298 related articles for article (PubMed ID: 23138764)
1. Ubiquilin 2 mutations in Italian patients with amyotrophic lateral sclerosis and frontotemporal dementia.
Gellera C; Tiloca C; Del Bo R; Corrado L; Pensato V; Agostini J; Cereda C; Ratti A; Castellotti B; Corti S; Bagarotti A; Cagnin A; Milani P; Gabelli C; Riboldi G; Mazzini L; Sorarù G; D'Alfonso S; Taroni F; Comi GP; Ticozzi N; Silani V;
J Neurol Neurosurg Psychiatry; 2013 Feb; 84(2):183-7. PubMed ID: 23138764
[TBL] [Abstract][Full Text] [Related]
2. Screening in ALS and FTD patients reveals 3 novel UBQLN2 mutations outside the PXX domain and a pure FTD phenotype.
Synofzik M; Maetzler W; Grehl T; Prudlo J; Vom Hagen JM; Haack T; Rebassoo P; Munz M; Schöls L; Biskup S
Neurobiol Aging; 2012 Dec; 33(12):2949.e13-7. PubMed ID: 22892309
[TBL] [Abstract][Full Text] [Related]
3. Mutation spectrum of chinese amyotrophic lateral sclerosis patients with frontotemporal dementia.
Yang X; Sun X; Liu Q; Liu L; Li J; Cai Z; Zhang K; Liu S; He D; Shen D; Liu M; Cui L; Zhang X
Orphanet J Rare Dis; 2022 Nov; 17(1):404. PubMed ID: 36345033
[TBL] [Abstract][Full Text] [Related]
4. Mutations in UBQLN2 and SIGMAR1 genes are rare in Korean patients with amyotrophic lateral sclerosis.
Kim HJ; Kwon MJ; Choi WJ; Oh KW; Oh SI; Ki CS; Kim SH
Neurobiol Aging; 2014 Aug; 35(8):1957.e7-8. PubMed ID: 24684794
[TBL] [Abstract][Full Text] [Related]
5. Distribution of ubiquilin 2 and TDP-43 aggregates throughout the CNS in UBQLN2 p.T487I-linked amyotrophic lateral sclerosis and frontotemporal dementia.
Nementzik LR; Thumbadoo KM; Murray HC; Gordon D; Yang S; Blair IP; Turner C; Faull RLM; Curtis MA; McLean C; Nicholson GA; Swanson MEV; Scotter EL
Brain Pathol; 2024 May; 34(3):e13230. PubMed ID: 38115557
[TBL] [Abstract][Full Text] [Related]
6. Novel UBQLN2 mutations linked to amyotrophic lateral sclerosis and atypical hereditary spastic paraplegia phenotype through defective HSP70-mediated proteolysis.
Teyssou E; Chartier L; Amador MD; Lam R; Lautrette G; Nicol M; Machat S; Da Barroca S; Moigneu C; Mairey M; Larmonier T; Saker S; Dussert C; Forlani S; Fontaine B; Seilhean D; Bohl D; Boillée S; Meininger V; Couratier P; Salachas F; Stevanin G; Millecamps S
Neurobiol Aging; 2017 Oct; 58():239.e11-239.e20. PubMed ID: 28716533
[TBL] [Abstract][Full Text] [Related]
7. No Evidence for Pathogenic Role of UBQLN2 Mutations in Sporadic Amyotrophic Lateral Sclerosis in the Mainland Chinese Population.
Huang X; Shen S; Fan D
PLoS One; 2017; 12(1):e0170943. PubMed ID: 28125704
[TBL] [Abstract][Full Text] [Related]
8. Striking phenotypic variation in a family with the P506S UBQLN2 mutation including amyotrophic lateral sclerosis, spastic paraplegia, and frontotemporal dementia.
