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Molecular Genetics and Metabolism
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June 19, 2026
High prevalence of GAA c.[752C > T;761C > T] haplotype complicates high-risk screening for Pompe disease in the Chinese population
Kexin Jiao, Yang Wang, Jueru Zhou, et al.
Neuromuscular Disorders : NMD
|
December 31, 2025
Expanded spectrum of MEGF10 related myopathies: late-onset myofibrillar myopathy-like phenotype with novel variants
Bochen Zhu, Kexin Jiao, Darrel Sou Li, et al.
Nature Communications
|
February 10, 2018
IL-6/STAT3 pathway induced deficiency of RFX1 contributes to Th17-dependent autoimmune diseases via epigenetic regulation
Ming Zhao, Yixin Tan, Qiao Peng, et al.
Health Information Science and Systems
|
April 21, 2026
PhenoRareAI: Phenotype-based intelligent diagnosis for rare neuromuscular disorders of glycogen storage disease and spinal muscular atrophy
Weiqi Zhai, Kexin Jiao, Ningning Wang, et al.
Clinical Epigenetics
|
July 8, 2015
DNA methylation profiling of the X chromosome reveals an aberrant demethylation on CXCR3 promoter in primary biliary cirrhosis
Ana Lleo, Weici Zhang, Ming Zhao, et al.
Muscle & Nerve
|
April 1, 2024
Pseudoexon activation by deep intronic variation in GNE myopathy with thrombocytopenia
Kexin Jiao, Nachuan Cheng, Xiao Huan, et al.
The Journal of Molecular Diagnostics : JMD
|
March 20, 2025
4qA D4Z4 Methylation Test as a Valuable Complement for Differential Diagnosis in Patients with a Facioscapulohumeral Muscular Dystrophy-Like Phenotype
Xingyu Xia, Nachuan Cheng, Yiqi Liu, et al.
Cell Discovery
|
April 15, 2025
Senescence-induced p21<sup>high</sup> macrophages contributed to CD8<sup>+</sup> T cells-related immune hyporesponsiveness in kidney transplantation via Zfp36/IL-27 axis
Tingting Zhu, Qixia Shen, Lingling Shen, et al.
Annals of the Rheumatic Diseases
|
January 21, 2016
IFI44L promoter methylation as a blood biomarker for systemic lupus erythematosus
Ming Zhao, Yin Zhou, Bochen Zhu, et al.
Journal of Medical Genetics
|
September 27, 2024
Novel variants and genotype-phenotype correlation in a multicentre cohort of GNE myopathy in China
Kexin Jiao, Jialong Zhang, Qiuxiang Li, et al.
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Showing results (11-20 of 22) with videos related to
Sort By:
Page
of 3
Molecular Genetics and Metabolism
|
June 19, 2026
High prevalence of GAA c.[752C > T;761C > T] haplotype complicates high-risk screening for Pompe disease in the Chinese population
Kexin Jiao, Yang Wang, Jueru Zhou, et al.
Neuromuscular Disorders : NMD
|
December 31, 2025
Expanded spectrum of MEGF10 related myopathies: late-onset myofibrillar myopathy-like phenotype with novel variants
Bochen Zhu, Kexin Jiao, Darrel Sou Li, et al.
Nature Communications
|
February 10, 2018
IL-6/STAT3 pathway induced deficiency of RFX1 contributes to Th17-dependent autoimmune diseases via epigenetic regulation
Ming Zhao, Yixin Tan, Qiao Peng, et al.
Health Information Science and Systems
|
April 21, 2026
PhenoRareAI: Phenotype-based intelligent diagnosis for rare neuromuscular disorders of glycogen storage disease and spinal muscular atrophy
Weiqi Zhai, Kexin Jiao, Ningning Wang, et al.
Clinical Epigenetics
|
July 8, 2015
DNA methylation profiling of the X chromosome reveals an aberrant demethylation on CXCR3 promoter in primary biliary cirrhosis
Ana Lleo, Weici Zhang, Ming Zhao, et al.
Muscle & Nerve
|
April 1, 2024
Pseudoexon activation by deep intronic variation in GNE myopathy with thrombocytopenia
Kexin Jiao, Nachuan Cheng, Xiao Huan, et al.
The Journal of Molecular Diagnostics : JMD
|
March 20, 2025
4qA D4Z4 Methylation Test as a Valuable Complement for Differential Diagnosis in Patients with a Facioscapulohumeral Muscular Dystrophy-Like Phenotype
Xingyu Xia, Nachuan Cheng, Yiqi Liu, et al.
Cell Discovery
|
April 15, 2025
Senescence-induced p21<sup>high</sup> macrophages contributed to CD8<sup>+</sup> T cells-related immune hyporesponsiveness in kidney transplantation via Zfp36/IL-27 axis
Tingting Zhu, Qixia Shen, Lingling Shen, et al.
Annals of the Rheumatic Diseases
|
January 21, 2016
IFI44L promoter methylation as a blood biomarker for systemic lupus erythematosus
Ming Zhao, Yin Zhou, Bochen Zhu, et al.
Journal of Medical Genetics
|
September 27, 2024
Novel variants and genotype-phenotype correlation in a multicentre cohort of GNE myopathy in China
Kexin Jiao, Jialong Zhang, Qiuxiang Li, et al.
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of 3