Zobrazeno 1 - 10
of 110
pro vyhledávání: '"Hassan, Rouba"'
Autor:
Houda Harmak, Salaheddine Redouane, Hicham Charoute, Ouafaa Aniq Filali, Abdelhamid Barakat, Hassan Rouba
Publikováno v:
Journal of Biomolecular Structure and Dynamics. :1-24
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2955de0640ffc98f2672a0485618a12c
https://doi.org/10.1080/07391102.2023.2193995
https://doi.org/10.1080/07391102.2023.2193995
Autor:
Imane Morjane, Hicham Charoute, Sanaa Ouatou, Lamiae Elkhattabi, Houda Benrahma, Rachid Saile, Hassan Rouba, Abdelhamid Barakat
Publikováno v:
Cardiology Research and Practice, Vol 2020 (2020)
Purpose. Coronary artery diseases (CAD) are clinical cardiovascular events associated with dyslipidemia in common. The interaction between environmental and genetic factors can be responsible for CAD. The present paper aimed to examine the associatio
Externí odkaz:
https://doaj.org/article/4ae80b7ce2d74100ad093ab5b8f8a891
Autor:
Salaheddine Redouane, Hicham Charoute, Houda Harmak, Abderrahim Malki, Abdelhamid Barakat, Hassan Rouba
Publikováno v:
Journal of Biomolecular Structure and Dynamics. :1-20
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9dc49e653ffa2e44493ade60c3d15c20
https://doi.org/10.1080/07391102.2022.2142846
https://doi.org/10.1080/07391102.2022.2142846
Autor:
Soukaina Essadssi, Al Mehdi Krami, Lamiae Elkhattabi, Zouhair Elkarhat, Ghita Amalou, Houria Abdelghaffar, Hassan Rouba, Abdelhamid Barakat
Publikováno v:
Journal of Immunology Research, Vol 2019 (2019)
Severe combined immunodeficiency (SCID) is the most severe form of primary immunodeficiency (PID), characterized by fatal opportunistic infections. The ADA gene encodes adenosine deaminase, an enzyme that catalyzes the irreversible deamination of ade
Externí odkaz:
https://doaj.org/article/e85042a2409444ac95a68039de425c73
Autor:
Lamiae Elkhattabi, Imane Morjane, Hicham Charoute, Soumaya Amghar, Hind Bouafi, Zouhair Elkarhat, Rachid Saile, Hassan Rouba, Abdelhamid Barakat
Publikováno v:
Journal of Diabetes Research, Vol 2019 (2019)
Resistin (RETN) is a gene coding for proinflammatory adipokine called resistin secreted by macrophages in humans. Single nucleotide polymorphisms (SNPs) in RETN are linked to obesity and insulin resistance in various populations. Using dbSNP, 78 nons
Externí odkaz:
https://doaj.org/article/41e98608f08d48dd86d2f849c1857432
Autor:
Imane AitRaise, Ghita Amalou, Amale Bousfiha, Hicham Charoute, Hassan Rouba, Houria Abdelghaffar, Crystel Bonnet, Christine Petit, Adbelhamid Barakat
Publikováno v:
Molecular Biology Reports
Molecular Biology Reports, 2022, 49 (5), pp.3949-3954. ⟨10.1007/s11033-022-07245-z⟩
Molecular Biology Reports, 2022, 49 (5), pp.3949-3954. ⟨10.1007/s11033-022-07245-z⟩
International audience; Background: Deafness is the most prevalent human sensorineural defect. It may occur as a result of an external auditory canal involvement, or a deficiency in the sound conduction mechanism, or an impairment of the cochlea, the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46a7013bd19b08c22094a168078bf3c5
https://doi.org/10.1007/s11033-022-07245-z
https://doi.org/10.1007/s11033-022-07245-z
Autor:
Amina Bakhchane, Majida Charif, Amale Bousfiha, Redouane Boulouiz, Halima Nahili, Hassan Rouba, Hicham Charoute, Guy Lenaers, Abdelhamid Barakat
Publikováno v:
PLoS ONE, Vol 12, Iss 5, p e0176516 (2017)
The MYO7A gene encodes a protein belonging to the unconventional myosin super family. Mutations within MYO7A can lead to either non syndromic hearing loss or to the Usher syndrome type 1B (USH1B). Here, we report the results of genetic analyses perfo
Externí odkaz:
https://doaj.org/article/82f455cff15345659651dafe589d5c76
Autor:
Salazar Orvig, Anne, Marcos, Haydée, Caët, Stéphanie, Corlateanu, Cristina, da Silva, Christine, Hassan, Rouba, Heurdier, Julien, le Mené, Marine, Leber-Marin, Jocelyne, Morgenstern, Aliyah
Publikováno v:
In Journal of Pragmatics September 2013 56:88-112
Publikováno v:
Journal of Biomolecular Structure and Dynamics
The SARS-cov-2 RNA dependent RNA polymerase (nsp12) is a crucial viral enzyme that catalyzes the replication of RNA from RNA templates. The fixation of some ligands in the active site may alter the viral life cycle. The aim of the present study is to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e4f41432b5c28f8a72339e16a8a47fc
https://doi.org/10.1080/07391102.2020.1813628
https://doi.org/10.1080/07391102.2020.1813628
Autor:
Houda Harmak, Hicham Charoute, Salaheddine Redouane, Ouafaa Aniq Filali, Abdelhamid Barakat, Hassan Rouba
Publikováno v:
BioMed Research International.
Meiotic chromosomes endure rapid prophase movements that ease the formation of interhomologue recombination intermediates that drive synapsis, crossing over, and segregation process. To generate these fast moves, the meiotic telomere complex (MTC) en
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae661cb3ec6f9a194230999849ba8786