Human Genome Epidemiology Literature Finder
Records 1 - 12 (of 12 Records) |
Query Trace: Neurodegenerative Diseases and TARDBP[original query] |
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Neuronal inclusion protein TDP-43 has no primary genetic role in FTD and ALS. Neurobiology of aging 2009 Aug 30 (8): 1329-31. Gijselinck Ilse, Sleegers Kristel, Engelborghs Sebastiaan, Robberecht Wim, Martin Jean-Jacques, Vandenberghe Rik, Sciot Raf, Dermaut Bart, Goossens Dirk, van der Zee Julie, De Pooter Tim, Del-Favero Jurgen, Santens Patrick, De Jonghe Peter, De Deyn Peter P, Van Broeckhoven Christine, Cruts Ma |
Novel mutations in TARDBP (TDP-43) in patients with familial amyotrophic lateral sclerosis. PLoS genetics 2008 4 (9): e1000193. Rutherford Nicola J, Zhang Yong-Jie, Baker Matt, Gass Jennifer M, Finch Nicole A, Xu Ya-Fei, Stewart Heather, Kelley Brendan J, Kuntz Karen, Crook Richard J P, Sreedharan Jemeen, Vance Caroline, Sorenson Eric, Lippa Carol, Bigio Eileen H, Geschwind Daniel H, Knopman David S, Mitsumoto Hiroshi, Petersen Ronald C, Cashman Neil R, Hutton Mike, Shaw Christopher E, Boylan Kevin B, Boeve Bradley, Graff-Radford Neill R, Wszolek Zbigniew K, Caselli Richard J, Dickson Dennis W, Mackenzie Ian R, Petrucelli Leonard, Rademakers Ro |
Mutational analysis of TARDBP in neurodegenerative diseases. Neurobiology of aging 2011 Nov 32 (11): 2096-9. Ticozzi Nicola, LeClerc Ashley Lyn, van Blitterswijk Marka, Keagle Pamela, McKenna-Yasek Diane M, Sapp Peter C, Silani Vincenzo, Wills Anne-Marie, Brown Robert H, Landers John |
A genetic association study of two genes linked to neurodegeneration in a Sardinian multiple sclerosis population: the TARDBP Ala382Thr mutation and C9orf72 expansion. Journal of the neurological sciences 2015 Oct 357 (1-2): 229-34. Lorefice L, Murru , Fenu G, Corongiu D, Frau J, Cuccu S, Coghe G C, Tranquilli S, Cocco E, Marrosu M |
Oligogenic inheritance of optineurin (OPTN) and C9ORF72 mutations in ALS highlights localisation of OPTN in the TDP-43-negative inclusions of C9ORF72-ALS. Neuropathology : official journal of the Japanese Society of Neuropathology 2015 Aug . Bury Joanna J, Highley J Robin, Cooper-Knock Johnathan, Goodall Emily F, Higginbottom Adrian, McDermott Christopher J, Ince Paul G, Shaw Pamela J, Kirby Jani |
Mutational analysis of TARDBP gene in patients affected by Parkinson's disease from Calabria. Journal of the neurological sciences 2018 Jul 390 209-211. Gagliardi Monica, Arabia Gennarina, Nisticò Rita, Iannello Grazia, Procopio Radha, Manfredini Lucia, Annesi Grazia, Quattrone Al |
Reduced mitochondrial D-loop methylation levels in sporadic amyotrophic lateral sclerosis. Clinical epigenetics 2020 9 12 (1): 137. Stoccoro Andrea, Smith Adam R, Mosca Lorena, Marocchi Alessandro, Gerardi Francesca, Lunetta Christian, Cereda Cristina, Gagliardi Stella, Lunnon Katie, Migliore Lucia, Coppedè Fab |
Targeted sequencing panels in Italian ALS patients support different etiologies in the ALS/FTD continuum. Journal of neurology 2021 Mar . Bartoletti-Stella Anna, Vacchiano Veria, De Pasqua Silvia, Mengozzi Giacomo, De Biase Dario, Bartolomei Ilaria, Avoni Patrizia, Rizzo Giovanni, Parchi Piero, Donadio Vincenzo, Chiò Adriano, Pession Annalisa, Oppi Federico, Salvi Fabrizio, Liguori Rocco, Capellari Sabina, |
A molecular view of amyotrophic lateral sclerosis through the lens of interaction network modules. PloS one 2022 5 17 (5): e0268159. Jensen Klaus Højgaard, Stalder Anna Katharina, Wernersson Rasmus, Roloff-Handschin Tim-Christoph, Hansen Daniel Hvidberg, Groenen Peter M |
TARDBP mutations in a cohort of Italian patients with Parkinson's disease and atypical parkinsonisms. Frontiers in aging neuroscience 2022 10 14 1020948. Tiloca Cinzia, Goldwurm Stefano, Calcagno Narghes, Verde Federico, Peverelli Silvia, Calini Daniela, Zecchinelli Anna Lena, Sangalli Davide, Ratti Antonia, Pezzoli Gianni, Silani Vincenzo, Ticozzi Nico |
Genetic Screening of Patients with Sporadic Alzheimer's Disease and Frontotemporal Lobar Degeneration in the Chinese Population. Journal of Alzheimer's disease : JAD 2024 5 . Yaoru Li, Ziying Yang, Yanxin Zhang, Fang Liu, Jing Xu, Yaping Meng, Gebeili Xing, Xuqin Ruan, Jun Sun, Nan Zha |
Gene specific effects on brain volume and cognition of TMEM106B in frontotemporal lobar degeneration. medRxiv : the preprint server for health sciences 2024 4 . Marijne Vandebergh, Eliana Marisa Ramos, Nick Corriveau-Lecavalier, Vijay K Ramanan, John Kornak, Carly Mester, Tyler Kolander, Danielle Brushaber, Adam M Staffaroni, Daniel Geschwind, Amy Wolf, Kejal Kantarci, Tania F Gendron, Leonard Petrucelli, Marleen Van den Broeck, Sarah Wynants, Matthew C Baker, Sergi Borrego-Écija, Brian Appleby, Sami Barmada, Andrea Bozoki, David Clark, R Ryan Darby, Bradford C Dickerson, Kimiko Domoto-Reilly, Julie A Fields, Douglas R Galasko, Nupur Ghoshal, Neill Graff-Radford, Ian M Grant, Lawrence S Honig, Ging-Yuek Robin Hsiung, Edward D Huey, David Irwin, David S Knopman, Justin Y Kwan, Gabriel C Léger, Irene Litvan, Joseph C Masdeu, Mario F Mendez, Chiadi Onyike, Belen Pascual, Peter Pressman, Aaron Ritter, Erik D Roberson, Allison Snyder, Anna Campbell Sullivan, M Carmela Tartaglia, Dylan Wint, Hilary W Heuer, Leah K Forsberg, Adam L Boxer, Howard J Rosen, Bradley F Boeve, Rosa Rademake |
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- Page last updated:Jun 24, 2024
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