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 *

209 related articles for article (PubMed ID: 31630804)

  • 1. 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]  

  • 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. 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]  

  • 4. 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]  

  • 5. Clinical features of a family with late-onset distal hereditary motor neuropathy harboring p.Pro39Leu variant of HSPB1.
    Naruse H; Okubo S; Sudo A; Mitsui J; Mikata T; Ishiura H; Morishita S; Tsuji S; Toda T
    J Peripher Nerv Syst; 2023 Sep; 28(3):518-521. PubMed ID: 37249095
    [TBL] [Abstract][Full Text] [Related]  

  • 6. HSPB1 and HSPB8 in inherited neuropathies: study of an Italian cohort of dHMN and CMT2 patients.
    Capponi S; Geroldi A; Fossa P; Grandis M; Ciotti P; Gulli R; Schenone A; Mandich P; Bellone E
    J Peripher Nerv Syst; 2011 Dec; 16(4):287-94. PubMed ID: 22176143
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Pilot phenotype and natural history study of hereditary neuropathies caused by mutations in the HSPB1 gene.
    Rossor AM; Morrow JM; Polke JM; Murphy SM; Houlden H; ; Laura M; Manji H; Blake J; Reilly MM
    Neuromuscul Disord; 2017 Jan; 27(1):50-56. PubMed ID: 27816334
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Further evidence for genetic heterogeneity of distal HMN type V, CMT2 with predominant hand involvement and Silver syndrome.
    Rohkamm B; Reilly MM; Lochmüller H; Schlotter-Weigel B; Barisic N; Schöls L; Nicholson G; Pareyson D; Laurà M; Janecke AR; Miltenberger-Miltenyi G; John E; Fischer C; Grill F; Wakeling W; Davis M; Pieber TR; Auer-Grumbach M
    J Neurol Sci; 2007 Dec; 263(1-2):100-6. PubMed ID: 17663003
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 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. PINK1 and Parkin rescue motor defects and mitochondria dysfunction induced by a patient-derived HSPB3 mutant in Drosophila models.
    Han JE; Kang KH; Kim H; Hong YB; Choi BO; Koh H
    Biochem Biophys Res Commun; 2023 Nov; 682():71-76. PubMed ID: 37804589
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. The distal hereditary motor neuropathies.
    Rossor AM; Kalmar B; Greensmith L; Reilly MM
    J Neurol Neurosurg Psychiatry; 2012 Jan; 83(1):6-14. PubMed ID: 22028385
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Heterogeneous Clinical Phenotypes of dHMN Caused by Mutation in
    Shen X; Zhang J; Zhan F; Tian W; Jiang Q; Luan X; Zhang X; Cao L
    Biomolecules; 2022 Sep; 12(10):. PubMed ID: 36291591
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Molecular analysis and clinical diversity of distal hereditary motor neuropathy.
    Liu X; Duan X; Zhang Y; Sun A; Fan D
    Eur J Neurol; 2020 Jul; 27(7):1319-1326. PubMed ID: 32298515
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular genetics and mechanisms of disease in distal hereditary motor neuropathies: insights directing future genetic studies.
    Drew AP; Blair IP; Nicholson GA
    Curr Mol Med; 2011 Nov; 11(8):650-65. PubMed ID: 21902652
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mutations in the HSP27 (HSPB1) gene cause dominant, recessive, and sporadic distal HMN/CMT type 2.
    Houlden H; Laura M; Wavrant-De Vrièze F; Blake J; Wood N; Reilly MM
    Neurology; 2008 Nov; 71(21):1660-8. PubMed ID: 18832141
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Relative contribution of mutations in genes for autosomal dominant distal hereditary motor neuropathies: a genotype-phenotype correlation study.
    Dierick I; Baets J; Irobi J; Jacobs A; De Vriendt E; Deconinck T; Merlini L; Van den Bergh P; Rasic VM; Robberecht W; Fischer D; Morales RJ; Mitrovic Z; Seeman P; Mazanec R; Kochanski A; Jordanova A; Auer-Grumbach M; Helderman-van den Enden AT; Wokke JH; Nelis E; De Jonghe P; Timmerman V
    Brain; 2008 May; 131(Pt 5):1217-27. PubMed ID: 18325928
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.