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↑ 4.04.1Sun X, Fontaine JM, Rest JS, Shelden EA, Welsh MJ, Benndorf R (Jan 2004). "Interaction of human HSP22 (HSPB8) with other small heat shock proteins". J. Biol. Chem. 279 (4): 2394–402. doi:10.1074/jbc.M311324200. PMID14594798.
↑Benndorf R, Sun X, Gilmont RR, Biederman KJ, Molloy MP, Goodmurphy CW, Cheng H, Andrews PC, Welsh MJ (Jul 2001). "HSP22, a new member of the small heat shock protein superfamily, interacts with mimic of phosphorylated HSP27 ((3D)HSP27)". J. Biol. Chem. 276 (29): 26753–61. doi:10.1074/jbc.M103001200. PMID11342557.
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Further reading
Hu Z, Chen L, Zhang J, Li T, Tang J, Xu N, Wang X (2007). "Structure, function, property, and role in neurologic diseases and other diseases of the sHsp22". J. Neurosci. Res. 85 (10): 2071–9. doi:10.1002/jnr.21231. PMID17304582.
Timmerman V, Raeymaekers P, Nelis E, De Jonghe P, Muylle L, Ceuterick C, Martin JJ, Van Broeckhoven C (1992). "Linkage analysis of distal hereditary motor neuropathy type II (distal HMN II) in a single pedigree". J. Neurol. Sci. 109 (1): 41–8. doi:10.1016/0022-510X(92)90091-X. PMID1517763.
Berciano J, Combarros O, Figols J, Calleja J, Cabello A, Silos I, Coria F (1986). "Hereditary motor and sensory neuropathy type II. Clinicopathological study of a family". Brain. 109 ( Pt 5) (5): 897–914. doi:10.1093/brain/109.5.897. PMID3022865.
Jansen PH, Joosten EM, Jaspar HH, Vingerhoets HM (1986). "A rapidly progressive autosomal dominant scapulohumeral form of spinal muscular atrophy". Ann. Neurol. 20 (4): 538–40. doi:10.1002/ana.410200417. PMID3789668.
Meadows JC, Marsden CD (1969). "A distal form of chronic spinal muscular atrophy". Neurology. 19 (1): 53–8. doi:10.1212/wnl.19.1.53. PMID5813127.
D'Alessandro R, Montagna P, Govoni E, Pazzaglia P (1982). "Benign familial spinal muscular atrophy with hypertrophy of the calves". Arch. Neurol. 39 (10): 657–60. doi:10.1001/archneur.1982.00510220055013. PMID7125978.
Groen RJ, Sie OG, van Weerden TW (1993). "Dominant inherited distal spinal muscular atrophy with atrophic and hypertrophic calves". J. Neurol. Sci. 114 (1): 81–4. doi:10.1016/0022-510X(93)90053-2. PMID8433103.
Timmerman V, De Jonghe P, Simokovic S, Löfgren A, Beuten J, Nelis E, Ceuterick C, Martin JJ, Van Broeckhoven C (1997). "Distal hereditary motor neuropathy type II (distal HMN II): mapping of a locus to chromosome 12q24". Hum. Mol. Genet. 5 (7): 1065–9. doi:10.1093/hmg/5.7.1065. PMID8817349.
Irobi J, Tissir F, De Jonghe P, De Vriendt E, Van Broeckhoven C, Timmerman V, Beuten J (2000). "A clone contig of 12q24.3 encompassing the distal hereditary motor neuropathy type II gene". Genomics. 65 (1): 34–43. doi:10.1006/geno.2000.6149. PMID10777663.
Aurelian L, Smith CC, Winchurch R, Kulka M, Gyotoku T, Zaccaro L, Chrest FJ, Burnett JW (2001). "A novel gene expressed in human keratinocytes with long-term in vitro growth potential is required for cell growth". J. Invest. Dermatol. 116 (2): 286–95. doi:10.1046/j.1523-1747.2001.00191.x. PMID11180006.
Yu YX, Heller A, Liehr T, Smith CC, Aurelian L (2001). "Expression analysis and chromosome location of a novel gene (H11) associated with the growth of human melanoma cells". Int. J. Oncol. 18 (5): 905–11. doi:10.3892/ijo.18.5.905. PMID11295034.
Benndorf R, Sun X, Gilmont RR, Biederman KJ, Molloy MP, Goodmurphy CW, Cheng H, Andrews PC, Welsh MJ (2001). "HSP22, a new member of the small heat shock protein superfamily, interacts with mimic of phosphorylated HSP27 ((3D)HSP27)". J. Biol. Chem. 276 (29): 26753–61. doi:10.1074/jbc.M103001200. PMID11342557.
Kappé G, Verschuure P, Philipsen RL, Staalduinen AA, Van de Boogaart P, Boelens WC, De Jong WW (2001). "Characterization of two novel human small heat shock proteins: protein kinase-related HspB8 and testis-specific HspB9". Biochim. Biophys. Acta. 1520 (1): 1–6. doi:10.1016/s0167-4781(01)00237-8. PMID11470154.
Molloy MP, Andrews PC (2002). "Phosphopeptide derivatization signatures to identify serine and threonine phosphorylated peptides by mass spectrometry". Anal. Chem. 73 (22): 5387–94. doi:10.1021/ac0104227. PMID11816564.
Depre C, Hase M, Gaussin V, Zajac A, Wang L, Hittinger L, Ghaleh B, Yu X, Kudej RK, Wagner T, Sadoshima J, Vatner SF (2002). "H11 kinase is a novel mediator of myocardial hypertrophy in vivo". Circ. Res. 91 (11): 1007–14. doi:10.1161/01.RES.0000044380.54893.4B. PMID12456486.