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Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, ISSN 2167-8421, 10/2019, Volume 20, Issue 7-8, pp. 568 - 575
Mutations in the TANK binding kinase 1 gene (TBK1) are associated with amyotrophic lateral sclerosis and/or frontotemporal dementia; however, the range of... 
TBK1 | primary lateral sclerosis | TDP-43 | primary progressive aphasia | neuropathology
Journal Article
Neuron, ISSN 0896-6273, 08/2017, Volume 95, Issue 4, pp. 808 - 816.e9
Amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) are age-related neurodegenerative disorders with shared genetic etiologies and... 
low-complexity domain | liquid-liquid phase separation | TDP-43 | T cell-restricted intracellular antigen-1 | stress granules | frontotemporal dementia | amyotrophic lateral sclerosis | membrane-less organelle | frontotemporal lobar degeneration | MULTISYSTEM PROTEINOPATHY | DISTAL MYOPATHY | MESSENGER-RNA | LIQUID DROPLETS | SEQUENCING DATA | HEXANUCLEOTIDE REPEAT | DOMAINS | C9ORF72 | NEUROSCIENCES | FAMILIAL ALS | Humans | Middle Aged | Family Health | Male | Green Fluorescent Proteins - genetics | DNA-Binding Proteins - metabolism | Transfection | Time Factors | Adult | Female | T-Cell Intracellular Antigen-1 | Frontotemporal Dementia - pathology | Frontotemporal Dementia - genetics | Stress, Physiological - physiology | Green Fluorescent Proteins - metabolism | Poly(A)-Binding Proteins - genetics | Amyotrophic Lateral Sclerosis - genetics | Heterogeneous-Nuclear Ribonucleoprotein Group A-B - metabolism | RNA-Binding Protein FUS - metabolism | Mutation - genetics | Heterogeneous Nuclear Ribonucleoprotein A1 | Microscopy, Confocal | Amyotrophic Lateral Sclerosis - pathology | Aged | HeLa Cells | Nervous system diseases | RNA | Analysis | Genetic research | Development and progression | Amyotrophic lateral sclerosis | Genetic aspects | T cells | Binding proteins | Protein binding | Dementia | Disease | Pathogenesis | Genes | Disorders | Lymphocytes T | Phase transitions | Proteins | Consortia | DNA-binding protein | Etiology | Dementia disorders | Age | Deoxyribonucleic acid--DNA | Phase transformations | Neurodegenerative diseases | Metabolism | Ribonucleic acid--RNA | Pathology | Phase separation | Mutation | Frontotemporal dementia | Dismantling | Phase transition | T-cell-restricted intracellular antigen-1
Journal Article
Nature Neuroscience, ISSN 1097-6256, 08/2015, Volume 18, Issue 8, pp. 1175 - 1182
Journal Article
Journal of Phycology, ISSN 0022-3646, 12/2011, Volume 47, Issue 6, pp. 1397 - 1412
Journal Article
by Pottier, Cyril and Ren, Yingxue and Perkerson III, Ralph B and Baker, Matt and Jenkins, Gregory D and van Blitterswijk, Marka and DeJesus-Hernandez, Mariely and van Rooij, Jeroen G. J and Murray, Melissa E and Christopher, Elizabeth and McDonnell, Shannon K and Fogarty, Zachary and Batzler, Anthony and Tian, Shulan and Vicente, Cristina T and Matchett, Billie and Karydas, Anna M and Hsiung, Ging-Yuek Robin and Seelaar, Harro and Mol, Merel O and Finger, Elizabeth C and Graff, Caroline and Öijerstedt, Linn and Neumann, Manuela and Heutink, Peter and Synofzik, Matthis and Wilke, Carlo and Prudlo, Johannes and Rizzu, Patrizia and Simon-Sanchez, Javier and Edbauer, Dieter and Roeber, Sigrun and Diehl-Schmid, Janine and Evers, Bret M and King, Andrew and Mesulam, M Marsel and Weintraub, Sandra and Geula, Changiz and Bieniek, Kevin F and Petrucelli, Leonard and Ahern, Geoffrey L and Reiman, Eric M and Woodruff, Bryan K and Caselli, Richard J and Huey, Edward D and Farlow, Martin R and Grafman, Jordan and Mead, Simon and Grinberg, Lea T and Spina, Salvatore and Grossman, Murray and Irwin, David J and Lee, Edward B and Suh, EunRan and Snowden, Julie and Mann, David and Ertekin-Taner, Nilufer and Uitti, Ryan J and Wszolek, Zbigniew K and Josephs, Keith A and Parisi, Joseph E and Knopman, David S and Petersen, Ronald C and Hodges, John R and Piguet, Olivier and Geier, Ethan G and Yokoyama, Jennifer S and Rissman, Robert A and Rogaeva, Ekaterina and Keith, Julia and Zinman, Lorne and Tartaglia, Maria Carmela and Cairns, Nigel J and Cruchaga, Carlos and Ghetti, Bernardino and Kofler, Julia and Lopez, Oscar L and Beach, Thomas G and Arzberger, Thomas and Herms, Jochen and Honig, Lawrence S and Vonsattel, Jean Paul and Halliday, Glenda M and Kwok, John B and White III, Charles L and Gearing, Marla and Glass, Jonathan and Rollinson, Sara and Pickering-Brown, Stuart and Rohrer, Jonathan D and Trojanowski, John Q and Van Deerlin, Vivianna and Bigio, Eileen H and Troakes, Claire and Al-Sarraj, Safa and Asmann, Yan and Miller, Bruce L and Graff-Radford, Neill R and Boeve, Bradley F and Seeley, William W and ...
