These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
9. Advances and challenges in understanding the multifaceted pathogenesis of amyotrophic lateral sclerosis. Laferriere F; Polymenidou M Swiss Med Wkly; 2015; 145():w14054. PubMed ID: 25635517 [TBL] [Abstract][Full Text] [Related]
10. SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotype-phenotype correlations. Millecamps S; Salachas F; Cazeneuve C; Gordon P; Bricka B; Camuzat A; Guillot-Noël L; Russaouen O; Bruneteau G; Pradat PF; Le Forestier N; Vandenberghe N; Danel-Brunaud V; Guy N; Thauvin-Robinet C; Lacomblez L; Couratier P; Hannequin D; Seilhean D; Le Ber I; Corcia P; Camu W; Brice A; Rouleau G; LeGuern E; Meininger V J Med Genet; 2010 Aug; 47(8):554-60. PubMed ID: 20577002 [TBL] [Abstract][Full Text] [Related]
12. New Model System Offers Clues to ALS. Kuehn BM JAMA; 2011 Oct; 306(14):1534. PubMed ID: 21990293 [No Abstract] [Full Text] [Related]
13. Examining the relationship between astrocyte dysfunction and neurodegeneration in ALS using hiPSCs. Halpern M; Brennand KJ; Gregory J Neurobiol Dis; 2019 Dec; 132():104562. PubMed ID: 31381978 [TBL] [Abstract][Full Text] [Related]
16. Aberrant axon branching via Fos-B dysregulation in FUS-ALS motor neurons. Akiyama T; Suzuki N; Ishikawa M; Fujimori K; Sone T; Kawada J; Funayama R; Fujishima F; Mitsuzawa S; Ikeda K; Ono H; Shijo T; Osana S; Shirota M; Nakagawa T; Kitajima Y; Nishiyama A; Izumi R; Morimoto S; Okada Y; Kamei T; Nishida M; Nogami M; Kaneda S; Ikeuchi Y; Mitsuhashi H; Nakayama K; Fujii T; Warita H; Okano H; Aoki M EBioMedicine; 2019 Jul; 45():362-378. PubMed ID: 31262712 [TBL] [Abstract][Full Text] [Related]
17. Astrocytes drive upregulation of the multidrug resistance transporter ABCB1 (P-Glycoprotein) in endothelial cells of the blood-brain barrier in mutant superoxide dismutase 1-linked amyotrophic lateral sclerosis. Qosa H; Lichter J; Sarlo M; Markandaiah SS; McAvoy K; Richard JP; Jablonski MR; Maragakis NJ; Pasinelli P; Trotti D Glia; 2016 Aug; 64(8):1298-313. PubMed ID: 27158936 [TBL] [Abstract][Full Text] [Related]
18. Minimally invasive transplantation of iPSC-derived ALDHhiSSCloVLA4+ neural stem cells effectively improves the phenotype of an amyotrophic lateral sclerosis model. Nizzardo M; Simone C; Rizzo F; Ruggieri M; Salani S; Riboldi G; Faravelli I; Zanetta C; Bresolin N; Comi GP; Corti S Hum Mol Genet; 2014 Jan; 23(2):342-54. PubMed ID: 24006477 [TBL] [Abstract][Full Text] [Related]
19. The fused in sarcoma protein forms cytoplasmic aggregates in motor neurons derived from integration-free induced pluripotent stem cells generated from a patient with familial amyotrophic lateral sclerosis carrying the FUS-P525L mutation. Liu X; Chen J; Liu W; Li X; Chen Q; Liu T; Gao S; Deng M Neurogenetics; 2015 Jul; 16(3):223-31. PubMed ID: 25912081 [TBL] [Abstract][Full Text] [Related]
20. Pericytes Extend Survival of ALS SOD1 Mice and Induce the Expression of Antioxidant Enzymes in the Murine Model and in IPSCs Derived Neuronal Cells from an ALS Patient. Coatti GC; Frangini M; Valadares MC; Gomes JP; Lima NO; Cavaçana N; Assoni AF; Pelatti MV; Birbrair A; de Lima ACP; Singer JM; Rocha FMM; Da Silva GL; Mantovani MS; Macedo-Souza LI; Ferrari MFR; Zatz M Stem Cell Rev Rep; 2017 Oct; 13(5):686-698. PubMed ID: 28710685 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]