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Mobile DNA
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January 1, 2016
Transposable element detection from whole genome sequence data
Adam D Ewing
Genome Research
|
May 22, 2010
High-throughput sequencing reveals extensive variation in human-specific L1 content in individual human genomes
Adam D Ewing, Haig H Kazazian
Genome Research
|
October 29, 2010
Whole-genome resequencing allows detection of many rare LINE-1 insertion alleles in humans
Adam D Ewing, Haig H Kazazian
Bioinformatics (Oxford, England)
|
April 28, 2022
Methylartist: tools for visualizing modified bases from nanopore sequence data
Seth W Cheetham, Michaela Kindlova, Adam D Ewing
Human Molecular Genetics
|
May 23, 2013
Enrichment of processed pseudogene transcripts in L1-ribonucleoprotein particles
Prabhat 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 syndrome
Paul A Dawson, Soohyun Lee, Adam D Ewing, et al.
Genome Research
|
July 29, 2009
Exon-trapping mediated by the human retrotransposon SVA
Dustin 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 burden
Jay 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 cancer
Janet Hardy, Ristan Greer, Karyn Foster, et al.
Human Mutation
|
November 19, 2011
Pathogenic orphan transduction created by a nonreference LINE-1 retrotransposon
Szilvia Solyom, Adam D Ewing, Dustin C Hancks, et al.
Page
of 5
Search research articles
Search
Showing results (1-10 of 47) with videos related to
Sort By:
Page
of 5
Mobile DNA
|
January 1, 2016
Transposable element detection from whole genome sequence data
Adam D Ewing
Genome Research
|
May 22, 2010
High-throughput sequencing reveals extensive variation in human-specific L1 content in individual human genomes
Adam D Ewing, Haig H Kazazian
Genome Research
|
October 29, 2010
Whole-genome resequencing allows detection of many rare LINE-1 insertion alleles in humans
Adam D Ewing, Haig H Kazazian
Bioinformatics (Oxford, England)
|
April 28, 2022
Methylartist: tools for visualizing modified bases from nanopore sequence data
Seth W Cheetham, Michaela Kindlova, Adam D Ewing
Human Molecular Genetics
|
May 23, 2013
Enrichment of processed pseudogene transcripts in L1-ribonucleoprotein particles
Prabhat 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 syndrome
Paul A Dawson, Soohyun Lee, Adam D Ewing, et al.
Genome Research
|
July 29, 2009
Exon-trapping mediated by the human retrotransposon SVA
Dustin 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 burden
Jay 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 cancer
Janet Hardy, Ristan Greer, Karyn Foster, et al.
Human Mutation
|
November 19, 2011
Pathogenic orphan transduction created by a nonreference LINE-1 retrotransposon
Szilvia Solyom, Adam D Ewing, Dustin C Hancks, et al.
Page
of 5