Acta Neuropathologica, ISSN 0001-6322, 6/2019, Volume 137, Issue 6, pp. 879 - 899
Journal Article
Amyotrophic lateral sclerosis & frontotemporal degeneration, 06/2019, p. 1
Mutations in the TANK binding kinase 1 gene ( ) are associated with amyotrophic lateral sclerosis and/or frontotemporal dementia; however, the range of... 
Journal Article
by Pottier, Cyril and Zhou, Xiaolai and Perkerson, Ralph B and Baker, Matt and Jenkins, Gregory D and Serie, Daniel J and Ghidoni, Roberta and Benussi, Luisa and Binetti, Giuliano and López de Munain, Adolfo and Zulaica, Miren and Moreno, Fermin and Le Ber, Isabelle and Pasquier, Florence and Hannequin, Didier and Sánchez-Valle, Raquel and Antonell, Anna and Lladó, Albert and Parsons, Tammee M and Finch, NiCole A and Finger, Elizabeth C and Lippa, Carol F and Huey, Edward D and Neumann, Manuela and Heutink, Peter and Synofzik, Matthis and Wilke, Carlo and Rissman, Robert A and Slawek, Jaroslaw and Sitek, Emilia and Johannsen, Peter and Nielsen, Jørgen E and Ren, Yingxue and van Blitterswijk, Marka and DeJesus-Hernandez, Mariely and Christopher, Elizabeth and Murray, Melissa E and Bieniek, Kevin F and Evers, Bret M and Ferrari, Raffaele and Ferrari, Camilla and Rollinson, Sara and Richardson, Anna and Scarpini, Elio and Fumagalli, Giorgio G and Padovani, Alessandro and Hardy, John and Momeni, Parastoo and Frangipane, Francesca and Maletta, Raffaele and Anfossi, Maria and Gallo, Maura and Petrucelli, Leonard and Suh, EunRan and Lopez, Oscar L and Wong, Tsz H and van Rooij, Jeroen G J and Seelaar, Harro and Mead, Simon and Caselli, Richard J and Reiman, Eric M and Noel Sabbagh, Marwan and Kjolby, Mads and Nykjaer, Anders and Karydas, Anna M and Boxer, Adam L and Grinberg, Lea T and Grafman, Jordan and Spina, Salvatore and Oblak, Adrian and Mesulam, M-Marsel and Weintraub, Sandra and Geula, Changiz and Hodges, John R and Piguet, Olivier and Brooks, William S and Irwin, David J and Trojanowski, John Q and Lee, Edward B and Josephs, Keith A and Parisi, Joseph E and Ertekin-Taner, Nilüfer and Knopman, David S and Nacmias, Benedetta and Piaceri, Irene and Bagnoli, Silvia and Sorbi, Sandro and Gearing, Marla and Glass, Jonathan and Beach, Thomas G and Black, Sandra E and Masellis, Mario and Rogaeva, Ekaterina and Vonsattel, Jean-Paul and Honig, Lawrence S and Kofler, Julia and Bruni, Amalia C and Snowden, Julie and Mann, David and Pickering-Brown, Stuart and ...
The Lancet Neurology, ISSN 1474-4422, 06/2018, Volume 17, Issue 6, pp. 548 - 558
Loss-of-function mutations in cause frontotemporal lobar degeneration (FTLD). Patients with mutations present with a uniform subtype of TAR DNA-binding protein... 
GDNF FAMILY | PROTEIN-LEVELS | DEMENTIA | THERAPY | PLASMA | TMEM106B | COMMON | AMYOTROPHIC-LATERAL-SCLEROSIS | CLINICAL NEUROLOGY | PARKINSONS-DISEASE | Genetic research | Physiological aspects | Genetic aspects | Genomics | Aging | Mutation
Journal Article
Journal of Neurochemistry, ISSN 0022-3042, 09/2013, Volume 126, Issue 6, pp. 781 - 791
Journal Article
Journal of Phycology, ISSN 0022-3646, 12/2011, Volume 47, Issue 6, pp. 1397 - 1412
Journal Article
Nature Communications, ISSN 2041-1723, 06/2016, Volume 7, Issue 1, p. 11992
Journal Article