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Janine Altmüller

Showing results (71-80 of 326) with videos related to

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Human Genetics|September 15, 2014
STIL mutation causes autosomal recessive microcephalic lobar holoprosencephalyNaseebullah Kakar, Jamil Ahmad, Deborah J Morris-Rosendahl, et al.
Clinical Epigenetics|April 29, 2019
Loss of Msh2 and a single-radiation hit induce common, genome-wide, and persistent epigenetic changes in the intestineMaria Herberg, Susann Siebert, Marianne Quaas, et al.
Fungal Genetics and Biology : FG & B|May 18, 2021
Coregulation of gene expression by White collar 1 and phytochrome in Ustilago maydisAnnika Brych, Fabian B Haas, Katharina Parzefall, et al.
Plos One|January 21, 2016
Increased Probability of Co-Occurrence of Two Rare Diseases in Consanguineous Families and Resolution of a Complex Phenotype by Next Generation SequencingDennis Lal, Bernd A Neubauer, Mohammad R Toliat, et al.
Scientific Reports|November 5, 2016
The mutation p.E113K in the Schiff base counterion of rhodopsin is associated with two distinct retinal phenotypes within the same familyCharlotte Reiff, Marta Owczarek-Lipska, Georg Spital, et al.
The Lancet. Neurology|August 2, 2012
Heterozygous de-novo mutations in ATP1A3 in patients with alternating hemiplegia of childhood: a whole-exome sequencing gene-identification studyHendrik Rosewich, Holger Thiele, Andreas Ohlenbusch, et al.
Plos One|November 22, 2013
Comprehensive RNA-Seq expression analysis of sensory ganglia with a focus on ion channels and GPCRs in Trigeminal gangliaStavros Manteniotis, Ramona Lehmann, Caroline Flegel, et al.
Environment International|July 13, 2024
Pathogen dynamics and discovery of novel viruses and enzymes by deep nucleic acid sequencing of wastewaterEmanuel Wyler, Chris Lauber, Artür Manukyan, et al.
Acta Neuropathologica|March 20, 2016
Neuropathological signs of inflammation correlate with mitochondrial DNA deletions in mesial temporal lobe epilepsyElisa Volmering, Pitt Niehusmann, Viktoriya Peeva, et al.
Molecular Cell|November 3, 2018
Exon Junction Complexes Suppress Spurious Splice Sites to Safeguard Transcriptome IntegrityVolker Boehm, Thiago Britto-Borges, Anna-Lena Steckelberg, et al.
Pageof 33

Showing results (71-80 of 326) with videos related to

Sort By:
Pageof 33
Human Genetics|September 15, 2014
STIL mutation causes autosomal recessive microcephalic lobar holoprosencephalyNaseebullah Kakar, Jamil Ahmad, Deborah J Morris-Rosendahl, et al.
Clinical Epigenetics|April 29, 2019
Loss of Msh2 and a single-radiation hit induce common, genome-wide, and persistent epigenetic changes in the intestineMaria Herberg, Susann Siebert, Marianne Quaas, et al.
Fungal Genetics and Biology : FG & B|May 18, 2021
Coregulation of gene expression by White collar 1 and phytochrome in Ustilago maydisAnnika Brych, Fabian B Haas, Katharina Parzefall, et al.
Plos One|January 21, 2016
Increased Probability of Co-Occurrence of Two Rare Diseases in Consanguineous Families and Resolution of a Complex Phenotype by Next Generation SequencingDennis Lal, Bernd A Neubauer, Mohammad R Toliat, et al.
Scientific Reports|November 5, 2016
The mutation p.E113K in the Schiff base counterion of rhodopsin is associated with two distinct retinal phenotypes within the same familyCharlotte Reiff, Marta Owczarek-Lipska, Georg Spital, et al.
The Lancet. Neurology|August 2, 2012
Heterozygous de-novo mutations in ATP1A3 in patients with alternating hemiplegia of childhood: a whole-exome sequencing gene-identification studyHendrik Rosewich, Holger Thiele, Andreas Ohlenbusch, et al.
Plos One|November 22, 2013
Comprehensive RNA-Seq expression analysis of sensory ganglia with a focus on ion channels and GPCRs in Trigeminal gangliaStavros Manteniotis, Ramona Lehmann, Caroline Flegel, et al.
Environment International|July 13, 2024
Pathogen dynamics and discovery of novel viruses and enzymes by deep nucleic acid sequencing of wastewaterEmanuel Wyler, Chris Lauber, Artür Manukyan, et al.
Acta Neuropathologica|March 20, 2016
Neuropathological signs of inflammation correlate with mitochondrial DNA deletions in mesial temporal lobe epilepsyElisa Volmering, Pitt Niehusmann, Viktoriya Peeva, et al.
Molecular Cell|November 3, 2018
Exon Junction Complexes Suppress Spurious Splice Sites to Safeguard Transcriptome IntegrityVolker Boehm, Thiago Britto-Borges, Anna-Lena Steckelberg, et al.
Pageof 33