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Eileen Remold-O'Donnell

Eileen Remold-O'Donnell

D-Index & Metrics

Biology and Biochemistry

D-Index
58
Citations
12154
World Ranking
13168
National Ranking
5617

Research.com Recognitions

  • 1999 - Fellow of the American Association for the Advancement of Science (AAAS)

Overview

Eileen Remold-O'Donnell is affiliated with Harvard University in the United States. Their research spans multiple areas within biochemistry, genetics, molecular biology, and medicine, with particular attention to protease mechanisms and blood properties.

Their publication record includes a notable paper titled The Serpins Are an Expanding Superfamily of Structurally Similar but Functionally Diverse Proteins: EVOLUTION, MECHANISM OF INHIBITION, NOVEL FUNCTIONS, AND A REVISED NOMENCLATURE, published in 2021 in UNC Libraries. This work has attracted citations and contributes to understanding the diverse functionality and evolution of serpin proteins.

Frequent co-authors collaborating with Remold-O'Donnell include:

  • Gary A. Silverman
  • Phillip I. Bird
  • Robin W. Carrell
  • Frank Church
  • Paul Coughlin

Their publications have appeared predominantly in UNC Libraries, reflecting a focused dissemination channel for their research outputs.

Main fields of study associated with Remold-O'Donnell's work comprise:

  • Biochemistry, Genetics and Molecular Biology
  • Medicine

Within these broader fields, subfields of research include:

  • Cancer Research
  • Cell Biology
  • Pulmonary and Respiratory Medicine

The core research topics covered by Remold-O'Donnell encompass:

  • Protease and Inhibitor Mechanisms
  • Calpain Protease Function and Regulation
  • Blood properties and coagulation

In recognition of contributions to the scientific community, Remold-O'Donnell was awarded the title of Fellow of the American Association for the Advancement of Science (AAAS) in 1999.

Best Publications

  • The serpins are an expanding superfamily of structurally similar but functionally diverse proteins - Evolution, mechanism of inhibition, novel functions, and a revised nomenclature

    Gary A. Silverman;Phillip I. Bird;Robin W. Carrell;Frank C. Church

  • Platelets Amplify Inflammation in Arthritis via Collagen-Dependent Microparticle Production

    Eric Boilard;Peter A. Nigrovic;Peter A. Nigrovic;Katherine Larabee;Gerald F. M. Watts

  • Inflammation induces hemorrhage in thrombocytopenia

    Tobias Goerge;Benoit Ho-Tin-Noe;Carla Carbo;Charaf Benarafa

  • Wiskott–Aldrich syndrome protein is required for NK cell cytotoxicity and colocalizes with actin to NK cell-activating immunologic synapses

    Jordan S. Orange;Narayanaswamy Ramesh;Eileen Remold-O'Donnell;Yoji Sasahara

  • The ovalbumin family of serpin proteins

    Eileen Remold-O'Donnell

  • Characterization of a human lymphocyte surface sialoglycoprotein that is defective in Wiskott-Aldrich syndrome.

    E Remold-O'Donnell;D M Kenney;R Parkman;L Cairns

  • T cells of patients with the Wiskott-Aldrich syndrome have a restricted defect in proliferative responses.

    I J Molina;J Sancho;C Terhorst;F S Rosen

  • Stimulation and desensitization of macrophage adenylate cyclase by prostaglandins and catecholamines.

    E. Remold-O'Donnell

  • Role of Caspase in a Subset of Human Platelet Activation Responses

    Anna Shcherbina;Eileen Remold-O’Donnell

  • The serpin MNEI inhibits elastase-like and chymotrypsin-like serine proteases through efficient reactions at two active sites.

    Jessica Cooley;Thomas K. Takayama;Steven D. Shapiro;Norman M. Schechter

  • SerpinB1 Promotes Pancreatic β Cell Proliferation

    Abdelfattah El Ouaamari;Ercument Dirice;Nicholas Gedeon;Jiang Hu

  • Sialophorin, a surface sialoglycoprotein defective in the Wiskott-Aldrich syndrome, is involved in human T lymphocyte proliferation.

    S. J. Mentzer;E. Remold-O'donnell;M. A. V. Crimmins;B. E. Bierer

  • Sequence and molecular characterization of human monocyte/neutrophil elastase inhibitor.

    E Remold-O'Donnell;J Chin;M Alberts

  • Molecular characterization of sialophorin (CD43), the lymphocyte surface sialoglycoprotein defective in Wiskott-Aldrich syndrome.

    C.S. Shelley;E. Remold-O'Donnell;A.E. Davis;G.A.P. Bruns

  • Morphological abnormalities in the lymphocytes of patients with the Wiskott-Aldrich syndrome

    Dianne Kenney;Lloyd Cairns;Eileen Remold-O’Donnell;Jeffrey Peterson

  • T cell lines characterize events in the pathogenesis of the Wiskott-Aldrich syndrome.

    I J Molina;D M Kenney;F S Rosen;E Remold-O'Donnell

  • Expression on blood cells of sialophorin, the surface glycoprotein that is defective in Wiskott-Aldrich syndrome.

    E Remold-O'Donnell;C Zimmerman;D Kenney;FS Rosen

  • SURFACE PROTEIN ABNORMALITIES IN LYMPHOCYTES AND PLATELETS FROM PATIENTS WITH WISKOTT-ALDRICH SYNDROME

    Robertson Parkman;DianneM. Kenney;Eileen Remold-O'Donnell;Susan Perrine

  • Moesin, the major ERM protein of lymphocytes and platelets, differs from ezrin in its insensitivity to calpain

    Anna Shcherbina;Anthony Bretscher;Dianne M. Kenney;Eileen Remold-O'Donnell

  • A monoclonal antibody to sialophorin (CD43) induces homotypic adhesion and activation of human monocytes.

    Yu-Hua Nong;E. Remold-O'donnell;T. W. Lebien;H. G. Remold

Frequent Co-Authors

Fred S. Rosen
Fred S. Rosen Harvard University
Robertson Parkman
Robertson Parkman University of Southern California
Denisa D. Wagner
Denisa D. Wagner Boston Children's Hospital
Phillip I. Bird
Phillip I. Bird Monash University
Peter A. Nigrovic
Peter A. Nigrovic Boston Children's Hospital
Heinz G. Remold
Heinz G. Remold Brigham and Women's Hospital
Barbara E. Bierer
Barbara E. Bierer Brigham and Women's Hospital
Jaime Sancho
Jaime Sancho Spanish National Research Council
Erika C. Crouch
Erika C. Crouch Washington University in St. Louis
Anthony Bretscher
Anthony Bretscher Cornell University

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