Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Alan Stepto"'
Autor:
Gerald Vinatier, Vincenzo G. Fiore, Edgar Buhl, Danielle C. Diaper, Benjamin L. de Bivort, Chenghao Chen, Raymond J. Dolan, Frank Hirth, Zoe N. Ludlow, Keita Endo, Yoshitsugu Adachi, Sheena Brown, James J L Hodge, Kei Ito, Nicholas J. Strausfeld, Stephan J. Sigrist, Daniel A. Solomon, Jean-René Martin, Alan Stepto, Katherine E. White, Dickon M. Humphrey, Sean M. Buchanan, Richard Faville, Ralf Stanewsky, Benjamin Kottler, Jonah Dearlove
Publikováno v:
BioRxiv
The insect central complex and vertebrate basal ganglia are forebrain centres involved in selection and maintenance of behavioural actions. However, little is known about the formation of the underlying circuits, or how they integrate sensory informa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a2989c701ca55944611538ce5283e21
https://hal.archives-ouvertes.fr/hal-02413547
https://hal.archives-ouvertes.fr/hal-02413547
Autor:
Pranetha Baskaran, Leonard Petrucelli, Frank Hirth, Bradley N. Smith, Claire Troakes, Alan Stepto, Youn-Bok Lee, Agnes L. Nishimura, Christopher Shaw, Jorge Gomez-Deza, Boris Rogelj, Yoshitsugu Adachi, Sarah Guthrie, Han-Jou Chen, Jean-Marc Gallo
Publikováno v:
Human Molecular Genetics
Hum Mol Genet
Hum Mol Genet
An intronic GGGGCC (G4C2) hexanucleotide repeat expansion inC9orf72 is the most common genetic cause of amyotrophic lateral sclerosis and frontotemporal dementia (C9ALS/FTD). Repeat-associated non-AUG (RAN) translation of G4C2 RNA can result in five
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf7c0fa820b4838afa99fa708bb71ee8
Publikováno v:
Acta Neuropathologica; Vol 127
GGGGCC (G4C2) hexanucleotide repeat expansion in chromosome 9 open reading frame 72 (C9ORF72) has been identified as the most common genetic abnormality in both frontotemporal lobar degeneration (FTLD) and amyotrophic lateral sclerosis (ALS). To inve
Autor:
Iain M. Robinson, Alan Stepto, Lies Vanden Broeck, Patrick Callaerts, Ben Sutcliffe, Zoe N. Ludlow, Christopher Shaw, Dickon M. Humphrey, Frank Hirth, Christopher J. H. Elliott, Bart Dermaut, Ammar Al-Chalabi, Danielle Diaper, Yoshitsugu Adachi
Publikováno v:
Human Molecular Genetics
HUMAN MOLECULAR GENETICS
HUMAN MOLECULAR GENETICS
Cytoplasmic accumulation and nuclear clearance of TDP-43 characterize familial and sporadic forms of amyotrophic lateral sclerosis and frontotemporal lobar degeneration, suggesting that either loss or gain of TDP-43 function, or both, cause disease f
Autor:
Sancho, Rosa M.1 r.sancho@alzheimersresearchuk.org, Cox, Carla J.1, Ridley, Simon H.1, Phipps, Laura E.1, Karran, Eric1
Publikováno v:
Alzheimer's Research & Therapy. Jul2015, Vol. 7 Issue 1, p1-4. 4p.
Autor:
Lee, Youn-Bok, Baskaran, Pranetha, Gomez-Deza, Jorge, Chen, Han-Jou, Nishimura, Agnes L, Smith, Bradley N, Troakes, Claire, Adachi, Yoshitsugu, Stepto, Alan, Petrucelli, Leonard, Gallo, Jean-Marc, Hirth, Frank, Rogelj, Boris, Guthrie, Sarah, Shaw, Christopher E
Publikováno v:
Human Molecular Genetics; Feb2021, Vol. 30 Issue 3/4, p318-320, 3p
Autor:
Solomon, Daniel A, Stepto, Alan, Au, Wing Hei, Adachi, Yoshitsugu, Diaper, Danielle C, Hall, Rachel, Rekhi, Anjeet, Boudi, Adel, Tziortzouda, Paraskevi, Lee, Youn-Bok, Smith, Bradley, Bridi, Jessika C, Spinelli, Greta, Dearlove, Jonah, Humphrey, Dickon M, Gallo, Jean-Marc, Troakes, Claire, Fanto, Manolis, Soller, Matthias, Rogelj, Boris
Publikováno v:
Brain: A Journal of Neurology; Oct2018, Vol. 141 Issue 10, p2908-2924, 17p
Publikováno v:
Acta Neuropathologica; Mar2014, Vol. 127 Issue 3, p377-389, 13p
Autor:
Guy Warner
651 was the first Air Observation Post (AOP) Squadron, formed at Old Sarum on August 1 1941 to work closely with army units in artillery spotting and liaison. It was still part of the RAF but all the pilots, drivers and signalers were from the Royal