BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

219 related articles for article (PubMed ID: 23062600)

  • 1. Mutation analysis of PFN1 in familial amyotrophic lateral sclerosis patients.
    Daoud H; Dobrzeniecka S; Camu W; Meininger V; Dupré N; Dion PA; Rouleau GA
    Neurobiol Aging; 2013 Apr; 34(4):1311.e1-2. PubMed ID: 23062600
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mutation analysis and immunopathological studies of PFN1 in familial and sporadic amyotrophic lateral sclerosis.
    Yang S; Fifita JA; Williams KL; Warraich ST; Pamphlett R; Nicholson GA; Blair IP
    Neurobiol Aging; 2013 Sep; 34(9):2235.e7-10. PubMed ID: 23635659
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mutations in the PFN1 gene are not a common cause in patients with amyotrophic lateral sclerosis and frontotemporal lobar degeneration in France.
    Lattante S; Le Ber I; Camuzat A; Brice A; Kabashi E
    Neurobiol Aging; 2013 Jun; 34(6):1709.e1-2. PubMed ID: 23182804
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Screening of VCP mutations in Chinese amyotrophic lateral sclerosis patients.
    Zou ZY; Liu MS; Li XG; Cui LY
    Neurobiol Aging; 2013 May; 34(5):1519.e3-4. PubMed ID: 23102936
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Analysis of the SORT1 gene in familial amyotrophic lateral sclerosis.
    Belzil VV; André-Guimont C; Atallah MR; Daoud H; Dupré N; Bouchard JP; Camu W; Dion PA; Rouleau GA
    Neurobiol Aging; 2012 Aug; 33(8):1845.e7-9. PubMed ID: 22361451
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mutations of the ANG gene in French patients with sporadic amyotrophic lateral sclerosis.
    Paubel A; Violette J; Amy M; Praline J; Meininger V; Camu W; Corcia P; Andres CR; Vourc'h P;
    Arch Neurol; 2008 Oct; 65(10):1333-6. PubMed ID: 18852347
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Rare and common paraoxonase gene variants in amyotrophic lateral sclerosis patients.
    van Blitterswijk M; Blokhuis A; van Es MA; van Vught PW; Rowicka PA; Schelhaas HJ; van der Kooi AJ; de Visser M; Veldink JH; van den Berg LH
    Neurobiol Aging; 2012 Aug; 33(8):1845.e1-3. PubMed ID: 22330174
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Screening of the PFN1 gene in sporadic amyotrophic lateral sclerosis and in frontotemporal dementia.
    Tiloca C; Ticozzi N; Pensato V; Corrado L; Del Bo R; Bertolin C; Fenoglio C; Gagliardi S; Calini D; Lauria G; Castellotti B; Bagarotti A; Corti S; Galimberti D; Cagnin A; Gabelli C; Ranieri M; Ceroni M; Siciliano G; Mazzini L; Cereda C; Scarpini E; Sorarù G; Comi GP; D'Alfonso S; Gellera C; Ratti A; Landers JE; Silani V;
    Neurobiol Aging; 2013 May; 34(5):1517.e9-10. PubMed ID: 23063648
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Novel deletion mutations of OPTN in amyotrophic lateral sclerosis in Japanese.
    Iida A; Hosono N; Sano M; Kamei T; Oshima S; Tokuda T; Nakajima M; Kubo M; Nakamura Y; Ikegawa S
    Neurobiol Aging; 2012 Aug; 33(8):1843.e19-24. PubMed ID: 22402017
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Analysis of the C9orf72 hexanucleotide repeat expansion in Korean patients with familial and sporadic amyotrophic lateral sclerosis.
    Jang JH; Kwon MJ; Choi WJ; Oh KW; Koh SH; Ki CS; Kim SH
    Neurobiol Aging; 2013 Apr; 34(4):1311.e7-9. PubMed ID: 23088937
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. A novel phosphorylation site mutation in profilin 1 revealed in a large screen of US, Nordic, and German amyotrophic lateral sclerosis/frontotemporal dementia cohorts.
    Ingre C; Landers JE; Rizik N; Volk AE; Akimoto C; Birve A; Hübers A; Keagle PJ; Piotrowska K; Press R; Andersen PM; Ludolph AC; Weishaupt JH
    Neurobiol Aging; 2013 Jun; 34(6):1708.e1-6. PubMed ID: 23141414
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A novel optineurin truncating mutation and three glaucoma-associated missense variants in patients with familial amyotrophic lateral sclerosis in Germany.
    Weishaupt JH; Waibel S; Birve A; Volk AE; Mayer B; Meyer T; Ludolph AC; Andersen PM
    Neurobiol Aging; 2013 May; 34(5):1516.e9-15. PubMed ID: 23062601
    [TBL] [Abstract][Full Text] [Related]  

