Journal of Neuropathology & Experimental Neurology, ISSN 0022-3069, 07/2015, Volume 74, Issue 7, pp. 653 - 671
Fetal-onset hydrocephalus affects 1 to 3 per 1,000 live births. It is not only a disorder of cerebrospinal fluid dynamics but also a brain disorder that...
Human | HUMAN FETAL EPENDYMA | Cerebrospinal fluid | SUBVENTRICULAR ZONE | CEREBROSPINAL-FLUID | CORTICAL DEVELOPMENT | NEUROBLAST MIGRATION | HTx rat | ARNOLD-CHIARI MALFORMATION | Ventricular zone disruption | Neurospheres | Congenital hydrocephalus | BLOOD-VESSELS | Neural stem cells | CENTRAL-NERVOUS-SYSTEM | Junction pathology | ADHERENS JUNCTIONS | EPENDYMAL DENUDATION | SUBCOMMISSURAL ORGAN | PATHOLOGY | NEUROSCIENCES | CLINICAL NEUROLOGY | Age Factors | Embryo, Mammalian | Humans | Hydrocephalus - pathology | Male | Glial Fibrillary Acidic Protein - metabolism | Neural Stem Cells - ultrastructure | Ventricular Outflow Obstruction - pathology | Telencephalon - growth & development | Intercellular Junctions - pathology | Telencephalon - pathology | Female | Fetus | Cell Differentiation | Animals, Newborn | Cells, Cultured | Rats | Telencephalon - embryology | Microscopy, Electron | Gestational Age | Neural Stem Cells - pathology | Animals | Neurogenesis - physiology | Intercellular Junctions - ultrastructure | Telencephalon - ultrastructure | Cell Movement
Human | HUMAN FETAL EPENDYMA | Cerebrospinal fluid | SUBVENTRICULAR ZONE | CEREBROSPINAL-FLUID | CORTICAL DEVELOPMENT | NEUROBLAST MIGRATION | HTx rat | ARNOLD-CHIARI MALFORMATION | Ventricular zone disruption | Neurospheres | Congenital hydrocephalus | BLOOD-VESSELS | Neural stem cells | CENTRAL-NERVOUS-SYSTEM | Junction pathology | ADHERENS JUNCTIONS | EPENDYMAL DENUDATION | SUBCOMMISSURAL ORGAN | PATHOLOGY | NEUROSCIENCES | CLINICAL NEUROLOGY | Age Factors | Embryo, Mammalian | Humans | Hydrocephalus - pathology | Male | Glial Fibrillary Acidic Protein - metabolism | Neural Stem Cells - ultrastructure | Ventricular Outflow Obstruction - pathology | Telencephalon - growth & development | Intercellular Junctions - pathology | Telencephalon - pathology | Female | Fetus | Cell Differentiation | Animals, Newborn | Cells, Cultured | Rats | Telencephalon - embryology | Microscopy, Electron | Gestational Age | Neural Stem Cells - pathology | Animals | Neurogenesis - physiology | Intercellular Junctions - ultrastructure | Telencephalon - ultrastructure | Cell Movement
Journal Article
Cellular and Molecular Life Sciences, ISSN 1420-682X, 2/2013, Volume 70, Issue 4, pp. 631 - 659
The gastrointestinal epithelium forms the boundary between the body and external environment. It effectively provides a selective permeable barrier that limits...
