Publications by authors named "Hongdou Li"

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The variants identified in a short stature cohort compromise the dephosphorylation ability of on SMAD5 to up-regulate BMP signaling.
Kai Yang, Hongdou Li, Rui Peng, Bo Wu, Yiping Shen, Chentao Li

Genes Dis· July 2025

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Elevated microRNA-187 causes cardiac endothelial dysplasia to promote congenital heart disease through inhibition of NIPBL.
Chao Li, Zizheng Tan, Hongdou Li, Xiaoying Yao, Chuyue Peng, Chentao Li

J Clin Invest· November 2024

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Downregulated nuclear lncRNA NRON inhibits SHP2/Wnt/β-catenin signaling and cardiomyocyte differentiation during the development of Tetralogy of Fallot.
Hui Zhang, Lei Lu, Chao Li, Hongdou Li, Jie Tian

Genes Dis· May 2023

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Master microRNA-222 regulates cardiac microRNA maturation and triggers Tetralogy of Fallot.
Chao Li, Hongdou Li, Xiaoying Yao, Dong Liu, Yongming Wang

Signal Transduct Target Ther· May 2022

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Beyond samples: A metric revealing more connections of gut microbiota between individuals.
Zhen Yang, Feng Xu, Hongdou Li, Yungang He

Comput Struct Biotechnol J· July 2021

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The first familial NSD2 cases with a novel variant in a Chinese father and daughter with atypical WHS facial features and a 7.5-year follow-up of growth hormone therapy.
Xuyun Hu, Di Wu, Yuchuan Li, Liya Wei, Xiaoqiao Li, Hongdou Li, Mengting Li

BMC Med Genomics· December 2020

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Vertically Aligned and Ordered Arrays of 2D MCoS@Metal with Ultrafast Ion/Electron Transport for Thickness-Independent Pseudocapacitive Energy Storage.
Zongbin Hao, Xingchen He, Hongdou Li, Denis Trefilov, Yangyang Song, Yang Li

ACS Nano· October 2020

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Age-Dependent Risks of Incidence and Mortality of COVID-19 in Hubei Province and Other Parts of China.
Hongdou Li, Shuang Wang, Fan Zhong, Wuyin Bao, Yipeng Li, Lei Liu

Front Med (Lausanne)· April 2020

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The first two Chinese Myhre syndrome patients with the recurrent SMAD4 pathogenic variants: Functional consequences and clinical diversity.
Hongdou Li, Bingjuan Cheng, Xuyun Hu, Chao Li, Jiasun Su, Ling Li, Mengting Li, Geli Liu

Clin Chim Acta· January 2020

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A report on a girl of Noonan syndrome 9 presenting with bilateral lower limbs lymphedema.
Yuan Ding, Xu-Yun Hu, Yan-Ning Song, Bing-Yan Cao, Xue-Jun Liang, Hong-Dou Li

Chin Med J (Engl)· February 2019

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Novel pathogenic RECQL4 variants in Chinese patients with Rothmund-Thomson syndrome.
Baoheng Gui, Yanning Song, Xuyun Hu, Hongdou Li, Zailong Qin, Chuan Li, Mengting Li, Liping Song

Gene· May 2018

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Prenatal and early diagnosis of Chinese 3-M syndrome patients with novel pathogenic variants.
Xuyun Hu, Hongdou Li, Baoheng Gui, Yufei Xu, Jin Wang, Niu Li

Clin Chim Acta· November 2017

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Mosaic UPD(7q)mat in a patient with silver Russell syndrome.
Jiasun Su, Jin Wang, Xin Fan, Chunyun Fu, ShuJie Zhang, Hongdou Li, Chuan Li

Mol Cytogenet· October 2017

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Novel pathogenic ACAN variants in non-syndromic short stature patients.
Xuyun Hu, Baoheng Gui, Jiasun Su, Hongdou Li, Niu Li, Guoqiang Li, Yulin Chen, Chuan Li, Juan Li

Clin Chim Acta· June 2017

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Thyroglobulin gene mutations in Chinese patients with congenital hypothyroidism.
Xuyun Hu, Rongyu Chen, Chunyun Fu, Xin Fan, Jin Wang, Chuan Li, Yunli Lai, Hongdou Li

Mol Cell Endocrinol· March 2016

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