| 1 | CMT2L, HSPB8
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| HspB8 mutation causing hereditary distal motor neuropathy impairs lysosomal delivery of autophagosomes.
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| Kwok AS, Phadwal K, Turner BJ, Oliver PL, Raw A, Simon AK, Talbot K, Agashe VR.
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| J Neurochem 119(6):1155-61. doi: 10.1111/j.1471-4159.2011.07521.x. Epub 2011 Nov 3.
2011
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| 2 | DDX20, HSPB8
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| Abnormal interaction of motor neuropathy-associated mutant HspB8 (Hsp22) forms with the RNA helicase Ddx20 (gemin3).
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| Sun X, Fontaine JM, Hoppe AD, Carra S, DeGuzman C, Martin JL, Simon S, Vicart P, Welsh MJ, Landry J, Benndorf R.
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| Cell Stress Chaperones 15(5):567-82. Epub 2010 Feb 17.PMID: 20157854 2010
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| 3 | HSPB8
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| The small heat shock protein B8 (HspB8) promotes autophagic removal of misfolded proteins involved in amyotrophic lateral sclerosis (ALS).
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| Crippa V, Sau D, Rusmini P, Boncoraglio A, Onesto E, Bolzoni E, Galbiati M, Fontana E, Marino M, Carra S, Bendotti C, De Biasi S, Poletti A.
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| Hum Mol Genet 19(17):3440-56. Epub 2010 Jun 22.PMID: 20570967 2010
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| 4 | HSPB8
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| Identification of the Drosophila ortholog of HSPB8: implication of HSPB8 loss of function in protein folding diseases.
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| Carra S, Boncoraglio A, Kanon B, Brunsting JF, Minoia M, Rana A, Vos MJ, Seidel K, Sibon OC, Kampinga HH.
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| J Biol Chem 285(48):37811-22. Epub 2010 Sep 21.PMID: 20858900 2010
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| 5 | HSPB8
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| A role of small heat shock protein B8 (HspB8) in the autophagic removal of misfolded proteins responsible for neurodegenerative diseases.
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| Crippa V, Carra S, Rusmini P, Sau D, Bolzoni E, Bendotti C, De Biasi S, Poletti A.
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| Autophagy 6(7):958-60. Epub 2010 Oct 16.PMID: 20699640 2010
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| 6 | CMT2L, HSPB8
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| Mutant HSPB8 causes motor neuron-specific neurite degeneration.
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| Irobi J, Almeida-Souza L, Asselbergh B, De Winter V, Goethals S, Dierick I, Krishnan J, Timmermans JP, Robberecht W, De Jonghe P, Van Den Bosch L, Janssens S, Timmerman V.
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| Hum Mol Genet 19(16):3254-65. Epub 2010 Jun 10.PMID: 20538880 2010
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| 7 | HSPB7, HSPB8
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| HSPB7 is the most potent polyQ aggregation suppressor within the HSPB family of molecular chaperones.
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| Vos MJ, Zijlstra MP, Kanon B, van Waarde-Verhagen MA, Brunt ER, Oosterveld-Hut HM, Carra S, Sibon OC, Kampinga HH.
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| Hum Mol Genet 19(23):4677-93. Epub 2010 Sep 15. 2010
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| 8 | BAG3, HSPB6, HSPB8
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| Identification of the key structural motifs involved in HspB8/HspB6-Bag3 interaction.
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| Fuchs M, Poirier DJ, Seguin SJ, Lambert H, Carra S, Charette SJ, Landry J.
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| Biochem J 425(1):245-55. Erratum in: Biochem J. 2010 Aug 27;430(3):559. PMID: 19845507 2009
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| 9 | BAG3, HSPB8
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| HspB8 and Bag3: a new chaperone complex targeting misfolded proteins to macroautophagy.
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| Carra S, Seguin SJ, Landry J.
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| Autophagy 4(2):237-9. Epub 2007 Dec 11. Review.PMID: 18094623 2008
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| 10 | HSPB8
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| HspB8 chaperone activity toward poly(Q)-containing proteins depends on its association with Bag3, a stimulator of macroautophagy.
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| Carra S, Seguin SJ, Lambert H, Landry J.
