198 related articles for article (PubMed ID: 26465396)
1. TUBA4A may not be a significant genetic factor in Chinese ALS patients.
Li J; He J; Tang L; Chen L; Xu L; Ma Y; Zhang N; Fan D
Amyotroph Lateral Scler Frontotemporal Degener; 2015; 17(1-2):148-50. PubMed ID: 26465396
[TBL] [Abstract][Full Text] [Related]
2. Screening of VCP mutations in Chinese amyotrophic lateral sclerosis patients.
Zou ZY; Liu MS; Li XG; Cui LY
Neurobiol Aging; 2013 May; 34(5):1519.e3-4. PubMed ID: 23102936
[TBL] [Abstract][Full Text] [Related]
3. Association of the functional SNP rs2275294 in ZNF512B with risk of amyotrophic lateral sclerosis and Parkinson's disease in Han Chinese.
Yang X; Zhao Q; An R; Zheng J; Tian S; Xu Y
Amyotroph Lateral Scler Frontotemporal Degener; 2015; 17(1-2):142-7. PubMed ID: 26313240
[TBL] [Abstract][Full Text] [Related]
4. Rare and common paraoxonase gene variants in amyotrophic lateral sclerosis patients.
van Blitterswijk M; Blokhuis A; van Es MA; van Vught PW; Rowicka PA; Schelhaas HJ; van der Kooi AJ; de Visser M; Veldink JH; van den Berg LH
Neurobiol Aging; 2012 Aug; 33(8):1845.e1-3. PubMed ID: 22330174
[TBL] [Abstract][Full Text] [Related]
5. De novo FUS gene mutations are associated with juvenile-onset sporadic amyotrophic lateral sclerosis in China.
Zou ZY; Cui LY; Sun Q; Li XG; Liu MS; Xu Y; Zhou Y; Yang XZ
Neurobiol Aging; 2013 Apr; 34(4):1312.e1-8. PubMed ID: 23046859
[TBL] [Abstract][Full Text] [Related]
6. ATAXIN2 CAG-repeat length in Italian patients with amyotrophic lateral sclerosis: risk factor or variant phenotype? Implication for genetic testing and counseling.
Gellera C; Ticozzi N; Pensato V; Nanetti L; Castucci A; Castellotti B; Lauria G; Taroni F; Silani V; Mariotti C
Neurobiol Aging; 2012 Aug; 33(8):1847.e15-21. PubMed ID: 22425256
[TBL] [Abstract][Full Text] [Related]
7. Mutation analysis of PFN1 in familial amyotrophic lateral sclerosis patients.
Daoud H; Dobrzeniecka S; Camu W; Meininger V; Dupré N; Dion PA; Rouleau GA
Neurobiol Aging; 2013 Apr; 34(4):1311.e1-2. PubMed ID: 23062600
[TBL] [Abstract][Full Text] [Related]
8. Excess of rare damaging TUBA4A variants suggests cytoskeletal defects in ALS.
Rademakers R; van Blitterswijk M
Neuron; 2014 Oct; 84(2):241-3. PubMed ID: 25374348
[TBL] [Abstract][Full Text] [Related]
9. Investigating the role of ALS genes CHCHD10 and TUBA4A in Belgian FTD-ALS spectrum patients.
Perrone F; Nguyen HP; Van Mossevelde S; Moisse M; Sieben A; Santens P; De Bleecker J; Vandenbulcke M; Engelborghs S; Baets J; Cras P; Vandenberghe R; De Jonghe P; De Deyn PP; Martin JJ; Van Damme P; Van Broeckhoven C; van der Zee J;
Neurobiol Aging; 2017 Mar; 51():177.e9-177.e16. PubMed ID: 28069311
[TBL] [Abstract][Full Text] [Related]
10. Analysis of the C9orf72 hexanucleotide repeat expansion in Korean patients with familial and sporadic amyotrophic lateral sclerosis.
Jang JH; Kwon MJ; Choi WJ; Oh KW; Koh SH; Ki CS; Kim SH
Neurobiol Aging; 2013 Apr; 34(4):1311.e7-9. PubMed ID: 23088937
[TBL] [Abstract][Full Text] [Related]
11. Novel deletion mutations of OPTN in amyotrophic lateral sclerosis in Japanese.
Iida A; Hosono N; Sano M; Kamei T; Oshima S; Tokuda T; Nakajima M; Kubo M; Nakamura Y; Ikegawa S
Neurobiol Aging; 2012 Aug; 33(8):1843.e19-24. PubMed ID: 22402017
[TBL] [Abstract][Full Text] [Related]
