Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Mouza M. Al-Ameri"'
Autor:
Thom Huppertz, Abdelmoneim Abdalla, Mouza M. Al-Ameri, Mohd Affan Baig, Jaleel Kizhakkayil, Mutamed M. Ayyash, Gang Chen, Afaf Kamal-Eldin
Publikováno v:
Journal of Dairy Science 104 (2021) 9
Journal of Dairy Science, 104(9), 9450-9464
Journal of Dairy Science, 104(9), 9450-9464
The objective of this study was to assess protein degradation and biological activities of the water-soluble extract (WSE) and the 10 kDa permeable and nonpermeable fractions of in vitro digesta of low-fat Akawi cheese made from blends (100:0, 85:15,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eef4f5e876aa4a413a42e6fa045d3aa6
https://research.wur.nl/en/publications/biological-activities-of-the-bioaccessible-compounds-after-in-vit
https://research.wur.nl/en/publications/biological-activities-of-the-bioaccessible-compounds-after-in-vit
Autor:
Bassam R Ali, Imen Ben-Rebeh, Anne John, Nadia A Akawi, Reham M Milhem, Nouf A Al-Shehhi, Mouza M Al-Ameri, Shamma A Al-Shamisi, Lihadh Al-Gazali
Publikováno v:
PLoS ONE, Vol 6, Iss 10, p e26206 (2011)
Hereditary haemorrhagic telangiectasia (HHT) is an autosomal dominant genetic condition affecting the vascular system and is characterised by epistaxis, arteriovenous malformations and mucocutaneous and gastrointestinal telangiectases. This disorder
Externí odkaz:
https://doaj.org/article/0c1361e492a343028561c1a1d16335c9
Autor:
Nadia Akawi, Imen Ben-Rebeh, Shamma A. Al-Shamisi, Bassam R. Ali, Anne John, Reham M. Milhem, Mouza M. Al-Ameri, Nouf Ahmed Alshehhi, Lihadh Al-Gazali
Publikováno v:
PLoS ONE
PLoS ONE, Vol 6, Iss 10, p e26206 (2011)
PLoS ONE, Vol 6, Iss 10, p e26206 (2011)
Hereditary haemorrhagic telangiectasia (HHT) is an autosomal dominant genetic condition affecting the vascular system and is characterised by epistaxis, arteriovenous malformations and mucocutaneous and gastrointestinal telangiectases. This disorder
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f47a53089e63c9fa74696c5967d36bf
https://doi.org/10.1371/journal.pone.0026206
https://doi.org/10.1371/journal.pone.0026206