Zobrazeno 1 - 10
of 90
pro vyhledávání: '"Faisal A. AL-ALLAF"'
Autor:
Abdellatif Bouazzaoui, Neda M. Bogari, Faisal A. Al-Allaf, Samar N. Ekram, Mohammad Athar, Anas Dannoun, Thomas Schubert, Shahzad N. Syed, Abdel-Rahman Youssef, Mashael Alqahtani, Ahmed A.H. Abdellatif
Publikováno v:
Heliyon, Vol 9, Iss 3, Pp e13876- (2023)
Graft versus host disease (GVHD) remains the major cause of morbidity and mortality after allogeneic stem cell transplantation, especially for intestinal GVHD, as steroid resistant GVHD results in high mortality. For this reason, new treatments of GV
Externí odkaz:
https://doaj.org/article/f6fd174e49ba49b0a8a216e18a7f33a0
Autor:
Mohammad Athar, Mawaddah Toonsi, Zainularifeen Abduljaleel, Abdellatif Bouazzaoui, Neda M. Bogari, Anas Dannoun, Faisal A. Al-Allaf
Publikováno v:
Life, Vol 13, Iss 7, p 1542 (2023)
Background: Familial Hypercholesterolemia (FH) is a hereditary condition that causes a rise in blood cholesterol throughout a person’s life. FH can result in myocardial infarction and even sudden death if not treated. FH is thought to be caused mai
Externí odkaz:
https://doaj.org/article/07372f2235cf4103b06a7c00c6c43dd7
Autor:
Neda M. Bogari, Amr A. Amin, Husni H. Rayes, Ahmed Abdelmotelb, Faisal A. Al-Allaf, Anas Dannoun, Hiba S. Al-Amodi, Anas A. Sedayo, Hilal Almalk, Amna Moulana, Rania Balkhair, Fatma Jambi, Fakhriah Madani, Mwafaq Abutalib, Mohiuddin M. Taher, Abdellatif Bouazzaoui, Ashwag Aljohani, Mustafa N. Bogari, Udaya Raja G.K., Ahmed Fawzy, Khalid Khalaf Alharbi, Imran Ali Khan
Publikováno v:
Journal of Infection and Public Health, Vol 13, Iss 1, Pp 27-33 (2020)
Background: Eczema is also known as atopic dermatitis is well-known for the skin disease globally. In Saudi Arabia, exome sequencing studies have not been documented. The purpose of this study was to scrutinize the disease causing mutations in childr
Externí odkaz:
https://doaj.org/article/ffb8dd7690a6478fbe33b25b4360e95a
Autor:
Zainularifeen Abduljaleel, Mohammad Athar, Faisal A. Al-Allaf, Saied Al-Dehlawi, Jose R. Vazquez
Publikováno v:
Non-coding RNA Research, Vol 4, Iss 4, Pp 155-173 (2019)
The human gene MUTYH codes for a DNA glycosylase involved in the repair of oxidative DNA damage. Faulty MUTYH protein activity causes the accumulation of G→T transversions due to unrepaired 8-oxoG:A mismatches. MUTYH germ-line mutations in humans a
Externí odkaz:
https://doaj.org/article/909510f86f44451f83914f540141fff7
Autor:
Khaled Ali Baniyaseen, Muhammad Saeed, Ahmed Omar Albonni, Bothaina Mohammed Abdulshakour, Ghida Dairi, Faisal A. Al-Allaf, Mohiuddin M. Taher
Publikováno v:
Middle East Journal of Digestive Diseases, Vol 11, Iss 3, Pp 166-173 (2019)
Anorectal melanomas are exceptionally uncommon and only 30% of anorectal melanomas are amelanotic. We report here a case of an anorectal amelanotic melanoma in a female patient. An 84-year-old patient complained of anal mass for 3 months. On examinat
Externí odkaz:
https://doaj.org/article/f71f787b6ef647c2a6c78eae4d42df64
Autor:
