BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

599 related articles for article (PubMed ID: 25299611)

  • 21. De novo nonsense mutation of the FUS gene in an apparently familial amyotrophic lateral sclerosis case.
    Calvo A; Moglia C; Canosa A; Brunetti M; Barberis M; Traynor BJ; Carrara G; Valentini C; Restagno G; Chiò A
    Neurobiol Aging; 2014 Jun; 35(6):1513.e7-11. PubMed ID: 24439481
    [TBL] [Abstract][Full Text] [Related]  

  • 22. The NGS technology for the identification of genes associated with the ALS. A systematic review.
    Pecoraro V; Mandrioli J; Carone C; Chiò A; Traynor BJ; Trenti T
    Eur J Clin Invest; 2020 May; 50(5):e13228. PubMed ID: 32293029
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Genetic counselling is relevant in familial as well as sporadic cases of amyotrophic lateral sclerosis].
    Lindquist SG; Dunø M; Svenstrup K; Nielsen JE
    Ugeskr Laeger; 2014 Oct; 176(43):. PubMed ID: 25353674
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Genetic and Pathological Assessment of hnRNPA1, hnRNPA2/B1, and hnRNPA3 in Familial and Sporadic Amyotrophic Lateral Sclerosis.
    Fifita JA; Zhang KY; Galper J; Williams KL; McCann EP; Hogan AL; Saunders N; Bauer D; Tarr IS; Pamphlett R; Nicholson GA; Rowe D; Yang S; Blair IP
    Neurodegener Dis; 2017; 17(6):304-312. PubMed ID: 29131108
    [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. Identification of novel FUS mutations in sporadic cases of amyotrophic lateral sclerosis.
    Belzil VV; Daoud H; St-Onge J; Desjarlais A; Bouchard JP; Dupre N; Lacomblez L; Salachas F; Pradat PF; Meininger V; Camu W; Dion PA; Rouleau GA
    Amyotroph Lateral Scler; 2011 Mar; 12(2):113-7. PubMed ID: 21261515
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. Studies of Genetic and Proteomic Risk Factors of Amyotrophic Lateral Sclerosis Inspire Biomarker Development and Gene Therapy.
    Bagyinszky E; Hulme J; An SSA
    Cells; 2023 Jul; 12(15):. PubMed ID: 37566027
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Novel FUS mutations identified through molecular screening in a large cohort of familial and sporadic amyotrophic lateral sclerosis.
    Tarlarini C; Lunetta C; Mosca L; Avemaria F; Riva N; Mantero V; Maestri E; Quattrini A; Corbo M; Melazzini MG; Penco S
    Eur J Neurol; 2015 Nov; 22(11):1474-81. PubMed ID: 26176978
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Genetic Epidemiology of Amyotrophic Lateral Sclerosis in Norway: A 2-Year Population-Based Study.
    Olsen CG; Busk ØL; Aanjesen TN; Alstadhaug KB; Bjørnå IK; Braathen GJ; Breivik KL; Demic N; Flemmen HØ; Hallerstig E; HogenEsch I; Holla ØL; Jøntvedt AB; Kampman MT; Kleveland G; Kvernmo HB; Ljøstad U; Maniaol A; Morsund ÅH; Nakken O; Novy C; Rekand T; Schlüter K; Schüler S; Tveten K; Tysnes OB; Holmøy T; Høyer H
    Neuroepidemiology; 2022; 56(4):271-282. PubMed ID: 35576897
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Gene mutations in familial amyotrophic lateral sclerosis].
    Oda M; Izumi Y; Kaji R
    Brain Nerve; 2011 Feb; 63(2):165-70. PubMed ID: 21301041
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. 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]  

  • 34. Amyotrophic lateral sclerosis onset is influenced by the burden of rare variants in known amyotrophic lateral sclerosis genes.
    Cady J; Allred P; Bali T; Pestronk A; Goate A; Miller TM; Mitra RD; Ravits J; Harms MB; Baloh RH
    Ann Neurol; 2015 Jan; 77(1):100-13. PubMed ID: 25382069
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Mutations in the 3' untranslated region of FUS causing FUS overexpression are associated with amyotrophic lateral sclerosis.
    Sabatelli M; Moncada A; Conte A; Lattante S; Marangi G; Luigetti M; Lucchini M; Mirabella M; Romano A; Del Grande A; Bisogni G; Doronzio PN; Rossini PM; Zollino M
    Hum Mol Genet; 2013 Dec; 22(23):4748-55. PubMed ID: 23847048
    [TBL] [Abstract][Full Text] [Related]  

  • 36. A serum microRNA sequence reveals fragile X protein pathology in amyotrophic lateral sclerosis.
    Freischmidt A; Goswami A; Limm K; Zimyanin VL; Demestre M; Glaß H; Holzmann K; Helferich AM; Brockmann SJ; Tripathi P; Yamoah A; Poser I; Oefner PJ; Böckers TM; Aronica E; Ludolph AC; Andersen PM; Hermann A; Weis J; Reinders J; Danzer KM; Weishaupt JH
    Brain; 2021 May; 144(4):1214-1229. PubMed ID: 33871026
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Identification of mutations in Korean patients with amyotrophic lateral sclerosis using multigene panel testing.
    Kim HJ; Oh KW; Kwon MJ; Oh SI; Park JS; Kim YE; Choi BO; Lee S; Ki CS; Kim SH
    Neurobiol Aging; 2016 Jan; 37():209.e9-209.e16. PubMed ID: 26601740
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Genetic analysis of GLT8D1 and ARPP21 in Australian familial and sporadic amyotrophic lateral sclerosis.
    Chan Moi Fat S; McCann EP; Williams KL; Henden L; Twine NA; Bauer DC; Pamphlett R; Kiernan MC; Rowe DB; Nicholson GA; Fifita JA; Blair IP
    Neurobiol Aging; 2021 May; 101():297.e9-297.e11. PubMed ID: 33581934
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Accuracy of a machine learning method based on structural and locational information from AlphaFold2 for predicting the pathogenicity of TARDBP and FUS gene variants in ALS.
    Hatano Y; Ishihara T; Onodera O
    BMC Bioinformatics; 2023 May; 24(1):206. PubMed ID: 37208601
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Frameshift and novel mutations in FUS in familial amyotrophic lateral sclerosis and ALS/dementia.
    Yan J; Deng HX; Siddique N; Fecto F; Chen W; Yang Y; Liu E; Donkervoort S; Zheng JG; Shi Y; Ahmeti KB; Brooks B; Engel WK; Siddique T
    Neurology; 2010 Aug; 75(9):807-14. PubMed ID: 20668259
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 30.