المؤلفون: Marc‐Olivier Deguise, Giovanni Baranello, Chiara Mastella, Ariane Beauvais, Jean Michaud, Alessandro Leone, Ramona De Amicis, Alberto Battezzati, Christopher Dunham, Kathryn Selby, Jodi Warman Chardon, Hugh J. McMillan, Yu‐Ting Huang, Natalie L. Courtney, Alannah J. Mole, Sabrina Kubinski, Peter Claus, Lyndsay M. Murray, Melissa Bowerman, Thomas H. Gillingwater, Simona Bertoli, Simon H. Parson, Rashmi Kothary

المصدر: Annals of Clinical and Translational Neurology, Vol 6, Iss 8, Pp 1519-1532 (2019)

مصطلحات موضوعية: Neurosciences. Biological psychiatry. Neuropsychiatry, RC321-571, Neurology. Diseases of the nervous system, RC346-429

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2328-9503

URL الوصول: https://doaj.org/article/fc27db022435433fb87c7d2bb5016994

المؤلفون: Rachel A. Kline, Kosala N. Dissanayake, Maica Llavero Hurtado, Nicolás W. Martínez, Alexander Ahl, Alannah J. Mole, Douglas J. Lamont, Felipe A. Court, Richard R. Ribchester, Thomas M. Wishart, Lyndsay M. Murray

المصدر: Neurobiology of Disease, Vol 130, Iss , Pp 104496- (2019)

مصطلحات موضوعية: Neurodegeneration, Wallerian, Neonate, Axon degeneration, Neuromuscular junction, NMJ, Neurosciences. Biological psychiatry. Neuropsychiatry, RC321-571

وصف الملف: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S0969996119301512; https://doaj.org/toc/1095-953X

URL الوصول: https://doaj.org/article/d7943619d6c0470097d6e53fe51e0db3

المؤلفون: Alison K. Thomson, Lyndsay M. Murray, Natalie L. Courtney, Alannah J. Mole

المصدر: Cell Death and Disease, Vol 10, Iss 7, Pp 1-14 (2019)
Cell Death & Disease
Courtney, N L, Mole, A J, Thomson, A K & Murray, L M 2019, ' Reduced P53 levels ameliorate neuromuscular junction loss without affecting motor neuron pathology in a mouse model of spinal muscular atrophy ', Cell Death and Disease, vol. 10, 515 . https://doi.org/10.1038/s41419-019-1727-6

مصطلحات موضوعية: 0301 basic medicine, Cancer Research, Pathology, medicine.medical_specialty, Immunology, Cell death in the nervous system, Neuromuscular Junction, Degeneration (medical), SMN1, Biology, Neuromuscular junction, Article, Muscular Atrophy, Spinal, 03 medical and health sciences, Cellular and Molecular Neuroscience, 0302 clinical medicine, Downregulation and upregulation, medicine, Animals, RNA, Messenger, lcsh:QH573-671, Motor Neurons, lcsh:Cytology, Cell Biology, Spinal muscular atrophy, Motor neuron, medicine.disease, SMA, Motor unit, Mice, Inbred C57BL, Disease Models, Animal, 030104 developmental biology, medicine.anatomical_structure, Phenotype, nervous system, Diseases of the nervous system, Tumor Suppressor Protein p53, 030217 neurology & neurosurgery, Signal Transduction

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c4d488ddf6adc52730522225f1ff245
http://link.springer.com/article/10.1038/s41419-019-1727-6

المؤلفون: Richard R. Ribchester, Lyndsay M. Murray, Sarah Bell, Alison K. Thomson, Alannah J. Mole, Kosala N. Dissanayake

المصدر: Journal of Anatomy
Mole, A J, Bell, S, Thomson, A K, Dissanayake, K N, Ribchester, R R & Murray, L M 2020, ' Synaptic withdrawal following nerve injury is influenced by postnatal maturity, muscle-specific properties, and the presence of underlying pathology in mice ', Journal of Anatomy, vol. 237, no. 2, pp. 263-274 . https://doi.org/10.1111/joa.13187

