Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Testsuro Noguchi"'
Autor:
Mohamed Adnène Laatiri, Walid Sabri Hamadou, Abderrahim Khelif, Violaine Bourdon, Yosra Ben Youssef, Hagay Sobol, Zohra Soua, Sawsen Besbes, Testsuro Noguchi
Publikováno v:
Familial Cancer. 16:153-157
Mutations are responsible for familial cancer syndromes which account for approximately 5–10 % of all types of cancers. Familial cancers are often caused by genetic alterations occurring either in tumor suppressor or genomic stability genes such as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a53a7923587d75a4229d05706813beec
https://doi.org/10.1007/s10689-016-9931-3
https://doi.org/10.1007/s10689-016-9931-3
Autor:
Valérie Bonadona, Chaker Ben Salem, Paul Gesta, Sawsen Besbes, Fabienne Brenet, Hagay Sobol, François Eisinger, Catherine Dugast, Hélène Dreyfus, Mohamed-Adnène Laatiri, Abderrahim Khélif, Testsuro Noguchi, Patrice Dubreuil, Hélène Zattara, Muriel D. David, Sébastien Letard, Laurence Faivre, Angelo Paci, Véronique Mari, Virginie Penard-Lacronique, Sofien Laarif, Violaine Bourdon, Walid-Sabri Hamadou, Yosra Ben Youssef, Zohra Soua
Publikováno v:
Annals of Hematology. 95:1943-1947
Isocitrate dehydrogenase IDH 1 and IDH 2 mutations were reported in several cancer forms, especially in hematological malignancies, but were never been investigated in familial aggregation. The aim of this study is to determine whether germline isoci
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14bb8f443e5c67a1bf490089f3d86726
https://doi.org/10.1007/s00277-016-2813-9
https://doi.org/10.1007/s00277-016-2813-9
Autor:
Walid Sabri Hamadou, Yosra Ben Youssef, Paul Gesta, Aurelie Fabre, Abderrahim Khelif, Testsuro Noguchi, François Eisinger, Mohamed Adnène Laatiri, Zohra Soua, Hélène Dreyfus, Sawsen Besbes, Véronique Mari, Laurence Faivre, Hagay Sobol, Pascaline Gaildrat, Hélène Zattara, Violaine Bourdon, Saloua Yacoub Jemni, Catherine Dugast, Valérie Bonadona, H. Regaieg
Publikováno v:
Annals of Hematology. 95:1043-1050
Familial aggregation of hematological malignancies has been reported highlighting inherited genetic predisposition. In this study, we targeted four candidate genes: JAK2 and RUNX1 genes assuring a prominent function in hematological process and CBL a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::371a1460270631669f693dd47f4fbe09
https://doi.org/10.1007/s00277-016-2678-y
https://doi.org/10.1007/s00277-016-2678-y
Autor:
A. Fabre, V. Bourdon, Hélène Dreyfus, F. Eisinger, S. Y. Jemni, Testsuro Noguchi, Walid-Sabri Hamadou, V. Bonadona, Yosra Ben Youssef, Laurence Faivre, V. Mari, Zohra Soua, M. A. Laatiri, C. Dugast, Abderrahim Khelif, Rym El Abed, Paul Gesta, Hélène Zattara, Sawsen Besbes, H. Sobol
Publikováno v:
Clinical and Translational Oncology. 18:385-390
Purpose Familial aggregation among patients with several hematological malignancies has been revealed. This emphasizes the importance of genetic factors. Only few genes predisposing to familial hematological malignancies have been reported until now
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e810b8a245ee2bbfa3e73ca244d1e8a9
https://doi.org/10.1007/s12094-015-1379-7
https://doi.org/10.1007/s12094-015-1379-7
Autor:
Paul Gesta, Véronique Mari, Testsuro Noguchi, Abderrahim Khelif, Sawsen Besbes, Rahma Mani, Hélène Zattara, Yosra Ben Youssef, Hagay Sobol, François Eisinger, Laurence Faivre, Zohra Soua, Violaine Bourdon, Valérie Bonadona, Hélène Dreyfus, Walid Sabri Hamadou, Catherine Dugast
