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1
المؤلفون: Jean-Marc Burgunder, M. Weber, Th Lauterburg, Irene Tobler
المصدر: Neuroscience Letters. 358:17-20
مصطلحات موضوعية: medicine.medical_specialty, Substantia nigra, Dynorphin, Motor Activity, Biology, Rats, Sprague-Dawley, Dopamine receptor D1, Dopamine, Dopamine receptor D2, Internal medicine, medicine, Animals, Neurotransmitter Agents, Tyrosine hydroxylase, General Neuroscience, Dopaminergic, Brain, Circadian Rhythm, Rats, Receptors, Neurotransmitter, Ventral tegmental area, Endocrinology, medicine.anatomical_structure, Gene Expression Regulation, Neuroscience, medicine.drug
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10fdecc9b1ec678973c8488de23457cdTest
https://doi.org/10.1016/j.neulet.2003.12.053Test -
2
المؤلفون: Li-Yen Lee, Akhlaq A. Farooqui, Gavin S. Dawe, Wei-Yi Ong, Jean-Marc Burgunder
المصدر: Neuroscience Letters. 453:6-8
مصطلحات موضوعية: Male, Reflex, Startle, medicine.medical_specialty, Phospholipase A2 Inhibitors, Striatum, Phospholipase A2, Internal medicine, Moro reflex, medicine, Animals, Enzyme Inhibitors, Rats, Wistar, Prepulse inhibition, Analysis of Variance, Phospholipase A, biology, Chemistry, General Neuroscience, Oligonucleotides, Antisense, Startle reaction, Rats, Phospholipases A2, Endocrinology, Acoustic Stimulation, Quinacrine, Acoustic Startle Reflex, Phospholipases A2, Calcium-Independent, Reflex, biology.protein, Neuroscience
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dd83756bcd4d5c25bafaaa498dab49c8Test
https://doi.org/10.1016/j.neulet.2009.01.069Test -
3
المؤلفون: Jean-Marc Burgunder, A. Richter, W. Löscher
المصدر: Experimental Brain Research. 129:114-120
مصطلحات موضوعية: Central Nervous System, medicine.medical_specialty, Tyrosine 3-Monooxygenase, Glutamate decarboxylase, Gene Expression, Hamster, Substantia nigra, Striatum, Biology, GAP-43 Protein, Cricetinae, Internal medicine, Basal ganglia, medicine, Animals, RNA, Messenger, Thyrotropin-Releasing Hormone, Mesocricetus, Tyrosine hydroxylase, Glutamate Decarboxylase, General Neuroscience, Hormones, Enzymes, Dystonia, Endocrinology, Cholecystokinin, Somatostatin, Pars reticulata, Golden hamster
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb3cab505da4ab93092f15ed9f0f75eaTest
https://doi.org/10.1007/s002210050941Test -
4
المصدر: Journal of Child Neurology. 21:253-255
مصطلحات موضوعية: Genetics, medicine.medical_specialty, Ataxia, Muscular hypotonia, Hearing loss, Point mutation, Respiratory chain complex, Biology, medicine.disease, Short stature, 03 medical and health sciences, 0302 clinical medicine, Endocrinology, 030225 pediatrics, Internal medicine, Diabetes mellitus, Pediatrics, Perinatology and Child Health, medicine, Sensorineural hearing loss, Neurology (clinical), medicine.symptom, 030217 neurology & neurosurgery
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::9b44ba3cfb4bba5311348c149659ee76Test
https://doi.org/10.2310/7010.2006.00047Test -
5
المؤلفون: Jean-Marc Burgunder
المصدر: Developmental Brain Research. 78:109-122
مصطلحات موضوعية: medicine.medical_specialty, Central nervous system, Gene Expression, In situ hybridization, Biology, Rats, Sprague-Dawley, Diencephalon, Prosencephalon, Developmental Neuroscience, Pregnancy, Internal medicine, medicine, Animals, RNA, Messenger, In Situ Hybridization, Cerebral Cortex, Neocortex, Histocytochemistry, Cerebrum, Allocortex, Rats, medicine.anatomical_structure, Endocrinology, Somatostatin, nervous system, Forebrain, Autoradiography, Female, Oligonucleotide Probes, Developmental Biology
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a09f36cdc84ca10e81fc95fc726903e3Test
https://doi.org/10.1016/0165-3806Test(94)90015-9 -
6
المؤلفون: Kai M. Rösler, Séverine Petitprez, Lie Chen, Liliane Kappeler, D Schorderet, Hugues Abriel, Jean-Marc Burgunder, L Tiab
المصدر: Neurology. 71(21)
مصطلحات موضوعية: medicine.medical_specialty, Nav1.4, DNA Mutational Analysis, Transfection, Sodium Channels, Cell Line, Membrane Potentials, Myotonia, Internal medicine, medicine, Humans, Hyperkalemic periodic paralysis, Patch clamp, Isoleucine, NAV1.4 Voltage-Gated Sodium Channel, Membrane potential, Family Health, biology, Sodium channel, Valine, medicine.disease, Cell biology, Transmembrane domain, Protein Subunits, Endocrinology, Paramyotonia congenita, Mutation, biology.protein, Female, Neurology (clinical)
