDUCIBLE GENE H3 | ARRIVE GUIDELINES | DELIVERY | Recombinant Proteins - therapeutic use | NIH 3T3 Cells | Arthritis, Experimental - drug therapy | RANK Ligand - metabolism | Recombinant Fusion Proteins - pharmacology | Recombinant Fusion Proteins - therapeutic use | Molecular Sequence Data | Male | Recombinant Proteins - biosynthesis | RNA, Messenger - metabolism | Arthritis, Experimental - metabolism | Arthritis, Experimental - pathology | Transforming Growth Factor beta - therapeutic use | Mice, Inbred DBA | Vascular Cell Adhesion Molecule-1 - genetics | Chemokine CCL2 - metabolism | Extracellular Matrix Proteins - therapeutic use | Severity of Illness Index | Amino Acid Sequence | Matrix Metalloproteinase 2 - metabolism | Extracellular Matrix Proteins - genetics | Extracellular Matrix Proteins - pharmacology | Chemokine CCL2 - genetics | Recombinant Proteins - pharmacology | Cell Adhesion - drug effects | Down-Regulation - drug effects | RANK Ligand - genetics | Cell Movement - drug effects | Transforming Growth Factor beta - pharmacology | Animals | Transforming Growth Factor beta - genetics | Recombinant Fusion Proteins - genetics | Mice | Vascular Cell Adhesion Molecule-1 - metabolism | Chronic Disease | Microscopy, Fluorescence | Rheumatoid factor | Peptides | Proteases | Analysis | Collagen | Bone morphogenetic proteins | Arthritis | Glycine | Health aspects | Matrix metalloproteinases | Pathogenesis | Transforming growth factor | Matrix metalloproteinase | Synovium | Cell adhesion & migration | Proteins | Angiogenesis | Metalloproteinase | Localization | Growth factors | Enzymes | Sequences | Immunoglobulins | Effectiveness | Internal medicine | Cloning | Rheumatology | Pharmacology | Inflammation | Chemical compounds | Adhesion | Gelatinase A | Medicine | Rheumatoid arthritis | In vivo methods and tests | Cell migration | Index Medicus
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3. Full Text Cell Homing for Pulp Tissue Engineering with Endogenous Dentin Matrix Proteins
by Widbiller, Matthias and Driesen, Ronald B and Eidt, Andreas and Lambrichts, Ivo and Hiller, Karl-Anton and Buchalla, Wolfgang and Schmalz, Gottfried and Galler, Kerstin M
Journal of Endodontics, ISSN 0099-2399, 06/2018, Volume 44, Issue 6, pp. 956 - 962.e2
Compelling evidence pinpoints that pulp tissue engineering after the transplantation of stem cells is possible. Although intriguing, severe problems regarding... 
plasma rich in growth factors | tissue engineering | Cell homing | fibrin | self-assembling peptide | pulp regeneration | SURVIVAL | APICAL PAPILLA | APEXIFICATION | MESENCHYMAL STEM-CELLS | DELIVERY | DENTISTRY, ORAL SURGERY & MEDICINE | GROWTH-FACTORS | PERSPECTIVES | OUTCOMES | REGENERATIVE ENDODONTICS | IMMATURE PERMANENT TEETH | Tissue Engineering - methods | Dentin - metabolism | Humans | Regenerative Endodontics - methods | Male | Dental Pulp - metabolism | Mice, Inbred Strains | Tissue Scaffolds | Animals | Dental Pulp - physiology | Tooth Root - physiology | Adult | Female | Mice | Extracellular Matrix Proteins - therapeutic use | Cell Movement | Fibrin | Transplantation | Root canal therapy | Cell differentiation | Tissue engineering | Stem cells | Dentistry
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4. Full Text The use of sodium trimetaphosphate as a biomimetic analog of matrix phosphoproteins for remineralization of artificial caries-like dentin
by Liu, Yan and Li, Nan and Qi, Yipin and Niu, Li-na and Elshafiy, Sally and Mao, Jing and Breschi, Lorenzo and Pashley, David H and Tay, Franklin R
Dental Materials, ISSN 0109-5641, 2011, Volume 27, Issue 5, pp. 465 - 477
Abstract Objectives This study examined the use of sodium trimetaphosphate (STMP) as a biomimetic analog of matrix phosphoproteins for remineralization of... 
