4.7 Article

NMJ Analyser: a novel method to quantify neuromuscular junction morphology in zebrafish

相关参考文献

注意:仅列出部分参考文献,下载原文获取全部文献信息。
Article Medicine, Research & Experimental

A multilevel screening pipeline in zebrafish identifies therapeutic drugs for GAN

Lea Lescouzeres et al.

Summary: Giant axonal neuropathy (GAN) is a fatal neurodegenerative disorder without effective treatment. Using the gan zebrafish model, researchers conducted a pharmacological screening and identified five drugs that restored locomotion and axonal outgrowth in GAN. The results provide potential drug candidates for the treatment of GAN and may also benefit other neuromuscular diseases.

EMBO MOLECULAR MEDICINE (2023)

Article Agriculture, Dairy & Animal Science

Effects of ferulic acid on muscle development and intestinal microbiota of zebrafish

Xiaoyu Yin et al.

Summary: Ferulic acid (FA) is a common ingredient in Chinese herbal medicine that has been found to promote growth and improve meat quality in animals, particularly in the skeletal muscles. It enhances feed assimilation, increases muscle fiber width, and regulates gut cell and microbiota composition. The gene expression changes induced by FA are beneficial for fatty acid metabolism and reduction of fat deposition.

JOURNAL OF ANIMAL PHYSIOLOGY AND ANIMAL NUTRITION (2022)

Review Neurosciences

Modeling neuromuscular diseases in zebrafish

Jaskaran Singh et al.

Summary: Neuromuscular diseases are a diverse group of conditions that affect the motor system. Despite being individually rare, their combined prevalence is similar to Parkinson's disease. Limited understanding of the molecular mechanisms behind most NMDs has hindered the development of effective therapies. Zebrafish models have emerged as a valuable tool for studying the genetics and pathogenesis of NMDs and for developing therapeutic interventions.

FRONTIERS IN MOLECULAR NEUROSCIENCE (2022)

Article Biology

Three-dimensional mapping reveals heterochronic development of the neuromuscular system in postnatal mouse skeletal muscles

Jianyi Xu et al.

Summary: This study investigated the structural features of the neuromuscular system in mice using tissue clearing and optical imaging techniques. The results showed that different muscles have heterochronic development, corresponding to their motor function. These structural data provide a new perspective for understanding the structural status during motor development.

COMMUNICATIONS BIOLOGY (2022)

Article Biology

Reduced C9orf72 function leads to defective synaptic vesicle release and neuromuscular dysfunction in zebrafish

Zoe Butti et al.

Summary: Butti et al. generated a C9orf72 loss-of-function model in zebrafish and found that C9orf72 is crucial for maintaining presynaptic vesicle trafficking and release at the larval neuromuscular junctions. This study provides functional insights into the pathogenesis of ALS and FTD.

COMMUNICATIONS BIOLOGY (2021)

Review Developmental Biology

Development, functional organization, and evolution of vertebrate axial motor circuits

Kristen P. D'Elia et al.

NEURAL DEVELOPMENT (2018)

Article Medicine, Research & Experimental

Role of Zebrafish fhl1A in Satellite Cell and Skeletal Muscle Development

F. Chen et al.

CURRENT MOLECULAR MEDICINE (2017)

Article Medicine, Research & Experimental

Neuroleptics as therapeutic compounds stabilizing neuromuscular transmission in amyotrophic lateral sclerosis

Shunmoogum A. Patten et al.

JCI INSIGHT (2017)

Review Biochemistry & Molecular Biology

Zebrafish: A Model for the Study of Toxicants Affecting Muscle Development and Function

Magda Dubinska-Magiera et al.

INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES (2016)

Article Multidisciplinary Sciences

Effective heritable gene knockdown in zebrafish using synthetic microRNAs

Jean Giacomotto et al.

NATURE COMMUNICATIONS (2015)

Article Multidisciplinary Sciences

Zebrafish ambra1a and ambra1b Knockdown Impairs Skeletal Muscle Development

Tatjana Skobo et al.

PLOS ONE (2014)

Article Oncology

Synaptic defects in type I spinal muscular atrophy in human development

Rebeca Martinez-Hernandez et al.

JOURNAL OF PATHOLOGY (2013)

Article Multidisciplinary Sciences

The zebrafish reference genome sequence and its relationship to the human genome

Kerstin Howe et al.

NATURE (2013)

Article Multidisciplinary Sciences

Plexin A3 and Turnout Regulate Motor Axonal Branch Morphogenesis in Zebrafish

Rajiv Sainath et al.

PLOS ONE (2013)

Article Marine & Freshwater Biology

BDE-47 disrupts axonal growth and motor behavior in developing zebrafish

Xiaojuan Chen et al.

AQUATIC TOXICOLOGY (2012)

Article Biochemical Research Methods

Fiji: an open-source platform for biological-image analysis

Johannes Schindelin et al.

NATURE METHODS (2012)

Article Biochemistry & Molecular Biology

HDAC6 inhibitors reverse axonal loss in a mouse model of mutant HSPB1-induced Charcot-Marie-Tooth disease

Constantin d'Ydewalle et al.

NATURE MEDICINE (2011)

Article Developmental Biology

Neuromuscular synaptogenesis in wild-type and mutant zebrafish

JA Panzer et al.

DEVELOPMENTAL BIOLOGY (2005)

Review Neurosciences

Wiring the zebrafish: axon guidance and synaptogenesis

LD Hutson et al.

CURRENT OPINION IN NEUROBIOLOGY (2002)