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Adam Ameur

Showing results (61-70 of 103) with videos related to

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Life Science Alliance|May 22, 2024
A multiomic characterization of the leukemia cell line REH using short- and long-read sequencingMariya Lysenkova Wiklander, Gustav Arvidsson, Ignas Bunikis, et al.
Haematologica|October 29, 2017
Single-molecule DNA sequencing of acute myeloid leukemia and myelodysplastic syndromes with multiple <i>TP53</i> alterationsLaurence Lodé, Adam Ameur, Thibault Coste, et al.
NAR Genomics and Bioinformatics|May 28, 2026
Whole-genome sequencing with AVITI and NovaSeq X Plus reveals comparable performance with contextual biasesPontus Höjer, Johannes Alneberg, Pär Lundin, et al.
Human Molecular Genetics|February 4, 2017
Revertant mosaicism repairs skin lesions in a patient with keratitis-ichthyosis-deafness syndrome by second-site mutations in connexin 26Sanna Gudmundsson, Maria Wilbe, Sara Ekvall, et al.
Scientific Reports|March 19, 2014
Comprehensive profiling of the vaginal microbiome in HIV positive women using massive parallel semiconductor sequencingAdam Ameur, Tracy L Meiring, Ignas Bunikis, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|January 13, 2009
Transcriptional profiling reveals a critical role for tyrosine phosphatase VE-PTP in regulation of VEGFR2 activity and endothelial cell morphogenesisSofie Mellberg, Anna Dimberg, Fuad Bahram, et al.
Human Mutation|January 26, 2013
Welander distal myopathy caused by an ancient founder mutation in TIA1 associated with perturbed splicingJoakim Klar, Maria Sobol, Atle Melberg, et al.
The Journal of Clinical Investigation|October 21, 2014
Abolished InsP3R2 function inhibits sweat secretion in both humans and miceJoakim Klar, Chihiro Hisatsune, Shahid M Baig, et al.
American Journal of Medical Genetics. Part A|February 15, 2022
Loss of Nexilin function leads to a recessive lethal fetal cardiomyopathy characterized by cardiomegaly and endocardial fibroelastosisJosefin Johansson, Carina Frykholm, Katharina Ericson, et al.
Neuro-Oncology|June 23, 2022
Novel cancer gene discovery using a forward genetic screen in RCAS-PDGFB-driven gliomasHolger Weishaupt, Matko Čančer, Gabriela Rosén, et al.
Pageof 11

Showing results (61-70 of 103) with videos related to

Sort By:
Pageof 11
Life Science Alliance|May 22, 2024
A multiomic characterization of the leukemia cell line REH using short- and long-read sequencingMariya Lysenkova Wiklander, Gustav Arvidsson, Ignas Bunikis, et al.
Haematologica|October 29, 2017
Single-molecule DNA sequencing of acute myeloid leukemia and myelodysplastic syndromes with multiple <i>TP53</i> alterationsLaurence Lodé, Adam Ameur, Thibault Coste, et al.
NAR Genomics and Bioinformatics|May 28, 2026
Whole-genome sequencing with AVITI and NovaSeq X Plus reveals comparable performance with contextual biasesPontus Höjer, Johannes Alneberg, Pär Lundin, et al.
Human Molecular Genetics|February 4, 2017
Revertant mosaicism repairs skin lesions in a patient with keratitis-ichthyosis-deafness syndrome by second-site mutations in connexin 26Sanna Gudmundsson, Maria Wilbe, Sara Ekvall, et al.
Scientific Reports|March 19, 2014
Comprehensive profiling of the vaginal microbiome in HIV positive women using massive parallel semiconductor sequencingAdam Ameur, Tracy L Meiring, Ignas Bunikis, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|January 13, 2009
Transcriptional profiling reveals a critical role for tyrosine phosphatase VE-PTP in regulation of VEGFR2 activity and endothelial cell morphogenesisSofie Mellberg, Anna Dimberg, Fuad Bahram, et al.
Human Mutation|January 26, 2013
Welander distal myopathy caused by an ancient founder mutation in TIA1 associated with perturbed splicingJoakim Klar, Maria Sobol, Atle Melberg, et al.
The Journal of Clinical Investigation|October 21, 2014
Abolished InsP3R2 function inhibits sweat secretion in both humans and miceJoakim Klar, Chihiro Hisatsune, Shahid M Baig, et al.
American Journal of Medical Genetics. Part A|February 15, 2022
Loss of Nexilin function leads to a recessive lethal fetal cardiomyopathy characterized by cardiomegaly and endocardial fibroelastosisJosefin Johansson, Carina Frykholm, Katharina Ericson, et al.
Neuro-Oncology|June 23, 2022
Novel cancer gene discovery using a forward genetic screen in RCAS-PDGFB-driven gliomasHolger Weishaupt, Matko Čančer, Gabriela Rosén, et al.
Pageof 11