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André Schaller

Showing results (1-10 of 57) with videos related to

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Biochemical and Biophysical Research Communications|June 12, 2012
qPCR-based mitochondrial DNA quantification: influence of template DNA fragmentation on accuracyChristopher B Jackson, Sabina Gallati, André Schaller
Ophthalmic Genetics|March 4, 2020
Longitudinal case study and phenotypic multimodal characterization of McArdle disease-linked retinopathy: insight into pathomechanismsVeronika Vaclavik, Francine Naderi, André Schaller, et al.
Klinische Monatsblatter Fur Augenheilkunde|May 10, 2023
Clinical Heterogeneity in Two Siblings Harbouring a Heterozygous PRPH2 Pathogenic VariantAyse Sanlialp, Pascal Escher, André Schaller, et al.
BMC Microbiology|August 16, 2011
Physiologic cold shock of Moraxella catarrhalis affects the expression of genes involved in the iron acquisition, serum resistance and immune evasionVioleta Spaniol, Rolf Troller, André Schaller, et al.
Molecular Genetics and Metabolism Reports|December 6, 2023
Induced pluripotent stem cell technology as diagnostic tool in patients with suspected ornithine transcarbamylase deficiency lacking genetic confirmationAdhuresa Ramosaj, Palak Singhal, André Schaller, et al.
Annals of Noninvasive Electrocardiology : the Official Journal of the International Society for Holter and Noninvasive Electrocardiology, Inc|December 2, 2017
Late-onset severe long QT syndromeBabken Asatryan, André Schaller, Deborah Bartholdi, et al.
Human Mutation|July 9, 2004
The role of common single-nucleotide polymorphisms on exon 9 and exon 12 skipping in nonmutated CFTR allelesBernhard Steiner, Kaspar Truninger, Javier Sanz, et al.
European Journal of Human Genetics : EJHG|October 7, 2006
Rapid and reliable genotyping of polymorphic loci modifying correct splicing of CFTR pre-mRNA using mass spectrometryAndré Schaller, Thomas von Känel, Benedikt Gehr, et al.
European Journal of Human Genetics : EJHG|August 16, 2012
Identification of SNPs in the cystic fibrosis interactome influencing pulmonary progression in cystic fibrosisFranziska M Gisler, Thomas von Kanel, Richard Kraemer, et al.
European Journal of Human Genetics : EJHG|June 13, 2018
Broad phenotypes in heterozygous NR5A1 46,XY patients with a disorder of sex development: an oligogenic origin?Núria Camats, Mónica Fernández-Cancio, Laura Audí, et al.
Pageof 6

Showing results (1-10 of 57) with videos related to

Sort By:
Pageof 6
Biochemical and Biophysical Research Communications|June 12, 2012
qPCR-based mitochondrial DNA quantification: influence of template DNA fragmentation on accuracyChristopher B Jackson, Sabina Gallati, André Schaller
Ophthalmic Genetics|March 4, 2020
Longitudinal case study and phenotypic multimodal characterization of McArdle disease-linked retinopathy: insight into pathomechanismsVeronika Vaclavik, Francine Naderi, André Schaller, et al.
Klinische Monatsblatter Fur Augenheilkunde|May 10, 2023
Clinical Heterogeneity in Two Siblings Harbouring a Heterozygous PRPH2 Pathogenic VariantAyse Sanlialp, Pascal Escher, André Schaller, et al.
BMC Microbiology|August 16, 2011
Physiologic cold shock of Moraxella catarrhalis affects the expression of genes involved in the iron acquisition, serum resistance and immune evasionVioleta Spaniol, Rolf Troller, André Schaller, et al.
Molecular Genetics and Metabolism Reports|December 6, 2023
Induced pluripotent stem cell technology as diagnostic tool in patients with suspected ornithine transcarbamylase deficiency lacking genetic confirmationAdhuresa Ramosaj, Palak Singhal, André Schaller, et al.
Annals of Noninvasive Electrocardiology : the Official Journal of the International Society for Holter and Noninvasive Electrocardiology, Inc|December 2, 2017
Late-onset severe long QT syndromeBabken Asatryan, André Schaller, Deborah Bartholdi, et al.
Human Mutation|July 9, 2004
The role of common single-nucleotide polymorphisms on exon 9 and exon 12 skipping in nonmutated CFTR allelesBernhard Steiner, Kaspar Truninger, Javier Sanz, et al.
European Journal of Human Genetics : EJHG|October 7, 2006
Rapid and reliable genotyping of polymorphic loci modifying correct splicing of CFTR pre-mRNA using mass spectrometryAndré Schaller, Thomas von Känel, Benedikt Gehr, et al.
European Journal of Human Genetics : EJHG|August 16, 2012
Identification of SNPs in the cystic fibrosis interactome influencing pulmonary progression in cystic fibrosisFranziska M Gisler, Thomas von Kanel, Richard Kraemer, et al.
European Journal of Human Genetics : EJHG|June 13, 2018
Broad phenotypes in heterozygous NR5A1 46,XY patients with a disorder of sex development: an oligogenic origin?Núria Camats, Mónica Fernández-Cancio, Laura Audí, et al.
Pageof 6