Life Sciences | Biochemistry, general | Life Sciences, general | Cytokine | Tight junction | Nutrient | Intestinal epithelium | Pathogen | Biomedicine general | Cell Biology | ACETALDEHYDE-INDUCED INCREASE | PROTEIN-KINASE-C | KAPPA-B ACTIVATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | CLOSTRIDIUM-PERFRINGENS ENTEROTOXIN | NECROSIS-FACTOR-ALPHA | CELL BIOLOGY | INFLAMMATORY-BOWEL-DISEASE | ENTEROPATHOGENIC ESCHERICHIA-COLI | CHAIN FATTY-ACIDS | EPIDERMAL-GROWTH-FACTOR | CACO-2 CELL MONOLAYERS | Tight Junctions - metabolism | Intestinal Mucosa - metabolism | Tight Junctions - microbiology | Cytokines - metabolism | Humans | Nutritional Physiological Phenomena | Intestinal Mucosa - microbiology | Permeability | Intercellular Signaling Peptides and Proteins - metabolism | Animals | Tight Junctions - immunology | Intestinal Mucosa - immunology | Intercellular Signaling Peptides and Proteins - immunology | Tight Junctions - pathology | Cytokines - immunology | Intestinal Mucosa - pathology | Analysis | Pathology | Immunology | Cytokines | Cellular biology | Digestive system | Nutrients
Life Sciences | Biochemistry, general | Life Sciences, general | Cytokine | Tight junction | Nutrient | Intestinal epithelium | Pathogen | Biomedicine general | Cell Biology | ACETALDEHYDE-INDUCED INCREASE | PROTEIN-KINASE-C | KAPPA-B ACTIVATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | CLOSTRIDIUM-PERFRINGENS ENTEROTOXIN | NECROSIS-FACTOR-ALPHA | CELL BIOLOGY | INFLAMMATORY-BOWEL-DISEASE | ENTEROPATHOGENIC ESCHERICHIA-COLI | CHAIN FATTY-ACIDS | EPIDERMAL-GROWTH-FACTOR | CACO-2 CELL MONOLAYERS | Tight Junctions - metabolism | Intestinal Mucosa - metabolism | Tight Junctions - microbiology | Cytokines - metabolism | Humans | Nutritional Physiological Phenomena | Intestinal Mucosa - microbiology | Permeability | Intercellular Signaling Peptides and Proteins - metabolism | Animals | Tight Junctions - immunology | Intestinal Mucosa - immunology | Intercellular Signaling Peptides and Proteins - immunology | Tight Junctions - pathology | Cytokines - immunology | Intestinal Mucosa - pathology | Analysis | Pathology | Immunology | Cytokines | Cellular biology | Digestive system | Nutrients
Journal Article
Biological research, ISSN 0716-9760, 2012, Volume 45, Issue 3, pp. 231 - 242
Most cells of the developing mammalian brain derive from the ventricular (VZ) and the subventricular (SVZ) zones. The VZ is formed by the multipotent radial...
GAP-JUNCTION | NEURONAL MIGRATION | hydrocephalus | EMBRYONIC CEREBROSPINAL-FLUID | INJURED SPINAL-CORD | neural stem cells | H-TX RAT | stem cell transplantation | PERIVENTRICULAR NODULAR HETEROTOPIA | CONGENITAL HYDROCEPHALUS | SUBVENTRICULAR ZONE | UMCG Approved | CEREBRAL-CORTEX | abnormal neurogenesis | ALPHA-SNAP | Stem cell transplantation | Abnormal neurogenesis | Neural stem cells | Hydrocephalus | EPENDYMAL DENUDATION | POINT MUTATION | SPINAL-CORD | CEREBROSPINAL-FLUID | CORTICAL DEVELOPMENT | BIOLOGY | Cerebral Ventricles - pathology | Cell Proliferation | Humans | Rats | Hydrocephalus - pathology | Hydrocephalus - therapy | Neural Stem Cells - pathology | Neurogenesis | Cerebral Aqueduct - pathology | Stem Cell Transplantation - methods | Animals | Intercellular Junctions - pathology | Neural Stem Cells - transplantation | Cell Differentiation | Cerebral Ventricles - embryology
GAP-JUNCTION | NEURONAL MIGRATION | hydrocephalus | EMBRYONIC CEREBROSPINAL-FLUID | INJURED SPINAL-CORD | neural stem cells | H-TX RAT | stem cell transplantation | PERIVENTRICULAR NODULAR HETEROTOPIA | CONGENITAL HYDROCEPHALUS | SUBVENTRICULAR ZONE | UMCG Approved | CEREBRAL-CORTEX | abnormal neurogenesis | ALPHA-SNAP | Stem cell transplantation | Abnormal neurogenesis | Neural stem cells | Hydrocephalus | EPENDYMAL DENUDATION | POINT MUTATION | SPINAL-CORD | CEREBROSPINAL-FLUID | CORTICAL DEVELOPMENT | BIOLOGY | Cerebral Ventricles - pathology | Cell Proliferation | Humans | Rats | Hydrocephalus - pathology | Hydrocephalus - therapy | Neural Stem Cells - pathology | Neurogenesis | Cerebral Aqueduct - pathology | Stem Cell Transplantation - methods | Animals | Intercellular Junctions - pathology | Neural Stem Cells - transplantation | Cell Differentiation | Cerebral Ventricles - embryology
Journal Article
Journal of the National Cancer Institute, ISSN 0027-8874, 03/2012, Volume 104, Issue 6, pp. 461 - 475
Background Angiopoietin-2 (Ang2), a ligand for endothelial TEK (Tie2) tyrosine kinase receptor, is induced in hypoxic endothelial cells of tumors, where it...
