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Cheryl A. Janson

Cheryl A. Janson

D-Index & Metrics

Chemistry

D-Index
54
Citations
9141
World Ranking
12751
National Ranking
229

Overview

Cheryl A. Janson is affiliated with Roche in Switzerland. Their research spans several interconnected fields within medicine and the biological sciences, focusing on infectious diseases and molecular biology.

The main fields of study in Janson's work include:

  • Medicine
  • Biochemistry, Genetics and Molecular Biology

Their subfields of study further specify their focus on:

  • Infectious Diseases
  • Molecular Biology
  • Parasitology
  • Epidemiology
  • Materials Chemistry

Janson's research covers a range of topics relevant to disease mechanisms, drug targeting, and biochemical processes. Key topics include:

  • Tuberculosis Research and Epidemiology
  • Parasitic Diseases Research and Treatment
  • Parasites and Host Interactions
  • Trypanosoma species research and implications
  • Biochemical and Molecular Research
  • Enzyme Structure and Function
  • HIV/AIDS drug development and treatment

Their recent publications illustrate this multidisciplinary approach. Notable papers include:

  • "Crystal structure of dihydrofolate reductase from the filarial nematode W. bancrofti in complex with NADPH and folate," published in 2023 in PLoS neglected tropical diseases
  • "Investigating the Roles of Active Site Residues in Mycobacterium tuberculosis Indole-3-glycerol Phosphate Synthase, a Potential Target for Antitubercular Agents," published in 2023 in ACS Bio & Med Chem Au
  • "Mutational analysis confirms the presence of distal inhibitor-selectivity determining residues in B. stearothermophilus dihydrofolate reductase," published in 2020 in Archives of Biochemistry and Biophysics

Janson has frequently collaborated with several scientists, including:

  • Nina M. Goodey
  • Tyler Eck
  • Ueli Gubler
  • Thomas Candela
  • Jaclyn Catalano

These collaborations appear across different studies and contribute to advancing knowledge in enzymology, infectious disease mechanisms, and molecular targets for drug development.

The venues where Janson publishes are specialized journals in the fields of tropical diseases, biochemistry, and biomedical chemistry, which include:

  • PLoS neglected tropical diseases
  • ACS Bio & Med Chem Au
  • Archives of Biochemistry and Biophysics

Best Publications

  • Novel subunit-subunit interactions in the structure of glutamine synthetase.

    Robert J. Almassy;Cheryl A. Janson;R. Hamlin;N. H. Xuong

  • Potent and selective nonpeptide inhibitors of caspases 3 and 7 inhibit apoptosis and maintain cell functionality.

    Dennis Lee;Scott A. Long;Jerry L. Adams;George Chan

  • Structure of and kinetic channelling in bifunctional dihydrofolate reductase-thymidylate synthase.

    Daniel R. Knighton;Chen-Chen Kan;Eleanor Howland;Cheryl A. Janson

  • Refined structures of beta-ketoacyl-acyl carrier protein synthase III.

    Xiayang Qiu;Cheryl A Janson;Ward W Smith;Martha Head

  • 4-Aryl-1,2,3-triazole: a novel template for a reversible methionine aminopeptidase 2 inhibitor, optimized to inhibit angiogenesis in vivo.

    Lara S. Kallander;Qing Lu;Wenfang Chen;Thaddeus Tomaszek

  • Crystal structure of Staphylococcus aureus tyrosyl-tRNA synthetase in complex with a class of potent and specific inhibitors.

    Xiayang Qiu;Cheryl A. Janson;Ward W. Smith;Susan M. Green

  • Design of thymidylate synthase inhibitors using protein crystal structures: the synthesis and biological evaluation of a novel class of 5-substituted quinazolinones.

    Stephen E. Webber;Ted M. Bleckman;John Attard;Judith G. Deal

  • Discovery of a Novel and Potent Class of FabI-Directed Antibacterial Agents

    David J. Payne;William H. Miller;Valerie Berry;John Brosky

  • Structure of the C-terminally truncated human ProMMP9, a gelatin-binding matrix metalloproteinase

    Patricia A. Elkins;Yen Sen Ho;Ward W. Smith;Cheryl A. Janson

  • Indole naphthyridinones as inhibitors of bacterial enoyl-ACP reductases FabI and FabK.

    Mark A. Seefeld;William H. Miller;Kenneth A. Newlander;Walter J. Burgess

  • Unique fold and active site in cytomegalovirus protease

    Xiayang Qiu;Jeffrey S. Culp;Anthony G. DiLella;Brian Hellmig

  • Refined atomic model of glutamine synthetase at 3.5 A resolution.

    M M Yamashita;R J Almassy;C A Janson;D Cascio

  • Crystal structure of beta-ketoacyl-acyl carrier protein synthase III. A key condensing enzyme in bacterial fatty acid biosynthesis.

    Xiayang Qiu;Cheryl A. Janson;Alex K. Konstantinidis;Silas Nwagwu

  • Design of potent and selective human cathepsin K inhibitors that span the active site

    S K Thompson;S M Halbert;M J Bossard;T A Tomaszek

  • Crystal structure and substrate specificity of the beta-ketoacyl-acyl carrier protein synthase III (FabH) from Staphylococcus aureus.

    Xiayang Qiu;Anthony E. Choudhry;Cheryl A. Janson;Michael Grooms

  • Stereochemical mechanism of action for thymidylate synthase based on the X-ray structure of the covalent inhibitory ternary complex with 5-fluoro-2′-deoxyuridylate and 5,10-methylenetetrahydrofolate

    D.A. Matthews;J.E. Villafranca;C.A. Janson;W.W. Smith

  • Molecular basis for triclosan activity involves a flipping loop in the active site.

    Xiayang Qiu;Cheryl A. Janson;Robert I. Court;Martin G. Smyth

  • Discovery of aminopyridine-based inhibitors of bacterial enoyl-ACP reductase (FabI).

    William H. Miller;Mark A. Seefeld;Kenneth A. Newlander;Irene N. Uzinskas

  • Crystal structure of human osteoclast cathepsin K complex with E-64.

    Baoguang Zhao;Cheryl A. Janson;Bernard Y. Amegadzie;Karla D'Alessio

  • 1,4-Disubstituted imidazoles are potential antibacterial agents functioning as inhibitors of enoyl acyl carrier protein reductase (FabI).

    Dirk A Heerding;George Chan;Walter E DeWolf;Andrew P Fosberry

  • Identification of a Series of Tricyclic Natural Products as Potent Broad-Spectrum Inhibitors of Metallo-β-Lactamases

    David J. Payne;Juan Antonio Hueso-Rodríguez;Helen Boyd;Néstor O. Concha

Frequent Co-Authors

Daniel F. Veber
Daniel F. Veber GlaxoSmithKline (United Kingdom)
David J. Payne
David J. Payne GlaxoSmithKline (United Kingdom)
Christine Debouck
Christine Debouck GlaxoSmithKline (United Kingdom)
David Eisenberg
David Eisenberg Harvard University
Paul M. Keller
Paul M. Keller MSD (United States)
J. M. White
J. M. White The University of Texas at Austin
Steven A. Carr
Steven A. Carr Broad Institute
Stephen E. Webber
Stephen E. Webber The University of Texas at Austin

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