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1
المؤلفون: Li, Jia-Yi, Popovic, Natalija, Brundin, Patrik
المصدر: NeuroRx. 2(3):64-447
مصطلحات موضوعية: Huntington Disease: psychology, Huntington Disease: therapy, Mice, Huntington Disease: pathology, Behavior, Animal, Humans, Huntington Disease: diet therapy, Huntington Disease: genetics, Animals, Anti-Inflammatory Agents: therapeutic use, Apoptosis: drug effects, Brain: pathology, Disease Models, Transgenic: physiology, Protease Inhibitors: therapeutic use, Protein Folding, Research Support, Non-U.S. Gov't, Tissue Therapy, Transglutaminases: antagonists & inhibitors, Medicin och hälsovetenskap, Medicinska och farmaceutiska grundvetenskaper, Neurovetenskaper, Medical and Health Sciences, Basic Medicine, Neurosciences
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2
المؤلفون: Virginie Zimmer, Sebastian Kügler, Shi Cheng, Frank Streit, Catherine Pythoud, Jolanda M. Liefhebber, Anupam Raina, Pavlina Konstantinova, Nicole Déglon, Maria Rey, Gabriel Vachey, Julia Tereshchenko, Andrzej Mazur, Mathias Bähr
المصدر: Experimental neurology, vol. 309, pp. 79-90
مصطلحات موضوعية: 0301 basic medicine, Parkinson's disease, Transgene, Genetic enhancement, Green Fluorescent Proteins, Synucleins, Mice, Transgenic, Gene product, Mice, 03 medical and health sciences, Transduction (genetics), Adrenergic Agents, Hormone Antagonists, 0302 clinical medicine, 3,4-Dihydroxyphenylacetic Acid/metabolism, Adrenergic Agents/toxicity, Animals, Disease Models, Animal, Gene Expression Regulation/drug effects, Gene Expression Regulation/genetics, Glial Cell Line-Derived Neurotrophic Factor/genetics, Glial Cell Line-Derived Neurotrophic Factor/metabolism, Green Fluorescent Proteins/genetics, Green Fluorescent Proteins/metabolism, Homovanillic Acid/metabolism, Hormone Antagonists/therapeutic use, Huntingtin Protein/genetics, Huntingtin Protein/metabolism, Huntington Disease/genetics, Huntington Disease/metabolism, Huntington Disease/pathology, Huntington Disease/therapy, Mifepristone/therapeutic use, Oxidopamine/toxicity, Parkinson Disease/etiology, Parkinson Disease/genetics, Parkinson Disease/metabolism, Parkinson Disease/therapy, Synapsins/genetics, Synapsins/metabolism, Synucleins/genetics, Synucleins/metabolism, Transduction, Genetic, AAV, GDNF, GeneSwitch, Huntington's disease, Mifepristone, Regulated expression, Developmental Neuroscience, Neurotrophic factors, medicine, Glial cell line-derived neurotrophic factor, Glial Cell Line-Derived Neurotrophic Factor, Oxidopamine, Huntingtin Protein, biology, business.industry, Homovanillic Acid, Parkinson Disease, Synapsins, medicine.disease, 3. Good health, Huntington Disease, 030104 developmental biology, Gene Expression Regulation, Neurology, Cancer research, biology.protein, 3,4-Dihydroxyphenylacetic Acid, business, 030217 neurology & neurosurgery
وصف الملف: application/pdf
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3رسالة جامعية
المؤلفون: Bacos, Karl
المساهمون: Lunds universitet. Medicinska fakulteten
مصطلحات موضوعية: Huntington disease -- pathology, Huntington disease -- genetics, Insulin -- metabolism, Insulin-secreting cells -- pathology, Islets of Langerhans -- pathology, Islets of Langerhans -- metabolism, Diabetes mellitus -- genetics, Exocytosis -- physiology
Degree: Diss. (sammanfattning) Lund : Lunds universitet, 2009
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4رسالة جامعية
المؤلفون: van der Burg, Jorien Maria Margaretha
مصطلحات موضوعية: Huntington Disease -- pathology, Huntington Disease -- metabolism, Weight Loss
Degree: Diss. Lund : Lunds universitet, 2008
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5
المؤلفون: Meunier, C., Merienne, N., Jollé, C., Déglon, N., Pellerin, L.
