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Biology and Biochemistry

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Overview

Stephen J. DeArmond is affiliated with the University of California, San Francisco in the United States. Their research primarily resides within the broad field of Biochemistry, Genetics and Molecular Biology, with specific focus on Molecular Biology, Cognitive Neuroscience, and Infectious Diseases.

Their research topics center around Prion Diseases and Protein Misfolding, Functional Brain Connectivity Studies, and Infectious Encephalopathies and Encephalitis.

The frequent co-authors who have collaborated with Stephen J. DeArmond include:

  • Matteo Paoletti
  • Eduardo Caverzasi
  • Maria Luisa Mandelli
  • Jesse A. Brown
  • Roland G. Henry

Their research has been published in various scientific venues, notably:

  • Human Brain Mapping
  • Journal of Molecular Biology

Recent papers by Stephen J. DeArmond include:

  • Default Mode Network quantitative diffusion and resting-state functional magnetic resonance imaging correlates in sporadic Creutzfeldt-Jakob disease, 2022, Human Brain Mapping
  • Corrigendum to "Conformational Transformation and Selection of Synthetic Prion Strains" [J. Mol. Biol. 413(3) (2011) 527-542], 2025, Journal of Molecular Biology

Best Publications

  • Normal development and behaviour of mice lacking the neuronal cell-surface PrP protein

    Hansruedi Büeler;Marek Fischer;Yolande Lang;Yolande Lang;Horst Bluethmann;Horst Bluethmann

  • Synthetic Mammalian Prions

    Giuseppe Legname;Ilia V. Baskakov;Hoang-Oanh B. Nguyen;Detlev Riesner

  • Prion protein biology.

    Stanley B Prusiner;Michael R Scott;Stephen J DeArmond;Fred E Cohen

  • Transgenetic studies implicate interactions between homologous PrP isoforms in scrapie prion replication.

    Stanley B. Prusiner;Michael Scott;Dallas Foster;Keh-Ming Pan

  • Prion propagation in mice expressing human and chimeric PrP transgenes implicates the interaction of cellular PrP with another protein

    Glenn C. Telling;Michael Scott;James Mastrianni;Ruth Gabizon

  • Evidence for the Conformation of the Pathologic Isoform of the Prion Protein Enciphering and Propagating Prion Diversity

    Glenn C. Telling;Piero Parchi;Stephen J. DeArmond;Pietro Cortelli

  • Transgenic mice expressing hamster prion protein produce species-specific scrapie infectivity and amyloid plaques

    Michael Scott;Dallas Foster;Carol Mirenda;Dan Serban

  • A transmembrane form of the prion protein in neurodegenerative disease.

    Ramanujan S. Hegde;James A. Mastrianni;Michael R. Scott;Kathryn A. DeFea

  • Compelling transgenetic evidence for transmission of bovine spongiform encephalopathy prions to humans.

    Michael R. Scott;Robert Will;James Ironside;Hoang-Oanh B. Nguyen

  • Spontaneous neurodegeneration in transgenic mice with mutant prion protein.

    Karen K. Hsiao;Michael Scott;Dallas Foster;Darlene F. Groth

  • Ablation of the prion protein (PrP) gene in mice prevents scrapie and facilitates production of anti-PrP antibodies

    Stanley B. Prusiner;Darlene Groth;Ana Serban;Ruth Koehler

  • Subcellular colocalization of the cellular and scrapie prion proteins in caveolae-like membranous domains

    Martin Vey;Susanne Pilkuhn;Holger Wille;Randal Nixon

  • Scrapie prion proteins are synthesized in neurons.

    H. A. Kretzschmar;S. B. Prusiner;L. E. Stowring;S. J. DeArmond

  • Linkage of prion protein and scrapie incubation time genes

    George A. Carlson;David T. Kingsbury;Patricia A. Goodman;Sherrie Coleman

  • Regional mapping of prion proteins in brain.

    Albert Taraboulos;Klaus Jendroska;Dan Serban;Shu-Lian Yang

  • Binding of neural cell adhesion molecules (N-CAMs) to the cellular prion protein.

    Gerold Schmitt-Ulms;Giuseppe Legname;Michael A Baldwin;Haydn L Ball

  • Molecular cloning of a human prion protein cDNA.

    Hans A. Kretzschmar;Linda E. Stowring;David Westaway;William H. Stubblebine

  • Propagation of prions with artificial properties in transgenic mice expressing chimeric PrP genes.

    Michael Scott;Darlene Groth;Dallas Foster;Marilyn Torchia

  • Transmission of Creutzfeldt-Jakob disease from humans to transgenic mice expressing chimeric human-mouse prion protein

    Glenn C. Telling;Michael Scott;Karen K. Hsiao;Dallas Foster

  • Transmission of multiple system atrophy prions to transgenic mice

    Joel C. Watts;Kurt Giles;Abby Oehler;Lefkos Middleton

Frequent Co-Authors

Stanley B. Prusiner
Stanley B. Prusiner University of California, San Francisco
Darlene Groth
Darlene Groth University of California, San Francisco
Bruce L. Miller
Bruce L. Miller University of California, San Francisco
George A. Carlson
George A. Carlson University of California, San Francisco
Giuseppe Legname
Giuseppe Legname International School for Advanced Studies
Fred E. Cohen
Fred E. Cohen University of California, San Francisco
Holger Wille
Holger Wille University of Alberta
William C. Mobley
William C. Mobley University of California, San Diego
William W. Seeley
William W. Seeley University of California, San Francisco
Smita S. Patel
Smita S. Patel Rutgers, The State University of New Jersey

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