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C Besmond

Showing results (21-30 of 41) with videos related to

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Biochemical and Biophysical Research Communications|April 30, 1984
Analysis of fibrinogen genes in patients with congenital afibrinogenemiaG Uzan, G Courtois, C Besmond, et al.
Human Genetics|August 1, 1997
Polymorphism in exon 10 of the human coagulation factor V gene in a population at risk for sickle cell diseaseD Helley, C Besmond, R Ducrocq, et al.
The Journal of Biological Chemistry|February 10, 1984
Dietary control of aldolase B and L-type pyruvate kinase mRNAs in rat. Study of translational activity and hybridization with cloned cDNA probesA Weber, J Marie, D Cottreau, et al.
Biochemical and Biophysical Research Communications|December 16, 1983
Nucleotide sequence of a cDNA clone for human aldolase BC Besmond, J C Dreyfus, C Gregori, et al.
Hemoglobin|February 24, 2001
A simple approach to the characterization of three common Indian beta-thalassemia mutations by artificially created restriction sitesA R Pawar, C Y Lu, C Besmond, et al.
Diabetes & Metabolism|April 2, 2005
Polymorphisms of the receptor of advanced glycation endproducts (RAGE) and the development of nephropathy in type 1 diabetic patientsG Prevost, I Fajardy, C Besmond, et al.
Biochemical and Biophysical Research Communications|February 29, 1984
Molecular cloning and sequence analysis of cDNA for human transferrinG Uzan, M Frain, I Park, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|September 12, 2019
RMND1 mutations in two siblings: Severe renal hypoplasia but different levels of extrarenal abnormality severity: The ethics of decision makingE Broenen, B Ranchin, C Besmond, et al.
Annals of Human Genetics|July 1, 1985
The structural gene for aldolase B (ALDB) maps to 9q13----32I Henry, P Gallano, C Besmond, et al.
The Journal of Clinical Endocrinology and Metabolism|January 1, 1995
Lipoatrophic diabetes: genetic exclusion of the insulin receptor geneC Desbois-Mouthon, J Magré, S Amselem, et al.
Pageof 5

Showing results (21-30 of 41) with videos related to

Sort By:
Pageof 5
Biochemical and Biophysical Research Communications|April 30, 1984
Analysis of fibrinogen genes in patients with congenital afibrinogenemiaG Uzan, G Courtois, C Besmond, et al.
Human Genetics|August 1, 1997
Polymorphism in exon 10 of the human coagulation factor V gene in a population at risk for sickle cell diseaseD Helley, C Besmond, R Ducrocq, et al.
The Journal of Biological Chemistry|February 10, 1984
Dietary control of aldolase B and L-type pyruvate kinase mRNAs in rat. Study of translational activity and hybridization with cloned cDNA probesA Weber, J Marie, D Cottreau, et al.
Biochemical and Biophysical Research Communications|December 16, 1983
Nucleotide sequence of a cDNA clone for human aldolase BC Besmond, J C Dreyfus, C Gregori, et al.
Hemoglobin|February 24, 2001
A simple approach to the characterization of three common Indian beta-thalassemia mutations by artificially created restriction sitesA R Pawar, C Y Lu, C Besmond, et al.
Diabetes & Metabolism|April 2, 2005
Polymorphisms of the receptor of advanced glycation endproducts (RAGE) and the development of nephropathy in type 1 diabetic patientsG Prevost, I Fajardy, C Besmond, et al.
Biochemical and Biophysical Research Communications|February 29, 1984
Molecular cloning and sequence analysis of cDNA for human transferrinG Uzan, M Frain, I Park, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|September 12, 2019
RMND1 mutations in two siblings: Severe renal hypoplasia but different levels of extrarenal abnormality severity: The ethics of decision makingE Broenen, B Ranchin, C Besmond, et al.
Annals of Human Genetics|July 1, 1985
The structural gene for aldolase B (ALDB) maps to 9q13----32I Henry, P Gallano, C Besmond, et al.
The Journal of Clinical Endocrinology and Metabolism|January 1, 1995
Lipoatrophic diabetes: genetic exclusion of the insulin receptor geneC Desbois-Mouthon, J Magré, S Amselem, et al.
Pageof 5