Expression and methylation status of vascular endothelial growth factor and thrombospondin-1 genes in congenital factor XIII-deficient patients with intracranial hemorrhage-Reference-Cited by-同舟云学术

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Expression and methylation status of vascular endothelial growth factor and thrombospondin-1 genes in congenital factor XIII-deficient patients with intracranial hemorrhage

Published:2021-06-07 Issue:5 Volume:32 Page:317-322
ISSN:0957-5235
Container-title:Blood Coagulation & Fibrinolysis
language:en
Short-container-title:

Author:

Noroozi-Aghideh Ali,Kashanikhatib Zahra,Naderi Majid,Dorgalaleh Akbar,Azad Mehdi,Alizadeh Shaban

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Hematology,General Medicine

Reference31 articles.

1. Blood coagulation factor XIII and factor XIII deficiency;Dorgalaleh;Blood Rev,2016

2. Advances of coagulation factor XIII;Shi;Chin Med J (Engl),2017

3. Molecular basis of congenital factor XIII deficiency in Iran;Dorgalaleh;Clin Appl Thromb Hemost,2018

4. Intracranial hemorrhage: a devastating outcome of congenital bleeding disorders – prevalence, diagnosis, and management, with a special focus on congenital factor XIII deficiency;Alavi;Semin Thromb Hemost,2018

5. Laboratory diagnosis of factor XIII deficiency, routine coagulation tests with quantitative and qualitative methods;Dorgalaleh;Clin Lab,2016

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Dual role of microRNAs in cancer metastasis;Human Gene;2023-12

2. The most common disease-causing mutation of factor XIII deficiency is corrected by CRISPR/CAS9 gene editing system;Blood Coagulation & Fibrinolysis;2022-02-25

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