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Lindsay M Payer

Showing results (1-10 of 12) with videos related to

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Nature Reviews. Genetics|September 14, 2019
Transposable elements in human genetic diseaseLindsay M Payer, Kathleen H Burns
Mobile DNA|April 29, 2017
Insertion and deletion polymorphisms of the ancient <i>AluS</i> family in the human genomeMaria S Kryatova, Jared P Steranka, Kathleen H Burns, et al.
Nucleic Acids Research|January 10, 2019
SQuIRE reveals locus-specific regulation of interspersed repeat expressionWan R Yang, Daniel Ardeljan, Clarissa N Pacyna, et al.
Genome Biology|July 29, 2020
Polymorphic mobile element insertions contribute to gene expression and alternative splicing in human tissuesXiaolong Cao, Yeting Zhang, Lindsay M Payer, et al.
Genome Research|November 20, 2021
<i>Alu</i> insertion variants alter gene transcript levelsLindsay M Payer, Jared P Steranka, Maria S Kryatova, et al.
Nucleic Acids Research|November 13, 2018
Alu insertion variants alter mRNA splicingLindsay M Payer, Jared P Steranka, Daniel Ardeljan, et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|February 21, 2020
Human transposon insertion profiling by sequencing (TIPseq) to map LINE-1 insertions in single cellsWilson McKerrow, Zuojian Tang, Jared P Steranka, et al.
Nucleic Acids Research|February 19, 2020
TypeTE: a tool to genotype mobile element insertions from whole genome resequencing dataClément Goubert, Jainy Thomas, Lindsay M Payer, et al.
EMBO Reports|November 11, 2022
Retrotransposon insertions associated with risk of neurologic and psychiatric diseasesHyo Won Ahn, Zelia F Worman, Arianna Lechsinska, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 4, 2017
Structural variants caused by <i>Alu</i> insertions are associated with risks for many human diseasesLindsay M Payer, Jared P Steranka, Wan Rou Yang, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Nature Reviews. Genetics|September 14, 2019
Transposable elements in human genetic diseaseLindsay M Payer, Kathleen H Burns
Mobile DNA|April 29, 2017
Insertion and deletion polymorphisms of the ancient <i>AluS</i> family in the human genomeMaria S Kryatova, Jared P Steranka, Kathleen H Burns, et al.
Nucleic Acids Research|January 10, 2019
SQuIRE reveals locus-specific regulation of interspersed repeat expressionWan R Yang, Daniel Ardeljan, Clarissa N Pacyna, et al.
Genome Biology|July 29, 2020
Polymorphic mobile element insertions contribute to gene expression and alternative splicing in human tissuesXiaolong Cao, Yeting Zhang, Lindsay M Payer, et al.
Genome Research|November 20, 2021
<i>Alu</i> insertion variants alter gene transcript levelsLindsay M Payer, Jared P Steranka, Maria S Kryatova, et al.
Nucleic Acids Research|November 13, 2018
Alu insertion variants alter mRNA splicingLindsay M Payer, Jared P Steranka, Daniel Ardeljan, et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|February 21, 2020
Human transposon insertion profiling by sequencing (TIPseq) to map LINE-1 insertions in single cellsWilson McKerrow, Zuojian Tang, Jared P Steranka, et al.
Nucleic Acids Research|February 19, 2020
TypeTE: a tool to genotype mobile element insertions from whole genome resequencing dataClément Goubert, Jainy Thomas, Lindsay M Payer, et al.
EMBO Reports|November 11, 2022
Retrotransposon insertions associated with risk of neurologic and psychiatric diseasesHyo Won Ahn, Zelia F Worman, Arianna Lechsinska, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 4, 2017
Structural variants caused by <i>Alu</i> insertions are associated with risks for many human diseasesLindsay M Payer, Jared P Steranka, Wan Rou Yang, et al.
Pageof 2