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Annals of Anatomy = Anatomischer Anzeiger : Official Organ of the Anatomische Gesellschaft
|
November 5, 2023
Interference of MDM2 attenuates vascular endothelial dysfunction in hypertension partly through blocking Notch1/NLRP3 inflammasome pathway
Rongyan Sun, Yubo Zhou, Jiao Liang, et al.
Frontiers in Pediatrics
|
June 26, 2023
Case report: A case of immune thrombocytopenia combined with Hashimoto's thyroiditis and Helicobacter pylori infection in a child
Lihong Yang, Dongqiong Xiao, Xihong Li, et al.
Hematology (Amsterdam, Netherlands)
|
February 16, 2017
Phenotypic and genetic analysis of dysprothrombinemia due to a novel homozygous mutation
Kankan Su, Yanhui Jin, Zhihai Miao, et al.
Cytotechnology
|
October 5, 2019
Bioactive molecule Icariin inhibited proliferation while enhanced apoptosis and autophagy of rat airway smooth muscle cells in vitro
Lihong Yang, Bo Xiao, Lixia Hou, et al.
Acta Biochimica Et Biophysica Sinica
|
June 7, 2019
Alteration of the microRNA expression profile and identification of miRNA/mRNA negative regulation pairs in neural tube defects
Juan Zhang, Lihong Yang, Juan Yu, et al.
International Journal of Hematology
|
February 1, 2018
Genetic analysis of a novel missense mutation (Gly542Ser) with factor XII deficiency in a Chinese patient of consanguineous marriage
Anqing Zou, Mingshan Wang, Yanhui Jin, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis
|
December 19, 2017
A novel factor X mutation Cys81 by Arg and a reported factor VII polymorphism Arg353 replaced by Gln co-occured in a patient
Yanhui Jin, Xiaoli Cheng, Jiayong Zheng, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis
|
August 18, 2022
A novel F13A1 gene mutation (Arg208Pro) in a Chinese patient with factor XIII deficiency
Haixiao Xie, Mingshan Wang, Yanhui Jin, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis
|
November 20, 2021
Genetic analysis of compound heterozygous pathogenic variants of the F11 gene in two Chinese patients with hereditary factor XI deficiency
Huanhuan Wang, Shuting Jiang, Haixiao Xie, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
December 26, 2025
[Genetic analysis of a family with inheritary coagulation factor Ⅹ deficiency due to compound heterozygous variants p.Phe71Ser and p.Val424Phe]
Shuangnyu Lin, Bile Chen, Zuoting Xie, et al.
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of 33
Search research articles
Search
Showing results (61-70 of 330) with videos related to
Sort By:
Page
of 33
Annals of Anatomy = Anatomischer Anzeiger : Official Organ of the Anatomische Gesellschaft
|
November 5, 2023
Interference of MDM2 attenuates vascular endothelial dysfunction in hypertension partly through blocking Notch1/NLRP3 inflammasome pathway
Rongyan Sun, Yubo Zhou, Jiao Liang, et al.
Frontiers in Pediatrics
|
June 26, 2023
Case report: A case of immune thrombocytopenia combined with Hashimoto's thyroiditis and Helicobacter pylori infection in a child
Lihong Yang, Dongqiong Xiao, Xihong Li, et al.
Hematology (Amsterdam, Netherlands)
|
February 16, 2017
Phenotypic and genetic analysis of dysprothrombinemia due to a novel homozygous mutation
Kankan Su, Yanhui Jin, Zhihai Miao, et al.
Cytotechnology
|
October 5, 2019
Bioactive molecule Icariin inhibited proliferation while enhanced apoptosis and autophagy of rat airway smooth muscle cells in vitro
Lihong Yang, Bo Xiao, Lixia Hou, et al.
Acta Biochimica Et Biophysica Sinica
|
June 7, 2019
Alteration of the microRNA expression profile and identification of miRNA/mRNA negative regulation pairs in neural tube defects
Juan Zhang, Lihong Yang, Juan Yu, et al.
International Journal of Hematology
|
February 1, 2018
Genetic analysis of a novel missense mutation (Gly542Ser) with factor XII deficiency in a Chinese patient of consanguineous marriage
Anqing Zou, Mingshan Wang, Yanhui Jin, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis
|
December 19, 2017
A novel factor X mutation Cys81 by Arg and a reported factor VII polymorphism Arg353 replaced by Gln co-occured in a patient
Yanhui Jin, Xiaoli Cheng, Jiayong Zheng, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis
|
August 18, 2022
A novel F13A1 gene mutation (Arg208Pro) in a Chinese patient with factor XIII deficiency
Haixiao Xie, Mingshan Wang, Yanhui Jin, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis
|
November 20, 2021
Genetic analysis of compound heterozygous pathogenic variants of the F11 gene in two Chinese patients with hereditary factor XI deficiency
Huanhuan Wang, Shuting Jiang, Haixiao Xie, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
December 26, 2025
[Genetic analysis of a family with inheritary coagulation factor Ⅹ deficiency due to compound heterozygous variants p.Phe71Ser and p.Val424Phe]
Shuangnyu Lin, Bile Chen, Zuoting Xie, et al.
Page
of 33