367 related articles for article (PubMed ID: 32403313)
21. Co-aggregation of RNA binding proteins in ALS spinal motor neurons: evidence of a common pathogenic mechanism.
Keller BA; Volkening K; Droppelmann CA; Ang LC; Rademakers R; Strong MJ
Acta Neuropathol; 2012 Nov; 124(5):733-47. PubMed ID: 22941224
[TBL] [Abstract][Full Text] [Related]
22. Impairment of Mitochondrial Calcium Buffering Links Mutations in C9ORF72 and TARDBP in iPS-Derived Motor Neurons from Patients with ALS/FTD.
Dafinca R; Barbagallo P; Farrimond L; Candalija A; Scaber J; Ababneh NA; Sathyaprakash C; Vowles J; Cowley SA; Talbot K
Stem Cell Reports; 2020 May; 14(5):892-908. PubMed ID: 32330447
[TBL] [Abstract][Full Text] [Related]
23. Gene Therapy in Amyotrophic Lateral Sclerosis.
Fang T; Je G; Pacut P; Keyhanian K; Gao J; Ghasemi M
Cells; 2022 Jun; 11(13):. PubMed ID: 35805149
[TBL] [Abstract][Full Text] [Related]
24. Multiple variants in families with amyotrophic lateral sclerosis and frontotemporal dementia related to C9orf72 repeat expansion: further observations on their oligogenic nature.
Giannoccaro MP; Bartoletti-Stella A; Piras S; Pession A; De Massis P; Oppi F; Stanzani-Maserati M; Pasini E; Baiardi S; Avoni P; Parchi P; Liguori R; Capellari S
J Neurol; 2017 Jul; 264(7):1426-1433. PubMed ID: 28620717
[TBL] [Abstract][Full Text] [Related]
25. Improving the knowledge of amyotrophic lateral sclerosis genetics: novel SOD1 and FUS variants.
Bertolin C; D'Ascenzo C; Querin G; Gaiani A; Boaretto F; Salvoro C; Vazza G; Angelini C; Cagnin A; Pegoraro E; Sorarù G; Mostacciuolo ML
Neurobiol Aging; 2014 May; 35(5):1212.e7-1212.e10. PubMed ID: 24325798
[TBL] [Abstract][Full Text] [Related]
26. Dysregulation of AMPA receptor subunit expression in sporadic ALS post-mortem brain.
Gregory JM; Livesey MR; McDade K; Selvaraj BT; Barton SK; Chandran S; Smith C
J Pathol; 2020 Jan; 250(1):67-78. PubMed ID: 31579943
[TBL] [Abstract][Full Text] [Related]
27. The distinct manifestation of young-onset amyotrophic lateral sclerosis in China.
Lin J; Chen W; Huang P; Xie Y; Zheng M; Yao X
Amyotroph Lateral Scler Frontotemporal Degener; 2021 Feb; 22(1-2):30-37. PubMed ID: 32729724
[TBL] [Abstract][Full Text] [Related]
28. Phenotype difference between ALS patients with expanded repeats in C9ORF72 and patients with mutations in other ALS-related genes.
Millecamps S; Boillée S; Le Ber I; Seilhean D; Teyssou E; Giraudeau M; Moigneu C; Vandenberghe N; Danel-Brunaud V; Corcia P; Pradat PF; Le Forestier N; Lacomblez L; Bruneteau G; Camu W; Brice A; Cazeneuve C; Leguern E; Meininger V; Salachas F
J Med Genet; 2012 Apr; 49(4):258-63. PubMed ID: 22499346
[TBL] [Abstract][Full Text] [Related]
29. [Genetic architecture of amyotrophic lateral sclerosis and frontotemporal dementia : Overlap and differences].
