Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Makia J. Marafie"'
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 16, Iss 1, Pp 95-99 (2015)
Background: Primary ciliary dyskinesia is a genetically heterogeneous autosomal recessive disorder with variable clinical manifestations, including chronic rhinosinusitis, otitis media, bronchitis, pneumonia, bronchiectasis, situs inversus totalis, r
Externí odkaz:
https://doaj.org/article/7759f467ccc94b948cbef3d935f5d1dd
Autor:
Rola H. Ali, Makia J. Marafie, Milad S. Bitar, Fahad Al-Dousari, Samar Ismael, Hussain Bin Haider, Waleed Al-Ali, Sindhu P. Jacob, Fahd Al-Mulla
Publikováno v:
International Journal of Molecular Sciences, Vol 15, Iss 10, Pp 17344-17365 (2014)
Gender-related differences in colorectal cancer (CRC) are not fully understood. Recent studies have shown that CRC arising in females are significantly associated with CpG island methylator phenotype (CIMP-high). Using array comparative genomic hybri
Externí odkaz:
https://doaj.org/article/de2ce7e8aa9146cd808e29247d97ae30
Autor:
Makia J Marafie, Fahd Al-Mulla
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 15, Iss 2, Pp 203-207 (2014)
Background: Rare autosomal recessive disorders of variable severity are segregating in many highly consanguineous families from the Arab population. One of these deleterious diseases is Senior-Loken syndrome, a hereditary heterogeneous multiorgan dis
Externí odkaz:
https://doaj.org/article/4363c23bc4a944319c615cac5c070956
Autor:
Rabeah A. Al-Temaimi, Tuan Zea Tan, Makia J. Marafie, Jean Paul Thiery, Philip Quirke, Fahd Al-Mulla
Publikováno v:
International Journal of Molecular Sciences, Vol 17, Iss 5, p 598 (2016)
Colorectal cancer (CRC) is one of the leading causes of cancer mortality. Metastasis remains the primary cause of CRC death. Predicting the possibility of metastatic relapse in early-stage CRC is of paramount importance to target therapy for patients
Externí odkaz:
https://doaj.org/article/027833bd44254c01b24f7a640b166c37
Autor:
Mary E. Velthuizen, Amal Abedrabbo, Demetra Georgiou, Ala I. Sharara, Keivan Majidzadeh-A, Carol Jabari, Laila Rifai, Andreas Hadjisavvas, Fahd Al-Mulla, Hans F. A. Vasen, Zeinab Ghorbanoghli, Rihab Ben Sghaier, Suzan M Talaat, Rania Abu Seir, Gurbankhan Muslumov, Wail Hammoudeh, Maria A. Loizidou, Hadia Ziada-Bouchaar, George Cortas, Berrin Tunca, Makia J. Marafie, Aysel Ahadova, Waseem Hamoudi, Ladan Goshayeshi, Marie-Pierre Buisine, Mohammad Sina
Publikováno v:
Familial Cancer, 20, 215-221. SPRINGER
Familial Cancer
Familial Cancer
Background Lynch syndrome (LS), the most common inherited form of colorectal cancer (CRC), is responsible for 3% of all cases of CRC. LS is caused by a mismatch repair gene defect and is characterized by a high risk for CRC, endometrial cancer and se
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a90eb967f7206c8653eb4ab4f227ba8
https://link.springer.com/article/10.1007/s10689-020-00211-3
https://link.springer.com/article/10.1007/s10689-020-00211-3
Publikováno v:
PLoS ONE, Vol 12, Iss 2, p e0171690 (2017)
PLoS ONE
PLoS ONE
Array-based comparative genomic hybridization (aCGH) emerged as a powerful technology for studying copy number variations at higher resolution in many cancers including colorectal cancer. However, the lack of standardized systematic protocols includi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac83d1e35d46e87de48bfcfa3e488344
http://europepmc.org/articles/PMC5322957?pdf=render
http://europepmc.org/articles/PMC5322957?pdf=render
Autor:
Xiong Yang, Fahd Al-Mulla, Shuhua Xu, Makia J. Marafie, Qidi Feng, Zhi-Ming Ma, Wei Guo, Sindhu Jacob, Suzanne A. Al-Bustan
Publikováno v:
Journal of Human Genetics. 59:615-622
The Middle East (ME) is an important crossroad where modern humans migrated 'out of Africa' and spread into Europe and Asia. After the initial peopling and long-term isolation leading to well-differentiated populations, the ME also had a crucial role
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db787ab906b2b8619ff0008007276607
https://doi.org/10.1038/jhg.2014.81
https://doi.org/10.1038/jhg.2014.81
Autor:
Fahd Al-Mulla, Makia J. Marafie
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 15, Iss 2, Pp 203-207 (2014)
Background : Rare autosomal recessive disorders of variable severity are segregating in many highly consanguineous families from the Arab population. One of these deleterious diseases is Senior-Loken syndrome, a hereditary heterogeneous multiorgan di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::435a967fc3690bd58329f48d43f464bd
http://www.sciencedirect.com/science/article/pii/S1110863013000967
http://www.sciencedirect.com/science/article/pii/S1110863013000967
Publikováno v:
Journal of Cellular Biochemistry. 115:488-497
In this study, we examined the association between the RKIP expression and the molecular subtypes of breast cancer. Microarray gene expression data of 2,333 human breast cancer from 26 different cohorts performed on Affymetrix U133A or U133Plus2 plat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::464afa822aa0c89efab86e610273f5f6
https://doi.org/10.1002/jcb.24682
https://doi.org/10.1002/jcb.24682
Publikováno v:
Middle East Journal of Medical Genetics. 3:31-36
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::34567330eb273b3cb9e560619325982b
https://doi.org/10.1097/01.mxe.0000441099.60123.9c
https://doi.org/10.1097/01.mxe.0000441099.60123.9c