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M Schloesser

Showing results (1-10 of 21) with videos related to

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Molecular Biology & Medicine|August 1, 1990
Direct gene diagnosis of cystic fibrosis by allele-specific polymerase chain reactionsM Wagner, M Schloesser, J Reiss
Nucleic Acids Research|November 25, 1988
Cloning, molecular characterization and chromosome localization of the inorganic pyrophosphatase (PPA) gene from S. cerevisiaeL F Kolakowski, M Schloesser, B S Cooperman
Journal of Medical Genetics|October 1, 1991
A cystic fibrosis patient homozygous for the nonsense mutation R553XJ Bal, M Stuhrmann, M Schloesser, et al.
Journal of Interferon & Cytokine Research : the Official Journal of the International Society for Interferon and Cytokine Research|January 19, 2002
Effects of antithrombin III on tumor necrosis factor-alpha and interleukin-1beta synthesis in vascular smooth muscle cellsG Totzke, W Schobersberger, M Schloesser, et al.
Human Genetics|July 1, 1991
Detection of human spermatid-specific transcripts in peripheral blood lymphocytes of males and femalesR Slomski, M Schloesser, H Chlebowska, et al.
Nucleic Acids Research|February 25, 1990
The effect of replication errors on the mismatch analysis of PCR-amplified DNAJ Reiss, M Krawczak, M Schloesser, et al.
Journal of Medical Genetics|December 1, 1991
A cystic fibrosis patient with the nonsense mutation G542X and the splice site mutation 1717-1M Schloesser, S Arleth, U Lenz, et al.
Archives of Gynecology and Obstetrics|December 29, 2000
Homozygous factor V Leiden mutation in a woman with multiple adverse pregnancy outcomesH U Pauer, J Neesen, M Schloesser, et al.
Human Genetics|June 1, 1996
A novel 5'-upstream mutation in the factor XII gene is associated with a TaqI restriction site in an Alu repeat in factor XII-deficient patientsS Hofferbert, J Müller, H Köstering, et al.
Human Molecular Genetics|July 1, 1995
The novel acceptor splice site mutation 11396(G-->A) in the factor XII gene causes a truncated transcript in cross-reacting material negative patientsM Schloesser, S Hofferbert, U Bartz, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
Molecular Biology & Medicine|August 1, 1990
Direct gene diagnosis of cystic fibrosis by allele-specific polymerase chain reactionsM Wagner, M Schloesser, J Reiss
Nucleic Acids Research|November 25, 1988
Cloning, molecular characterization and chromosome localization of the inorganic pyrophosphatase (PPA) gene from S. cerevisiaeL F Kolakowski, M Schloesser, B S Cooperman
Journal of Medical Genetics|October 1, 1991
A cystic fibrosis patient homozygous for the nonsense mutation R553XJ Bal, M Stuhrmann, M Schloesser, et al.
Journal of Interferon & Cytokine Research : the Official Journal of the International Society for Interferon and Cytokine Research|January 19, 2002
Effects of antithrombin III on tumor necrosis factor-alpha and interleukin-1beta synthesis in vascular smooth muscle cellsG Totzke, W Schobersberger, M Schloesser, et al.
Human Genetics|July 1, 1991
Detection of human spermatid-specific transcripts in peripheral blood lymphocytes of males and femalesR Slomski, M Schloesser, H Chlebowska, et al.
Nucleic Acids Research|February 25, 1990
The effect of replication errors on the mismatch analysis of PCR-amplified DNAJ Reiss, M Krawczak, M Schloesser, et al.
Journal of Medical Genetics|December 1, 1991
A cystic fibrosis patient with the nonsense mutation G542X and the splice site mutation 1717-1M Schloesser, S Arleth, U Lenz, et al.
Archives of Gynecology and Obstetrics|December 29, 2000
Homozygous factor V Leiden mutation in a woman with multiple adverse pregnancy outcomesH U Pauer, J Neesen, M Schloesser, et al.
Human Genetics|June 1, 1996
A novel 5'-upstream mutation in the factor XII gene is associated with a TaqI restriction site in an Alu repeat in factor XII-deficient patientsS Hofferbert, J Müller, H Köstering, et al.
Human Molecular Genetics|July 1, 1995
The novel acceptor splice site mutation 11396(G-->A) in the factor XII gene causes a truncated transcript in cross-reacting material negative patientsM Schloesser, S Hofferbert, U Bartz, et al.
Pageof 3