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C Besmond

Showing results (31-40 of 41) with videos related to

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Analytical Biochemistry|November 1, 1984
Immunological screening of standard cDNA libraries in pBR322 vectors: detection of human fibrinogen and prothrombin cDNA clonesH Plaisancié, Y Alexandre, G Uzan, et al.
American Journal of Human Genetics|July 27, 1999
Evaluation of parental mitochondrial inheritance in neonates born after intracytoplasmic sperm injectionC Danan, D Sternberg, A Van Steirteghem, et al.
Biochemical and Biophysical Research Communications|November 30, 1984
Cyclic AMP as a transcriptional inhibitor of upper eukaryotic gene transcriptionS Vaulont, A Munnich, J Marie, et al.
American Journal of Hematology|June 15, 1999
Potential of denaturing gradient gel electrophoresis for scanning of beta-thalassemia mutations in IndiaA C Gorakshakar, A R Pawar, A H Nadkarni, et al.
The Journal of Clinical Endocrinology and Metabolism|February 1, 1996
Deletion of Asn281 in the alpha-subunit of the human insulin receptor causes constitutive activation of the receptor and insulin desensitizationC Desbois-Mouthon, C Sert-Langeron, J Magre, et al.
The Journal of Biological Chemistry|December 10, 1983
Molecular cloning of cDNA for rat L-type pyruvate kinase and aldolase BM P Simon, C Besmond, D Cottreau, et al.
Human Genetics|January 1, 1996
A novel mutation in exon 17 of the beta-subunit of rod phosphodiesterase in two RP sisters of a consanguineous familyD Valverde, T Solans, D Grinberg, et al.
Metabolism: Clinical and Experimental|December 1, 1996
Severe resistance to insulin and insulin-like growth factor-I in cells from a patient with leprechaunism as a result of two mutations in the tyrosine kinase domain of the insulin receptorC Desbois-Mouthon, C Danan, S Amselem, et al.
Prenatal Diagnosis|July 1, 1997
Molecular analysis of the insulin receptor gene for prenatal diagnosis of leprechaunism in two familiesC Desbois-Mouthon, E Girodon, N Ghanem, et al.
European Journal of Human Genetics : EJHG|September 14, 1999
Genetic polymorphism of the mannose-binding protein gene in children with sickle cell disease: identification of three new variant alleles and relationship to infectionsM G Neonato, C Y Lu, M Guilloud-Bataille, et al.
Pageof 5

Showing results (31-40 of 41) with videos related to

Sort By:
Pageof 5
Analytical Biochemistry|November 1, 1984
Immunological screening of standard cDNA libraries in pBR322 vectors: detection of human fibrinogen and prothrombin cDNA clonesH Plaisancié, Y Alexandre, G Uzan, et al.
American Journal of Human Genetics|July 27, 1999
Evaluation of parental mitochondrial inheritance in neonates born after intracytoplasmic sperm injectionC Danan, D Sternberg, A Van Steirteghem, et al.
Biochemical and Biophysical Research Communications|November 30, 1984
Cyclic AMP as a transcriptional inhibitor of upper eukaryotic gene transcriptionS Vaulont, A Munnich, J Marie, et al.
American Journal of Hematology|June 15, 1999
Potential of denaturing gradient gel electrophoresis for scanning of beta-thalassemia mutations in IndiaA C Gorakshakar, A R Pawar, A H Nadkarni, et al.
The Journal of Clinical Endocrinology and Metabolism|February 1, 1996
Deletion of Asn281 in the alpha-subunit of the human insulin receptor causes constitutive activation of the receptor and insulin desensitizationC Desbois-Mouthon, C Sert-Langeron, J Magre, et al.
The Journal of Biological Chemistry|December 10, 1983
Molecular cloning of cDNA for rat L-type pyruvate kinase and aldolase BM P Simon, C Besmond, D Cottreau, et al.
Human Genetics|January 1, 1996
A novel mutation in exon 17 of the beta-subunit of rod phosphodiesterase in two RP sisters of a consanguineous familyD Valverde, T Solans, D Grinberg, et al.
Metabolism: Clinical and Experimental|December 1, 1996
Severe resistance to insulin and insulin-like growth factor-I in cells from a patient with leprechaunism as a result of two mutations in the tyrosine kinase domain of the insulin receptorC Desbois-Mouthon, C Danan, S Amselem, et al.
Prenatal Diagnosis|July 1, 1997
Molecular analysis of the insulin receptor gene for prenatal diagnosis of leprechaunism in two familiesC Desbois-Mouthon, E Girodon, N Ghanem, et al.
European Journal of Human Genetics : EJHG|September 14, 1999
Genetic polymorphism of the mannose-binding protein gene in children with sickle cell disease: identification of three new variant alleles and relationship to infectionsM G Neonato, C Y Lu, M Guilloud-Bataille, et al.
Pageof 5