LYMPHATIC VESSELS | TRANSGENE EXPRESSION | ANGIOGENESIS | ONCOLOGY | IN-VIVO | GENE-THERAPY | VEGF-C | TUMOR-GROWTH | CANCER | RECEPTOR TYROSINE KINASE | TIE2 RECEPTOR | Immunohistochemistry | Antibodies, Blocking - metabolism | Up-Regulation | Immunoprecipitation | Melanoma - blood supply | Coculture Techniques | Endothelium, Vascular - drug effects | Immunoblotting | Transplantation, Heterologous | Antibodies, Blocking - pharmacology | Angiopoietin-2 - metabolism | Cell Hypoxia | Retinal Vessels - pathology | Lung Neoplasms - secondary | Intercellular Junctions - pathology | Female | Neovascularization, Pathologic - prevention & control | Receptor, TIE-2 - metabolism | Lymphangiogenesis | Lung Neoplasms - blood supply | Microscopy, Electron, Transmission | Retinal Vessels - metabolism | Intercellular Junctions - metabolism | Angiogenesis Inhibitors - pharmacology | Mice, Transgenic | Lymphatic Metastasis | Retinal Vessels - drug effects | Mice, SCID | Melanoma - secondary | Animals | Neovascularization, Pathologic - drug therapy | Intercellular Junctions - drug effects | Endothelium, Vascular - pathology | Mice | Mice, Inbred BALB C | Neovascularization, Pathologic - metabolism | Angiopoietin-2 - antagonists & inhibitors | Endothelial Cells - pathology | Endothelial Cells - drug effects | Junctional complexes (Epithelium) | Lung cancer | Cell junctions | Physiological aspects | Development and progression | Models | Metastasis | Research | Growth factor receptors
LYMPHATIC VESSELS | TRANSGENE EXPRESSION | ANGIOGENESIS | ONCOLOGY | IN-VIVO | GENE-THERAPY | VEGF-C | TUMOR-GROWTH | CANCER | RECEPTOR TYROSINE KINASE | TIE2 RECEPTOR | Immunohistochemistry | Antibodies, Blocking - metabolism | Up-Regulation | Immunoprecipitation | Melanoma - blood supply | Coculture Techniques | Endothelium, Vascular - drug effects | Immunoblotting | Transplantation, Heterologous | Antibodies, Blocking - pharmacology | Angiopoietin-2 - metabolism | Cell Hypoxia | Retinal Vessels - pathology | Lung Neoplasms - secondary | Intercellular Junctions - pathology | Female | Neovascularization, Pathologic - prevention & control | Receptor, TIE-2 - metabolism | Lymphangiogenesis | Lung Neoplasms - blood supply | Microscopy, Electron, Transmission | Retinal Vessels - metabolism | Intercellular Junctions - metabolism | Angiogenesis Inhibitors - pharmacology | Mice, Transgenic | Lymphatic Metastasis | Retinal Vessels - drug effects | Mice, SCID | Melanoma - secondary | Animals | Neovascularization, Pathologic - drug therapy | Intercellular Junctions - drug effects | Endothelium, Vascular - pathology | Mice | Mice, Inbred BALB C | Neovascularization, Pathologic - metabolism | Angiopoietin-2 - antagonists & inhibitors | Endothelial Cells - pathology | Endothelial Cells - drug effects | Junctional complexes (Epithelium) | Lung cancer | Cell junctions | Physiological aspects | Development and progression | Models | Metastasis | Research | Growth factor receptors
Journal Article
Journal of Neuroscience, ISSN 0270-6474, 06/2011, Volume 31, Issue 26, pp. 9456 - 9465
HIV infection of the CNS is an early event after primary infection, resulting in neurological complications in a significant number of individuals despite...
