Suchergebnisse - "Neuromuscular Junction/metabolism"
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1
Autoren: et al.
Weitere Verfasser: et al.
Quelle: Science Signaling. 18
Schlagwörter: RNA, Messenger/genetics, Motor Neurons, Synapses/metabolism, Neuromuscular Junction, Gene Expression Regulation, Developmental, Mice, Transgenic, Mice, Protein Biosynthesis, Synapses, Journal Article, Animals, Ribosomes/metabolism, RNA, Messenger, Neuromuscular Junction/metabolism, Ribosomes, Motor Neurons/metabolism
Dateibeschreibung: application/pdf
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2
Autoren: et al.
Quelle: Sci Rep
Scientific Reports, Vol 15, Iss 1, Pp 1-17 (2025)Schlagwörter: Mice, Knockout, Science, Neuromuscular Junction, Receptor Protein-Tyrosine Kinases / metabolism, Receptor Protein-Tyrosine Kinases, Muscle, Skeletal / metabolism, Article, Mice, Receptor Protein-Tyrosine Kinases / genetics, Receptors, Cholinergic / metabolism, Calcium-Calmodulin-Dependent Protein Kinase Type 2 / genetics, Medicine, Animals, Humans, Receptors, Cholinergic, Neuromuscular Junction / metabolism, Phosphorylation, Calcium-Calmodulin-Dependent Protein Kinase Type 2, Muscle, Skeletal, Calcium-Calmodulin-Dependent Protein Kinase Type 2 / metabolism
Dateibeschreibung: application/pdf
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3
Autoren: et al.
Quelle: J Cell Sci
Gavrilova, A, Boström, A, Korabel, N, Fedotov, S, Poulin, G B & Allan, V J 2024, 'The role of kinesin-1 in neuronal dense core vesicle transport, locomotion and lifespan regulation in C. elegans', Journal of Cell Science, vol. 137, no. 17, jcs262148. https://doi.org/10.1242/jcs.262148Schlagwörter: 0301 basic medicine, Kinesins/metabolism, Mutation/genetics, Longevity, Neurons/metabolism, Neuromuscular Junction, Kinesins, Genetically Modified, Cell Cycle Proteins, Axonal Transport, Animals, Genetically Modified, 03 medical and health sciences, Animals, Neuromuscular Junction/metabolism, Caenorhabditis elegans, Caenorhabditis elegans Proteins, Secretory Vesicles/metabolism, Neurons, Caenorhabditis elegans/metabolism, 0303 health sciences, Secretory Vesicles, Longevity/genetics, Locomotion/genetics, Mutation, Caenorhabditis elegans Proteins/metabolism, Locomotion, Research Article
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4
Autoren: et al.
Quelle: Mol Neurodegener
Molecular Neurodegeneration, Vol 19, Iss 1, Pp 1-23 (2024)
Molecular neurodegeneration 19(1), 50 (2024). doi:10.1186/s13024-024-00735-7Schlagwörter: metabolism [Zebrafish Proteins], pathology [Motor Neurons], TDP-43, Hypothalamus, Neuromuscular Junction, metabolism [Neuromuscular Junction], genetics [DNA-Binding Proteins], genetics [Zebrafish Proteins], Zebrafish Proteins/genetics [MeSH], Amyotrophic Lateral Sclerosis/pathology [MeSH], Neuromuscular Junction/pathology [MeSH], Animal model, Zebrafish, Motor Neurons/pathology [MeSH], Neuromuscular Junction/metabolism [MeSH], Amyotrophic Lateral Sclerosis/metabolism [MeSH], Animals [MeSH], DNA-Binding Proteins/genetics [MeSH], Metabolic dysfunction, DNA-Binding Proteins/metabolism [MeSH], Neurodegeneration, Animals, Genetically Modified [MeSH], Zebrafish [MeSH], ALS, Amyotrophic Lateral Sclerosis/genetics [MeSH], Motor Neurons/metabolism [MeSH], Disease Models, Animal [MeSH], Research Article, Zebrafish Proteins/metabolism [MeSH], pathology [Neuromuscular Junction], Animals, Genetically Modified, ddc:570, Tardbp protein, zebrafish, Animals, pathology [Amyotrophic Lateral Sclerosis], RC346-429, Motor Neurons, metabolism [Amyotrophic Lateral Sclerosis], Amyotrophic Lateral Sclerosis, RC952-954.6, metabolism [Motor Neurons], Zebrafish Proteins, DNA-Binding Proteins, genetics [Amyotrophic Lateral Sclerosis], Disease Models, Animal, Geriatrics, Neurology. Diseases of the nervous system, metabolism [DNA-Binding Proteins]
Dateibeschreibung: application/pdf
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5
Autoren: et al.
