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pro vyhledávání: '"Factor VII a"'
Akademický článek
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Akademický článek
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Autor:
Giorgio Rosati, Sofia Camerlo, Alessandro Fornari, Valerio Marci, Barbara Montaruli, Alessandro Morotti
Publikováno v:
Hematology Reports, Vol 16, Iss 1, Pp 132-139 (2024)
Factor VII (FVII) deficiency is a rare bleeding disorder that can be classified as congenital or acquired, and the majority of acquired cases are due to vitamin K deficiency or liver disease. Isolated acquired FVII deficiency is a rare occurrence and
Externí odkaz:
https://doaj.org/article/8e7ccde3a88b4db38caf0214755c38c8
Autor:
Liya Wang, Wenshan Zeng, Yeqing Qian, Yixi Sun, Min Chen, Bei Liu, Junjie Hu, Ping Yu, Minyue Dong
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 12, Iss 7, Pp n/a-n/a (2024)
Abstract Background Synonymous variants are non‐pathogenic due to non‐substitution of amino acids. However, synonymous exonic terminal nucleotide substitutions may affect splicing. Splicing variants are easily analyzed at RNA level for genes expr
Externí odkaz:
https://doaj.org/article/6f4cba715eea42ca9af755ba0ed8026e
Publikováno v:
Iranian Journal of Parasitology, Vol 19, Iss 2 (2024)
Background: Iranian Lizard Leishmania (I.L.L) is a nonpathogenic Leishmania strain. Due to its advantages, several recombinant proteins have been produced in this host. However, I.L.L shows a lower yield of recombinant protein expression compared to
Externí odkaz:
https://doaj.org/article/a4af028573ba48d4b6191b41beab9e82
Publikováno v:
Haemophilia. Mar2017, Vol. 23 Issue 2, p300-308. 9p.
Autor:
Yamada, Shinya1 (AUTHOR) abacus3shinya@gmail.com, Arahata, Masahisa1 (AUTHOR), Morishita, Eriko1 (AUTHOR), Ichinose, Akitada2 (AUTHOR), Asakura, Hidesaku1 (AUTHOR)
Publikováno v:
Haemophilia. Sep2019, Vol. 25 Issue 5, pe350-e352. 3p. 2 Graphs.
Autor:
Sara Moruzzi, Annalisa Castagna, Marianna Spizzo, Silvia Udali, Patrizia Pattini, Francesca Pizzolo, Simonetta Friso, Nicola Martinelli
Publikováno v:
Diagnostics, Vol 14, Iss 16, p 1711 (2024)
Tissue factor (TF) is a transmembrane glycoprotein that represents the fundamental physiological initiator of the coagulation cascade through its interaction with factor VII. TF belongs to the cytokine receptor protein superfamily and contributes to
Externí odkaz:
https://doaj.org/article/f5fb15af30ec43f79dae8cac1d54f1de
Autor:
See, W. ‐ S. Q.1, Chang, K. ‐ O2, Cheuk, D. K. ‐ L.1, Leung, Y. ‐ Y. R.3, Chan, G. C. ‐ F.1, Chan, S. ‐ C.4, Ha, S. ‐ Y.1 syha@hku.hk
Publikováno v:
Haemophilia. Sep2016, Vol. 22 Issue 5, pe417-e422. 6p. 1 Diagram, 2 Charts, 1 Graph.
Publikováno v:
Thrombosis Journal, Vol 21, Iss 1, Pp 1-6 (2023)
Abstract Background Factor VII deficiency is a rare bleeding disorder caused by a deficiency of clotting factor VII. However, there have been some case reports of venous thrombosis in patients with factor VII deficiency, especially underlying the pro
Externí odkaz:
https://doaj.org/article/8c2f9a756a6144628a1a673ed740d451