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C Junien

Showing results (271-280 of 284) with videos related to

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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 14, 1999
[Persistent hyperinsulinemic hypoglycemia in the newborn and infants]P de Lonlay-Debeney, J C Fournet, D Martin, et al.
Nucleic Acids Research|January 1, 1997
Marfan Database (second edition): software and database for the analysis of mutations in the human FBN1 geneG Collod-Béroud, C Béroud, L Adès, et al.
European Journal of Human Genetics : EJHG|August 22, 2000
Autosomal dominant type IIa hypercholesterolemia: evaluation of the respective contributions of LDLR and APOB gene defects as well as a third major group of defectsB Saint-Jore, M Varret, C Dachet, et al.
Journal De La Societe De Biologie|December 7, 2000
[Prevention of renal carcinoma: the nutri-genetic approach]C Junien, J M Dupret, C Gallou, et al.
Placenta|July 10, 2010
Placental BDNF/TrkB signaling system is modulated by fetal growth disturbances in rat and humanS Mayeur, M Silhol, E Moitrot, et al.
The Journal of Clinical Investigation|August 15, 1997
Somatic deletion of the imprinted 11p15 region in sporadic persistent hyperinsulinemic hypoglycemia of infancy is specific of focal adenomatous hyperplasia and endorses partial pancreatectomyP de Lonlay, J C Fournet, J Rahier, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 1, 1982
Human type I procollagen genes are located on different chromosomesC Huerre, C Junien, D Weil, et al.
Nucleic Acids Research|February 21, 1998
LDLR Database (second edition): new additions to the database and the software, and results of the first molecular analysisM Varret, J P Rabés, R Thiart, et al.
Endocrine Reviews|October 26, 2010
Child health, developmental plasticity, and epigenetic programmingZ Hochberg, R Feil, M Constancia, et al.
Nucleic Acids Research|February 21, 1998
Marfan Database (third edition): new mutations and new routines for the softwareG Collod-Béroud, C Béroud, L Ades, et al.
Pageof 29

Showing results (271-280 of 284) with videos related to

Sort By:
Pageof 29
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 14, 1999
[Persistent hyperinsulinemic hypoglycemia in the newborn and infants]P de Lonlay-Debeney, J C Fournet, D Martin, et al.
Nucleic Acids Research|January 1, 1997
Marfan Database (second edition): software and database for the analysis of mutations in the human FBN1 geneG Collod-Béroud, C Béroud, L Adès, et al.
European Journal of Human Genetics : EJHG|August 22, 2000
Autosomal dominant type IIa hypercholesterolemia: evaluation of the respective contributions of LDLR and APOB gene defects as well as a third major group of defectsB Saint-Jore, M Varret, C Dachet, et al.
Journal De La Societe De Biologie|December 7, 2000
[Prevention of renal carcinoma: the nutri-genetic approach]C Junien, J M Dupret, C Gallou, et al.
Placenta|July 10, 2010
Placental BDNF/TrkB signaling system is modulated by fetal growth disturbances in rat and humanS Mayeur, M Silhol, E Moitrot, et al.
The Journal of Clinical Investigation|August 15, 1997
Somatic deletion of the imprinted 11p15 region in sporadic persistent hyperinsulinemic hypoglycemia of infancy is specific of focal adenomatous hyperplasia and endorses partial pancreatectomyP de Lonlay, J C Fournet, J Rahier, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 1, 1982
Human type I procollagen genes are located on different chromosomesC Huerre, C Junien, D Weil, et al.
Nucleic Acids Research|February 21, 1998
LDLR Database (second edition): new additions to the database and the software, and results of the first molecular analysisM Varret, J P Rabés, R Thiart, et al.
Endocrine Reviews|October 26, 2010
Child health, developmental plasticity, and epigenetic programmingZ Hochberg, R Feil, M Constancia, et al.
Nucleic Acids Research|February 21, 1998
Marfan Database (third edition): new mutations and new routines for the softwareG Collod-Béroud, C Béroud, L Ades, et al.
Pageof 29