Weitere Verfasser: et al.
Quelle: Theranostics
Theranostics, vol 12, iss 12Schlagwörter: Male, 0301 basic medicine, amyotrophic lateral sclerosis, Medical Biotechnology, Caveolin 1, Neurodegenerative, 01 natural sciences, Transgenic, Motor Neurons / metabolism, Mice, 0302 clinical medicine, 2.1 Biological and endogenous factors, membrane/lipid raft, Motor Neurons, Dependovirus / genetics, neuromuscular junction, hSOD1G93A, Gene Transfer Techniques, Gene Therapy, Dependovirus, gene therapy, Synapsins* / genetics, 3. Good health, Synapsins* / therapeutic use, Superoxide Dismutase / genetics, Neurological, Superoxide Dismutase / metabolism, Female, Neuromuscular Junction / metabolism, Synapsins* / metabolism, Biotechnology, Research Paper, caveolin-1, Oncology and Carcinogenesis, Neuromuscular Junction, Mice, Transgenic, Amyotrophic Lateral Sclerosis* / therapy, 03 medical and health sciences, Rare Diseases, Caveolin 1* / genetics, Genetics, Animals, Humans, membrane/lipid raft (MLRs), Dependovirus / metabolism, motor neuron, Caveolin 1* / metabolism, Biomedical and Clinical Sciences, Caveolin 1* / therapeutic use, Animal, Superoxide Dismutase, Amyotrophic Lateral Sclerosis, Neurosciences, Oncology and carcinogenesis, Synapsins, Brain Disorders, 0104 chemical sciences, Rats, Disease Models, Animal, Orphan Drug, Amyotrophic Lateral Sclerosis* / genetics, Disease Models, hSOD1(G93A), ALS
Dateibeschreibung: application/pdf
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6
Autoren: et al.
Schlagwörter: Agrin/physiology, Animals, Newborn, Cells, Cultured, Genes, erbB, erbB-2, Membrane Potentials, Mice, Motor Endplate/metabolism, Motor Endplate/physiology, Muscle, Skeletal/innervation, Skeletal/ultrastructure, Mutation, Neuregulins/metabolism, Neuromuscular Junction/embryology, Neuromuscular Junction/metabolism, Presynaptic Terminals/physiology, RNA, Messenger/genetics, Messenger/metabolism, Receptor, Epidermal Growth Factor/genetics, Epidermal Growth Factor/physiology, ErbB-2/genetics, ErbB-2/physiology, ErbB-4, Receptors
Relation: Science; https://iris.unil.ch/handle/iris/241166; serval:BIB_EE8AE266DF25
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7
Autoren: et al.