Advanced Basic Science | Dentistry | Degradation | Biomimetic | Artificial carious lesion | Collagen | Remineralization | Sodium trimetaphosphate | CARIOUS DENTIN | MATERIALS SCIENCE, BIOMATERIALS | CONFOCAL RAMAN MICROSPECTROSCOPY | IN-VITRO REMINERALIZATION | LESIONS | CALCIUM-PHOSPHATE | CRYSTAL-GROWTH | DENTISTRY, ORAL SURGERY & MEDICINE | ADHESIVE SYSTEMS | BOND STRENGTH | 2 LAYERS | Cariostatic Agents - therapeutic use | Humans | Composite Resins - chemistry | Dental Cements - chemistry | Methacrylates - chemistry | Calcium - chemistry | X-Ray Microtomography | Tooth Remineralization - methods | Dental Caries - pathology | Collagen - drug effects | Time Factors | Phosphoproteins - therapeutic use | Extracellular Matrix Proteins - therapeutic use | Dentin-Bonding Agents - chemistry | Biomimetic Materials - therapeutic use | Microscopy, Electron, Transmission | Hydroxides - chemistry | Collagen - ultrastructure | Silicon Dioxide - chemistry | Calcium Phosphates - chemistry | Dentin - ultrastructure | Materials Testing | Minerals - analysis | Acrylic Resins - chemistry | Dentin - drug effects | Tooth Demineralization - drug therapy | Dental Caries - drug therapy | Tooth Demineralization - pathology | Saliva, Artificial - chemistry | Polyphosphates - therapeutic use | Phosphates | Dental caries | Usage | Biomimetics | Phosphoproteins | Dentin | Adhesives | Dental materials | Transmission electron microscopy | Sodium | Collagens | Nanostructure | Lesions | remineralization | collagen | sodium trimetaphosphate | degradation | biomimetic | artificial carious lesion
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5. Full Text Antitumor Potential of Fibulin-5 in Breast Cancer Cells Depends on Its RGD Cell Adhesion Motif
by Mohamedi, Yamina and Fontanil, Tania and Cobo, Teresa and Vega, José A and Cobo, Juan Luis and Pérez-Basterrechea, Marcos and Cobo, Juan and Obaya, Álvaro J and Cal, Santiago
Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology, ISSN 1015-8987, 2019, Volume 53, Issue 1, pp. 87 - 100
Different components of the tumor microenvironment can be either tumor-promoting or tumor-suppressive agents depending on factors which are not fully... 
Recombinant Proteins - therapeutic use | Cadherins - metabolism | Vimentin - metabolism | Humans | Male | Recombinant Proteins - biosynthesis | Transplantation, Homologous | Breast Neoplasms - metabolism | Female | Extracellular Matrix Proteins - therapeutic use | Extracellular Matrix Proteins - metabolism | Mutagenesis, Site-Directed | Oligopeptides - genetics | Extracellular Matrix Proteins - pharmacology | Oligopeptides - metabolism | Recombinant Proteins - pharmacology | Cell Adhesion - drug effects | Neoplasms - drug therapy | Animals | Breast Neoplasms - pathology | Cell Line, Tumor | Cell Proliferation - drug effects | Mice | Mice, Inbred BALB C | Neoplasms - pathology | Cell Movement | Index Medicus
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6. Full Text COMP-Angiopoietin-1 Promotes Wound Healing through Enhanced Angiogenesis, Lymphangiogenesis, and Blood Flow in a Diabetic Mouse Model
by Chung-Hyun Cho and Hoon-Ki Sung and Kyung-Tae Kim and Hyae Gyeong Cheont and Goo Taeg Oh and Hyo Jeong Hong and Ook-Joon Yoo and Gou Young Koh
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 3/2006, Volume 103, Issue 13, pp. 4946 - 4951
Microvascular dysfunction is a major cause of impaired wound healing seen in diabetic patients. Therefore, reestablishment of structural and functional... 