Synofzik M; Otto M; Ludolph A; Weishaupt JH
Nervenarzt; 2017 Jul; 88(7):728-735. PubMed ID: 28573364
[TBL] [Abstract][Full Text] [Related]
30. ALS-causing mutations differentially affect PGC-1α expression and function in the brain vs. peripheral tissues.
Bayer H; Lang K; Buck E; Higelin J; Barteczko L; Pasquarelli N; Sprissler J; Lucas T; Holzmann K; Demestre M; Lindenberg KS; Danzer KM; Boeckers T; Ludolph AC; Dupuis L; Weydt P; Witting A
Neurobiol Dis; 2017 Jan; 97(Pt A):36-45. PubMed ID: 27818323
[TBL] [Abstract][Full Text] [Related]
31. FUS mutations in amyotrophic lateral sclerosis: clinical, pathological, neurophysiological and genetic analysis.
Blair IP; Williams KL; Warraich ST; Durnall JC; Thoeng AD; Manavis J; Blumbergs PC; Vucic S; Kiernan MC; Nicholson GA
J Neurol Neurosurg Psychiatry; 2010 Jun; 81(6):639-45. PubMed ID: 19965854
[TBL] [Abstract][Full Text] [Related]
32. Downstream Effects of Mutations in
Dash BP; Freischmidt A; Weishaupt JH; Hermann A
Int J Mol Sci; 2022 Aug; 23(17):. PubMed ID: 36077049
[TBL] [Abstract][Full Text] [Related]
33. The multistep hypothesis of ALS revisited: The role of genetic mutations.
Chiò A; Mazzini L; D'Alfonso S; Corrado L; Canosa A; Moglia C; Manera U; Bersano E; Brunetti M; Barberis M; Veldink JH; van den Berg LH; Pearce N; Sproviero W; McLaughlin R; Vajda A; Hardiman O; Rooney J; Mora G; Calvo A; Al-Chalabi A
Neurology; 2018 Aug; 91(7):e635-e642. PubMed ID: 30045958
[TBL] [Abstract][Full Text] [Related]
34. State of play in amyotrophic lateral sclerosis genetics.
Renton AE; Chiò A; Traynor BJ
Nat Neurosci; 2014 Jan; 17(1):17-23. PubMed ID: 24369373
[TBL] [Abstract][Full Text] [Related]
35. Connecting RNA-Modifying Similarities of TDP-43, FUS, and SOD1 with MicroRNA Dysregulation Amidst A Renewed Network Perspective of Amyotrophic Lateral Sclerosis Proteinopathy.
Pham J; Keon M; Brennan S; Saksena N
Int J Mol Sci; 2020 May; 21(10):. PubMed ID: 32422969
[TBL] [Abstract][Full Text] [Related]
36. Amyotrophic Lateral Sclerosis Genes in
Layalle S; They L; Ourghani S; Raoul C; Soustelle L
Int J Mol Sci; 2021 Jan; 22(2):. PubMed ID: 33477509
[TBL] [Abstract][Full Text] [Related]
37. Genotype-phenotype correlation in Tunisian patients with Amyotrophic Lateral Sclerosis.
Kacem I; Sghaier I; Peverelli S; Souissi E; Ticozzi N; Gharbi A; Ratti A; Berrechid AG; Silani V; Gouider R
Neurobiol Aging; 2022 Dec; 120():27-33. PubMed ID: 36108486
[TBL] [Abstract][Full Text] [Related]
38. Familial Amyotrophic Lateral Sclerosis.
Boylan K
Neurol Clin; 2015 Nov; 33(4):807-30. PubMed ID: 26515623
[TBL] [Abstract][Full Text] [Related]
39. [Familial Amyotrophic Lateral Sclerosis].
Suzuki N; Nishiyama A; Kato M; Warita H; Aoki M
Brain Nerve; 2019 Nov; 71(11):1169-1181. PubMed ID: 31722303
[TBL] [Abstract][Full Text] [Related]
40. Motor neurons from ALS patients with mutations in C9ORF72 and SOD1 exhibit distinct transcriptional landscapes.
Wong CO; Venkatachalam K
Hum Mol Genet; 2019 Aug; 28(16):2799-2810. PubMed ID: 31107959
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
