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Cancer Causes & Control : CCC|March 1, 1996
Diet and cancers of the larynx and hypopharynx: the IARC multi-center study in southwestern EuropeJ Estève, E Riboli, G Péquignot, et al.
The Journal of Investigative Dermatology|March 14, 2017
TNF-α Antagonist and Vascular Inflammation in Patients with Psoriasis Vulgaris: A Randomized Placebo-Controlled StudyRobert Bissonnette, François Harel, James G Krueger, et al.
The Science of the Total Environment|February 21, 2025
Chemical responses of small boreal lakes to atmospheric and catchment drivers over four decadesLauri Arvola, Martti Rask, Jussi Huotari, et al.
Journal of Gynecology Obstetrics and Human Reproduction|January 22, 2023
Embryo transfer learning using medical simulation tools: a comparison of two embryo transfer simulatorsMathilde Bourdon, Marion Ouazana, Chloe Maignien, et al.
Journal of Neuroinflammation|March 5, 2020
Pathological modeling of TBEV infection reveals differential innate immune responses in human neurons and astrocytes that correlate with their susceptibility to infectionMazigh Fares, Marielle Cochet-Bernoin, Gaëlle Gonzalez, et al.
Environmental Science and Pollution Research International|November 20, 2014
Changes in bacterial community metabolism and composition during the degradation of dissolved organic matter from the jellyfish Aurelia aurita in a Mediterranean coastal lagoonMarine Blanchet, Olivier Pringault, Marc Bouvy, et al.
Targeted Oncology|May 21, 2017
Circulating Tumor DNA Measurement by Picoliter Droplet-Based Digital PCR and Vemurafenib Plasma Concentrations in Patients with Advanced BRAF-Mutated MelanomaFanny Garlan, Benoit Blanchet, Nora Kramkimel, et al.
Bioinformatics (Oxford, England)|September 9, 2010
BioXSD: the common data-exchange format for everyday bioinformatics web servicesMatús Kalas, Pål Puntervoll, Alexandre Joseph, et al.
Journal of Synchrotron Radiation|May 5, 2021
Anomalous SAXS at P12 beamline EMBL Hamburg: instrumentation and applicationsAndrey Yu Gruzinov, Martin A Schroer, Karen Manalastas-Cantos, et al.
European Journal of Ophthalmology|May 31, 2011
Cataract as a phenotypic marker for a mutation in WFS1, the Wolfram syndrome geneSalah Mohamed Cherif Titah, Isabelle Meunier, Catherine Blanchet, et al.
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