Angiogenesis | Wound healing | Diabetes complications | Blood vessels | Mice | Skin | Diabetes | Lymphatic vessels | Blood | Blood flow | Therapeutic protein | Nitric oxide | Cutaneous wound | Growth factor | LONG-TERM | therapeutic protein | nitric oxide | MULTIDISCIPLINARY SCIENCES | cutaneous wound | ANGIOPOIETIN-1 | growth factor | STIMULATES ANGIOGENESIS | REPAIR | COMP-ANG1 | NITRIC-OXIDE | MICE | COMPLICATIONS | diabetes | EXPRESSION | TIE2 RECEPTOR | Diabetes Mellitus - pathology | Recombinant Proteins - therapeutic use | Tail - pathology | Matrilin Proteins | Regional Blood Flow - drug effects | Tail - blood supply | Extracellular Matrix Proteins - therapeutic use | Ear - blood supply | Wound Healing - drug effects | Skin - pathology | Disease Models, Animal | Tail - drug effects | Glycoproteins - genetics | Wounds and Injuries - pathology | Wounds and Injuries - blood | Extracellular Matrix Proteins - genetics | Glycoproteins - therapeutic use | Mice, Inbred C57BL | Nitric Oxide Synthase Type II - deficiency | Diabetes Mellitus - drug therapy | Nitric Oxide Synthase Type III | Recombinant Proteins - genetics | Mice, Knockout | Lymphangiogenesis - drug effects | Skin - blood supply | Angiopoietin-1 - genetics | Animals | Nitric Oxide Synthase Type II - genetics | Wounds and Injuries - drug therapy | Angiopoietin-1 - therapeutic use | Ear - pathology | Skin - drug effects | Nitric Oxide Synthase Type II - metabolism | Blood circulation disorders | Research | Proteins | Cellular biology | Rodents | Injuries | Index Medicus | Biological Sciences
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7. Full Text Preferential enhancement of sensory and motor axon regeneration by combining extracellular matrix components with neurotrophic factors
by Santos, Daniel and González-Pérez, Francisco and Giudetti, Guido and Micera, Silvestro and Udina, Esther and Del Valle, Jaume and Navarro, Xavier
International Journal of Molecular Sciences, ISSN 1661-6596, 01/2017, Volume 18, Issue 1, pp. 65 - 65
After peripheral nerve injury, motor and sensory axons are able to regenerate but inaccuracy of target reinnervation leads to poor functional recovery.... 
BDNF | Motor axons | Extracellular matrix | Reinnervation | Neurotrophic factors | NGF | NT3 | Nerve regeneration | Sensory axons | TUBE REPAIR | FUNCTIONAL RECOVERY | RAT | NEURONS IN-VITRO | BIOCHEMISTRY & MOLECULAR BIOLOGY | INJURY | RELEASE | CHEMISTRY, MULTIDISCIPLINARY | NERVE GROWTH-FACTOR | PERIPHERAL-NERVE | NEURITE OUTGROWTH | neurotrophic factors | nerve regeneration | reinnervation | SCHWANN-CELLS | extracellular matrix | motor axons | sensory axons | Motor Neurons - physiology | Cells, Cultured | Extracellular Matrix Proteins - pharmacology | Rats | Nerve Growth Factors - administration & dosage | Axons - physiology | Rats, Sprague-Dawley | Nerve Growth Factors - therapeutic use | Nerve Growth Factors - pharmacology | Microspheres | Animals | Sensory Receptor Cells - physiology | Nerve Regeneration - drug effects | Female | Extracellular Matrix Proteins - therapeutic use | Peripheral Nerve Injuries - drug therapy | Extracellular Matrix Proteins - administration & dosage | Motor neurons | Spinal cord | Axonogenesis | Brain slice preparation | Recovery of function | Nerve growth factor | Neurotrophin 3 | Motor task performance | Fibronectin | Polylactide-co-glycolide | Regeneration | Laminin | Brain-derived neurotrophic factor | Rodents | Glycolic acid | Collagen | Sensory neurons | Axon guidance | Silicones | Sciatic nerve | Index Medicus
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8. Full Text Proline/arginine‐rich end leucine‐rich repeat protein N‐terminus is a novel osteoclast antagonist that counteracts bone loss
by Rucci, Nadia and Capulli, Mattia and Ventura, Luca and Angelucci, Adriano and Peruzzi, Barbara and Tillgren, Viveka and Muraca, Maurizio and Heinegård, Dick and Teti, Anna and Department of Rheumatology and Lund University and Reumatologi och molekylär skelettbiologi and Lunds universitet
Journal of Bone and Mineral Research, ISSN 0884-0431, 09/2013, Volume 28, Issue 9, pp. 1912 - 1924
(PRELP)-P-hbd is a peptide corresponding to the N-terminal heparin binding domain of the matrix protein proline/arginine-rich end leucine-rich repeat protein... 
