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Xuyun Hu

Showing results (31-40 of 62) with videos related to

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Molecular Therapy. Nucleic Acids|May 26, 2022
Retraction Notice to: Silencing of Long Non-coding RNA HOTTIP Reduces Inflammation in Rheumatoid Arthritis by Demethylation of SFRP1Xumin Hu, Jianhua Tang, Xuyun Hu, et al.
Genetic Testing and Molecular Biomarkers|December 28, 2022
Newborn Genetic Screening Revealed Increased Levels of Biochemical Indicators in Carriers of Heterozygous VariantsWenyan Zhang, Feng Jin, Ruolan Guo, et al.
Molecular Therapy. Nucleic Acids|January 7, 2020
Silencing of Long Non-coding RNA HOTTIP Reduces Inflammation in Rheumatoid Arthritis by Demethylation of SFRP1Xumin Hu, Jianhua Tang, Xuyun Hu, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|July 13, 2026
Novel <i>NPR2</i> heterozygous variant in a familial short stature and the therapeutic response to rhGH: a case reportDongmei Wang, Xuyun Hu, Shan Su, et al.
BMC Medical Genomics|December 5, 2020
The first familial NSD2 cases with a novel variant in a Chinese father and daughter with atypical WHS facial features and a 7.5-year follow-up of growth hormone therapyXuyun Hu, Di Wu, Yuchuan Li, et al.
European Journal of Human Genetics : EJHG|October 24, 2024
Targeted gene sequencing and hearing follow-up in 7501 newborns reveals an improved strategy for newborn hearing screeningChanjuan Hao, Xuyun Hu, Ruolan Guo, et al.
Biochemical and Biophysical Research Communications|March 5, 2014
TALE nickase mediates high efficient targeted transgene integration at the human multi-copy ribosomal DNA locusYong Wu, Tieli Gao, Xiaolin Wang, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao|June 3, 2020
Severe cases of BCGosis-susceptible primary immunodeficiency diseases identified by next-generation sequencing: Implications for adjustment of BCG vaccination timing in ChinaGang Liu, Haijuan Xiao, Linlin Liu, et al.
Molecular Cytogenetics|May 10, 2016
de novo interstitial deletions at the 11q23.3-q24.2 regionJiasun Su, Rongyu Chen, Jingsi Luo, et al.
Scientific Reports|January 9, 2016
In situ genetic correction of F8 intron 22 inversion in hemophilia A patient-specific iPSCsYong Wu, Zhiqing Hu, Zhuo Li, et al.
Pageof 7

Showing results (31-40 of 62) with videos related to

Sort By:
Pageof 7
Molecular Therapy. Nucleic Acids|May 26, 2022
Retraction Notice to: Silencing of Long Non-coding RNA HOTTIP Reduces Inflammation in Rheumatoid Arthritis by Demethylation of SFRP1Xumin Hu, Jianhua Tang, Xuyun Hu, et al.
Genetic Testing and Molecular Biomarkers|December 28, 2022
Newborn Genetic Screening Revealed Increased Levels of Biochemical Indicators in Carriers of Heterozygous VariantsWenyan Zhang, Feng Jin, Ruolan Guo, et al.
Molecular Therapy. Nucleic Acids|January 7, 2020
Silencing of Long Non-coding RNA HOTTIP Reduces Inflammation in Rheumatoid Arthritis by Demethylation of SFRP1Xumin Hu, Jianhua Tang, Xuyun Hu, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|July 13, 2026
Novel <i>NPR2</i> heterozygous variant in a familial short stature and the therapeutic response to rhGH: a case reportDongmei Wang, Xuyun Hu, Shan Su, et al.
BMC Medical Genomics|December 5, 2020
The first familial NSD2 cases with a novel variant in a Chinese father and daughter with atypical WHS facial features and a 7.5-year follow-up of growth hormone therapyXuyun Hu, Di Wu, Yuchuan Li, et al.
European Journal of Human Genetics : EJHG|October 24, 2024
Targeted gene sequencing and hearing follow-up in 7501 newborns reveals an improved strategy for newborn hearing screeningChanjuan Hao, Xuyun Hu, Ruolan Guo, et al.
Biochemical and Biophysical Research Communications|March 5, 2014
TALE nickase mediates high efficient targeted transgene integration at the human multi-copy ribosomal DNA locusYong Wu, Tieli Gao, Xiaolin Wang, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao|June 3, 2020
Severe cases of BCGosis-susceptible primary immunodeficiency diseases identified by next-generation sequencing: Implications for adjustment of BCG vaccination timing in ChinaGang Liu, Haijuan Xiao, Linlin Liu, et al.
Molecular Cytogenetics|May 10, 2016
de novo interstitial deletions at the 11q23.3-q24.2 regionJiasun Su, Rongyu Chen, Jingsi Luo, et al.
Scientific Reports|January 9, 2016
In situ genetic correction of F8 intron 22 inversion in hemophilia A patient-specific iPSCsYong Wu, Zhiqing Hu, Zhuo Li, et al.
Pageof 7