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 *

117 related articles for article (PubMed ID: 16036429)

  • 1. Primary lateral sclerosis, hereditary spastic paraplegia, and mutations in the alsin gene: historical background for the first International Conference.
    Rowland LP
    Amyotroph Lateral Scler Other Motor Neuron Disord; 2005 Jun; 6(2):67-76. PubMed ID: 16036429
    [No Abstract]   [Full Text] [Related]  

  • 2. Infantile-onset ascending hereditary spastic paraplegia with bulbar involvement due to the novel ALS2 mutation c.2761C>T.
    Wakil SM; Ramzan K; Abuthuraya R; Hagos S; Al-Dossari H; Al-Omar R; Murad H; Chedrawi A; Al-Hassnan ZN; Finsterer J; Bohlega S
    Gene; 2014 Feb; 536(1):217-20. PubMed ID: 24315819
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Alsin and the molecular pathways of amyotrophic lateral sclerosis.
    Chandran J; Ding J; Cai H
    Mol Neurobiol; 2007 Dec; 36(3):224-31. PubMed ID: 17955197
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Are alsin and spartin novel interaction partners?
    Çobanoğlu G; Ozansoy M; Başak AN
    Biochem Biophys Res Commun; 2012 Oct; 427(1):1-4. PubMed ID: 22982304
    [TBL] [Abstract][Full Text] [Related]  

  • 5. An ALS2 gene mutation causes hereditary spastic paraplegia in a Pakistani kindred.
    Gros-Louis F; Meijer IA; Hand CK; Dubé MP; MacGregor DL; Seni MH; Devon RS; Hayden MR; Andermann F; Andermann E; Rouleau GA
    Ann Neurol; 2003 Jan; 53(1):144-5. PubMed ID: 12509863
    [No Abstract]   [Full Text] [Related]  

  • 6. Absence of alsin function leads to corticospinal motor neuron vulnerability via novel disease mechanisms.
    Gautam M; Jara JH; Sekerkova G; Yasvoina MV; Martina M; Özdinler PH
    Hum Mol Genet; 2016 Mar; 25(6):1074-87. PubMed ID: 26755825
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Infantile-onset ascending hereditary spastic paralysis is associated with mutations in the alsin gene.
    Eymard-Pierre E; Lesca G; Dollet S; Santorelli FM; di Capua M; Bertini E; Boespflug-Tanguy O
    Am J Hum Genet; 2002 Sep; 71(3):518-27. PubMed ID: 12145748
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genotype-phenotype correlation in seven motor neuron disease families with novel ALS2 mutations.
    Sprute R; Jergas H; Ölmez A; Alawbathani S; Karasoy H; Dafsari HS; Becker K; Daimagüler HS; Nürnberg P; Muntoni F; Topaloglu H; Uyanik G; Cirak S
    Am J Med Genet A; 2021 Feb; 185(2):344-354. PubMed ID: 33155358
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Adult-onset primary lateral sclerosis is not associated with mutations in the ALS2 gene.
    Brugman F; Eymard-Pierre E; van den Berg LH; Wokke JH; Gauthier-Barichard F; Boespflug-Tanguy O
    Neurology; 2007 Aug; 69(7):702-4. PubMed ID: 17698795
    [No Abstract]   [Full Text] [Related]  

  • 10. Molecular and cellular function of ALS2/alsin: implication of membrane dynamics in neuronal development and degeneration.
    Hadano S; Kunita R; Otomo A; Suzuki-Utsunomiya K; Ikeda JE
    Neurochem Int; 2007; 51(2-4):74-84. PubMed ID: 17566607
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The various forms of hereditary motor neuron disorders and their historical descriptions.
    Mathis S; Beauvais D; Duval F; Solé G; Le Masson G
    J Neurol; 2024 Jul; 271(7):3978-3990. PubMed ID: 38816479
    [TBL] [Abstract][Full Text] [Related]  

  • 12. ALS2/alsin knockout mice and motor neuron diseases.
    Cai H; Shim H; Lai C; Xie C; Lin X; Yang WJ; Chandran J
    Neurodegener Dis; 2008; 5(6):359-66. PubMed ID: 18714162
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Identification of two novel ALS2 mutations in infantile-onset ascending hereditary spastic paraplegia.
    Daud S; Kakar N; Goebel I; Hashmi AS; Yaqub T; Nürnberg G; Nürnberg P; Morris-Rosendahl DJ; Wasim M; Volk AE; Kubisch C; Ahmad J; Borck G
    Amyotroph Lateral Scler Frontotemporal Degener; 2016; 17(3-4):260-5. PubMed ID: 26751646
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Astrocytic protection of spinal motor neurons but not cortical neurons against loss of Als2/alsin function.
    Jacquier A; Bellouze S; Blanchard S; Bohl D; Haase G
    Hum Mol Genet; 2009 Jun; 18(12):2127-39. PubMed ID: 19304783
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A novel locus for an autosomal recessive hereditary spastic paraplegia (SPG35) maps to 16q21-q23.
    Dick KJ; Al-Mjeni R; Baskir W; Koul R; Simpson MA; Patton MA; Raeburn S; Crosby AH
    Neurology; 2008 Jul; 71(4):248-52. PubMed ID: 18463364
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The first ALS2 missense mutation associated with JPLS reveals new aspects of alsin biological function.
    Panzeri C; De Palma C; Martinuzzi A; Daga A; De Polo G; Bresolin N; Miller CC; Tudor EL; Clementi E; Bassi MT
    Brain; 2006 Jul; 129(Pt 7):1710-9. PubMed ID: 16670179
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Primary lateral sclerosis: the era of international diagnosis criteria].
    Le Forestier N; Meininger V
    Rev Neurol (Paris); 2009 May; 165(5):415-29. PubMed ID: 18842276
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The expanding clinical and genetic spectrum of alsin-related disorders: the first cohort of Brazilian patients.
    Alves De Siqueira Carvalho A; Antônio Troccoli Chieia M; Braga Farias I; Bulle Oliveira AS; Pinto WBVR; Souza PVS
    Amyotroph Lateral Scler Frontotemporal Degener; 2022 Feb; 23(1-2):16-24. PubMed ID: 34738851
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Human-induced pluripotent stem cells pave the road for a better understanding of motor neuron disease.
    Winner B; Marchetto MC; Winkler J; Gage FH
    Hum Mol Genet; 2014 Sep; 23(R1):R27-34. PubMed ID: 24821704
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Exome Sequencing Identifies a Mutation (Y740C) in Spastic Paraplegia 7 Gene Associated with Adult-Onset Primary Lateral Sclerosis in a Chinese Family.
    Liu Y; Xu J; Tao W; Fu C; Liu J; Yu R; Zhang X
    Eur Neurol; 2019; 81(1-2):87-93. PubMed ID: 31117107
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.