PRELP | BONE LOSS | BREAST CANCER METASTASIS | hbd | OSTEOPOROSIS | (PRELP)-P-hbd | PRELP BINDS | DENOSUMAB | ENDOCRINOLOGY & METABOLISM | CANCER | Bone and Bones - pathology | Humans | Bone Neoplasms - secondary | Osteoporosis - drug therapy | Structure-Activity Relationship | Glycoproteins - pharmacology | Bone and Bones - drug effects | Bone and Bones - metabolism | Protein Binding - drug effects | Mammary Neoplasms, Experimental - pathology | Extracellular Matrix Proteins - adverse effects | Female | Bone Neoplasms - drug therapy | Extracellular Matrix Proteins - therapeutic use | Glycoproteins - chemistry | Mammary Neoplasms, Experimental - complications | Extracellular Matrix Proteins - chemistry | Osteoclasts - pathology | Glycoproteins - therapeutic use | Bone Resorption - drug therapy | Extracellular Matrix Proteins - pharmacology | Glycoproteins - adverse effects | Bone Resorption - complications | Osteoclasts - metabolism | Animals | Osteoporosis - pathology | Mice, Nude | Osteoporosis - complications | Bone Resorption - pathology | Cell Line, Tumor | Cell Proliferation - drug effects | Mice | Mice, Inbred BALB C | Osteoclasts - drug effects | Glycosaminoglycans | Peptides | Analysis | Estrogen | Amino acids | Development and progression | Anticoagulants (Medicine) | Sulfates | Protein binding | Tretinoin | Tumors | Proteins | Osteoporosis | Breast cancer | Index Medicus | Rheumatology and Autoimmunity | Clinical Medicine | Medical and Health Sciences | Medicin och hälsovetenskap | Reumatologi och inflammation | Klinisk medicin
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9. Full Text Decorin gene delivery inhibits cardiac fibrosis in spontaneously hypertensive rats by modulation of transforming growth factor-beta/Smad and p38 mitogen-activated protein kinase signaling pathways
by Yan, Wen and Wang, Peihua and Zhao, Chun Xia and Tang, Jiarong and Xiao, Xiao and Wang, Dao Wen
Human gene therapy, ISSN 1043-0342, 2009, Volume 20, Issue 10, pp. 1190 - 1200
Fibrosis is the response of heart and other organs to injuries. Excessive fibrosis can cause organ dysfunction or even failure. Transforming-growth factor... 
