128 related articles for article (PubMed ID: 15296780)
1. Neuronal diseases: small heat shock proteins calm your nerves.
Der Perng M; Quinlan RA
Curr Biol; 2004 Aug; 14(15):R625-6. PubMed ID: 15296780
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. 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]
5. Novel insights in the disease biology of mutant small heat shock proteins in neuromuscular diseases.
Adriaenssens E; Geuens T; Baets J; Echaniz-Laguna A; Timmerman V
Brain; 2017 Oct; 140(10):2541-2549. PubMed ID: 28969372
[TBL] [Abstract][Full Text] [Related]
6. Small heat shock protein 27 mutation in a Japanese patient with distal hereditary motor neuropathy.
Kijima K; Numakura C; Goto T; Takahashi T; Otagiri T; Umetsu K; Hayasaka K
J Hum Genet; 2005; 50(9):473-476. PubMed ID: 16155736
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Hereditary motor neuropathy and heat shock proteins: a shocking transformation.
Gooch C; Shy M
Neurology; 2008 Nov; 71(21):1656-7. PubMed ID: 19015482
[No Abstract] [Full Text] [Related]
9. Axonal Neuropathies due to Mutations in Small Heat Shock Proteins: Clinical, Genetic, and Functional Insights into Novel Mutations.
Echaniz-Laguna A; Geuens T; Petiot P; Péréon Y; Adriaenssens E; Haidar M; Capponi S; Maisonobe T; Fournier E; Dubourg O; Degos B; Salachas F; Lenglet T; Eymard B; Delmont E; Pouget J; Juntas Morales R; Goizet C; Latour P; Timmerman V; Stojkovic T
Hum Mutat; 2017 May; 38(5):556-568. PubMed ID: 28144995
[TBL] [Abstract][Full Text] [Related]
10. HspB8, a small heat shock protein mutated in human neuromuscular disorders, has in vivo chaperone activity in cultured cells.
Carra S; Sivilotti M; Chávez Zobel AT; Lambert H; Landry J
Hum Mol Genet; 2005 Jun; 14(12):1659-69. PubMed ID: 15879436
[TBL] [Abstract][Full Text] [Related]
11. Abnormal small heat shock protein interactions involving neuropathy-associated HSP22 (HSPB8) mutants.
Fontaine JM; Sun X; Hoppe AD; Simon S; Vicart P; Welsh MJ; Benndorf R
FASEB J; 2006 Oct; 20(12):2168-70. PubMed ID: 16935933
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. Chaperoning motor neurons.
Pleasure D
Arch Neurol; 2005 Aug; 62(8):1193. PubMed ID: 16087756
[No Abstract] [Full Text] [Related]
15. [Study on aggregate formation mechanism of HSPB8 gene mutation resulting in CMT2L].
Zhang RX; Tang BS; Zi XH; Xia K; Pan Q; Zhang FF; Li SJ; Zhao GH; Guo K
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Dec; 23(6):601-4. PubMed ID: 17160934
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Abnormal interaction of motor neuropathy-associated mutant HspB8 (Hsp22) forms with the RNA helicase Ddx20 (gemin3).
Sun X; Fontaine JM; Hoppe AD; Carra S; DeGuzman C; Martin JL; Simon S; Vicart P; Welsh MJ; Landry J; Benndorf R
Cell Stress Chaperones; 2010 Sep; 15(5):567-82. PubMed ID: 20157854
[TBL] [Abstract][Full Text] [Related]
18. Altered TDP-43-dependent splicing in HSPB8-related distal hereditary motor neuropathy and myofibrillar myopathy.
Cortese A; Laurà M; Casali C; Nishino I; Hayashi YK; Magri S; Taroni F; Stuani C; Saveri P; Moggio M; Ripolone M; Prelle A; Pisciotta C; Sagnelli A; Pichiecchio A; Reilly MM; Buratti E; Pareyson D
Eur J Neurol; 2018 Jan; 25(1):154-163. PubMed ID: 29029362
[TBL] [Abstract][Full Text] [Related]
19. The Role of the Arginine in the Conserved N-Terminal Domain RLFDQxFG Motif of Human Small Heat Shock Proteins HspB1, HspB4, HspB5, HspB6, and HspB8.
Shatov VM; Weeks SD; Strelkov SV; Gusev NB
Int J Mol Sci; 2018 Jul; 19(7):. PubMed ID: 30036999
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]