Hongkun Jiang

发表

Silencing of TBX20 gene expression in rat myocardial and human embryonic kidney cells leads to cell cycle arrest in G2 phase

G. Qiu, G. Qiu, Yueling Sun, 2016, Molecular medicine reports.

Diagnosed but Not Undiagnosed Diabetes Is Associated with Depression in Rural Areas

Z. Li, M. Abraham, Xiao-fan Guo, 2016, International journal of environmental research and public health.

Prenatal diagnosis for a novel splice mutation of PHEX gene in a large Han Chinese family affected with X-linked hypophosphatemic rickets.

Jun Wang, Caixia Liu, J. Li-Ling, 2010, Genetic testing and molecular biomarkers.

Novel compound heterozygous COG5 mutations in a Chinese male patient with severe clinical symptoms and type IIi congenital disorder of glycosylation: A case report.

Y. Lv, Liying Gong, S. Yin, 2019, Experimental and therapeutic medicine.

MicroRNA-144 Regulates Cardiomyocyte Proliferation and Apoptosis by Targeting TBX1 through the JAK2/STAT1 Pathway

G. Qiu, Yuanyuan Sun, W. Fu, 2020, Cytogenetic and Genome Research.

Acute Lymphoblastic Leukemia in Combined Methylmalonic Acidemia and Homocysteinemia (cblC Type): A Case Report and Literature Review

Y. Lv, Xue-ni Zhao, Hongkun Jiang, 2022, Frontiers in Genetics.

The TBX1/miR-193a-3p/TGF-β2 Axis Mediates CHD by Promoting Ferroptosis

W. Fu, Xiuju Sun, Huiqin Yang, 2022, Oxidative Medicine and Cellular Longevity.

A novel CLCNKB mutation in a Chinese girl with classic Bartter syndrome: a case report

Hong Jiang, Hongkun Jiang, Xueqi Zhao, 2019, BMC Medical Genetics.

Severe Recurrent Fever Episodes With Clinical Diagnosis of Hemophagocytic Lymphohistiocytosis, Incomplete Kawasaki Disease and Systemic-Onset Juvenile Idiopathic Arthritis: A Case Report and Literature Review

Hongkun Jiang, Zhiliang Yang, 2020, Frontiers in Pediatrics.

Whole‐exome sequencing identifies a donor splice‐site variant in SMPX that causes rare X‐linked congenital deafness

Jia Gu, Y. Lv, S. Yin, 2019, Molecular genetics & genomic medicine.

Radiological and histopathological features of short rib‑polydactyly syndrome type III and identification of two novel DYNC2H1 variants.

J. Li-Ling, Yuan Lyu, Chun-ling Xia, 2021, Molecular medicine reports.

Influencing factors of self-directed learning abilities of medical students of mainland China: a cross-sectional study

Yaxin Zhu, B. Qu, Hongkun Jiang, 2021, BMJ Open.

ALG3-CDG: lethal phenotype and novel variants in Chinese siblings

C. Qiao, Yue Bian, J. Li-Ling, 2020, Journal of Human Genetics.

TBX3 deficiency accelerates apoptosis in cardiomyoblasts through regulation of P21 expression.

Yuanyuan Sun, W. Fu, Hongkun Jiang, 2019, Life sciences.

ALG3-CDG: lethal phenotype and novel variants in Chinese siblings

C. Qiao, Yue Bian, J. Li-Ling, 2020, Journal of Human Genetics.

Competitive Binding of Transcription Factors Underlies Flexibility of T Peripheral Helper Cells and T Follicular Helper Cells in SLE.

Wei Li, Xiaoxue Ma, Yu Shan, 2022, Rheumatology.