Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Mohammed T Tayeb"'
Autor:
Nasser A. Elhawary, Essam H. Jiffri, Samira Jambi, Ahmad H. Mufti, Anas Dannoun, Hassan Kordi, Asim Khogeer, Osama H. Jiffri, Abdelrahman N. Elhawary, Mohammed T. Tayeb
Publikováno v:
Human Genomics, Vol 12, Iss 1, Pp 1-11 (2018)
Abstract Background In individuals with Duchenne muscular dystrophy (DMD), exon skipping treatment to restore a wild-type phenotype or correct the frame shift of the mRNA transcript of the dystrophin (DMD) gene are mutation-specific. To explore the m
Externí odkaz:
https://doaj.org/article/a0ad8400a7a945fd9970a2e02136f578
Autor:
Hind Naffadi, Ahmed O. Babalghith, Samar N. Ekram, Nasser A. Elhawary, Ezzeldin N. Elhawary, Munaifah Alenezi, Mohammed T. Tayeb, Ahmad H. Mufti, Ikhlas A. Sindi
Publikováno v:
International Journal of General Medicine. 14:1311-1323
Ikhlas A Sindi,1 Ahmed O Babalghith,2 Mohammed T Tayeb,2 Ahmad H Mufti,2 Hind Naffadi,3 Samar N Ekram,2,4 Ezzeldin N Elhawary,5,6 Munaifah Alenezi,2 Nasser A Elhawary2,7 1Department of Biotechnology, Faculty of Science, King Abdulaziz University, Jed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b5d7b7d436f28c30a29a870f39a52cf
https://doi.org/10.2147/ijgm.s294802
https://doi.org/10.2147/ijgm.s294802
Autor:
Ahmad H Mufti, Imad A AlJahdali, Nasser A Elhawary, Samar N Ekram, Iman Abumansour, Ikhlas A Sindi, Hind Naffadi, Ezzeldin N Elhawary, Najiah M Alyamani, Ghydda Alghamdi, Wafaa Alosaimi, Ghufran Rawas, Amaal Alharbi, Mohammed T Tayeb
Publikováno v:
International Journal of General Medicine.
Ahmad H Mufti, 1 Imad A AlJahdali, 2 Nasser A Elhawary, 1 Samar N Ekram, 1 Iman Abumansour, 1 Ikhlas A Sindi, 3 Hind Naffadi, 4 Ezzeldin N Elhawary, 5 Najiah M Alyamani, 6 Ghydda Alghamdi, 1 Wafaa Alosaimi, 7 Ghufran Rawas, 8 Amaal Alharbi, 9 Mohamme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1988d062ae9d9e442565e038a84c232f
https://www.dovepress.com/variations-in-tap1-and-psmb9-genes-involved-in-antigen-processing-and--peer-reviewed-fulltext-article-IJGM
https://www.dovepress.com/variations-in-tap1-and-psmb9-genes-involved-in-antigen-processing-and--peer-reviewed-fulltext-article-IJGM
Autor:
Ahmad H, Mufti, Imad A, AlJahdali, Nasser A, Elhawary, Samar N, Ekram, Iman, Abumansour, Ikhlas A, Sindi, Hind, Naffadi, Ezzeldin N, Elhawary, Najiah M, Alyamani, Ghydda, Alghamdi, Wafaa, Alosaimi, Ghufran, Rawas, Amaal, Alharbi, Mohammed T, Tayeb
Publikováno v:
International Journal of General Medicine
Background The antigen processing 1 (TAP1) and proteasome 20S subunit beta 9 (PSMB9) genes are associated with strong susceptibility to many autoimmune diseases. Here, we explored whether TAP1/PSMB9 genetic variants, individually or combined, affecte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f7b6601a3dde10811f3cab21533d5c79
https://pubmed.ncbi.nlm.nih.gov/34984025
https://pubmed.ncbi.nlm.nih.gov/34984025
Autor:
Ikhlas A, Sindi, Ahmed O, Babalghith, Mohammed T, Tayeb, Ahmad H, Mufti, Hind, Naffadi, Samar N, Ekram, Ezzeldin N, Elhawary, Munaifah, Alenezi, Nasser A, Elhawary
Publikováno v:
International Journal of General Medicine
