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Xiao Dang

Showing results (21-30 of 40) with videos related to

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Human Genetics|June 22, 2026
Investigating the shared genetic architecture between selective immunoglobulin A deficiency and autoimmune diseasesXiao Dang, Frank Qingyun Wang, Caicai Zhang, et al.
Pathogens (Basel, Switzerland)|June 25, 2026
Clinical Characteristics and Risk Factors for Cryptococcal Meningitis in Non-Acquired Immunodeficiency Syndrome Patients with Pulmonary Cryptococcosis: A 12-Year Hospital-Based StudyXiao Dang, Sha-Sha Wu, Lan Zhang, et al.
Nucleic Acids Research|November 3, 2025
DisCP-Atlas: a comprehensive resource mapping cellular processes to complex diseasesFrank Qingyun Wang, Caicai Zhang, Hangchen Zhang, et al.
Frontiers in Neurology|February 19, 2025
Clinical and biochemical characteristics for patients with polyneuropathy, organomegaly, endocrinopathy, M-protein, and skin changes syndrome: a pilot observational studyPei Li, Ye Zhang, Li-Min Luo, et al.
Journal of Geriatric Cardiology : JGC|July 3, 2023
Identification of an <i>LDLR</i> variant in a Chinese familial hypercholesterolemia and its relation to ROS/NLRP3-Mediated pyroptosis in hepatic cellsWen-Zhuo Cheng, Wei-Hua Wang, Ai-Ping Deng, et al.
Frontiers in Genetics|September 1, 2023
Corrigendum: A heterozygous mutation in <i>NOTCH3</i> in a Chinese family with CADASILJuyi Li, Tao Luo, Xiufang Wang, et al.
Frontiers in Genetics|December 19, 2022
A heterozygous mutation in <i>NOTCH3</i> in a Chinese family with CADASILJuyi Li, Tao Luo, Xiufang Wang, et al.
Cardiology|May 12, 2017
Mutation Load of Multiple Ion Channel Gene Mutations in Brugada SyndromeFrancesca Gualandi, Fatima Zaraket, Michele Malagù, et al.
Mobile DNA|October 19, 2024
Association of hyperactivated transposon expression with exacerbated immune activation in systemic lupus erythematosusFrank Qingyun Wang, Xiao Dang, Huidong Su, et al.
Translational Research : the Journal of Laboratory and Clinical Medicine|January 8, 2016
Search for the potential "second-hit" mechanism underlying the onset of familial hemophagocytic lymphohistiocytosis type 2 by whole-exome sequencing analysisLili Gao, Xiao Dang, Liang Huang, et al.
Pageof 4

Showing results (21-30 of 40) with videos related to

Sort By:
Pageof 4
Human Genetics|June 22, 2026
Investigating the shared genetic architecture between selective immunoglobulin A deficiency and autoimmune diseasesXiao Dang, Frank Qingyun Wang, Caicai Zhang, et al.
Pathogens (Basel, Switzerland)|June 25, 2026
Clinical Characteristics and Risk Factors for Cryptococcal Meningitis in Non-Acquired Immunodeficiency Syndrome Patients with Pulmonary Cryptococcosis: A 12-Year Hospital-Based StudyXiao Dang, Sha-Sha Wu, Lan Zhang, et al.
Nucleic Acids Research|November 3, 2025
DisCP-Atlas: a comprehensive resource mapping cellular processes to complex diseasesFrank Qingyun Wang, Caicai Zhang, Hangchen Zhang, et al.
Frontiers in Neurology|February 19, 2025
Clinical and biochemical characteristics for patients with polyneuropathy, organomegaly, endocrinopathy, M-protein, and skin changes syndrome: a pilot observational studyPei Li, Ye Zhang, Li-Min Luo, et al.
Journal of Geriatric Cardiology : JGC|July 3, 2023
Identification of an <i>LDLR</i> variant in a Chinese familial hypercholesterolemia and its relation to ROS/NLRP3-Mediated pyroptosis in hepatic cellsWen-Zhuo Cheng, Wei-Hua Wang, Ai-Ping Deng, et al.
Frontiers in Genetics|September 1, 2023
Corrigendum: A heterozygous mutation in <i>NOTCH3</i> in a Chinese family with CADASILJuyi Li, Tao Luo, Xiufang Wang, et al.
Frontiers in Genetics|December 19, 2022
A heterozygous mutation in <i>NOTCH3</i> in a Chinese family with CADASILJuyi Li, Tao Luo, Xiufang Wang, et al.
Cardiology|May 12, 2017
Mutation Load of Multiple Ion Channel Gene Mutations in Brugada SyndromeFrancesca Gualandi, Fatima Zaraket, Michele Malagù, et al.
Mobile DNA|October 19, 2024
Association of hyperactivated transposon expression with exacerbated immune activation in systemic lupus erythematosusFrank Qingyun Wang, Xiao Dang, Huidong Su, et al.
Translational Research : the Journal of Laboratory and Clinical Medicine|January 8, 2016
Search for the potential "second-hit" mechanism underlying the onset of familial hemophagocytic lymphohistiocytosis type 2 by whole-exome sequencing analysisLili Gao, Xiao Dang, Liang Huang, et al.
Pageof 4