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Journal Articles

Standardization of zebrafish drug testing parameters for muscle diseases

In collection:

Drug Discovery , Zebrafish as a Disease Model

Muthukumar Karuppasamy, Katherine G. English, Clarissa A. Henry, M. Chiara Manzini, John M. Parant, Melissa A. Wright, Avnika A. Ruparelia, Peter D. Currie, Vandana A. Gupta, James J. Dowling, Lisa Maves, Matthew S. Alexander

Dis Model Mech (2024) 17 (1): dmm050339.

https://doi.org/10.1242/dmm.050339

Published: 18 January 2024

View article titled, Standardization of zebrafish drug testing parameters for muscle diseases

Journal Articles

Natural history of a mouse model of X-linked myotubular myopathy

In collection:

Neuromuscular Disease

Ege Sarikaya, Nesrin Sabha, Jonathan Volpatti, Emanuela Pannia, Nika Maani, Hernan D. Gonorazky, Alper Celik, Yijng Liang, Paula Onofre-Oliveira, James J. Dowling

Dis Model Mech (2022) 15 (7): dmm049342.

https://doi.org/10.1242/dmm.049342

Published: 25 July 2022

View article titled, Natural history of a mouse model of X-linked myotubular myopathy

Includes: Supplementary data

Journal Articles

Characterization of a novel zebrafish model of SPEG -related centronuclear myopathy

In collection:

Neuromuscular Disease , Zebrafish as a Disease Model

Karla G. Espinosa, Salma Geissah, Linda Groom, Jonathan Volpatti, Ian C. Scott, Robert T. Dirksen, Mo Zhao, James J. Dowling

Dis Model Mech (2022) 15 (5): dmm049437.

https://doi.org/10.1242/dmm.049437

Published: 9 May 2022

View article titled, Characterization of a novel zebrafish model of SPEG -related centronuclear myopathy

Includes: Supplementary data

Journal Articles

Moving neuromuscular disorders research forward: from novel models to clinical studies

In collection:

Heart Disease , Neuromuscular Disease

Maaike van Putten, Julija Hmeljak, Annemieke Aartsma-Rus, James J. Dowling

Dis Model Mech (2020) 13 (2): dmm044370.

https://doi.org/10.1242/dmm.044370

Published: 25 February 2020

View article titled, Moving neuromuscular disorders research forward: from novel models to clinical studies

Journal Articles

The expanding spectrum of neurological disorders of phosphoinositide metabolism

Jonathan R. Volpatti, Almundher Al-Maawali, Lindsay Smith, Aqeela Al-Hashim, Julie A. Brill, James J. Dowling

Dis Model Mech (2019) 12 (8): dmm038174.

https://doi.org/10.1242/dmm.038174

Published: 13 August 2019

View article titled, The expanding spectrum of neurological disorders of phosphoinositide metabolism

Includes: Supplementary data

Journal Articles

Impaired embryonic motility in dusp27 mutants reveals a developmental defect in myofibril structure

Kandice Fero, Sadie A. Bergeron, Eric J. Horstick, Hiba Codore, Grace H. Li, Fumihito Ono, James J. Dowling, Harold A. Burgess

Dis Model Mech (2014) 7 (2): 289–298.

https://doi.org/10.1242/dmm.013235

Published: 1 February 2014

View article titled, Impaired embryonic motility in dusp27 mutants reveals a developmental defect in myofibril structure

Includes: Supplementary data

Journal Articles

The myopathy-causing mutation DNM2-S619L leads to defective tubulation in vitro and in developing zebrafish

Elizabeth M. Gibbs, Ann E. Davidson, William R. Telfer, Eva L. Feldman, James J. Dowling

Dis Model Mech (2014) 7 (1): 157–161.

https://doi.org/10.1242/dmm.012286

Published: 1 January 2014

View article titled, The myopathy-causing mutation DNM2-S619L leads to defective tubulation in vitro and in developing zebrafish

Includes: Supplementary data

Journal Articles

Transcriptional changes and developmental abnormalities in a zebrafish model of myotonic dystrophy type 1

Peter K. Todd, Feras Y. Ackall, Junguk Hur, Kush Sharma, Henry L. Paulson, James J. Dowling

Dis Model Mech (2014) 7 (1): 143–155.

https://doi.org/10.1242/dmm.012427

Published: 1 January 2014

View article titled, Transcriptional changes and developmental abnormalities in a zebrafish model of myotonic dystrophy type 1

Includes: Supplementary data

Journal Articles

Myotubular myopathy and the neuromuscular junction: a novel therapeutic approach from mouse models

James J. Dowling, Romain Joubert, Sean E. Low, Ashley N. Durban, Nadia Messaddeq, Xingli Li, Ashley N. Dulin-Smith, Andrew D. Snyder, Morgan L. Marshall, Jordan T. Marshall, Alan H. Beggs, Anna Buj-Bello, Christopher R. Pierson

Dis Model Mech (2012) 5 (6): 852–859.

https://doi.org/10.1242/dmm.009746

Published: 1 November 2012

View article titled, Myotubular myopathy and the neuromuscular junction: a novel therapeutic approach from mouse models

Journal Articles

neb : a zebrafish model of nemaline myopathy due to nebulin mutation

William R. Telfer, Darcee D. Nelson, Trent Waugh, Susan V. Brooks, James J. Dowling

Dis Model Mech (2012) 5 (3): 389–396.

https://doi.org/10.1242/dmm.008631

Published: 1 May 2012

View article titled, neb : a zebrafish model of nemaline myopathy due to nebulin mutation

Includes: Multimedia, Supplementary data

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Standardization of zebrafish drug testing parameters for muscle diseases

Natural history of a mouse model of X-linked myotubular myopathy

Characterization of a novel zebrafish model of SPEG -related centronuclear myopathy

Moving neuromuscular disorders research forward: from novel models to clinical studies

The expanding spectrum of neurological disorders of phosphoinositide metabolism

Impaired embryonic motility in dusp27 mutants reveals a developmental defect in myofibril structure

The myopathy-causing mutation DNM2-S619L leads to defective tubulation in vitro and in developing zebrafish

Transcriptional changes and developmental abnormalities in a zebrafish model of myotonic dystrophy type 1

Myotubular myopathy and the neuromuscular junction: a novel therapeutic approach from mouse models

neb : a zebrafish model of nemaline myopathy due to nebulin mutation

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