Výsledky vyhledávání - "Nadia Ben Jemii"

Akademický článek

Dysregulated PDGFR alpha expression and novel somatic mutations in colorectal cancer: association to RAS wild type status and tumor size

Autor: Nadia Ben Jemii, Haifa Tounsi-Kettiti, Hamza Yaiche, Najla Mezghanni, Amira Jaballah Gabteni, Emna Fehri, Chayma Ben Fayala, Sonia Abdelhak, Samir Boubaker

Publikováno v: Journal of Translational Medicine, Vol 18, Iss 1, Pp 1-20 (2020)

Abstract Background Platelet derived growth factor receptor alpha (PDGFRα) has been considered as a relevant factor in tumor proliferation, angiogenesis and metastatic dissemination. It was a target of tyrosine kinase (TK) inhibitors emerged in the

Externí odkaz: https://doaj.org/article/7e61269da7af403081e048bae78af069

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Akademický článek

Identification of novel pathogenic MSH2 mutation and new DNA repair genes variants: investigation of a Tunisian Lynch syndrome family with discordant twins

Autor: Amira Jaballah-Gabteni, Haifa Tounsi, Maria Kabbage, Yosr Hamdi, Sahar Elouej, Ines Ben Ayed, Mouna Medhioub, Moufida Mahmoudi, Hamza Dallali, Hamza Yaiche, Nadia Ben Jemii, Afifa Maaloul, Najla Mezghani, Sonia Abdelhak, Lamine Hamzaoui, Mousaddak Azzouz, Samir Boubaker

Publikováno v: Journal of Translational Medicine, Vol 17, Iss 1, Pp 1-13 (2019)

Abstract Background Lynch syndrome (LS) is a highly penetrant inherited cancer predisposition syndrome, characterized by autosomal dominant inheritance and germline mutations in DNA mismatch repair genes. Despite several genetic variations that have

Externí odkaz: https://doaj.org/article/a09c2b09894543cfad966473641e0ab2

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BRAF V600E and Novel Somatic Mutations in Thyroid Cancer of Libyan Patients

Autor: Haifa Tounsi Guettiti, Hanan Traina, Ines Ben Ayed, Nadia Ben Jemii, Samir Boubaker, Musa Alrageeg, Omar Alqawi

Publikováno v: Asian Pacific journal of cancer prevention : APJCP. 23(12)

Thyroid cancer (TC) is a common endocrine malignancy that frequently harbours the oncogenic V600E BRAF mutation. This mutation has received considerable attention in recent years for its potential utility in the risk stratification and management of

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef582615bc7bfaabb58f4995e2acf274
https://pubmed.ncbi.nlm.nih.gov/36579983

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Dysregulated PDGFR alpha expression and novel somatic mutations in colorectal cancer: association to RAS wild type status and tumor size

Autor: Najla Mezghanni, Amira Jaballah Gabteni, Emna Fehri, Hamza Yaiche, Nadia Ben Jemii, Sonia Abdelhak, Chayma Ben Fayala, Haifa Tounsi-Kettiti, Samir Boubaker

Publikováno v: Journal of Translational Medicine
Journal of Translational Medicine, Vol 18, Iss 1, Pp 1-20 (2020)

Background Platelet derived growth factor receptor alpha (PDGFRα) has been considered as a relevant factor in tumor proliferation, angiogenesis and metastatic dissemination. It was a target of tyrosine kinase (TK) inhibitors emerged in the therapy o

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b930dfa71daaf6b0f3d3eea93b0afdc
https://doi.org/10.1186/s12967-020-02614-3

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New insights in the clinical implication of HOXA5 as prognostic biomarker in patients with colorectal cancer

Autor: Samir Boubaker, Afifa Maaloul, Emna Fehri, Najla Mezghanni, Monia Ardhaoui, Nadia Ben Jemii, Amira Jaballah Gabteni, Hamza Yaiche, Sonia Abdelhak, Haifa Tounsi-Kettiti

Publikováno v: Cancer biomarkers : section A of Disease markers. 30(2)

Background Homeobox A5 (HOXA5) is a member of the HOX protein family which is involved in several pathways of carcinogenesis, and is dysregulated in many types of cancers. However, its expression and function in human colorectal cancer (CRC) is still

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::325a229e038afab068e650233295206e
https://pubmed.ncbi.nlm.nih.gov/33136093

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Identification of novel pathogenic MSH2 mutation and new DNA repair genes variants: investigation of a Tunisian Lynch syndrome family with discordant twins

Autor: M Mahmoudi, Samir Boubaker, Amira Jaballah-Gabteni, Haifa Tounsi, Mousaddak Azzouz, Hamza Dallali, Hamza Yaiche, Sahar Elouej, Maria Kabbage, Ines Ben Ayed, Lamine Hamzaoui, Mouna Medhioub, Sonia Abdelhak, Afifa Maaloul, Yosr Hamdi, Nadia Ben Jemii, Najla Mezghani

Publikováno v: Journal of Translational Medicine, Vol 17, Iss 1, Pp 1-13 (2019)
Journal of Translational Medicine
Journal of Translational Medicine, BioMed Central, 2019, 17 (1), pp.212. ⟨10.1186/s12967-019-1961-9⟩

Background Lynch syndrome (LS) is a highly penetrant inherited cancer predisposition syndrome, characterized by autosomal dominant inheritance and germline mutations in DNA mismatch repair genes. Despite several genetic variations that have been iden

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3714aec0aaa66ec377220ed5bbeb7de9
https://doi.org/10.1186/s12967-019-1961-9

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