La représentation du corps dans la peinture du Moyen-Âge à nos jours.

Most Common Irregular Verbs

A prokaryotic proton-gated ion channel from the nicotinic acetylcholine receptor family

Cysteine Crosslinking to Study Allosteric Transitions of a Bacterial Homolog of Pentameric Channel-Receptors

Study of the Interaction Between General Anesthetics and a Bacterial Homologue to the Human Nicotinic Receptor

X-Ray Structures of General Anaesthetics Bound to a Pentameric Ligand-Gated Ion Channel

On the complexity of solving quadratic Boolean systems

Me, myself and I: Sartre and Husserl on elusiveness of the self

[IEEE IGARSS 2008 - 2008 IEEE International Geoscience and Remote Sensing Symposium - Boston, MA, USA (2008.07.7-2008.07.11)] IGARSS 2008 - 2008 IEEE International Geoscience and Remote

The HER2 amplicon in breast cancer: Topoisomerase IIA and beyond

Model-based decoupling control method for dual-drive gantry stages: A case study with experimental validations

[ACM Press the 2009 ACM symposium - Honolulu, Hawaii (2009.03.08-2008.03.12)] Proceedings of the 2009 ACM symposium on Applied Computing - SAC '09 - Learners automated evaluation with

Precise determination of Rb, Sr, Ba, and Pb in geological materials by isotope dilution and ICP-quadrupole mass spectrometry following selective separation of the analytes

Biomechanics of thoracolumbar junction vertebral fractures from various kinematic conditions

A locally closed conformation of a bacterial pentameric proton-gated ion channel

Physicians' Knowledge and Practice of Lung Cancer Screening: A Cross-Sectional Survey Comparing General Practitioners, Thoracic Oncologists, and Pulmonologists in France

Sur la nature et la signification des dolerites du bassin precambrien de sembe-ouesso (republique du congo)

Central and Eastern European health care financing: report of a visit

Cryoglobulinaemia and hepatitis C infection

Primary lung adenocarcinoma occurring in a PTEN related syndrome (Cowden's disease): Routine EGFR sequencing also highlights two rare somatic mutations S768I and V769L