Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Omar Askander"'
Autor:
Ahmed Bouhouche, Omar Askander, Hicham Charoute, Mouna Sabib, Abdeljalil El Quessar, Amine El Hassani, Naima Erreimi
Publikováno v:
Journal of Clinical and Translational Endocrinology Case Reports, Vol 28, Iss , Pp 100144- (2023)
Introduction: In humans, there is considerable individual variability in ethanol metabolism, and these differences have been partially attributed to genetic variability at the ADH locus at 4q22-23, where seven genes are found. They encode ADH enzymes
Externí odkaz:
https://doaj.org/article/128eb9956a514944882c508dfe0c2a06
Autor:
Taha Chouati, Mouhssine Hemlali, Marouane Melloul, Sanaa Alaoui-Amine, Safae Rhoulam, Hamza Ghamaz, Maha Ouarab, Omar Askander, Lamiae Belayachi, Nadia Touil, Bouchra El Mchichi, Hicham Elannaz, Abdelillah Laraqui, Mostafa Elouennass, Khalid Ennibi, Elmostafa El Fahime
Publikováno v:
Microbiology resource announcements. 11(5)
Here, we describe the coding-complete sequence of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) strain HM36, identified as a strain of concern of B.1.1.529+BA (Omicron).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4670dc7001b9659973154578e39708e3
https://pubmed.ncbi.nlm.nih.gov/35420465
https://pubmed.ncbi.nlm.nih.gov/35420465
Autor:
Ahmed Bouhouche, Yasmin Tabache, Omar Askander, Hicham Charoute, Nada Mesnaoui, Lamiae Belayachi, Naima El Hafidi, Houyam Hardizi, Elmostafa El Fahime, Naima Erreimi, Abdelhamid Barakat, Mohammed Khattab, Fouad Seghrouchni, Amine El Hassani
Publikováno v:
BioMed Research International.
Leukocyte adhesion deficiency type 1 (LAD1) is a rare autosomal recessive hereditary disorder characterized by recurrent infections, impaired pus formation, delayed wound healing, omphalitis, and delayed separation of the umbilical cord as hallmark f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c6629c4f900704ce4490b6c7d341067b
Autor:
Ahmed, Bouhouche, Yasmin, Tabache, Omar, Askander, Hicham, Charoute, Nada, Mesnaoui, Lamiae, Belayachi, Naima, El Hafidi, Houyam, Hardizi, Elmostafa, El Fahime, Naima, Erreimi, Abdelhamid, Barakat, Mohammed, Khattab, Fouad, Seghrouchni, Amine, El Hassani
Publikováno v:
BioMed research international. 2022
Leukocyte adhesion deficiency type 1 (LAD1) is a rare autosomal recessive hereditary disorder characterized by recurrent infections, impaired pus formation, delayed wound healing, omphalitis, and delayed separation of the umbilical cord as hallmark f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fa98e7b3587364832a77cf6901efd6b4
https://pubmed.ncbi.nlm.nih.gov/35281597
https://pubmed.ncbi.nlm.nih.gov/35281597
Autor:
Ahmed Bouhouche, My Abdelaziz El Alaoui, Elmostafa El Fahime, Nada Albaroudi, Amine El Hassani, Mohammed Belmekki, Zineb Habbadi, Omar Askander, Hinde Iraqi
Publikováno v:
Experimental eye research. 209
Hereditary connective tissue diseases form a heterogeneous group of disorders that affect collagen and extracellular matrix components. The cornea and the skin are among the major forms of connective tissues, and syndromes affecting both organs are o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::05f08e189149cc1fd1564284636ca32a
https://pubmed.ncbi.nlm.nih.gov/34133966
https://pubmed.ncbi.nlm.nih.gov/34133966