Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Mohamed, Zghal"'
Autor:
Asma Chikhaoui, Meriem Jones, Tadeja Režen, Melika Ben Ahmed, Chokri Naouali, Radovan Komel, Mohamed Zghal, Samir Boubaker, Sonia Abdelhak, Houda Yacoub-Youssef
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-13 (2022)
Abstract Xeroderma pigmentosum (XP) is a DNA repair disease that predisposes to early skin cancers as cutaneous melanoma. Melanoma microenvironment contains inflammatory mediators, which would be interesting biomarkers for the prognosis or for the id
Externí odkaz:
https://doaj.org/article/35dad24228624691ae99529e8ee5fcb5
Autor:
Najlaa Khalat, Olfa Messaoud, Mariem Ben Rekaya, Mariem Chargui, Mohamed Zghal, Bashir Zendah, Najat Saqer, Mourad Mokni, Sonia Abdelhak, Othman A. Mohamed
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 11, Iss 6, Pp n/a-n/a (2023)
Abstract Background Xeroderma pigmentosum is an autosomal recessive disease characterized by a high sensitivity to UV radiations. The disease is clinically and genetically heterogeneous, thus making accurate early clinical diagnosis difficult. Althou
Externí odkaz:
https://doaj.org/article/38ec3159672749948c32a81fc0e52b3f
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
Autor:
Rym Benmously Mlika, Mohamed Zghal, Nadia Kerkeni, Samy Fenniche, Achraf Debbiche, Mohamed Ben Ayed, Amel Jebali, Insaf Mokhtar
Publikováno v:
Annales de Pathologie. 31:32-35
Resume Introduction La muqueuse labiale est un siege inhabituel du carcinome basocellulaire. L’emergence de cette tumeur au sein du vermillon de la levre, depourvu de follicules pilo-sebaces, parait peu compatible avec la theorie de sa genese a par
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bcaacc5610d23c9d588525e9c837b6b6
https://doi.org/10.1016/j.annpat.2010.08.024
https://doi.org/10.1016/j.annpat.2010.08.024
Publikováno v:
Molecular Carcinogenesis. 11:98-105
Mutations in Ha-ras, Ki-ras, and N-ras genes in squamous and basal cell carcinomas in patients with xeroderma pigmentosum (XP) were examined by the polymerase chain reaction followed by single-strand conformation polymorphism analysis and direct base
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dddf7b6d61ae06a1fc1184c976308e45
https://doi.org/10.1002/mc.2940110207
https://doi.org/10.1002/mc.2940110207
Autor:
Yoichiro Kusunoki, Nori Nakamura, Alec J. Jeffreys, Hiraku Takebe, Yuko Hirai, Mohamed Ridha Kamoun, Kouichi Tatsumi, Takayuki Kurihara, Jun-ichi Kushiro, Mitoshi Akiyama, Mohamed Zghal, Tomonori Hayashi
Publikováno v:
Japanese Journal of Cancer Research : Gann
Bloom's syndrome (BS) is an autosomal recessive disorder conferring high propensity for cancer and displaying a high degree of genetic instability; the frequency of sister chromatid exchange is characteristically 10 times above background. The symmet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a79256fc479adb4ebe2913b5de754b1
https://doi.org/10.1111/j.1349-7006.1994.tb02403.x
https://doi.org/10.1111/j.1349-7006.1994.tb02403.x
Autor:
Olfa, Messaoud, Mariem, Ben Rekaya, Wafa, Cherif, Faten, Talmoudi, Hammouda, Boussen, Inçaf, Mokhtar, Samir, Boubaker, Ahlem, Amouri, Sonia, Abdelhak, Mohamed, Zghal
Publikováno v:
International journal of dermatology. 49(5)
Xeroderma Pigmentosum (XP) is a rare autosomal recessive disorder characterized by cutaneous and ocular alterations. Eight genes, Xeroderma Pigmentosum group A (XPA) to Xeroderma Pigmentosum group G (XPG) and Xeroderma Pigmentosum group V (XPV), are
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d169f97b628016e5b57244660a27e44c
https://pubmed.ncbi.nlm.nih.gov/20534089
https://pubmed.ncbi.nlm.nih.gov/20534089
Autor:
Rym Benmously, Mlika, Nadia, Kerkeni, Amel, Jebali, Mohamed, Zghal, Achraf, Debbiche, Mohamed Ben, Ayed, Insaf, Mokhtar, Samy, Fenniche
Publikováno v:
Annales de pathologie. 31(1)
Labial mucosa is an atypical site of basal cell carcinoma. The involvement of the vermilion lip, devoid of hair follicles and sweat glands, contrasts with the concept of its origin from pilar structures. We report a case of basal cell carcinoma devel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ee1285bee07bd8dfd50919d2b0120919
https://pubmed.ncbi.nlm.nih.gov/21349386
https://pubmed.ncbi.nlm.nih.gov/21349386
Autor:
Elhem, Khelifa, Rym, Benmously, Samy, Fenniche, Hayet, Marrak, Mohamed, Zghal, Insaf, Mokhtar
Publikováno v:
La Tunisie medicale. 85(8)
Dermatomyositis (DM) is a rare but serious disease. The aim was to evaluate the epidemiology, presenting clinical manifestations, therapeutic features and outcome of patients with DM.From January 1986 to December 2003, we collected retrospectively ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ba5ce4cf3bf008946122cfe6b138f001
https://pubmed.ncbi.nlm.nih.gov/18254286
https://pubmed.ncbi.nlm.nih.gov/18254286