المؤلفون: Penelope J Boyd, Wen-Yo Tu, Hannah K Shorrock, Ewout J N Groen, Roderick N Carter, Rachael A Powis, Sophie R Thomson, Derek Thomson, Laura C Graham, Anna A L Motyl, Thomas M Wishart, J Robin Highley, Nicholas M Morton, Thomas Becker, Catherina G Becker, Paul R Heath, Thomas H Gillingwater

المصدر: PLoS Genetics, Vol 13, Iss 4, p e1006744 (2017)

مصطلحات موضوعية: Genetics, QH426-470

وصف الملف: electronic resource

Relation: http://europepmc.org/articles/PMC5417717?pdf=render; https://doaj.org/toc/1553-7390; https://doaj.org/toc/1553-7404

URL الوصول: https://doaj.org/article/6a1994812232441a91ce50a3acc16685

المؤلفون: Sophie R Thomson, Joya E Nahon, Chantal A Mutsaers, Derek Thomson, Gillian Hamilton, Simon H Parson, Thomas H Gillingwater

المصدر: PLoS ONE, Vol 7, Iss 12, p e52605 (2012)

مصطلحات موضوعية: Medicine, Science

وصف الملف: electronic resource

Relation: http://europepmc.org/articles/PMC3527597?pdf=render; https://doaj.org/toc/1932-6203

URL الوصول: https://doaj.org/article/aab6160554fc4e56b50d92d147aa2b51

المؤلفون: Gemma Molinaro, Kimberly M. Huber, Elizabeth A. McCullagh, Sophie R. Thomson

المصدر: Frontiers in Neuroscience, Vol 17 (2023)

مصطلحات موضوعية: E/I imbalance, autism spectrum disorders (ASDs), Fragile X Syndrome (FXS), therapeutics, microbiome, Neurosciences. Biological psychiatry. Neuropsychiatry, RC321-571

وصف الملف: electronic resource

Relation: https://www.frontiersin.org/articles/10.3389/fnins.2023.1187799/full; https://doaj.org/toc/1662-453X

URL الوصول: https://doaj.org/article/fd63178a6f2e4da4b5c77fd5fe215f58

المؤلفون: Sang S. Seo, Susana R. Louros, Natasha Anstey, Miguel A. Gonzalez-Lozano, Callista B. Harper, Nicholas C. Verity, Owen Dando, Sophie R. Thomson, Jennifer C. Darnell, Peter C. Kind, Ka Wan Li

المصدر: Nature, Nature Communications. 13(1):1-18

الإتاحة: https://ideas.repec.org/a/nat/natcom/v13y2022i1d10.1038_s41467-022-30979-0.html

المؤلفون: Sang S. Seo, Susana R. Louros, Natasha Anstey, Miguel A. Gonzalez-Lozano, Callista B. Harper, Nicholas C. Verity, Owen Dando, Sophie R. Thomson, Jennifer C. Darnell, Peter C. Kind, Ka Wan Li, Emily K. Osterweil

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::2190637137306e7721ec36cd611bab07
https://doi.org/10.1101/2022.04.07.487442

المؤلفون: Sophie R, Thomson, Sang S, Seo, Stephanie A, Barnes, Susana R, Louros, Melania, Muscas, Owen, Dando, Caoimhe, Kirby, David J A, Wyllie, Giles E, Hardingham, Peter C, Kind, Emily K, Osterweil

المصدر: Neuron

مصطلحات موضوعية: Neurons, protein synthesis, Long-Term Synaptic Depression, fragile X, autism, Mice, Transgenic, Receptors, Metabotropic Glutamate, Hippocampus, Article, Methoxyhydroxyphenylglycol, TRAP, Disease Models, Animal, Fragile X Mental Retardation Protein, muscarinic receptor, Fragile X Syndrome, Protein Biosynthesis, m4, LTD, Animals, mglur theory, FMRP, FMR1

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::f0e24f707a0dd29785472d4b32c95581
https://pubmed.ncbi.nlm.nih.gov/28772121

المؤلفون: Stephanie A. Barnes, Silvia Bassani, Àlex Bayés, Elizabeth Berry-Kravis, Luigi Boccuto, Thomas Bourgeron, Jamel Chelly, Bice Chini, Jérôme Ezan, Jozef Gecz, Valentina Gigliucci, Xiaohong Gong, Seth G.N. Grant, Anne Hoffmann, Claire Homan, Elaine Y. Hsiao, Guillaume Huguet, Lachlan Jolly, Eunjoon Kim, Peter C. Kind, Jaewon Ko, Janine M. Lamonica, Marianna Leonzino, Natalia V. Malkova, Carla Marini, Caterina Michetti, Caterina Montani, Mireille Montcouquiol, Maïté M. Moreau, Edoardo Moretto, Alysson Renato Muotri, Emily K. Osterweil, Maria Passafaro, Olga Peñagarikano, Alan K. Percy, Duyen Pham, Katy Phelan, Laura Ricceri, Yoann Saillour, Carlo Sala, Nathalie Sans, Sara Sarasua, Maria Luisa Scattoni, Michael J. Schmeisser, Charles E. Schwartz, Yiping Shen, Chuan Tan, Daniel C. Tarquinio, Sophie R. Thomson, Chiara Verpelli, Kazuhiro Yamakawa, Zhaolan Zhou

