Results 191 to 200 of about 22,140 (207)

Shared brain transcriptomic signature in TDP-43 type A FTLD patients with or without GRN mutations

Brain, 2022
Cyril Pottier, Ligia Mateiu, Matthew C Baker   +2 more
exaly  

Microglial lysosome dysfunction contributes to white matter pathology and TDP-43 proteinopathy in GRN-associated FTD

Cell Reports, 2021
Yanwei Wu, Wei Shao, Jimei Tong
exaly  

Homozygous GRN mutations: new phenotypes and new insights into pathological and molecular mechanisms

Brain, 2020
Vincent Huin, Mathieu Barbier, Armand Bottani   +2 more
exaly  

Generation and Characterization of Novel iPSC Lines from a Portuguese Family Bearing Heterozygous and Homozygous GRN Mutations

Biomedicines, 2022
Maria Rosario Almeida, Maria Do Carmo Macário, Isabel Santana   +2 more
exaly  

Plasma Small Extracellular Vesicles with Complement Alterations in GRN/C9orf72 and Sporadic Frontotemporal Lobar Degeneration

Cells, 2022
Sonia Bellini, Claudia Saraceno, Luisa Benussi   +2 more
exaly  

Progranulin gene (GRN) promoter methylation is increased in patients with sporadic frontotemporal lobar degeneration

Neurological Sciences, 2012
Daniela Galimberti, Bernardo Dell'Osso, Chiara Fenoglio   +2 more
exaly  

GRN 3′UTR+78 C>T is not associated with risk for Parkinson’s disease

European Journal of Neurology, 2009
C Wider, Grzegorz Opala, M Barcikowska   +2 more
exaly  

A new phenotype associated with homozygous GRN mutations: complicated spastic paraplegia

European Journal of Neurology, 2017
Alberto R M Martinez, Iscia Lopes-Cendes, Marcondes C Franca   +2 more
exaly  

Genetic and functional characters of GRN p.T487I mutation in Taiwanese patients with atypical parkinsonian disorders

Parkinsonism and Related Disorders, 2018
Kuo-Hsuan Chang, Guan-Chiun Lee, Chin-Chang Huang   +2 more
exaly  

Isolated parkinsonism is an atypical presentation of GRN and C9orf72 gene mutations

Parkinsonism and Related Disorders, 2020
Dario Saracino, Vincent Huin, Fabienne Clot   +2 more
exaly