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 *

175 related articles for article (PubMed ID: 36619669)

  • 1. Survival motor neuron protein and neurite degeneration are regulated by Gemin3 in spinal muscular atrophy motoneurons.
    Miralles MP; Sansa A; Beltran M; Soler RM; Garcera A
    Front Cell Neurosci; 2022; 16():1054270. PubMed ID: 36619669
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Regulation of Survival Motor Neuron Protein by the Nuclear Factor-Kappa B Pathway in Mouse Spinal Cord Motoneurons.
    Arumugam S; Mincheva-Tasheva S; Periyakaruppiah A; de la Fuente S; Soler RM; Garcera A
    Mol Neurobiol; 2018 Jun; 55(6):5019-5030. PubMed ID: 28808928
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Calpain Inhibition Increases SMN Protein in Spinal Cord Motoneurons and Ameliorates the Spinal Muscular Atrophy Phenotype in Mice.
    de la Fuente S; Sansa A; Periyakaruppiah A; Garcera A; Soler RM
    Mol Neurobiol; 2019 Jun; 56(6):4414-4427. PubMed ID: 30327977
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Intracellular pathways involved in cell survival are deregulated in mouse and human spinal muscular atrophy motoneurons.
    Sansa A; de la Fuente S; Comella JX; Garcera A; Soler RM
    Neurobiol Dis; 2021 Jul; 155():105366. PubMed ID: 33845129
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Survival motor neuron protein reduction deregulates autophagy in spinal cord motoneurons in vitro.
    Garcera A; Bahi N; Periyakaruppiah A; Arumugam S; Soler RM
    Cell Death Dis; 2013 Jun; 4(6):e686. PubMed ID: 23788043
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Calpain system is altered in survival motor neuron-reduced cells from in vitro and in vivo spinal muscular atrophy models.
    de la Fuente S; Sansa A; Hidalgo I; Vivancos N; Romero-Guevara R; Garcera A; Soler RM
    Cell Death Dis; 2020 Jun; 11(6):487. PubMed ID: 32587237
    [TBL] [Abstract][Full Text] [Related]  

  • 7. ERK MAPK signaling pathway inhibition as a potential target to prevent autophagy alterations in Spinal Muscular Atrophy motoneurons.
    Sansa A; Miralles MP; Beltran M; Celma-Nos F; Calderó J; Garcera A; Soler RM
    Cell Death Discov; 2023 Apr; 9(1):113. PubMed ID: 37019880
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Spinal Muscular Atrophy autophagy profile is tissue-dependent: differential regulation between muscle and motoneurons.
    Sansa A; Hidalgo I; Miralles MP; de la Fuente S; Perez-Garcia MJ; Munell F; Soler RM; Garcera A
    Acta Neuropathol Commun; 2021 Jul; 9(1):122. PubMed ID: 34217376
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Disruption of snRNP biogenesis factors Tgs1 and pICln induces phenotypes that mirror aspects of SMN-Gemins complex perturbation in Drosophila, providing new insights into spinal muscular atrophy.
    Borg RM; Fenech Salerno B; Vassallo N; Bordonne R; Cauchi RJ
    Neurobiol Dis; 2016 Oct; 94():245-58. PubMed ID: 27388936
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Spinal motor neuron loss occurs through a p53-and-p21-independent mechanism in the Smn
    Reedich EJ; Kalski M; Armijo N; Cox GA; DiDonato CJ
    Exp Neurol; 2021 Mar; 337():113587. PubMed ID: 33382987
    [TBL] [Abstract][Full Text] [Related]  

  • 12. HuD and the Survival Motor Neuron Protein Interact in Motoneurons and Are Essential for Motoneuron Development, Function, and mRNA Regulation.
    Hao le T; Duy PQ; An M; Talbot J; Iyer CC; Wolman M; Beattie CE
    J Neurosci; 2017 Nov; 37(48):11559-11571. PubMed ID: 29061699
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Spinal astrocyte dysfunction drives motor neuron loss in late-onset spinal muscular atrophy.
    Schmitt LI; David C; Steffen R; Hezel S; Roos A; Schara-Schmidt U; Kleinschnitz C; Leo M; Hagenacker T
    Acta Neuropathol; 2023 May; 145(5):611-635. PubMed ID: 36930296
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Deficiency of the Survival of Motor Neuron Protein Impairs mRNA Localization and Local Translation in the Growth Cone of Motor Neurons.
    Fallini C; Donlin-Asp PG; Rouanet JP; Bassell GJ; Rossoll W
    J Neurosci; 2016 Mar; 36(13):3811-20. PubMed ID: 27030765
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Splicing changes in SMA mouse motoneurons and SMN-depleted neuroblastoma cells: evidence for involvement of splicing regulatory proteins.
    Huo Q; Kayikci M; Odermatt P; Meyer K; Michels O; Saxena S; Ule J; Schümperli D
    RNA Biol; 2014; 11(11):1430-46. PubMed ID: 25692239
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Chronic treatment with lithium does not improve neuromuscular phenotype in a mouse model of severe spinal muscular atrophy.
    Dachs E; Piedrafita L; Hereu M; Esquerda JE; Calderó J
    Neuroscience; 2013 Oct; 250():417-33. PubMed ID: 23876328
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Decreased microRNA levels lead to deleterious increases in neuronal M2 muscarinic receptors in Spinal Muscular Atrophy models.
    O'Hern PJ; do Carmo G Gonçalves I; Brecht J; López Soto EJ; Simon J; Chapkis N; Lipscombe D; Kye MJ; Hart AC
    Elife; 2017 May; 6():. PubMed ID: 28463115
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Activating ATF6 in spinal muscular atrophy promotes SMN expression and motor neuron survival through the IRE1α-XBP1 pathway.
    D'Amico D; Biondi O; Januel C; Bezier C; Sapaly D; Clerc Z; El Khoury M; Sundaram VK; Houdebine L; Josse T; Della Gaspera B; Martinat C; Massaad C; Weill L; Charbonnier F
    Neuropathol Appl Neurobiol; 2022 Aug; 48(5):e12816. PubMed ID: 35338505
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Gemin3: A novel DEAD box protein that interacts with SMN, the spinal muscular atrophy gene product, and is a component of gems.
    Charroux B; Pellizzoni L; Perkinson RA; Shevchenko A; Mann M; Dreyfuss G
    J Cell Biol; 1999 Dec; 147(6):1181-94. PubMed ID: 10601333
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Triptolide increases transcript and protein levels of survival motor neurons in human SMA fibroblasts and improves survival in SMA-like mice.
    Hsu YY; Jong YJ; Tsai HH; Tseng YT; An LM; Lo YC
    Br J Pharmacol; 2012 Jun; 166(3):1114-26. PubMed ID: 22220673
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.