Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Ezzeldin N, Elhawary"'
Autor:
Nasser A. Elhawary, Imad A. AlJahdali, Iman S. Abumansour, Ezzeldin N. Elhawary, Nagwa Gaboon, Mohammed Dandini, Abdulelah Madkhali, Wafaa Alosaimi, Abdulmajeed Alzahrani, Fawzia Aljohani, Ehab M. Melibary, Osama A. Kensara
Publikováno v:
Human Genomics, Vol 16, Iss 1, Pp 1-17 (2022)
Abstract This review discusses the epidemiology, pathophysiology, genetic etiology, and management of phenylketonuria (PKU). PKU, an autosomal recessive disease, is an inborn error of phenylalanine (Phe) metabolism caused by pathogenic variants in th
Externí odkaz:
https://doaj.org/article/4583e2e4e7bb46e0adcd2247e7f26fe4
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:
Hisham Saada, Abdulaziz Baazeem, MohammedT. Tayeb, Nasser A. Elhawary, Ahmad H. Mufti, Ezzeldin N. Elhawary, Anmar M. Nassir, Ikhlas A. Sindi, Samar N. Ekram, Asim Khogeer, Hatem Adel Sembawa
Publikováno v:
Biomedical Journal of Scientific & Technical Research. 23
Growing knowledge supports the importance of microRNAs in cell growth regulation, differentiation ...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ffa1c8906633ecc245f2b38c80cc516f
https://doi.org/10.26717/bjstr.2019.23.003966
https://doi.org/10.26717/bjstr.2019.23.003966
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