The abnormal phosphorylation of the Rac1, Lim-kinase 1, and Cofilin proteins in the pathogenesis of Hirschsprung’s disease
Author:
Affiliation:
1. Department of Pediatric General, Thoracic & Urological Surgery II Ward, Affiliated Hospital of Zunyi Medical University, Zunyi, China
2. Gastrointestinal Surgery, The Second Affiliated Hospital of Zunyi Medical University, Zunyi, China
Funder
Guizhou Science & Technology Foundation Project
Zunyi Science & Technology Program
Publisher
Informa UK Limited
Subject
Applied Microbiology and Biotechnology,General Medicine,Bioengineering,Biotechnology
Link
https://www.tandfonline.com/doi/pdf/10.1080/21655979.2022.2051882
Reference32 articles.
1. Molecular Genetic Anatomy and Risk Profile of Hirschsprung’s Disease
2. What is new about the genetic background of Hirschsprung disease?
3. Enteric nervous system development: A crest cell’s journey from neural tube to colon
4. Long-term functional outcomes and quality of life in patients with Hirschsprung's disease
5. Long-term Outcome of Hirschsprung Disease: Impact on Quality of Life and Social Condition at Adult Age
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1. Advances in the study of long non-coding RNAs in Hirschsprung disease;Journal of Pediatric Surgery Open;2024-01
2. Silencing of purinergic receptor P2Y2 inhibited enteric neural crest cell proliferation, invasion and migration via suppressing ERK signaling pathway in Hirschsprung disease;3 Biotech;2023-08-23
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