Abdel-Rahman Youssef, Ramy Emara, Mohiuddin M. Taher, Faisal A. Al-Allaf, Majed Almalki, Mazen A. Almasri, Shahid S. Siddiqui
Publikováno v:
BMC Oral Health, Vol 19, Iss 1, Pp 1-9 (2019)
Abstract Background Vital pulp therapy preserves and maintains the integrity and the health of dental pulp tissue that has been injured by trauma, caries or restorative procedures. The enhancement of cells viability and formation of reparative dentin
Externí odkaz:
https://doaj.org/article/47dfe00b7a8c47abb2d33ef2798a69be
Autor:
Faisal A. Al-Allaf, Zainularifeen Abduljaleel, Mohammad Athar, Mohiuddin M. Taher, Wajahatullah Khan, Huseyin Mehmet, Mukaddes Colakogullari, Sophia Apostolidou, Brian Bigger, Simon Waddington, Charles Coutelle, Michael Themis, Mohammed N. Al-Ahdal, Futwan A. Al-Mohanna, Zuhair N. Al-Hassnan, Abdellatif Bouazzaoui
Publikováno v:
Non-coding RNA Research, Vol 4, Iss 1, Pp 1-14 (2019)
Internal ribosome entry site (IRES) sequences have become a valuable tool in the construction of gene transfer and therapeutic vectors for multi-cistronic gene expression from a single mRNA transcript. The optimal conditions for effective use of this
Externí odkaz:
https://doaj.org/article/e7460ad473a841058174a80c260fe241
Autor:
Neda M. Bogari, Ashwag Aljohani, Amr A. Amin, Faisal A. Al-Allaf, Anas Dannoun, Mohiuddin M. Taher, Atalla Elsayed, Dareen ibrahim Rednah, Osama Elkhatee, Massimo Porqueddu, Francesco Alamanni, Soud Abdulraof A. Khogeer, Ahmed Fawzy
Publikováno v:
BMC Cardiovascular Disorders, Vol 19, Iss 1, Pp 1-6 (2019)
Abstract Background Elevated plasma triglycerides (TGs) are widely used as a major cardiovascular risk predictor and are thought to play an important role in the progression of coronary heart disease (CHD). It has been demonstrated that lipid lowerin
Externí odkaz:
https://doaj.org/article/172040f6ef5440169966fd38446027d2
Autor:
Mohammad Athar PhD, Zainularifeen Abduljaleel PhD, Ibrahim S. Ghita MD, Amani A. Albagenny MD, Saeed H. Halawani PhD, Mohammad M. Alkazmi MD, Wafa M. Elbjeirami PhD, Khalid Alquthami PhD, Mohammad M. Alkhuzae BLM, Fadel M. Ragab MS, Faisal A. Al-Allaf PhD
Publikováno v:
Clinical and Applied Thrombosis/Hemostasis, Vol 27 (2021)
The rare Gln534 (Factor V Leiden; FVL) allele (1:169,519,049 T>C) is associated with an increased risk of venous thrombosis. The purpose of this study was to measure the prevalence of Factor V Leiden mutation in thrombophilia patients with deep vein
Externí odkaz:
https://doaj.org/article/e394647bb9664e38a5acbaa68b2fea43
Autor:
Neda M. Bogari, Faisal A. Al-Allaf, Ashwag Aljohani, Mohiuddin M. Taher, Nermeen A. Qutub, Suhair Alhelfawi, Amal Alobaidi, Derar M. Alqudah, Hussain Banni, Ghida Dairi, Amr A. Amin
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
Attention-deficit/hyperactivity disorder (ADHD) is one of the most common neurodevelopmental disorders. Several studies have confirmed the co-existence of other neuropsychiatric disorders with ADHD. Out of 106 individuals suspected to have ADHD, eigh
Externí odkaz:
https://doaj.org/article/822edafe550c4dad9ca01151753dbca7