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Mengqiu Li

Showing results (61-70 of 68) with videos related to

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Orphanet Journal of Rare Diseases|September 2, 2022
Late-onset cblC deficiency around puberty: a retrospective study of the clinical characteristics, diagnosis, and treatmentZhehui Chen, Hui Dong, Yupeng Liu, et al.
Free Radical Biology & Medicine|April 8, 2018
Hepatocyte-specific deletion of LASS2 protects against diet-induced hepatic steatosis and insulin resistanceShaohua Fan, Yanyan Wang, Cun Wang, et al.
Plos One|March 31, 2022
Comparing amniotic fluid mass spectrometry assays and amniocyte gene analyses for the prenatal diagnosis of methylmalonic aciduriaYupeng Liu, Zhehui Chen, Lulu Kang, et al.
Journal of Inherited Metabolic Disease|October 18, 2019
A study on a cohort of 301 Chinese patients with isolated methylmalonic acidemiaLulu Kang, Yupeng Liu, Ming Shen, et al.
Nature Communications|February 21, 2019
The structure of a prokaryotic viral envelope protein expands the landscape of membrane fusion proteinsKamel El Omari, Sai Li, Abhay Kotecha, et al.
Neurology|September 18, 2020
Analysis of 70 patients with hydrocephalus due to cobalamin C deficiencyRuxuan He, Hongwu Zhang, Lulu Kang, et al.
Orphanet Journal of Rare Diseases|August 5, 2020
Variable phenotypes and outcomes associated with the MMACHC c.609G>A homologous mutation: long term follow-up in a large cohort of casesRuxuan He, Ruo Mo, Ming Shen, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|July 1, 2022
[Factors affecting phenotypes in the patients with MMACHC gene c.609G>A homozygous variant cblC type methylmalonic acidemia combined with homocysteinuria]Ruxuan He, Ruo Mo, Yao Zhang, et al.
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Showing results (61-70 of 68) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 68 results.
Orphanet Journal of Rare Diseases|September 2, 2022
Late-onset cblC deficiency around puberty: a retrospective study of the clinical characteristics, diagnosis, and treatmentZhehui Chen, Hui Dong, Yupeng Liu, et al.
Free Radical Biology & Medicine|April 8, 2018
Hepatocyte-specific deletion of LASS2 protects against diet-induced hepatic steatosis and insulin resistanceShaohua Fan, Yanyan Wang, Cun Wang, et al.
Plos One|March 31, 2022
Comparing amniotic fluid mass spectrometry assays and amniocyte gene analyses for the prenatal diagnosis of methylmalonic aciduriaYupeng Liu, Zhehui Chen, Lulu Kang, et al.
Journal of Inherited Metabolic Disease|October 18, 2019
A study on a cohort of 301 Chinese patients with isolated methylmalonic acidemiaLulu Kang, Yupeng Liu, Ming Shen, et al.
Nature Communications|February 21, 2019
The structure of a prokaryotic viral envelope protein expands the landscape of membrane fusion proteinsKamel El Omari, Sai Li, Abhay Kotecha, et al.
Neurology|September 18, 2020
Analysis of 70 patients with hydrocephalus due to cobalamin C deficiencyRuxuan He, Hongwu Zhang, Lulu Kang, et al.
Orphanet Journal of Rare Diseases|August 5, 2020
Variable phenotypes and outcomes associated with the MMACHC c.609G>A homologous mutation: long term follow-up in a large cohort of casesRuxuan He, Ruo Mo, Ming Shen, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|July 1, 2022
[Factors affecting phenotypes in the patients with MMACHC gene c.609G>A homozygous variant cblC type methylmalonic acidemia combined with homocysteinuria]Ruxuan He, Ruo Mo, Yao Zhang, et al.
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