Human Genome Epidemiology Literature Finder
Records 1 - 7 (of 7 Records) |
Query Trace: Death and FUS[original query] |
---|
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 |
Argyrophilic Grain Pathology in Frontotemporal Lobar Degeneration: Demographic, Clinical, Neuropathological, and Genetic Features. Journal of Alzheimer's disease : JAD 2018 5 63 (3): 1109-1117. Gil María José, Manzano María Sagrario, Cuadrado María Luz, Fernández Cristina, Góméz Elena, Matesanz Carmen, Calero Miguel, Rábano Alber |
Generation of six induced pluripotent stem cell lines from patients with amyotrophic lateral sclerosis with associated genetic mutations in either FUS or ANXA11. Stem cell research 2021 2 52 102246. Hedges Erin C, Topp Simon, Shaw Christopher E, Nishimura Agnes |
UBTF-internal tandem duplication as a novel poor prognostic factor in pediatric acute myeloid leukemia. Genes, chromosomes & cancer 2022 11 62 (4): 202-209. Kaburagi Taeko, Shiba Norio, Yamato Genki, Yoshida Kenichi, Tabuchi Ken, Ohki Kentaro, Ishikita Etsuko, Hara Yusuke, Shiraishi Yuichi, Kawasaki Hirohide, Sotomatsu Manabu, Takizawa Takumi, Taki Tomohiko, Kiyokawa Nobutaka, Tomizawa Daisuke, Horibe Keizo, Miyano Satoru, Taga Takashi, Adachi Souichi, Ogawa Seishi, Hayashi Yasuhi |
Spectrum and frequency of genetic variants in sporadic amyotrophic lateral sclerosis. Brain communications 2023 5 5 (3): fcad152. Wolfgang P Ruf, Matej Boros, Axel Freischmidt, David Brenner, Veselin Grozdanov, Joao de Meirelles, Thomas Meyer, Torsten Grehl, Susanne Petri, Julian Grosskreutz, Ute Weyen, Rene Guenther, Martin Regensburger, Tim Hagenacker, Jan C Koch, Alexander Emmer, Annekathrin Roediger, Robert Steinbach, Joachim Wolf, Jochen H Weishaupt, Paul Lingor, Marcus Deschauer, Isabell Cordts, Thomas Klopstock, Peter Reilich, Florian Schoeberl, Berthold Schrank, Daniel Zeller, Andreas Hermann, Antje Knehr, Kornelia Günther, Johannes Dorst, Joachim Schuster, Reiner Siebert, Albert C Ludolph, Kathrin Müll |
FUS gene mutation in amyotrophic lateral sclerosis: a new case report and systematic review. Amyotrophic lateral sclerosis & frontotemporal degeneration 2023 11 1-15. Xin Xiao, Min Li, Zhi Ye, Xiaoyan He, Jun Wei, Yunhong Z |
Integrative genetic analysis illuminates ALS heritability and identifies risk genes. Nature communications 2023 1 14 (1): 342. Megat Salim, Mora Natalia, Sanogo Jason, Roman Olga, Catanese Alberto, Alami Najwa Ouali, Freischmidt Axel, Mingaj Xhuljana, De Calbiac Hortense, Muratet François, Dirrig-Grosch Sylvie, Dieterle Stéphane, Van Bakel Nick, Müller Kathrin, Sieverding Kirsten, Weishaupt Jochen, Andersen Peter Munch, Weber Markus, Neuwirth Christoph, Margelisch Markus, Sommacal Andreas, Van Eijk Kristel R, Veldink Jan H, , Lautrette Géraldine, Couratier Philippe, Camuzat Agnès, Le Ber Isabelle, Grassano Maurizio, Chio Adriano, Boeckers Tobias, Ludolph Albert C, Roselli Francesco, Yilmazer-Hanke Deniz, Millecamps Stéphanie, Kabashi Edor, Storkebaum Erik, Sellier Chantal, Dupuis L |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
- Content source: