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Biology and Biochemistry

D-Index
75
Citations
21327
World Ranking
5289
National Ranking
2512

Overview

Lawrence J. Stern is affiliated with the University of Massachusetts Chan Medical School in the United States. Their research spans multiple fields including Immunology and Microbiology, Medicine, and Biochemistry, Genetics and Molecular Biology. Within these domains, their work focuses particularly on Immunology, Molecular Biology, Epidemiology, Infectious Diseases, and Radiology, Nuclear Medicine and Imaging.

The scientist's recent significant publications include:

  • "Pleiotropic consequences of metabolic stress for the major histocompatibility complex class II molecule antigen processing and presentation machinery," 2021, Immunity
  • "PDIA3 epitope-driven immune autoreactivity contributes to hepatic damage in type 2 diabetes," 2022, Science Immunology
  • "Conformational dynamics linked to domain closure and substrate binding explain the ERAP1 allosteric regulation mechanism," 2021, Nature Communications
  • "Broadly recognized, cross-reactive SARS-CoV-2 CD4 T cell epitopes are highly conserved across human coronaviruses and presented by common HLA alleles," 2022, Cell Reports
  • "Non-mutational neoantigens in disease," 2024, Nature Immunology

The primary topics addressed in their research include:

  • Immunotherapy and Immune Responses
  • Vaccines and immunoinformatics approaches
  • Immune Cell Function and Interaction
  • T-cell and B-cell Immunology
  • SARS-CoV-2 and COVID-19 Research
  • Monoclonal and Polyclonal Antibodies Research
  • Diabetes and associated disorders

Frequent coauthors collaborating with the scientist are:

  • Padma P. Nanaware
  • Cristina C. Clement
  • Laura Santambrogio
  • Grant C. Weaver
  • Richa Arya

The scientist's publications are often found in the following venues:

  • The Journal of Immunology
  • Frontiers in Immunology
  • Molecular Immunology
  • Cell Reports
  • bioRxiv (Cold Spring Harbor Laboratory)

Best Publications

  • Three-dimensional structure of the human class II histocompatibility antigen HLA-DR1

    Jerry H. Brown;Theodore S. Jardetzky;Joan C. Gorga;Joan C. Gorga;Lawrence J. Stern;Lawrence J. Stern

  • Crystal structure of the human class II MHC protein HLA-DR1 complexed with an influenza virus peptide

    Lawrence J. Stern;Jerry H. Brown;Theodore S. Jardetzky;Joan C. Gorga

  • Predominant naturally processed peptides bound to HLA-DR1 are derived from MHC-related molecules and are heterogeneous in size

    Roman M. Chicz;Robert G. Urban;William S. Lane;Joan C. Gorga;Joan C. Gorga

  • Three-dimensional structure of a human class II histocompatibility molecule complexed with superantigen.

    Theodore S Jardetzky;Jerry H Brown;Jerry H Brown;Joan C Gorga;Lawrence J Stern

  • Vibrational spectroscopy of bacteriorhodopsin mutants: light-driven proton transport involves protonation changes of aspartic acid residues 85, 96, and 212

    Mark S. Braiman;Tatsushi M. Mogi;Thomas M. Marti;Lawrence J. Stern

  • Antigenic peptide binding by class I and class II histocompatibility proteins

    Lawrence J Stern;Don C Wiley

  • Proteomic Analysis of Microglia-Derived Exosomes: Metabolic Role of the Aminopeptidase CD13 in Neuropeptide Catabolism

    Ilaria Potolicchio;Gregory J. Carven;Xiaonan Xu;Christopher Stipp

  • The human class II MHC protein HLA-DR1 assembles as empty αβ heterodimers in the absence of antigenic peptide

    Lawrence J. Stern;Don C. Wiley;Don C. Wiley

  • Developmental plasticity of CNS microglia

    L. Santambrogio;S. L. Belyanskaya;F. R. Fischer;B. Cipriani

  • Aspartic acid substitutions affect proton translocation by bacteriorhodopsin.

    T Mogi;L J Stern;T Marti;B H Chao

  • Crystallographic analysis of endogenous peptides associated with HLA-DR1 suggests a common, polyproline II-like conformation for bound peptides

    Theodore S. Jardetzky;Jerry H. Brown;Joan C. Gorga;Lawrence J. Stern

  • The relationship of MHC-peptide binding and T cell activation probed using chemically defined MHC class II oligomers.

    Jennifer R Cochran;Thomas O Cameron;Lawrence J Stern

  • Phosphorylation of T cell receptor zeta is regulated by a lipid dependent folding transition.

    Dikran Aivazian;Lawrence J. Stern

  • Substitution of amino acids Asp-85, Asp-212, and Arg-82 in bacteriorhodopsin affects the proton release phase of the pump and the pK of the Schiff base.

    H Otto;T Marti;M Holz;T Mogi

  • Model studies of iron―tyrosinate proteins

    Joseph W. Pyrz;A. Lawrence Roe;Lawrence J. Stern;Lawrence Que

  • Extracellular antigen processing and presentation by immature dendritic cells

    Laura Santambrogio;Aaron K. Sato;Gregory J. Carven;Svetlana L. Belyanskaya

  • Peptide immunotherapy in allergic asthma generates IL-10–dependent immunological tolerance associated with linked epitope suppression

    John D M Campbell;Karen F. Buckland;Sarah J. McMillan;Jennifer Kearley

  • Structural Basis For Antigenic Peptide Precursor Processing by the Endoplasmic Reticulum Aminopeptidase ERAP1

    Tina T Nguyen;Shih‐Chung Chang;Irini Evnouchidou;Ian York

  • Binary and ternary complexes between T-cell receptor, class II MHC and superantigen in vitro

    Alpna Seth;Lawrence J. Stern;Tom H. M. Ottenhoff;Isaac Engel;Isaac Engel

  • The class II MHC protein HLA-DR1 in complex with an endogenous peptide: implications for the structural basis of the specificity of peptide binding.

    Venkatesh L Murthy;Lawrence J Stern

Frequent Co-Authors

Laura Santambrogio
Laura Santambrogio Cornell University
Don C. Wiley
Don C. Wiley Harvard University
Jack L. Strominger
Jack L. Strominger Harvard University
Elizabeth D. Mellins
Elizabeth D. Mellins Stanford University
Theodore S. Jardetzky
Theodore S. Jardetzky Stanford University
Kenneth J. Rothschild
Kenneth J. Rothschild Boston University
Francis A. Ennis
Francis A. Ennis University of Massachusetts Chan Medical School
Liisa K. Selin
Liisa K. Selin University of Massachusetts Chan Medical School

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