Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Ayda Bennour"'
Autor:
Yosr Hamdi, Mediha Trabelsi, Kais Ghedira, Maroua Boujemaa, Ikhlas Ben Ayed, Cherine Charfeddine, Amal Souissi, Imen Rejeb, Wafa Kammoun Rebai, Chaima Hkimi, Fadoua Neifar, Nouha Jandoubi, Rahma Mkaouar, Melek Chaouch, Ayda Bennour, Selim Kamoun, Hend Chaker Masmoudi, Nabil Abid, Maha Mezghani Khemakhem, On behalf of the GTCA Consortium, Saber Masmoudi, Ali Saad, Lamia BenJemaa, Alia BenKahla, Samir Boubaker, Ridha Mrad, Hassen Kamoun, Sonia Abdelhak, Moez Gribaa, Neila Belguith, Najla Kharrat, Dorra Hmida, Ahmed Rebai
Publikováno v:
Genome Medicine, Vol 16, Iss 1, Pp 1-19 (2024)
Abstract Background Key discoveries and innovations in the field of human genetics have led to the foundation of molecular and personalized medicine. Here, we present the Genome Tunisia Project, a two-phased initiative (2022–2035) which aims to del
Externí odkaz:
https://doaj.org/article/d62ab665af394533b93e1685ae93dc5f
Autor:
Hamza Chouk, Sarra Saad, Sarra Dimassi, Nadia Ghariani Fetoui, Ayda Bennour, Rima Gammoudi, Haifa Elmabrouk, Ali Saad, Mohamed Denguezli, Dorra H’mida
Publikováno v:
BMC Medical Genomics, Vol 15, Iss 1, Pp 1-9 (2022)
Abstract Introduction X-linked recessive ichthyosis (XLI) is a genodermatosis, caused by a deficiency of the steroid sulphatase enzyme encoded by the STS gene (OMIM # 300,747). Adopted XLI molecular diagnosis approaches differ from one laboratory to
Externí odkaz:
https://doaj.org/article/f20217f90c3d4b5999fb0fefe2380ac1
Autor:
Ayda Bennour, Ikram Tabka, Yosra Ben Youssef, Zahra Kmeira, Abderrahim Khelif, Ali Saad, Halima Sennana
Publikováno v:
Cancer Biology & Medicine, Vol 10, Iss 1, Pp 47-51 (2013)
The acquisition of secondary chromosomal aberrations in chronic myeloid leukemia (CML) patients with Philadelphia chromosome-positive (Ph+) karyotype signifies clonal evolution associated with the progression of the disease to its accelerated or blas
Externí odkaz:
https://doaj.org/article/ad4d88c947ad4b19ab2c793f31c924d9
Autor:
Moez Elloumi, Halima Sennana, Hatem Bellâaj, Yosra Ben Youssef, Ali Saad, Ayda Bennour, Abderrahim Khelif
Publikováno v:
Journal of Cancer Research and Clinical Oncology. 137:1329-1336
The BCR/ABL gene rearrangement is generated by a reciprocal translocation t(9;22)(q34;q11) in chronic myeloid leukemia (CML) patients. In most cases, it is cytogenetically visualized by the Philadelphia (Ph) chromosome. About 5-10% of CML patients la
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::224dd1d02e9b03b6e623159040dc097b
https://doi.org/10.1007/s00432-011-1002-4
https://doi.org/10.1007/s00432-011-1002-4
Publikováno v:
Journal of Clinical Pathology. 63:737-740
The development of imatinib is a milestone in the treatment of chronic myeloid leukaemia (CML), and its therapeutic effect has been extensively investigated in patients with CML who carry M-bcr and m-bcrBCR–ABL fusion transcripts. However, knowledg
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb2ade8a20f95205430cf846417cea56
https://doi.org/10.1136/jcp.2010.078311
https://doi.org/10.1136/jcp.2010.078311
Publikováno v:
Cancer Genetics and Cytogenetics. 194:30-37
The mechanisms for the formation of variant Philadelphia (Ph) translocations that occur in 5-10% of patients with chronic myeloid leukemia (CML) are not fully characterized. Studies on the prognosis of these variant translocations have yielded confli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e3c3f8a812c4760b11175b36077b695d
https://doi.org/10.1016/j.cancergencyto.2009.05.010
https://doi.org/10.1016/j.cancergencyto.2009.05.010
Autor:
Ali Saad, Ayda Bennour, Halima Sennana, Abderrahim Khelif, Monia Zaier, Zannouba Mrad, Ines Ouahchi, Yosra Ben Youssef
Publikováno v:
Medical Oncology. 29:1134-1136
Sex chromosomes are infrequently involved in patients with hematologic malignancies. In most instances, the abnormality is either duplication in the q arm or deletion and translocation involving the q13 and q24 regions. We report herein a rare transl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c83219c17d4f88c8b3764e7ea994096
https://doi.org/10.1007/s12032-011-9908-x
https://doi.org/10.1007/s12032-011-9908-x
Publikováno v:
Cancer Genetics and Cytogenetics. 181:72-74
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e81dca39a95564f280d9a7e4a48e5bb8
https://doi.org/10.1016/j.cancergencyto.2007.11.007
https://doi.org/10.1016/j.cancergencyto.2007.11.007
Autor:
Abderrahim Khelif, Monia Zaier, Ali Saad, Halima Sennana, Sondess Hizem, Ikram Tabka, Ayda Bennour, Yosra Ben Youssef
Publikováno v:
Medical oncology (Northwood, London, England). 30(1)
Acute promyelocytic leukemia (APL) is genetically characterized by a reciprocal translocation between chromosomes 15 and 17, t(15;17)(q22;q21), which results in the fusion gene PML-RARA. A small proportion of patients with APL have complex or simple
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa6a604b98a8d1e4e3f552bb231c837a
https://pubmed.ncbi.nlm.nih.gov/23292868
https://pubmed.ncbi.nlm.nih.gov/23292868
Autor:
Ayda, Bennour, Ines, Ouahchi, Medhaffar, Moez, Moez, Elloumi, Abderrahim, Khelif, Ali, Saad, Halima, Sennana
Publikováno v:
Clinical laboratory. 58(5-6)
A specific chromosomal abnormality, the Philadelphia chromosome (Ph), is present in 90 - 95% of patients with chronic myeloid leukemia (CML). This aberration results from a reciprocal translocation between chromosomes 9 and 22, creating a BCR/ABL fus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cf02a7a66fabce91021411c6a41875fd
https://pubmed.ncbi.nlm.nih.gov/22783572
https://pubmed.ncbi.nlm.nih.gov/22783572