المصدر: Glia, vol. 64, no. 11, pp. 1841-1856
مصطلحات موضوعية: Neurons, Dopamine and cAMP-Regulated Phosphoprotein 32, Huntingtin Protein, Glutamine, Brain, Glutamic Acid, Nuclear Proteins, Mice, Transgenic, Nerve Tissue Proteins, DNA-Binding Proteins, Disease Models, Animal, Mice, Huntington Disease, nervous system, Gene Expression Regulation, Glutamate-Ammonia Ligase, Astrocytes, Glial Fibrillary Acidic Protein, Mutation, Animals, Humans, Astrocytes/metabolism, Astrocytes/pathology, Brain/pathology, Cyclophilin A/metabolism, Dopamine and cAMP-Regulated Phosphoprotein 32/metabolism, Gene Expression Regulation/genetics, Glial Fibrillary Acidic Protein/metabolism, Glutamate-Ammonia Ligase/genetics, Glutamate-Ammonia Ligase/metabolism, Glutamic Acid/metabolism, Glutamine/metabolism, Huntingtin Protein/genetics, Huntingtin Protein/metabolism, Huntington Disease/complications, Huntington Disease/genetics, Huntington Disease/pathology, Locomotion/genetics, Locomotion/physiology, Mutation/genetics, Nerve Tissue Proteins/metabolism, Neurons/pathology, Nuclear Proteins/metabolism, adenoassociated viral vectors, glia, mouse model, polyglutamine expansion, striatum, Cyclophilin A, Locomotion
وصف الملف: application/pdf
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6
المؤلفون: Petersén, Åsa, Chase, K, Puschban, Zoe, DiFiglia, M, Brundin, Patrik, Aronin, N
المصدر: Experimental Neurology. 175(1):297-300
مصطلحات موضوعية: Huntington Disease : complications, Heterozygote, Huntington Disease : chemically induced, Human, Huntington Disease : genetics, P.H.S., U.S. Gov't, Support, Non-P.H.S., Non-U.S. Gov't, Species Specificity, Quinolinic Acid : administration & dosage, Neurons : pathology, Neurons : drug effects, Neurodegenerative Diseases : pathology, Neurodegenerative Diseases : complications, Neurodegenerative Diseases : chemically induced, Microinjections, Transgenic, Mice, Huntington Disease : pathology, Disease Susceptibility, Animal, Disease Models, Corpus Striatum : pathology, Cell Count, Cell Death, Corpus Striatum : drug effects, Medicin och hälsovetenskap, Klinisk medicin, Neurologi, Medical and Health Sciences, Clinical Medicine, Neurology
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7
المؤلفون: Nicole Déglon, Luís Pereira de Almeida, Patrick Aebischer, Christopher A. Ross, Diana Zala
المصدر: Scopus-Elsevier
Journal of Neuroscience, vol. 22, no. 9, pp. 3473-3483
Nicole Déglonمصطلحات موضوعية: Huntingtin, Mutant, Wistar, Gene Expression, Peptides/ genetics, Neural degeneration, Cell Nucleus/pathology, Corpus Striatum/drug effects/metabolism/ pathology, Inclusion Bodies/pathology, Nerve Tissue Proteins/biosynthesis/ genetics/toxicity, Tissue Distribution, Phosphoglycerate kinase 1, Promoter Regions, Genetic, Inclusion Bodies, education.field_of_study, Huntingtin Protein, Huntington Disease/genetics/ pathology, Blotting, General Neuroscience, Gene Transfer Techniques, Nuclear Proteins, Genetic Vectors/administration & dosage/genetics, Phosphoproteins/metabolism, Huntington Disease, Female, Promoter Regions (Genetics), Drug, Western, congenital, hereditary, and neonatal diseases and abnormalities, Dopamine and cAMP-Regulated Phosphoprotein 32, Microinjections, Blotting, Western, Genetic Vectors, Nerve Tissue Proteins, Biology, Animals, Cell Line, Corpus Striatum/drug effects, Corpus Striatum/metabolism, Disease Models, Animal, Dose-Response Relationship, Drug, Genetic Vectors/administration & dosage, Genetic Vectors/genetics, Humans, Huntington Disease/genetics, Huntington Disease/pathology, Lentivirus/genetics, Mutation, Nerve Tissue Proteins/biosynthesis, Nerve Tissue Proteins/genetics, Nuclear Proteins/biosynthesis, Nuclear Proteins/genetics, Peptides/genetics, Rats, Rats, Wistar, Trinucleotide Repeat Expansion, Dose-Response Relationship, Huntington's disease, Genetic model, mental disorders, medicine, ARTICLE, education, Cell Nucleus, Animal, Lentivirus, medicine.disease, Phosphoproteins, Molecular biology, Nuclear Proteins/biosynthesis/ genetics/toxicity, Corpus Striatum, nervous system diseases, nervous system, Disease Models, Trinucleotide repeat expansion, Peptides
وصف الملف: application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::58821be6197c8d2c965a1e6ac372bc70
https://infoscience.epfl.ch/record/101270 -
8
المؤلفون: Novati, Arianna, Hentrich, Thomas, Wassouf, Zinah, Weber, Jonasz J., Yu-Taeger, Libo, Déglon, Nicole, Nguyen, Huu Phuc, Schulze-Hentrich, Julia M.
