Stephen M. Lyon

Emergency Medicine

1900 Pine St
Abilene, TX 79601

Last Updated: 09/26/2026

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Found 11 publications

Structural insights into the ubiquitin-independent midnolin-proteasome pathway.

Structural insights into the ubiquitin-independent midnolin-proteasome pathway.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: May 08, 2025

Deep Learning-Based Automated Measurement of Murine Bone Length in Radiographs.

Deep Learning-Based Automated Measurement of Murine Bone Length in Radiographs.

Journal: Bioengineering (Basel, Switzerland)

Published: April 30, 2024

Obesity caused by an OVOL2 mutation reveals dual roles of OVOL2 in promoting thermogenesis and limiting white adipogenesis.

Obesity caused by an OVOL2 mutation reveals dual roles of OVOL2 in promoting thermogenesis and limiting white adipogenesis.

Journal: Cell metabolism

Published: March 03, 2022

De novo germline mutation in the dual specificity phosphatase 10 gene accelerates autoimmune diabetes.

De novo germline mutation in the dual specificity phosphatase 10 gene accelerates autoimmune diabetes.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: September 28, 2021

Thousands of induced germline mutations affecting immune cells identified by automated meiotic mapping coupled with machine learning.

Thousands of induced germline mutations affecting immune cells identified by automated meiotic mapping coupled with machine learning.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: July 14, 2021

Germline Saturation Mutagenesis Induces Skeletal Phenotypes in Mice.

Germline Saturation Mutagenesis Induces Skeletal Phenotypes in Mice.

Journal: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research

Published: October 06, 2020

Forward genetic analysis using OCT screening identifies Sfxn3 mutations leading to progressive outer retinal degeneration in mice.

Forward genetic analysis using OCT screening identifies Sfxn3 mutations leading to progressive outer retinal degeneration in mice.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: May 28, 2020

Probability of phenotypically detectable protein damage by ENU-induced mutations in the Mutagenetix database.

Probability of phenotypically detectable protein damage by ENU-induced mutations in the Mutagenetix database.

Journal: Nature communications

Published: June 01, 2017

Comparison of predicted and actual consequences of missense mutations.

Comparison of predicted and actual consequences of missense mutations.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: August 14, 2015

NLRP3 activation and mitosis are mutually exclusive events coordinated by NEK7, a new inflammasome component.

NLRP3 activation and mitosis are mutually exclusive events coordinated by NEK7, a new inflammasome component.

Journal: Nature immunology

Published: August 04, 2015

Real-time resolution of point mutations that cause phenovariance in mice.

Real-time resolution of point mutations that cause phenovariance in mice.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: January 22, 2015

Showing 1-11 of 11

Last Updated: 09/26/2026