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J L Perignon

Showing results (1-10 of 26) with videos related to

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Archives Francaises De Pediatrie|October 1, 1980
[Hereditary anomalies of purine metabolism. Current biochemical aspects]J L Perignon, P Cartier
La Nouvelle Presse Medicale|April 22, 1978
[Xanthinuria (author's transl)]P Cartier, J L Perignon
Biochemical and Biophysical Research Communications|June 15, 1983
5'-Deoxy-5'-methylthioadenosine inhibition of rat T lymphocyte phosphodiesterase: correlation with inhibition of Con A induced proliferationL Christa, L Thuillier, J L Perignon
Lancet (London, England)|April 20, 1991
Transient neonatal hypertrypsinaemia as test for delta F508 heterozygosityG Lucotte, J L Perignon, G Lenoir
La Nouvelle Presse Medicale|June 7, 1980
[Hereditary deficiency in adenine phosphoribosyltransferase: a metabolic cause of urinary lithiasis in children (author's transl)]P Cartier, M Hamet, J L Perignon
Birth Defects Original Article Series|January 1, 1983
Hereditary orotic aciduria: a defect of pyrimidine metabolism with cellular immunodeficiencyR Girot, A Durandy, J L Perignon, et al.
Advances in Experimental Medicine and Biology|January 1, 1980
Complete adenine phosphoribosyltransferase (APRT) deficiency in two siblings: report of a new caseP Cartier, M Hamet, A Vincens, et al.
Advances in Experimental Medicine and Biology|January 1, 1980
Complete adenosine deaminase (ADA) deficiency without immunodeficiency, and primary hyperoxaluria, in a 12-year-old boyJ L Perignon, M Hamet, P Cartier, et al.
Biochimica Et Biophysica Acta|February 17, 1984
Salvage of 5'-deoxy-methylthioadenosine into purines and methionine by lymphoid cells and inhibition of cell proliferationL Christa, L Thuillier, A Munier, et al.
Biochemical and Biophysical Research Communications|February 26, 1986
Salvage of 5'-deoxy-5'-methylthioadenosine and L-homocysteine into methionine in cells cultured in a methionine-free medium: a study of "methionine-dependence"L Christa, J Kersual, J Auge, et al.
Pageof 3

Showing results (1-10 of 26) with videos related to

Sort By:
Pageof 3
Archives Francaises De Pediatrie|October 1, 1980
[Hereditary anomalies of purine metabolism. Current biochemical aspects]J L Perignon, P Cartier
La Nouvelle Presse Medicale|April 22, 1978
[Xanthinuria (author's transl)]P Cartier, J L Perignon
Biochemical and Biophysical Research Communications|June 15, 1983
5'-Deoxy-5'-methylthioadenosine inhibition of rat T lymphocyte phosphodiesterase: correlation with inhibition of Con A induced proliferationL Christa, L Thuillier, J L Perignon
Lancet (London, England)|April 20, 1991
Transient neonatal hypertrypsinaemia as test for delta F508 heterozygosityG Lucotte, J L Perignon, G Lenoir
La Nouvelle Presse Medicale|June 7, 1980
[Hereditary deficiency in adenine phosphoribosyltransferase: a metabolic cause of urinary lithiasis in children (author's transl)]P Cartier, M Hamet, J L Perignon
Birth Defects Original Article Series|January 1, 1983
Hereditary orotic aciduria: a defect of pyrimidine metabolism with cellular immunodeficiencyR Girot, A Durandy, J L Perignon, et al.
Advances in Experimental Medicine and Biology|January 1, 1980
Complete adenine phosphoribosyltransferase (APRT) deficiency in two siblings: report of a new caseP Cartier, M Hamet, A Vincens, et al.
Advances in Experimental Medicine and Biology|January 1, 1980
Complete adenosine deaminase (ADA) deficiency without immunodeficiency, and primary hyperoxaluria, in a 12-year-old boyJ L Perignon, M Hamet, P Cartier, et al.
Biochimica Et Biophysica Acta|February 17, 1984
Salvage of 5'-deoxy-methylthioadenosine into purines and methionine by lymphoid cells and inhibition of cell proliferationL Christa, L Thuillier, A Munier, et al.
Biochemical and Biophysical Research Communications|February 26, 1986
Salvage of 5'-deoxy-5'-methylthioadenosine and L-homocysteine into methionine in cells cultured in a methionine-free medium: a study of "methionine-dependence"L Christa, J Kersual, J Auge, et al.
Pageof 3