GLIOVASCULAR INTERFACE | POLYMERASE-CHAIN-REACTION | INTERCELLULAR COMMUNICATION | ENDOTHELIAL-CELLS | IN-VIVO | HUMAN FETAL ASTROCYTES | CENTRAL-NERVOUS-SYSTEM | CHEMOATTRACTANT PROTEIN-1 | CEREBROSPINAL-FLUID | HIV-1 INFECTION | NEUROSCIENCES | HIV-1 | In Situ Nick-End Labeling | Gap Junctions - pathology | Macaca nemestrina | Cell Count | Humans | Astrocytes - pathology | Cells, Cultured | Brain - virology | Blood-Brain Barrier - pathology | Simian Acquired Immunodeficiency Syndrome - virology | Animals | Fluorescent Antibody Technique | Brain - pathology | Blood-Brain Barrier - virology | Gap Junctions - virology | Endothelial Cells - pathology | Endothelial Cells - virology | Simian Acquired Immunodeficiency Syndrome - pathology | Astrocytes - virology
GLIOVASCULAR INTERFACE | POLYMERASE-CHAIN-REACTION | INTERCELLULAR COMMUNICATION | ENDOTHELIAL-CELLS | IN-VIVO | HUMAN FETAL ASTROCYTES | CENTRAL-NERVOUS-SYSTEM | CHEMOATTRACTANT PROTEIN-1 | CEREBROSPINAL-FLUID | HIV-1 INFECTION | NEUROSCIENCES | HIV-1 | In Situ Nick-End Labeling | Gap Junctions - pathology | Macaca nemestrina | Cell Count | Humans | Astrocytes - pathology | Cells, Cultured | Brain - virology | Blood-Brain Barrier - pathology | Simian Acquired Immunodeficiency Syndrome - virology | Animals | Fluorescent Antibody Technique | Brain - pathology | Blood-Brain Barrier - virology | Gap Junctions - virology | Endothelial Cells - pathology | Endothelial Cells - virology | Simian Acquired Immunodeficiency Syndrome - pathology | Astrocytes - virology
Journal Article
Cardiovascular Research, ISSN 0008-6363, 03/2017, Volume 113, Issue 3, pp. 259 - 275
This review presents an extensively integrated model of the cardiac intercalated disc (ID), a highly orchestrated structure that connects adjacent...
Cardiac arrhythmia | Wnt signaling | Arrhythmogenic cardiomyopathy | Brugada syndrome | Physiology | Cardiology and Cardiovascular Medicine | Physiology (medical) | Intercalated disc | ANKYRIN-G | CARDIAC & CARDIOVASCULAR SYSTEMS | AREA-COMPOSITA | HEART-MUSCLE CELLS | SODIUM-CHANNEL NA(V)1.5 | 3-DIMENSIONAL STRUCTURE | GAP-JUNCTIONS | ADENOVIRUS RECEPTOR | ARRHYTHMOGENIC CARDIOMYOPATHIES | RIGHT-VENTRICULAR CARDIOMYOPATHY | Gap Junctions - metabolism | Humans | Adherens Junctions - metabolism | Arrhythmias, Cardiac - physiopathology | Arrhythmias, Cardiac - pathology | Desmosomes - pathology | Intercellular Junctions - pathology | Membrane Proteins - metabolism | Arrhythmias, Cardiac - genetics | Arrhythmias, Cardiac - metabolism | Desmosomes - metabolism | Gap Junctions - pathology | Genetic Predisposition to Disease | Signal Transduction | Membrane Proteins - genetics | Intercellular Junctions - metabolism | Cell Communication | Intercellular Junctions - genetics | Adherens Junctions - pathology | Mechanotransduction, Cellular | Myocytes, Cardiac - pathology | Animals | Ion Channels - metabolism | Myocytes, Cardiac - metabolism | Mutation