Purpose Colorectal carcinoma (CRC) represents a considerable public health burden in Saudi Arabia. Several candidate genes and genetic variants have been associated with morbidity and mortality among patients with CRC. We explored whether allelic var
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::66cfafeee98270f0ad7723a854510b11
https://pubmed.ncbi.nlm.nih.gov/33883929
https://pubmed.ncbi.nlm.nih.gov/33883929
Autor:
Samira Jambi, Anas Dannoun, Essam H. Jiffri, Nasser A. Elhawary, Hassan Kordi, Asim Khogeer, Ahmad H. Mufti, Osama H. Jiffri, Mohammed T. Tayeb, Abdelrahman N. Elhawary
Publikováno v:
Human Genomics, Vol 12, Iss 1, Pp 1-11 (2018)
Human Genomics
Human Genomics
Background In individuals with Duchenne muscular dystrophy (DMD), exon skipping treatment to restore a wild-type phenotype or correct the frame shift of the mRNA transcript of the dystrophin (DMD) gene are mutation-specific. To explore the molecular
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::37b1bcdded8362a0e9efb6600ee9a919
http://link.springer.com/article/10.1186/s40246-018-0152-8
http://link.springer.com/article/10.1186/s40246-018-0152-8
Autor:
Arwa H. Arab, Nasser A. Elhawary, Neda M. Bogari, Mona Rashad, Ezzeldin N. Elhawary, Mohammed T. Tayeb, Ahmad H. Mufti, Anas Dannoun, Ikhlas A. Sindi, Nermeen Qutub, Asim Khogeer
Publikováno v:
Cogent Biology, Vol 5, Iss 1 (2019)
Objective: To determine whether individual or interactive single nucleotide polymorphisms (SNPs) may influence the development of autism spectrum disorder (ASD). Methods: DNA from buccal cells of 212 participants (110 cases and 102 controls) were sub
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3802c06a1689179b0b38df8b89a32d21
https://doi.org/10.1080/23312025.2019.1606555
https://doi.org/10.1080/23312025.2019.1606555
Autor:
Mona Rashad, Nasser A. Elhawary, Mohammed T. Tayeb, Shereen Abdel-Ghafar, Abdel-Aziz Alkhotani
Publikováno v:
Pediatric Pulmonology. 48:699-706
Summary. Bronchopulmonary dysplasia (BPD) remains as a major and increasing burden in Egypt. Rationale: To determine whether alleles of TNFa-238G > A affect the risk of BPD or the severity of BPD in preterm infants in Egypt. Study Design: We prospect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e0a024a1d218c68d5efad94fe7292a06
https://doi.org/10.1002/ppul.22748
https://doi.org/10.1002/ppul.22748
Autor:
Mohammed T. Tayeb
Publikováno v:
Egyptian Journal of Medical Human Genetics; Vol 13, No 3 (2012); 263-268
This unreeled study aimed to examine the relationship between the genetic polymorphisms C677T in MTHFR gene and mapped this figure with other ethnic populations. The present study examined 70 Saudi females (30 mothers with DS children plus 40 healthy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::451930a030cd04c3b27890139b995f51
Publikováno v:
Egyptian Journal of Medical Human Genetics; Vol 12, No 2 (2011); 187-192
Reported to date, strong evidence exists in multiple studies for genetic predisposing in the development of diabetic nephropathy, and no studies addressed this issue among Egyptian population. The results of angiotensin converting enzyme gene (ACE) i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c75a2956356f10178a4fa5485f0f0b3
https://doi.org/10.1016/j.ejmhg.2011.07.008
https://doi.org/10.1016/j.ejmhg.2011.07.008