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::677b1aeb0f489949f8a9ef705e45ab19Test
https://pubmed.ncbi.nlm.nih.gov/19015483Test -
7
المؤلفون: W. Scott Young, Jean-Marc Burgunder
المصدر: Developmental Brain Research. 52:85-93
مصطلحات موضوعية: medicine.medical_specialty, Tyrosine 3-Monooxygenase, Ontogeny, Substantia nigra, Biology, Midbrain, Embryonic and Fetal Development, Developmental Neuroscience, Mesencephalon, Dopamine, Internal medicine, medicine, Animals, RNA, Messenger, Gene, Tyrosine hydroxylase, Nucleic Acid Hybridization, Rats, Inbred Strains, Molecular biology, Rats, Ventral tegmental area, Endocrinology, medicine.anatomical_structure, Gene Expression Regulation, nervous system, Immunohistochemistry, Cholecystokinin, Developmental Biology, medicine.drug
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::856f9c892b12f1afea714f261e94d40fTest
https://doi.org/10.1016/0165-3806Test(90)90224-m -
8
المؤلفون: Benjamin K.C. Ong, Raymond C.S. Seet, Roland Baur, Chew Soh Eng, Shang Huifang, Erle C.H. Lim, Walter Hunziker, Pascal Béguin, Erwin Sigel, Jean-Marc Burgunder
المصدر: Neuromuscular disorders : NMD. 18(8)
مصطلحات موضوعية: musculoskeletal diseases, Male, congenital, hereditary, and neonatal diseases and abnormalities, medicine.medical_specialty, China, DNA, Complementary, Adolescent, Xenopus, Pain, Biology, Compound heterozygosity, medicine.disease_cause, Myotonia, Variable features, Chloride Channels, Internal medicine, medicine, Animals, Humans, Muscle, Skeletal, Exercise, Genetics (clinical), Genetics, Neurologic Examination, CLCN1, Mutation, Myotonia congenita, Electromyography, Reverse Transcriptase Polymerase Chain Reaction, medicine.disease, biology.organism_classification, Electrophysiology, Endocrinology, Neurology, Pediatrics, Perinatology and Child Health, Chloride channel, biology.protein, Oocytes, Female, Neurology (clinical)
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f0c2fdf4dfca35d7248e8e99f8ec0c33Test
https://pubmed.ncbi.nlm.nih.gov/18579381Test -
9
المؤلفون: Li-Yen Lee, Akhlaq A. Farooqui, Wei-Yi Ong, Jean-Marc Burgunder
المصدر: Lee, Li-Yen; Ong, Wei-Yi; Farooqui, Akhlaq A; Burgunder, Jean-Marc (2007). Role of calcium-independent phospholipase A2 in cortex striatum thalamus cortex circuitry-enzyme inhibition causes vacuous chewing movements in rats. Psychopharmacology, 195(3), pp. 387-95. Berlin: Springer 10.1007/s00213-007-0912-y <http://dx.doi.org/10.1007/s00213-007-0912-yTest>
مصطلحات موضوعية: Male, medicine.medical_specialty, Cerebellum, Phosphodiesterase Inhibitors, Central nervous system, Thalamus, Organophosphonates, chemistry.chemical_element, Striatum, Arachidonic Acids, Biology, Calcium, Naphthalenes, Dopamine Uptake Inhibitors, Internal medicine, Cortex (anatomy), Basal ganglia, medicine, Animals, Enzyme Inhibitors, Rats, Wistar, Pharmacology, Benztropine, Cerebral Cortex, Behavior, Animal, Drug Administration Routes, Oligonucleotides, Antisense, Corpus Striatum, Rats, medicine.anatomical_structure, Endocrinology, nervous system, chemistry, Cerebral cortex, Organ Specificity, Pyrones, Phospholipases A2, Calcium-Independent, Stereotyped Behavior, Neuroscience
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::25babd4f6fd63dcb641e59b2d1647178Test
https://pubmed.ncbi.nlm.nih.gov/17768607Test -
10
المؤلفون: Huifang Shang, Dong Zhou, Qin Chen, Jean-Marc Burgunder, Xiao-Feng Jiang
المصدر: Movement disorders : official journal of the Movement Disorder Society. 21(12)
مصطلحات موضوعية: medicine.medical_specialty, DNA Mutational Analysis, Gene mutation, Diabetes Complications, Exon, Diabetes mellitus, Internal medicine, medicine, Serine, Humans, Aceruloplasminemia, Movement Disorders, biology, Cognitive disorder, Homozygote, Tryptophan, Ceruloplasmin, Exons, Middle Aged, medicine.disease, Phenotype, Magnetic Resonance Imaging, Endocrinology, Neurology, Mutation (genetic algorithm), Mutation, biology.protein, Female, Neurology (clinical), Psychology, Cognition Disorders
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a3da30cccc0fa854513e1d71baf09b51Test
https://pubmed.ncbi.nlm.nih.gov/17013908Test