المؤلفون: Zsofia I. Laszlo, Nicole Hindley, Anna Sanchez Avila, Rachel A. Kline, Samantha L. Eaton, Douglas J. Lamont, Colin Smith, Tara L. Spires-Jones, Thomas M. Wishart, Christopher M. Henstridge

المصدر: Acta Neuropathologica Communications, Vol 10, Iss 1, Pp 1-20 (2022)

مصطلحات موضوعية: ALS, Synapse, Proteomics, FTD, C9ORF72, Human brain, Neurology. Diseases of the nervous system, RC346-429

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2051-5960

URL الوصول: https://doaj.org/article/a5dc3dda62ae45789b1d7df6f27a7cc3

المؤلفون: Sharon J. Brown, Rachel A. Kline, Silvia A. Synowsky, Sally L. Shirran, Ian Holt, Kelly A. Sillence, Peter Claus, Brunhilde Wirth, Thomas M. Wishart, Heidi R. Fuller

المصدر: Cells, Vol 11, Iss 17, p 2624 (2022)

مصطلحات موضوعية: Spinal muscular atrophy, SMA, fibroblasts, severity, proteomics, biomarkers, Cytology, QH573-671

وصف الملف: electronic resource

Relation: https://www.mdpi.com/2073-4409/11/17/2624; https://doaj.org/toc/2073-4409

URL الوصول: https://doaj.org/article/3cd4a33860b94e2dbe9ab7ac17ec3748

المؤلفون: Rachel A. Kline, Lena Lößlein, Dominic Kurian, Judit Aguilar Martí, Samantha L. Eaton, Felipe A. Court, Thomas H. Gillingwater, Thomas M. Wishart

المصدر: Cells, Vol 11, Iss 17, p 2653 (2022)

مصطلحات موضوعية: proteomics, systems biology, experimental design, neurodegeneration, pathway analysis, data filtering, Cytology, QH573-671

وصف الملف: electronic resource

Relation: https://www.mdpi.com/2073-4409/11/17/2653; https://doaj.org/toc/2073-4409

URL الوصول: https://doaj.org/article/bf309651417e499eb255c76a496cd0b7

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: Laura C. Graham, Rachel A. Kline, Douglas J. Lamont, Thomas H. Gillingwater, Neil A. Mabbott, Paul A. Skehel, Thomas M. Wishart

المصدر: Cells, Vol 10, Iss 12, p 3403 (2021)

مصطلحات موضوعية: mitochondria, synapse, aging, proteomics, neuron, Cytology, QH573-671

وصف الملف: electronic resource

Relation: https://www.mdpi.com/2073-4409/10/12/3403; https://doaj.org/toc/2073-4409

URL الوصول: https://doaj.org/article/4016d2637beb42f992bd8d2a5e864fad

المؤلفون: Laura H Comley, Rachel A Kline, Alison K Thomson, Victoria Woschitz, Eric Villalón Landeros, Erkan Y Osman, Christian L Lorson, Lyndsay M Murray

المصدر: Human Molecular Genetics. 31:3107-3119

مصطلحات موضوعية: Motor Neurons, Muscular Atrophy, Spinal, Disease Models, Animal, Mice, Oligonucleotides, Genetics, Animals, General Medicine, Oligonucleotides, Antisense, Tumor Suppressor Protein p53, Survival of Motor Neuron 1 Protein, Molecular Biology, Genetics (clinical)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ecc408e57e9db246ad93fb393ecb8c8e
https://doi.org/10.1093/hmg/ddac097

المؤلفون: Felipe A. Court, Thomas M. Wishart, Waldo Cerpa, J César Cárdenas, Sebastián Bernales, Gonzalo Ureta, Hernán Huerta, Douglas J Lamont, Rachel A Kline, Samantha L Eaton, Somya Iqbal, Gabriel Quiroz, Matías Lira, Macarena S. Arrázola

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::21bb5423093d534bb98a447468cb2e45
https://doi.org/10.15252/rc.2022284456

