Jieya Shao

Jieya Shao

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Jieya Shao

Jieya Shao

Publications by authors named "Jieya Shao"

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21Publications

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TYK2 promotes malignant peripheral nerve sheath tumor progression through inhibition of cell death.

Cancer Med 2019 Sep 6;8(11):5232-5241. Epub 2019 Jul 6.

Division of Oncology, Department of Internal Medicine, Washington University School of Medicine, St. Louis, Missouri.

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http://dx.doi.org/10.1002/cam4.2386DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6718590PMC
September 2019

Subcellular localization and Ser-137 phosphorylation regulate tumor-suppressive activity of profilin-1.

J Biol Chem 2015 Apr 13;290(14):9075-86. Epub 2015 Feb 13.

Breast Oncology Program, Division of Oncology, Department of Internal Medicine, Washington University School of Medicine, St. Louis, Missouri 63110

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http://dx.doi.org/10.1074/jbc.M114.619874DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4423694PMC
April 2015

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

Hum Mol Genet 2014 Jan 19;23(1):157-70. Epub 2013 Aug 19.

Department of Neurology, Washington University School of Medicine, 660 South Euclid Avenue, St Louis, MO 63110, USA.

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http://dx.doi.org/10.1093/hmg/ddt408DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3857952PMC
January 2014

Protein phosphatase 1 dephosphorylates profilin-1 at Ser-137.

PLoS One 2012 30;7(3):e32802. Epub 2012 Mar 30.

Department of Neurology, School of Medicine, Washington University, St. Louis, Missouri, United States of America.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0032802PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3316545PMC
August 2012

Interaction with polyglutamine aggregates reveals a Q/N-rich domain in TDP-43.

J Biol Chem 2010 Aug 16;285(34):26304-14. Epub 2010 Jun 16.

Department of Neurology, Washington University School of Medicine, St. Louis, Missouri 63110, USA.

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http://dx.doi.org/10.1074/jbc.M110.125039DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2924052PMC
August 2010

F-actin binding regions on the androgen receptor and huntingtin increase aggregation and alter aggregate characteristics.

PLoS One 2010 Feb 4;5(2):e9053. Epub 2010 Feb 4.

Department of Neurology, University of California San Francisco, San Francisco, California, United States of America.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0009053PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2816219PMC
February 2010

Phosphorylation of profilin by ROCK1 regulates polyglutamine aggregation.

Mol Cell Biol 2008 Sep 23;28(17):5196-208. Epub 2008 Jun 23.

Departments of Neurology and Cellular and Molecular Pharmacology, UCSF, San Francisco, California 94143, USA.

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http://mcb.asm.org/content/28/17/5196.full.pdf
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http://mcb.asm.org/cgi/doi/10.1128/MCB.00079-08
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http://dx.doi.org/10.1128/MCB.00079-08DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2519718PMC
September 2008

A common motif targets huntingtin and the androgen receptor to the proteasome.

J Biol Chem 2008 Aug 27;283(35):23950-5. Epub 2008 Jun 27.

Departments of Neurology and Cellular and Molecular Pharmacology, University of California-San Francisco, 600 16th Street, San Francisco, CA 94143, USA.

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http://www.jbc.org/lookup/doi/10.1074/jbc.M800467200
Publisher Site
http://dx.doi.org/10.1074/jbc.M800467200DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2527109PMC
August 2008

ROCK and PRK-2 mediate the inhibitory effect of Y-27632 on polyglutamine aggregation.

FEBS Lett 2008 May 16;582(12):1637-42. Epub 2008 Apr 16.

Department of Neurology, UCSF, GH-S572B, 600 16th Street, San Francisco, CA 94143, United States.

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http://dx.doi.org/10.1016/j.febslet.2008.04.009DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2693003PMC
May 2008

Polyglutamine diseases: emerging concepts in pathogenesis and therapy.

Hum Mol Genet 2007 Oct;16 Spec No. 2:R115-23

Department of Neurology, UCSF, San Francisco, CA 94143, USA.

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http://dx.doi.org/10.1093/hmg/ddm213DOI Listing
October 2007

Evidence for chaperone heterocomplexes containing both Hsp90 and VCP.

Biochem Biophys Res Commun 2005 Jun;331(4):1331-7

Department of Biochemistry and Molecular Biology, Oklahoma State University, Stillwater, OK 74078-3035, USA.

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http://dx.doi.org/10.1016/j.bbrc.2005.04.047DOI Listing
June 2005

High affinity binding of Hsp90 is triggered by multiple discrete segments of its kinase clients.

Biochemistry 2003 Nov;42(43):12550-61

Department of Biochemistry and Molecular Biology, Oklahoma State University, Stillwater, Oklahoma 74078-3035, USA.

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http://dx.doi.org/10.1021/bi035001tDOI Listing
November 2003

Functional dissection of cdc37: characterization of domain structure and amino acid residues critical for protein kinase binding.

Biochemistry 2003 Nov;42(43):12577-88

Department of Biochemistry and Molecular Biology, Oklahoma State University, Stillwater, Oklahoma 74078-3035, USA.

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http://dx.doi.org/10.1021/bi035138jDOI Listing
November 2003

Phosphorylation of serine 13 is required for the proper function of the Hsp90 co-chaperone, Cdc37.

J Biol Chem 2003 Oct 20;278(40):38117-20. Epub 2003 Aug 20.

Department of Biochemistry and Molecular Biology, Oklahoma State University, Stillwater, Oklahoma 74078-3035, USA.

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http://dx.doi.org/10.1074/jbc.C300330200DOI Listing
October 2003

Evidence that protein phosphatase 5 functions to negatively modulate the maturation of the Hsp90-dependent heme-regulated eIF2alpha kinase.

Biochemistry 2002 May;41(21):6770-9

Department of Biochemistry and Molecular Biology, Oklahoma State University, Stillwater, OK 74078-3035, USA.

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http://dx.doi.org/10.1021/bi025737aDOI Listing
May 2002