Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Mohamed Ali, Mosrati"'
Autor:
Moufida Chaari, Sarra Akermi, Khaoula Elhadef, Monia Ennouri, Lobna Jlaiel, Mohamed Ali Mosrati, Lotfi Mellouli, Walid Elfalleh, Theodoros Varzakas, Slim Smaoui
Publikováno v:
Heliyon, Vol 10, Iss 21, Pp e39784- (2024)
Given consumers', environmental and sustainability apprehensions, the meat industry investigated the natural colorant resources. As proof, betalain, Opuntia stricta peels (OSP) pigment, is premeditated in the meat industry. Here, OSP betalains were q
Externí odkaz:
https://doaj.org/article/b86616e1b9894ead90d705e4971c31c8
Autor:
Amal Souissi, Mariem Ben Said, Ikhlas Ben Ayed, Ines Elloumi, Amal Bouzid, Mohamed Ali Mosrati, Mehdi Hasnaoui, Malek Belcadhi, Nabil Idriss, Hassen Kamoun, Nourhene Gharbi, Abdullah A. Gibriel, Abdelaziz Tlili, Saber Masmoudi
Publikováno v:
Journal of Advanced Research, Vol 31, Iss , Pp 13-24 (2021)
Introduction: Hearing impairment (HI) is characterized by complex genetic heterogeneity. The evolution of next generation sequencing, including targeted enrichment panels, has revolutionized HI diagnosis. Objectives: In this study, we investigated ge
Externí odkaz:
https://doaj.org/article/d83cd2772882444aaeaa06063629e58a
Autor:
Amal Bouzid, Adel Tekari, Fida Jbeli, Amine Chakroun, Kirtal Hansdah, Amal Souissi, Neha Singh, Mohamed Ali Mosrati, Imen Achour, Abdelmonem Ghorbel, Ilhem Charfeddine, Puppala Venkat Ramchander, Saber Masmoudi
Publikováno v:
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-10 (2020)
Abstract Background Otosclerosis (OTSC) is among the most common causes of a late-onset hearing loss in adults and is characterized by an abnormal bone growth in the otic capsule. Alteration in the osteoprotegerin (OPG) expression has been suggested
Externí odkaz:
https://doaj.org/article/f0fdfec8b41144259354249c5a32eceb
Autor:
Mohamed Ali Mosrati, Karima Fadhlaoui‐Zid, Amel Benammar‐Elgaaied, Abdullah Ahmed Gibriel, Mariem Ben Said, Saber Masmoudi
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 10, Pp n/a-n/a (2021)
Abstract Autosomal recessive non‐syndromic hearing loss (ARNSHL) is the most common inherited sensory impairment. It is particularly frequent in North African populations who have a high rate of consanguineous marriage. The c.242G>A homozygous vari
Externí odkaz:
https://doaj.org/article/29daf1cf4ebf4f7b903815af2e77e718
Autor:
Mariem Ben Said, Abdelaziz Tlili, Saber Masmoudi, Ikhlas Ben Ayed, Amal Bouzid, Hassen Kamoun, Malek Belcadhi, Amal Souissi, Mohamed Ali Mosrati, Abdullah A.Y. Gibriel, Mehdi Hasnaoui, Ines Elloumi, Nabil Idriss, N. Gharbi
Publikováno v:
Journal of Advanced Research, Vol 31, Iss, Pp 13-24 (2021)
Journal of Advanced Research
Journal of Advanced Research
Graphical abstract
Introduction Hearing impairment (HI) is characterized by complex genetic heterogeneity. The evolution of next generation sequencing, including targeted enrichment panels, has revolutionized HI diagnosis. Objectives In this stu
Introduction Hearing impairment (HI) is characterized by complex genetic heterogeneity. The evolution of next generation sequencing, including targeted enrichment panels, has revolutionized HI diagnosis. Objectives In this stu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49b22b0998b87a76309abc3face7c791
http://www.sciencedirect.com/science/article/pii/S2090123221000126
http://www.sciencedirect.com/science/article/pii/S2090123221000126
Autor:
Ilhem Charfeddine, Fida Jbeli, Puppala Venkat Ramchander, Kirtal Hansdah, Neha Singh, Amal Souissi, A. Chakroun, Adel Tekari, Abdelmonem Ghorbel, Mohamed Ali Mosrati, Saber Masmoudi, Amal Bouzid, I. Achour
Publikováno v:
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-10 (2020)
BMC Medical Genetics
BMC Medical Genetics
Background Otosclerosis (OTSC) is among the most common causes of a late-onset hearing loss in adults and is characterized by an abnormal bone growth in the otic capsule. Alteration in the osteoprotegerin (OPG) expression has been suggested in the im
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1590ca9edc6f53aecb78e66e0baefe1b
http://link.springer.com/article/10.1186/s12881-020-01036-8
http://link.springer.com/article/10.1186/s12881-020-01036-8
Autor:
Amal, Souissi, Dorra, Abdelmalek Driss, Imen, Chakchouk, Mariem, Ben Said, Ikhlas, Ben Ayed, Mohamed Ali, Mosrati, Ines, Elloumi, Abdelaziz, Tlili, Sami, Aifa, Saber, Masmoudi
Publikováno v:
Journal of biomolecular structuredynamics. 40(21)
Hereditary hearing impairment (HI) is a common disease with the highest incidence among sensory defects. Several genes have been identified to affect stereocilia structure causing HI, including the unconventional myosin3A. Interestingly, we noticed t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6a7c5cda996df8922e56163b6c4f9f00
https://pubmed.ncbi.nlm.nih.gov/34423747
https://pubmed.ncbi.nlm.nih.gov/34423747
Autor:
Abdullah A.Y. Gibriel, Saber Masmoudi, Amel Benammar-Elgaaied, Karima Fadhlaoui-Zid, Mariem Ben Said, Mohamed Ali Mosrati
Publikováno v:
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine, Vol 9, Iss 10, Pp n/a-n/a (2021)
Molecular Genetics & Genomic Medicine, Vol 9, Iss 10, Pp n/a-n/a (2021)
Autosomal recessive non‐syndromic hearing loss (ARNSHL) is the most common inherited sensory impairment. It is particularly frequent in North African populations who have a high rate of consanguineous marriage. The c.242G>A homozygous variant in LR
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6b907ee74f1e75ebe2c615cbf659cd2
https://pubmed.ncbi.nlm.nih.gov/34514748
https://pubmed.ncbi.nlm.nih.gov/34514748
Autor:
Dorra Driss, Mariem Ben Said, Mohamed Ali Mosrati, Imen Chakchouk, Sami Aifa, Amal Souissi, Ikhlas Ben Ayed, Saber Masmoudi, Abdelaziz Tlili, Ines Elloumi
Hereditary hearing impairment (HI) is a common disease with the highest incidence among sensory defects. Several genes have been identified to affect stereocilia structure causing HI, including the unconventional myosin3A. Interestingly, we noticed t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7099d0aa4b51b20ba420d3e4d4517819
Autor:
Saber Masmoudi, Erik Fransen, Mohamed Ali Mosrati, Ilhem Charfeddine, Hassen Kamoun, Abdelmonem Ghorbel, Guy Van Camp, Isabelle Schrauwen
Publikováno v:
Gene
Hearing loss is a common congenital anomaly with an incidence of 1 in 1000 live births. It has been described together with several other clinical features as fortuitous association or commune genetic syndrome. In this study, we investigated a consan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ddb44d74e5f0206e76109fcd386dc86c
https://doi.org/10.1016/j.gene.2012.09.006
https://doi.org/10.1016/j.gene.2012.09.006