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Alexandre Reymond

Showing results (11-20 of 169) with videos related to

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The International Journal of Developmental Biology|March 21, 2002
Chromosome 21: a small land of fascinating disorders with unknown pathophysiologyStylianos E Antonarakis, Robert Lyle, Samuel Deutsch, et al.
Human Molecular Genetics|May 28, 2004
The subcellular localization of the ChoRE-binding protein, encoded by the Williams-Beuren syndrome critical region gene 14, is regulated by 14-3-3Giuseppe Merla, Cédric Howald, Stylianos E Antonarakis, et al.
Genomics Insights|May 3, 2019
<i>De Novo</i> Duplication in the <i>CHD7</i> Gene Associated With Severe CHARGE SyndromeLaura Pranckėnienė, Eglė Preikšaitienė, Lucie Gueneau, et al.
Methods in Molecular Biology (Clifton, N.J.)|September 23, 2011
Detecting long-range chromatin interactions using the chromosome conformation capture sequencing (4C-seq) methodNele Gheldof, Marion Leleu, Daan Noordermeer, et al.
Mechanisms of Development|April 19, 2002
TRIM9 is specifically expressed in the embryonic and adult nervous systemCaterina Berti, Silvia Messali, Andrea Ballabio, et al.
Advances in Experimental Medicine and Biology|May 1, 2013
The tripartite motif: structure and functionLucia Micale, Evelyne Chaignat, Carmela Fusco, et al.
BMC Genomics|February 11, 2017
Diversity and regulatory impact of copy number variation in the primate Macaca fascicularisAndreas R Gschwind, Anjali Singh, Ulrich Certa, et al.
Plos Biology|October 6, 2005
Emergence of young human genes after a burst of retroposition in primatesAna Claudia Marques, Isabelle Dupanloup, Nicolas Vinckenbosch, et al.
Nature Reviews. Genetics|October 29, 2004
Chromosome 21 and down syndrome: from genomics to pathophysiologyStylianos E Antonarakis, Robert Lyle, Emmanouil T Dermitzakis, et al.
American Journal of Medical Genetics. Part A|February 2, 2021
Ophthalmic phenotypes associated with biallelic loss-of-function PCDH12 variantsFrancesca Mattioli, Norine Voisin, Eglė Preikšaitienė, et al.
Pageof 17

Showing results (11-20 of 169) with videos related to

Sort By:
Pageof 17
The International Journal of Developmental Biology|March 21, 2002
Chromosome 21: a small land of fascinating disorders with unknown pathophysiologyStylianos E Antonarakis, Robert Lyle, Samuel Deutsch, et al.
Human Molecular Genetics|May 28, 2004
The subcellular localization of the ChoRE-binding protein, encoded by the Williams-Beuren syndrome critical region gene 14, is regulated by 14-3-3Giuseppe Merla, Cédric Howald, Stylianos E Antonarakis, et al.
Genomics Insights|May 3, 2019
<i>De Novo</i> Duplication in the <i>CHD7</i> Gene Associated With Severe CHARGE SyndromeLaura Pranckėnienė, Eglė Preikšaitienė, Lucie Gueneau, et al.
Methods in Molecular Biology (Clifton, N.J.)|September 23, 2011
Detecting long-range chromatin interactions using the chromosome conformation capture sequencing (4C-seq) methodNele Gheldof, Marion Leleu, Daan Noordermeer, et al.
Mechanisms of Development|April 19, 2002
TRIM9 is specifically expressed in the embryonic and adult nervous systemCaterina Berti, Silvia Messali, Andrea Ballabio, et al.
Advances in Experimental Medicine and Biology|May 1, 2013
The tripartite motif: structure and functionLucia Micale, Evelyne Chaignat, Carmela Fusco, et al.
BMC Genomics|February 11, 2017
Diversity and regulatory impact of copy number variation in the primate Macaca fascicularisAndreas R Gschwind, Anjali Singh, Ulrich Certa, et al.
Plos Biology|October 6, 2005
Emergence of young human genes after a burst of retroposition in primatesAna Claudia Marques, Isabelle Dupanloup, Nicolas Vinckenbosch, et al.
Nature Reviews. Genetics|October 29, 2004
Chromosome 21 and down syndrome: from genomics to pathophysiologyStylianos E Antonarakis, Robert Lyle, Emmanouil T Dermitzakis, et al.
American Journal of Medical Genetics. Part A|February 2, 2021
Ophthalmic phenotypes associated with biallelic loss-of-function PCDH12 variantsFrancesca Mattioli, Norine Voisin, Eglė Preikšaitienė, et al.
Pageof 17