L. Thuillier

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The activation of protein kinase C is not necessary for the monoclonalantibody‐induced modulation of CD3 and CD4 antigens

F. Selz, J. Pérignon, F. Selz, 1990, European journal of immunology.

Salvage of 5'-deoxy-methylthioadenosine into purines and methionine by lymphoid cells and inhibition of cell proliferation.

L. Christa, J. Pérignon, L. Thuillier, 1984, Biochimica et biophysica acta.

Defects in activation and transport of fatty acids

D. Rabier, J. Saudubray, A. Slama, 1999, Journal of Inherited Metabolic Disease.

Genotype/phenotype correlation in carnitine palmitoyl transferase II deficiency: lessons from a compound heterozygous patient

D. Rabier, J. Saudubray, P. Kamoun, 2000, Neuromuscular Disorders.

Ligation of CD4 surface antigen induces rapid tyrosine phosphorylation of the cytoskeletal protein ezrin.

P. Mangeat, R. Fagard, C. Hivroz, 1994, Cellular immunology.

Correction of Fatty Acid Oxidation in Carnitine Palmitoyl Transferase 2–Deficient Cultured Skin Fibroblasts by Bezafibrate

A. Munnich, J. Bonnefont, F. Djouadi, 2003, Pediatric Research.

Opposing effects of protein tyrosine kinase inhibitors on the monoclonal antibody induced internalization of CD3 and CD4 antigens

C. Griscelli, F. Selz, J. Pérignon, 1991, European journal of immunology.

Correlation between genotype, metabolic data, and clinical presentation in carnitine palmitoyltransferase 2 (CPT2) deficiency

J. Saudubray, J. Bonnefont, M. Brivet, 2003, Human mutation.

Functional and Structural Basis of Carnitine Palmitoyltransferase 1A Deficiency*

L. Tong, J. Girard, J. Bonnefont, 2003, Journal of Biological Chemistry.

Prenatal diagnosis of carnitine palmitoyltransferase 2 deficiency in chorionic villi: a novel approach

J. Saudubray, T. Attié-Bitach, J. Bonnefont, 2003, Prenatal diagnosis.

Uridine as the only alternative to pyrimidine de novo synthesis in rat T lymphocytes

G. Bismuth, J. Pérignon, L. Thuillier, 1982, FEBS letters.

Molecular and enzymatic characterization of a unique carnitine palmitoyltransferase 1A mutation in the Hutterite community.

J. Girard, C. Greenberg, P. Kamoun, 2001, Molecular genetics and metabolism.

Consequences of adenosine deaminase deficiency on thymocyte metabolism

F. Garreau, L. Thuillier, P. Cartier, 1981, European journal of immunology.

Purification and kinetic properties of human erythrocyte Mg2+-dependent inorganic pyrophosphatase.

L. Thuillier, 1978, Biochimica et biophysica acta.

Hepatic carnitine palmitoyl transferase 1 (CPT1 A) deficiency in North American Hutterites (Canadian and American): evidence for a founder effect and results of a pilot study on a DNA-based newborn screening program.

J. Thompson, C. Greenberg, C. Prasad, 2001, Molecular genetics and metabolism.

Carnitine palmitoyltransferase deficiencies.

J. Saudubray, J. Bonnefont, J M Saudubray, 1999, Molecular genetics and metabolism.

MINIREVIEW Carnitine Palmitoyltransferase Deficiencies

J. Saudubray, J. Bonnefont, C. Prip-Buus, 1999 .

Energy metabolism in adenosine deaminase-inhibited human erythrocytes.

A. Moncion, H. Buc, F. Garreau, 1986, Clinica chimica acta; international journal of clinical chemistry.

Metabolism of pyrimidine bases and nucleosides by pyrimidine-nucleoside phosphorylases in cultured human lymphoid cells.

A. Houllier, D. Bories, J. Pérignon, 1987, Biochimica et biophysica acta.

Synergistic toxicity of pyrazofurin and cytidine in cytidine deaminase deficient lymphoid cells (Raji).

A. Houllier, J. Pérignon, L. Thuillier, 1986, International journal of immunopharmacology.

Cytidine deaminase activity of human normal and malignant lymphoid cells.

G. Leverger, A. Houllier, J. Pérignon, 1985, Clinica chimica acta; international journal of clinical chemistry.

Cytidine deaminase deficiency in a child with combined immunodeficiency: more than a coincidence?

A. Fischer, C. Griscelli, F. Arenzana‐Seisdedos, 1986, Advances in experimental medicine and biology.

Consequences of the salvage of purine compounds on the proliferation of rat T-lymphocytes with normal or inhibited purine de novo synthesis.

A. Houllier, J. Pérignon, L. Thuillier, 1984, Biochimica et biophysica acta.

Does the polymorphism 677C-T of the 5,10-methylenetetrahydrofolate reductase gene contribute to homocysteine-related vascular disease?

G. Montalescot, P. Kamoun, B. Chadefaux-Vekemans, 1998, Journal of Inherited Metabolic Disease.

Phenotypic and functional characteristics of human newborns' B lymphocytes.

A. Fischer, M. Forveille, A. Durandy, 1990, Journal of immunology.

Organization of the human liver carnitine palmitoyltransferase 1 gene (CPT1A) and identification of novel mutations in hypoketotic hypoglycaemia

S. Cederbaum, W. Nyhan, J. Girard, 2002, Human Genetics.

New radiochemical method for assay of inorganic pyrophosphatase.

L. Thuillier, P. Cartier, 1971, Analytical biochemistry.

Inability of immunocompetent thymocytes to produce T-cell growth factor under adenosine deaminase deficiency conditions.

F. Garreau, L. Thuillier, P. Cartier, 1981, Cellular immunology.

De novo purine and pyrimidine biosynthesis during thymocyte concanavalin A stimulation.

F. Garreau, L. Thuillier, M. Hamet, 1982, Experimental cell research.

Measurement of inorganic pyrophosphate in biological fluids and bone tissues.

L. Thuillier, P. Cartier, 1974, Analytical biochemistry.

5'-Deoxy-5'-methylthioadenosine inhibition of rat T lymphocyte phosphodiesterase: correlation with inhibition of Con A induced proliferation.

L. Christa, J. Pérignon, L. Thuillier, 1983, Biochemical and biophysical research communications.

Novel CFTR mutations in black cystic fibrosis patients

J. Steffann, I. Sermet, G. Lenoir, 2004, Clinical genetics.

Study of rat lymphocytes by use of peanut agglutinin.

F. Garreau, J. London, L. Thuillier, 1981, Thymus.

Prenatal diagnosis of cystic fibrosis

A. Munnich, N. Gigarel, M. Briard, 1997, Pediatric pulmonology. Supplement.