Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Hong-Kun Jiang"'
Autor:
Chun-Ling Xia, Yuan Lyu, Chuang Li, Huan Li, Zhi-Tao Zhang, Shao-Wei Yin, Yan Mao, Wen Li, Ling-Yin Kong, Bo Liang, Hong-Kun Jiang, Jesse Li-Ling, Cai-Xia Liu, Jun Wei
Publikováno v:
Frontiers in Genetics, Vol 10 (2019)
Silver–Russell syndrome (SRS) is a rare, well-recognized disorder characterized by growth restriction, including intrauterine and postnatal growth. Most SRS cases are caused by hypomethylation of the paternal imprinting center 1 (IC1) in chromosome
Externí odkaz:
https://doaj.org/article/d6ff355a6b4044d3875a554ca15e865f
Autor:
Shi-Qi Xiao, Yuan Lyu, Caixia Liu, Hong-Kun Jiang, Xue Yang, Hao Qiu, Jesse Li-Ling, Chun-Ling Xia
Publikováno v:
Molecular Medicine Reports. 23
Short rib‑polydactyly syndrome type III (SRPS3) is a lethal perinatal skeletal disorder consisting of polydactyly and multi‑system organ abnormalities. To further assess the pathogenicity of two pairs of compound heterozygotes and to search for n
Publikováno v:
Cytogenetic and Genome Research. 159:190-200
It is currently believed that the TBX1 gene is one of the core genes of congenital heart disease (CHD). However, there are few studies on the abnormal regulation of TBX1 gene expression. The purpose of this work was to investigate the role of miR-144
Publikováno v:
BIBM
The automatic identification of traditional Chinese medicine decoction pieces is of great significance in the objectification of Chinese medicine quality control. Common methods are traditional features of artificial design and machine learning algor
Autor:
Chun-Ling, Xia, Shi-Qi, Xiao, Xue, Yang, Cai-Xia, Liu, Hao, Qiu, Hong-Kun, Jiang, Jesse, Li-Ling, Yuan, Lyu
Publikováno v:
Molecular medicine reports. 23(6)
Short rib‑polydactyly syndrome type III (SRPS3) is a lethal perinatal skeletal disorder consisting of polydactyly and multi‑system organ abnormalities. To further assess the pathogenicity of two pairs of compound heterozygotes and to search for n
Autor:
ShuGuang Zheng, Jesse Li-Ling, Yue Bian, Caixia Liu, Yuan Lyu, Huan Li, Zhitao Zhang, Hong-Kun Jiang, Chong Qiao, Shaowei Yin, Hao Qiu
Publikováno v:
J Hum Genet
Congenital disorders of glycosylation (CDG) are a group of genetic, mostly multisystem disorders, which often involve the central nervous system. ALG3-CDG is one the some 130 known CDG. Here we report two siblings with a severe phenotype and intraute
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4cb8daa550301986e176f9ae2b8a435f
https://europepmc.org/articles/PMC7605439/
https://europepmc.org/articles/PMC7605439/
Publikováno v:
Cytogenetic and genome research. 159(4)
It is currently believed that the TBX1 gene is one of the core genes of congenital heart disease (CHD). However, there are few studies on the abnormal regulation of TBX1 gene expression. The purpose of this work was to investigate the role of miR-144
Autor:
Jun Wei, Huan Li, Chun-Ling Xia, Wen Li, Hong-Kun Jiang, Caixia Liu, Zhitao Zhang, Yan Mao, Chuang Li, Kong Lingyin, Shaowei Yin, Yuan Lyu, Bo Liang, Jesse Li-Ling
Publikováno v:
Frontiers in Genetics, Vol 10 (2019)
Frontiers in Genetics
Frontiers in Genetics
Silver–Russell syndrome (SRS) is a rare, well-recognized disorder characterized by growth restriction, including intrauterine and postnatal growth. Most SRS cases are caused by hypomethylation of the paternal imprinting center 1 (IC1) in chromosome
Autor:
Yinglong Bai, Wanqiu Zhu, Mingxia Wang, Zhao Li, Hong-Kun Jiang, Samantha J. Caton, Xin Niu, Chuntao Li
Publikováno v:
Diabetes, Metabolic Syndrome and Obesity: Targets and Therapy, Vol Volume 12, Pp 1625-1638 (2019)
Diabetes, Metabolic Syndrome and Obesity: Targets and Therapy
Diabetes, Metabolic Syndrome and Obesity: Targets and Therapy
Wanqiu Zhu,1,* Xin Niu,1,* Mingxia Wang,1 Zhao Li,2 Hong-Kun Jiang,3 Chuntao Li,4 Samantha J Caton,5 Yinglong Bai11Department of Maternal and Child Health, School of Public Health, China Medical University, Shenyang, Liaoning, People’s Republic of
Autor:
Shaowei Yin, Caixia Liu, Yuan Lv, Yan Mao, Ling‑Yin Kong, Bo Liang, Hong-kun Jiang, Hao Qiu, Yan Zhang, Liying Gong, Yan Zhao
In the current study, one case of COG5-CDG involving a Chinese male patient with severe neurological symptoms, who had previously been misdiagnosed with congenital gyrus malformation, is described. A clinical investigation was performed and targeted
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba8e1b8dcd76329fad604c297cde1388
https://europepmc.org/articles/PMC6755449/
https://europepmc.org/articles/PMC6755449/