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Fengxiao Bu

Showing results (1-10 of 34) with videos related to

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Genes|May 4, 2026
A Cross-Species Single-Cell Atlas Reveals Conserved Regulatory Networks and Candidate Hearing Loss Genes in the CochleaHui Cheng, Fandi Ai, Wan Hua, et al.
Journal of Medical Genetics|September 19, 2025
Calibration and refinement of ACMG/AMP criteria for variant classification with BayesQuantifySihan Liu, Xiaoshu Feng, Yang Wu, et al.
Clinical & Developmental Immunology|December 20, 2012
Familial atypical hemolytic uremic syndrome: a review of its genetic and clinical aspectsFengxiao Bu, Nicolo Borsa, Ardissino Gianluigi, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao|December 24, 2023
NCAD v1.0: a database for non-coding variant annotation and interpretationXiaoshu Feng, Sihan Liu, Ke Li, et al.
Case Reports in Nephrology and Dialysis|October 9, 2025
A Complement Factor B Mutation in a Chinese Family with Atypical Hemolytic Uremic Syndrome: A Case Report and Systematic ReviewWan Peng, Xicui Long, Haoran Lei, et al.
Science China. Life Sciences|January 22, 2025
Sequencing and characterizing human mitochondrial genomes in the biobank-based genomic research paradigmLintao Luo, Mengge Wang, Yunhui Liu, et al.
Journal of the American Society of Nephrology : JASN|September 14, 2013
Comprehensive genetic analysis of complement and coagulation genes in atypical hemolytic uremic syndromeFengxiao Bu, Tara Maga, Nicole C Meyer, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao|January 5, 2024
Exploring noncoding variants in genetic diseases: from detection to functional insightsKe Wu, Fengxiao Bu, Yang Wu, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao|April 6, 2025
Multiple nucleotide variants in genetic diagnosis: implications from 11,467 cases of hearing lossFandi Ai, Jiayi Zeng, Qian Zhang, et al.
Frontiers in Genetics|March 21, 2022
seGMM: A New Tool for Gender Determination From Massively Parallel Sequencing DataSihan Liu, Yuanyuan Zeng, Chao Wang, et al.
Pageof 4

Showing results (1-10 of 34) with videos related to

Sort By:
Pageof 4
Genes|May 4, 2026
A Cross-Species Single-Cell Atlas Reveals Conserved Regulatory Networks and Candidate Hearing Loss Genes in the CochleaHui Cheng, Fandi Ai, Wan Hua, et al.
Journal of Medical Genetics|September 19, 2025
Calibration and refinement of ACMG/AMP criteria for variant classification with BayesQuantifySihan Liu, Xiaoshu Feng, Yang Wu, et al.
Clinical & Developmental Immunology|December 20, 2012
Familial atypical hemolytic uremic syndrome: a review of its genetic and clinical aspectsFengxiao Bu, Nicolo Borsa, Ardissino Gianluigi, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao|December 24, 2023
NCAD v1.0: a database for non-coding variant annotation and interpretationXiaoshu Feng, Sihan Liu, Ke Li, et al.
Case Reports in Nephrology and Dialysis|October 9, 2025
A Complement Factor B Mutation in a Chinese Family with Atypical Hemolytic Uremic Syndrome: A Case Report and Systematic ReviewWan Peng, Xicui Long, Haoran Lei, et al.
Science China. Life Sciences|January 22, 2025
Sequencing and characterizing human mitochondrial genomes in the biobank-based genomic research paradigmLintao Luo, Mengge Wang, Yunhui Liu, et al.
Journal of the American Society of Nephrology : JASN|September 14, 2013
Comprehensive genetic analysis of complement and coagulation genes in atypical hemolytic uremic syndromeFengxiao Bu, Tara Maga, Nicole C Meyer, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao|January 5, 2024
Exploring noncoding variants in genetic diseases: from detection to functional insightsKe Wu, Fengxiao Bu, Yang Wu, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao|April 6, 2025
Multiple nucleotide variants in genetic diagnosis: implications from 11,467 cases of hearing lossFandi Ai, Jiayi Zeng, Qian Zhang, et al.
Frontiers in Genetics|March 21, 2022
seGMM: A New Tool for Gender Determination From Massively Parallel Sequencing DataSihan Liu, Yuanyuan Zeng, Chao Wang, et al.
Pageof 4