HEART | MEDICINE, RESEARCH & EXPERIMENTAL | FACTOR-BETA | TGF-BETA | COLLAGEN | MYOCARDIAL-INFARCTION | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | DIASTOLIC FUNCTION | GENETICS & HEREDITY | EXTRACELLULAR-MATRIX | EXPRESSION | FIBROBLASTS | Dependovirus - genetics | Genetic Therapy | Decorin | Humans | Protective Agents - therapeutic use | Dependovirus - drug effects | Time Factors | Protective Agents - pharmacology | p38 Mitogen-Activated Protein Kinases - metabolism | Extracellular Matrix Proteins - therapeutic use | Rats, Inbred SHR | Gene Transfer Techniques | Kidney - drug effects | Extracellular Matrix Proteins - genetics | Cardiomegaly - physiopathology | Extracellular Matrix Proteins - pharmacology | Rats | Myocardium - pathology | Cardiomegaly - enzymology | Myocardium - enzymology | Proteoglycans - therapeutic use | Animals | Cardiomegaly - prevention & control | MAP Kinase Signaling System - drug effects | Proteoglycans - pharmacology | Fibroblasts - drug effects | Fibrosis | Hemodynamics - drug effects | Smad Proteins - metabolism | Transforming Growth Factor beta - metabolism | Proteoglycans - genetics | Index Medicus
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10. Full Text Maxillary sinus floor augmentation and dental implant placement using dentin matrix protein-1 gene-modified bone marrow stromal cells mixed with deproteinized boving bone: A comparative study in beagles
by Liu, Xin and Li, Qiong and Wang, Fang and Wang, Zuolin
Archives of Oral Biology, ISSN 0003-9969, 2016, Volume 64, pp. 102 - 108
Highlights • bMSCs were transduced with a lentiviral vector overexpressing DMP1 gene. • Bio-Oss® was used as the scaffold for DMP1 mediated bMSCs. • bMSCs... 
Advanced Basic Science | Dentistry | Bone marrow stromal cells | Dentin matrix protein 1 | Gene therapy | Maxillary sinus floor augmentation | Dental implant | SURVIVAL | GRAFTS | DENTISTRY, ORAL SURGERY & MEDICINE | AUTOGENOUS BONE | IN-VIVO | ELEVATION | HYDROXYAPATITE | Osseointegration | Tissue Engineering - methods | Extracellular Matrix Proteins - biosynthesis | Extracellular Matrix Proteins - genetics | Sinus Floor Augmentation - methods | Male | Bone Regeneration | Green Fluorescent Proteins - genetics | Maxilla - surgery | Minerals | Mesenchymal Stem Cell Transplantation - methods | Animals | Mesenchymal Stromal Cells | Green Fluorescent Proteins - biosynthesis | Bone Substitutes - therapeutic use | Dogs | Extracellular Matrix Proteins - therapeutic use | Dental Implantation, Endosseous - methods | Bone Transplantation - methods | Osteogenesis | Genetic Therapy - methods | Genetic research | Genetic vectors | Comparative analysis | Implant dentures | Genes | Index Medicus
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11. Full Text Co-expression of fibulin-5 and VEGF165 increases long-term patency of synthetic vascular grafts seeded with autologous endothelial cells
by Preis, M and Schneiderman, J and Koren, B and Ben-Yosef, Y and Levin-Ashkenazi, D and Shapiro, S and Cohen, T and Blich, M and Israeli-Amit, M and Sarnatzki, Y and Gershtein, D and Shofti, R and Lewis, B S and Shaul, Y and Flugelman, M Y
Gene therapy, ISSN 0969-7128, 03/2016, Volume 23, Issue 3, pp. 237 - 246
Small caliber synthetic vascular grafts are commonly used for bypass surgery and dialysis access sites but have high failure rates because of neointima... 
Vascular Grafting - methods | Peripheral Vascular Diseases - therapy | Extracellular Matrix Proteins - genetics | Humans | Vascular Endothelial Growth Factor A - therapeutic use | Endothelial Cells - transplantation | Rats | Vascular Endothelial Growth Factor A - genetics | Animals | Models, Animal | Sheep | Extracellular Matrix Proteins - therapeutic use | Endothelial Cells - physiology | Vascular Patency | Cellular biology | Heart surgery | Hemodialysis | Skin & tissue grafts | Index Medicus
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12. Full Text Exogenous reelin prevents granule cell dispersion in experimental epilepsy
by Müller, Martin C and Osswald, Matthias and Tinnes, Stefanie and Häussler, Ute and Jacobi, Anne and Förster, Eckart and Frotscher, Michael and Haas, Carola A
Experimental Neurology, ISSN 0014-4886, 2009, Volume 216, Issue 2, pp. 390 - 397
Temporal lobe epilepsy (TLE) is often accompanied by granule cell dispersion (GCD), a migration defect of granule cells in the dentate gyrus. We have... 
