Zobrazeno 1 - 10
of 39
pro vyhledávání: '"Mostafa Kandil"'
Autor:
Aymane Bouzidi, Hicham Charoute, Majida Charif, Ghita Amalou, Mostafa Kandil, Abdelhamid Barakat, Guy Lenaers
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-21 (2022)
Abstract Background Inherited retinal dystrophies (IRD) and optic neuropathies (ION) are the two major causes world-wide of early visual impairment, frequently leading to legal blindness. These two groups of pathologies are highly heterogeneous and r
Externí odkaz:
https://doaj.org/article/db52d4935dcd4f328ef4486bf0a50f6e
Autor:
Outmane Bouhlal, Andrea Visioni, Ramesh Pal Singh Verma, Mostafa Kandil, Sanjaya Gyawali, Flavio Capettini, Miguel Sanchez-Garcia
Publikováno v:
Frontiers in Plant Science, Vol 13 (2022)
Breeding programs in developing countries still cannot afford the new genotyping technologies, hindering their research. We aimed to assemble an Association Mapping panel to serve as CGIAR Barley Breeding Toolbox (CBBT), especially for the Developing
Externí odkaz:
https://doaj.org/article/5ab2dd42600d4cdc95829c6bc7af934f
Autor:
Andrea Visioni, Fatima El Otmani, Adil El-Baouchi, Damiano Puglisi, Mostafa Kandil, Outmane Bouhlal, Mesut Keser, Miguel Sanchez-Garcia, Jean Raymond Affricot, Abdellatif Hafidi
Publikováno v:
Journal of the American Society of Brewing Chemists. 80:401-412
The use of barley (Hordeum vulgare L.) in Morocco is still limited to food and feed despite the amplified demand by local industries for imported malt. This study aims to evaluate 36 barley elite l...
Autor:
Aymane Bouzidi, Hicham Charoute, Majida Charif, Ghita Amalou, Mostafa Kandil, Abdelhamid Barakat, Guy Lenaers
Publikováno v:
Orphanet journal of rare diseases. 17(1)
BackgroundInherited retinal dystrophies (IRD) and optic neuropathies (ION) are the two major causes world-wide of early visual impairment, frequently leading to legal blindness. These two groups of pathologies are highly heterogeneous and require com
Autor:
Zied Riahi, Majida Charif, Christine Petit, Amale Bousfiha, Ghita Amalou, Aymane Bouzidi, Crystel Bonnet, Guy Lenaers, Soukaina Elrharchi, Abdelhamid Barakat, Mostafa Kandil
Publikováno v:
International Journal of Pediatric Otorhinolaryngology
International Journal of Pediatric Otorhinolaryngology, 2021, 140, pp.110481. ⟨10.1016/j.ijporl.2020.110481⟩
International Journal of Pediatric Otorhinolaryngology, Elsevier, 2021, 140, pp.110481. ⟨10.1016/j.ijporl.2020.110481⟩
International Journal of Pediatric Otorhinolaryngology, 2021, 140, pp.110481. ⟨10.1016/j.ijporl.2020.110481⟩
International Journal of Pediatric Otorhinolaryngology, Elsevier, 2021, 140, pp.110481. ⟨10.1016/j.ijporl.2020.110481⟩
International audience; Adhesion glycoproteins are implicated in the pathophysiology of hearing loss, the most frequent inherited sensory disorder, affecting 1 in 1000 new-borns. Exome sequencing of a consanguineous Moroccan patient with mild hearing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2714a64f1edb3db0e7d4dcc08c8bb538
https://hal-pasteur.archives-ouvertes.fr/pasteur-03215242
https://hal-pasteur.archives-ouvertes.fr/pasteur-03215242
Publikováno v:
2020 6th International Conference on Electric Power and Energy Conversion Systems (EPECS).
This paper aims to investigate the effect of integrating short term Energy Storage System (ESS) on the transient stability of the power system with high levels of wind power penetration. The wind power technology considered in this study is of type I
Autor:
Aymane, Bouzidi, Majida, Charif, Adil, Bouzidi, Ghita, Amalou, Mostafa, Kandil, Abdelhamid, Barakat, Guy, Lenaers
Publikováno v:
Molecular Vision
Purpose Progressive inherited retinal dystrophies, characterized by degeneration of rod photoreceptors and then cone photoreceptors, are known as retinitis pigmentosa (RP), for which 89 genes have been identified. Today, only five Moroccan families w
Autor:
Nisrine Aboussair, Céline Bris, Mostafa Kandil, Halima Nahili, David Goudenège, Patrizia Amati-Bonneau, Abdelhamid Barakat, Majida Charif, Aymane Bouzidi, Najat Sifeddine, Guy Lenaers, Kenza Dafir, Vincent Procaccio, Valérie Desquiret-Dumas, Ghita Amalou, Meriem Elqabli
Publikováno v:
Eye
Eye, Nature Publishing Group: Open Access Hybrid Model Option B, 2020, ⟨10.1038/s41433-019-0755-x⟩
Eye (Lond)
Eye, Nature Publishing Group: Open Access Hybrid Model Option B, 2020, ⟨10.1038/s41433-019-0755-x⟩
Eye (Lond)
International audience
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1bc53b748f5b3ea0cb05e901295fcb5c
https://hal.archives-ouvertes.fr/hal-02942813
https://hal.archives-ouvertes.fr/hal-02942813
Autor:
Houda Benrahma, Mostafa Kandil, Abdelhakim Ainahi, Hassan Rouba, Hicham Charoute, Imane Morjane, Hajar Sefri, F. Lakbakbi el Yaagoubi, Abdelhamid Barakat
Publikováno v:
Current Research in Translational Medicine. 65:121-125
This study aimed to analyze the association between UBE2E2, G6PC2, PROX1, DUSP9, ADCY5 and APOC3 polymorphisms and the risk of metabolic syndrome (MetS) in Moroccan patients. The study was applied on 316 unrelated individuals from Morocco, 177 MetS p
Autor:
Amina Bakhchane, Mostafa Kandil, Houda Benrahma, Rym Kefi, Hassan Rouba, Safaa Bounaceur, Ahmed Reguig, Hicham Charoute, Sonia Abdelhak, Abdelhamid Barakat
Publikováno v:
Mitochondrial DNA Part A
Mitochondrial DNA Part A, Taylor and Francis, 2017, 29 (1), pp.9-13. ⟨10.1080/24701394.2016.1233530⟩
Mitochondrial DNA Part A, Taylor and Francis, 2017, 29 (1), pp.9-13. ⟨10.1080/24701394.2016.1233530⟩
International audience; In this study, we investigated the association of mtDNA variants and haplogroups with Type 2 diabetes (T2D) in Moroccan patients. The Hypervariable Segments 1 of the mtDNA was sequenced in 108 diabetic patients and 97 controls
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b80fb21243ef78eaf933810ae2a983a3
https://hal-riip.archives-ouvertes.fr/pasteur-01966344
https://hal-riip.archives-ouvertes.fr/pasteur-01966344