BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

200 related articles for article (PubMed ID: 38554151)

  • 1. Pathogenic effects of Leu200Pro and Arg387His VRK1 protein variants on phosphorylation targets and H4K16 acetylation in distal hereditary motor neuropathy.
    Campos-Díaz A; Morejón-García P; Monte-Serrano E; Ros-Pardo D; Marcos-Alcalde I; Gómez-Puertas P; Lazo PA
    J Mol Med (Berl); 2024 Jun; 102(6):801-817. PubMed ID: 38554151
    [TBL] [Abstract][Full Text] [Related]  

  • 2. VRK1 functional insufficiency due to alterations in protein stability or kinase activity of human VRK1 pathogenic variants implicated in neuromotor syndromes.
    Martín-Doncel E; Rojas AM; Cantarero L; Lazo PA
    Sci Rep; 2019 Sep; 9(1):13381. PubMed ID: 31527692
    [TBL] [Abstract][Full Text] [Related]  

  • 3. VRK1 variants at the cross road of Cajal body neuropathogenic mechanisms in distal neuropathies and motor neuron diseases.
    Lazo PA; Morejón-García P
    Neurobiol Dis; 2023 Jul; 183():106172. PubMed ID: 37257665
    [TBL] [Abstract][Full Text] [Related]  

  • 4. VRK1 (Y213H) homozygous mutant impairs Cajal bodies in a hereditary case of distal motor neuropathy.
    Marcos AT; Martín-Doncel E; Morejón-García P; Marcos-Alcalde I; Gómez-Puertas P; Segura-Puimedon M; Armengol L; Navarro-Pando JM; Lazo PA
    Ann Clin Transl Neurol; 2020 May; 7(5):808-818. PubMed ID: 32365420
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Loss of Cajal bodies in motor neurons from patients with novel mutations in VRK1.
    El-Bazzal L; Rihan K; Bernard-Marissal N; Castro C; Chouery-Khoury E; Desvignes JP; Atkinson A; Bertaux K; Koussa S; Lévy N; Bartoli M; Mégarbané A; Jabbour R; Delague V
    Hum Mol Genet; 2019 Jul; 28(14):2378-2394. PubMed ID: 31090908
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Nuclear functions regulated by the VRK1 kinase.
    Lazo PA
    Nucleus; 2024 Dec; 15(1):2353249. PubMed ID: 38753965
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Motor neuron diseases caused by a novel VRK1 variant - A genotype/phenotype study.
    Sedghi M; Moslemi AR; Olive M; Etemadifar M; Ansari B; Nasiri J; Emrahi L; Mianesaz HR; Laing NG; Tajsharghi H
    Ann Clin Transl Neurol; 2019 Nov; 6(11):2197-2204. PubMed ID: 31560180
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A novel
    Feng SY; Li LY; Feng SM; Zou ZY
    Ann Clin Transl Neurol; 2019 Feb; 6(2):401-405. PubMed ID: 30847374
    [TBL] [Abstract][Full Text] [Related]  

  • 9.
    Silva DP; Soeiro E Sá M; Silveira F; Pinto S; Gromicho M; Sousa AB; Leão M; De Carvalho M
    Amyotroph Lateral Scler Frontotemporal Degener; 2020 May; 21(3-4):291-295. PubMed ID: 32242460
    [No Abstract]   [Full Text] [Related]  

  • 10. VRK1 Kinase Activity Modulating Histone H4K16 Acetylation Inhibited by SIRT2 and VRK-IN-1.
    Monte-Serrano E; Lazo PA
    Int J Mol Sci; 2023 Mar; 24(5):. PubMed ID: 36902348
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Olaparib and ionizing radiation trigger a cooperative DNA-damage repair response that is impaired by depletion of the VRK1 chromatin kinase.
    Campillo-Marcos I; Lazo PA
    J Exp Clin Cancer Res; 2019 May; 38(1):203. PubMed ID: 31101118
    [TBL] [Abstract][Full Text] [Related]  

  • 12. VRK1 chromatin kinase phosphorylates H2AX and is required for foci formation induced by DNA damage.
    Salzano M; Sanz-García M; Monsalve DM; Moura DS; Lazo PA
    Epigenetics; 2015; 10(5):373-83. PubMed ID: 25923214
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Identification of a homozygous VRK1 mutation in two patients with adult-onset distal hereditary motor neuropathy.
    Greenbaum L; Barel O; Nikitin V; Hersalis-Eldar A; Kol N; Reznik-Wolf H; Dominissini D; Pras E; Dori A
    Muscle Nerve; 2020 Mar; 61(3):395-400. PubMed ID: 31837156
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Substrate profiling of human vaccinia-related kinases identifies coilin, a Cajal body nuclear protein, as a phosphorylation target with neurological implications.
    Sanz-García M; Vázquez-Cedeira M; Kellerman E; Renbaum P; Levy-Lahad E; Lazo PA
    J Proteomics; 2011 Dec; 75(2):548-60. PubMed ID: 21920476
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Depletion of the protein kinase VRK1 disrupts nuclear envelope morphology and leads to BAF retention on mitotic chromosomes.
    Molitor TP; Traktman P
    Mol Biol Cell; 2014 Mar; 25(6):891-903. PubMed ID: 24430874
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Dysfunctional Homozygous VRK1-D263G Variant Impairs the Assembly of Cajal Bodies and DNA Damage Response in Hereditary Spastic Paraplegia.
    Morejon-Garcia P; Keren B; Marcos-Alcalde I; Gomez-Puertas P; Mochel F; Lazo PA
    Neurol Genet; 2021 Oct; 7(5):e624. PubMed ID: 34504951
    [TBL] [Abstract][Full Text] [Related]  

  • 17. VRK1 Regulates Sensitivity to Oxidative Stress by Altering Histone Epigenetic Modifications and the Nuclear Phosphoproteome in Tumor Cells.
    Navarro-Carrasco E; Monte-Serrano E; Campos-Díaz A; Rolfs F; de Goeij-de Haas R; Pham TV; Piersma SR; González-Alonso P; Jiménez CR; Lazo PA
    Int J Mol Sci; 2024 Apr; 25(9):. PubMed ID: 38732093
    [TBL] [Abstract][Full Text] [Related]  

  • 18. VRK1 regulates Cajal body dynamics and protects coilin from proteasomal degradation in cell cycle.
    Cantarero L; Sanz-García M; Vinograd-Byk H; Renbaum P; Levy-Lahad E; Lazo PA
    Sci Rep; 2015 Jun; 5():10543. PubMed ID: 26068304
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Novel motor phenotypes in patients with VRK1 mutations without pontocerebellar hypoplasia.
    Stoll M; Teoh H; Lee J; Reddel S; Zhu Y; Buckley M; Sampaio H; Roscioli T; Farrar M; Nicholson G
    Neurology; 2016 Jul; 87(1):65-70. PubMed ID: 27281532
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The human VRK1 chromatin kinase in cancer biology.
    Campillo-Marcos I; García-González R; Navarro-Carrasco E; Lazo PA
    Cancer Lett; 2021 Apr; 503():117-128. PubMed ID: 33516791
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.