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Liu, D. HSPB8 Gene. Encyclopedia. Available online: https://encyclopedia.pub/entry/4117 (accessed on 29 September 2026).
Liu D. HSPB8 Gene. Encyclopedia. Available at: https://encyclopedia.pub/entry/4117. Accessed September 29, 2026.
Liu, Dean. "HSPB8 Gene" Encyclopedia, https://encyclopedia.pub/entry/4117 (accessed September 29, 2026).
Liu, D. (2020, December 23). HSPB8 Gene. In Encyclopedia. https://encyclopedia.pub/entry/4117
Liu, Dean. "HSPB8 Gene." Encyclopedia. Web. 23 December, 2020.
HSPB8 Gene
Edit

Heat shock protein family B (small) member 8

genes

References

  1. Bird TD. Charcot-Marie-Tooth (CMT) Hereditary Neuropathy Overview. 1998 Sep 28[updated 2020 May 14]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): Universityof Washington, Seattle; 1993-2020. Available fromhttp://www.ncbi.nlm.nih.gov/books/NBK1358/
  2. Datskevich PN, Nefedova VV, Sudnitsyna MV, Gusev NB. Mutations of small heatshock proteins and human congenital diseases. Biochemistry (Mosc). 2012Dec;77(13):1500-14. doi: 10.1134/S0006297912130081. Review.
  3. 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 denEnden AT, Wokke JH, Nelis E, De Jonghe P, Timmerman V. Relative contribution ofmutations in genes for autosomal dominant distal hereditary motor neuropathies: agenotype-phenotype correlation study. Brain. 2008 May;131(Pt 5):1217-27. doi:10.1093/brain/awn029.
  4. Drew AP, Blair IP, Nicholson GA. Molecular genetics and mechanisms of disease in distal hereditary motor neuropathies: insights directing future geneticstudies. Curr Mol Med. 2011 Nov;11(8):650-65. Review.
  5. Fontaine JM, Sun X, Hoppe AD, Simon S, Vicart P, Welsh MJ, Benndorf R.Abnormal small heat shock protein interactions involving neuropathy-associatedHSP22 (HSPB8) mutants. FASEB J. 2006 Oct;20(12):2168-70.
  6. Hu Z, Chen L, Zhang J, Li T, Tang J, Xu N, Wang X. Structure, function,property, and role in neurologic diseases and other diseases of the sHsp22. JNeurosci Res. 2007 Aug 1;85(10):2071-9. Review.
  7. Irobi J, Van Impe K, Seeman P, Jordanova A, Dierick I, Verpoorten N, Michalik A, De Vriendt E, Jacobs A, Van Gerwen V, Vennekens K, Mazanec R, Tournev I,Hilton-Jones D, Talbot K, Kremensky I, Van Den Bosch L, Robberecht W, VanVandekerckhove J, Van Broeckhoven C, Gettemans J, De Jonghe P, Timmerman V.Hot-spot residue in small heat-shock protein 22 causes distal motor neuropathy.Nat Genet. 2004 Jun;36(6):597-601.
  8. Nefedova VV, Muranova LK, Sudnitsyna MV, Ryzhavskaya AS, Gusev NB. Small Heat Shock Proteins and Distal Hereditary Neuropathies. Biochemistry (Mosc). 2015Dec;80(13):1734-47. doi: 10.1134/S000629791513009X. Review.
  9. Shemetov AA, Seit-Nebi AS, Gusev NB. Structure, properties, and functions ofthe human small heat-shock protein HSP22 (HspB8, H11, E2IG1): a critical review. J Neurosci Res. 2008 Feb 1;86(2):264-9. Review.
  10. Tang BS, Zhao GH, Luo W, Xia K, Cai F, Pan Q, Zhang RX, Zhang FF, Liu XM, ChenB, Zhang C, Shen L, Jiang H, Long ZG, Dai HP. Small heat-shock protein 22 mutatedin autosomal dominant Charcot-Marie-Tooth disease type 2L. Hum Genet. 2005Feb;116(3):222-4.
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