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| J Biol Chem 283(3):1437-44. Epub 2007 Nov 15.PMID: 18006506 2008
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| 11 | HSPB8
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| Structure, properties, and functions of the human small heat-shock protein HSP22 (HspB8, H11, E2IG1): a critical review.
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| Shemetov AA, Seit-Nebi AS, Gusev NB.
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| J Neurosci Res 86(2):264-9. Review.PMID: 17722063 2008
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| 12 | HSPB8
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| Structure, function, property, and role in neurologic diseases and other diseases of the sHsp22.
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| Hu Z, Chen L, Zhang J, Li T, Tang J, Xu N, Wang X.
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| J Neurosci Res 85(10):2071-9. Review.PMID: 17304582 2007
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| 13 | CMT2L, HSPB8
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| Abnormal small heat shock protein interactions involving neuropathy-associated HSP22 (HSPB8) mutants.
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| Fontaine JM, Sun X, Hoppe AD, Simon S, Vicart P, Welsh MJ, Benndorf R.
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| FASEB J 20(12):2168-70. Epub 2006 Aug 25.PMID: 16935933 2006
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| 14 | CMT2L, HSPB8
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| Small heat-shock protein 22 mutated in autosomal dominant Charcot-Marie-Tooth disease type 2L.
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| Tang BS, Zhao GH, Luo W, Xia K, Cai F, Pan Q, Zhang RX, Zhang FF, Liu XM, Chen B, Zhang C, Shen L, Jiang H, Long ZG, Dai HP.
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| Hum Genet 116(3):222-224. Epub 2004 Nov 23. 2005
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| 15 | HSPB8
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| HspB8, a small heat shock protein mutated in human neuromuscular disorders, has in vivo chaperone activity in cultured cells.
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| Carra S, Sivilotti M, Chavez Zobel AT, Lambert H, Landry J.
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| Hum Mol Genet 14(12):1659-69. Epub 2005 May 6. 2005
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| 16 | CRYAB, HSPB1, HSPB3, HSPB6, HSPB8
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| Interactions of HSP22 (HSPB8) with HSP20, alphaB-crystallin, and HSPB3.
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| Fontaine JM, Sun X, Benndorf R, Welsh MJ.
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| Biochem Biophys Res Commun 337(3):1006-11. Epub 2005 Oct 3. 2005
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| 17 | HSPB8, HMN2
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| Hot-spot residue in small heat-shock protein 22 causes distal motor neuropathy.
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| 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, Van Vandekerckhove J, Broeckhoven C, Gettemans J, De Jonghe P, Timmerman V.
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| Nat Genet 36(6):597-601. Epub 2004 May 02. 2004
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| 18 | HSPB8, HSPB1
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| Interaction of human HSP22 (HSPB8) with other small heat shock proteins.
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| Sun X, Fontaine JM, Rest JS, Shelden EA, Welsh MJ, Benndorf R.
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| J Biol Chem 279(4):2394-402. Epub 2003 Oct 31. 2004
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| 19 | HSPB8, HSPB9
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| Expression analysis and chromosome location of a novel gene (H11) associated with the growth of human melanoma cells.
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| Yu YX, Heller A, Liehr T, Smith CC, Aurelian L.
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| Int J Oncol 18(5):905-11. 2001
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| 20 | HSPB8
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| HSP22, a new member of the small heat shock protein superfamily, interacts with mimic of phosphorylated HSP27 ((3D)HSP27).
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| Benndorf R, Sun X, Gilmont RR, Biederman KJ, Molloy MP, Goodmurphy CW, Cheng H, Andrews PC, Welsh MJ.
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| J Biol Chem 276(29):26753-61. 2001
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| 21 | HSPB8, HSPB9
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| Characterization of two novel human small heat shock proteins: protein kinase-related HspB8 and testis-specific HspB9.
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| Kappe G, Verschuure P, Philipsen RL, Staalduinen AA, Van de Boogaart P, Boelens WC, De Jong WW.
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| Biochim Biophys Acta 1520(1):1-6. 2001
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| 22 | CBSMA, HSPB8
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| Localisation of the gene for a dominant congenital spinal muscular atrophy predominantly affecting the lower limbs to chromosome 12q23-q24.
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| van der Vleuten AJ, van Ravenswaaij-Arts CM, Frijns CJ, Smits AP, Hageman G, Padberg GW, Kremer H.
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| Eur J Hum Genet 6(4):376-82. 1998
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