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 *

129 related articles for article (PubMed ID: 26203661)

  • 1. A Dutch family with autosomal recessively inherited lower motor neuron predominant motor neuron disease due to optineurin mutations.
    Beeldman E; van der Kooi AJ; de Visser M; van Maarle MC; van Ruissen F; Baas F
    Amyotroph Lateral Scler Frontotemporal Degener; 2015; 16(5-6):410-1. PubMed ID: 26203661
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Novel optineurin mutations in patients with familial and sporadic amyotrophic lateral sclerosis.
    Del Bo R; Tiloca C; Pensato V; Corrado L; Ratti A; Ticozzi N; Corti S; Castellotti B; Mazzini L; Sorarù G; Cereda C; D'Alfonso S; Gellera C; Comi GP; Silani V;
    J Neurol Neurosurg Psychiatry; 2011 Nov; 82(11):1239-43. PubMed ID: 21613650
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Novel optineurin mutations in sporadic amyotrophic lateral sclerosis patients.
    van Blitterswijk M; van Vught PW; van Es MA; Schelhaas HJ; van der Kooi AJ; de Visser M; Veldink JH; van den Berg LH
    Neurobiol Aging; 2012 May; 33(5):1016.e1-7. PubMed ID: 21802176
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Screening of OPTN in French familial amyotrophic lateral sclerosis.
    Millecamps S; Boillée S; Chabrol E; Camu W; Cazeneuve C; Salachas F; Pradat PF; Danel-Brunaud V; Vandenberghe N; Corcia P; Le Forestier N; Lacomblez L; Bruneteau G; Seilhean D; Brice A; Feingold J; Meininger V; LeGuern E
    Neurobiol Aging; 2011 Mar; 32(3):557.e11-3. PubMed ID: 21220178
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Novel heterozygous nonsense mutation of the OPTN gene segregating in a Danish family with ALS.
    Tümer Z; Bertelsen B; Gredal O; Magyari M; Nielsen KC; Lucamp ; Grønskov K; Brøndum-Nielsen K
    Neurobiol Aging; 2012 Jan; 33(1):208.e1-5. PubMed ID: 21852022
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A novel amyotrophic lateral sclerosis mutation in OPTN induces ER stress and Golgi fragmentation in vitro.
    Fifita JA; Williams KL; Sundaramoorthy V; Mccann EP; Nicholson GA; Atkin JD; Blair IP
    Amyotroph Lateral Scler Frontotemporal Degener; 2017 Feb; 18(1-2):126-133. PubMed ID: 27534431
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Absence of the OPTN mutation in a patient with ALS and familial primary open angle glaucoma.
    Corcia P; Praline J; Guennoc AM; Thépault RA; Gordon PH; Blasco H; Andres CR; Vourc'h P
    J Neurol Sci; 2011 Oct; 309(1-2):16-7. PubMed ID: 21851955
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mutation analysis of the optineurin gene in familial amyotrophic lateral sclerosis.
    Solski JA; Williams KL; Yang S; Nicholson GA; Blair IP
    Neurobiol Aging; 2012 Jan; 33(1):210.e9-10. PubMed ID: 22015311
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Screening for OPTN mutations in a cohort of British amyotrophic lateral sclerosis patients.
    Johnson L; Miller JW; Gkazi AS; Vance C; Topp SD; Newhouse SJ; Al-Chalabi A; Smith BN; Shaw CE
    Neurobiol Aging; 2012 Dec; 33(12):2948.e15-7. PubMed ID: 22892313
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Inflammatory mechanisms in amyotrophic lateral sclerosis].
    Fujita K; Izumi Y; Kaji R
    Brain Nerve; 2012 Mar; 64(3):273-8. PubMed ID: 22402721
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Screening for OPTN mutations in amyotrophic lateral sclerosis in a mainly Caucasian population.
    Sugihara K; Maruyama H; Kamada M; Morino H; Kawakami H
    Neurobiol Aging; 2011 Oct; 32(10):1923.e9-10. PubMed ID: 21550138
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Clinicopathologic features of autosomal recessive amyotrophic lateral sclerosis associated with optineurin mutation.
    Kamada M; Izumi Y; Ayaki T; Nakamura M; Kagawa S; Kudo E; Sako W; Maruyama H; Nishida Y; Kawakami H; Ito H; Kaji R
    Neuropathology; 2014 Feb; 34(1):64-70. PubMed ID: 23889540
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Dysfunction of Optineurin in Amyotrophic Lateral Sclerosis and Glaucoma.
    Toth RP; Atkin JD
    Front Immunol; 2018; 9():1017. PubMed ID: 29875767
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mutational analysis of familial and sporadic amyotrophic lateral sclerosis with OPTN mutations in Japanese population.
    Naruse H; Takahashi Y; Kihira T; Yoshida S; Kokubo Y; Kuzuhara S; Ishiura H; Amagasa M; Murayama S; Tsuji S; Goto J
    Amyotroph Lateral Scler; 2012 Oct; 13(6):562-6. PubMed ID: 22708870
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Association of a paraneoplastic motor neuron disease with anti-Ri antibodies and a novel SOD1 I18del mutation.
    Diard-Detoeuf C; Dangoumau A; Limousin N; Biberon J; Vourc'h P; Andres CR; de Toffol B; Praline J
    J Neurol Sci; 2014 Feb; 337(1-2):212-4. PubMed ID: 24296360
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Functional analysis of optineurin and some of its disease-associated mutants.
    Bansal M; Swarup G; Balasubramanian D
    IUBMB Life; 2015 Feb; 67(2):120-8. PubMed ID: 25855473
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Primary lateral sclerosis may occur within familial amyotrophic lateral sclerosis pedigrees.
    Praline J; Guennoc AM; Vourc'h P; De Toffol B; Corcia P
    Amyotroph Lateral Scler; 2010; 11(1-2):154-6. PubMed ID: 20184517
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Treatment for familial amyotrophic lateral sclerosis/motor neuron disease.
    Benatar M; Kurent J; Moore DH
    Cochrane Database Syst Rev; 2009 Jan; 2009(1):CD006153. PubMed ID: 19160266
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.