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Adam D Ewing

Showing results (1-10 of 47) with videos related to

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Mobile DNA|January 1, 2016
Transposable element detection from whole genome sequence dataAdam D Ewing
Genome Research|May 22, 2010
High-throughput sequencing reveals extensive variation in human-specific L1 content in individual human genomesAdam D Ewing, Haig H Kazazian
Genome Research|October 29, 2010
Whole-genome resequencing allows detection of many rare LINE-1 insertion alleles in humansAdam D Ewing, Haig H Kazazian
Bioinformatics (Oxford, England)|April 28, 2022
Methylartist: tools for visualizing modified bases from nanopore sequence dataSeth W Cheetham, Michaela Kindlova, Adam D Ewing
Human Molecular Genetics|May 23, 2013
Enrichment of processed pseudogene transcripts in L1-ribonucleoprotein particlesPrabhat K Mandal, Adam D Ewing, Dustin C Hancks, et al.
Molecular Genetics and Metabolism Reports|May 9, 2020
Whole genome investigation of an atypical autism case identifies a novel <i>ANOS1</i> mutation with subsequent diagnosis of Kallmann syndromePaul A Dawson, Soohyun Lee, Adam D Ewing, et al.
Genome Research|July 29, 2009
Exon-trapping mediated by the human retrotransposon SVADustin C Hancks, Adam D Ewing, Jesse E Chen, et al.
Brain Pathology (Zurich, Switzerland)|August 31, 2021
An early proinflammatory transcriptional response to tau pathology is age-specific and foreshadows reduced tau burdenJay Rasmussen, Adam D Ewing, Liviu-Gabriel Bodea, et al.
BMJ Supportive & Palliative Care|December 18, 2025
Genomic variation in symptom expression in castrate-resistant prostate cancerJanet Hardy, Ristan Greer, Karyn Foster, et al.
Human Mutation|November 19, 2011
Pathogenic orphan transduction created by a nonreference LINE-1 retrotransposonSzilvia Solyom, Adam D Ewing, Dustin C Hancks, et al.
Pageof 5

Showing results (1-10 of 47) with videos related to

Sort By:
Pageof 5
Mobile DNA|January 1, 2016
Transposable element detection from whole genome sequence dataAdam D Ewing
Genome Research|May 22, 2010
High-throughput sequencing reveals extensive variation in human-specific L1 content in individual human genomesAdam D Ewing, Haig H Kazazian
Genome Research|October 29, 2010
Whole-genome resequencing allows detection of many rare LINE-1 insertion alleles in humansAdam D Ewing, Haig H Kazazian
Bioinformatics (Oxford, England)|April 28, 2022
Methylartist: tools for visualizing modified bases from nanopore sequence dataSeth W Cheetham, Michaela Kindlova, Adam D Ewing
Human Molecular Genetics|May 23, 2013
Enrichment of processed pseudogene transcripts in L1-ribonucleoprotein particlesPrabhat K Mandal, Adam D Ewing, Dustin C Hancks, et al.
Molecular Genetics and Metabolism Reports|May 9, 2020
Whole genome investigation of an atypical autism case identifies a novel <i>ANOS1</i> mutation with subsequent diagnosis of Kallmann syndromePaul A Dawson, Soohyun Lee, Adam D Ewing, et al.
Genome Research|July 29, 2009
Exon-trapping mediated by the human retrotransposon SVADustin C Hancks, Adam D Ewing, Jesse E Chen, et al.
Brain Pathology (Zurich, Switzerland)|August 31, 2021
An early proinflammatory transcriptional response to tau pathology is age-specific and foreshadows reduced tau burdenJay Rasmussen, Adam D Ewing, Liviu-Gabriel Bodea, et al.
BMJ Supportive & Palliative Care|December 18, 2025
Genomic variation in symptom expression in castrate-resistant prostate cancerJanet Hardy, Ristan Greer, Karyn Foster, et al.
Human Mutation|November 19, 2011
Pathogenic orphan transduction created by a nonreference LINE-1 retrotransposonSzilvia Solyom, Adam D Ewing, Dustin C Hancks, et al.
Pageof 5