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 *

263 related articles for article (PubMed ID: 19437551)

  • 1. Mitochondrial dysfunction in a neural cell model of spinal muscular atrophy.
    Acsadi G; Lee I; Li X; Khaidakov M; Pecinova A; Parker GC; Hüttemann M
    J Neurosci Res; 2009 Sep; 87(12):2748-56. PubMed ID: 19437551
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Stathmin, a microtubule-destabilizing protein, is dysregulated in spinal muscular atrophy.
    Wen HL; Lin YT; Ting CH; Lin-Chao S; Li H; Hsieh-Li HM
    Hum Mol Genet; 2010 May; 19(9):1766-78. PubMed ID: 20176735
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A new model to study spinal muscular atrophy: neurite degeneration and cell death is counteracted by BCL-X(L) Overexpression in motoneurons.
    Garcera A; Mincheva S; Gou-Fabregas M; Caraballo-Miralles V; Lladó J; Comella JX; Soler RM
    Neurobiol Dis; 2011 Jun; 42(3):415-26. PubMed ID: 21333739
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Synthesis and biological evaluation of novel 2,4-diaminoquinazoline derivatives as SMN2 promoter activators for the potential treatment of spinal muscular atrophy.
    Thurmond J; Butchbach ME; Palomo M; Pease B; Rao M; Bedell L; Keyvan M; Pai G; Mishra R; Haraldsson M; Andresson T; Bragason G; Thosteinsdottir M; Bjornsson JM; Coovert DD; Burghes AH; Gurney ME; Singh J
    J Med Chem; 2008 Feb; 51(3):449-69. PubMed ID: 18205293
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Spinal muscular atrophy: a deficiency in a ubiquitous protein; a motor neuron-specific disease.
    Monani UR
    Neuron; 2005 Dec; 48(6):885-96. PubMed ID: 16364894
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Smn deficiency causes neuritogenesis and neurogenesis defects in the retinal neurons of a mouse model of spinal muscular atrophy.
    Liu H; Beauvais A; Baker AN; Tsilfidis C; Kothary R
    Dev Neurobiol; 2011 Feb; 71(2):153-69. PubMed ID: 20862739
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A role for complexes of survival of motor neurons (SMN) protein with gemins and profilin in neurite-like cytoplasmic extensions of cultured nerve cells.
    Sharma A; Lambrechts A; Hao le T; Le TT; Sewry CA; Ampe C; Burghes AH; Morris GE
    Exp Cell Res; 2005 Sep; 309(1):185-97. PubMed ID: 15975577
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Restoring Bcl-x(L) levels benefits a mouse model of spinal muscular atrophy.
    Tsai LK; Tsai MS; Ting CH; Wang SH; Li H
    Neurobiol Dis; 2008 Sep; 31(3):361-7. PubMed ID: 18590823
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Transgenic inactivation of murine myostatin does not decrease the severity of disease in a model of Spinal Muscular Atrophy.
    Rindt H; Buckley DM; Vale SM; Krogman M; Rose FF; Garcia ML; Lorson CL
    Neuromuscul Disord; 2012 Mar; 22(3):277-85. PubMed ID: 22079083
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mitochondrial defects in the respiratory complex I contribute to impaired translational initiation via ROS and energy homeostasis in SMA motor neurons.
    Thelen MP; Wirth B; Kye MJ
    Acta Neuropathol Commun; 2020 Dec; 8(1):223. PubMed ID: 33353564
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Survival motor neuron SMN1 and SMN2 gene promoters: identical sequences and differential expression in neurons and non-neuronal cells.
    Boda B; Mas C; Giudicelli C; Nepote V; Guimiot F; Levacher B; Zvara A; Santha M; LeGall I; Simonneau M
    Eur J Hum Genet; 2004 Sep; 12(9):729-37. PubMed ID: 15162126
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Degenerative diseases, oxidative stress and cytochrome c oxidase function.
    Kadenbach B; Ramzan R; Vogt S
    Trends Mol Med; 2009 Apr; 15(4):139-47. PubMed ID: 19303362
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Co-regulation of survival of motor neuron and Bcl-xL expression: implications for neuroprotection in spinal muscular atrophy.
    Anderton RS; Price LL; Turner BJ; Meloni BP; Mitrpant C; Mastaglia FL; Goh C; Wilton SD; Boulos S
    Neuroscience; 2012 Sep; 220():228-36. PubMed ID: 22732506
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Polyglutamine tract-binding protein-1 dysfunction induces cell death of neurons through mitochondrial stress.
    Marubuchi S; Wada Y; Okuda T; Hara Y; Qi ML; Hoshino M; Nakagawa M; Kanazawa I; Okazawa H
    J Neurochem; 2005 Nov; 95(3):858-70. PubMed ID: 16104847
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Fishing for a mechanism: using zebrafish to understand spinal muscular atrophy.
    Beattie CE; Carrel TL; McWhorter ML
    J Child Neurol; 2007 Aug; 22(8):995-1003. PubMed ID: 17761655
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Hypomorphic Smn knockdown C2C12 myoblasts reveal intrinsic defects in myoblast fusion and myotube morphology.
    Shafey D; Côté PD; Kothary R
    Exp Cell Res; 2005 Nov; 311(1):49-61. PubMed ID: 16219305
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mitochondria, metabolic disturbances, oxidative stress and the kynurenine system, with focus on neurodegenerative disorders.
    Sas K; Robotka H; Toldi J; Vécsei L
    J Neurol Sci; 2007 Jun; 257(1-2):221-39. PubMed ID: 17462670
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Characterization of Ighmbp2 in motor neurons and implications for the pathomechanism in a mouse model of human spinal muscular atrophy with respiratory distress type 1 (SMARD1).
    Grohmann K; Rossoll W; Kobsar I; Holtmann B; Jablonka S; Wessig C; Stoltenburg-Didinger G; Fischer U; Hübner C; Martini R; Sendtner M
    Hum Mol Genet; 2004 Sep; 13(18):2031-42. PubMed ID: 15269181
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The spinal muscular atrophy disease protein SMN is linked to the Rho-kinase pathway via profilin.
    Nölle A; Zeug A; van Bergeijk J; Tönges L; Gerhard R; Brinkmann H; Al Rayes S; Hensel N; Schill Y; Apkhazava D; Jablonka S; O'mer J; Srivastav RK; Baasner A; Lingor P; Wirth B; Ponimaskin E; Niedenthal R; Grothe C; Claus P
    Hum Mol Genet; 2011 Dec; 20(24):4865-78. PubMed ID: 21920940
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Downregulation of glutaredoxin but not glutathione loss leads to mitochondrial dysfunction in female mice CNS: implications in excitotoxicity.
    Diwakar L; Kenchappa RS; Annepu J; Ravindranath V
    Neurochem Int; 2007 Jul; 51(1):37-46. PubMed ID: 17512091
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.