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Wanyang Liu

Showing results (31-40 of 52) with videos related to

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Frontiers in Public Health|December 6, 2019
The Play of Genes and Non-genetic Factors on Type 2 DiabetesMichael Mambiya, Mengke Shang, Yue Wang, et al.
Stroke|April 17, 2010
Confirmation of an association of single-nucleotide polymorphism rs1333040 on 9p21 with familial and sporadic intracranial aneurysms in Japanese patientsHirokuni Hashikata, Wanyang Liu, Kayoko Inoue, et al.
Journal of Human Genetics|March 29, 2013
Combined linkage analysis and exome sequencing identifies novel genes for familial goiterJunxia Yan, Tsutomu Takahashi, Toshihiro Ohura, et al.
European Journal of Neurology|November 11, 2020
Meta-analysis of genotype and phenotype studies to confirm the predictive role of the RNF213 p.R4810K variant for moyamoya diseaseYue Wang, Luping Yang, Xiaotong Wang, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|May 6, 2020
Effects of TNF-α-308G/A Polymorphism on the Risk of Diabetic Nephropathy and Diabetic Retinopathy: An Updated Meta-AnalysisMengwei Liu, Mengke Shang, Yue Wang, et al.
Molecular Genetics & Genomic Medicine|March 7, 2019
Association between ADIPOQ G276T and C11377G polymorphisms and the risk of non-alcoholic fatty liver disease: An updated meta-analysisMengwei Liu, Shan Liu, Mengke Shang, et al.
Bioscience Reports|December 10, 2019
Association of single nucleotide polymorphisms of MTHFR, TCN2, RNF213 with susceptibility to hypertension and blood pressureShan Liu, Mengwei Liu, Qian Li, et al.
Pulmonary Circulation|May 3, 2018
Rare variants in RNF213, a susceptibility gene for moyamoya disease, are found in patients with pulmonary hypertension and aggravate hypoxia-induced pulmonary hypertension in miceHatasu Kobayashi, Risako Kabata, Hideyuki Kinoshita, et al.
European Journal of Neurology|September 24, 2024
HAPLN3 p.T34A contributes to incomplete penetrance of moyamoya disease in Chinese carrying RNF213 p.R4810KJun Xu, Zhengxing Zou, Wanyang Liu, et al.
Journal of Genetics|December 28, 2013
Genomewide association study identifies no major founder variant in Caucasian moyamoya diseaseWanyang Liu, S T M L D Senevirathna, Toshiaki Hitomi, et al.
Pageof 6

Showing results (31-40 of 52) with videos related to

Sort By:
Pageof 6
Frontiers in Public Health|December 6, 2019
The Play of Genes and Non-genetic Factors on Type 2 DiabetesMichael Mambiya, Mengke Shang, Yue Wang, et al.
Stroke|April 17, 2010
Confirmation of an association of single-nucleotide polymorphism rs1333040 on 9p21 with familial and sporadic intracranial aneurysms in Japanese patientsHirokuni Hashikata, Wanyang Liu, Kayoko Inoue, et al.
Journal of Human Genetics|March 29, 2013
Combined linkage analysis and exome sequencing identifies novel genes for familial goiterJunxia Yan, Tsutomu Takahashi, Toshihiro Ohura, et al.
European Journal of Neurology|November 11, 2020
Meta-analysis of genotype and phenotype studies to confirm the predictive role of the RNF213 p.R4810K variant for moyamoya diseaseYue Wang, Luping Yang, Xiaotong Wang, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|May 6, 2020
Effects of TNF-α-308G/A Polymorphism on the Risk of Diabetic Nephropathy and Diabetic Retinopathy: An Updated Meta-AnalysisMengwei Liu, Mengke Shang, Yue Wang, et al.
Molecular Genetics & Genomic Medicine|March 7, 2019
Association between ADIPOQ G276T and C11377G polymorphisms and the risk of non-alcoholic fatty liver disease: An updated meta-analysisMengwei Liu, Shan Liu, Mengke Shang, et al.
Bioscience Reports|December 10, 2019
Association of single nucleotide polymorphisms of MTHFR, TCN2, RNF213 with susceptibility to hypertension and blood pressureShan Liu, Mengwei Liu, Qian Li, et al.
Pulmonary Circulation|May 3, 2018
Rare variants in RNF213, a susceptibility gene for moyamoya disease, are found in patients with pulmonary hypertension and aggravate hypoxia-induced pulmonary hypertension in miceHatasu Kobayashi, Risako Kabata, Hideyuki Kinoshita, et al.
European Journal of Neurology|September 24, 2024
HAPLN3 p.T34A contributes to incomplete penetrance of moyamoya disease in Chinese carrying RNF213 p.R4810KJun Xu, Zhengxing Zou, Wanyang Liu, et al.
Journal of Genetics|December 28, 2013
Genomewide association study identifies no major founder variant in Caucasian moyamoya diseaseWanyang Liu, S T M L D Senevirathna, Toshiaki Hitomi, et al.
Pageof 6