J. Chassé

发表

Urinary Retinol Binding Protein Is a Marker of the Extent of Interstitial Kidney Fibrosis

J. Olivo-Marin, P. Beaune, V. Meas-Yedid, 2014, PloS one.

Spatial and temporal expression of the cystathionine beta-synthase gene during early human development.

P. Kamoun, J. Demaille, J. Dufier, 1999, Biochemical and biophysical research communications.

Inverse correlation between phenylacetate hydrolase activity of the serum PON1 protein and homocysteinemia in humans

R. Barouki, K. Robert, N. Janel, 2005, Thrombosis and Haemostasis.

Homocysteine is not detected in normal human vessel walls.

K. Robert, N. Janel, D. Damotte, 2005, Atherosclerosis.

Genomic organization of the human cystathionine beta-synthase gene: evidence for various cDNAs.

P. Kamoun, P. Sinet, D. Paris, 1995, Biochemical and biophysical research communications.

Methylenetetrahydrofolate reductase thermolabile variant and human longevity.

P. Kamoun, O. Guerassimenko, J. Zittoun, 1997, American journal of human genetics.

Human cystathionine β-synthase: gene organization and expression of different 5′ alternative splicing

P. Kamoun, J. Chassé, V. Paul, 1997, Mammalian Genome.

The neuronal SAPK/JNK pathway is altered in a murine model of hyperhomocysteinemia

K. Robert, N. Janel, P. Kamoun, 2004, Journal of neurochemistry.

Low Serum Creatine Kinase Level Predicts Mortality in Patients with a Chronic Kidney Disease

P. Houillier, B. Stengel, J. Haymann, 2016, PloS one.

Mouse liver paraoxonase-1 gene expression is downregulated in hyperhomocysteinemia

R. Barouki, K. Robert, J. Delabar, 2004, Thrombosis and Haemostasis.

Altered Gene Expression in Liver from a Murine Model of Hyperhomocysteinemia*

K. Robert, N. Janel, N. Maeda, 2003, Journal of Biological Chemistry.

[Homocysteine, 5,10-methylenetetrahydrofolate reductase and deep venous thrombosis. Survey of 120 patients in internal medicine].

I. Quéré, C. Janbon, G. Tobelem, 1998, La Revue de medecine interne.

Linkage disequilibrium at the cystathionine β synthase (CBS) locus and the association between genetic variation at the CBS locus and plasma levels of homocysteine

V. Gudnason, S. Humphries, V. Nicaud, 1998 .

Linkage disequilibrium at the cystathionine beta synthase (CBS) locus and the association between genetic variation at the CBS locus and plasma levels of homocysteine. The Ears II Group. European Atherosclerosis Research Study.

V. Gudnason, S. Humphries, V. Nicaud, 1998, Annals of human genetics.

Characterisation of a human liver cystathionine beta synthase mRNA sequence corresponding to the c.[833T>C;844_845ins68] mutation in CBS gene

R. Barouki, J. Chassé, 2009, Molecular and Cellular Biochemistry.

Evaluation of the transfer and expression in mice of an enzyme-encoding gene using a human adenovirus vector.

M. Perricaudet, M. Levrero, P. Briand, 1990, Human gene therapy.

Identification of a new stilbene-derived inducer of paraoxonase 1 and ligand of the Aryl hydrocarbon Receptor.

X. Coumoul, R. Barouki, M. Poirot, 2012, Biochemical pharmacology.

Correction of mouse ornithine transcarbamylase deficiency by gene transfer into the germ line.

C. Cavard, G. Grimber, P. Briand, 1988, Nucleic acids research.

Two novel mutations (K384E and L539S) in the C‐terminal moiety of the cystathionine β‐synthase protein in two French pyridoxine‐responsive homocystinuria patients

P. Kamoun, B. Chadefaux-Vekemans, B. Aral, 1997, Human mutation.

Compared expression levels of ornithine transcarbamylase and carbamylphosphate synthetase in liver and small intestine of normal and mutant mice.

C. Cavard, P. Briand, P. Kamoun, 1988, Biochimica et biophysica acta.