Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Hanane, Sayel"'
Autor:
Meriame Abbassi, Hanane Sayel, Nadia Senhaji, Said Trhanint, Hanane Bay Bay, Laila Bouguenouch, Fatima Zahra Mernisi
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 23, Iss 1, Pp 1-10 (2022)
Abstract Background Xeroderma pigmentosum (XP) is a rare autosomal recessive skin disorder characterized by hyperpigmentation, premature skin aging, ocular and cutaneous photosensitivity with increased risk of skin tumors. XP is caused by mutations i
Externí odkaz:
https://doaj.org/article/5c5e91126bd44e1fba166f7c3cd899e8
Autor:
Laila Bouguenouch, Imane Samri, Meryem Abbassi, Hasna Hamdaoui, Ihssane El Otmani, Hanane Sayel, Said Trhanint, Sara Benmiloud, Moncif Amrani, Sanae Bennis, Karim Ouldim, Mustapha Hida
Publikováno v:
The Pan African Medical Journal, Vol 28, Iss 286 (2017)
L'anémie de Fanconi est une maladie récessive associée à une instabilité chromosomique, elle est marquée par une hétérogénéité phénotypique qui inclut une insuffisance médullaire, un syndrome malformatif variable, une prédisposition à
Externí odkaz:
https://doaj.org/article/705f1be34f42472c840423bdc2691a67
Autor:
Hanae Daha Belghiti, Meriame Abbassi, Hanane Sayel, Mohamed Ahakoud, Badr Eddine El Makhzen, Norman Lee, Silvia Russo, Sana Chaouki, Laila Bouguenouch
Publikováno v:
Journal of Pediatric Genetics.
Angelman syndrome (AS) is a rare neurodevelopmental disorder due to genetic defects involving chromosome 15, known by intellectual disability, cognitive and behavioral disorders, ataxia, delayed motor development, and seizures. This study highlights
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8484f172826cd6ad49cf2c8f9e4d9df9
https://doi.org/10.1055/s-0042-1751268
https://doi.org/10.1055/s-0042-1751268
Autor:
Laila Bouguenouch, Imane Samri, Khadija Belhassan, Hanane Sayel, Meriame Abbassi, Sanae Bennis, Dafr Allah Benajah, Adil Ibrahimi, Afaf Amarti, Karim Ouldim
Publikováno v:
The Pan African Medical Journal, Vol 24, Iss 142 (2016)
Le syndrome de Lynch, ou cancer colorectal héréditaire sans polypose ou HNPCC (hereditary non-polyposis colorectal cancer), est la forme la plus fréquente de cancer colorectal héréditaire. Il conduit à une augmentation de la susceptibilité à
Externí odkaz:
https://doaj.org/article/69779e19152e440e8af1490eb9c53989
Autor:
N. El Ghachtouli, Hanane Sayel, N. Tahri Joutey, Meryem Asri, Nabil Tirry, Wifak Bahafid, A. Kouchou
Publikováno v:
Journal of Genetic Engineering & Biotechnology
Journal of Genetic Engineering and Biotechnology, Vol 16, Iss 2, Pp 613-619 (2018)
Journal of Genetic Engineering and Biotechnology, Vol 16, Iss 2, Pp 613-619 (2018)
Phytoremediation is considered as a novel environmental friendly technology, which uses plants to remove or immobilize heavy metals. The use of metal-resistant plant growth-promoting bacteria (PGPB) constitutes an important technology for enhancing b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::508221a044fa931ddb7e6a06c8bcba97
https://doi.org/10.1016/j.jgeb.2018.06.004
https://doi.org/10.1016/j.jgeb.2018.06.004
Autor:
Wifak Bahafid, Hanane Sayel, Nezha Tahri Joutey, Faouzi Errachidi, Hajar Maâtaoui, Naïma El Ghachtouli
Publikováno v:
Soil and Sediment Contamination: An International Journal. 24:129-142
Hexavalent chromium Cr(VI) is regularly introduced into the environment through diverse anthropogenic activities. It is highly toxic, mutagenic and carcinogenic, and because of its solubility in water, chromate contamination can be difficult to conta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c9b21654fcf43930ee01e8244146c69c
https://doi.org/10.1080/15320383.2014.922931
https://doi.org/10.1080/15320383.2014.922931
Autor:
Laila Bouguenouch, Saaid Trhanint, Mohammed Iraqui Houssaini, Ihssane El Bouchikhi, Imane Samri, Moustapha Hida, Hanane Sayel, Karim Ouldim, Samir Atmani
Publikováno v:
Volume: 45, Issue: 2 306-312
Turkish Journal of Medical Sciences
Turkish Journal of Medical Sciences
Background/aim: Noonan syndrome is an autosomal dominant disorder with an incidence of 1/1000?2500. It results from protein-tyrosine phosphatase, nonreceptor type 11 (PTPN11) mutations in roughly 50% of cases. Mutational screening of PTPN11 has been
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7bc458c666998df73b4c865c8f21ac1
https://doi.org/10.3906/sag-1310-50
https://doi.org/10.3906/sag-1310-50
Autor:
Hanane Sayel, Meryem Asri, Naïma El Ghachtouli, Wifak Bahafid, Nabil Tirry, Nezha Tahri Joutey
Publikováno v:
Yeast-Industrial Applications
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::359c6d00cc52cc8518fed49998c7893d
https://doi.org/10.5772/intechopen.70559
https://doi.org/10.5772/intechopen.70559
Autor:
Hasna Hamdaoui, Moncif Amrani, Hanane Sayel, Said Trhanint, Karim Ouldim, Ihssane El Otmani, Imane Samri, Meryem Abbassi, Sara Benmiloud, S. Bennis, M. Hida, Laila Bouguenouch
Publikováno v:
Pan African Medical Journal; Vol 28, No 1 (2017)
The Pan African Medical Journal
The Pan African Medical Journal
L'anémie de Fanconi est une maladie récessive associée à une instabilité chromosomique, elle est marquée par une hétérogénéité phénotypique qui inclut une insuffisance médullaire, un syndrome malformatif variable, une prédisposition à
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2199eea7792a3a413c95d55b37545d1
https://www.ajol.info/index.php/pamj/article/view/167044
https://www.ajol.info/index.php/pamj/article/view/167044
Autor:
M. Hida, Laila Bouguenouch, Driss Couissi, Jamila El-Akhal, Ihssane El Bouchikhi, Karim Ouldim, Hanane Sayel, Touhami Mejtoute, Fatima Zahra Moufid
Publikováno v:
Human Genome Variation. 4
Familial Mediterranean fever (FMF) is a hereditary autoinflammatory disease that is inherited in an autosomal recessive manner and is caused by mutations in the MEFV gene. As the name indicates, FMF occurs within families and is more common in indivi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0921183f962fb0f41df75f7ef5c4ded0
https://doi.org/10.1038/hgv.2017.23
https://doi.org/10.1038/hgv.2017.23