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C Benelli

Showing results (31-40 of 42) with videos related to

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American Journal of Human Genetics|December 18, 1997
Mutations in PDX1, the human lipoyl-containing component X of the pyruvate dehydrogenase-complex gene on chromosome 11p1, in congenital lactic acidosisB Aral, C Benelli, G Ait-Ghezala, et al.
Pediatric Nephrology (Berlin, Germany)|June 19, 2001
Effects of growth hormone on growth factors after renal transplantationJ P Clot, H Crosnier, G Guest, et al.
The Journal of Clinical Endocrinology and Metabolism|March 1, 1994
Nonparallel changes of growth hormone (GH) and insulin-like growth factor-I, insulin-like growth factor binding protein-3, and GH-binding protein, after craniospinal irradiation and chemotherapyS Nivot, C Benelli, J P Clot, et al.
Pediatric Research|December 1, 1994
Aberrant splicing of exon 6 in the pyruvate dehydrogenase-E1 alpha mRNA linked to a silent mutation in a large family with Leigh's encephalomyelopathyL De Meirleir, W Lissens, C Benelli, et al.
Journal of Inherited Metabolic Disease|March 21, 1998
Pyruvate dehydrogenase complex deficiency and absence of subunit XL De Meirleir, W Lissens, C Benelli, et al.
Pediatric Research|March 1, 1993
E1 pyruvate dehydrogenase deficiency in a child with motor neuropathyG Bonne, C Benelli, L De Meirleir, et al.
Prenatal Diagnosis|December 11, 1999
First prenatal diagnosis of defects in the HsPDX1 gene encoding protein X, an additional lipoyl-containing subunit of the human pyruvate dehydrogenase complexC Rouillac, B Aral, F Fouque, et al.
The Journal of Biological Chemistry|March 30, 2001
New splicing-site mutations in the SURF1 gene in Leigh syndrome patientsM O Pequignot, I Desguerre, R Dey, et al.
Human Mutation|January 1, 1996
Mutation analysis of the pyruvate dehydrogenase E1 alpha gene in eight patients with a pyruvate dehydrogenase complex deficiencyW Lissens, L De Meirleir, S Seneca, et al.
Diabetologia|January 24, 2007
Acute and selective regulation of glyceroneogenesis and cytosolic phosphoenolpyruvate carboxykinase in adipose tissue by thiazolidinediones in type 2 diabetesT Cadoudal, J M Blouin, M Collinet, et al.
Pageof 5

Showing results (31-40 of 42) with videos related to

Sort By:
Pageof 5
American Journal of Human Genetics|December 18, 1997
Mutations in PDX1, the human lipoyl-containing component X of the pyruvate dehydrogenase-complex gene on chromosome 11p1, in congenital lactic acidosisB Aral, C Benelli, G Ait-Ghezala, et al.
Pediatric Nephrology (Berlin, Germany)|June 19, 2001
Effects of growth hormone on growth factors after renal transplantationJ P Clot, H Crosnier, G Guest, et al.
The Journal of Clinical Endocrinology and Metabolism|March 1, 1994
Nonparallel changes of growth hormone (GH) and insulin-like growth factor-I, insulin-like growth factor binding protein-3, and GH-binding protein, after craniospinal irradiation and chemotherapyS Nivot, C Benelli, J P Clot, et al.
Pediatric Research|December 1, 1994
Aberrant splicing of exon 6 in the pyruvate dehydrogenase-E1 alpha mRNA linked to a silent mutation in a large family with Leigh's encephalomyelopathyL De Meirleir, W Lissens, C Benelli, et al.
Journal of Inherited Metabolic Disease|March 21, 1998
Pyruvate dehydrogenase complex deficiency and absence of subunit XL De Meirleir, W Lissens, C Benelli, et al.
Pediatric Research|March 1, 1993
E1 pyruvate dehydrogenase deficiency in a child with motor neuropathyG Bonne, C Benelli, L De Meirleir, et al.
Prenatal Diagnosis|December 11, 1999
First prenatal diagnosis of defects in the HsPDX1 gene encoding protein X, an additional lipoyl-containing subunit of the human pyruvate dehydrogenase complexC Rouillac, B Aral, F Fouque, et al.
The Journal of Biological Chemistry|March 30, 2001
New splicing-site mutations in the SURF1 gene in Leigh syndrome patientsM O Pequignot, I Desguerre, R Dey, et al.
Human Mutation|January 1, 1996
Mutation analysis of the pyruvate dehydrogenase E1 alpha gene in eight patients with a pyruvate dehydrogenase complex deficiencyW Lissens, L De Meirleir, S Seneca, et al.
Diabetologia|January 24, 2007
Acute and selective regulation of glyceroneogenesis and cytosolic phosphoenolpyruvate carboxykinase in adipose tissue by thiazolidinediones in type 2 diabetesT Cadoudal, J M Blouin, M Collinet, et al.
Pageof 5