Characterization of gastrointestinal pathologies in the dystonia musculorum mouse model for hereditary sensory and autonomic neuropathy type VI-Reference-Cited by-同舟云学术

Characterization of gastrointestinal pathologies in the dystonia musculorum mouse model for hereditary sensory and autonomic neuropathy type VI

Published:2019-12-09 Issue:4 Volume:32 Page:
ISSN:1350-1925
Container-title:Neurogastroenterology & Motility
language:en
Short-container-title:Neurogastroenterology & Motility

Author:

Lynch‐Godrei Anisha¹²^ORCID,De Repentigny Yves¹^ORCID,Yaworski Rebecca A.¹^ORCID,Gagnon Sabrina¹^ORCID,Butcher James³^ORCID,Manoogian Juliana³,Stintzi Alain³^ORCID,Kothary Rashmi¹²³⁴⁵^ORCID

Affiliation:

1. Regenerative Medicine Program Ottawa Hospital Research Institute Ottawa ON Canada

2. Department of Cellular and Molecular Medicine Faculty of Medicine University of Ottawa Ottawa ON Canada

3. Department of Biochemistry, Microbiology, and Immunology Faculty of Medicine University of Ottawa Ottawa ON Canada

4. Department of Medicine University of Ottawa Ottawa ON Canada

5. Centre for Neuromuscular Disease University of Ottawa Ottawa ON Canada

Funder

Genome Canada

Canadian Institutes of Health Research

Publisher

Wiley

Subject

Gastroenterology,Endocrine and Autonomic Systems,Physiology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/nmo.13773

Reference51 articles.

1. Hereditary sensory autonomic neuropathy caused by a mutation in dystonin

2. Novel mutations in dystonin provide clues to the pathomechanisms of HSAN-VI

3. Recessive mutations in the neuronal isoforms of DST , encoding dystonin, lead to abnormal actin cytoskeleton organization and HSAN type VI

4. Expanding the phenotype of DST ‐related disorder: A case report suggesting a genotype/phenotype correlation

5. Dystonin-A3 upregulation is responsible for maintenance of tubulin acetylation in a less severedystonia musculorummouse model for hereditary sensory and autonomic neuropathy type VI

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1. Sensory-motor circuit is a therapeutic target for dystonia musculorum mice, a model of hereditary sensory and autonomic neuropathy 6;Science Advances;2024-07-26