299 related articles for article (PubMed ID: 28595321)
1. Mitochondrial deficits and abnormal mitochondrial retrograde axonal transport play a role in the pathogenesis of mutant Hsp27-induced Charcot Marie Tooth Disease.
Kalmar B; Innes A; Wanisch K; Kolaszynska AK; Pandraud A; Kelly G; Abramov AY; Reilly MM; Schiavo G; Greensmith L
Hum Mol Genet; 2017 Sep; 26(17):3313-3326. PubMed ID: 28595321
[TBL] [Abstract][Full Text] [Related]
2. Mitochondrial dynamics and inherited peripheral nerve diseases.
Pareyson D; Saveri P; Sagnelli A; Piscosquito G
Neurosci Lett; 2015 Jun; 596():66-77. PubMed ID: 25847151
[TBL] [Abstract][Full Text] [Related]
3. Charcot-Marie-Tooth causing HSPB1 mutations increase Cdk5-mediated phosphorylation of neurofilaments.
Holmgren A; Bouhy D; De Winter V; Asselbergh B; Timmermans JP; Irobi J; Timmerman V
Acta Neuropathol; 2013 Jul; 126(1):93-108. PubMed ID: 23728742
[TBL] [Abstract][Full Text] [Related]
4. Altered axonal mitochondrial transport in the pathogenesis of Charcot-Marie-Tooth disease from mitofusin 2 mutations.
Baloh RH; Schmidt RE; Pestronk A; Milbrandt J
J Neurosci; 2007 Jan; 27(2):422-30. PubMed ID: 17215403
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Decreased ceramide underlies mitochondrial dysfunction in Charcot-Marie-Tooth 2F.
Schwartz NU; Linzer RW; Truman JP; Gurevich M; Hannun YA; Senkal CE; Obeid LM
FASEB J; 2018 Mar; 32(3):1716-1728. PubMed ID: 29133339
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Characterization of New Transgenic Mouse Models for Two Charcot-Marie-Tooth-Causing HspB1 Mutations using the Rosa26 Locus.
Bouhy D; Geuens T; De Winter V; Almeida-Souza L; Katona I; Weis J; Hochepied T; Goossens S; Haigh JJ; Janssens S; Timmerman V
J Neuromuscul Dis; 2016 May; 3(2):183-200. PubMed ID: 27854215
[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. Charcot-Marie-Tooth 2F (Hsp27 mutations): A review.
Schwartz NU
Neurobiol Dis; 2019 Oct; 130():104505. PubMed ID: 31212070
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Mutation analysis of the small heat shock protein 27 gene in chinese patients with Charcot-Marie-Tooth disease.
Tang B; Liu X; Zhao G; Luo W; Xia K; Pan Q; Cai F; Hu Z; Zhang C; Chen B; Zhang F; Shen L; Zhang R; Jiang H
Arch Neurol; 2005 Aug; 62(8):1201-7. PubMed ID: 16087758
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Overexpression of mutant HSP27 causes axonal neuropathy in mice.
Lee J; Jung SC; Joo J; Choi YR; Moon HW; Kwak G; Yeo HK; Lee JS; Ahn HJ; Jung N; Hwang S; Rheey J; Woo SY; Kim JY; Hong YB; Choi BO
J Biomed Sci; 2015 Jun; 22(1):43. PubMed ID: 26141737
[TBL] [Abstract][Full Text] [Related]
15. Mitochondrial and axonal abnormalities precede disruption of the neurofilament network in a model of charcot-marie-tooth disease type 2E and are prevented by heat shock proteins in a mutant-specific fashion.
Tradewell ML; Durham HD; Mushynski WE; Gentil BJ
J Neuropathol Exp Neurol; 2009 Jun; 68(6):642-52. PubMed ID: 19458545
[TBL] [Abstract][Full Text] [Related]
16. A mutation in the small heat-shock protein HSPB1 leading to distal hereditary motor neuronopathy disrupts neurofilament assembly and the axonal transport of specific cellular cargoes.
Ackerley S; James PA; Kalli A; French S; Davies KE; Talbot K
Hum Mol Genet; 2006 Jan; 15(2):347-54. PubMed ID: 16368711
[TBL] [Abstract][Full Text] [Related]
17. Mitofusin 2 is necessary for transport of axonal mitochondria and interacts with the Miro/Milton complex.
Misko A; Jiang S; Wegorzewska I; Milbrandt J; Baloh RH
J Neurosci; 2010 Mar; 30(12):4232-40. PubMed ID: 20335458
[TBL] [Abstract][Full Text] [Related]
18. Heat shock protein 27 R127W mutation: evidence of a continuum between axonal Charcot-Marie-Tooth and distal hereditary motor neuropathy.
Solla P; Vannelli A; Bolino A; Marrosu G; Coviello S; Murru MR; Tranquilli S; Corongiu D; Benedetti S; Marrosu MG
J Neurol Neurosurg Psychiatry; 2010 Sep; 81(9):958-62. PubMed ID: 20660910
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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]
[Next] [New Search]