Gkazi SA; Troakes C; Topp S; Miller JW; Vance CA; Sreedharan J; Al-Chalabi A; Kirby J; Shaw PJ; Al-Sarraj S; King A; Smith BN; Shaw CE
Neurobiol Aging; 2019 Jan; 73():229.e5-229.e9. PubMed ID: 30348461
[TBL] [Abstract][Full Text] [Related]
9. Mutations in UBQLN2 are rare in French amyotrophic lateral sclerosis.
Millecamps S; Corcia P; Cazeneuve C; Boillée S; Seilhean D; Danel-Brunaud V; Vandenberghe N; Pradat PF; Le Forestier N; Lacomblez L; Bruneteau G; Camu W; Brice A; Meininger V; LeGuern E; Salachas F
Neurobiol Aging; 2012 Apr; 33(4):839.e1-3. PubMed ID: 22169395
[TBL] [Abstract][Full Text] [Related]
10. Evidence of a link between ubiquilin 2 and optineurin in amyotrophic lateral sclerosis.
Osaka M; Ito D; Yagi T; Nihei Y; Suzuki N
Hum Mol Genet; 2015 Mar; 24(6):1617-29. PubMed ID: 25398946
[TBL] [Abstract][Full Text] [Related]
11. Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia.
Deng HX; Chen W; Hong ST; Boycott KM; Gorrie GH; Siddique N; Yang Y; Fecto F; Shi Y; Zhai H; Jiang H; Hirano M; Rampersaud E; Jansen GH; Donkervoort S; Bigio EH; Brooks BR; Ajroud K; Sufit RL; Haines JL; Mugnaini E; Pericak-Vance MA; Siddique T
Nature; 2011 Aug; 477(7363):211-5. PubMed ID: 21857683
[TBL] [Abstract][Full Text] [Related]
12. UBQLN2 variant of unknown significance in frontotemporal lobar degeneration.
Ugwu F; Rollinson S; Harris J; Gerhard A; Richardson A; Jones M; Mann D; Snowden J; Pickering-Brown S
Neurobiol Aging; 2015 Jan; 36(1):546.e15-6. PubMed ID: 25179229
[TBL] [Abstract][Full Text] [Related]
13. Novel TARDBP missense mutation caused familial amyotrophic lateral sclerosis with frontotemporal dementia and parkinsonism.
Chen S; Zhou RL; Zhang W; Che CH; Feng SY; Huang HP; Liu CY; Zou ZY
Neurobiol Aging; 2021 Nov; 107():168-173. PubMed ID: 34175147
[TBL] [Abstract][Full Text] [Related]
14. UBQLN2/ubiquilin 2 mutation and pathology in familial amyotrophic lateral sclerosis.
Williams KL; Warraich ST; Yang S; Solski JA; Fernando R; Rouleau GA; Nicholson GA; Blair IP
Neurobiol Aging; 2012 Oct; 33(10):2527.e3-10. PubMed ID: 22717235
[TBL] [Abstract][Full Text] [Related]
15. UBQLN2 mutations are rare in French and French-Canadian amyotrophic lateral sclerosis.
Daoud H; Suhail H; Szuto A; Camu W; Salachas F; Meininger V; Bouchard JP; Dupré N; Dion PA; Rouleau GA
Neurobiol Aging; 2012 Sep; 33(9):2230.e1-2230.e5. PubMed ID: 22560112
[TBL] [Abstract][Full Text] [Related]
16. UBQLN2/P62 cellular recycling pathways in amyotrophic lateral sclerosis and frontotemporal dementia.
Fecto F; Siddique T
Muscle Nerve; 2012 Feb; 45(2):157-62. PubMed ID: 22246868
[TBL] [Abstract][Full Text] [Related]
17. VCP mutations are not a major cause of familial amyotrophic lateral sclerosis in the UK.
Kwok CT; Wang HY; Morris AG; Smith B; Shaw C; de Belleroche J
J Neurol Sci; 2015 Feb; 349(1-2):209-13. PubMed ID: 25618255
[TBL] [Abstract][Full Text] [Related]
18. Serpin neuropathology in the P497S UBQLN2 mouse model of ALS/FTD.
Higgins NR; Greenslade JE; Wu JJ; Miranda E; Galliciotti G; Monteiro MJ
Brain Pathol; 2021 Sep; 31(5):e12948. PubMed ID: 33780087
[TBL] [Abstract][Full Text] [Related]
19. Making connections: pathology and genetics link amyotrophic lateral sclerosis with frontotemporal lobe dementia.
Fecto F; Siddique T
J Mol Neurosci; 2011 Nov; 45(3):663-75. PubMed ID: 21901496
[TBL] [Abstract][Full Text] [Related]
20. First case of an
Raggi A; Bartoletti-Stella A; Parchi P; Capellari S
Amyotroph Lateral Scler Frontotemporal Degener; 2020 Aug; 21(5-6):467-469. PubMed ID: 32290710
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]