MYH 3‐associated distal arthrogryposis zebrafish model is normalized with para‐aminoblebbistatin-Reference-Cited by-同舟云学术

MYH 3‐associated distal arthrogryposis zebrafish model is normalized with para‐aminoblebbistatin

Published:2020-10-05 Issue:11 Volume:12 Page:
ISSN:1757-4676
Container-title:EMBO Molecular Medicine
language:en
Short-container-title:EMBO Mol Med

Author:

Whittle Julia¹^ORCID,Antunes Lilian¹,Harris Mya²,Upshaw Zachary²,Sepich Diane S³,Johnson Aaron N³,Mokalled Mayssa³,Solnica‐Krezel Lilianna³,Dobbs Matthew B⁴,Gurnett Christina A¹²⁵^ORCID

Affiliation:

1. Department of Neurology Washington University in St. Louis St. Louis MO USA

2. Department of Orthopedic Surgery Washington University in St. Louis St. Louis MO USA

3. Department of Developmental Biology Washington University in St. Louis St. Louis MO USA

4. Paley Institute West Palm Beach FL USA

5. Department of Pediatrics Washington University in St. Louis St. Louis MO USA

Funder

National Institute of Arthritis and Musculoskeletal and Skin Diseases

Eunice Kennedy Shriver National Institute of Child Health and Human Development

National Center for Advancing Translational Sciences

Publisher

EMBO

Subject

Molecular Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.15252/emmm.202012356

Reference39 articles.

1. Exome Sequencing Identifies an MYH3 Mutation in a Family with Distal Arthrogryposis Type 1

2. Spectrum of mutations that cause distal arthrogryposis types 1 and 2B

3. Six1a is required for the onset of fast muscle differentiation in zebrafish

4. Early Results of the Ponseti Method for the Treatment of Clubfoot in Distal Arthrogryposis

Cited by 18 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Spinal scoliosis: insights into developmental mechanisms and animal models;Spine Deformity;2024-08-20

2. Functional role of myosin-binding protein H in thick filaments of developing vertebrate fast-twitch skeletal muscle;2024-05-13

3. Piezo1 mutant zebrafish as a model of idiopathic scoliosis;Frontiers in Genetics;2024-01-08

4. ERBB3 deficiency causes a multisystemic syndrome in human patient and zebrafish;Clinical Genetics;2023-11-27

5. Musculoskeletal defects associated with myosin heavy chain‐embryonic loss of function are mediated by the YAP signaling pathway;EMBO Molecular Medicine;2023-07-26