Zobrazeno 1 - 10
of 309
pro vyhledávání: '"Pros1"'
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 11 (2024)
BackgroundGenetic variation plays an extremely important pathogenic role in the development of venous thromboembolism (VTE). Genetic protein S (PS) deficiency caused by PROS1 gene mutation is an important risk factor for hereditary thrombophilia.Case
Externí odkaz:
https://doaj.org/article/60f21a0ae2494529809f0977d798c7ef
Publikováno v:
Journal of Medical Case Reports, Vol 18, Iss 1, Pp 1-4 (2024)
Abstract Background Lower limb deep vein thrombosis (DVT) concurrent with pulmonary embolism (PE) is perilous, particularly in the elderly, exhibiting heterogeneity with thrombophilia mutations. Tailored treatment is essential, yet sudden deaths comp
Externí odkaz:
https://doaj.org/article/b5a895251dd5478a9c60a1925307a7b1
Autor:
Peng Ding, Yuan Zhou, Kai-Chen Zhang, Sheng Li, Kun-lan Long, Jun Chen, Ying-jie Chen, Pei-yang Gao
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 10 (2023)
BackgroundGenetic and acquired risk factors are fundamental to developing venous thromboembolism. Autosomal dominant protein S deficiency caused by pathogenic mutations in the PROS1 gene is a well-known risk factor for thrombophilia.Case presentation
Externí odkaz:
https://doaj.org/article/b12567bdc65149edabd4753c89e14f2f
Publikováno v:
World Journal of Surgical Oncology, Vol 20, Iss 1, Pp 1-11 (2022)
Abstract Background AXL, a TAM tyrosine kinase receptor, plays an essential role in the pathogenesis of various solid tumours. This study explores the role of AXL and its ligand PROS1 in the generation and biological behaviour of papillary thyroid ca
Externí odkaz:
https://doaj.org/article/c9506091a7784ff0a9bc2d57c8621c7e
Autor:
Marcello Baroni, Silvia Beltrami, Giovanna Schiuma, Paolo Ferraresi, Sabrina Rizzo, Angelina Passaro, Juana Maria Sanz Molina, Roberta Rizzo, Dario Di Luca, Daria Bortolotti
Publikováno v:
Life, Vol 14, Iss 2, p 237 (2024)
Background: Coagulation decompensation is one of the complications most frequently encountered in COVID-19 patients with a poor prognosis or long-COVID syndrome, possibly due to the persistence of SARS-CoV-2 infection in the cardiovascular system. To
Externí odkaz:
https://doaj.org/article/477b5347df5e41099823bce48f88c1e1
Akademický článek
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Autor:
Jinxiang Wang, Nisha Wu, Xiaowei Feng, Yanling Liang, Meijin Huang, Wenle Li, Lingmi Hou, Chengliang Yin
Publikováno v:
Frontiers in Immunology, Vol 13 (2023)
BackgroundGlioma is the most malignant cancer in the brain. As a major vitamin-K-dependent protein in the central nervous system, PROS1 not only plays a vital role in blood coagulation, and some studies have found that it was associated with tumor im
Externí odkaz:
https://doaj.org/article/c5f9d7eaeb374902bca7cd7d464e3955
Akademický článek
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Autor:
Yan-ping Zhang, Bin Lin, Yuan-yuan Ji, Ya-nan Hu, Xin-fu Lin, Yi Tang, Jian-hui Zhang, Shao-jie Wu, Sen-lin Cai, Yan-feng Zhou, Ting Chen, Zhu-ting Fang, Jie-wei Luo
Publikováno v:
Thrombosis Journal, Vol 19, Iss 1, Pp 1-11 (2021)
Abstract Background Protein S deficiency (PSD) is an autosomal dominant hereditary disease. In 1984, familial PSD was reported to be prone to recurrent thrombosis. Follow-up studies have shown that heterozygous protein S (PROS1) mutations increase th
Externí odkaz:
https://doaj.org/article/e43aa8efc6064882ada55ad2c1ad2693
Akademický článek
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