Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Meriem Ben Rekaya"'
Autor:
Farah Sassi, Meriem Ben Rekaya, Ayed Belarbi, Dalia Chilla, Nada Mansouri, Leila Achouri, Essia Saied, Reda Kassa, Linda Belhaj Kacem, Manel Ouezani, Nadjiba Debabeche, Fatima Rebhi, Soumaya Rammeh
Publikováno v:
Cancer Reports, Vol 6, Iss S1, Pp n/a-n/a (2023)
Abstract Background Breast cancer (BC) is the most frequent malignancy among women in Tunisia and Algeria. Clinical and pathological characteristics of this cancer among these populations are not widely reported. The aim of the study was to report cl
Externí odkaz:
https://doaj.org/article/6e09eac241f2452fb244bce75ccd44a8
Autor:
Imen Nabouli, Asma Chikhaoui, Houcemeddine Othman, Sahar Elouej, Meriem Jones, Arnaud Lagarde, Meriem Ben Rekaya, Olfa Messaoud, Mohamed Zghal, Valerie Delague, Nicolas Levy, Annachiara De Sandre-Giovannoli, Sonia Abdelhak, Houda Yacoub-Youssef
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
Xeroderma Pigmentosum (XP) is a rare genetic disorder affecting the nucleotide excision repair system (NER). It is characterized by an extreme sensitivity to sunlight that induces cutaneous disorders such as severe sunburn, freckling and cancers. In
Externí odkaz:
https://doaj.org/article/11ab2c55985a43ec9f2dd01bbfa4aed3
Autor:
Asma Chikhaoui, Sahar Elouej, Imen Nabouli, Meriem Jones, Arnaud Lagarde, Meriem Ben Rekaya, Olfa Messaoud, Yosr Hamdi, Mohamed Zghal, Valerie Delague, Nicolas Levy, Annachiara De Sandre-Giovannoli, Sonia Abdelhak, Houda Yacoub-Youssef
Publikováno v:
Frontiers in Genetics, Vol 10 (2019)
Xeroderma pigmentosum (XP) is a rare autosomal recessive disorder due to a defect in the nucleotide excision repair (NER) DNA repair pathway, characterized by severe sunburn development of freckles, premature skin aging, and susceptibility to develop
Externí odkaz:
https://doaj.org/article/1096c163093a4f33ae06d009de8bb509