المصدر: Scientific Reports, Vol 8, Iss 1, Pp 1-15 (2018)
Scientific reports, vol. 8, no. 1, pp. 5803
Scientific Reportsمصطلحات موضوعية: Huntingtin Protein, Sequence Analysis, RNA, Gene Expression Profiling, lcsh:R, Gene Expression, lcsh:Medicine, Environmental Exposure, Animals, Corpus Striatum/pathology, Disease Models, Animal, Disease Progression, Gene Regulatory Networks, Huntingtin Protein/deficiency, Huntington Disease/pathology, Mice, Rats, Article, Corpus Striatum, Huntington Disease, lcsh:Q, lcsh:Science
وصف الملف: application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::d3fe5c6d2db3386dd91d45fe2683279c
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9مورد إلكتروني
المصدر: NeuroImage, 49 (1
مصطلحات الفهرس: Sciences bio-médicales et agricoles, Adolescent, Adult, Age of Onset, Aged, Atrophy -- pathology, Brain -- pathology, Brain Stem -- pathology, Cerebellum -- pathology, DNA -- genetics, Diagnosis, Differential, Disease Progression, Female, Humans, Huntington Disease -- pathology, Linear Models, Magnetic Resonance Imaging, Male, Middle Aged, Repetitive Sequences, Nucleic Acid, Sex Characteristics, Spinocerebellar Ataxias -- diagnosis, Spinocerebellar Ataxias -- genetics, Spinocerebellar Ataxias -- pathology, Young Adult, Repeat length, Spinocerebellar ataxia, Volumetry, Voxel-based morphometry, info:eu-repo/semantics/article, info:ulb-repo/semantics/articlePeerReview, info:ulb-repo/semantics/openurl/article
URL:
https://dipot.ulb.ac.be/dspace/bitstream/2013/51459/1/Elsevier_26551.pdf http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/51459 http://worldcat.org/search?q=on:EQY+http://difusion-oai.ulb.ac.be/oai/request+DCG_ENTIRE_REPOSITORY+CNTCOLL -
10مورد إلكتروني
المصدر: NeuroImage, 49 (1
مصطلحات الفهرس: Sciences bio-médicales et agricoles, Adolescent, Adult, Age of Onset, Aged, Atrophy -- pathology, Brain -- pathology, Brain Stem -- pathology, Cerebellum -- pathology, DNA -- genetics, Diagnosis, Differential, Disease Progression, Female, Humans, Huntington Disease -- pathology, Linear Models, Magnetic Resonance Imaging, Male, Middle Aged, Repetitive Sequences, Nucleic Acid, Sex Characteristics, Spinocerebellar Ataxias -- diagnosis, Spinocerebellar Ataxias -- genetics, Spinocerebellar Ataxias -- pathology, Young Adult, Repeat length, Spinocerebellar ataxia, Volumetry, Voxel-based morphometry, info:eu-repo/semantics/article, info:ulb-repo/semantics/articlePeerReview, info:ulb-repo/semantics/openurl/article
URL:
https://dipot.ulb.ac.be/dspace/bitstream/2013/51459/1/Elsevier_26551.pdf http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/51459 http://worldcat.org/search?q=on:EQY+http://difusion-oai.ulb.ac.be/oai/request+DCG_ENTIRE_REPOSITORY+CNTCOLL
