BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

306 related articles for article (PubMed ID: 25353674)

  • 21. CRISPR/Cas9-Mediated Gene Correction to Understand ALS.
    Yun Y; Ha Y
    Int J Mol Sci; 2020 May; 21(11):. PubMed ID: 32471232
    [TBL] [Abstract][Full Text] [Related]  

  • 22. De novo FUS mutations are the most frequent genetic cause in early-onset German ALS patients.
    Hübers A; Just W; Rosenbohm A; Müller K; Marroquin N; Goebel I; Högel J; Thiele H; Altmüller J; Nürnberg P; Weishaupt JH; Kubisch C; Ludolph AC; Volk AE
    Neurobiol Aging; 2015 Nov; 36(11):3117.e1-3117.e6. PubMed ID: 26362943
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Protein folding alterations in amyotrophic lateral sclerosis.
    Parakh S; Atkin JD
    Brain Res; 2016 Oct; 1648(Pt B):633-649. PubMed ID: 27064076
    [TBL] [Abstract][Full Text] [Related]  

  • 24. A Systematic and Comprehensive Review on Disease-Causing Genes in Amyotrophic Lateral Sclerosis.
    Srinivasan E; Rajasekaran R
    J Mol Neurosci; 2020 Nov; 70(11):1742-1770. PubMed ID: 32415434
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Motoneuron Disease: Basic Science.
    Ilieva H; Maragakis NJ
    Adv Neurobiol; 2017; 15():163-190. PubMed ID: 28674981
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Genetic analysis of the SOD1 and C9ORF72 genes in Hungarian patients with amyotrophic lateral sclerosis.
    Tripolszki K; Csányi B; Nagy D; Ratti A; Tiloca C; Silani V; Kereszty É; Török N; Vécsei L; Engelhardt JI; Klivényi P; Nagy N; Széll M
    Neurobiol Aging; 2017 May; 53():195.e1-195.e5. PubMed ID: 28222900
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. 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]  

  • 29. Genetic testing in ALS: A survey of current practices.
    Vajda A; McLaughlin RL; Heverin M; Thorpe O; Abrahams S; Al-Chalabi A; Hardiman O
    Neurology; 2017 Mar; 88(10):991-999. PubMed ID: 28159885
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Comparison of the clinical and cognitive features of genetically positive ALS patients from the largest tertiary center in Serbia.
    Marjanović IV; Selak-Djokić B; Perić S; Janković M; Arsenijević V; Basta I; Lavrnić D; Stefanova E; Stević Z
    J Neurol; 2017 Jun; 264(6):1091-1098. PubMed ID: 28444446
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Mutations in FUS are the most frequent genetic cause in juvenile sporadic ALS patients of Chinese origin.
    Zou ZY; Liu MS; Li XG; Cui LY
    Amyotroph Lateral Scler Frontotemporal Degener; 2016; 17(3-4):249-52. PubMed ID: 26972116
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. The distinct genetic pattern of ALS in Turkey and novel mutations.
    Özoğuz A; Uyan Ö; Birdal G; Iskender C; Kartal E; Lahut S; Ömür Ö; Agim ZS; Eken AG; Sen NE; Kavak P; Saygı C; Sapp PC; Keagle P; Parman Y; Tan E; Koç F; Deymeer F; Oflazer P; Hanağası H; Gürvit H; Bilgiç B; Durmuş H; Ertaş M; Kotan D; Akalın MA; Güllüoğlu H; Zarifoğlu M; Aysal F; Döşoğlu N; Bilguvar K; Günel M; Keskin Ö; Akgün T; Özçelik H; Landers JE; Brown RH; Başak AN
    Neurobiol Aging; 2015 Apr; 36(4):1764.e9-1764.e18. PubMed ID: 25681989
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Genetic Convergence Brings Clarity to the Enigmatic Red Line in ALS.
    Cook C; Petrucelli L
    Neuron; 2019 Mar; 101(6):1057-1069. PubMed ID: 30897357
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Genetics of amyotrophic lateral sclerosis].
    Hübers A; Weishaupt JH; Ludolph AC
    Nervenarzt; 2013 Oct; 84(10):1213-9. PubMed ID: 24072096
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Clinical genetics of amyotrophic lateral sclerosis in Japan: an update].
    Aoki M; Warita H; Suzuki N; Kato M
    Rinsho Shinkeigaku; 2012; 52(11):844-7. PubMed ID: 23196439
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Genotype-phenotype relationships in familial amyotrophic lateral sclerosis with FUS/TLS mutations in Japan.
    Akiyama T; Warita H; Kato M; Nishiyama A; Izumi R; Ikeda C; Kamada M; Suzuki N; Aoki M
    Muscle Nerve; 2016 Sep; 54(3):398-404. PubMed ID: 26823199
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Metabolomics: A Tool to Understand the Impact of Genetic Mutations in Amyotrophic Lateral Sclerosis.
    Lanznaster D; Veyrat-Durebex C; Vourc'h P; Andres CR; Blasco H; Corcia P
    Genes (Basel); 2020 May; 11(5):. PubMed ID: 32403313
    [TBL] [Abstract][Full Text] [Related]  

  • 39. De novo truncating FUS gene mutation as a cause of sporadic amyotrophic lateral sclerosis.
    DeJesus-Hernandez M; Kocerha J; Finch N; Crook R; Baker M; Desaro P; Johnston A; Rutherford N; Wojtas A; Kennelly K; Wszolek ZK; Graff-Radford N; Boylan K; Rademakers R
    Hum Mutat; 2010 May; 31(5):E1377-89. PubMed ID: 20232451
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Classification of familial amyotrophic lateral sclerosis by family history: effects on frequency of genes mutation.
    Conte A; Lattante S; Luigetti M; Del Grande A; Romano A; Marcaccio A; Marangi G; Rossini PM; Neri G; Zollino M; Sabatelli M
    J Neurol Neurosurg Psychiatry; 2012 Dec; 83(12):1201-3. PubMed ID: 22773853
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 16.