المؤلفون: Jonathan D. Cooper, Thomas M. Wishart, Maica Llavero Hurtado, Hemanth R. Nelvagal, Mark S. Sands, Samantha L. Eaton, Douglas J. Lamont, Rachel A. Kline

المصدر: Scientific Reports, Vol 10, Iss 1, Pp 1-16 (2020)
Scientific Reports
Nelvagal, H R, Llavero Hurtado, M, Eaton, S, Kline, R, Lamont, D J, Sands, M S, Wishart, T & Cooper, J D 2020, ' Comparative proteomic profiling reveals mechanisms for early spinal cord vulnerability in CLN1 disease ', Scientific Reports . https://doi.org/10.1038/s41598-020-72075-7

مصطلحات موضوعية: Batten disease, Proteome, Protein Array Analysis, lcsh:Medicine, Lipofuscinoses, Disease, Bioinformatics, Article, Mice, Neuroinflammation, Neuronal Ceroid-Lipofuscinoses, Comparative proteomics, medicine, Lysosomal storage disease, Animals, Humans, Lipid-storage diseases, Neurodegeneration, lcsh:Science, Pathological, Neuronal Ceroid, Mice, Knockout, Multidisciplinary, business.industry, Proteomic Profiling, lcsh:R, Membrane Proteins, Batten Disease, medicine.disease, Spinal cord, Mice, Inbred C57BL, Disease Models, Animal, medicine.anatomical_structure, Spinal Cord, Disease Progression, lcsh:Q, Thiolester Hydrolases, business

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e504a052048e5f04230b1f8bcd449c3
http://link.springer.com/article/10.1038/s41598-020-72075-7

المؤلفون: Thomas H. Gillingwater, Helena Chaytow, Yu-Ting Huang, Leire M. Ledahawsky, Anna A L Motyl, Thomas M. Wishart, Samantha L. Eaton, Kiterie M. E. Faller, Douglas J. Lamont, Ewout J N Groen, Rachel A. Kline

المصدر: Human Molecular Genetics
Motyl, A A L, Faller, K, Groen, E J N, Kline, R, Eaton, S, Ledahawsky, L, Chaytow, H, Lamont, D J, Wishart, T, Huang, Y & Gillingwater, T 2020, ' Pre-natal manifestation of systemic developmental abnormalities in spinal muscular atrophy ', Human Molecular Genetics, vol. 29, no. 16, pp. 2674-2683 . https://doi.org/10.1093/hmg/ddaa146

مصطلحات موضوعية: Proteomics, AcademicSubjects/SCI01140, Pathology, Disease, SMN1, Pathogenesis, Mice, 0302 clinical medicine, Prenatal Diagnosis, congenital abnormality, Genetics (clinical), spinal muscular atrophy, Motor Neurons, 0303 health sciences, Brain, Heart, General Medicine, SMA, Phenotype, heart ventricle, developmental delay, medicine.anatomical_structure, Liver, General Article, microtomography, medicine.medical_specialty, mice, Neuromuscular disease, phenotype, brain, embryo, neuromuscular diseases, heart, Biology, liver, Muscular Atrophy, Spinal, 03 medical and health sciences, proteomics, perturbations, Genetics, medicine, Animals, Humans, motor neurons, Molecular Biology, 030304 developmental biology, Myocardium, X-Ray Microtomography, Spinal muscular atrophy, Motor neuron, medicine.disease, Survival of Motor Neuron 1 Protein, Disease Models, Animal, x-ray, mutation, 030217 neurology & neurosurgery

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::254e0fb675dafec618503b1ba725a930
http://europepmc.org/articles/PMC7530529

المؤلفون: null Leire M. Ledahawsky, null Maria Eirini Terzenidou, null Ruairidh Edwards, null Rachel A. Kline, null Laura C. Graham, null Samantha L. Eaton, null Dinja van der Hoorn, null Helena Chaytow, null Yu‐Ting Huang, null Ewout J.N. Groen, null Anna A. L. Motyl, null Douglas J. Lamont, null Kostas Tokatlidis, null Thomas M. Wishart, null Thomas H. Gillingwater

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::03143649c9c435da9090c5a119d02f6c
https://doi.org/10.1111/febs.16377/v2/response1