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C Lenzner

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

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Clinical and Experimental Immunology|March 20, 2004
Antibodies to TSH-receptor in thyroid autoimmune disease interact with monoclonal antibodies whose epitopes are broadly distributed on the receptorW B Minich, C Lenzner, N G Morgenthaler
DNA Sequence : the Journal of DNA Sequencing and Mapping|January 1, 1997
Complete genomic sequence of the human PK-L/R-gene includes four intragenic polymorphisms defining different haplotype backgrounds of normal and mutant PK-genesC Lenzner, P Nürnberg, G Jacobasch, et al.
Clinical Endocrinology|January 1, 1996
A novel mutation in the coding region for neurophysin-II is associated with autosomal dominant neurohypophyseal diabetes insipidusF Rauch, C Lenzner, P Nürnberg, et al.
Human Molecular Genetics|March 1, 1994
Trinucleotide repeat polymorphism at the PKLR locusC Lenzner, G Jacobasch, A Reis, et al.
Blood|March 1, 1997
Molecular analysis of 29 pyruvate kinase-deficient patients from central Europe with hereditary hemolytic anemiaC Lenzner, P Nürnberg, G Jacobasch, et al.
European Journal of Biochemistry|November 3, 1998
Structure of the promoter and complete sequence of the gene coding for the rabbit translationally controlled tumor protein (TCTP) P23H Thiele, M Berger, C Lenzner, et al.
Diabetes|June 26, 2001
Hepatocyte nuclear factor-4alpha involved in type 1 maturity-onset diabetes of the young is a novel target of AMP-activated protein kinaseI Leclerc, C Lenzner, L Gourdon, et al.
Nucleic Acids Research|November 1, 2000
Cre-mediated germline mosaicism: a method allowing rapid generation of several alleles of a target geneM Holzenberger, C Lenzner, P Leneuve, et al.
Blood|May 15, 1994
Mutations in the pyruvate kinase L gene in patients with hereditary hemolytic anemiaC Lenzner, P Nürnberg, B J Thiele, et al.
Electrophoresis|February 1, 1991
Monitoring genomic alterations with a panel of oligonucleotide probes specific for various simple repeat motifsP Nürnberg, I Barth, E Fuhrmann, et al.
Pageof 1

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

Sort By:
Pageof 1
Clinical and Experimental Immunology|March 20, 2004
Antibodies to TSH-receptor in thyroid autoimmune disease interact with monoclonal antibodies whose epitopes are broadly distributed on the receptorW B Minich, C Lenzner, N G Morgenthaler
DNA Sequence : the Journal of DNA Sequencing and Mapping|January 1, 1997
Complete genomic sequence of the human PK-L/R-gene includes four intragenic polymorphisms defining different haplotype backgrounds of normal and mutant PK-genesC Lenzner, P Nürnberg, G Jacobasch, et al.
Clinical Endocrinology|January 1, 1996
A novel mutation in the coding region for neurophysin-II is associated with autosomal dominant neurohypophyseal diabetes insipidusF Rauch, C Lenzner, P Nürnberg, et al.
Human Molecular Genetics|March 1, 1994
Trinucleotide repeat polymorphism at the PKLR locusC Lenzner, G Jacobasch, A Reis, et al.
Blood|March 1, 1997
Molecular analysis of 29 pyruvate kinase-deficient patients from central Europe with hereditary hemolytic anemiaC Lenzner, P Nürnberg, G Jacobasch, et al.
European Journal of Biochemistry|November 3, 1998
Structure of the promoter and complete sequence of the gene coding for the rabbit translationally controlled tumor protein (TCTP) P23H Thiele, M Berger, C Lenzner, et al.
Diabetes|June 26, 2001
Hepatocyte nuclear factor-4alpha involved in type 1 maturity-onset diabetes of the young is a novel target of AMP-activated protein kinaseI Leclerc, C Lenzner, L Gourdon, et al.
Nucleic Acids Research|November 1, 2000
Cre-mediated germline mosaicism: a method allowing rapid generation of several alleles of a target geneM Holzenberger, C Lenzner, P Leneuve, et al.
Blood|May 15, 1994
Mutations in the pyruvate kinase L gene in patients with hereditary hemolytic anemiaC Lenzner, P Nürnberg, B J Thiele, et al.
Electrophoresis|February 1, 1991
Monitoring genomic alterations with a panel of oligonucleotide probes specific for various simple repeat motifsP Nürnberg, I Barth, E Fuhrmann, et al.
Pageof 1