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Maximilian Radtke

Showing results (1-10 of 18) with videos related to

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RNA Biology|January 18, 2013
U1 snRNP-mediated poly(A) site suppression: beneficial and deleterious for mRNA fateJörg Langemeier, Maximilian Radtke, Jens Bohne
BMC Bioinformatics|September 12, 2024
altAFplotter: a web app for reliable UPD detection in NGS diagnosticsMaximilian Radtke, Johanna Moch, Julia Hentschel, et al.
European Journal of Human Genetics : EJHG|October 25, 2021
Exome first approach to reduce diagnostic costs and time - retrospective analysis of 111 individuals with rare neurodevelopmental disordersJulia Klau, Rami Abou Jamra, Maximilian Radtke, et al.
Genes|January 21, 2023
Approach to Cohort-Wide Re-Analysis of Exome Data in 1000 Individuals with Neurodevelopmental DisordersInsa Halfmeyer, Tobias Bartolomaeus, Bernt Popp, et al.
Human Genetics|July 16, 2024
Automatized detection of uniparental disomies in a large cohortJohanna Moch, Maximilian Radtke, Thomas Liehr, et al.
Epilepsia Open|November 21, 2024
Exome sequencing in Nigerian children with early-onset epilepsy syndromesIbitayo Abigail Ademuwagun, Yagoub Adam, Solomon Oladapo Rotimi, et al.
Frontiers in Genetics|January 8, 2024
Case report: Complete paternal isodisomy on chromosome 18 induces methylation changes in <i>PARD6G-AS1</i> promotor in a case with arthrogryposisJohanna Moch, Maximilian Radtke, Janina Gburek-Augustat, et al.
The EMBO Journal|September 13, 2012
A complex immunodeficiency is based on U1 snRNP-mediated poly(A) site suppressionJörg Langemeier, Eva-Maria Schrom, Alona Rabner, et al.
Transcription|July 15, 2020
RNA polymerase II-binding aptamers in human ACRO1 satellites disrupt transcription <i>in cis</i>Jennifer L Boots, Frederike von Pelchrzim, Adam Weiss, et al.
Bioinformatics (Oxford, England)|April 27, 2023
CNV-ClinViewer: enhancing the clinical interpretation of large copy-number variants onlineMarie Macnee, Eduardo Pérez-Palma, Tobias Brünger, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
RNA Biology|January 18, 2013
U1 snRNP-mediated poly(A) site suppression: beneficial and deleterious for mRNA fateJörg Langemeier, Maximilian Radtke, Jens Bohne
BMC Bioinformatics|September 12, 2024
altAFplotter: a web app for reliable UPD detection in NGS diagnosticsMaximilian Radtke, Johanna Moch, Julia Hentschel, et al.
European Journal of Human Genetics : EJHG|October 25, 2021
Exome first approach to reduce diagnostic costs and time - retrospective analysis of 111 individuals with rare neurodevelopmental disordersJulia Klau, Rami Abou Jamra, Maximilian Radtke, et al.
Genes|January 21, 2023
Approach to Cohort-Wide Re-Analysis of Exome Data in 1000 Individuals with Neurodevelopmental DisordersInsa Halfmeyer, Tobias Bartolomaeus, Bernt Popp, et al.
Human Genetics|July 16, 2024
Automatized detection of uniparental disomies in a large cohortJohanna Moch, Maximilian Radtke, Thomas Liehr, et al.
Epilepsia Open|November 21, 2024
Exome sequencing in Nigerian children with early-onset epilepsy syndromesIbitayo Abigail Ademuwagun, Yagoub Adam, Solomon Oladapo Rotimi, et al.
Frontiers in Genetics|January 8, 2024
Case report: Complete paternal isodisomy on chromosome 18 induces methylation changes in <i>PARD6G-AS1</i> promotor in a case with arthrogryposisJohanna Moch, Maximilian Radtke, Janina Gburek-Augustat, et al.
The EMBO Journal|September 13, 2012
A complex immunodeficiency is based on U1 snRNP-mediated poly(A) site suppressionJörg Langemeier, Eva-Maria Schrom, Alona Rabner, et al.
Transcription|July 15, 2020
RNA polymerase II-binding aptamers in human ACRO1 satellites disrupt transcription <i>in cis</i>Jennifer L Boots, Frederike von Pelchrzim, Adam Weiss, et al.
Bioinformatics (Oxford, England)|April 27, 2023
CNV-ClinViewer: enhancing the clinical interpretation of large copy-number variants onlineMarie Macnee, Eduardo Pérez-Palma, Tobias Brünger, et al.
Pageof 2