BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

256 related articles for article (PubMed ID: 32301006)

  • 1. Mutations in HspB1 and hereditary neuropathies.
    Muranova LK; Sudnitsyna MV; Strelkov SV; Gusev NB
    Cell Stress Chaperones; 2020 Jul; 25(4):655-665. PubMed ID: 32301006
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Neuropathy-causing mutations in HSPB1 impair autophagy by disturbing the formation of SQSTM1/p62 bodies.
    Haidar M; Asselbergh B; Adriaenssens E; De Winter V; Timmermans JP; Auer-Grumbach M; Juneja M; Timmerman V
    Autophagy; 2019 Jun; 15(6):1051-1068. PubMed ID: 30669930
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Characterization of Mutants of Human Small Heat Shock Protein HspB1 Carrying Replacements in the N-Terminal Domain and Associated with Hereditary Motor Neuron Diseases.
    Muranova LK; Weeks SD; Strelkov SV; Gusev NB
    PLoS One; 2015; 10(5):e0126248. PubMed ID: 25965061
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Characterization of human small heat shock protein HSPB1 α-crystallin domain localized mutants associated with hereditary motor neuron diseases.
    Weeks SD; Muranova LK; Heirbaut M; Beelen S; Strelkov SV; Gusev NB
    Sci Rep; 2018 Jan; 8(1):688. PubMed ID: 29330367
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Structure and properties of G84R and L99M mutants of human small heat shock protein HspB1 correlating with motor neuropathy.
    Nefedova VV; Sudnitsyna MV; Strelkov SV; Gusev NB
    Arch Biochem Biophys; 2013 Oct; 538(1):16-24. PubMed ID: 23948568
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mutant HSPB1 causes loss of translational repression by binding to PCBP1, an RNA binding protein with a possible role in neurodegenerative disease.
    Geuens T; De Winter V; Rajan N; Achsel T; Mateiu L; Almeida-Souza L; Asselbergh B; Bouhy D; Auer-Grumbach M; Bagni C; Timmerman V
    Acta Neuropathol Commun; 2017 Jan; 5(1):5. PubMed ID: 28077174
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Disruption of neurofilament network with aggregation of light neurofilament protein: a common pathway leading to motor neuron degeneration due to Charcot-Marie-Tooth disease-linked mutations in NFL and HSPB1.
    Zhai J; Lin H; Julien JP; Schlaepfer WW
    Hum Mol Genet; 2007 Dec; 16(24):3103-16. PubMed ID: 17881652
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mutations in heat shock protein beta-1 (HSPB1) are associated with a range of clinical phenotypes related to different patterns of motor neuron dysfunction: A case series.
    Katz M; Davis M; Garton FC; Henderson R; Bharti V; Wray N; McCombe P
    J Neurol Sci; 2020 Jun; 413():116809. PubMed ID: 32334137
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mutant small heat-shock protein 27 causes axonal Charcot-Marie-Tooth disease and distal hereditary motor neuropathy.
    Evgrafov OV; Mersiyanova I; Irobi J; Van Den Bosch L; Dierick I; Leung CL; Schagina O; Verpoorten N; Van Impe K; Fedotov V; Dadali E; Auer-Grumbach M; Windpassinger C; Wagner K; Mitrovic Z; Hilton-Jones D; Talbot K; Martin JJ; Vasserman N; Tverskaya S; Polyakov A; Liem RK; Gettemans J; Robberecht W; De Jonghe P; Timmerman V
    Nat Genet; 2004 Jun; 36(6):602-6. PubMed ID: 15122254
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Increased monomerization of mutant HSPB1 leads to protein hyperactivity in Charcot-Marie-Tooth neuropathy.
    Almeida-Souza L; Goethals S; de Winter V; Dierick I; Gallardo R; Van Durme J; Irobi J; Gettemans J; Rousseau F; Schymkowitz J; Timmerman V; Janssens S
    J Biol Chem; 2010 Apr; 285(17):12778-86. PubMed ID: 20178975
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A Charcot-Marie-Tooth-Causing Mutation in HSPB1 Decreases Cell Adaptation to Repeated Stress by Disrupting Autophagic Clearance of Misfolded Proteins.
    Zhang X; Qiao Y; Han R; Gao Y; Yang X; Zhang Y; Wan Y; Yu W; Pan X; Xing J
    Cells; 2022 Sep; 11(18):. PubMed ID: 36139461
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Charcot-Marie-Tooth disease type 2F associated with biallelic HSPB1 mutations.
    Abati E; Magri S; Meneri M; Manenti G; Velardo D; Balistreri F; Pisciotta C; Saveri P; Bresolin N; Comi GP; Ronchi D; Pareyson D; Taroni F; Corti S
    Ann Clin Transl Neurol; 2021 May; 8(5):1158-1164. PubMed ID: 33943041
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Characterization of human small heat shock protein HspB1 that carries C-terminal domain mutations associated with hereditary motor neuron diseases.
    Chalova AS; Sudnitsyna MV; Strelkov SV; Gusev NB
    Biochim Biophys Acta; 2014 Dec; 1844(12):2116-26. PubMed ID: 25220807
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mutant HSPB1 overexpression in neurons is sufficient to cause age-related motor neuronopathy in mice.
    Srivastava AK; Renusch SR; Naiman NE; Gu S; Sneh A; Arnold WD; Sahenk Z; Kolb SJ
    Neurobiol Dis; 2012 Aug; 47(2):163-73. PubMed ID: 22521462
    [TBL] [Abstract][Full Text] [Related]  

  • 15. HSPB1 mutations causing hereditary neuropathy in humans disrupt non-cell autonomous protection of motor neurons.
    Heilman PL; Song S; Miranda CJ; Meyer K; Srivastava AK; Knapp A; Wier CG; Kaspar BK; Kolb SJ
    Exp Neurol; 2017 Nov; 297():101-109. PubMed ID: 28797631
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Human HSPB1 mutation recapitulates features of distal hereditary motor neuropathy (dHMN) in Drosophila.
    Kang KH; Han JE; Hong YB; Nam SH; Choi BO; Koh H
    Biochem Biophys Res Commun; 2020 Jan; 521(1):220-226. PubMed ID: 31630804
    [TBL] [Abstract][Full Text] [Related]  

  • 17. HDAC6 inhibitors reverse axonal loss in a mouse model of mutant HSPB1-induced Charcot-Marie-Tooth disease.
    d'Ydewalle C; Krishnan J; Chiheb DM; Van Damme P; Irobi J; Kozikowski AP; Vanden Berghe P; Timmerman V; Robberecht W; Van Den Bosch L
    Nat Med; 2011 Jul; 17(8):968-74. PubMed ID: 21785432
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Specific sequences in the N-terminal domain of human small heat-shock protein HSPB6 dictate preferential hetero-oligomerization with the orthologue HSPB1.
    Heirbaut M; Lermyte F; Martin EM; Beelen S; Sobott F; Strelkov SV; Weeks SD
    J Biol Chem; 2017 Jun; 292(24):9944-9957. PubMed ID: 28487364
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Heterooligomeric complexes formed by human small heat shock proteins HspB1 (Hsp27) and HspB6 (Hsp20).
    Bukach OV; Glukhova AE; Seit-Nebi AS; Gusev NB
    Biochim Biophys Acta; 2009 Mar; 1794(3):486-95. PubMed ID: 19100870
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A novel p.T139M mutation in HSPB1 highlighting the phenotypic spectrum in a family.
    Amornvit J; Yalvac ME; Chen L; Sahenk Z
    Brain Behav; 2017 Aug; 7(8):e00774. PubMed ID: 28828227
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.