Schlagwörter: Adult, Agrin/chemistry, Agrin/genetics, Animals, Biopsy, Cell Line, DNA Mutational Analysis, Dystroglycans/metabolism, Female, Humans, Male, Models, Chemical, Muscle Fibers, Skeletal/cytology, Skeletal/metabolism, Muscle, Skeletal/pathology, Mutation, Missense, Myasthenic Syndromes, Congenital/genetics, Neuromuscular Junction/genetics, Neuromuscular Junction/metabolism, Pedigree, Protein Structure, Tertiary, Rats, Receptors, Cholinergic/genetics
Dateibeschreibung: application/pdf
Relation: American Journal of Human Genetics; 1537-6605[electronic]; https://iris.unil.ch/handle/iris/195599; serval:BIB_7B8117A7C642; 000269332900005
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8
Autoren: et al.
Weitere Verfasser: et al.
Schlagwörter: Animals, Motor Neurons/metabolism, Mice, Neuromuscular Junction/metabolism, Protein Biosynthesis, RNA, Messenger/genetics, Synapses/metabolism, Ribosomes/metabolism, Gene Expression Regulation, Developmental, Transgenic, Journal Article
Dateibeschreibung: application/pdf
Verfügbarkeit: https://dspace.library.uu.nl/handle/1874/461138
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9
Autoren: et al.
Quelle: Brain
Devoy, A, Kalmar, B, Stewart, M, Park, H, Burke, B, Noy, S J, Redhead, Y, Humphrey, J, Lo, K, Jaeger, J, Mejia Maza, A, Sivakumar, P, Bertolin, C, Soraru, G, Plagnol, V, Greensmith, L, Acevedo Arozena, A, Isaacs, A M, Davies, B, Fratta, P & Fisher, E M C 2017, ' Humanized mutant FUS drives progressive motor neuron degeneration without aggregation in 'FUSDelta14' knockin mice ', Brain : a journal of neurology, vol. 140, no. 11, pp. 2797-2805 . https://doi.org/10.1093/brain/awx248
CONCYTEC-Institucional
Consejo Nacional de Ciencia Tecnología e Innovación Tecnológica
instacron:CONCYTECSchlagwörter: 0301 basic medicine, amyotrophic lateral sclerosis, frameshift mutation, RNA binding protein FUS, nerve degeneration, Gene Dosage, Endoplasmic Reticulum, gene targeting, transcriptomics, Mice, antibody, mitochondrion, animal, genetics, proteinosis, Gene Knock-In Techniques, progressive motor neuron degeneration, Neuromuscular Junction/metabolism, Frameshift Mutation, motoneuron, Motor Neurons, epitope, 0303 health sciences, neuromuscular junction, pathogenesis, Delta14, Amyotrophic Lateral Sclerosis/genetics, Rough/metabolism, peptide, Mitochondria, 3. Good health, female, priority journal, Endoplasmic Reticulum, Rough, Pathological/genetics, Ribosomal Proteins, Heterozygote, humanization, animal experiment, Neuromuscular Junction, rough endoplasmic reticulum, gene dosage, Protein Aggregation, Pathological, Article, 03 medical and health sciences, ribosome protein, male, Mitochondria/metabolism, gene expression profiling, heterozygosity, Animals, Humans, controlled study, mutant, human, mouse, FUS, nerve cell degeneration, nonhuman, Animal, animal model, disease model, Gene Expression Profiling, Amyotrophic Lateral Sclerosis, Protein Aggregation, heterozygote, Endoplasmic Reticulum, Rough/metabolism, Protein Aggregation, Pathological/genetics, Disease Models, Animal, Disease Models, Ribosomal Proteins/genetics, RNA-Binding Protein FUS, ALS, metabolism, RNA-Binding Protein FUS/genetics, Motor Neurons/metabolism, Reports
Dateibeschreibung: application/pdf
Zugangs-URL: https://academic.oup.com/brain/article-pdf/140/11/2797/24174428/awx248.pdf
https://pubmed.ncbi.nlm.nih.gov/29053787
https://discovery.ucl.ac.uk/10035275/
https://core.ac.uk/display/132208430
https://www.well.ox.ac.uk/publications/738162
http://europepmc.org/abstract/MED/29053787
https://www.ncbi.nlm.nih.gov/pubmed/29053787
https://academic.oup.com/brain/article/140/11/2797/4372144
https://ora.ox.ac.uk/objects/uuid:94f34271-1c43-4c96-b532-abb16c4ba4fa
https://doi.org/10.1093/brain/awx248
https://kclpure.kcl.ac.uk/en/publications/57c6b9d4-8280-4a7e-9515-3f29eca70861
https://kclpure.kcl.ac.uk/portal/en/publications/57c6b9d4-8280-4a7e-9515-3f29eca70861
http://hdl.handle.net/20.500.12390/640
https://discovery-pp.ucl.ac.uk/id/eprint/10035275/ -
10
Autoren: et al.