  • 14. PFN1 mutations are rare in Han Chinese populations with amyotrophic lateral sclerosis.
    Chen Y; Zheng ZZ; Huang R; Chen K; Song W; Zhao B; Chen X; Yang Y; Yuan L; Shang HF
    Neurobiol Aging; 2013 Jul; 34(7):1922.e1-5. PubMed ID: 23428184
    [TBL] [Abstract][Full Text] [Related]  

  • 15. VCP mutations in familial and sporadic amyotrophic lateral sclerosis.
    Koppers M; van Blitterswijk MM; Vlam L; Rowicka PA; van Vught PW; Groen EJ; Spliet WG; Engelen-Lee J; Schelhaas HJ; de Visser M; van der Kooi AJ; van der Pol WL; Pasterkamp RJ; Veldink JH; van den Berg LH
    Neurobiol Aging; 2012 Apr; 33(4):837.e7-13. PubMed ID: 22078486
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosis.
    Wu CH; Fallini C; Ticozzi N; Keagle PJ; Sapp PC; Piotrowska K; Lowe P; Koppers M; McKenna-Yasek D; Baron DM; Kost JE; Gonzalez-Perez P; Fox AD; Adams J; Taroni F; Tiloca C; Leclerc AL; Chafe SC; Mangroo D; Moore MJ; Zitzewitz JA; Xu ZS; van den Berg LH; Glass JD; Siciliano G; Cirulli ET; Goldstein DB; Salachas F; Meininger V; Rossoll W; Ratti A; Gellera C; Bosco DA; Bassell GJ; Silani V; Drory VE; Brown RH; Landers JE
    Nature; 2012 Aug; 488(7412):499-503. PubMed ID: 22801503
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Gain-of-function profilin 1 mutations linked to familial amyotrophic lateral sclerosis cause seed-dependent intracellular TDP-43 aggregation.
    Tanaka Y; Nonaka T; Suzuki G; Kametani F; Hasegawa M
    Hum Mol Genet; 2016 Apr; 25(7):1420-33. PubMed ID: 26908597
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A novel Angiogenin gene mutation in a sporadic patient with amyotrophic lateral sclerosis from southern Italy.
    Conforti FL; Sprovieri T; Mazzei R; Ungaro C; La Bella V; Tessitore A; Patitucci A; Magariello A; Gabriele AL; Tedeschi G; Simone IL; Majorana G; Valentino P; Condino F; Bono F; Monsurrò MR; Muglia M; Quattrone A
    Neuromuscul Disord; 2008 Jan; 18(1):68-70. PubMed ID: 17703939
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The occurrence of mutations in FUS in a Belgian cohort of patients with familial ALS.
    Damme PV; Goris A; Race V; Hersmus N; Dubois B; Bosch LV; Matthijs G; Robberecht W
    Eur J Neurol; 2010 May; 17(5):754-6. PubMed ID: 19922450
    [TBL] [Abstract][Full Text] [Related]  

  • 20. ATAXIN2 CAG-repeat length in Italian patients with amyotrophic lateral sclerosis: risk factor or variant phenotype? Implication for genetic testing and counseling.
    Gellera C; Ticozzi N; Pensato V; Nanetti L; Castucci A; Castellotti B; Lauria G; Taroni F; Silani V; Mariotti C
    Neurobiol Aging; 2012 Aug; 33(8):1847.e15-21. PubMed ID: 22425256
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.