Cardiac arrhythmia | Wnt signaling | Arrhythmogenic cardiomyopathy | Brugada syndrome | Physiology | Cardiology and Cardiovascular Medicine | Physiology (medical) | Intercalated disc | ANKYRIN-G | CARDIAC & CARDIOVASCULAR SYSTEMS | AREA-COMPOSITA | HEART-MUSCLE CELLS | SODIUM-CHANNEL NA(V)1.5 | 3-DIMENSIONAL STRUCTURE | GAP-JUNCTIONS | ADENOVIRUS RECEPTOR | ARRHYTHMOGENIC CARDIOMYOPATHIES | RIGHT-VENTRICULAR CARDIOMYOPATHY | Gap Junctions - metabolism | Humans | Adherens Junctions - metabolism | Arrhythmias, Cardiac - physiopathology | Arrhythmias, Cardiac - pathology | Desmosomes - pathology | Intercellular Junctions - pathology | Membrane Proteins - metabolism | Arrhythmias, Cardiac - genetics | Arrhythmias, Cardiac - metabolism | Desmosomes - metabolism | Gap Junctions - pathology | Genetic Predisposition to Disease | Signal Transduction | Membrane Proteins - genetics | Intercellular Junctions - metabolism | Cell Communication | Intercellular Junctions - genetics | Adherens Junctions - pathology | Mechanotransduction, Cellular | Myocytes, Cardiac - pathology | Animals | Ion Channels - metabolism | Myocytes, Cardiac - metabolism | Mutation
Journal Article
The Journal of Immunology, ISSN 0022-1767, 12/2003, Volume 171, Issue 11, pp. 6164 - 6172
It is well known that inflammatory conditions of the intestinal mucosa result in compromised barrier function. Inflammation is characterized by an influx into...
FACTOR TNF RECEPTORS | TIGHT JUNCTIONS | INTERCELLULAR-ADHESION MOLECULE-1 | INFLAMMATORY-BOWEL-DISEASE | INTERFERON-GAMMA | CROHNS-DISEASE | IFN-GAMMA | CD95 (APO-1/FAS)-MEDIATED APOPTOSIS | NECROSIS-FACTOR-ALPHA | IMMUNOLOGY | INTESTINAL PERMEABILITY | Inflammation - pathology | Intestinal Mucosa - metabolism | Membrane Microdomains - metabolism | Fluoresceins - metabolism | Humans | Adherens Junctions - immunology | Adherens Junctions - metabolism | Membrane Microdomains - immunology | Inflammation - metabolism | Intestinal Mucosa - immunology | Octoxynol | Dextrans - metabolism | Tight Junctions - metabolism | Solubility | Interferon-gamma - physiology | Inflammation - immunology | Detergents | Adherens Junctions - pathology | Cell Membrane Permeability - immunology | Apoptosis - immunology | Tight Junctions - immunology | Up-Regulation - immunology | Tumor Necrosis Factor-alpha - physiology | Cell Line, Tumor | Membrane Microdomains - pathology | Tight Junctions - pathology | Intestinal Mucosa - pathology
FACTOR TNF RECEPTORS | TIGHT JUNCTIONS | INTERCELLULAR-ADHESION MOLECULE-1 | INFLAMMATORY-BOWEL-DISEASE | INTERFERON-GAMMA | CROHNS-DISEASE | IFN-GAMMA | CD95 (APO-1/FAS)-MEDIATED APOPTOSIS | NECROSIS-FACTOR-ALPHA | IMMUNOLOGY | INTESTINAL PERMEABILITY | Inflammation - pathology | Intestinal Mucosa - metabolism | Membrane Microdomains - metabolism | Fluoresceins - metabolism | Humans | Adherens Junctions - immunology | Adherens Junctions - metabolism | Membrane Microdomains - immunology | Inflammation - metabolism | Intestinal Mucosa - immunology | Octoxynol | Dextrans - metabolism | Tight Junctions - metabolism | Solubility | Interferon-gamma - physiology | Inflammation - immunology | Detergents | Adherens Junctions - pathology | Cell Membrane Permeability - immunology | Apoptosis - immunology | Tight Junctions - immunology | Up-Regulation - immunology | Tumor Necrosis Factor-alpha - physiology | Cell Line, Tumor | Membrane Microdomains - pathology | Tight Junctions - pathology | Intestinal Mucosa - pathology
Journal Article
BBA - Biomembranes, ISSN 0005-2736, 01/2018, Volume 1860, Issue 1, pp. 83 - 90
Gap junctions are specialized membrane domains containing tens to thousands of intercellular channels. These channels permit exchange of small molecules (<...