Quelle: European Journal of Paediatric Neurology. 15:189-196
Schlagwörter: Myasthenic Syndromes, Congenital, 0301 basic medicine, Myasthenic Syndromes, Congenital / genetics, Acetylcholinesterase / genetics, Myasthenic Syndromes, Congenital / metabolism, Neuromuscular Junction, Neuromuscular Junction / physiopathology, Neuromuscular Junction / genetics, Myasthenic Syndromes, Congenital / physiopathology, Acetylcholine, 3. Good health, Genetic Heterogeneity, 03 medical and health sciences, 0302 clinical medicine, Acetylcholine / genetics, Receptors, Cholinergic / genetics, Acetylcholinesterase, Humans, Receptors, Cholinergic, Neuromuscular Junction / metabolism
Dateibeschreibung: application/pdf
Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/21498094
https://pubmed.ncbi.nlm.nih.gov/21498094/
https://core.ac.uk/display/11700041
http://eprint.ncl.ac.uk/pub_details2.aspx?pub_id=183826
https://europepmc.org/article/MED/21498094
https://www.sciencedirect.com/science/article/pii/S1090379811000419
https://www.ncbi.nlm.nih.gov/pubmed/21498094
https://urn.nsk.hr/urn:nbn:hr:105:062922
https://doi.org/10.1016/j.ejpn.2011.03.006 -
11
Autoren:
Quelle: Molecular Biology of the Cell. 19:150-158
Schlagwörter: Carbonyl Cyanide p-Trifluoromethoxyphenylhydrazone, 0301 basic medicine, Spinal Cord: cytology, Cells, Xenopus, Presynaptic Terminals: drug effects, Intracellular Space, Neuromuscular Junction, Presynaptic Terminals, Actins: metabolism, Carbonyl Cyanide p-Trifluoromethoxyphenylhydrazone: pharmacology, Membrane Potential, Mitochondrial: drug effects, Adenosine Triphosphate: metabolism, Synaptic Vesicles: drug effects, 03 medical and health sciences, Adenosine Triphosphate, Animals, Mitochondria: drug effects, Cells, Cultured, Synaptic Vesicles: metabolism, Membrane Potential, Mitochondrial, Intracellular Space: drug effects, 0303 health sciences, Cultured, Creatine, Creatine: pharmacology, Actins, Microspheres, Mitochondria, Neuromuscular Junction: drug effects, Spinal Cord, Neuromuscular Junction: metabolism, Presynaptic Terminals: metabolism, Mitochondria: metabolism, Intracellular Space: metabolism, Synaptic Vesicles
Zugangs-URL: https://europepmc.org/articles/pmc2174173?pdf=render
https://pubmed.ncbi.nlm.nih.gov/17942598
https://pubmed.ncbi.nlm.nih.gov/17942598/
https://www.molbiolcell.org/doi/full/10.1091/mbc.e07-05-0515
https://hub.hku.hk/handle/10722/225409
https://www.molbiolcell.org/content/19/1/150.full
http://repository.ust.hk/ir/Record/1783.1-3529
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2174173/
http://hdl.handle.net/10722/225409 -
12
Autoren: et al.
