受强制性开放获取政策约束的文章 - Frank Baas了解详情
无法在其他位置公开访问的文章：5 篇
查看
Neuroblastoma is composed of two super-enhancer-associated differentiation states
T van Groningen, J Koster, LJ Valentijn, DA Zwijnenburg, N Akogul, ...
Nature genetics 49 (8), 1261-1266, 2017
强制性开放获取政策： European Commission, Dutch Cancer Society
查看
Genome‐wide association study in musician's dystonia: A risk variant at the arylsulfatase G locus?
K Lohmann, A Schmidt, A Schillert, S Winkler, A Albanese, F Baas, ...
Movement Disorders 29 (7), 921-927, 2014
强制性开放获取政策： German Research Foundation, Government of Spain, Government of Italy
查看
Recurrent GNAO1 Mutations Associated With Developmental Delay and a Movement Disorder
LA Menke, M Engelen, M Alders, VJJ Odekerken, F Baas, JM Cobben
Journal of child neurology 31 (14), 1598-1601, 2016
强制性开放获取政策： US National Institutes of Health
查看
Plasminogen activator inhibitor-1 influences cerebrovascular complications and death in pneumococcal meningitis
MC Brouwer, JCM Meijers, F Baas, A van der Ende, HW Pfister, A Giese, ...
Acta neuropathologica 127, 553-564, 2014
强制性开放获取政策： European Commission, Netherlands Organisation for Health Research and …
查看
Variation in coagulation and fibrinolysis genes evaluated for their contribution to cerebrovascular complications in adults with bacterial meningitis in the Netherlands
AT Kloek, HN Khan, MV Seron, A Jongejan, AH Zwinderman, F Baas, ...
Journal of Infection 77 (1), 54-59, 2018
强制性开放获取政策： Netherlands Organisation for Scientific Research, European Commission …
可在其他位置公开访问的文章：87 篇
查看
Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways
ET Cirulli, BN Lasseigne, S Petrovski, PC Sapp, PA Dion, CS Leblond, ...
Science 347 (6229), 1436-1441, 2015
强制性开放获取政策： US National Institutes of Health, Motor Neurone Disease Association, UK, UK …
查看
Genome-wide analyses identify KIF5A as a novel ALS gene
A Nicolas, KP Kenna, AE Renton, N Ticozzi, F Faghri, R Chia, ...
Neuron 97 (6), 1268-1283. e6, 2018
强制性开放获取政策： US National Institutes of Health, US Department of Veterans Affairs, Howard …
查看
Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALS
BN Smith, N Ticozzi, C Fallini, AS Gkazi, S Topp, KP Kenna, EL Scotter, ...
Neuron 84 (2), 324-331, 2014
强制性开放获取政策： US National Institutes of Health, National Health and Medical Research …
查看
Schwann cell autophagy, myelinophagy, initiates myelin clearance from injured nerves
JA Gomez-Sanchez, L Carty, M Iruarrizaga-Lejarreta, M Palomo-Irigoyen, ...
Journal of Cell Biology 210 (1), 153-168, 2015
强制性开放获取政策： US National Institutes of Health, Cancer Research UK, UK Medical Research …
查看
Recessive mutations in the putative calcium-activated chloride channel Anoctamin 5 cause proximal LGMD2L and distal MMD3 muscular dystrophies
V Bolduc, G Marlow, KM Boycott, K Saleki, H Inoue, J Kroon, M Itakura, ...
The American Journal of Human Genetics 86 (2), 213-221, 2010
强制性开放获取政策： Canadian Institutes of Health Research, Genome Canada
查看
NEK1 variants confer susceptibility to amyotrophic lateral sclerosis
KP Kenna, PTC Van Doormaal, AM Dekker, N Ticozzi, BJ Kenna, ...
Nature genetics 48 (9), 1037-1042, 2016
强制性开放获取政策： US National Institutes of Health, Howard Hughes Medical Institute, National …
查看
CLP1 Founder Mutation Links tRNA Splicing and Maturation to Cerebellar Development and Neurodegeneration
AE Schaffer, VRC Eggens, AO Caglayan, MS Reuter, E Scott, NG Coufal, ...
Cell 157 (3), 651-663, 2014
强制性开放获取政策： US National Institutes of Health, Howard Hughes Medical Institute
查看
ITPR2 as a susceptibility gene in sporadic amyotrophic lateral sclerosis: a genome-wide association study
MA Van Es, PW Van Vught, HM Blauw, L Franke, CG Saris, PM Andersen, ...
The Lancet Neurology 6 (10), 869-877, 2007
强制性开放获取政策： Research Foundation (Flanders)
查看
Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis
MA Van Es, PWJ Van Vught, HM Blauw, L Franke, CGJ Saris, ...
Nature genetics 40 (1), 29-31, 2008
强制性开放获取政策： Research Foundation (Flanders)
查看
The C9ORF72 expansion mutation is a common cause of ALS+/− FTD in Europe and has a single founder
BN Smith, S Newhouse, A Shatunov, C Vance, S Topp, L Johnson, ...
European Journal of Human Genetics 21 (1), 102-108, 2013
强制性开放获取政策： US National Institutes of Health, Motor Neurone Disease Association, UK
查看
Postmortem cortex samples identify distinct molecular subtypes of als: retrotransposon activation, oxidative stress, and activated glia
OH Tam, NV Rozhkov, R Shaw, D Kim, I Hubbard, S Fennessey, N Propp, ...
Cell reports 29 (5), 1164-1177. e5, 2019
强制性开放获取政策： US National Institutes of Health, Chan Zuckerberg Initiative
查看
Clinical, neuroradiological and genetic findings in pontocerebellar hypoplasia
Y Namavar, PG Barth, PR Kasher, F Van Ruissen, K Brockmann, ...
Brain 134 (1), 143-156, 2011
强制性开放获取政策： US National Institutes of Health, Howard Hughes Medical Institute
查看
C3-dependent mechanism of microglial priming relevant to multiple sclerosis
V Ramaglia, TR Hughes, RM Donev, MM Ruseva, X Wu, I Huitinga, ...
Proceedings of the National Academy of Sciences 109 (3), 965-970, 2012
强制性开放获取政策： US National Institutes of Health
查看
Mutations in the vesicular trafficking protein annexin A11 are associated with amyotrophic lateral sclerosis
BN Smith, SD Topp, C Fallini, H Shibata, HJ Chen, C Troakes, A King, ...
Science translational medicine 9 (388), eaad9157, 2017
强制性开放获取政策： US National Institutes of Health, Howard Hughes Medical Institute …
查看
Mechanisms for nonrecurrent genomic rearrangements associated with CMT1A or HNPP: rare CNVs as a cause for missing heritability
F Zhang, P Seeman, P Liu, MAJ Weterman, C Gonzaga-Jauregui, ...
The American Journal of Human Genetics 86 (6), 892-903, 2010
强制性开放获取政策： US National Institutes of Health, Research Foundation (Flanders)
出版信息和资助信息由计算机程序自动确定