541 related articles for article (PubMed ID: 29313812)
1. Pathogenic commonalities between spinal muscular atrophy and amyotrophic lateral sclerosis: Converging roads to therapeutic development.
Bowerman M; Murray LM; Scamps F; Schneider BL; Kothary R; Raoul C
Eur J Med Genet; 2018 Nov; 61(11):685-698. PubMed ID: 29313812
[TBL] [Abstract][Full Text] [Related]
2. Enhancing survival motor neuron expression extends lifespan and attenuates neurodegeneration in mutant TDP-43 mice.
Perera ND; Sheean RK; Crouch PJ; White AR; Horne MK; Turner BJ
Hum Mol Genet; 2016 Sep; 25(18):4080-4093. PubMed ID: 27466204
[TBL] [Abstract][Full Text] [Related]
3. TDP-43 expression in mouse models of amyotrophic lateral sclerosis and spinal muscular atrophy.
Turner BJ; Bäumer D; Parkinson NJ; Scaber J; Ansorge O; Talbot K
BMC Neurosci; 2008 Oct; 9():104. PubMed ID: 18957104
[TBL] [Abstract][Full Text] [Related]
4. ALS-associated mutations in FUS disrupt the axonal distribution and function of SMN.
Groen EJ; Fumoto K; Blokhuis AM; Engelen-Lee J; Zhou Y; van den Heuvel DM; Koppers M; van Diggelen F; van Heest J; Demmers JA; Kirby J; Shaw PJ; Aronica E; Spliet WG; Veldink JH; van den Berg LH; Pasterkamp RJ
Hum Mol Genet; 2013 Sep; 22(18):3690-704. PubMed ID: 23681068
[TBL] [Abstract][Full Text] [Related]
5. Overexpression of survival motor neuron improves neuromuscular function and motor neuron survival in mutant SOD1 mice.
Turner BJ; Alfazema N; Sheean RK; Sleigh JN; Davies KE; Horne MK; Talbot K
Neurobiol Aging; 2014 Apr; 35(4):906-15. PubMed ID: 24210254
[TBL] [Abstract][Full Text] [Related]
6. Survival motor neuron deficiency enhances progression in an amyotrophic lateral sclerosis mouse model.
Turner BJ; Parkinson NJ; Davies KE; Talbot K
Neurobiol Dis; 2009 Jun; 34(3):511-7. PubMed ID: 19332122
[TBL] [Abstract][Full Text] [Related]
7. Mutant superoxide dismutase 1 (SOD1), a cause of amyotrophic lateral sclerosis, disrupts the recruitment of SMN, the spinal muscular atrophy protein to nuclear Cajal bodies.
Kariya S; Re DB; Jacquier A; Nelson K; Przedborski S; Monani UR
Hum Mol Genet; 2012 Aug; 21(15):3421-34. PubMed ID: 22581780
[TBL] [Abstract][Full Text] [Related]
8. Phenotypic and genotypic studies of ALS cases in ALS-SMA families.
Corcia P; Vourc'h P; Blasco H; Couratier P; Dangoumau A; Bellance R; Desnuelle C; Viader F; Pautot V; Millecamps S; Bakkouche S; Salachas F; Andres CR; Meininger V; Camu W
Amyotroph Lateral Scler Frontotemporal Degener; 2018 Aug; 19(5-6):432-437. PubMed ID: 29493298
[TBL] [Abstract][Full Text] [Related]
9. SMN complex member Gemin3 self-interacts and has a functional relationship with ALS-linked proteins TDP-43, FUS and Sod1.
