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Frontiers in Cellular and Infection Microbiology
|
October 8, 2025
Tissue-resident memory CD8+T cells might enhance HBV DNA clearance in CHB patients with MASLD complication and normal ALT via the CCL-CCR pathways
Chao Cai, Wen-Xuan Shang, Si-Jie Zheng, et al.
Human Mutation
|
September 30, 2016
Mutation in SSUH2 Causes Autosomal-Dominant Dentin Dysplasia Type I
Fu Xiong, Zhisong Ji, Yanhui Liu, et al.
Msystems
|
March 4, 2026
EEG and gut microbiota response patterns in high-altitude indigenous populations
Ke Bai, Ting Ge, Chen-Xi Wang, et al.
Human Mutation
|
July 10, 2019
LOVD-DASH: A comprehensive LOVD database coupled with diagnosis and an at-risk assessment system for hemoglobinopathies
Li Zhang, Qianqian Zhang, Yaohua Tang, et al.
Angiogenesis
|
June 28, 2025
Semaphorin 3A protects against thoracic aortic aneurysm dissection by suppressing aortic angiogenesis
Li-Fei Wu, Jiao-Jiao Zhang, Xing Zhang, et al.
European Journal of Human Genetics : EJHG
|
September 5, 2020
NGS-based spinal muscular atrophy carrier screening of 10,585 diverse couples in China: a pan-ethnic study
Sumin Zhao, Wanyang Wang, Yaoshen Wang, et al.
Brain : a Journal of Neurology
|
June 15, 2019
Mutations in C1orf194, encoding a calcium regulator, cause dominant Charcot-Marie-Tooth disease
Shun-Chang Sun, Di Ma, Mei-Yi Li, et al.
European Journal of Human Genetics : EJHG
|
October 3, 2018
Pilot study of expanded carrier screening for 11 recessive diseases in China: results from 10,476 ethnically diverse couples
Sumin Zhao, Jiale Xiang, Chunna Fan, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao
|
April 26, 2026
Genetic dissection of clinical heterogeneity in Hemoglobin H patients by targeted long-read sequencing
Yuhua Ye, Chao Niu, Aiping Mao, et al.
Ebiomedicine
|
September 4, 2017
Rapid Targeted Next-Generation Sequencing Platform for Molecular Screening and Clinical Genotyping in Subjects with Hemoglobinopathies
Xuan Shang, Zhiyu Peng, Yuhua Ye, et al.
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of 11
Search research articles
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Showing results (101-110 of 110) with videos related to
Sort By:
Page
of 11
You have reached the last page of results.
This site can display upto 110 results.
Frontiers in Cellular and Infection Microbiology
|
October 8, 2025
Tissue-resident memory CD8+T cells might enhance HBV DNA clearance in CHB patients with MASLD complication and normal ALT via the CCL-CCR pathways
Chao Cai, Wen-Xuan Shang, Si-Jie Zheng, et al.
Human Mutation
|
September 30, 2016
Mutation in SSUH2 Causes Autosomal-Dominant Dentin Dysplasia Type I
Fu Xiong, Zhisong Ji, Yanhui Liu, et al.
Msystems
|
March 4, 2026
EEG and gut microbiota response patterns in high-altitude indigenous populations
Ke Bai, Ting Ge, Chen-Xi Wang, et al.
Human Mutation
|
July 10, 2019
LOVD-DASH: A comprehensive LOVD database coupled with diagnosis and an at-risk assessment system for hemoglobinopathies
Li Zhang, Qianqian Zhang, Yaohua Tang, et al.
Angiogenesis
|
June 28, 2025
Semaphorin 3A protects against thoracic aortic aneurysm dissection by suppressing aortic angiogenesis
Li-Fei Wu, Jiao-Jiao Zhang, Xing Zhang, et al.
European Journal of Human Genetics : EJHG
|
September 5, 2020
NGS-based spinal muscular atrophy carrier screening of 10,585 diverse couples in China: a pan-ethnic study
Sumin Zhao, Wanyang Wang, Yaoshen Wang, et al.
Brain : a Journal of Neurology
|
June 15, 2019
Mutations in C1orf194, encoding a calcium regulator, cause dominant Charcot-Marie-Tooth disease
Shun-Chang Sun, Di Ma, Mei-Yi Li, et al.
European Journal of Human Genetics : EJHG
|
October 3, 2018
Pilot study of expanded carrier screening for 11 recessive diseases in China: results from 10,476 ethnically diverse couples
Sumin Zhao, Jiale Xiang, Chunna Fan, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao
|
April 26, 2026
Genetic dissection of clinical heterogeneity in Hemoglobin H patients by targeted long-read sequencing
Yuhua Ye, Chao Niu, Aiping Mao, et al.
Ebiomedicine
|
September 4, 2017
Rapid Targeted Next-Generation Sequencing Platform for Molecular Screening and Clinical Genotyping in Subjects with Hemoglobinopathies
Xuan Shang, Zhiyu Peng, Yuhua Ye, et al.
Page
of 11