Showing results (91-100 of 101) with videos related to
Sort By:
Pageof 11
Frontiers in Aging Neuroscience|March 31, 2018
Atrophy in the Thalamus But Not Cerebellum Is Specific for C9orf72 FTD and ALS Patients - An Atlas-Based Volumetric MRI StudySonja Schönecker, Christiane Neuhofer, Markus Otto, et al.Science Translational Medicine|June 5, 2024
Peripheral expression of brain-penetrant progranulin rescues pathologies in mouse models of frontotemporal lobar degenerationMarvin Reich, Matthew J Simon, Beate Polke, et al.Science (New York, N.Y.)|May 16, 2015
Neurodegeneration. C9ORF72 repeat expansions in mice cause TDP-43 pathology, neuronal loss, and behavioral deficitsJeannie Chew, Tania F Gendron, Mercedes Prudencio, et al.Nature Communications|June 7, 2024
Multiomic ALS signatures highlight subclusters and sex differences suggesting the MAPK pathway as therapeutic targetLucas Caldi Gomes, Sonja Hänzelmann, Fabian Hausmann, et al.Molecular Psychiatry|September 25, 2021
Clinico-genetic findings in 509 frontotemporal dementia patientsMatias Wagner, Georg Lorenz, Alexander E Volk, et al.Acta Neuropathologica|September 10, 2015
Cerebellar c9RAN proteins associate with clinical and neuropathological characteristics of C9ORF72 repeat expansion carriersTania F Gendron, Marka van Blitterswijk, Kevin F Bieniek, et al.Nature Neuroscience|March 22, 2016
C9ORF72 poly(GA) aggregates sequester and impair HR23 and nucleocytoplasmic transport proteinsYong-Jie Zhang, Tania F Gendron, Jonathan C Grima, et al.Neuron|April 27, 2016
Gain of Toxicity from ALS/FTD-Linked Repeat Expansions in C9ORF72 Is Alleviated by Antisense Oligonucleotides Targeting GGGGCC-Containing RNAsJie Jiang, Qiang Zhu, Tania F Gendron, et al.Acta Neuropathologica|February 11, 2019
Genome-wide analyses as part of the international FTLD-TDP whole-genome sequencing consortium reveals novel disease risk factors and increases support for immune dysfunction in FTLDCyril Pottier, Yingxue Ren, Ralph B Perkerson, et al.Medrxiv : the Preprint Server for Health Sciences|July 9, 2024
Deciphering Distinct Genetic Risk Factors for FTLD-TDP Pathological Subtypes via Whole-Genome SequencingCyril Pottier, Fahri Küçükali, Matt Baker, et al.Pageof 11