AI Chat Paper
Note: Please note that the following content is generated by AMiner AI. SciOpen does not take any responsibility related to this content.
{{lang === 'zh_CN' ? '文章概述' : 'Summary'}}
{{lang === 'en_US' ? '中' : 'Eng'}}
Chat more with AI
Powered by AMiner. Clicking this button will take you away from SciOpen.
Home Genes & Diseases Article
PDF (624 KB)
Cite
EndNote(RIS) BibTeX
Collect
Submit Manuscript AI Chat Paper
Show Outline
Outline
Show full outline
Hide outline
Outline
Show full outline
Hide outline
Rapid Communication | Open Access

C. elegans model of riboflavin transporter deficiency (RTD) disorder reveals deficits in synaptic transmission and movement

Ramesh K. Narayanana,b( ), Gonzalo Perez-silesa,b , Kamila A. Marzecc, Alexandra Boylinga,b, Brent Neumannd, Manoj P. Menezese,f,1, Marina L. Kennersona,b,g,1
Northcott Neuroscience Laboratory, ANZAC Research Institute - Sydney Local Health District, Sydney, NSW 2139, Australia
Sydney Medical School, University of Sydney, Sydney, NSW 2050, Australia
ANZAC Research Institute - Sydney Local Health District, Sydney, NSW 2139, Australia
Neuroscience Program, Monash Biomedicine Discovery Institute and Department of Anatomy and Developmental Biology, Monash University, Melbourne, Victoria 3800, Australia
TY Nelson Department of Neurology and Neurosurgery and Kids Neuroscience, Children's Hospital at Westmead, Westmead, Sydney, NSW 2145, Australia
Paediatrics and Child Health, The University of Sydney, Sydney, Sydney, NSW 2145, Australia
Molecular Medicine Laboratory, Concord General Repatriation Hospital, Sydney, NSW 2139, Australia

Peer review under responsibility of Chongqing Medical University.

1 Co-senior authors.

Show Author Information

References

【1】
【1】
 
 
Crossref Google Scholar
Genes & Diseases
Volume 11 Issue 4,
July 2024
Article number: 101071
DOI: 10.1016/j.gendis.2023.06.038

{{item.num}}

Comments on this article

Go to comment

< Back to all reports

Review Status: {{reviewData.commendedNum}} Commended , {{reviewData.revisionRequiredNum}} Revision Required , {{reviewData.notCommendedNum}} Not Commended Under Peer Review

Review Comment

Cite this Report
Close
Close
Cite this article:
Narayanan RK, Perez-siles G, Marzec KA, et al. C. elegans model of riboflavin transporter deficiency (RTD) disorder reveals deficits in synaptic transmission and movement. Genes & Diseases, 2024, 11(4): 101071. https://doi.org/10.1016/j.gendis.2023.06.038

607

Views

5

Downloads

0

Crossref

0

Web of Science

0

Scopus

0

CSCD
Received: 11 April 2023
Published: 08 August 2023
© 2023 The Authors.

This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).