Phosphorylation | Connexin43 | Kinase | Gap junction | ROUS-SARCOMA VIRUS | BIOCHEMISTRY & MOLECULAR BIOLOGY | CARDIAC MYOCYTES | PLASMA-MEMBRANE | PROTEIN CONNEXIN43 | ISCHEMIA-REPERFUSION INJURY | BIOPHYSICS | INTERCELLULAR COMMUNICATION | V-SRC | MOLECULAR-BASIS | ZONULA OCCLUDENS-1 | LIVING CELLS | Arrhythmias, Cardiac - metabolism | Arrhythmias, Cardiac - pathology | Gap Junctions - metabolism | Gap Junctions - pathology | Biological Transport, Active | Animals | Connexin 43 - metabolism | Humans | Heart Failure - metabolism | Heart Failure - pathology | Second Messenger Systems | Physiological aspects | Epidermal growth factor | Metabolites | Cyclic guanylic acid | Protein kinases | Membrane proteins
Phosphorylation | Connexin43 | Kinase | Gap junction | ROUS-SARCOMA VIRUS | BIOCHEMISTRY & MOLECULAR BIOLOGY | CARDIAC MYOCYTES | PLASMA-MEMBRANE | PROTEIN CONNEXIN43 | ISCHEMIA-REPERFUSION INJURY | BIOPHYSICS | INTERCELLULAR COMMUNICATION | V-SRC | MOLECULAR-BASIS | ZONULA OCCLUDENS-1 | LIVING CELLS | Arrhythmias, Cardiac - metabolism | Arrhythmias, Cardiac - pathology | Gap Junctions - metabolism | Gap Junctions - pathology | Biological Transport, Active | Animals | Connexin 43 - metabolism | Humans | Heart Failure - metabolism | Heart Failure - pathology | Second Messenger Systems | Physiological aspects | Epidermal growth factor | Metabolites | Cyclic guanylic acid | Protein kinases | Membrane proteins
Journal Article
9.
Full Text
The role of differential VE-cadherin dynamics in cell rearrangement during angiogenesis
Nature Cell Biology, ISSN 1465-7392, 2014, Volume 16, Issue 4, pp. 309 - 321
Endothelial cells show surprising cell rearrangement behaviour during angiogenic sprouting; however, the underlying mechanisms and functional importance remain...
MIGRATION | MORPHOGENESIS | REGULATES FORMATION | JUNCTIONS | MOUSE | PERMEABILITY IN-VIVO | ADHESION HYPOTHESIS | MODEL | ADAPTER PROTEIN | VASCULAR ENDOTHELIAL-CADHERIN | CELL BIOLOGY | Cadherins - metabolism | Signal Transduction | Endothelial Cells - metabolism | Receptors, Notch - metabolism | Humans | Cells, Cultured | Vascular Endothelial Growth Factor Receptor-2 - metabolism | Male | Mice, Transgenic | Vascular Endothelial Growth Factor A - metabolism | Diabetic Retinopathy - pathology | Cell Movement - physiology | Diabetic Retinopathy - metabolism | Antigens, CD - metabolism | Neovascularization, Pathologic - pathology | Animals | Image Processing, Computer-Assisted | Cell Adhesion - physiology | Computer Simulation | Intercellular Junctions - pathology | Female | Mice | Neovascularization, Pathologic - metabolism | Endothelial Cells - pathology | Cell research | Cellular control mechanisms | Physiological aspects | Cadherins | Neovascularization | Research | Properties | Medical and Health Sciences | Medicin och hälsovetenskap
MIGRATION | MORPHOGENESIS | REGULATES FORMATION | JUNCTIONS | MOUSE | PERMEABILITY IN-VIVO | ADHESION HYPOTHESIS | MODEL | ADAPTER PROTEIN | VASCULAR ENDOTHELIAL-CADHERIN | CELL BIOLOGY | Cadherins - metabolism | Signal Transduction | Endothelial Cells - metabolism | Receptors, Notch - metabolism | Humans | Cells, Cultured | Vascular Endothelial Growth Factor Receptor-2 - metabolism | Male | Mice, Transgenic | Vascular Endothelial Growth Factor A - metabolism | Diabetic Retinopathy - pathology | Cell Movement - physiology | Diabetic Retinopathy - metabolism | Antigens, CD - metabolism | Neovascularization, Pathologic - pathology | Animals | Image Processing, Computer-Assisted | Cell Adhesion - physiology | Computer Simulation | Intercellular Junctions - pathology | Female | Mice | Neovascularization, Pathologic - metabolism | Endothelial Cells - pathology | Cell research | Cellular control mechanisms | Physiological aspects | Cadherins | Neovascularization | Research | Properties | Medical and Health Sciences | Medicin och hälsovetenskap
