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Journal Articles

The predictive value of models of neuromuscular disorders to potentiate clinical translation

Maaike van Putten

Dis Model Mech (2022) 15 (7): dmm049788.

DOI: https://doi.org/10.1242/dmm.049788

Published: 1 August 2022

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Journal Articles

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

In collection:

Moving Heart Failure to Heart Success , Neuromuscular Disease Models

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

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

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

Published: 25 February 2020

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Journal Articles

Mouse models for muscular dystrophies: an overview

In collection:

Model Systems in Drug Discovery , Moving Heart Failure to Heart Success , Tools and Resources for Mouse Studies , Neuromuscular Disease Models

Maaike van Putten, Erin M. Lloyd, Jessica C. de Greef, Vered Raz, Raffaella Willmann, Miranda D. Grounds

Dis Model Mech (2020) 13 (2): dmm043562.

DOI: https://doi.org/10.1242/dmm.043562

Published: 21 February 2020

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Journal Articles

Improving translatability of preclinical studies for neuromuscular disorders: lessons from the TREAT-NMD Advisory Committee for Therapeutics (TACT)

In collection:

Model Systems in Drug Discovery , Neuromuscular Disease Models

Raffaella Willmann, Joanne Lee, Cathy Turner, Kanneboyina Nagaraju, Annemieke Aartsma-Rus, Dominic J. Wells, Kathryn R. Wagner, Cristina Csimma, Volker Straub, Miranda D. Grounds, Annamaria De Luca

Dis Model Mech (2020) 13 (2): dmm042903.

DOI: https://doi.org/10.1242/dmm.042903

Published: 7 February 2020

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Journal Articles

Integrated lipidomic and transcriptomic analyses identify altered nerve triglycerides in mouse models of prediabetes and type 2 diabetes

In collection:

Metabolic Disorders , Neuromuscular Disease Models

Phillipe D. O'Brien, Kai Guo, Stephanie A. Eid, Amy E. Rumora, Lucy M. Hinder, John M. Hayes, Faye E. Mendelson, Junguk Hur, Eva L. Feldman

Dis Model Mech (2020) 13 (2): dmm042101.

DOI: https://doi.org/10.1242/dmm.042101

Published: 24 January 2020

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Includes: Supplementary data

Journal Articles

Modelling the pathogenesis of X-linked distal hereditary motor neuropathy using patient-derived iPSCs

In collection:

Neuromuscular Disease Models , Stem Cells

Gonzalo Perez-Siles, Anthony Cutrupi, Melina Ellis, Jakob Kuriakose, Sharon La Fontaine, Di Mao, Motonari Uesugi, Reinaldo I. Takata, Carlos E. Speck-Martins, Garth Nicholson, Marina L. Kennerson

Dis Model Mech (2020) 13 (2): dmm041541.

DOI: https://doi.org/10.1242/dmm.041541

Published: 13 January 2020

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Includes: Supplementary data

Journal Articles

A comparison of the bone and growth phenotype of mdx , mdx:Cmah −/− and mdx:Utrn +/− murine models with the C57BL/10 wild-type mouse

In collection:

Neuromuscular Disease Models

Claire L. Wood, Karla J. Suchacki, Rob van ’t Hof, Will P. Cawthorn, Scott Dillon, Volker Straub, Sze Choong Wong, Syed F. Ahmed, Colin Farquharson

Dis Model Mech (2020) 13 (2): dmm040659.

DOI: https://doi.org/10.1242/dmm.040659

Published: 10 January 2020

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Includes: Supplementary data

Journal Articles

Altered in vitro muscle differentiation in X-linked myopathy with excessive autophagy

In collection:

Neuromuscular Disease Models

Stephanie A. Fernandes, Camila F. Almeida, Lucas S. Souza, Monize Lazar, Paula Onofre-Oliveira, Guilherme L. Yamamoto, Letícia Nogueira, Letícia Y. Tasaki, Rafaela R. Cardoso, Rita C. M. Pavanello, Helga C. A. Silva, Merari F. R. Ferrari, Anne Bigot, Vincent Mouly, Mariz Vainzof

Dis Model Mech (2020) 13 (2): dmm041244.

DOI: https://doi.org/10.1242/dmm.041244

Published: 10 January 2020

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Includes: Supplementary data

Journal Articles

To dystrophin and beyond: an interview with Louis Kunkel

In collection:

Neuromuscular Disease Models

Louis M. Kunkel

Dis Model Mech (2020) 13 (2): dmm043018.

DOI: https://doi.org/10.1242/dmm.043018

Published: 12 December 2019

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Journal Articles

The use of genetically humanized animal models for personalized medicine approaches

In collection:

Neuromuscular Disease Models

Annemieke Aartsma-Rus, Maaike van Putten

Dis Model Mech (2020) 13 (2): dmm041673.

DOI: https://doi.org/10.1242/dmm.041673

Published: 1 October 2019

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Journal Articles

At the heart of genetic disease: an interview with Elizabeth McNally

Elizabeth McNally

Dis Model Mech (2020) 13 (2): dmm041566.

DOI: https://doi.org/10.1242/dmm.041566

Published: 18 September 2019

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Journal Articles

Interactions among ryanodine receptor isotypes contribute to muscle fiber type development and function

Alexis A. Chagovetz, Dana Klatt Shaw, Erin Ritchie, Kazuyuki Hoshijima, David J. Grunwald

Dis Model Mech (2020) 13 (2): dmm038844.

DOI: https://doi.org/10.1242/dmm.038844

Published: 18 September 2019

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Includes: Supplementary data

NARROW

The predictive value of models of neuromuscular disorders to potentiate clinical translation

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

Mouse models for muscular dystrophies: an overview

Improving translatability of preclinical studies for neuromuscular disorders: lessons from the TREAT-NMD Advisory Committee for Therapeutics (TACT)

Integrated lipidomic and transcriptomic analyses identify altered nerve triglycerides in mouse models of prediabetes and type 2 diabetes

Modelling the pathogenesis of X-linked distal hereditary motor neuropathy using patient-derived iPSCs

A comparison of the bone and growth phenotype of mdx , mdx:Cmah −/− and mdx:Utrn +/− murine models with the C57BL/10 wild-type mouse

Altered in vitro muscle differentiation in X-linked myopathy with excessive autophagy

To dystrophin and beyond: an interview with Louis Kunkel

The use of genetically humanized animal models for personalized medicine approaches

At the heart of genetic disease: an interview with Elizabeth McNally

Interactions among ryanodine receptor isotypes contribute to muscle fiber type development and function

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