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Hongying Ma

Showing results (61-70 of 66) with videos related to

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Tobacco Induced Diseases|August 17, 2022
Study on the effects of combined tea drinking and mental activity after dinner on smokers in ChinaZhongbo Chen, Xuechan Yu, Hanlu Gao, et al.
Chest|March 9, 2026
Prophylactic haemostatic treatment to control iatrogenic bleeding during endobronchial biopsy (PROTECT study): a multicentre, randomised, single-blind, placebo-controlled studyBei Li, Li He, Wei Wu, et al.
Epilepsia|July 17, 2018
A PRRT2 variant in a Chinese family with paroxysmal kinesigenic dyskinesia and benign familial infantile seizures results in loss of interaction with STX1BHongying Ma, Shenglei Feng, Xuejun Deng, et al.
Science China. Life Sciences|April 18, 2023
Functional characterization of novel NPRL3 mutations identified in three families with focal epilepsyShiyue Du, Sheng Zeng, Li Song, et al.
American Journal of Human Genetics|November 12, 2013
Gain-of-function mutations in SCN11A cause familial episodic painXiang Yang Zhang, Jingmin Wen, Wei Yang, et al.
Nature Genetics|February 14, 2012
Mutations in SLC20A2 link familial idiopathic basal ganglia calcification with phosphate homeostasisCheng Wang, Yulei Li, Lei Shi, et al.
Pageof 7

Showing results (61-70 of 66) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 66 results.
Tobacco Induced Diseases|August 17, 2022
Study on the effects of combined tea drinking and mental activity after dinner on smokers in ChinaZhongbo Chen, Xuechan Yu, Hanlu Gao, et al.
Chest|March 9, 2026
Prophylactic haemostatic treatment to control iatrogenic bleeding during endobronchial biopsy (PROTECT study): a multicentre, randomised, single-blind, placebo-controlled studyBei Li, Li He, Wei Wu, et al.
Epilepsia|July 17, 2018
A PRRT2 variant in a Chinese family with paroxysmal kinesigenic dyskinesia and benign familial infantile seizures results in loss of interaction with STX1BHongying Ma, Shenglei Feng, Xuejun Deng, et al.
Science China. Life Sciences|April 18, 2023
Functional characterization of novel NPRL3 mutations identified in three families with focal epilepsyShiyue Du, Sheng Zeng, Li Song, et al.
American Journal of Human Genetics|November 12, 2013
Gain-of-function mutations in SCN11A cause familial episodic painXiang Yang Zhang, Jingmin Wen, Wei Yang, et al.
Nature Genetics|February 14, 2012
Mutations in SLC20A2 link familial idiopathic basal ganglia calcification with phosphate homeostasisCheng Wang, Yulei Li, Lei Shi, et al.
Pageof 7