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Cell Reports|July 2, 2014
Human-chromatin-related protein interactions identify a demethylase complex required for chromosome segregationEdyta Marcon, Zuyao Ni, Shuye Pu, et al.Nature Structural & Molecular Biology|July 7, 2014
RPRD1A and RPRD1B are human RNA polymerase II C-terminal domain scaffolds for Ser5 dephosphorylationZuyao Ni, Chao Xu, Xinghua Guo, et al.Parkinsonism & Related Disorders|March 27, 2018
LRRK2 protective haplotype and full sequencing study in REM sleep behavior disorderBouchra Ouled Amar Bencheikh, Jennifer A Ruskey, Isabelle Arnulf, et al.Molecular Cancer Therapeutics|June 6, 2018
Development of MGD007, a gpA33 x CD3-Bispecific DART Protein for T-Cell Immunotherapy of Metastatic Colorectal CancerPaul A Moore, Kalpana Shah, Yinhua Yang, et al.Nature Genetics|September 28, 2005
Mutations in SEPT9 cause hereditary neuralgic amyotrophyGregor Kuhlenbäumer, Mark C Hannibal, Eva Nelis, et al.Neurogenetics|March 18, 2009
Identification of the variant Ala335Val of MED25 as responsible for CMT2B2: molecular data, functional studies of the SH3 recognition motif and correlation between wild-type MED25 and PMP22 RNA levels in CMT1A animal modelsAlejandro Leal, Kathrin Huehne, Finn Bauer, et al.Sleep|September 10, 2020
New 2013 incidence peak in childhood narcolepsy: more than vaccination?Zhongxing Zhang, Jari K Gool, Rolf Fronczek, et al.Disease Models & Mechanisms|January 22, 2017
Blood RNA biomarkers in prodromal PARK4 and rapid eye movement sleep behavior disorder show role of complexin 1 loss for risk of Parkinson's diseaseSuna Lahut, Suzana Gispert, Özgür Ömür, et al.Journal of Sleep Research|January 27, 2016
The European Narcolepsy Network (EU-NN) databaseRamin Khatami, Gianina Luca, Christian R Baumann, et al.Journal of Neurology, Neurosurgery, and Psychiatry|September 2, 2017
Biomarkers predict outcome in Charcot-Marie-Tooth disease 1ARobert Fledrich, Manoj Mannil, Andreas Leha, et al.Pageof 31