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Items: 1 to 20 of 24


Modulation the alternative splicing of GLA (IVS4+919G>A) in Fabry disease.

Chang WH, Niu DM, Lu CY, Lin SY, Liu TC, Chang JG.

PLoS One. 2017 Apr 21;12(4):e0175929. doi: 10.1371/journal.pone.0175929. eCollection 2017.


Cytosolic splice isoform of Hsp70 nucleotide exchange factor Fes1 is required for the degradation of misfolded proteins in yeast.

Gowda NK, Kaimal JM, Masser AE, Kang W, Friedländer MR, Andréasson C.

Mol Biol Cell. 2016 Apr 15;27(8):1210-9. doi: 10.1091/mbc.E15-10-0697. Epub 2016 Feb 24.


Widespread use of non-productive alternative splice sites in Saccharomyces cerevisiae.

Kawashima T, Douglass S, Gabunilas J, Pellegrini M, Chanfreau GF.

PLoS Genet. 2014 Apr 10;10(4):e1004249. doi: 10.1371/journal.pgen.1004249. eCollection 2014 Apr.


Prion-like nuclear aggregation of TDP-43 during heat shock is regulated by HSP40/70 chaperones.

Udan-Johns M, Bengoechea R, Bell S, Shao J, Diamond MI, True HL, Weihl CC, Baloh RH.

Hum Mol Genet. 2014 Jan 1;23(1):157-70. doi: 10.1093/hmg/ddt408. Epub 2013 Aug 19.


Quercetin suppresses drug-resistant spheres via the p38 MAPK-Hsp27 apoptotic pathway in oral cancer cells.

Chen SF, Nieh S, Jao SW, Liu CL, Wu CH, Chang YC, Yang CY, Lin YS.

PLoS One. 2012;7(11):e49275. doi: 10.1371/journal.pone.0049275. Epub 2012 Nov 12.


Dual effect of heat shock on DNA replication and genome integrity.

Velichko AK, Petrova NV, Kantidze OL, Razin SV.

Mol Biol Cell. 2012 Sep;23(17):3450-60. doi: 10.1091/mbc.E11-12-1009. Epub 2012 Jul 11.


The elusive middle domain of Hsp104 and ClpB: location and function.

Desantis ME, Shorter J.

Biochim Biophys Acta. 2012 Jan;1823(1):29-39. doi: 10.1016/j.bbamcr.2011.07.014. Epub 2011 Jul 24. Review.


Diverse environmental stresses elicit distinct responses at the level of pre-mRNA processing in yeast.

Bergkessel M, Whitworth GB, Guthrie C.

RNA. 2011 Aug;17(8):1461-78. doi: 10.1261/rna.2754011. Epub 2011 Jun 22.


Heat shock-induced SRSF10 dephosphorylation displays thermotolerance mediated by Hsp27.

Shi Y, Nishida K, Campigli Di Giammartino D, Manley JL.

Mol Cell Biol. 2011 Feb;31(3):458-65. doi: 10.1128/MCB.01123-10. Epub 2010 Dec 6.


Role of the heat shock transcription factor, Hsf1, in a major fungal pathogen that is obligately associated with warm-blooded animals.

Nicholls S, Leach MD, Priest CL, Brown AJ.

Mol Microbiol. 2009 Nov;74(4):844-61. doi: 10.1111/j.1365-2958.2009.06883.x. Epub 2009 Oct 8.


Spp382p interacts with multiple yeast splicing factors, including possible regulators of Prp43 DExD/H-Box protein function.

Pandit S, Paul S, Zhang L, Chen M, Durbin N, Harrison SM, Rymond BC.

Genetics. 2009 Sep;183(1):195-206. doi: 10.1534/genetics.109.106955. Epub 2009 Jul 6.


The 2008 Genetics Society of America Medal. Susan Lindquist.

Hopkins N.

Genetics. 2008 Mar;178(3):1125-8. doi: 10.1534/genetics.104.017834. No abstract available.


Role of glutathione in heat-shock-induced cell death of Saccharomyces cerevisiae.

Sugiyama K, Kawamura A, Izawa S, Inoue Y.

Biochem J. 2000 Nov 15;352 Pt 1:71-8.


The role of the ClpA chaperone in proteolysis by ClpAP.

Hoskins JR, Pak M, Maurizi MR, Wickner S.

Proc Natl Acad Sci U S A. 1998 Oct 13;95(21):12135-40.


Regulation of yeast glycogen metabolism and sporulation by Glc7p protein phosphatase.

Ramaswamy NT, Li L, Khalil M, Cannon JF.

Genetics. 1998 May;149(1):57-72.


Leishmania major Hsp100 is required chiefly in the mammalian stage of the parasite.

Hübel A, Krobitsch S, Hörauf A, Clos J.

Mol Cell Biol. 1997 Oct;17(10):5987-95.

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