C. Lasselin

发表

REDD2 Gene Is Upregulated by Modified LDL or Hypoxia and Mediates Human Macrophage Cell Death

M. Jaye, A. Nègre-Salvayre, J. Fruchart, 2004, Arteriosclerosis, thrombosis, and vascular biology.

Adipophilin increases triglyceride storage in human macrophages by stimulation of biosynthesis and inhibition of β‐oxidation

M. Jaye, J. Fruchart, M. Rouis, 2006, The FEBS journal.

Molecular relationships between virulence plasmids of Salmonella serotypes typhimurium and dublin and large plasmids of other Salmonella serotypes.

M. Popoff, P. Pardon, C. Coynault, 1984, Annales de microbiologie.

Effects of alcohol on the major steps of reverse cholesterol transport.

M. Jauhiainen, G. Castro, N. Perova, 2000, Biochemistry. Biokhimiia.

Reexpression of cartilage-specific genes by dedifferentiated human articular chondrocytes cultured in alginate beads.

J. Bonaventure, P. Freisinger, K. Ng, 1994, Experimental cell research.

Abnormal procollagen synthesis in fibroblasts from three patients of the same family with a severe form of osteogenesis imperfecta (type III).

J. Bonaventure, P. Maroteaux, C. Lasselin, 1986, Biochimica et biophysica acta.

Linkage studies of four fibrillar collagen genes in three pedigrees with Larsen-like syndrome.

J. Bonaventure, P. Maroteaux, C. Lasselin, 1992, Journal of medical genetics.

Adipophilin Enhances Lipid Accumulation and Prevents Lipid Efflux From THP-1 Macrophages: Potential Role in Atherogenesis

M. Jaye, J. Fruchart, M. Rouis, 2004, Arteriosclerosis, thrombosis, and vascular biology.

Influence of shielding blocks on the output of photon beams as a function of energy and type of treatment unit.

N. Blanckaert, A. Dutreix, A. Bridier, 1992, Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology.

A new lethal brittle bone syndrome with increased amount of type V collagen in a patient.

J. Bonaventure, P. Maroteaux, L. Zylberberg, 1989, American journal of medical genetics.

A dominant mutation in the COL1A1 gene that substitutes glycine for valine causes recurrent lethal osteogenesis imperfecta

J. Bonaventure, P. Maroteaux, C. Lasselin, 1992, Human Genetics.

Linkage study in a large pedigree with Stickler syndrome: exclusion of COL2A1 as the mutant gene

J. Bonaventure, C. Philippe, G. Plessis, 1992, Human Genetics.