المؤلفون: O'Meara, Gillian, Coumis, Urania, Ma, Shuang Y., Kehr, Jan, Mahoney, Sally, Bacon, Andrea, Allen, Shelley J., Holmes, Fiona, Kahl, Ulrika, Wang, Fu H., Kearns, Ian R., Ove-Ogren, Sven, Dawbarn, David, Mufson, Elliott J., Davies, Ceri, Dawson, Gerard, Wynick, David

المصدر: Proceedings of the National Academy of Sciences of the United States of America, 2000 Oct 01. 97(21), 11569-11574.

URL الوصول: https://www.jstor.org/stable/123437

المؤلفون: Crompton, Lucy A., Byrne, Meg L., Taylor, Hannah, Kerrigan, Talitha L., Bru-Mercier, Gilles, Badger, Jennifer L., Barbuti, Peter A., Jo, Jihoon, Tyler, Sue J., Allen, Shelley J., Kunath, Tilo, Cho, Kwangwook, Caldwell, Maeve A.

المصدر: In Stem Cell Research November 2013 11(3):1206-1221

المؤلفون: McNamee, Kay E., Burleigh, Annika, Gompels, Luke L., Feldmann, Marc, Allen, Shelley J., Williams, Richard O., Dawbarn, David, Vincent, Tonia L., Inglis, Julia J.

المصدر: In Pain May 2010 149(2):386-392

المؤلفون: Wang, Hao, Sessions, Richard B., Prime, Stephen S., Shoemark, Deborah K., Allen, Shelley J., Hong, Wei, Narayanan, Sathya, Paterson, Ian C.

المصدر: Journal of Computer-Aided Molecular Design: Incorporating Perspectives in Drug Discovery and Design. April 2013 27(4):365-372

المؤلفون: Watson, Judy J., Allen, Shelley J., Dawbarn, DrDavid

المصدر: BioDrugs. November 2008 22(6):349-359

المؤلفون: Allen, Shelley J.

المساهمون: Dawbarn, David, editor, Allen, Shelley J., editor

المصدر: Neurobiology of Alzheimer‘s Disease: (Molecular and Cellular Neurobiology).

الإتاحة: https://doi.org/10.1093/oso/9780198566618.003.0001

المؤلفون: Love, Seth, Siew, L. Khai, Dawbarn, David, Wilcock, Gordon K., Ben-Shlomo, Yoav, Allen, Shelley J.

المصدر: In Neurobiology of Aging 2006 27(6):797-803

المؤلفون: Fahey, Mark S., Dawbarn, David, Allen, Shelley J., Paterson, Ian C., Prime, Stephen S.

المصدر: In Analytical Biochemistry 15 March 2001 290(2):272-276

المؤلفون: Allen, Shelley J ^*, Robertson, Alan G.S, Tyler, Sue J, Wilcock, Gordon K, Dawbarn, David

المصدر: In Journal of Biochemical and Biophysical Methods 2001 47(3):239-255

المؤلفون: Kailainathan, Sumangali, Piers, Thomas M., Yi, Jee Hyun, Choi, Seongmin, Fahey, Mark S., Borger, Eva, Gunn-Moore, Frank J., O’Neill, Laurie, Lever, Michael, Whitcomb, Daniel J., Cho, Kwangwook, Allen, Shelley J.

المساهمون: University of St Andrews. School of Biology, University of St Andrews. Institute of Behavioural and Neural Sciences, University of St Andrews. Biomedical Sciences Research Complex

المصدر: Kailainathan, S, Piers, T M, Yi, J H, Choi, S, Fahey, M S, Borger, E, Gunn-Moore, F J, O'Neill, L, Lever, M, Whitcomb, D J, Cho, K & Allen, S J 2016, ' Activation of a synapse weakening pathway by human Val66 but not Met66 pro-brain-derived neurotrophic factor (proBDNF) ', Pharmacological Research, vol. 104, pp. 97-107 . https://doi.org/10.1016/j.phrs.2015.12.008
Kailainathan, S, Piers, T M, Yi, J H, Choi, S M, Fahey, M S, Borger, E, Gunn-Moore, F J, O'Neill, L, Lever, M, Whitcomb, D J, Cho, K & Allen, S J 2016, ' Activation of a synapse weakening pathway by human Val66 but not Met66 pro-brain-derived neurotrophic factor (proBDNF) ', Pharmacological Research, vol. 104, pp. 97-107 . https://doi.org/10.1016/j.phrs.2015.12.008
Kailainathan, S, Piers, T M, Yi, J H, Choi, S, Fahey, M S, Borger, E, Gunn-Moore, F J, O'Neill, L, Lever, M, Whitcomb, D J, Cho, K & Allen, S J 2016, ' Activation of a synapse weakening pathway by human Val66 but not Met66 pro-brain-derived neurotrophic factor (proBDNF) ', Pharmacological Research, vol. 104, no. 0, pp. 97-107 . https://doi.org/10.1016/j.phrs.2015.12.008
Pharmacological Research

مصطلحات موضوعية: Male, DIV, days in vitro, IPTG, isopropyl β-D-1-thiogalactopyranoside, Long-Term Potentiation, LD, luminal domain, chemical compounds studied in this article, Hippocampus, Mice, LTP, long-term potentiation, NAD, nicotinamide adenine dinucleotide, binding kinetics, CD, circular dichroism, ANOVA, analysis of variance, Cells, Cultured, Membrane Potential, Mitochondrial, Neurons, Pro-brain-derived neurotrophic factor (proBDNF), Neuronal Plasticity, LDH, lactate dehydrogenase, neurotrophin receptor, TrkB, tyrosine kinase B, fEPSP, field excitatory postsynaptic potentials, Neurotrophin receptors, SNP, single nucleotide polymorphism, Recombinant Proteins, aCSF, artificial cerebrospinal fluid, PMS, phenazinemethosulfate, Chemical compounds studied in this article, BDNF, brain-derived neurotrophic factor, Val66Met polymorphism, JC-1 dye, 5′,6,6′-tetrachloro-1,1′,3,3′-tetraethylbenzimidazolylcarbocyanine iodide, neurotrophin receptors, RM, LTD, long-term depression, NDAS, SPR, surface plasmon resonance, tau Proteins, QH426 Genetics, AD, Alzheimer’s disease, Article, SDG 3 - Good Health and Well-being, GSK3β, glycogen synthase kinase 3β, Animals, Humans, p75NTR, pan-neurotrophin receptor, FCR, furin cleavage-resistant, Protein Precursors, Rats, Wistar, QH426, ComputingMethodologies_COMPUTERGRAPHICS, Pharmacology, PONDR, predictor of naturally disordered regions, Glycogen Synthase Kinase 3 beta, Polymorphism, Genetic, L-Lactate Dehydrogenase, Brain-Derived Neurotrophic Factor, Long-term depression (LTD), ECD, extracellular domain, TrkBIg2, TrkB immunoglobulin-like domain 2, WT, wild-type, SDS PAGE, sodium dodecyl sulfate polyacrylamide electrophoresis, RM Therapeutics. Pharmacology, long-term depression (LTD), Binding kinetics, DTT, dithiothreitol, s.e.m., standard error of mean, Synapses, RU, response units

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URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::f16825268b801b7410012eba9db69263
https://hdl.handle.net/20.500.11820/4c394466-7f86-4195-98e2-7f20d1ae3435