مصطلحات موضوعية: 0301 basic medicine, Wallerian degeneration, peripheral neuropathy, medicine.medical_treatment, Mice, 0302 clinical medicine, Peripheral Nerve Injuries, Axon, spinal muscular atrophy, Denervation, Motor Neurons, axotomy, postnatal development, medicine.anatomical_structure, developmental regulation, motor neuron disease, Original Article, Anatomy, Axotomy, medicine.symptom, Histology, mouse model, synaptic degeneration, Neuromuscular Junction, Neuromuscular junction, Muscular Atrophy, Spinal, 03 medical and health sciences, differential vulnerability, medicine, Animals, Muscle, Skeletal, Molecular Biology, Ecology, Evolution, Behavior and Systematics, business.industry, Cell Biology, Spinal muscular atrophy, Original Articles, neuromuscular disease, Nerve injury, Motor neuron, medicine.disease, Survival of Motor Neuron 1 Protein, die‐back, Disease Models, Animal, 030104 developmental biology, Nerve Degeneration, ex vivo, business, Neuroscience, 030217 neurology & neurosurgery, Developmental Biology

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1eb43ec72532e4e77b5643ae44b92ab
https://pubmed.ncbi.nlm.nih.gov/32311115

المؤلفون: Kosala N. Dissanayake, Nicolas W. Martinez, Felipe A. Court, Douglas J. Lamont, Alannah J. Mole, Richard R. Ribchester, Lyndsay M. Murray, Rachel A. Kline, Thomas M. Wishart, Maria del carmen Llavero hurtado, Alexander Ahl

المصدر: Kline, R, Dissanayake, K, Llavero hurtado, M D C, Martínez, N W, Ahl, A, Mole, A J, Lamont, D J, Court, F A, Ribchester, R, Wishart, T & Murray, L 2019, ' Altered mitochondrial bioenergetics are responsible for the delay in Wallerian degeneration observed in neonatal mice. ', Neurobiology of disease, vol. 130, 104496 . https://doi.org/10.1016/j.nbd.2019.104496
Neurobiology of Disease
Neurobiology of Disease, Vol 130, Iss, Pp 104496-(2019)

مصطلحات موضوعية: Proteomics, 0301 basic medicine, ETC, Electron Transport Chain, Wallerian degeneration, MPS, Mammalian Physiological Saline, Bioenergetics, P, Post Natal Day, Degeneration (medical), 2H3, Neurofilament, Mitochondrion, DRG, Dorsal Root Ganglion, Oxidative Phosphorylation, Wallerian, WD, Wallerian Degeneration, Mice, Neonate, 0302 clinical medicine, Axon, TMT, Tandem Mass Tagging, Neurodegeneration, ROS, Reaction Oxygen Species, Mitochondria, medicine.anatomical_structure, Neurology, Axon degeneration, Neuromuscular Junction, AMPK, Adenosine Monophosphate Kinase, Oxidative phosphorylation, Biology, Article, Neuromuscular junction, lcsh:RC321-571, 03 medical and health sciences, medicine, Animals, lcsh:Neurosciences. Biological psychiatry. Neuropsychiatry, SV2, Synaptic Vesicle Protein 2, IPA, Ingenuity Pathway Analysis, OXPHOS, Oxidative Phosphorylation, NMJ, Neuromuscular Junction, TEAB, Tetraethylammonium Bromide, NMJ, QFWB, Quantitative Fluorescent Western Blotting, DHE, Dihydroethidium, ELISA, Enzyme Link Immuno, medicine.disease, Mice, Inbred C57BL, TMT-QMS, Tandem-Mass Tagging Quantitative Mass Spectrometry, 030104 developmental biology, Animals, Newborn, Wallerian Degeneration, Neuroscience, 030217 neurology & neurosurgery

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6698d39a711f14f5626dba5e52213e5a
https://www.pure.ed.ac.uk/ws/files/102228857/1_s2.0_S0969996119301512_main.pdf

