Chemistry Reference
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Duennwald ML, Echeverria A, Shorter J (2012) Small heat shock proteins potentiate amyloid dis-
solution by protein disaggregases from yeast and humans. PLoS Biol 10:e1001346
Ehrnsperger M, Graber S, Gaestel M et al (1997) Binding of non-native protein to Hsp25 during
heat shock creates a reservoir of folding intermediates for reactivation. EMBO J 16:221-229
Engert JC, Berube P, Mercier J et al (2000) ARSACS, a spastic ataxia common in northeastern
Quebec, is caused by mutations in a new gene encoding an 11.5-kb ORF. Nat Gen 24:120-125
Eriguchi M, Mizuta H, Kurohara K et al (2008) Identification of a new homozygous frameshift
insertion mutation in the SIL1 gene in 3 Japanese patients with Marinesco-Sj￶gren syndrome.
J Neurol Sci 270:197-200
Estaquier J, Arnoult D (2007) Inhibiting Drp1-mediated mitochondrial fission selectively prevents
the release of cytochrome c during apoptosis. Cell Death Diff 14:1086-1094
Evgrafov OV, Mersiyanova I, Irobi J et al (2004) Mutant small heat-shock protein 27 causes axonal
Charcot-Marie-Tooth disease and distal hereditary motor neuropathy. Nat Genet 36:602-606
Ezgu F, Krejci P, Li S et al (2014) Phenotype-genotype correlations in patients with Marinesco-
Sj￶gren syndrome. Clin Genet 86:74-84
Frank S, Gaume B, Bergmann-Leitner ES et al (2001) The role of dynamin-related protein 1, a
mediator of mitochondrial fission, in apoptosis. Dev Cell 1:515-525
Fujikake N, Nagai Y, Popiel HA et al (2008) Heat shock transcription factor 1-activating com-
pounds suppress polyglutamine-induced neurodegeneration through induction of multiple mo-
lecular chaperones. J Biol Chem 283:26188-26197
Gao XC, Zhou CJ, Zhou ZR et al (2011) Co-chaperone HSJ1a dually regulates the proteasomal
degradation of ataxin-3. PLoS One 6:e19763
Gebert N, Joshi AS, Kutik S et al (2009) Mitochondrial cardiolipin involved in outer-membrane
protein biogenesis: implications for Barth syndrome. Curr Biol 19:2133-2139
Girard M, Lariviere R, Parfitt DA et al (2012) Mitochondrial dysfunction and Purkinje cell loss in
autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS). Proc Nat Acad Sci U
S A 109:1661-1666
Greer PL, Hanayama R, Bloodgood BL et al (2010) The Angelman syndrome protein Ube3A
regulates synapse development by ubiquitinating arc. Cell 140:704-716
Grynberg M, Erlandsen H, Godzik A (2003) HEPN: a common domain in bacterial drug resistance
and human neurodegenerative proteins. Trends Bioch Sci 28:224-226
Hageman J, Rujano MA, van Waarde MAWH et al (2010) A DNAJB chaperone subfamily with
HDAC-dependent activities suppresses toxic protein aggregation. Mol Cell 37:355-369
Hansen JJ, Durr A, Cournu-Rebeix I et al (2002) Hereditary spastic paraplegia SPG13 is associ-
ated with a mutation in the gene encoding the mitochondrial chaperonin Hsp60. Am J Hum
Genet 70:1328-1332
Hansson O, Nylandsted J, Castilho RF et al (2003) Overexpression of heat shock protein 70 in
R6/2 Huntington's disease mice has only modest effects on disease progression. Brain Res
970:47-57
Hargitai J, Lewis H, Boros I et al (2003) Bimoclomol, a heat shock protein co-inducer, acts by
the prolonged activation of heat shock factor-1. Biochem Biophys Res Commun 307:689-695
Harms MB, Sommerville RB, Allred P et al (2012) Exome sequencing reveals DNAJB6 mutations
in dominantly-inherited myopathy. Ann Neurol 71:407-416
Hartl FU, Hayer-Hartl M (2002) Molecular chaperones in the cytosol: from nascent chain to folded
protein. Science 295:1852-1858
Haslbeck M, Miess A, Stromer T et al (2005) Disassembling protein aggregates in the yeast cyto-
sol. The cooperation of Hsp26 with Ssa1 and Hsp104. J Biol Chem 280:23861-23868
Hayashi M, Imanaka-Yoshida K, Yoshida T et al (2006) A crucial role of mitochondrial Hsp40 in
preventing dilated cardiomyopathy. Nat Med 12:128-132
He Q (2010) Tafazzin knockdown causes hypertrophy of neonatal ventricular myocytes. Am J
Physiol Heart Circ Physiol 299:H210-229
Hidalgo-de-Quintana J, Evans RJ, Cheetham ME et al (2008) The Leber congenital amaurosis
protein AIPL1 functions as part of a chaperone heterocomplex. Invest Ophthalmol Vis Sci
49:2878-2887
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