Journal Article
Acta Neuropathologica, ISSN 0001-6322, 08/2013, Volume 126, Issue 2, pp. 303 - 306
NATIONAL INSTITUTE | PROTEIN | EVOLUTION | DEPOSITION | NEUROFIBRILLARY DEGENERATION | ASSOCIATION GUIDELINES | PLAQUES | PATHOLOGY | MILD COGNITIVE IMPAIRMENT | NEUROSCIENCES | CLINICAL NEUROLOGY | NEUROPATHOLOGIC ASSESSMENT | Brain Stem - pathology | Axons - pathology | Humans | Intercellular Junctions - pathology | Alzheimer Disease - metabolism | Amyloid beta-Peptides - metabolism | Brain Stem - metabolism | Intercellular Junctions - metabolism | Axons - metabolism | tau Proteins - metabolism | Alzheimer Disease - pathology
Journal Article
Cardiovascular Research, ISSN 0008-6363, 07/2013, Volume 99, Issue 2, pp. 304 - 314
Connexins form a family of transmembrane proteins that consists of 20 members in humans and 21 members in mice. Six connexins assemble into a connexon that can...
Cardiovascular system | Connexins | Mechanotransduction | Gap junctions | CARDIAC & CARDIOVASCULAR SYSTEMS | PULMONARY ARTERIAL-HYPERTENSION | NITRIC-OXIDE SYNTHASE | CARDIAC MYOCYTES | ANGIOTENSIN-II | RAT AORTIC ENDOTHELIUM | ENDOTHELIUM-DEPENDENT RELAXATIONS | SHEAR-STRESS | MYOENDOTHELIAL GAP-JUNCTIONS | HYPERTROPHIED RIGHT VENTRICLES | RIGHT-VENTRICULAR CARDIOMYOPATHY | Humans | Intercellular Junctions - metabolism | Stress, Mechanical | Myocardium - pathology | Arteries - pathology | Regional Blood Flow | Hypertension - pathology | Hypertension - physiopathology | Arteries - metabolism | Connexins - metabolism | Hypertension - metabolism | Cardiovascular System - pathology | Mechanotransduction, Cellular | Biomechanical Phenomena | Cardiovascular System - physiopathology | Animals | Cardiovascular System - metabolism | Arteries - physiopathology | Intercellular Junctions - pathology | Myocardium - metabolism | Hemodynamics | Spotlight Reviews | Spotlight on Biomechanical Factors in Cardiovascular Disease
Cardiovascular system | Connexins | Mechanotransduction | Gap junctions | CARDIAC & CARDIOVASCULAR SYSTEMS | PULMONARY ARTERIAL-HYPERTENSION | NITRIC-OXIDE SYNTHASE | CARDIAC MYOCYTES | ANGIOTENSIN-II | RAT AORTIC ENDOTHELIUM | ENDOTHELIUM-DEPENDENT RELAXATIONS | SHEAR-STRESS | MYOENDOTHELIAL GAP-JUNCTIONS | HYPERTROPHIED RIGHT VENTRICLES | RIGHT-VENTRICULAR CARDIOMYOPATHY | Humans | Intercellular Junctions - metabolism | Stress, Mechanical | Myocardium - pathology | Arteries - pathology | Regional Blood Flow | Hypertension - pathology | Hypertension - physiopathology | Arteries - metabolism | Connexins - metabolism | Hypertension - metabolism | Cardiovascular System - pathology | Mechanotransduction, Cellular | Biomechanical Phenomena | Cardiovascular System - physiopathology | Animals | Cardiovascular System - metabolism | Arteries - physiopathology | Intercellular Junctions - pathology | Myocardium - metabolism | Hemodynamics | Spotlight Reviews | Spotlight on Biomechanical Factors in Cardiovascular Disease
Journal Article