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::8c97f80d4c0b770dbc0b6984c2acf55d
https://doi.org/10.1016/b978-0-12-800109-7.01002-5

المؤلفون: Sophie R. Thomson, Emily K. Osterweil, Peter C. Kind, Stephanie A. Barnes

مصطلحات موضوعية: Causes of autism, Genetics, congenital, hereditary, and neonatal diseases and abnormalities, education.field_of_study, Population, Biology, medicine.disease, FMR1, Fragile X syndrome, Metabotropic glutamate receptor, Intellectual disability, medicine, Metabotropic glutamate receptor 1, Spectrum disorder, education, Neuroscience

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::14d883e599bf119f614195be9194113c
https://doi.org/10.1016/b978-0-12-800109-7.00008-x

المؤلفون: Thomas H. Gillingwater, Siddharthan Chandran, Thomas M. Wishart, Rickie Patani, Sophie R. Thomson

المصدر: Journal of Anatomy. 220:122-130

مصطلحات موضوعية: Pathology, medicine.medical_specialty, Histology, Skeletal muscle, Cell Biology, Spinal muscular atrophy, Motor neuron, Disease pathogenesis, Biology, medicine.disease, Neuromuscular junction, medicine.anatomical_structure, medicine, Anatomy, Amyotrophic lateral sclerosis, Stem cell, Induced pluripotent stem cell, Molecular Biology, Neuroscience, Ecology, Evolution, Behavior and Systematics, Developmental Biology

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::bf2485fb0396e2ee00f6190f5812c8ed
https://doi.org/10.1111/j.1469-7580.2011.01459.x

المؤلفون: J. Robin Highley, Paul R. Heath, Nicholas M. Morton, Thomas Becker, Ewout J N Groen, Derek Thomson, Thomas M. Wishart, Rachael A. Powis, Penelope J Boyd, Catherina G. Becker, Roderick N. Carter, Wen-Yo Tu, Thomas H. Gillingwater, Anna A L Motyl, Sophie R. Thomson, Hannah K. Shorrock, Laura C. Graham

المصدر: PLoS Genetics, Vol 13, Iss 4, p e1006744 (2017)
Boyd, P J, Tu, W-Y, Shorrock, H K, Groen, E J N, Carter, R N, Powis, R A, Thomson, S R, Thomson, D, Graham, L C, Motyl, A A L, Wishart, T M, Highley, J R, Morton, N M, Becker, T, Becker, C G, Heath, P R & Gillingwater, T H 2017, ' Bioenergetic status modulates motor neuron vulnerability and pathogenesis in a zebrafish model of spinal muscular atrophy ', PLoS Genetics, vol. 13, no. 4, e1006744 . https://doi.org/10.1371/journal.pgen.1006744
PLoS Genetics

مصطلحات موضوعية: 0301 basic medicine, Embryology, Cancer Research, Biochemistry, Nervous System, Mice, Adenosine Triphosphate, Nerve Fibers, 0302 clinical medicine, Animal Cells, Medicine and Health Sciences, Axon, Phosphoglycerate kinase 1, Zebrafish, Energy-Producing Organelles, Genetics (clinical), Motor Neurons, Neurons, education.field_of_study, biology, Fishes, Gene Expression Regulation, Developmental, Animal Models, Gene Pool, Anatomy, SMA, Mitochondria, medicine.anatomical_structure, Spinal Cord, Experimental Organism Systems, Osteichthyes, Vertebrates, Disease Susceptibility, Cellular Types, Cellular Structures and Organelles, Research Article, lcsh:QH426-470, Bioenergetics, Research and Analysis Methods, Muscular Atrophy, Spinal, 03 medical and health sciences, Model Organisms, Genetics, medicine, Animals, Humans, Muscle, Skeletal, education, Molecular Biology, Ecology, Evolution, Behavior and Systematics, Evolutionary Biology, Population Biology, Embryos, Organisms, Biology and Life Sciences, Prazosin, Cell Biology, Spinal muscular atrophy, Motor neuron, biology.organism_classification, medicine.disease, Survival of Motor Neuron 1 Protein, Axons, Disease Models, Animal, Phosphoglycerate Kinase, Neuroanatomy, lcsh:Genetics, 030104 developmental biology, Mitochondrial biogenesis, Cellular Neuroscience, Axoplasmic transport, Energy Metabolism, Neuroscience, Population Genetics, 030217 neurology & neurosurgery, Developmental Biology

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ea50dbb34fd8d58066abee13b6d717f
https://doi.org/10.1371/journal.pgen.1006744