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Yanling Yang

Showing results (361-370 of 376) with videos related to

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Molecular Genetics and Metabolism Reports|June 28, 2018
Diversity in the incidence and spectrum of organic acidemias, fatty acid oxidation disorders, and amino acid disorders in Asian countries: Selective screening vs. expanded newborn screeningNaoaki Shibata, Yuki Hasegawa, Kenji Yamada, et al.
Journal of Human Genetics|August 2, 2005
Frequency and distribution in East Asia of 12 mutations identified in the SLC25A13 gene of Japanese patients with citrin deficiencyYao Bang Lu, Keiko Kobayashi, Miharu Ushikai, et al.
ACS Catalysis|April 17, 2023
Ex Situ Reconstruction-Shaped Ir/CoO/Perovskite Heterojunction for Boosted Water Oxidation ReactionHongquan Guo, Yanling Yang, Guangming Yang, 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.
Neurology|September 18, 2020
Analysis of 70 patients with hydrocephalus due to cobalamin C deficiencyRuxuan He, Hongwu Zhang, Lulu Kang, et al.
Metabolic Brain Disease|April 12, 2017
Identification of novel ATP7A mutations and prenatal diagnosis in Chinese patients with Menkes diseaseBinbin Cao, Xiaoping Yang, Yinyin Chen, et al.
Exploration (Beijing, China)|June 16, 2023
Atomic cerium modulated palladium nanoclusters exsolved ferrite catalysts for lean methane conversionYanling Yang, Si Wang, Xin Tu, et al.
Science (New York, N.Y.)|March 11, 2017
Synthesis, debugging, and effects of synthetic chromosome consolidation: synVI and beyondLeslie A Mitchell, Ann Wang, Giovanni Stracquadanio, et al.
Plos One|February 17, 2018
Hypomyelinating disorders in China: The clinical and genetic heterogeneity in 119 patientsHaoran Ji, Dongxiao Li, Ye Wu, 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.
Pageof 38

Showing results (361-370 of 376) with videos related to

Sort By:
Pageof 38
Molecular Genetics and Metabolism Reports|June 28, 2018
Diversity in the incidence and spectrum of organic acidemias, fatty acid oxidation disorders, and amino acid disorders in Asian countries: Selective screening vs. expanded newborn screeningNaoaki Shibata, Yuki Hasegawa, Kenji Yamada, et al.
Journal of Human Genetics|August 2, 2005
Frequency and distribution in East Asia of 12 mutations identified in the SLC25A13 gene of Japanese patients with citrin deficiencyYao Bang Lu, Keiko Kobayashi, Miharu Ushikai, et al.
ACS Catalysis|April 17, 2023
Ex Situ Reconstruction-Shaped Ir/CoO/Perovskite Heterojunction for Boosted Water Oxidation ReactionHongquan Guo, Yanling Yang, Guangming Yang, 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.
Neurology|September 18, 2020
Analysis of 70 patients with hydrocephalus due to cobalamin C deficiencyRuxuan He, Hongwu Zhang, Lulu Kang, et al.
Metabolic Brain Disease|April 12, 2017
Identification of novel ATP7A mutations and prenatal diagnosis in Chinese patients with Menkes diseaseBinbin Cao, Xiaoping Yang, Yinyin Chen, et al.
Exploration (Beijing, China)|June 16, 2023
Atomic cerium modulated palladium nanoclusters exsolved ferrite catalysts for lean methane conversionYanling Yang, Si Wang, Xin Tu, et al.
Science (New York, N.Y.)|March 11, 2017
Synthesis, debugging, and effects of synthetic chromosome consolidation: synVI and beyondLeslie A Mitchell, Ann Wang, Giovanni Stracquadanio, et al.
Plos One|February 17, 2018
Hypomyelinating disorders in China: The clinical and genetic heterogeneity in 119 patientsHaoran Ji, Dongxiao Li, Ye Wu, 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.
Pageof 38