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Peter Nürnberg

Showing results (181-190 of 517) with videos related to

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Cell & Bioscience|September 24, 2022
Reliable assessment of telomere maintenance mechanisms in neuroblastomaAlina Meeser, Christoph Bartenhagen, Lisa Werr, et al.
Clinical Genetics|February 26, 2022
Phenotypic spectrum of BLM- and RMI1-related Bloom syndromeIpek Ilgin Gönenc, Nursel H Elcioglu, Carolina Martinez Grijalva, et al.
Neuropediatrics|August 31, 2018
Dominant SCN2A Mutation Causes Familial Episodic Ataxia and Impairment of Speech DevelopmentWalid Fazeli, Kerstin Becker, Peter Herkenrath, et al.
Journal of Leukocyte Biology|July 8, 2019
Leukocyte transcriptional signatures dependent on LPS dosage in human endotoxemiaHina N Khan, Desiree Perlee, Lieke Schoenmaker, et al.
Pharmacogenomics|April 1, 2015
Association of NADPH oxidase polymorphisms with anthracycline-induced cardiotoxicity in the RICOVER-60 trial of patients with aggressive CD20(+) B-cell lymphomaAnnegret Reichwagen, Marita Ziepert, Markus Kreuz, 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.
Genome Medicine|June 26, 2020
cfNOMe - A single assay for comprehensive epigenetic analyses of cell-free DNAFlorian Erger, Deborah Nörling, Domenica Borchert, et al.
Investigative Ophthalmology & Visual Science|November 24, 2005
Three novel Pax6 alleles in the mouse leading to the same small-eye phenotype caused by different consequences at target promotersJochen Graw, Jana Löster, Oliver Puk, et al.
American Journal of Human Genetics|June 12, 2004
Mutations in the gene encoding gap junction protein alpha 12 (connexin 46.6) cause Pelizaeus-Merzbacher-like diseaseBirgit Uhlenberg, Markus Schuelke, Franz Rüschendorf, et al.
Plos One|September 17, 2013
RBFOX1 and RBFOX3 mutations in rolandic epilepsyDennis Lal, Eva M Reinthaler, Janine Altmüller, et al.
Pageof 52

Showing results (181-190 of 517) with videos related to

Sort By:
Pageof 52
Cell & Bioscience|September 24, 2022
Reliable assessment of telomere maintenance mechanisms in neuroblastomaAlina Meeser, Christoph Bartenhagen, Lisa Werr, et al.
Clinical Genetics|February 26, 2022
Phenotypic spectrum of BLM- and RMI1-related Bloom syndromeIpek Ilgin Gönenc, Nursel H Elcioglu, Carolina Martinez Grijalva, et al.
Neuropediatrics|August 31, 2018
Dominant SCN2A Mutation Causes Familial Episodic Ataxia and Impairment of Speech DevelopmentWalid Fazeli, Kerstin Becker, Peter Herkenrath, et al.
Journal of Leukocyte Biology|July 8, 2019
Leukocyte transcriptional signatures dependent on LPS dosage in human endotoxemiaHina N Khan, Desiree Perlee, Lieke Schoenmaker, et al.
Pharmacogenomics|April 1, 2015
Association of NADPH oxidase polymorphisms with anthracycline-induced cardiotoxicity in the RICOVER-60 trial of patients with aggressive CD20(+) B-cell lymphomaAnnegret Reichwagen, Marita Ziepert, Markus Kreuz, 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.
Genome Medicine|June 26, 2020
cfNOMe - A single assay for comprehensive epigenetic analyses of cell-free DNAFlorian Erger, Deborah Nörling, Domenica Borchert, et al.
Investigative Ophthalmology & Visual Science|November 24, 2005
Three novel Pax6 alleles in the mouse leading to the same small-eye phenotype caused by different consequences at target promotersJochen Graw, Jana Löster, Oliver Puk, et al.
American Journal of Human Genetics|June 12, 2004
Mutations in the gene encoding gap junction protein alpha 12 (connexin 46.6) cause Pelizaeus-Merzbacher-like diseaseBirgit Uhlenberg, Markus Schuelke, Franz Rüschendorf, et al.
Plos One|September 17, 2013
RBFOX1 and RBFOX3 mutations in rolandic epilepsyDennis Lal, Eva M Reinthaler, Janine Altmüller, et al.
Pageof 52