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Sebastian Lunke

Showing results (51-60 of 117) with videos related to

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Genome Research|September 6, 2011
Genome-wide analysis distinguishes hyperglycemia regulated epigenetic signatures of primary vascular cellsLuciano Pirola, Aneta Balcerczyk, Richard W Tothill, et al.
Epigenomics|October 4, 2024
Epigenomic newborn screening for conditions with intellectual disability and autistic features in Australian newbornsMohammed Alshawsh, Melissa Wake, Jozef Gecz, et al.
Seminars in Pediatric Neurology|July 3, 2018
Genetic, Radiologic, and Clinical Variability in Brown-Vialetto-van Laere SyndromeIan R Woodcock, Manoj P Menezes, Lee Coleman, et al.
Genome Research|April 16, 2014
Vascular histone deacetylation by pharmacological HDAC inhibitionHaloom Rafehi, Aneta Balcerczyk, Sebastian Lunke, et al.
The Australian & New Zealand Journal of Obstetrics & Gynaecology|March 24, 2025
The PreGen Research Program: Implementing Prenatal Genomic Testing in Australia-A CommentarySarah Long, Deborah Schofield, Josh Kraindler, et al.
Genome Medicine|July 29, 2015
Cpipe: a shared variant detection pipeline designed for diagnostic settingsSimon P Sadedin, Harriet Dashnow, Paul A James, et al.
European Journal of Human Genetics : EJHG|November 10, 2020
Correction: Exome sequencing in infants with congenital hearing impairment: a population-based cohort studyLilian Downie, Jane Halliday, Rachel Burt, et al.
Human Mutation|September 9, 2020
Rapid exome sequencing and adjunct RNA studies confirm the pathogenicity of a novel homozygous ASNS splicing variant in a critically ill neonateLauren S Akesson, Adam Bournazos, Andrew Fennell, et al.
European Journal of Human Genetics : EJHG|December 13, 2019
Exome sequencing in infants with congenital hearing impairment: a population-based cohort studyLilian Downie, Jane Halliday, Rachel Burt, et al.
NPJ Genomic Medicine|November 8, 2024
Benchmarking nanopore sequencing and rapid genomics feasibility: validation at a quaternary hospital in New ZealandDenis M Nyaga, Peter Tsai, Clare Gebbie, et al.
Pageof 12

Showing results (51-60 of 117) with videos related to

Sort By:
Pageof 12
Genome Research|September 6, 2011
Genome-wide analysis distinguishes hyperglycemia regulated epigenetic signatures of primary vascular cellsLuciano Pirola, Aneta Balcerczyk, Richard W Tothill, et al.
Epigenomics|October 4, 2024
Epigenomic newborn screening for conditions with intellectual disability and autistic features in Australian newbornsMohammed Alshawsh, Melissa Wake, Jozef Gecz, et al.
Seminars in Pediatric Neurology|July 3, 2018
Genetic, Radiologic, and Clinical Variability in Brown-Vialetto-van Laere SyndromeIan R Woodcock, Manoj P Menezes, Lee Coleman, et al.
Genome Research|April 16, 2014
Vascular histone deacetylation by pharmacological HDAC inhibitionHaloom Rafehi, Aneta Balcerczyk, Sebastian Lunke, et al.
The Australian & New Zealand Journal of Obstetrics & Gynaecology|March 24, 2025
The PreGen Research Program: Implementing Prenatal Genomic Testing in Australia-A CommentarySarah Long, Deborah Schofield, Josh Kraindler, et al.
Genome Medicine|July 29, 2015
Cpipe: a shared variant detection pipeline designed for diagnostic settingsSimon P Sadedin, Harriet Dashnow, Paul A James, et al.
European Journal of Human Genetics : EJHG|November 10, 2020
Correction: Exome sequencing in infants with congenital hearing impairment: a population-based cohort studyLilian Downie, Jane Halliday, Rachel Burt, et al.
Human Mutation|September 9, 2020
Rapid exome sequencing and adjunct RNA studies confirm the pathogenicity of a novel homozygous ASNS splicing variant in a critically ill neonateLauren S Akesson, Adam Bournazos, Andrew Fennell, et al.
European Journal of Human Genetics : EJHG|December 13, 2019
Exome sequencing in infants with congenital hearing impairment: a population-based cohort studyLilian Downie, Jane Halliday, Rachel Burt, et al.
NPJ Genomic Medicine|November 8, 2024
Benchmarking nanopore sequencing and rapid genomics feasibility: validation at a quaternary hospital in New ZealandDenis M Nyaga, Peter Tsai, Clare Gebbie, et al.
Pageof 12