BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

231 related articles for article (PubMed ID: 22752089)

  • 1. Oligoclonal bands in the cerebrospinal fluid of amyotrophic lateral sclerosis patients with disease-associated mutations.
    Ticozzi N; Tiloca C; Mencacci NE; Morelli C; Doretti A; Rusconi D; Colombrita C; Sangalli D; Verde F; Finelli P; Messina S; Ratti A; Silani V
    J Neurol; 2013 Jan; 260(1):85-92. PubMed ID: 22752089
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Extensive genetics of ALS: a population-based study in Italy.
    Chiò A; Calvo A; Mazzini L; Cantello R; Mora G; Moglia C; Corrado L; D'Alfonso S; Majounie E; Renton A; Pisano F; Ossola I; Brunetti M; Traynor BJ; Restagno G;
    Neurology; 2012 Nov; 79(19):1983-9. PubMed ID: 23100398
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Screening of the SOD1, FUS, TARDBP, ANG, and OPTN mutations in Korean patients with familial and sporadic ALS.
    Kwon MJ; Baek W; Ki CS; Kim HY; Koh SH; Kim JW; Kim SH
    Neurobiol Aging; 2012 May; 33(5):1017.e17-23. PubMed ID: 22244934
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Extensive molecular genetic survey of Taiwanese patients with amyotrophic lateral sclerosis.
    Soong BW; Lin KP; Guo YC; Lin CC; Tsai PC; Liao YC; Lu YC; Wang SJ; Tsai CP; Lee YC
    Neurobiol Aging; 2014 Oct; 35(10):2423.e1-6. PubMed ID: 24908169
    [TBL] [Abstract][Full Text] [Related]  

  • 6. SOD1, ANG, TARDBP and FUS mutations in amyotrophic lateral sclerosis: a United States clinical testing lab experience.
    Brown JA; Min J; Staropoli JF; Collin E; Bi S; Feng X; Barone R; Cao Y; O'Malley L; Xin W; Mullen TE; Sims KB
    Amyotroph Lateral Scler; 2012 Feb; 13(2):217-22. PubMed ID: 22292843
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Oligogenic inheritance of optineurin (OPTN) and C9ORF72 mutations in ALS highlights localisation of OPTN in the TDP-43-negative inclusions of C9ORF72-ALS.
    Bury JJ; Highley JR; Cooper-Knock J; Goodall EF; Higginbottom A; McDermott CJ; Ince PG; Shaw PJ; Kirby J
    Neuropathology; 2016 Apr; 36(2):125-34. PubMed ID: 26303227
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genetic architecture of ALS in Sardinia.
    Borghero G; Pugliatti M; Marrosu F; Marrosu MG; Murru MR; Floris G; Cannas A; Parish LD; Occhineri P; Cau TB; Loi D; Ticca A; Traccis S; Manera U; Canosa A; Moglia C; Calvo A; Barberis M; Brunetti M; Pliner HA; Renton AE; Nalls MA; Traynor BJ; Restagno G; Chiò A;
    Neurobiol Aging; 2014 Dec; 35(12):2882.e7-2882.e12. PubMed ID: 25123918
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Comprehensive targeted next-generation sequencing in Japanese familial amyotrophic lateral sclerosis.
    Nishiyama A; Niihori T; Warita H; Izumi R; Akiyama T; Kato M; Suzuki N; Aoki Y; Aoki M
    Neurobiol Aging; 2017 May; 53():194.e1-194.e8. PubMed ID: 28160950
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mutation analysis of SOD1, C9orf72, TARDBP and FUS genes in ethnically-diverse Malaysian patients with amyotrophic lateral sclerosis (ALS).
    Edgar S; Ellis M; Abdul-Aziz NA; Goh KJ; Shahrizaila N; Kennerson ML; Ahmad-Annuar A
    Neurobiol Aging; 2021 Dec; 108():200-206. PubMed ID: 34404558
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Mutations of optineurin in amyotrophic lateral sclerosis.
    Maruyama H; Morino H; Ito H; Izumi Y; Kato H; Watanabe Y; Kinoshita Y; Kamada M; Nodera H; Suzuki H; Komure O; Matsuura S; Kobatake K; Morimoto N; Abe K; Suzuki N; Aoki M; Kawata A; Hirai T; Kato T; Ogasawara K; Hirano A; Takumi T; Kusaka H; Hagiwara K; Kaji R; Kawakami H
    Nature; 2010 May; 465(7295):223-6. PubMed ID: 20428114
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Large proportion of amyotrophic lateral sclerosis cases in Sardinia due to a single founder mutation of the TARDBP gene.
    Chiò A; Borghero G; Pugliatti M; Ticca A; Calvo A; Moglia C; Mutani R; Brunetti M; Ossola I; Marrosu MG; Murru MR; Floris G; Cannas A; Parish LD; Cossu P; Abramzon Y; Johnson JO; Nalls MA; Arepalli S; Chong S; Hernandez DG; Traynor BJ; Restagno G;
    Arch Neurol; 2011 May; 68(5):594-8. PubMed ID: 21220647
    [TBL] [Abstract][Full Text] [Related]  

  • 15. State of play in amyotrophic lateral sclerosis genetics.
    Renton AE; Chiò A; Traynor BJ
    Nat Neurosci; 2014 Jan; 17(1):17-23. PubMed ID: 24369373
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. Screening of SOD1, FUS and TARDBP genes in patients with amyotrophic lateral sclerosis in central-southern China.
    Hou L; Jiao B; Xiao T; Zhou L; Zhou Z; Du J; Yan X; Wang J; Tang B; Shen L
    Sci Rep; 2016 Sep; 6():32478. PubMed ID: 27604643
    [TBL] [Abstract][Full Text] [Related]  

  • 19. FUS, TARDBP, and SOD1 mutations in a Taiwanese cohort with familial ALS.
    Tsai CP; Soong BW; Lin KP; Tu PH; Lin JL; Lee YC
    Neurobiol Aging; 2011 Mar; 32(3):553.e13-21. PubMed ID: 20472325
    [TBL] [Abstract][Full Text] [Related]  

  • 20. FUS mutations in amyotrophic lateral sclerosis: clinical, pathological, neurophysiological and genetic analysis.
    Blair IP; Williams KL; Warraich ST; Durnall JC; Thoeng AD; Manavis J; Blumbergs PC; Vucic S; Kiernan MC; Nicholson GA
    J Neurol Neurosurg Psychiatry; 2010 Jun; 81(6):639-45. PubMed ID: 19965854
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.