Aggressive non-Hodgkin's lymphoma: Concomitant evaluation of interleukin-2, soluble interleukin-2 receptor, interleukin-4, interleukin-6, interleukin-10 and correlation with outcome

Autor: Alain Monnereau, Elizabeth Fabre-Guillevin, Pierre Soubeyran, Valérie Coulon, Houchingue Eghbali, Isabelle Soubeyran, Reza Tabrizi

Publikováno v: Leukemia & lymphoma
Leukemia & lymphoma, Taylor & Francis, 2006, 47, pp.603--611. 〈10.1080/10428190500361029〉
Leukemia & lymphoma, Taylor & Francis, 2006, 47, pp.603--611. ⟨10.1080/10428190500361029⟩

International audience; The purpose of this study was to assess the prognostic value of a large panel of cytokines in aggressive non-Hodgkin's lymphoma (NHL) and to confront it to parameters of the International Prognostic Index (IPI). It investigate

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::317f84e1e5efbfed32d01450a23643d7
https://doi.org/10.1080/10428190500361029

Allelic imbalance, including deletion ofPTEN/MMAC1, at the Cowden disease locus on 10q22-23, in hamartomas from patients with cowden syndrome and germlinePTEN mutation

Autor: Rosalind A. Eeles, Valérie Coulon, Michel Longy, H. Christian Weber, Katherine M. Call, Anne Louise Richardson, Bruce G. Robinson, Zimu Zheng, Shirley Hodgson, Françoise Dorion-Bonnet, Deborah J. Marsh, Patricia L. M. Dahia, Charis Eng, Albert Y. Lin, Alisa M. Goldstein, Randall Little

Publikováno v: Genes, Chromosomes and Cancer. 21:61-69

Cowden disease (CD) is a rare, autosomal dominant inherited cancer syndrome characterized by multiple benign and malignant lesions in a wide spectrum of tissues. While individuals with CD have an increased risk of breast and thyroid neoplasms, the pr

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::5c2e801acd90ca57618be2f1680c8281
https://doi.org/10.1002/(sici)1098-2264(199801)21:1<61::aid-gcc8>3.0.co

Mutation spectrum and genotype-phenotype analyses in Cowden disease and Bannayan-Zonana syndrome, two hamartoma syndromes with germline PTEN mutation

Autor: Alan M. Yahanda, Jean Marie Bressieux, Robert J. Gorlin, Claude Toulouse, Rosalind A. Eeles, Anne Louise Richardson, Zimu Zheng, Agnés Cabarrot-Moreau, Patricia L. M. Dahia, Frédéric Leprat, C. Geoffrey Woods, Ramon Parsons, Shirley Hodgson, Olufunmilayo I. Olopade, Philippe Rocca-Serra, Michel Longy, Deborah J. Marsh, Kathryn L. Lunetta, Jean Marie Bonnetblanc, Valérie Coulon, Susan Huson, Albert Y. Lin, Sylvie Odent, Sigrid Tishler, Liliane Demange, Danny Liaw, Didier Lacombe, Eric R. Fearon, Hagay Sobol, Agnès Chompret, Stacey Caron, Charis Eng, Bernadette Duboué, Jean Pierre Fricker, H. Christian Weber, Monica Peacocke, Bruce G. Robinson

Publikováno v: Human molecular genetics. 7(3)

The tumour suppressor gene PTEN , which maps to 10q23.3 and encodes a 403 amino acid dual specificity phosphatase (protein tyrosine phosphatase; PTPase), was shown recently to play a broad role in human malignancy. Somatic PTEN deletions and mutation

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46c291d6467df699f89ea816dcaba43a
https://pubmed.ncbi.nlm.nih.gov/9467011

PP-1-15 Is Cowden disease gene a tumor suppressor gene or not?

Autor: Bernadette Duboué, Valérie Coulon, I. Hostein, F. Bonnet-Dorion, Michel Longy

Publikováno v: European Journal of Cancer. 32:12

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::d0c170fc46050c26181294a2acf865e3
https://doi.org/10.1016/0959-8049(96)84048-2