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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

115 related articles for article (PubMed ID: 20932227)

  • 1. The P413L chromogranin B variation in French patients with sporadic amyotrophic lateral sclerosis.
    Blasco H; Corcia P; Veyrat-Durebex C; Coutadeur C; Fournier C; Camu W; Gordon P; Praline J; Andres CR; Vourc'h P;
    Amyotroph Lateral Scler; 2011 May; 12(3):210-4. PubMed ID: 20932227
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Lack of relationship between the P413L chromogranin B variant and a SALS Italian cohort.
    Ricci C; Battistini S; Avemaria F; Benigni M; Tarlarini C; Giannini F; Corbo M; Lunetta C; Penco S
    Gene; 2015 Sep; 568(2):186-9. PubMed ID: 26003296
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Chromogranin B P413L variant as risk factor and modifier of disease onset for amyotrophic lateral sclerosis.
    Gros-Louis F; Andersen PM; Dupre N; Urushitani M; Dion P; Souchon F; D'Amour M; Camu W; Meininger V; Bouchard JP; Rouleau GA; Julien JP
    Proc Natl Acad Sci U S A; 2009 Dec; 106(51):21777-82. PubMed ID: 20007371
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Sex-dependent effects of chromogranin B P413L allelic variant as disease modifier in amyotrophic lateral sclerosis.
    Ohta Y; Soucy G; Phaneuf D; Audet JN; Gros-Louis F; Rouleau GA; Blasco H; Corcia P; Andersen PM; Nordin F; Yamashita T; Abe K; Julien JP
    Hum Mol Genet; 2016 Nov; 25(21):4771-4786. PubMed ID: 28175304
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Lack of association between the P413L variant of chromogranin B and ALS risk or age at onset: a meta-analysis.
    Yang X; Li S; Xing D; Li P; Li C; Qi L; Xu Y; Ren H
    Amyotroph Lateral Scler Frontotemporal Degener; 2018 Feb; 19(1-2):80-86. PubMed ID: 28795874
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. P413L CHGB is not associated with ALS susceptibility or age at onset in a Dutch population.
    van Vught PW; Veldink JH; van den Berg LH
    Proc Natl Acad Sci U S A; 2010 May; 107(19):E77; author reply E78. PubMed ID: 20431044
    [No Abstract]   [Full Text] [Related]  

  • 8. Association of APOE with age at onset of sporadic amyotrophic lateral sclerosis.
    Zetterberg H; Jacobsson J; Rosengren L; Blennow K; Andersen PM
    J Neurol Sci; 2008 Oct; 273(1-2):67-9. PubMed ID: 18656208
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mutational analysis of the Cu/Zn superoxide dismutase gene in a Catalan ALS population: should all sporadic ALS cases also be screened for SOD1?
    Gamez J; Corbera-Bellalta M; Nogales G; Raguer N; García-Arumí E; Badia-Canto M; Lladó-Carbó E; Alvarez-Sabín J
    J Neurol Sci; 2006 Aug; 247(1):21-8. PubMed ID: 16674979
    [TBL] [Abstract][Full Text] [Related]  

  • 10. An analysis of the entire SOD1 gene in sporadic ALS.
    Luquin N; Yu B; Trent RJ; Morahan JM; Pamphlett R
    Neuromuscul Disord; 2008 Jul; 18(7):545-52. PubMed ID: 18504130
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Clinical heterogeneity in Italian patients with amyotrophic lateral sclerosis.
    Piaceri I; Del Mastio M; Tedde A; Bagnoli S; Latorraca S; Massaro F; Paganini M; Corrado A; Sorbi S; Nacmias B
    Clin Genet; 2012 Jul; 82(1):83-7. PubMed ID: 21651514
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Molecular analysis of the superoxide dismutase 1 gene in Spanish patients with sporadic or familial amyotrophic lateral sclerosis.
    García-Redondo A; Bustos F; Juan Y Seva B; Del Hoyo P; Jiménez S; Campos Y; Martín MA; Rubio JC; Cañadillas F; Arenas J; Esteban J
    Muscle Nerve; 2002 Aug; 26(2):274-8. PubMed ID: 12210393
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Lack of evidence of monomer/misfolded superoxide dismutase-1 in sporadic amyotrophic lateral sclerosis.
    Liu HN; Sanelli T; Horne P; Pioro EP; Strong MJ; Rogaeva E; Bilbao J; Zinman L; Robertson J
    Ann Neurol; 2009 Jul; 66(1):75-80. PubMed ID: 19670443
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Contribution of major amyotrophic lateral sclerosis genes to the etiology of sporadic disease.
    Lattante S; Conte A; Zollino M; Luigetti M; Del Grande A; Marangi G; Romano A; Marcaccio A; Meleo E; Bisogni G; Rossini PM; Sabatelli M
    Neurology; 2012 Jul; 79(1):66-72. PubMed ID: 22722621
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A common functional allele of the Nogo receptor gene, reticulon 4 receptor (RTN4R), is associated with sporadic amyotrophic lateral sclerosis in a French population.
    Amy M; Staehlin O; René F; Blasco H; Marouillat S; Daoud H; Vourc'h P; Gordon PH; Camu W; Corcia P; Loeffler JP; Palkovits M; Sommer WH; Andres CR
    Amyotroph Lateral Scler Frontotemporal Degener; 2015; 16(7-8):490-6. PubMed ID: 26083872
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 50bp deletion in the promoter for superoxide dismutase 1 (SOD1) reduces SOD1 expression in vitro and may correlate with increased age of onset of sporadic amyotrophic lateral sclerosis.
    Broom WJ; Greenway M; Sadri-Vakili G; Russ C; Auwarter KE; Glajch KE; Dupre N; Swingler RJ; Purcell S; Hayward C; Sapp PC; McKenna-Yasek D; Valdmanis PN; Bouchard JP; Meininger V; Hosler BA; Glass JD; Polack M; Rouleau GA; Cha JH; Hardiman O; Brown RH
    Amyotroph Lateral Scler; 2008 Aug; 9(4):229-37. PubMed ID: 18608091
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Analysis of a genetic defect in the TATA box of the SOD1 gene in a patient with familial amyotrophic lateral sclerosis.
    Niemann S; Broom WJ; Brown RH
    Muscle Nerve; 2007 Nov; 36(5):704-7. PubMed ID: 17636481
    [TBL] [Abstract][Full Text] [Related]  

  • 19. N19S, a new SOD1 mutation in sporadic amyotrophic lateral sclerosis: no evidence for disease causation.
    Mayeux V; Corcia P; Besson G; Jafari-Schluep HF; Briolotti V; Camu W
    Ann Neurol; 2003 Jun; 53(6):815-8. PubMed ID: 12783432
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutations.
    Mackenzie IR; Bigio EH; Ince PG; Geser F; Neumann M; Cairns NJ; Kwong LK; Forman MS; Ravits J; Stewart H; Eisen A; McClusky L; Kretzschmar HA; Monoranu CM; Highley JR; Kirby J; Siddique T; Shaw PJ; Lee VM; Trojanowski JQ
    Ann Neurol; 2007 May; 61(5):427-34. PubMed ID: 17469116
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.