The role of polypeptide PDTLN1 in suppression of PI3K/AKT signaling causes cardiogenetic disorders in vitro and in vivo-Reference-Cited by-同舟云学术

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The role of polypeptide PDTLN1 in suppression of PI3K/AKT signaling causes cardiogenetic disorders in vitro and in vivo

Published:2022-01 Issue: Volume:289 Page:120244
ISSN:0024-3205
Container-title:Life Sciences
language:en
Short-container-title:Life Sciences

Author:

Yu Boshi,Yao Shuwen,Liu Linjie,Li Huimin,Zhu Jingai,Li Mengmeng,Han Shuping,Yu Zhangbin

Funder

Jiangsu Provincial Medical Youth Talent

National Natural Science Foundation of China

Medical Science and Technology Development Foundation, Nanjing Municipality Health Bureau

Publisher

Elsevier BV

Subject

General Pharmacology, Toxicology and Pharmaceutics,General Biochemistry, Genetics and Molecular Biology,General Medicine

Reference31 articles.

1. De novo variants in exomes of congenital heart disease patients identify risk genes and pathways;Sevim Bayrak;Genome Med.,2020

2. Achievements in congenital heart defect surgery: a prospective, 40-year study of 7038 patients;Erikssen;Circulation,2015

3. Fetal growth and neurodevelopmental outcome in congenital heart disease;Williams;Pediatr. Cardiol.,2015

4. Reduced fetal brain fissures depth in fetuses with congenital heart diseases: reduced fissures in CHD;Peng;Prenat. Diagn.,2016

5. Single-cell resolution of temporal gene expression during heart development;DeLaughter;Dev. Cell,2016

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1. Triadimenol promotes the production of reactive oxygen species and apoptosis with cardiotoxicity and developmental abnormalities in zebrafish;Science of The Total Environment;2023-03

2. Immunity of turbot Induced by inactivated vaccine of Aeromonas salmonicida from the perspective of DNA methylation;Frontiers in Immunology;2023-02-07

3. The casein-derived peptide YFYPEL alleviates intestinal epithelial cell dysfunction associated with NEC by regulating the PI3K/AKT signaling pathway;Food & Function;2023

4. Identifying shared genetic factors underlying epilepsy and congenital heart disease in Europeans;Human Genetics;2022-11-09

5. Genetic Diagnostic Yield and Novel Causal Genes of Congenital Heart Disease;Frontiers in Genetics;2022-07-13

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