Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Mohamed Amine Senhaji"'
Autor:
Zineb Kindil, Mohamed Amine Senhaji, Amina Bakhchane, Hicham Charoute, Soumia Chihab, Sellama Nadifi, Abdelhamid Barakat
Publikováno v:
BMC Research Notes, Vol 10, Iss 1, Pp 1-6 (2017)
Abstract Objective Xeroderma pigmentosum (XP) is a genetically and clinically heterogeneous disease, associated with an inherited defect in one of eight different genes (XPA to XPG and XPV). In addition to the early onset of the skin manifestations,
Externí odkaz:
https://doaj.org/article/0add5980e7164b9a8a081a7cfa58c7cb
Autor:
Sellama Nadifi, Zineb Kindil, Soumia Chihab, Hicham Charoute, Abdelhamid Barakat, Mohamed Amine Senhaji, Amina Bakhchane
Publikováno v:
BMC Research Notes
BMC Research Notes, Vol 10, Iss 1, Pp 1-6 (2017)
BMC Research Notes, Vol 10, Iss 1, Pp 1-6 (2017)
Objective Xeroderma pigmentosum (XP) is a genetically and clinically heterogeneous disease, associated with an inherited defect in one of eight different genes (XPA to XPG and XPV). In addition to the early onset of the skin manifestations, the XP gr
Autor:
Olfa Messaoud, Sellama Nadifi, Omar Abidi, Abdelmajid Eloualid, Mariem Ben Rekaya, Abdelhamid Barakat, Mohamed Amine Senhaji, Khadija Khadir, Hakima Benchikhi, Sonia Abdelhak
Publikováno v:
Archives of Dermatological Research. 305:53-57
Xeroderma pigmentosum is a rare autosomal recessive disease characterized by hypersensitivity to UV light which is due to alterations of the nucleotide excision repair pathway. Eight genes (XPA to XPG and XPV) are responsible for the disease. Among t
Autor:
Hassan Jouhadi, Abdallah Badou, Abdelhamid Barakat, Amina Bakhchane, Brehima Diakite, Abdellatif Benider, Mohamed Amine Senhaji, Meryam El Khachibi, Khalil Hamzi, Sellama Nadifi
Publikováno v:
BMC Cancer
Background Identification of specific mutations in cancer patients may lead to the discovery of genes, which can affect susceptibility and/or prognosis. It has previously been reported that mutations in BRCA1 and BRCA2 genes are linked to breast canc