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Year | Number of Results |
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2020 | 2 |
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Page 1
CDH1 Germline Variants in a Tunisian Cohort with Hereditary Diffuse Gastric Carcinoma.
Genes (Basel). 2022 Feb 23;13(3):400. doi: 10.3390/genes13030400.
Genes (Basel). 2022.
PMID: 35327954
Free PMC article.
New insights in the clinical implication of HOXA5 as prognostic biomarker in patients with colorectal cancer.
Yaiche H, Tounsi-Kettiti H, Ben Jemii N, Jaballah Gabteni A, Mezghanni N, Ardhaoui M, Fehri E, Maaloul A, Abdelhak S, Boubaker S.
Yaiche H, et al. Among authors: jaballah gabteni a.
Cancer Biomark. 2021;30(2):213-221. doi: 10.3233/CBM-201758.
Cancer Biomark. 2021.
PMID: 33136093
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A Rare MSH2 Variant as a Candidate Marker for Lynch Syndrome II Screening in Tunisia: A Case of Diffuse Gastric Carcinoma.
Kabbage M, Ben Aissa-Haj J, Othman H, Jaballah-Gabteni A, Laarayedh S, Elouej S, Medhioub M, Kettiti HT, Khsiba A, Mahmoudi M, BelFekih H, Maaloul A, Touinsi H, Hamzaoui L, Chelbi E, Abdelhak S, Boubaker MS, Azzouz MM.
Kabbage M, et al. Among authors: jaballah gabteni a.
Genes (Basel). 2022 Jul 28;13(8):1355. doi: 10.3390/genes13081355.
Genes (Basel). 2022.
PMID: 36011265
Free PMC article.
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Dysregulated PDGFR alpha expression and novel somatic mutations in colorectal cancer: association to RAS wild type status and tumor size.
Ben Jemii N, Tounsi-Kettiti H, Yaiche H, Mezghanni N, Jaballah Gabteni A, Fehri E, Ben Fayala C, Abdelhak S, Boubaker S.
Ben Jemii N, et al. Among authors: jaballah gabteni a.
J Transl Med. 2020 Nov 19;18(1):440. doi: 10.1186/s12967-020-02614-3.
J Transl Med. 2020.
PMID: 33213472
Free PMC article.
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Selective expression of KCNA5 and KCNB1 genes in gastric and colorectal carcinoma.
Farah A, Kabbage M, Atafi S, Gabteni AJ, Barbirou M, Madhioub M, Hamzaoui L, Mohamed MA, Touinsi H, Kchaou AO, Chelbi E, Boubaker S, Abderrazek RB, Bouhaouala-Zahar B.
Farah A, et al. Among authors: gabteni aj.
BMC Cancer. 2020 Dec 2;20(1):1179. doi: 10.1186/s12885-020-07647-x.
BMC Cancer. 2020.
PMID: 33267786
Free PMC article.
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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.
Jaballah-Gabteni A, Tounsi H, Kabbage M, Hamdi Y, Elouej S, Ben Ayed I, Medhioub M, Mahmoudi M, Dallali H, Yaiche H, Ben Jemii N, Maaloul A, Mezghani N, Abdelhak S, Hamzaoui L, Azzouz M, Boubaker S.
Jaballah-Gabteni A, et al.
J Transl Med. 2019 Jun 27;17(1):212. doi: 10.1186/s12967-019-1961-9.
J Transl Med. 2019.
PMID: 31248416
Free PMC article.
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