Neuronal migration | Dentate gyrus | dab1 | apoER2 | Temporal lobe epilepsy | Extracellular matrix | VLDLR | Neurogenesis | Ammon's horn sclerosis | LIPOPROTEIN RECEPTORS | PROTEIN | TEMPORAL-LOBE EPILEPSY | NEUROSCIENCES | DISRUPTION | NEURONAL MIGRATION DISORDERS | HIPPOCAMPAL SCLEROSIS | MOUSE MODEL | MICE | RADIAL GLIAL SCAFFOLD | Neuroprotective Agents - therapeutic use | Nerve Tissue Proteins - therapeutic use | LDL-Receptor Related Proteins | Male | RNA, Messenger - metabolism | Drug Delivery Systems | Receptors, Lipoprotein - metabolism | Adaptor Protein Complex 1 - metabolism | Adaptor Protein Complex 1 - genetics | Dentate Gyrus - drug effects | Time Factors | Cell Adhesion Molecules, Neuronal - therapeutic use | Cell Adhesion Molecules, Neuronal - metabolism | Extracellular Matrix Proteins - therapeutic use | Kainic Acid - toxicity | Neurons - drug effects | Extracellular Matrix Proteins - metabolism | Disease Models, Animal | Receptors, LDL - genetics | Mice, Inbred C57BL | Receptors, Lipoprotein - genetics | Receptors, LDL - metabolism | Gene Expression Regulation - drug effects | Nerve Tissue Proteins - metabolism | Cell Movement - drug effects | Animals | Cell Count - methods | Excitatory Amino Acid Agonists - toxicity | Analysis of Variance | Epilepsy - chemically induced | Serine Endopeptidases - therapeutic use | Epilepsy - drug therapy | Mice | Serine Endopeptidases - metabolism | Dentate Gyrus - pathology | Epilepsy - pathology | Neural Inhibition - drug effects | Prevention | Neurons | Epilepsy | Analysis | Index Medicus
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13. Full Text COMP-angiopoietin-1 ameliorates renal fibrosis in a unilateral ureteral obstruction model
by Kim, Won and Moon, Sang-Ok and Lee, Sang Yong and Jang, Kyu Yun and Cho, Chung-Hyun and Koh, Gou Young and Choi, Kyu-Sil and Yoon, Kwon-Ha and Sung, Mi Jeong and Kim, Duk Hoon and Lee, Sik and Kang, Kyung Pyo and Park, Sung Kwang
Journal of the American Society of Nephrology, ISSN 1046-6673, 09/2006, Volume 17, Issue 9, pp. 2474 - 2483
Injury to the renal microvasculature may be a major factor in the progression of renal disease; therefore, protection of endothelial cells (EC) in renal... 
APOPTOSIS | DESIGNED ANGIOPOIETIN-1 VARIANT | COMP-ANG1 | UROLOGY & NEPHROLOGY | BLOOD-FLOW | POTENTIAL ROLE | EXPRESSION | NEPHROPATHY | PROGRESSION | ENDOTHELIAL GROWTH-FACTOR | TIE2 RECEPTOR | Kidney - blood supply | Kidney - pathology | Recombinant Fusion Proteins - therapeutic use | Transforming Growth Factor beta1 - metabolism | Male | Smad3 Protein - metabolism | Microcirculation - drug effects | Renal Artery | Matrilin Proteins | Platelet Endothelial Cell Adhesion Molecule-1 - metabolism | Antigens, Differentiation - metabolism | Receptor, TIE-2 - metabolism | Extracellular Matrix Proteins - therapeutic use | Ureteral Obstruction - drug therapy | Proto-Oncogene Proteins c-akt - metabolism | Smad7 Protein - metabolism | Kidney - drug effects | Glycoproteins - therapeutic use | Smad2 Protein - metabolism | Animals | Fibrosis | Angiopoietin-1 - therapeutic use | Mice | Blood Flow Velocity - drug effects | Endothelial Cells - drug effects | Index Medicus
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