Intracellular readthrough of nonsense mutations by aminoglycosides in coagulation factor VII
Background: Nonsense mutations in coagulation factor (F) VII potentially cause a lethal hemorrhagic diathesis. Readthrough of nonsense mutations by aminoglycosides has been studied in a few human disease models with variable results. Objectives: We investigated the K316X and W364 FVII mutations, ass...
محفوظ في:
المؤلفون الرئيسيون: | Mirko Pinotti, L. Rizzotto, P. Pinton, P. Ferraresi, A. Chuansumrit, P. Charoenkwan, G. MarchettiI, R. Rizzoto, G. Mariani, F. Bernardi |
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التنسيق: | دورية |
منشور في: |
2018
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الموضوعات: | |
الوصول للمادة أونلاين: | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=33646758850&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/61865 |
الوسوم: |
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مواد مشابهة
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Intracellular readthrough of nonsense mutations by aminoglycosides in coagulation factor VII
بواسطة: Mirko Pinotti, وآخرون
منشور في: (2018) -
Gentamicin induces sub-therapeutic levels of coagulation factor VII in patients with nonsense mutations [1]
بواسطة: Mirko Pinotti, وآخرون
منشور في: (2018) -
Effects of gentamicin inducing readthrough premature stop Codons: A study of alpha-L-iduronidase nonsense variants in COS-7 Cells
بواسطة: Ngiwsara L.
منشور في: (2023) -
Activation of Endoplasmic Reticulum Stress and Unfolded Protein Response in Congenital Factor VII Deficiency
بواسطة: Elisabeth Andersen, وآخرون
منشور في: (2019) -
Activation of a cryptic splice site in a potentially lethal coagulation defect accounts for a functional protein variant
بواسطة: Nicola Cavallari, وآخرون
منشور في: (2018)