Investigation of dopaminergic signalling in Meis homeobox 1 ( Meis1 ) deficient mice as an animal model of restless legs syndrome-Reference-Cited by-同舟云学术

Investigation of dopaminergic signalling in Meis homeobox 1 ( Meis1 ) deficient mice as an animal model of restless legs syndrome

Published:2021-05-18 Issue:5 Volume:30 Page:
ISSN:0962-1105
Container-title:Journal of Sleep Research
language:en
Short-container-title:J Sleep Res

Author:

Cathiard Lucile¹,Fraulob Valerie¹,Lam Daniel D.²^ORCID,Torres Miguel³,Winkelmann Juliane²⁴,Krężel Wojciech¹^ORCID

Affiliation:

1. Institute of Genetics and Molecular and Cellular Biology, CNRS UMR7104, INSERM U1258, University of Strasbourg Illkirch France

2. Institute for Human Genetic, Klinikum rechts der Isar, Technische Universität München Munich Germany

3. Cardiovascular Development Program Centro Nacional de Investigaciones Cardiovasculares, CNIC Madrid Spain

4. Chair for Neucgenetic, Klinikum rechts der Isar Technische Universität München; Institute for Neurogenomics, Helmholtz Zentrum München; Munich Cluster for Systems Neurology (SyNergy) Munich Germany

Funder

Ministerio de Economía y Competitividad

Agence Nationale de la Recherche

Bundesministerium für Bildung und Forschung

Publisher

Wiley

Subject

Behavioral Neuroscience,Cognitive Neuroscience,General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/jsr.13311

Reference38 articles.

1. Animal models of RLS phenotypes

2. Defining the phenotype of the restless legs syndrome (RLS) using age-of-symptom-onset

3. Restless legs syndrome/Willis–Ekbom disease diagnostic criteria: updated International Restless Legs Syndrome Study Group (IRLSSG) consensus criteria – history, rationale, description, and significance

4. The homeodomain protein Meis1 is essential for definitive hematopoiesis and vascular patterning in the mouse embryo

5. Animal studies in restless legs syndrome

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