World's Best Scientists 2026 revealed!

D-Index & Metrics

Biology and Biochemistry

D-Index
85
Citations
32120
World Ranking
3098
National Ranking
1568

Overview

Jamey D. Marth is affiliated with the University of California, Santa Barbara in the United States. Their research spans multiple fields, including Medicine, Biochemistry, Genetics and Molecular Biology, and Immunology and Microbiology. Within these broad areas, they have contributed significantly to subfields such as Molecular Biology, Immunology, Epidemiology, Hematology, and Infectious Diseases.

The scientist's work focuses on several key topics, including:

  • Glycosylation and Glycoproteins Research
  • Complement system in diseases
  • Platelet Disorders and Treatments
  • Antimicrobial Resistance in Staphylococcus
  • Carbohydrate Chemistry and Synthesis
  • Lysosomal Storage Disorders Research
  • Probiotics and Fermented Foods

Jamey D. Marth's recent research output includes publications in notable scientific journals. These papers are:

  • "Macrophage galactose lectin is critical for Kupffer cells to clear aged platelets," 2020, The Journal of Experimental Medicine
  • "Kupffer cell receptor CLEC4F is important for the destruction of desialylated platelets in mice," 2021, Cell Death and Differentiation
  • "Repurposed drugs block toxin-driven platelet clearance by the hepatic Ashwell-Morell receptor to clear Staphylococcus aureus bacteremia," 2021, Science Translational Medicine
  • "Neu3 neuraminidase induction triggers intestinal inflammation and colitis in a model of recurrent human food-poisoning," 2021, Proceedings of the National Academy of Sciences
  • "Glycomic Analysis Reveals a Conserved Response to Bacterial Sepsis Induced by Different Bacterial Pathogens," 2022, ACS Infectious Diseases

The scientist frequently publishes in venues such as:

  • The FASEB Journal
  • Proceedings of the National Academy of Sciences
  • bioRxiv (Cold Spring Harbor Laboratory)
  • The Journal of Experimental Medicine
  • Cell Death and Differentiation

Collaboration forms a key part of Jamey D. Marth's research process. Frequent co-authors include:

  • Peter V. Aziz
  • Damien Restagno
  • Douglas M. Heithoff
  • Markus Sperandio
  • Won Ho Yang

Best Publications

  • Glycosylation in Cellular Mechanisms of Health and Disease

    Kazuaki Ohtsubo;Jamey D. Marth

  • Deletion of a DNA polymerase beta gene segment in T cells using cell type-specific gene targeting

    Hua Gu;Jamey D. Marth;Paul C. Orban;Horst Mossmann

  • Targeted disruption of the Huntington's disease gene results in embryonic lethality and behavioral and morphological changes in heterozygotes.

    Jamal Nasir;Stan B Floresco;John R O'Kusky;Virginia M Diewert

  • Symbol Nomenclature for Graphical Representations of Glycans.

    Ajit Varki;Richard D. Cummings;Markus Aebi;Nicole H. Packer

  • Tissue- and site-specific DNA recombination in transgenic mice

    Paul C. Orban;Daniel Chui;Jamey D. Marth

  • Mammalian glycosylation in immunity

    Jamey D. Marth;Prabhjit K. Grewal

  • The O-GlcNAc transferase gene resides on the X chromosome and is essential for embryonic stem cell viability and mouse ontogeny.

    Raheel Shafi;Sai Prasad N Iyer;Lesley G. Ellies;Niall O'Donnell

  • A Genetic Approach to Mammalian Glycan Function

    John B. Lowe;Jamey D. Marth

  • Ablation of NF1 function in neurons induces abnormal development of cerebral cortex and reactive gliosis in the brain

    Yuan Zhu;Mario I. Romero;Pritam Ghosh;Zhengyi Ye

  • A lymphocyte-specific protein-tyrosine kinase gene is rearranged and overexpressed in the murine T cell lymphoma LSTRA

    Jamey D. Marth;Richard Peet;Richard Peet;Edwin G. Krebs;Roger M. Perlmutter;Roger M. Perlmutter

  • Dynamic O-GlcNAc Modification of Nucleocytoplasmic Proteins in Response to Stress A SURVIVAL RESPONSE OF MAMMALIAN CELLS

    Natasha E. Zachara;Niall O'Donnell;Win D. Cheung;Jessica J. Mercer

  • Ogt-Dependent X-Chromosome-Linked Protein Glycosylation Is a Requisite Modification in Somatic Cell Function and Embryo Viability

    Niall O'Donnell;Natasha E. Zachara;Gerald W. Hart;Jamey D. Marth

  • Dietary and Genetic Control of Glucose Transporter 2 Glycosylation Promotes Insulin Secretion in Suppressing Diabetes

    Kazuaki Ohtsubo;Shinji Takamatsu;Mari T. Minowa;Aruto Yoshida

  • Genetic evidence for selective transport of opsin and arrestin by kinesin-II in mammalian photoreceptors.

    Joseph R Marszalek;Xinran Liu;Elizabeth A Roberts;Daniel Chui

  • Immune regulation by the ST6Gal sialyltransferase

    Thierry Hennet;Daniel Chui;James C. Paulson;Jamey D. Marth

  • Virus-assisted mapping of neural inputs to a feeding center in the hypothalamus.

    Jeff DeFalco;Mark Tomishima;Hongyan Liu;Connie Zhao

  • Updates to the Symbol Nomenclature for Glycans guidelines.

    Sriram Neelamegham;Kiyoko Aoki-Kinoshita;Evan Bolton;Martin Frank

  • The Ashwell receptor mitigates the lethal coagulopathy of sepsis

    Prabhjit K Grewal;Satoshi Uchiyama;David Ditto;Nissi Varki

  • Complex asparagine-linked oligosaccharides are required for morphogenic events during post-implantation development.

    M. Metzler;A. Gertz;M. Sarkar;H. Schachter

  • Core 2 Oligosaccharide Biosynthesis Distinguishes between Selectin Ligands Essential for Leukocyte Homing and Inflammation

    Lesley G Ellies;Shigeru Tsuboi;Bronislawa Petryniak;John B Lowe

Frequent Co-Authors

Victor Nizet
Victor Nizet University of California, San Diego
Ajit Varki
Ajit Varki University of California, San Diego
Anne Dell
Anne Dell Imperial College London
James C. Paulson
James C. Paulson Scripps Research Institute
Pamela Stanley
Pamela Stanley Albert Einstein College of Medicine
Gerald W. Hart
Gerald W. Hart University of Georgia
Minoru Fukuda
Minoru Fukuda Sanford Burnham Prebys Medical Discovery Institute
Lesley G. Ellies
Lesley G. Ellies University of California, San Diego
Jeffrey D. Esko
Jeffrey D. Esko University of California, San Diego
Hudson H. Freeze
Hudson H. Freeze Discovery Institute

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