Thomas Thompson

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Professor

University of Cincinnati Medical Center

United States

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Thomas Thompson is a Professor at the University of Cincinnati Medical Center in the United States. His research primarily focuses on the molecular mechanisms underlying growth factor signaling, particularly within the transforming growth factor β (TGF-β) family. Recent articles highlight his work on activin ligands, anti-Müllerian hormone synthesis, and the oligomeric states of various antagonists.

Recent Grants

Grant: Close

Structure-Function Investigation of DAN-mediated BMP Antagonism

Open Date: 2015-04-01

Close Date: 2019-01-31

Grant: Close

Structural basis of antagonism within the TGFbeta-superfamily

Open Date: 2008-04-01

Close Date: 2014-03-31

Grant: Close

Structural Studies of Inhibin/Activin Receptor Complexes

Open Date: 2002-05-01

Close Date: 2003-01-01

Articles (10)

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2024

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2024

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2024

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2022

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2021

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2021

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2021

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2020

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2020

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2020

Collaborators (3)

david pepin

Associate Professor

Massachusetts General Hospital

UNITED STATES

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Daniel J Bernard

McGill University

CANADA

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Kelly Walton

MONASH UNIVERSITY

AUSTRALIA

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Thomas Thompson

Research Interests

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About

Recent Grants

Articles (10)

Activin E is a transforming growth factor β ligand that signals specifically through activin receptor-like kinase 7

Characterization of erythroferrone oligomerization and its impact on BMP antagonism

Characterization of the molecular mechanisms that govern anti‐Müllerian hormone synthesis and activity

The orphan ligand, activin C, signals through activin receptor-like kinase 7

Structure of AMH bound to AMHR2 provides insight into a unique signaling pair in the TGF-β family

Characterization of tolloid-mediated cleavage of the GDF8 procomplex

Heparin-mediated dimerization of follistatin

Characterization of the different oligomeric states of the DAN family antagonists SOSTDC1 and SOST

Mutational Analysis of the Putative Anti-Müllerian Hormone (AMH) Binding Interface on its Type II Receptor, AMHR2

Functional recombinant apolipoprotein A5 that is stable at high concentrations at physiological pH

Collaborators (3)

david pepin

Daniel J Bernard

Kelly Walton

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