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Team 3 - Oncogenesis of cutaneous lymphomas (26 November 2020)

disease’s stages. Our team involves clinicians and researchers working in the Dermatology, Pathology and Tumor Genetic Departments of Bordeaux University Hospital with coordination of the Cancer Biobank. We

Group M. Bouchecareilh (25 February 2022)

Watch the video from ADAAT Alpha 1 France Research Alpha-1-antitrypsin (1AT) deficiency (1ATD) is a rare genetic disorder that manifests as pulmonary emphysema and liver damages (cirrhosis

Group 3- Enterohepatic Helicobacters CDT and Helicobacter phylogeny (PI: Armelle Ménard) (20 November 2020)

al., Syst Appl Microbiol 2016). In another study (manuscript in preparation), we investigated the genetic diversity and evolution of homD gene coding for H. pylori outer membrane protein (OMP

Translational Research (29 November 2020)

hepatocellular carcinomas. Nat Genet. 2015 Oct;47(10):1187-93. Pilati C, Letouzé E, Nault JC, Imbeaud S, Boulai A, Calderaro J, Poussin K, Franconi A, Couchy G, Morcrette G, Mallet M, Taouji S, Balabaud C, Terris