Cacciottolo R; Ciantar J; Lanfranco M; Borg RM; Vassallo N; Bordonné R; Cauchi RJ
Sci Rep; 2019 Dec; 9(1):18666. PubMed ID: 31822699
[TBL] [Abstract][Full Text] [Related]
10. FUS-SMN protein interactions link the motor neuron diseases ALS and SMA.
Yamazaki T; Chen S; Yu Y; Yan B; Haertlein TC; Carrasco MA; Tapia JC; Zhai B; Das R; Lalancette-Hebert M; Sharma A; Chandran S; Sullivan G; Nishimura AL; Shaw CE; Gygi SP; Shneider NA; Maniatis T; Reed R
Cell Rep; 2012 Oct; 2(4):799-806. PubMed ID: 23022481
[TBL] [Abstract][Full Text] [Related]
11. Cross-disease comparison of amyotrophic lateral sclerosis and spinal muscular atrophy reveals conservation of selective vulnerability but differential neuromuscular junction pathology.
Comley LH; Nijssen J; Frost-Nylen J; Hedlund E
J Comp Neurol; 2016 May; 524(7):1424-42. PubMed ID: 26502195
[TBL] [Abstract][Full Text] [Related]
12. Comparative interactomics analysis of different ALS-associated proteins identifies converging molecular pathways.
Blokhuis AM; Koppers M; Groen EJN; van den Heuvel DMA; Dini Modigliani S; Anink JJ; Fumoto K; van Diggelen F; Snelting A; Sodaar P; Verheijen BM; Demmers JAA; Veldink JH; Aronica E; Bozzoni I; den Hertog J; van den Berg LH; Pasterkamp RJ
Acta Neuropathol; 2016 Aug; 132(2):175-196. PubMed ID: 27164932
[TBL] [Abstract][Full Text] [Related]
13. From Mouse Models to Human Disease: An Approach for Amyotrophic Lateral Sclerosis.
Alrafiah AR
In Vivo; 2018; 32(5):983-998. PubMed ID: 30150420
[TBL] [Abstract][Full Text] [Related]
14. SMN1 gene study in three families in which ALS and spinal muscular atrophy co-exist.
Corcia P; Khoris J; Couratier P; Mayeux-Portas V; Bieth E; De Toffol B; Autret A; Müh JP; Andres C; Camu W
Neurology; 2002 Nov; 59(9):1464-6. PubMed ID: 12427909
[TBL] [Abstract][Full Text] [Related]
15. The importance of the SMN genes in the genetics of sporadic ALS.
Corcia P; Camu W; Praline J; Gordon PH; Vourch P; Andres C
Amyotroph Lateral Scler; 2009; 10(5-6):436-40. PubMed ID: 19922137
[TBL] [Abstract][Full Text] [Related]
16. Genetics of amyotrophic lateral sclerosis: A review.
Mathis S; Goizet C; Soulages A; Vallat JM; Masson GL
J Neurol Sci; 2019 Apr; 399():217-226. PubMed ID: 30870681
[TBL] [Abstract][Full Text] [Related]
17. Pathological Modification of TDP-43 in Amyotrophic Lateral Sclerosis with SOD1 Mutations.
Jeon GS; Shim YM; Lee DY; Kim JS; Kang M; Ahn SH; Shin JY; Geum D; Hong YH; Sung JJ
Mol Neurobiol; 2019 Mar; 56(3):2007-2021. PubMed ID: 29982983
[TBL] [Abstract][Full Text] [Related]
18. Spliceosome integrity is defective in the motor neuron diseases ALS and SMA.
Tsuiji H; Iguchi Y; Furuya A; Kataoka A; Hatsuta H; Atsuta N; Tanaka F; Hashizume Y; Akatsu H; Murayama S; Sobue G; Yamanaka K
EMBO Mol Med; 2013 Feb; 5(2):221-34. PubMed ID: 23255347
[TBL] [Abstract][Full Text] [Related]
19. Stress granules in the spinal muscular atrophy and amyotrophic lateral sclerosis: The correlation and promising therapy.
Hu L; Mao S; Lin L; Bai G; Liu B; Mao J
Neurobiol Dis; 2022 Aug; 170():105749. PubMed ID: 35568100
[TBL] [Abstract][Full Text] [Related]
20. Cellular and molecular approaches to motor neuron therapy in amyotrophic lateral sclerosis and spinal muscular atrophy.
O'Connor DM; Boulis NM
Neurosci Lett; 2012 Oct; 527(2):78-84. PubMed ID: 22579818
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]