James Goldenring

Professor of Surgery

Vanderbilt University Medical Center

United States

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James Goldenring is a Professor of Surgery at Vanderbilt University Medical Center in the United States. His research focuses on gastric biology and involves investigating the safety and efficacy of treatments for gastric precancerous lesions, the interaction of protein complexes in cellular functions, and the cell biology of intestinal epithelial disorders. Recent articles highlight his work on gastric mucosal regeneration, cellular metabolic pathways, and the role of specific proteins in gastric metaplasia and dysplasia.

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2020

Collaborators (7)

Brenda Hogue

Professor

Arizona State University

UNITED STATES

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Yoonkyung Won

Assistant Professor

Chonnam National University

SOUTH KOREA

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Eunyoung Choi

Associate professor

Vanderbilt University Medical Center

UNITED STATES

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Frederic Tangy

Head of Unit

Institut Pasteur

FRANCE

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Amy Engevik

Assistant Professor

Medical University of South Carolina

UNITED STATES

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Cornelis de Haan

Utrecht University

NETHERLANDS

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Izumi Kaji

Vanderbilt University

UNITED STATES

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James Goldenring

Research Interests

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Articles (20)

Hybrid identity and distinct methylation profiles of incomplete intestinal metaplasia in the stomach

Stratifin Is Necessary for Spasmolytic Polypeptide-Expressing Metaplasia Development After Acute Gastric Injury

Safety and Efficacy of MEK Inhibitor Treatment for Gastric Precancerous Lesions

The Interaction of pT73-Rab10 with Myosin Va, but Not Myosin Vb, Is Regulated Though a Site in the Globular Tail Domain

Microvillus inclusion disease-causing MYO5B point mutations exert differential effects on motor function

Coronavirus M Protein Trafficking in Epithelial Cells Utilizes a Myosin Vb Splice Variant and Rab10

Modeling the cell biology of monogenetic intestinal epithelial disorders

Dynamic tuft cell expansion during gastric metaplasia and dysplasia

Amphiregulin Switches Progenitor Cell Fate for Lineage Commitment During Gastric Mucosal Regeneration.

Alterations in cellular metabolic pathway and epithelial cell maturation induced by MYO5B defects are partially reversible by LPAR5 activation

Spasmolytic polypeptide‐expressing metaplasia (SPEM) cell lineages can be an origin of gastric cancer

NoH. pylori, no adenocarcinoma for patients with autoimmune gastritis

Rab11FIP1-deficient mice develop spontaneous inflammation and show increased susceptibility to colon damage

Cellular Plasticity, Reprogramming, and Regeneration: Metaplasia in the Stomach and Beyond

Altered MYO5B Function Underlies Microvillus Inclusion Disease: Opportunities for Intervention at a Cellular Level

Up-regulation of Aquaporin 5 Defines Spasmolytic Polypeptide-Expressing Metaplasia and Progression to Incomplete Intestinal Metaplasia

Cell differentiation is disrupted by MYO5B loss through Wnt/Notch imbalance

RAB11A-mediated YAP localization to adherens and tight junctions is essential for colonic epithelial integrity

Lysophosphatidic Acid Increases Maturation of Brush Borders and SGLT1 Activity in MYO5B-deficient Mice, a Model of Microvillus Inclusion Disease

Noggin regulates foregut progenitor cell programming and mis-expression leads to esophageal atresia

Collaborators (7)

Brenda Hogue

Yoonkyung Won

Eunyoung Choi

Frederic Tangy

Amy Engevik

Cornelis de Haan

Izumi Kaji

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