Quelle: The Journal of Neuroscience. 24:9105-9116
Schlagwörter: 0301 basic medicine, Patch-Clamp Techniques, Action Potentials -- physiology, Neuromuscular Junction, Presynaptic Terminals, Action Potentials, Glutamic Acid, Genetically Modified, Synapses -- metabolism -- physiology -- ultrastructure, Receptors, Metabotropic Glutamate, Synaptic Transmission, Feedback, Animals, Genetically Modified, 03 medical and health sciences, Receptors, Animals, Drosophila Proteins, Drosophila Proteins -- genetics -- metabolism, Physiological -- physiology, GTP-Binding Protein beta Subunits -- metabolism, Neuronal Plasticity -- genetics -- physiology, Feedback, Physiological, 0303 health sciences, Neuronal Plasticity, Glutamic Acid -- metabolism, Neuromuscular Junction -- metabolism -- physiology -- ultrastructure, GTP-Binding Protein beta Subunits, Synaptic Transmission -- physiology, Electric Stimulation, Drosophila melanogaster, Larva, Mutation, Synapses, Presynaptic Terminals -- metabolism -- ultrastructure, Biologie, Metabotropic Glutamate -- genetics -- metabolism -- physiology
Dateibeschreibung: 1 full-text file(s): application/pdf
Zugangs-URL: https://europepmc.org/articles/pmc6730051?pdf=render
https://pubmed.ncbi.nlm.nih.gov/15483129
https://europepmc.org/article/MED/15483129
https://www.jneurosci.org/content/24/41/9105.full.pdf
https://www.jneurosci.org/content/jneuro/24/41/9105.full.pdf
http://www.jneurosci.org/content/24/41/9105.abstract
http://www.ncbi.nlm.nih.gov/pubmed/15483129
https://www.jneurosci.org/content/24/41/9105 -
13
Autoren: et al.
Quelle: Molecular Pharmacology. 66:794-806
Schlagwörter: 0301 basic medicine, Protein Kinase C: metabolism, Purinergic P2Y1, Cells, Xenopus, Inositol Phosphates, Neuromuscular Junction, Gene Expression, Messenger: metabolism, Adenosine Diphosphate: physiology, Inositol Phosphates: metabolism, Receptors, Purinergic P2Y2, Receptors, Purinergic P2Y1, 03 medical and health sciences, Adenosine Triphosphate, Spinal Cord: metabolism, Mitogen-Activated Protein Kinases: metabolism, Uridine Triphosphate: physiology, Receptors, Animals, Receptors, Cholinergic, RNA, Messenger, Purinergic P2Y2, Phosphorylation, Cells, Cultured, Protein Kinase C, Cholinergic: metabolism, 0303 health sciences, Acetylcholinesterase: metabolism, Adenosine Triphosphate: physiology, Cultured, Purinergic P2: physiology, Cholinergic: genetics, Receptors, Purinergic P2, Muscles, Gene Expression: physiology, Acetylcholinesterase: genetics, Rats, Purinergic P2: metabolism, Adenosine Diphosphate, Muscles: metabolism, Spinal Cord, Neuromuscular Junction: metabolism, Acetylcholinesterase, RNA, Mitogen-Activated Protein Kinases, Chickens
Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/15258260
https://pubmed.ncbi.nlm.nih.gov/15258260/
http://europepmc.org/abstract/MED/15258260
https://molpharm.aspetjournals.org/content/66/4/794
https://repository.ust.hk/ir/Record/1783.1-29544
https://www.ncbi.nlm.nih.gov/pubmed/15258260
https://molpharm.aspetjournals.org/content/molpharm/early/2004/07/16/mol.104.003269.full.pdf -
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Autoren: et al.
