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Simone Schröder

Showing results (1-10 of 13) with videos related to

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Electrophoresis|May 11, 2011
Quantitative gel electrophoresis: new records in precision by elaborated staining and detection protocolsXi Deng, Simone Schröder, Sabine Redweik, et al.
Journal of Pharmaceutical and Biomedical Analysis|June 9, 2009
Improving precision in gel electrophoresis by stepwisely decreasing variance componentsSimone Schröder, Asita Brandmüller, Xi Deng, et al.
Journal of Proteome Research|January 29, 2008
Quantitative gel electrophoresis: sources of variationSimone Schröder, Hui Zhang, Edward S Yeung, et al.
American Journal of Medical Genetics. Part A|September 12, 2020
Evidence of pathogenicity for the leaky splice variant c.1066-6T>G in ATMSimone Schröder, Britta Wieland, Andreas Ohlenbusch, et al.
Electrophoresis|December 16, 2011
The challenge to quantify proteins with charge trains due to isoforms or conformersXi Deng, Thomas Hahne, Simone Schröder, et al.
Journal of Medical Genetics|August 19, 2018
Homozygosity for the c.428delG variant in <i>KIAA0586</i> in a healthy individual: implications for molecular testing in patients with Joubert syndromeSilke Pauli, Janine Altmüller, Simone Schröder, et al.
Neurobiology of Disease|July 13, 2020
Comparative analysis of alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism ATP1A3 mutations reveals functional deficits, which do not correlate with disease severityElinor Lazarov, Merle Hillebrand, Simone Schröder, et al.
Orphanet Journal of Rare Diseases|May 2, 2023
The genetic spectrum of congenital ocular motor apraxia type Cogan: an observational study, continuedSimone Schröder, Gökhan Yigit, Yun Li, et al.
Orphanet Journal of Rare Diseases|July 31, 2016
Nosological delineation of congenital ocular motor apraxia type Cogan: an observational studySarah Wente, Simone Schröder, Johannes Buckard, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 7, 2020
Heterozygous truncating variants in SUFU cause congenital ocular motor apraxiaSimone Schröder, Yun Li, Gökhan Yigit, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Electrophoresis|May 11, 2011
Quantitative gel electrophoresis: new records in precision by elaborated staining and detection protocolsXi Deng, Simone Schröder, Sabine Redweik, et al.
Journal of Pharmaceutical and Biomedical Analysis|June 9, 2009
Improving precision in gel electrophoresis by stepwisely decreasing variance componentsSimone Schröder, Asita Brandmüller, Xi Deng, et al.
Journal of Proteome Research|January 29, 2008
Quantitative gel electrophoresis: sources of variationSimone Schröder, Hui Zhang, Edward S Yeung, et al.
American Journal of Medical Genetics. Part A|September 12, 2020
Evidence of pathogenicity for the leaky splice variant c.1066-6T>G in ATMSimone Schröder, Britta Wieland, Andreas Ohlenbusch, et al.
Electrophoresis|December 16, 2011
The challenge to quantify proteins with charge trains due to isoforms or conformersXi Deng, Thomas Hahne, Simone Schröder, et al.
Journal of Medical Genetics|August 19, 2018
Homozygosity for the c.428delG variant in <i>KIAA0586</i> in a healthy individual: implications for molecular testing in patients with Joubert syndromeSilke Pauli, Janine Altmüller, Simone Schröder, et al.
Neurobiology of Disease|July 13, 2020
Comparative analysis of alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism ATP1A3 mutations reveals functional deficits, which do not correlate with disease severityElinor Lazarov, Merle Hillebrand, Simone Schröder, et al.
Orphanet Journal of Rare Diseases|May 2, 2023
The genetic spectrum of congenital ocular motor apraxia type Cogan: an observational study, continuedSimone Schröder, Gökhan Yigit, Yun Li, et al.
Orphanet Journal of Rare Diseases|July 31, 2016
Nosological delineation of congenital ocular motor apraxia type Cogan: an observational studySarah Wente, Simone Schröder, Johannes Buckard, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 7, 2020
Heterozygous truncating variants in SUFU cause congenital ocular motor apraxiaSimone Schröder, Yun Li, Gökhan Yigit, et al.
Pageof 2