Publications by authors named "Robert Tryon"

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Muscle fatigue arising intrinsically from SUR2- but not Kir6.1-dependent gain-of-function in Cantu syndrome mice.
Rosa Scala, Maya Mukadam, Yuezhou Chen, Courtney Frazier, Nathaniel W York, Robert C Tryon

J Gen Physiol· November 2025

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Novel loss-of-function variants expand ABCC9-related intellectual disability and myopathy syndrome.
Stephanie Efthymiou, Marcello Scala, Vini Nagaraj, Katarzyna Ochenkowska, Fenne L Komdeur, Robert C Tryon

Brain· May 2024

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Kir1.1 and SUR1 are not implicated as subunits of an adenosine triphosphate-sensitive potassium channel involved in diazoxide cardioprotection.
Jie Wang, Kyriakos Papanicolaou, Robert Tryon, Janelle Sangalang, Ben Salazar

JTCVS Open· September 2023

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Skeletal muscle delimited myopathy and verapamil toxicity in SUR2 mutant mouse models of AIMS.
Conor McClenaghan, Maya A Mukadam, Jacob Roeglin, Robert C Tryon, Manfred Grabner

EMBO Mol Med· June 2023

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Genome-edited zebrafish model of loss-of-function disease.
Jennifer M Ikle, Robert C Tryon, Soma S Singareddy, Nathaniel W York, Maria S Remedi

Islets· December 2022

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Isolation of Cardiac and Vascular Smooth Muscle Cells from Adult, Juvenile, Larval and Embryonic Zebrafish for Electrophysiological Studies.
Soma S Singareddy, Conor McClenaghan, Helen I Roessler, Robert Tryon, Colin G Nichols

J Vis Exp· February 2022

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ATP-sensitive potassium channels in zebrafish cardiac and vascular smooth muscle.
Soma S Singareddy, Helen I Roessler, Conor McClenaghan, Jennifer M Ikle, Robert C Tryon

J Physiol· January 2022

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Beta-cell excitability and excitability-driven diabetes in adult Zebrafish islets.
Christopher H Emfinger, Réka Lőrincz, Yixi Wang, Nathaniel W York, Soma S Singareddy, Robert C Tryon

Physiol Rep· June 2019

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Cx43 suppresses evx1 expression to regulate joint initiation in the regenerating fin.
Gabrielle Dardis, Robert Tryon, Quynh Ton, Stephen L Johnson, M Kathryn Iovine

Dev Dyn· September 2017

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Clonal analysis of kit ligand a functional expression reveals lineage-specific competence to promote melanocyte rescue in the mutant regenerating caudal fin.
Robert C Tryon, Stephen L Johnson

PLoS One· November 2015

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Clonal and lineage analysis of melanocyte stem cells and their progeny in the zebrafish.
Robert C Tryon, Stephen L Johnson

Methods Mol Biol· March 2013

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Development of translating ribosome affinity purification for zebrafish.
Robert C Tryon, Nilambari Pisat, Stephen L Johnson, Joseph D Dougherty

Genesis· March 2013

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Lineage relationship of direct-developing melanocytes and melanocyte stem cells in the zebrafish.
Robert C Tryon, Charles W Higdon, Stephen L Johnson

PLoS One· November 2011

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Evaluation of allele frequencies of inherited disease genes in subgroups of American Quarter Horses.
Robert C Tryon, M Cecilia T Penedo, Molly E McCue, Stephanie J Valberg, James R Mickelson

J Am Vet Med Assoc· January 2009

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Genetic test for HERDA.
Robert Tryon

Vet Rec· January 2008

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Homozygosity mapping approach identifies a missense mutation in equine cyclophilin B (PPIB) associated with HERDA in the American Quarter Horse.
Robert C Tryon, Stephen D White, Danika L Bannasch

Genomics· July 2007

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Inheritance of hereditary equine regional dermal asthenia in Quarter Horses.
Robert C Tryon, Stephen D White, Thomas R Famula, Patricia C Schultheiss, Dwayne W Hamar

Am J Vet Res· March 2005

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