Quelle: Journal of Biological Chemistry. 279:31081-31088
Schlagwörter: Purinergic P2 Receptor Agonists, 0301 basic medicine, Purinergic P2Y1, Agrin: administration & dosage, Cells, Muscle Fibers, Skeletal, Neuromuscular Junction, Chick Embryo, Muscle Fibers, Adenosine Triphosphate: metabolism, Receptors, Purinergic P2Y1, 03 medical and health sciences, Adenosine Triphosphate, Agrin: metabolism, Receptors, RhoA GTP-Binding Protein: metabolism, Purinergic P2 Receptor Antagonists, Animals, Receptors, Cholinergic, Agrin, Muscle, Skeletal, Cells, Cultured, Cholinergic: metabolism, Adenosine Triphosphate: administration & dosage, 0303 health sciences, Cultured, Skeletal: metabolism, Receptors, Purinergic P2, Skeletal: drug effects, Drug Synergism, Rats, 3. Good health, Purinergic P2: metabolism, Neuromuscular Junction: drug effects, Neuromuscular Junction: metabolism, Mutation, RhoA GTP-Binding Protein: genetics, Muscle, rhoA GTP-Binding Protein, Chickens, Signal Transduction
Zugangs-URL: http://www.jbc.org/content/279/30/31081.full.pdf
https://pubmed.ncbi.nlm.nih.gov/15145960
https://www.ncbi.nlm.nih.gov/pubmed/15145960
https://europepmc.org/abstract/MED/15145960
http://repository.ust.hk/ir/bitstream/1783.1-2464/1/JBC2.pdf
https://www.sciencedirect.com/science/article/pii/S002192581836160X
http://repository.ust.hk/ir/Record/1783.1-2464
https://www.jbc.org/content/279/30/31081.full -
15
Autoren: et al.
Quelle: Volynski, K E, Capogna, M, Ashton, A C, Thomson, D, Orlova, E V, Manser, C F, Ribchester, R R & Ushkaryov, Y A 2003, 'Mutant alpha-latrotoxin (LTXN4C) does not form pores and causes secretion by receptor stimulation : this action does not require neurexins', Journal of Biological Chemistry, vol. 278, no. 33, pp. 31058-66. https://doi.org/10.1074/jbc.M210395200
Schlagwörter: 0301 basic medicine, Calcium/metabolism, Patch-Clamp Techniques, Strontium/pharmacology, Chromaffin Cells, Neuromuscular Junction, Glutamic Acid, CHO Cells, Synaptosomes/metabolism, Hippocampus, Glutamic Acid/pharmacokinetics, Exocytosis, Membrane Potentials, Mice, 03 medical and health sciences, Catecholamines, Cricetinae, Animals, Black Widow Spider, Carbon Radioisotopes, Neuromuscular Junction/metabolism, Protein Structure, Quaternary, Receptors, Cell Surface/metabolism, Catecholamines/metabolism, 0303 health sciences, Cell Membrane/metabolism, Cell Membrane, Chromaffin Cells/metabolism, Acetylcholine, Rats, 3. Good health, Membrane Potentials/physiology, Spider Venoms/chemistry, COS Cells, Mutation, Acetylcholine/metabolism, Hippocampus/cytology, Calcium, Cattle
Zugangs-URL: http://www.jbc.org/content/278/33/31058.full.pdf
https://pubmed.ncbi.nlm.nih.gov/12782639
https://www.ncbi.nlm.nih.gov/pubmed/12782639
http://www.mrcbndu.ox.ac.uk/sites/default/files/pdfs/capognajbiolchem.pdf
https://www.neuroscience.ox.ac.uk/publications/329224
https://www.jbc.org/article/S0021-9258(20)84146-5/fulltext
http://www.jbc.org/content/early/2003/06/02/jbc.M210395200.full.pdf
https://www.sciencedirect.com/science/article/pii/S0021925820841465
https://ora.ox.ac.uk/objects/uuid:610cd61f-3778-4612-84a7-8944608eaa14
https://doi.org/10.1074/jbc.m210395200 -
16
Autoren:
Quelle: Journal of Neurocytology. 32:727-741
Schlagwörter: 0301 basic medicine, Synapses: genetics, 0303 health sciences, 03 medical and health sciences, Synapses: metabolism, Neuromuscular Junction: metabolism, Synapses, Neuromuscular Junction, Neuromuscular Junction: genetics, Animals, Humans, Signal Transduction: physiology, Signal Transduction
Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/15034264
https://dialnet.unirioja.es/servlet/articulo?codigo=839969
http://repository.ust.hk/ir/Record/1783.1-30500
https://link.springer.com/article/10.1023/B:NEUR.0000020620.62318.01
https://pubmed.ncbi.nlm.nih.gov/15034264/
http://europepmc.org/abstract/MED/15034264
http://hdl.handle.net/10722/196669 -
17
Autoren: et al.
