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Adam Ameur

Showing results (71-80 of 103) with videos related to

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Acta Oncologica (Stockholm, Sweden)|January 12, 2020
Molecular characterization of a large unselected cohort of metastatic colorectal cancers in relation to primary tumor location, rare metastatic sites and prognosisLuís Nunes, Kristine Aasebø, Lucy Mathot, et al.
Genome Biology|December 2, 2020
Amplification-free long-read sequencing reveals unforeseen CRISPR-Cas9 off-target activityIda Höijer, Josefin Johansson, Sanna Gudmundsson, et al.
Bioinformatics (Oxford, England)|February 19, 2026
Nallo: a Nextflow pipeline for comprehensive human long-read genome analysisFelix Lenner, Anders Jemt, Lucia Peña Pérez, et al.
Communications Biology|May 20, 2024
MDM2 amplification in rod-shaped chromosomes provides clues to early stages of circularized gene amplification in liposarcomaSaskia Sydow, Paul Piccinelli, Shamik Mitra, et al.
Nature Communications|August 24, 2023
Long-read whole-genome analysis of human single cellsJoanna Hård, Jeff E Mold, Jesper Eisfeldt, et al.
Medrxiv : the Preprint Server for Health Sciences|November 28, 2024
Single cell long read whole genome sequencing reveals somatic transposon activity in human brainMichal B Izydorczyk, Ester Kalef-Ezra, Dominic W Horner, et al.
Genome Research|June 15, 2007
Butyrate mediates decrease of histone acetylation centered on transcription start sites and down-regulation of associated genesAlvaro Rada-Iglesias, Stefan Enroth, Adam Ameur, et al.
American Journal of Human Genetics|November 30, 2023
Exonic trinucleotide repeat expansions in ZFHX3 cause spinocerebellar ataxia type 4: A poly-glycine diseaseJoel Wallenius, Efthymia Kafantari, Emma Jhaveri, et al.
Scientific Reports|July 18, 2020
Translating GWAS-identified loci for cardiac rhythm and rate using an in vivo image- and CRISPR/Cas9-based approachBenedikt von der Heyde, Anastasia Emmanouilidou, Eugenia Mazzaferro, et al.
European Journal of Human Genetics : EJHG|June 5, 2023
Gustavson syndrome is caused by an in-frame deletion in RBMX associated with potentially disturbed SH3 domain interactionsJosefin Johansson, Sarah Lidéus, Carina Frykholm, et al.
Pageof 11

Showing results (71-80 of 103) with videos related to

Sort By:
Pageof 11
Acta Oncologica (Stockholm, Sweden)|January 12, 2020
Molecular characterization of a large unselected cohort of metastatic colorectal cancers in relation to primary tumor location, rare metastatic sites and prognosisLuís Nunes, Kristine Aasebø, Lucy Mathot, et al.
Genome Biology|December 2, 2020
Amplification-free long-read sequencing reveals unforeseen CRISPR-Cas9 off-target activityIda Höijer, Josefin Johansson, Sanna Gudmundsson, et al.
Bioinformatics (Oxford, England)|February 19, 2026
Nallo: a Nextflow pipeline for comprehensive human long-read genome analysisFelix Lenner, Anders Jemt, Lucia Peña Pérez, et al.
Communications Biology|May 20, 2024
MDM2 amplification in rod-shaped chromosomes provides clues to early stages of circularized gene amplification in liposarcomaSaskia Sydow, Paul Piccinelli, Shamik Mitra, et al.
Nature Communications|August 24, 2023
Long-read whole-genome analysis of human single cellsJoanna Hård, Jeff E Mold, Jesper Eisfeldt, et al.
Medrxiv : the Preprint Server for Health Sciences|November 28, 2024
Single cell long read whole genome sequencing reveals somatic transposon activity in human brainMichal B Izydorczyk, Ester Kalef-Ezra, Dominic W Horner, et al.
Genome Research|June 15, 2007
Butyrate mediates decrease of histone acetylation centered on transcription start sites and down-regulation of associated genesAlvaro Rada-Iglesias, Stefan Enroth, Adam Ameur, et al.
American Journal of Human Genetics|November 30, 2023
Exonic trinucleotide repeat expansions in ZFHX3 cause spinocerebellar ataxia type 4: A poly-glycine diseaseJoel Wallenius, Efthymia Kafantari, Emma Jhaveri, et al.
Scientific Reports|July 18, 2020
Translating GWAS-identified loci for cardiac rhythm and rate using an in vivo image- and CRISPR/Cas9-based approachBenedikt von der Heyde, Anastasia Emmanouilidou, Eugenia Mazzaferro, et al.
European Journal of Human Genetics : EJHG|June 5, 2023
Gustavson syndrome is caused by an in-frame deletion in RBMX associated with potentially disturbed SH3 domain interactionsJosefin Johansson, Sarah Lidéus, Carina Frykholm, et al.
Pageof 11