Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Sana Alqarni"'
Publikováno v:
Case Reports in Medicine, Vol 2023 (2023)
Antithrombin (AT) deficiency is a blood disorder associated with an increased tendency to form thrombosis. Hereditary AT deficiency is frequently caused by mutations in SERPINC1 gene. It is usually inherited as an autosomal dominant with variable pen
Externí odkaz:
https://doaj.org/article/be2b6bd6677c445781c7bd805afa642a
Autor:
Sana Alqarni, Saleh Alqarni
Publikováno v:
EDULEARN Proceedings.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3f91e39d9ea09c4199affde8fa8dbb69
https://doi.org/10.21125/edulearn.2020.0639
https://doi.org/10.21125/edulearn.2020.0639
Autor:
Penelope M. Tsimbouri, Yazeed A. Al-Sheikh, Paul M. Lieberman, Lauren Jamieson, Adele Hannigan, Mariarca Bailo, Kate Armfield, Shelagh Boyle, Mark E. Drotar, Joanna B. Wilson, Andrew V. Kossenkov, Pawel Herzyk, Sana Alqarni, Donald Campbell
Publikováno v:
Oncogene
Epstein-Barr virus (EBV)-associated Burkitt's lymphoma is characterised by the deregulation of c-Myc expression and a restricted viral gene expression pattern in which the EBV nuclear antigen-1 (EBNA1) is the only viral protein to be consistently exp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5dd3427aff78151e3c85d3c39d77ed1a
https://eprints.gla.ac.uk/161780/13/161780.pdf
https://eprints.gla.ac.uk/161780/13/161780.pdf