Quelle: Journal of Neurocytology. 32:603-617
Schlagwörter: Gene Expression Regulation: physiology, 0301 basic medicine, Synapses: genetics, 0303 health sciences, Skeletal: metabolism, Neuromuscular Junction, Neuromuscular Junction: genetics, Skeletal: drug effects, Adenosine Triphosphate: pharmacology, Adenosine Triphosphate: metabolism, 03 medical and health sciences, Synapses: metabolism, Adenosine Triphosphate, Neuromuscular Junction: drug effects, Gene Expression Regulation, Neuromuscular Junction: metabolism, Synapses, Muscle, Animals, Humans, Synapses: drug effects, Muscle, Skeletal, Gene Expression Regulation: drug effects
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18
Autoren: et al.
Quelle: Groffen, A J, Ruegg, M A, Dijkman, H, Van De Velden, T J, Buskens, C A, Van Den Born, J, Assmann, K J, Monnens, L A, Veerkamp, J H & Van Den Heuvel, L P 1998, 'Agrin is a major heparan sulfate proteoglycan in the human glomerular basement membrane', Journal of Histochemistry and Cytochemistry, vol. 46, no. 1, pp. 19-27. https://doi.org/10.1177/002215549804600104
Journal of the American Society of Nephrology, 8, pp. A2396-A2396
Journal of Histochemistry and Cytochemistry, 46, pp. 19-27Schlagwörter: 0301 basic medicine, Immunologische ontstekingsprocessen in de nier, Kidney Glomerulus, Pathofysiologie, immunologie en behandeling van nieraandoeningen, Fluorescent Antibody Technique, Immune Sera/metabolism, Heparitin Sulfate/metabolism, Basement Membrane, Inflammatory reactions in the kidneys, Monoclonal, Neuromuscular Junction/metabolism, Fluorescent Antibody Technique, Indirect, Microscopy, Immunoelectron, Heparan Sulfate Proteoglycans/metabolism, Microscopy, 0303 health sciences, Structuur en functie van heparansulfaat proteoglycanen in de humane basaal membraan van de nier, Antibodies, Monoclonal, Pathophysiology, immunology and treatment of renal disease, 3. Good health, Kidney Glomerulus/cytology, Proteoglycans of renal basement membranes, Muscle, Proteoglycans, Adult, Indirect, Kidney Cortex, Heparan sulfate proteoglycan, Neuromuscular Junction, Kidney Cortex/cytology, Enzyme-Linked Immunosorbent Assay, Skeletal/metabolism, Antibodies, Fluorescence, Proteoglycanen van basaalmembranen van de nier, 03 medical and health sciences, Agrin/biosynthesis, Animals, Humans, Agrin, Muscle, Skeletal, Immunoelectron, Basement Membrane/metabolism, Bungarotoxins/metabolism, Immune Sera, Proteoglycans/metabolism, Bungarotoxins, Perlecan, Rats, Glomerular basement membrane, Microscopy, Fluorescence, Heparitin Sulfate, Structure and function of heparan sulphate proteoglycans in human renal basement membranes, Heparan Sulfate Proteoglycans
Dateibeschreibung: application/pdf
Zugangs-URL: http://journals.sagepub.com/doi/pdf/10.1177/002215549804600104
https://pubmed.ncbi.nlm.nih.gov/9405491
https://hdl.handle.net/1871.1/6eb00434-385e-41c1-8ad0-9f270b760d04
