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D-Index & Metrics

Biology and Biochemistry

D-Index
98
Citations
31293
World Ranking
1690
National Ranking
940

Overview

William B. Pratt was affiliated with the University of Michigan-Ann Arbor in the United States. Their research primarily contributed to the field of Biochemistry, Genetics and Molecular Biology, with a focus on several subfields including Molecular Biology, Computational Mechanics, Cell Biology, and Cancer Research.

The scientist's work covered a variety of topics related to cellular and molecular processes. Key topics investigated included Heat Shock Proteins Research, ATP Synthase and ATPases Research, Heat Transfer and Supercritical Fluids, Endoplasmic Reticulum Stress and Disease, Ubiquitin and Proteasome Pathways, Histone Deacetylase Inhibitors Research, and Cancer, Hypoxia, and Metabolism.

William B. Pratt authored several papers in notable venues, illustrating a focus on biochemical and molecular mechanisms with relevance to cancer and cellular stress responses. Some of these papers were:

  • "Low-Dose Hsp90 Inhibitor Selectively Radiosensitizes HNSCC and Pancreatic Xenografts," Clinical Cancer Research, 2020
  • "Dynamic cycling with a unique Hsp90/Hsp70-dependent chaperone machinery and GAPDH is needed for heme insertion and activation of neuronal NO synthase," Journal of Biological Chemistry, 2022
  • "Ubiquitylation of Neuronal Nitric-oxide Synthase by CHIP, a Chaperone-dependent E3 Ligase," UNC Libraries, 2021

Frequent coauthors collaborated with Pratt on multiple occasions, reflecting ongoing research partnerships. These collaborators included Yoshihiro Morishima, Yoichi Osawa, Miranda Lau, Ranjit K. Mehta, and Sanjima Pal.

The scientist's publications appeared predominantly in the Journal of Biological Chemistry, Clinical Cancer Research, and UNC Libraries, highlighting a consistent presence in respected biochemical and cancer research journals.

Best Publications

  • Steroid receptor interactions with heat shock protein and immunophilin chaperones.

    William B. Pratt;David O. Toft

  • Regulation of signaling protein function and trafficking by the hsp90/hsp70-based chaperone machinery.

    William B. Pratt;David O. Toft

  • HDAC6 Regulates Hsp90 Acetylation and Chaperone-Dependent Activation of Glucocorticoid Receptor

    Jeffrey J. Kovacs;Patrick J.M. Murphy;Stéphanie Gaillard;Xuan Zhao

  • The role of heat shock proteins in regulating the function, folding, and trafficking of the glucocorticoid receptor

    William B. Pratt

  • The hsp90-based chaperone system: Involvement in signal transduction from a variety of hormone and growth factor receptors

    William B. Pratt

  • Evidence that the 90-kDa phosphoprotein associated with the untransformed L-cell glucocorticoid receptor is a murine heat shock protein.

    E R Sanchez;D O Toft;M J Schlesinger;W B Pratt

  • The role of the hsp90-based chaperone system in signal transduction by nuclear receptors and receptors signaling via MAP kinase.

    William B. Pratt

  • Evidence that the 90-kDa heat shock protein is necessary for the steroid binding conformation of the L cell glucocorticoid receptor.

    E H Bresnick;F C Dalman;E R Sanchez;W B Pratt

  • Molybdate inhibition of glucocorticoid receptor inactivation and transformation.

    K L Leach;M K Dahmer;N D Hammond;J J Sando

  • Proof that the endogenous, heat-stable glucocorticoid receptor-activating factor is thioredoxin.

    J F Grippo;A Holmgren;W B Pratt

  • Raf exists in a native heterocomplex with hsp90 and p50 that can be reconstituted in a cell-free system

    L. F. Stancato;Yu-Hua Chow;K. A. Hutchison;G. H. Perdew

  • Folding of the glucocorticoid receptor by the heat shock protein (hsp) 90-based chaperone machinery. The role of p23 is to stabilize receptor.hsp90 heterocomplexes formed by hsp90.p60.hsp70.

    Kurt D. Dittmar;Damon R. Demady;Louis F. Stancato;Priti Krishna

  • Role of hsp90 and the hsp90-binding immunophilins in signalling protein movement.

    William B Pratt;Mario D Galigniana;Jennifer M Harrell;Donald B DeFranco

  • A region in the steroid binding domain determines formation of the non-DNA-binding, 9 S glucocorticoid receptor complex.

    W B Pratt;D J Jolly;D V Pratt;S M Hollenberg

  • Evidence That the Peptidylprolyl Isomerase Domain of the hsp90-binding Immunophilin FKBP52 Is Involved in Both Dynein Interaction and Glucocorticoid Receptor Movement to the Nucleus *

    Mario D. Galigniana;Christine Radanyi;Jack Michel Renoir;Paul R. Housley

  • Role of molecular chaperones in steroid receptor action.

    William B Pratt;Mario D Galigniana;Yoshihiro Morishima;Patrick J M Murphy

  • Protein Phosphatase 5 Is a Major Component of Glucocorticoid Receptor·hsp90 Complexes with Properties of an FK506-binding Immunophilin

    Adam M. Silverstein;Mario D. Galigniana;Mei-Shya Chen;Janet K. Owens-Grillo

  • Evidence for a mechanism of repression of heat shock factor 1 transcriptional activity by a multichaperone complex.

    Yongle Guo;Toumy Guettouche;Mary Fenna;Frank Boellmann

  • The Tetratricopeptide Repeat Domain of Protein Phosphatase 5 Mediates Binding to Glucocorticoid Receptor Heterocomplexes and Acts as a Dominant Negative Mutant

    Mei Shya Chen;Adam M. Silverstein;William B. Pratt;Michael Chinkers

  • Short Article HDAC6 Regulates Hsp90 Acetylation and Chaperone-Dependent Activation of Glucocorticoid Receptor

    Jeffrey J. Kovacs;Stéphanie Gaillard;Xuan Zhao;June-Tai Wu

Frequent Co-Authors

Mario D. Galigniana
Mario D. Galigniana Experimental Medicine and Biology Institute
Emery H. Bresnick
Emery H. Bresnick University of Wisconsin–Madison
Michael J. Welsh
Michael J. Welsh University of Michigan–Ann Arbor
Andrew P. Lieberman
Andrew P. Lieberman University of Michigan–Ann Arbor
S. Stoney Simons
S. Stoney Simons National Institutes of Health
Gary H. Perdew
Gary H. Perdew Pennsylvania State University
Alnawaz Rehemtulla
Alnawaz Rehemtulla University of Michigan–Ann Arbor
Priti Krishna
Priti Krishna University of Western Ontario
Jason E. Gestwicki
Jason E. Gestwicki University of California, San Francisco
Huda Akil
Huda Akil University of Michigan–Ann Arbor

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