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Peter Nürnberg

Showing results (11-20 of 517) with videos related to

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Cells|February 25, 2023
Congenital Microcephaly: A Debate on Diagnostic Challenges and Etiological Paradigm of the Shift from Isolated/Non-Syndromic to Syndromic MicrocephalyMaria Asif, Uzma Abdullah, Peter Nürnberg, et al.
Human Molecular Genetics|July 16, 2004
Gene-Ontology analysis reveals association of tissue-specific 5' CpG-island genes with development and embryogenesisPeter N Robinson, Ulrike Böhme, Rodrigo Lopez, et al.
Journal of Bioinformatics and Computational Biology|October 10, 2015
CoNCoS: copy number estimation in cancer with controlled supportAli T Abdallah, Matthias Fischer, Peter Nürnberg, et al.
Nucleic Acids Research|May 23, 2019
Simple ClinVar: an interactive web server to explore and retrieve gene and disease variants aggregated in ClinVar databaseEduardo Pérez-Palma, Marie Gramm, Peter Nürnberg, et al.
Electrophoresis|December 7, 2005
New universal primers facilitate PyrosequencingAtakan Aydin, Mohammad R Toliat, Sylvia Bähring, et al.
Journal of Molecular Medicine (Berlin, Germany)|February 23, 2010
Insights into lysosomal cobalamin trafficking: lessons learned from cblF diseaseSusann Gailus, Wolfgang Höhne, Bruno Gasnier, et al.
Cold Spring Harbor Molecular Case Studies|December 21, 2017
Late diagnosis of a truncating <i>WISP3</i> mutation entails a severe phenotype of progressive pseudorheumatoid dysplasiaSalem Alawbathani, Amit Kawalia, Mert Karakaya, et al.
Journal of Biomolecular Structure & Dynamics|June 19, 2012
Apoptotic cleavage of DNA in human lymphocyte chromatin shows high sequence specificityThomas Bettecken, Zakharia M Frenkel, Janine Altmüller, et al.
Genomics|February 4, 2006
Expression profiling of uniparental mouse embryos is inefficient in identifying novel imprinted genesNico Ruf, Ulrich Dünzinger, Anja Brinckmann, et al.
Molecular and Cellular Probes|July 18, 2015
Exome sequencing identifies a novel heterozygous TGFB3 mutation in a disorder overlapping with Marfan and Loeys-Dietz syndromeAlma Kuechler, Janine Altmüller, Peter Nürnberg, et al.
Pageof 52

Showing results (11-20 of 517) with videos related to

Sort By:
Pageof 52
Cells|February 25, 2023
Congenital Microcephaly: A Debate on Diagnostic Challenges and Etiological Paradigm of the Shift from Isolated/Non-Syndromic to Syndromic MicrocephalyMaria Asif, Uzma Abdullah, Peter Nürnberg, et al.
Human Molecular Genetics|July 16, 2004
Gene-Ontology analysis reveals association of tissue-specific 5' CpG-island genes with development and embryogenesisPeter N Robinson, Ulrike Böhme, Rodrigo Lopez, et al.
Journal of Bioinformatics and Computational Biology|October 10, 2015
CoNCoS: copy number estimation in cancer with controlled supportAli T Abdallah, Matthias Fischer, Peter Nürnberg, et al.
Nucleic Acids Research|May 23, 2019
Simple ClinVar: an interactive web server to explore and retrieve gene and disease variants aggregated in ClinVar databaseEduardo Pérez-Palma, Marie Gramm, Peter Nürnberg, et al.
Electrophoresis|December 7, 2005
New universal primers facilitate PyrosequencingAtakan Aydin, Mohammad R Toliat, Sylvia Bähring, et al.
Journal of Molecular Medicine (Berlin, Germany)|February 23, 2010
Insights into lysosomal cobalamin trafficking: lessons learned from cblF diseaseSusann Gailus, Wolfgang Höhne, Bruno Gasnier, et al.
Cold Spring Harbor Molecular Case Studies|December 21, 2017
Late diagnosis of a truncating <i>WISP3</i> mutation entails a severe phenotype of progressive pseudorheumatoid dysplasiaSalem Alawbathani, Amit Kawalia, Mert Karakaya, et al.
Journal of Biomolecular Structure & Dynamics|June 19, 2012
Apoptotic cleavage of DNA in human lymphocyte chromatin shows high sequence specificityThomas Bettecken, Zakharia M Frenkel, Janine Altmüller, et al.
Genomics|February 4, 2006
Expression profiling of uniparental mouse embryos is inefficient in identifying novel imprinted genesNico Ruf, Ulrich Dünzinger, Anja Brinckmann, et al.
Molecular and Cellular Probes|July 18, 2015
Exome sequencing identifies a novel heterozygous TGFB3 mutation in a disorder overlapping with Marfan and Loeys-Dietz syndromeAlma Kuechler, Janine Altmüller, Peter Nürnberg, et al.
Pageof 52