https://research.vu.nl/en/publications/6eb00434-385e-41c1-8ad0-9f270b760d04
https://doi.org/10.1177/002215549804600104
https://hdl.handle.net/11370/53e993fe-67b6-4829-bcd6-17100348ffbf
https://research.rug.nl/en/publications/53e993fe-67b6-4829-bcd6-17100348ffbf
https://doi.org/10.1177/002215549804600104
https://europepmc.org/abstract/MED/9405491
https://research.vu.nl/en/publications/agrin-is-a-major-heparan-sulfate-proteoglycan-in-the-human-glomer
https://www.ncbi.nlm.nih.gov/pubmed/9405491
http://europepmc.org/abstract/MED/9405491
https://journals.sagepub.com/doi/pdf/10.1177/002215549804600104
http://journals.sagepub.com/doi/abs/10.1177/002215549804600104
https://research.vumc.nl/en/publications/cec08d9f-43a6-4fc9-9782-57f553579ade
https://pure.amsterdamumc.nl/en/publications/14b55671-8ce6-4557-bb92-2e0d266f6f5b
https://doi.org/10.1177/002215549804600104
http://hdl.handle.net/2066/29421
https://hdl.handle.net/2066/224415 -
19
Weitere Verfasser: et al.
Quelle: T201205534.pdf
Schlagwörter: Action Potentials, Animals, Ataxia/genetics, Ataxia/metabolism, Ataxia/pathology, Ataxia/physiopathology, Brain/metabolism, Brain/pathology, Brain/physiopathology, Diaphragm/cytology, Diaphragm/metabolism, Electric Stimulation, Fluorescent Dyes/analysis, Gene Deletion, Homozygote, Mice, Knockout, Neuromuscular Junction/cytology, Neuromuscular Junction/metabolism, Neurons/cytology, Neurons/metabolism, Patch-Clamp Techniques, Peripheral Nervous System/metabolism, Peripheral Nervous System/pathology, Peripheral Nervous System/physiopathology, Proteasome Endopeptidase Complex/genetics, Proteasome Endopeptidase Complex/metabolism, Respiratory Muscles/cytology, Respiratory Muscles/metabolism, Synaptic Transmission
Relation: AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY; J00102; https://ir.ymlib.yonsei.ac.kr/handle/22282913/89439; T201205534; 31768
Verfügbarkeit: https://ir.ymlib.yonsei.ac.kr/handle/22282913/89439
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20
Autoren: et al.
Quelle: BioEssays. 23:372-374
Schlagwörter: CD4-Positive T-Lymphocytes: metabolism, Ions, 0301 basic medicine, 0303 health sciences, Tyrosine 3-Monooxygenase: metabolism, Calcium Signaling: physiology, Calcium: physiology, Gene Expression, Calmodulin: metabolism, Calcium: metabolism, Neuromuscular Junction: physiology, 03 medical and health sciences, 14-3-3 Proteins, Gastrula: physiology, Neuromuscular Junction: metabolism, Animals, Humans, Nitric Oxide: metabolism, Cyclic GMP: metabolism, Fertilization: physiology
Zugangs-URL: http://repository.ust.hk/ir/bitstream/1783.1-2258/1/8cal_in.pdf
https://philpapers.org/rec/WEBCID
https://www.ncbi.nlm.nih.gov/pubmed/11268044
https://repository.ust.hk/ir/Record/1783.1-2258
https://europepmc.org/article/MED/11268044
https://core.ac.uk/display/34060444
https://repository.ust.hk/ir/bitstream/1783.1-2258/1/8cal_in.pdf
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