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Wanling Yang

Showing results (131-140 of 168) with videos related to

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Cancers|October 14, 2023
Genome-Wide DNA Methylation Profiling as Frontline Diagnostics for Central Nervous System Embryonal Tumors in Hong KongOtto C H Tam, Ronnie S L Ho, Shing Chan, et al.
Cell|August 12, 2025
NRT1.1B acts as an abscisic acid receptor in integrating compound environmental cues for plantsXiaojun Ma, Wei Wang, Jingyi Zhang, et al.
The Journal of Allergy and Clinical Immunology|September 17, 2020
Excessive deubiquitination of NLRP3-R779C variant contributes to very-early-onset inflammatory bowel disease developmentLingli Zhou, Tao Liu, Bing Huang, et al.
Arthritis Research & Therapy|December 5, 2015
Discovery of a novel genetic susceptibility locus on X chromosome for systemic lupus erythematosusZhengwei Zhu, Zhuoyuan Liang, Herty Liany, et al.
Ebiomedicine|May 28, 2026
Translating transcriptomics analysis into diagnostic workflows: clinical variant identification and interpretation in hypothesis-driven and hypothesis-free approachesChingyiu Pang, Martin Man-Chun Chui, Wenshu Tang, et al.
Annals of Human Genetics|April 26, 2013
Epistatic interaction between genetic variants in susceptibility gene ETS1 correlates with IL-17 levels in SLE patientsJing Zhang, Yan Zhang, Lu Zhang, et al.
BMC Medical Genomics|October 26, 2018
Identifying the genetic causes for prenatally diagnosed structural congenital anomalies (SCAs) by whole-exome sequencing (WES)Gordon K C Leung, Christopher C Y Mak, Jasmine L F Fung, et al.
Communications Biology|November 21, 2025
Imputation disparities driven by recent selection and their impact on disease risk estimation in East and Southeast Asian populationsDingyang Li, Pattarin Tangtanatakul, Yao Lei, et al.
Molecular Genetics & Genomic Medicine|January 25, 2017
<i>CFTR</i> founder mutation causes protein trafficking defects in Chinese patients with cystic fibrosisGordon K C Leung, Dingge Ying, Christopher C Y Mak, et al.
Nature Genetics|November 15, 2011
Genome-wide association study identifies FCGR2A as a susceptibility locus for Kawasaki diseaseChiea Chuen Khor, Sonia Davila, Willemijn B Breunis, et al.
Pageof 17

Showing results (131-140 of 168) with videos related to

Sort By:
Pageof 17
Cancers|October 14, 2023
Genome-Wide DNA Methylation Profiling as Frontline Diagnostics for Central Nervous System Embryonal Tumors in Hong KongOtto C H Tam, Ronnie S L Ho, Shing Chan, et al.
Cell|August 12, 2025
NRT1.1B acts as an abscisic acid receptor in integrating compound environmental cues for plantsXiaojun Ma, Wei Wang, Jingyi Zhang, et al.
The Journal of Allergy and Clinical Immunology|September 17, 2020
Excessive deubiquitination of NLRP3-R779C variant contributes to very-early-onset inflammatory bowel disease developmentLingli Zhou, Tao Liu, Bing Huang, et al.
Arthritis Research & Therapy|December 5, 2015
Discovery of a novel genetic susceptibility locus on X chromosome for systemic lupus erythematosusZhengwei Zhu, Zhuoyuan Liang, Herty Liany, et al.
Ebiomedicine|May 28, 2026
Translating transcriptomics analysis into diagnostic workflows: clinical variant identification and interpretation in hypothesis-driven and hypothesis-free approachesChingyiu Pang, Martin Man-Chun Chui, Wenshu Tang, et al.
Annals of Human Genetics|April 26, 2013
Epistatic interaction between genetic variants in susceptibility gene ETS1 correlates with IL-17 levels in SLE patientsJing Zhang, Yan Zhang, Lu Zhang, et al.
BMC Medical Genomics|October 26, 2018
Identifying the genetic causes for prenatally diagnosed structural congenital anomalies (SCAs) by whole-exome sequencing (WES)Gordon K C Leung, Christopher C Y Mak, Jasmine L F Fung, et al.
Communications Biology|November 21, 2025
Imputation disparities driven by recent selection and their impact on disease risk estimation in East and Southeast Asian populationsDingyang Li, Pattarin Tangtanatakul, Yao Lei, et al.
Molecular Genetics & Genomic Medicine|January 25, 2017
<i>CFTR</i> founder mutation causes protein trafficking defects in Chinese patients with cystic fibrosisGordon K C Leung, Dingge Ying, Christopher C Y Mak, et al.
Nature Genetics|November 15, 2011
Genome-wide association study identifies FCGR2A as a susceptibility locus for Kawasaki diseaseChiea Chuen Khor, Sonia Davila, Willemijn B Breunis, et al.
Pageof 17