Publikováno v:
Annals of hematology. 96(10)
The genetic predisposition to familial hematological malignancies has been previously reported highlighting inherited gene mutations. Several genes have been reported but genetic basis remains not well defined. In this study, we extended our investig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc820a9ff92946870eca5f1dc144cab5
https://pubmed.ncbi.nlm.nih.gov/28752392
https://pubmed.ncbi.nlm.nih.gov/28752392
Autor:
Violaine Bourdon, Abderrahim Khelif, Hagay Sobol, Hélène Dreyfus, Walid Sabri Hamadou, Laurence Faivre, Véronique Mari, Valérie Bonadona, Catherine Dugast, Hélène Zattara, François Eisinger, Yosra Ben Youssef, B. Achour, Zohra Soua, Sawsen Besbes, Paul Gesta, H. Regaieg, Testsuro Noguchi, Rahma Mani
Publikováno v:
Bulletin du cancer. 104(2)
Summary Introduction Genetic predisposition to familial hematological malignancies was previously described through several epidemiological analyses, but the genetic basis remains unclear. The tumor-suppressor ARLTS1 gene was previously described in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b684e42fceff9f2298d00a395c808bcb
https://pubmed.ncbi.nlm.nih.gov/27866680
https://pubmed.ncbi.nlm.nih.gov/27866680
Autor:
Bruno Buecher, Cédrick Lefol, V Bourdon, Testsuro Noguchi, Hélène Zattara, Hagay Sobol, Adrien Briaux, Rosette Lidereau, Sylviane Olschwang, Etienne Rouleau
Publikováno v:
Clinical genetics. 80(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::973f83811fb1c9ae855b074e274018c5
https://pubmed.ncbi.nlm.nih.gov/21815886
https://pubmed.ncbi.nlm.nih.gov/21815886
Autor:
Hélène Zattara, Ilia Voskoboinik, Halima El Omri, Saloua Yacoub Jemni, Laurence Faivre, Hagay Sobol, Catherine Dugast, Valérie Bonadona, Hélène Dreyfus, Testsuro Noguchi, Laetitia Huiart, Yosra Ben Youssef, Rim El Abed, Marc Frenay, Liliane Demange, Violaine Bourdon, Paul Gesta, Mohamed Adnène Laatiri, François Eisinger, Laetitia Rabayrol, Monia Zaier, Zohra Soua
Publikováno v:
Hereditary Cancer in Clinical Practice
Hereditary Cancer in Clinical Practice, Vol 9, Iss 1, p 9 (2011)
Hereditary Cancer in Clinical Practice, Vol 9, Iss 1, p 9 (2011)
Perforin gene (PRF1) mutations have been identified in some patients diagnosed with the familial form of hemophagocytic lymphohistiocytosis (HLH) and in patients with lymphoma. The aim of the present study was to determine whether patients with a fam
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc247c4fdacd860b9b5b28afa8e697e9
https://pubmed.ncbi.nlm.nih.gov/21936944
https://pubmed.ncbi.nlm.nih.gov/21936944
Autor:
V. Bourdon, Hélène Zattara, Testsuro Noguchi, Laurence Faivre, Valérie Bonadona, Paul Gesta, François Eisinger, L. Huiart, Marc Frenay, Hagay Sobol, Liliane Demange, Zohra Soua, R. El Abed, Hélène Dreyfus, Catherine Dugast, Abderrahim Khelif, R. Sauvan
Publikováno v:
Familial Cancer
Familial Cancer, 2009, 8, pp.581-4. ⟨10.1007/s10689-009-9289-x⟩
Familial Cancer, 2009, 8, pp.581-4. ⟨10.1007/s10689-009-9289-x⟩
Familial aggregation in patients with several haematological malignancies has been described, but the genetic basis for this familial clustering is not known. Few genes predisposing to familial haematological malignancies have been identified, among
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66e07666db14718f7ebdebe9f3548063
https://pubmed.ncbi.nlm.nih.gov/19731081
https://pubmed.ncbi.nlm.nih.gov/19731081