Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Henry Robins"'
Autor:
Johnathan Cooper-Knock, Henry Robins, Isabell Niedermoser, Matthew Wyles, Paul R. Heath, Adrian Higginbottom, Theresa Walsh, Mbombe Kazoka, Project MinE ALS Sequencing Consortium, Paul G. Ince, Guillaume M. Hautbergue, Christopher J. McDermott, Janine Kirby, Pamela J. Shaw, Ahmad Al Kheifat, Ammar Al-Chalabi, Nazli Basak, Ian Blair, Annelot Dekker, Orla Hardiman, Winston Hide, Alfredo Iacoangeli, Kevin Kenna, John Landers, Russel McLaughlin, Jonathan Mill, Bas Middelkoop, Mattieu Moisse, Jesus Mora Pardina, Karen Morrison, Stephen Newhouse, Sara Pulit, Aleksey Shatunov, Chris Shaw, William Sproviero, Gijs Tazelaar, Philip van Damme, Leonard van den Berg, Rick van der Spek, Kristelvan Eijk, Michael van Es, Wouter van Rheenen, Joke van Vugt, Jan Veldink, Maarten Kooyman, Jonathan Glass, Wim Robberecht, Marc Gotkine, Vivian Drory, Matthew Kiernan, Miguel Mitne Neto, Mayana Ztaz, Philippe Couratier, Philippe Corcia, Vincenzo Silani, Adriano Chio, Mamede de Carvalho, Susana Pinto, Alberto Garcia Redondo, Peter Andersen, Markus Weber, Nicola Ticozzi
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 10 (2017)
Amyotrophic lateral sclerosis (ALS) is underpinned by an oligogenic rare variant architecture. Identified genetic variants of ALS include RNA-binding proteins containing prion-like domains (PrLDs). We hypothesized that screening genes encoding additi
Externí odkaz:
https://doaj.org/article/37b028ed777e4060add426ccea440b63
Autor:
Matthieu Moisse, Jesus S. Mora, Ian Fox, Tennore Ramesh, Philip Van Damme, Mbombe Kazoka, Abdelilah Assialioui, Karen E. Morrison, Orla Hardiman, Matthew Wyles, Mónica Povedano Panades, Christopher Shaw, John Landers, Janine Kirby, Christopher J McDermott, A. Nazli Basak, Henry Robins, Johnathan Cooper-Knock, Adrian Higginbottom, Lydia M. Castelli, Theresa Walsh, Isabell Niedermoser, Alexander Beer, Tobias Moll, Paul R. Heath, Pamela J. Shaw, Ammar Al-Chalabi, Wim Robberecht, Guillaume M. Hautbergue
Publikováno v:
Cell Reports
Cooper-Knock, J, Moll, T, Ramesh, T, Castelli, L, Beer, A, Robins, H, Fox, I, Niedermoser, I, Van Damme, P, Moisse, M, Robberecht, W, Hardiman, O, Panades, M P, Assialioui, A, Mora, J S, Basak, A N, Morrison, K E, Shaw, C E, Al-Chalabi, A, Landers, J E, Wyles, M, Heath, P R, Higginbottom, A, Walsh, T, Kazoka, M, McDermott, C J, Hautbergue, G M, Kirby, J & Shaw, P J 2019, ' Mutations in the glycosyltransferase domain of GLT8D1 are associated with familial amyotrophic lateral sclerosis ', Cell Reports, vol. 26, no. 9, pp. 2298-2306.e5 . https://doi.org/10.1016/j.celrep.2019.02.006
Cooper-Knock, J, Moll, T, Ramesh, T, Castelli, L, Beer, A, Robins, H, Fox, I, Niedermoser, I, Van Damme, P, Moisse, M, Robberecht, W, Hardiman, O, Panades, M P, Assialioui, A, Mora, J S, Basak, A N, Morrison, K E, Shaw, C E, Al-Chalabi, A, Landers, J E, Wyles, M, Heath, P R, Higginbottom, A, Walsh, T, Kazoka, M, McDermott, C J, Hautbergue, G M, Kirby, J & Shaw, P J 2019, ' Mutations in the glycosyltransferase domain of GLT8D1 are associated with familial amyotrophic lateral sclerosis ', Cell Reports, vol. 26, no. 9, pp. 2298-2306.e5 . https://doi.org/10.1016/j.celrep.2019.02.006
Summary Amyotrophic lateral sclerosis (ALS) is a severe neurodegenerative disorder without effective neuroprotective therapy. Known genetic variants impair pathways, including RNA processing, axonal transport, and protein homeostasis. We report ALS-c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::861d5712fbc95278be1a2cd90804a15c
https://eprints.whiterose.ac.uk/142642/8/PIIS2211124719301688.pdf
https://eprints.whiterose.ac.uk/142642/8/PIIS2211124719301688.pdf
Autor:
Pamela J. Shaw, Ammar Al-Chalabi, Orla Hardiman, Tobias Moll, Paul R. Heath, Mbombe Kazoka, Matthew Wyles, Mónica Povedano Panades, Jesus S. Mora, A. Nazli Basak, Ian Fox, Lydia M. Castelli, Philip Van Damme, Tennore Ramesh, John Landers, Wim Robberecht, Isabell Niedermoser, Karen E. Morrison, Theresa Walsh, Johnathan Cooper-Knock, Adrian Higginbottom, Alexander Beer, Christopher Shaw, Christopher J McDermott, Henry Robins, Guillaume M. Hautbergue, Janine Kirby
Publikováno v:
SSRN Electronic Journal.
Amyotrophic lateral sclerosis (ALS) is a severe neurodegenerative disorder without effective neuroprotective therapy. Known genetic variants impair pathways including RNA processing, axonal transport and protein homeostasis. Here we report mutations
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6ba5cbe9e26d95423de9f9de72702370
https://doi.org/10.2139/ssrn.3245222
https://doi.org/10.2139/ssrn.3245222
Autor:
Robert Henry Robins
Publikováno v:
The Prix Volney ISBN: 9789401057769
The Prix Volney
The Prix Volney
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2f484e857a5100cbd509a6cfdec241e1
https://doi.org/10.1007/978-94-011-4024-9_2
https://doi.org/10.1007/978-94-011-4024-9_2
Autor:
Robert Henry Robins
Publikováno v:
The Prix Volney ISBN: 9789401057769
The Prix Volney
The Prix Volney
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d7380091899222eb8d45d0d3634c364e
https://doi.org/10.1007/978-94-011-4024-9_3
https://doi.org/10.1007/978-94-011-4024-9_3
Autor:
Robert Henry Robins
Publikováno v:
The Prix Volney ISBN: 9789401057769
The Prix Volney
The Prix Volney
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::96cf10d723b316f71e654dbe6483e238
https://doi.org/10.1007/978-94-011-4024-9_1
https://doi.org/10.1007/978-94-011-4024-9_1
Autor:
Henry Robinson, Liewald Mathias
Publikováno v:
MATEC Web of Conferences, Vol 80, p 10007 (2016)
Hollow or tubular preforms are used to meet lightweight requirements and reduce production costs of cold formed components. In order to increase efficiency of manufacturing, a combined forming process was developed, which will be presented in this pa
Externí odkaz:
https://doaj.org/article/54dce3131e92429fa730542ee988899f