12. CGG-repeat expansion in FMR1 is not associated with amyotrophic lateral sclerosis.
Groen EJ; van Rheenen W; Koppers M; van Doormaal PT; Vlam L; Diekstra FP; Dooijes D; Pasterkamp RJ; van den Berg LH; Veldink JH
Neurobiol Aging; 2012 Aug; 33(8):1852.e1-3. PubMed ID: 22507827
[TBL] [Abstract][Full Text] [Related]
13. Genetic studies of Russian patients with amyotrophic lateral sclerosis.
Lysogorskaia EV; Abramycheva NY; Zakharova MN; Stepanova MS; Moroz AA; Rossokhin AV; Illarioshkin SN
Amyotroph Lateral Scler Frontotemporal Degener; 2015; 17(1-2):135-41. PubMed ID: 26551617
[TBL] [Abstract][Full Text] [Related]
14. Dysregulation of a novel miR-1825/TBCB/TUBA4A pathway in sporadic and familial ALS.
Helferich AM; Brockmann SJ; Reinders J; Deshpande D; Holzmann K; Brenner D; Andersen PM; Petri S; Thal DR; Michaelis J; Otto M; Just S; Ludolph AC; Danzer KM; Freischmidt A; Weishaupt JH
Cell Mol Life Sci; 2018 Dec; 75(23):4301-4319. PubMed ID: 30030593
[TBL] [Abstract][Full Text] [Related]
15. Possible gender-dependent association of vascular endothelial growth factor (VEGF) gene and ALS.
Fernández-Santiago R; Sharma M; Mueller JC; Gohlke H; Illig T; Anneser J; Münch C; Ludolph A; Kamm C; Gasser T
Neurology; 2006 Jun; 66(12):1929-31. PubMed ID: 16801663
[TBL] [Abstract][Full Text] [Related]
16. Assessing the role of TUBA4A gene in frontotemporal degeneration.
Dols-Icardo O; Iborra O; Valdivia J; Pastor P; Ruiz A; López de Munain A; Sánchez-Valle R; Álvarez V; Sánchez-Juan P; Lleó A; Fortea J; Blesa R; Cardona F; Baquero M; Alonso MD; Ortega-Cubero S; Pastor MA; Razquin C; Boada M; Hernández I; Gorostidi A; Moreno F; Zulaika M; Lladó A; Coto E; Combarros O; Pérez-Tur J; Clarimón J;
Neurobiol Aging; 2016 Feb; 38():215.e13-215.e14. PubMed ID: 26675813
[TBL] [Abstract][Full Text] [Related]
17. Analysis of the SORT1 gene in familial amyotrophic lateral sclerosis.
Belzil VV; André-Guimont C; Atallah MR; Daoud H; Dupré N; Bouchard JP; Camu W; Dion PA; Rouleau GA
Neurobiol Aging; 2012 Aug; 33(8):1845.e7-9. PubMed ID: 22361451
[TBL] [Abstract][Full Text] [Related]
18. Elevated Levels of Selenium Species in Cerebrospinal Fluid of Amyotrophic Lateral Sclerosis Patients with Disease-Associated Gene Mutations.
Mandrioli J; Michalke B; Solovyev N; Grill P; Violi F; Lunetta C; Conte A; Sansone VA; Sabatelli M; Vinceti M
Neurodegener Dis; 2017; 17(4-5):171-180. PubMed ID: 28478440
[TBL] [Abstract][Full Text] [Related]
19. Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALS.
Smith BN; Ticozzi N; Fallini C; Gkazi AS; Topp S; Kenna KP; Scotter EL; Kost J; Keagle P; Miller JW; Calini D; Vance C; Danielson EW; Troakes C; Tiloca C; Al-Sarraj S; Lewis EA; King A; Colombrita C; Pensato V; Castellotti B; de Belleroche J; Baas F; ten Asbroek AL; Sapp PC; McKenna-Yasek D; McLaughlin RL; Polak M; Asress S; Esteban-Pérez J; Muñoz-Blanco JL; Simpson M; ; van Rheenen W; Diekstra FP; Lauria G; Duga S; Corti S; Cereda C; Corrado L; Sorarù G; Morrison KE; Williams KL; Nicholson GA; Blair IP; Dion PA; Leblond CS; Rouleau GA; Hardiman O; Veldink JH; van den Berg LH; Al-Chalabi A; Pall H; Shaw PJ; Turner MR; Talbot K; Taroni F; García-Redondo A; Wu Z; Glass JD; Gellera C; Ratti A; Brown RH; Silani V; Shaw CE; Landers JE
Neuron; 2014 Oct; 84(2):324-31. PubMed ID: 25374358
[TBL] [Abstract][Full Text] [Related]
20. Screening for rare variants in the coding region of ALS-associated genes at 9p21.2 and 19p13.3.
Koppers M; Groen EJ; van Vught PW; van Rheenen W; Witteveen E; van Es MA; Pasterkamp RJ; van den Berg LH; Veldink JH
Neurobiol Aging; 2013 May; 34(5):1518.e5-7. PubMed ID: 23141412
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]