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Shasha Luo

Showing results (31-40 of 64) with videos related to

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Plos One|December 14, 2017
Fungal communities in ancient peatlands developed from different periods in the Sanjiang Plain, ChinaZhenqing Zhang, Xue Zhou, Lei Tian, et al.
Hematology (Amsterdam, Netherlands)|April 2, 2019
Compound heterozygous mutations Glu502Lys and Met527Thr of the FXII gene in a patient with factor XII deficiencyHaiyue Zhang, Siqi Liu, Chanchan Lin, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|May 31, 2020
[Analysis of a Chinese pedigree affected with hereditary factor VII deficiency caused by compound heterozygous variants of F7 gene]Meina Liu, Yanhui Jin, Lihong Yang, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|July 2, 2019
Phenotypic and genetic analysis of hypofibrinogenemia because of a novel missense mutation in the FGB: Leu121ArgHaiyue Zhang, Shasha Luo, Weiwei Fang, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 25, 2020
Analysis of phenotype and genotype of a family with hereditary coagulation factor V deficiency caused by the compound heterozygous mutationsShasha Luo, Siqi Liu, Mengjie Xu, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|December 3, 2019
A novel homozygous mutation (Gly1715Ser) causing hereditary factor V deficiency in a Chinese patientSiqi Liu, Shasha Luo, Lihong Yang, et al.
Journal of Ginseng Research|January 22, 2019
The effect of <i>Glomus intraradices</i> on the physiological properties of <i>Panax ginseng</i> and on rhizospheric microbial diversityLei Tian, Shaohua Shi, Lina Ma, et al.
International Journal of Molecular Medicine|January 8, 2021
ASK1/p38‑mediated NLRP3 inflammasome signaling pathway contributes to aberrant retinal angiogenesis in diabetic retinopathyWenjun Zou, Shasha Luo, Zhengwei Zhang, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|October 1, 2019
Genetic analysis of a pedigree with hereditary coagulation factor XI deficiencyXingxing Zhou, Haiyue Zhang, Mingshan Wang, et al.
Acta Haematologica|September 4, 2019
Two Novel Mutations Cause Hereditary Antithrombin Deficiency in a Chinese FamilyHaiyue Zhang, Siqi Liu, Shasha Luo, et al.
Pageof 7

Showing results (31-40 of 64) with videos related to

Sort By:
Pageof 7
Plos One|December 14, 2017
Fungal communities in ancient peatlands developed from different periods in the Sanjiang Plain, ChinaZhenqing Zhang, Xue Zhou, Lei Tian, et al.
Hematology (Amsterdam, Netherlands)|April 2, 2019
Compound heterozygous mutations Glu502Lys and Met527Thr of the FXII gene in a patient with factor XII deficiencyHaiyue Zhang, Siqi Liu, Chanchan Lin, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|May 31, 2020
[Analysis of a Chinese pedigree affected with hereditary factor VII deficiency caused by compound heterozygous variants of F7 gene]Meina Liu, Yanhui Jin, Lihong Yang, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|July 2, 2019
Phenotypic and genetic analysis of hypofibrinogenemia because of a novel missense mutation in the FGB: Leu121ArgHaiyue Zhang, Shasha Luo, Weiwei Fang, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 25, 2020
Analysis of phenotype and genotype of a family with hereditary coagulation factor V deficiency caused by the compound heterozygous mutationsShasha Luo, Siqi Liu, Mengjie Xu, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|December 3, 2019
A novel homozygous mutation (Gly1715Ser) causing hereditary factor V deficiency in a Chinese patientSiqi Liu, Shasha Luo, Lihong Yang, et al.
Journal of Ginseng Research|January 22, 2019
The effect of <i>Glomus intraradices</i> on the physiological properties of <i>Panax ginseng</i> and on rhizospheric microbial diversityLei Tian, Shaohua Shi, Lina Ma, et al.
International Journal of Molecular Medicine|January 8, 2021
ASK1/p38‑mediated NLRP3 inflammasome signaling pathway contributes to aberrant retinal angiogenesis in diabetic retinopathyWenjun Zou, Shasha Luo, Zhengwei Zhang, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|October 1, 2019
Genetic analysis of a pedigree with hereditary coagulation factor XI deficiencyXingxing Zhou, Haiyue Zhang, Mingshan Wang, et al.
Acta Haematologica|September 4, 2019
Two Novel Mutations Cause Hereditary Antithrombin Deficiency in a Chinese FamilyHaiyue Zhang, Siqi Liu, Shasha Luo, et al.
Pageof 7