Zobrazeno 1 - 7
of 7
pro vyhledávání: '"SALMA WAKIL"'
Publikováno v:
Saudi Pharmaceutical Journal, Vol 28, Iss 8, Pp 963-970 (2020)
Human estrogen receptor positive cancer cells have mutations and make an excess of the HER2 protein and are far more aggressive than others cancers. Neratinib, an irreversible tyrosine kinase inhibitor is used to treat HER2 positive cancers. Neratini
Externí odkaz:
https://doaj.org/article/a3fd516796aa499fa070253e79e8fb14
Autor:
Zuhair N. Al-Hassnan, Waad Albawardi, Faten Almutairi, Rawan AlMass, Albandary AlBakheet, Osama M. Mustafa, Laila AlQuait, Zarghuna M. A. Shinwari, Salma Wakil, Mustafa A. Salih, Majid Al-Fayyadh, Saeed M. Hassan, Mansour Aljoufan, Osima Al-Nakhli, Brynn Levy, Balsam AlMaarik, Hana A. Al-Hakami, Maysoon Alsagob, Dilek Colak, Namik Kaya
Publikováno v:
Molecular Cytogenetics, Vol 11, Iss 1, Pp 1-11 (2018)
Abstract Background Quick genetic diagnosis of a patient with congenital heart disease (CHD) is quite important for proper health care and management. Copy number variations (CNV), chromosomal imbalances and rearrangements have been frequently associ
Externí odkaz:
https://doaj.org/article/238fd9ac89634a798995c2454c74671b
Publikováno v:
Saudi Pharmaceutical Journal, Vol 28, Iss 8, Pp 963-970 (2020)
Saudi Pharmaceutical Journal : SPJ
Saudi Pharmaceutical Journal : SPJ
Human estrogen receptor positive cancer cells have mutations and make an excess of the HER2 protein and are far more aggressive than others cancers. Neratinib, an irreversible tyrosine kinase inhibitor is used to treat HER2 positive cancers. Neratini
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::41f563a230ec051cfe0203f5e99c70a9
http://www.sciencedirect.com/science/article/pii/S1319016420301365
http://www.sciencedirect.com/science/article/pii/S1319016420301365
Publikováno v:
Biomedical Reports. 1:883-888
Coronary artery disease (CAD) is one of the leading causes of mortality in developed countries. Adenosine triphosphate (ATP)-binding cassette A1 (ABCA1) belongs to the superfamily of membrane proteins that function as a key factor in the regulation o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8887fad2b6ff3c327d46e8fd0b60e09
https://doi.org/10.3892/br.2013.163
https://doi.org/10.3892/br.2013.163
Publikováno v:
Genome Biology
To understand the contribution of Mendelian mutations to the burden of undiagnosed diseases that are suspected to be genetic in origin, we developed a next-generation sequencing-based multiplexing assay that encompasses the ~3000 known Mendelian gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21b95f6debeae6307c8bdda2a64f43bc
http://europepmc.org/articles/PMC4605087
http://europepmc.org/articles/PMC4605087
Autor:
Nada Al Tassan, Hussien Elsiesy, RANAD SHAHEEN, Fahad A. Bashiri, SALMA WAKIL, Abbas Hawwari, Amal Alhashem, Mohammed Abdullah Aldahmesh, Iman Abumansour
Publikováno v:
Genome Biology
Background To understand the contribution of Mendelian mutations to the burden of undiagnosed diseases that are suspected to be genetic in origin, we developed a next-generation sequencing-based multiplexing assay that encompasses the ~3000 known Men
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7d0489643c9d15e0bf95906945d19ed
https://doi.org/10.1186/s13059-015-0693-2
https://doi.org/10.1186/s13059-015-0693-2
Autor:
SALMA WAKIL
Publikováno v:
Journal of Pharmacy and Pharmacology. 68:421-421
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::45cad78befc0a747e0cc1ad001d6f6a2
https://doi.org/10.1111/jphp.12546
https://doi.org/10.1111/jphp.12546