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D-Index & Metrics

Molecular Biology

D-Index
70
Citations
21700
World Ranking
1409
National Ranking
717

Research.com Recognitions

  • 2009 - Fellow of the American Association for the Advancement of Science (AAAS)

Overview

Michael R. Stallcup is affiliated with the University of Southern California in the United States and specializes in research within the fields of biochemistry, genetics, and molecular biology, as well as medicine. Their work spans several subfields including molecular biology, physiology, genetics, pulmonary and respiratory medicine, and endocrinology, diabetes, and metabolism.

The scientist has contributed to topics such as adipose tissue and metabolism, protein degradation and inhibitors, genetics and physical performance, cancer-related gene regulation, epigenetics and DNA methylation, prostate cancer treatment and research, and the effects of estrogen and related hormones.

Among the recently published papers attributed to Michael R. Stallcup are:

  • Gene-Specific Actions of Transcriptional Coregulators Facilitate Physiological Plasticity: Evidence for a Physiological Coregulator Code (2020, Trends in Biochemical Sciences)
  • How Protein Methylation Regulates Steroid Receptor Function (2021, Endocrine Reviews)
  • Transcriptional coactivation by EHMT2 restricts glucocorticoid-induced insulin resistance in a study with male mice (2023, Nature Communications)

Frequent co-authors collaborating with Michael R. Stallcup include:

  • Coralie Poulard
  • Lucie Malbeteau
  • Ha Thuy Pham
  • Louisane Eve
  • Muriel Le Romancer

The main publication venues for their work are:

  • Trends in Biochemical Sciences
  • Endocrine Reviews
  • Nature Communications

Michael R. Stallcup was awarded the honor of Fellow of the American Association for the Advancement of Science (AAAS) in 2009.

Best Publications

  • Regulation of transcription by a protein methyltransferase.

    Dagang Chen;Han Ma;Heng Hong;Stephen S. Koh

  • Human PAD4 regulates histone arginine methylation levels via demethylimination.

    Yanming Wang;Joanna Wysocka;Joyce Sayegh;Young-Ho Lee

  • Structure and specificity of nuclear receptor-coactivator interactions.

    Beatrice D. Darimont;Richard L. Wagner;James W. Apriletti;Michael R. Stallcup

  • GRIP1, a novel mouse protein that serves as a transcriptional coactivator in yeast for the hormone binding domains of steroid receptors.

    Heng Hong;Kulwant Kohli;Alpa Trivedi;Deborah L. Johnson

  • GRIP1, a transcriptional coactivator for the AF-2 transactivation domain of steroid, thyroid, retinoid, and vitamin D receptors.

    H Hong;K Kohli;M J Garabedian;M R Stallcup

  • Nuclear Receptor-Binding Sites of Coactivators Glucocorticoid Receptor Interacting Protein 1 (GRIP1) and Steroid Receptor Coactivator 1 (SRC-1): Multiple Motifs with Different Binding Specificities

    Xiu Fen Ding;Carol M. Anderson;Han Ma;Heng Hong

  • A functional MRI study of mental image generation.

    M D'Esposito;J.A Detre;G.K Aguirre;M Stallcup

  • Role of protein methylation in regulation of transcription.

    David Y. Lee;Catherine Teyssier;Brian D. Strahl;Michael R. Stallcup

  • Methylation of histone H4 at arginine 3 occurs in vivo and is mediated by the nuclear receptor coactivator PRMT1

    Brian D. Strahl;Scott D. Briggs;Cynthia J. Brame;Jennifer A. Caldwell

  • Estrogen Receptor Activation Function 1 Works by Binding p160 Coactivator Proteins

    Paul Webb;Phuong Nguyen;Jeanette Shinsako;Carol Anderson

  • Synergistic Enhancement of Nuclear Receptor Function by p160 Coactivators and Two Coactivators with Protein Methyltransferase Activities

    Stephen S. Koh;Dagang Chen;Young-Ho Lee;Michael R. Stallcup

  • Hormone-independent Transcriptional Activation and Coactivator Binding by Novel Orphan Nuclear Receptor ERR3

    Heng Hong;Lan Yang;Michael R. Stallcup

  • Molecular pathogenesis of chronic wounds: The role of β-catenin and c-myc in the inhibition of epithelialization and wound healing

    Olivera Stojadinovic;Harold Brem;Constantinos Vouthounis;Brian Lee

  • Methylation of Histone H3 by Coactivator-Associated Arginine Methyltransferase 1†

    Schurter Bt;Koh Ss;Chen D;Bunick Gj

  • Inhibition of p160-mediated coactivation with increasing androgen receptor polyglutamine length

    Ryan A. Irvine;Han Ma;Mimi C. Yu;Ronald K. Ross

  • Multiple signal input and output domains of the 160-kilodalton nuclear receptor coactivator proteins.

    Han Ma;Heng Hong;Shih Ming Huang;Ryan A. Irvine

  • Inhibitors and Inactivators of Protein Arginine Deiminase 4: Functional and Structural Characterization

    Yuan Luo;Kyouhei Arita;Monica Bhatia;Bryan Knuckley

  • Synergistic, p160 Coactivator-dependent Enhancement of Estrogen Receptor Function by CARM1 and p300

    Dagang Chen;Shih-Ming Huang;Michael R. Stallcup

  • The ankyrin repeats of G9a and GLP histone methyltransferases are mono- and dimethyllysine binding modules

    Robert E Collins;Jeffrey P Northrop;John R Horton;David Y Lee

  • Activation of nuclear receptor coactivator PGC-1α by arginine methylation

    Catherine Teyssier;Han Ma;Roger Emter;Anastasia Kralli

Frequent Co-Authors

Keith R. Yamamoto
Keith R. Yamamoto University of California, San Francisco
Gerhard A. Coetzee
Gerhard A. Coetzee University of Southern California
Kimberly D. Siegmund
Kimberly D. Siegmund University of Southern California
Brian D. Strahl
Brian D. Strahl University of North Carolina at Chapel Hill
Xiaodong Cheng
Xiaodong Cheng The University of Texas MD Anderson Cancer Center
C. David Allis
C. David Allis Rockefeller University
Donald B. DeFranco
Donald B. DeFranco University of Pittsburgh
Marjana Tomic-Canic
Marjana Tomic-Canic University of Miami
Axel H. Schönthal
Axel H. Schönthal University of Southern California
Xing Zhang
Xing Zhang The University of Texas MD Anderson Cancer Center

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