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Alexandre Reymond

Showing results (121-130 of 169) with videos related to

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BMC Biology|May 9, 2023
Secondary structure of the human mitochondrial genome affects formation of deletionsVictor Shamanskiy, Alina A Mikhailova, Evgenii O Tretiakov, et al.
JAMA|May 27, 2015
Copy number variations and cognitive phenotypes in unselected populationsKatrin Männik, Reedik Mägi, Aurélien Macé, et al.
Genome Research|September 27, 2007
Islands of euchromatin-like sequence and expressed polymorphic sequences within the short arm of human chromosome 21Robert Lyle, Paola Prandini, Kazutoyo Osoegawa, et al.
American Journal of Human Genetics|June 21, 2008
Infantile spasms is associated with deletion of the MAGI2 gene on chromosome 7q11.23-q21.11Christian R Marshall, Edwin J Young, Ariel M Pani, et al.
Science (New York, N.Y.)|October 19, 2013
Coordinated effects of sequence variation on DNA binding, chromatin structure, and transcriptionHelena Kilpinen, Sebastian M Waszak, Andreas R Gschwind, et al.
Nucleic Acids Research|September 21, 2022
A mitochondria-specific mutational signature of aging: increased rate of A > G substitutions on the heavy strandAlina G Mikhailova, Alina A Mikhailova, Kristina Ushakova, et al.
Journal of Medical Genetics|November 11, 2020
Inhibition of G-protein signalling in cardiac dysfunction of intellectual developmental disorder with cardiac arrhythmia (IDDCA) syndromePasquelena De Nittis, Stephanie Efthymiou, Alexandre Sarre, et al.
Biological Psychiatry|January 9, 2016
The Number of Genomic Copies at the 16p11.2 Locus Modulates Language, Verbal Memory, and InhibitionLoyse Hippolyte, Anne M Maillard, Borja Rodriguez-Herreros, et al.
Nature|August 4, 2016
Emergence of a Homo sapiens-specific gene family and chromosome 16p11.2 CNV susceptibilityXander Nuttle, Giuliana Giannuzzi, Michael H Duyzend, et al.
American Journal of Human Genetics|December 22, 2020
Rare and de novo coding variants in chromodomain genes in Chiari I malformationBrooke Sadler, Jackson Wilborn, Lilian Antunes, et al.
Pageof 17

Showing results (121-130 of 169) with videos related to

Sort By:
Pageof 17
BMC Biology|May 9, 2023
Secondary structure of the human mitochondrial genome affects formation of deletionsVictor Shamanskiy, Alina A Mikhailova, Evgenii O Tretiakov, et al.
JAMA|May 27, 2015
Copy number variations and cognitive phenotypes in unselected populationsKatrin Männik, Reedik Mägi, Aurélien Macé, et al.
Genome Research|September 27, 2007
Islands of euchromatin-like sequence and expressed polymorphic sequences within the short arm of human chromosome 21Robert Lyle, Paola Prandini, Kazutoyo Osoegawa, et al.
American Journal of Human Genetics|June 21, 2008
Infantile spasms is associated with deletion of the MAGI2 gene on chromosome 7q11.23-q21.11Christian R Marshall, Edwin J Young, Ariel M Pani, et al.
Science (New York, N.Y.)|October 19, 2013
Coordinated effects of sequence variation on DNA binding, chromatin structure, and transcriptionHelena Kilpinen, Sebastian M Waszak, Andreas R Gschwind, et al.
Nucleic Acids Research|September 21, 2022
A mitochondria-specific mutational signature of aging: increased rate of A > G substitutions on the heavy strandAlina G Mikhailova, Alina A Mikhailova, Kristina Ushakova, et al.
Journal of Medical Genetics|November 11, 2020
Inhibition of G-protein signalling in cardiac dysfunction of intellectual developmental disorder with cardiac arrhythmia (IDDCA) syndromePasquelena De Nittis, Stephanie Efthymiou, Alexandre Sarre, et al.
Biological Psychiatry|January 9, 2016
The Number of Genomic Copies at the 16p11.2 Locus Modulates Language, Verbal Memory, and InhibitionLoyse Hippolyte, Anne M Maillard, Borja Rodriguez-Herreros, et al.
Nature|August 4, 2016
Emergence of a Homo sapiens-specific gene family and chromosome 16p11.2 CNV susceptibilityXander Nuttle, Giuliana Giannuzzi, Michael H Duyzend, et al.
American Journal of Human Genetics|December 22, 2020
Rare and de novo coding variants in chromodomain genes in Chiari I malformationBrooke Sadler, Jackson Wilborn, Lilian Antunes, et al.
Pageof 17