المؤلفون: Natalie L. Courtney, Simon H. Parson, Giovanni Baranello, Peter Claus, Ramona De Amicis, Lyndsay M. Murray, Christopher Dunham, Jean Michaud, Ariane Beauvais, Rashmi Kothary, Melissa Bowerman, Simona Bertoli, Kathryn Selby, Alannah J. Mole, Marc-Olivier Deguise, Jodi Warman Chardon, Sabrina Kubinski, Yu-Ting Huang, Chiara Mastella, Hugh J. McMillan, Alessandro Leone, Alberto Battezzati, Thomas H. Gillingwater

المصدر: Deguise, M-O, Baranello, G, Mastella, C, Beauvais, A, Michaud, J, Leone, A, De Amicis, R, Battezzati, A, Dunham, C, Selby, K, Warman Chardon, J, McMillan, H J, Huang, Y-T, Courtney, N L, Mole, A J, Kubinski, S, Claus, P, Murray, L M, Bowerman, M, Gillingwater, T H, Bertoli, S, Parson, S H & Kothary, R 2019, ' Abnormal fatty acid metabolism is a core component of spinal muscular atrophy ', Annals of Clinical and Translational Neurology, vol. 6, no. 8, pp. 1519-1532 . https://doi.org/10.1002/acn3.50855
Annals of Clinical and Translational Neurology, Vol 6, Iss 8, Pp 1519-1532 (2019)
Annals of Clinical and Translational Neurology

مصطلحات موضوعية: 0301 basic medicine, Male, Pathology, medicine.medical_specialty, Mice, Transgenic, Neurosciences. Biological psychiatry. Neuropsychiatry, Muscular Atrophy, Spinal, 03 medical and health sciences, chemistry.chemical_compound, Mice, 0302 clinical medicine, medicine, Animals, Humans, Child, RC346-429, Pathological, Research Articles, Triglycerides, Dyslipidemias, Denervation, Fatty acid metabolism, business.industry, General Neuroscience, Fatty liver, Fatty Acids, Infant, Lipid metabolism, Spinal muscular atrophy, medicine.disease, SMA, Lipid Metabolism, R1, Survival of Motor Neuron 1 Protein, 3. Good health, Fatty Liver, Disease Models, Animal, 030104 developmental biology, chemistry, Child, Preschool, Female, Neurology (clinical), Neurology. Diseases of the nervous system, business, 030217 neurology & neurosurgery, Dyslipidemia, Research Article, RC321-571

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00ede6b8187b3bcdb3f1faeaf997bb54
https://www.pure.ed.ac.uk/ws/files/112110119/Gillingwater_T_Abnormal_fatty_acid....pdf

المؤلفون: Y De Repentigny, Alessandro Leone, Hugh J. McMillan, Mary-Ellen Harper, Alberto Battezzati, Alannah J. Mole, Lyndsay M. Murray, Rashmi Kothary, Thomas M. Wishart, Maica Llavero-Hurtado, R. De Amicis, Giovanni Baranello, Peter Claus, J Warman Chardon, Chantal A. Pileggi, Ariane Beauvais, Simona Bertoli, Simon H. Parson, Natalie L. Courtney, Chiara Mastella, Sabrina Kubinski, Yu-Ting Huang, Lucia Chehade, Alexandra Tierney, Douglas J. Lamont, Abdelmadjid Atrih, Thomas H. Gillingwater, Marc-Olivier Deguise, Melissa Bowerman

المصدر: Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 46:S32

مصطلحات موضوعية: medicine.medical_specialty, education.field_of_study, Fatty acid metabolism, business.industry, Population, Fatty liver, Lipid metabolism, General Medicine, Spinal muscular atrophy, medicine.disease, SMA, chemistry.chemical_compound, Liver disease, Endocrinology, Neurology, chemistry, Internal medicine, medicine, Neurology (clinical), Steatosis, education, business

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::330dbc26f9f4d4a51ed3743d7a2bbdec
https://doi.org/10.1017/cjn.2019.168