Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Manal Wilson"'
Autor:
Samea Rizk, Amal El-Mahdy, Manal Wilson, Amira Osama Abd El-Ghafar, Howayda Mohamed, Amira Noureldin, Hanan El-Hosseiny
Publikováno v:
Benha Medical Journal. 37:439-448
Background: Alpha-smooth muscle actin (α-SMA) is used as a marker for a subset of activated fibrogenic cells, myofibroblasts, which are regarded as important effector cells of tissue fibrogenesis. Purpose: We addressed whether ASMA gene (actin alpha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b40c68b23a0901d3dff805e57e707024
https://doi.org/10.21608/bmfj.2020.97897
https://doi.org/10.21608/bmfj.2020.97897
Autor:
Rabab El Hawary, Manar El-Baioumy, Safa Meshaal, Sherif Elanwary, Nancy El-Guindy, Ghada Ezzat, Manal Wilson, Inas Raafat
Publikováno v:
Gene Reports. 27:101620
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fa572ad45cfc46c6cc16d50f1d366384
https://doi.org/10.1016/j.genrep.2022.101620
https://doi.org/10.1016/j.genrep.2022.101620
Autor:
Hala Lotfy Fayed, Manal Wilson, Huda Marzouk, Amany A. Abou-Elalla, Mariam Onsy F. Hanna, Mervat Talaat Zakaria
Publikováno v:
Pathobiology. 83:295-300
Background: Since spontaneous inflammation is an important contributor to familial Mediterranean fever (FMF), genetic variants mediating inflammation are of interest. We investigated gene variants in the acute-phase serum amyloid A type 1 (SAA1), a s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ccb1377da1466a6f191de59dabb79554
https://doi.org/10.1159/000444933
https://doi.org/10.1159/000444933
Publikováno v:
Egyptian Journal of Medical Human Genetics; Vol 16, No 2 (2015); 129-133
Egyptian Journal of Medical Human Genetics, Vol 16, Iss 2, Pp 129-133 (2015)
Egyptian Journal of Medical Human Genetics, Vol 16, Iss 2, Pp 129-133 (2015)
Introduction: β-thalassemia is a common genetic disorder affecting the β-globin gene, characterized by ineffective erythropoiesis and iron overload. It is the most common hereditary hemolytic anemia in Egypt(85.1%)with a carrier rate of 5.3to 9% an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::41138189dd803595b73683a9d31fc0b9
Autor:
Luigi Terracciano, Druckerei Stückle, Fréderic Duprez, Joema Felipe Lima, Yasufumi Saito, Seiji Naito, Momoe Itsumi, Philippe Deron, Cynthia Aparecida Bueno de Toledo Osório, Masatoshi Kochi, João de Jesus Viana Pinheiro, Takao Hinoi, Tijl Vermassen, Yoko Takahashi, Kenichi Kohashi, Karen Zwaenepoel, Tatsuro Abe, Mervat Talaat Zakaria, Liliane Oliveira de Lima Amaral dos Santos, Huda Marzouk, Shoichiro Mukai, Valeria Perrina, Yuko Kusakabe, Kobori Masuko, Haruki Sada, Tomohiro Adachi, Amany A. Abou-Elalla, Maíra A. Lima, Suely Nonogaki, Kentaro Kuroiwa, Luigi Tornillo, Hiroko Inoue, Mariam Onsy F. Hanna, Sylvie Rottey, Masaki Shiota, Hideki Ohdan, Hala Lotfy Fayed, Ichiro Saito, Astrid De Meulenaere, JA Turri, Luca Quagliata, Fernando Augusto Soares, Yuichi Yamada, Kazuhiro Sentani, Satz Mengensatzproduktion, Masaaki Sugimoto, Vanessa Morais Freitas, Naohide Oue, Liesbeth Ferdinande, Yumiko Shindo, Yoshinao Oda, Wataru Yasui, Hiroaki Niitsu, Manal Wilson, Manuel Schlageter, Marcilei E. Buim, Sandrine Aspeslagh, Matthias S. Matter, Masashi Miguchi, Takayuki Kawai
Publikováno v:
Pathobiology. 83
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::71e3cf735d494d0221af4783d1bd2f0b
https://doi.org/10.1159/000448128
https://doi.org/10.1159/000448128
Autor:
Ghada A. Abdallah, Happy Sawires, Rania Fawzy, Manal Wilson, Eman Fathy, Ilham Youssry, Samuel H Makar
Publikováno v:
Pediatric nephrology (Berlin, Germany). 30(12)
Given the burden and poor outcome of end-stage renal disease in sickle cell disease (SCD), early markers of sickle cell nephropathy (SN) are desirable. Disordered angiogenesis underlies many complications of SCD. We aimed to determine the relationshi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b94ca51d5f46211b9018ff36a453332
https://pubmed.ncbi.nlm.nih.gov/26238275
https://pubmed.ncbi.nlm.nih.gov/26238275
Publikováno v:
Italian Journal of Pediatrics
Background: Asthma is the result of a complex interaction between environmental factors and genetic variants that confer susceptibility. The glutathione S-transferases (GSTT1 and GSTM1) are phase II enzymes thought to protect the airways from oxidati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d3b73d71f6af4c1162d42c33e41159e
https://doi.org/10.1186/1824-7288-40-22
https://doi.org/10.1186/1824-7288-40-22
Publikováno v:
Egyptian Journal of Medical Human Genetics; Vol 14, No 2 (2013)
The present study investigated the relationship between the genetic polymorphisms in MMP-9 and MMP-3 genes and acute myocardial infarction (AMI). We examined 40 patients with acute myocardial infarction and 40 age and sex matched controls for MMP-9 f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef67bfa2da2f147e9e257a4efcddf695
https://www.ajol.info/index.php/ejhg/article/view/87406
https://www.ajol.info/index.php/ejhg/article/view/87406
Autor:
Doha A. Mokhtar, Mona M. El-Falaki, Mohamed S. El Baz, Manal Wilson, Dina H. Hamed, Ghada M. Ezzat
Publikováno v:
Egyptian Journal of Medical Human Genetics. (1):55-62
A disintegrin and metalloproteinase-encoding gene (ADAM33), was recently identified as an asthma susceptibility gene. ADAM33 protein is expressed in smooth muscle cells of bronchi and pulmonary fibroblasts, playing a major role in airway remodeling.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc798e31bf734e57c0c462620e0e03cb