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Alexandre Reymond

Showing results (31-40 of 169) with videos related to

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Plos Computational Biology|February 10, 2011
Using transcription modules to identify expression clusters perturbed in Williams-Beuren syndromeCharlotte N Henrichsen, Gábor Csárdi, Marie-Thérèse Zabot, et al.
Genomics|July 6, 2004
The Caenorhabditis elegans ortholog of C21orf80, a potential new protein O-fucosyltransferase, is required for normal developmentOlivier Menzel, Tibor Vellai, Krisztina Takacs-Vellai, et al.
European Journal of Medical Genetics|February 29, 2012
2q34-qter duplication and 4q34.2-qter deletion in a patient with developmental delayAli Rashidi-Nezhad, Nima Parvaneh, Farideh Farzanfar, et al.
Gene|December 9, 2003
The TPTE gene family: cellular expression, subcellular localization and alternative splicingCaroline Tapparel, Alexandre Reymond, Christophe Girardet, et al.
Plos One|November 23, 2013
Structural variation-associated expression changes are paralleled by chromatin architecture modificationsNele Gheldof, Robert M Witwicki, Eugenia Migliavacca, et al.
Nucleic Acids Research|April 6, 2005
Comparative gene finding in chicken indicates that we are closing in on the set of multi-exonic widely expressed human genesRobert Castelo, Alexandre Reymond, Carine Wyss, et al.
Genome Research|November 19, 2010
Copy number variation modifies expression time coursesEvelyne Chaignat, Emilie Aït Yahya-Graison, Charlotte N Henrichsen, et al.
American Journal of Medical Genetics. Part A|April 29, 2010
A t(7;12) balanced translocation with breakpoints overlapping those of the Williams-Beuren and 12q14 microdeletion syndromesStefania Gimelli, Jacqueline Chrast, Anwar Baban, et al.
Gene|May 31, 2020
A de novo 13q31.3 microduplication encompassing the miR-17 ~ 92 cluster results in features mirroring those associated with Feingold syndrome 2Evelina Siavrienė, Eglė Preikšaitienė, Živilė Maldžienė, et al.
Human Molecular Genetics|July 1, 2005
LKB1 interacts with and phosphorylates PTEN: a functional link between two proteins involved in cancer predisposing syndromesHamid Mehenni, Nathalie Lin-Marq, Karine Buchet-Poyau, et al.
Pageof 17

Showing results (31-40 of 169) with videos related to

Sort By:
Pageof 17
Plos Computational Biology|February 10, 2011
Using transcription modules to identify expression clusters perturbed in Williams-Beuren syndromeCharlotte N Henrichsen, Gábor Csárdi, Marie-Thérèse Zabot, et al.
Genomics|July 6, 2004
The Caenorhabditis elegans ortholog of C21orf80, a potential new protein O-fucosyltransferase, is required for normal developmentOlivier Menzel, Tibor Vellai, Krisztina Takacs-Vellai, et al.
European Journal of Medical Genetics|February 29, 2012
2q34-qter duplication and 4q34.2-qter deletion in a patient with developmental delayAli Rashidi-Nezhad, Nima Parvaneh, Farideh Farzanfar, et al.
Gene|December 9, 2003
The TPTE gene family: cellular expression, subcellular localization and alternative splicingCaroline Tapparel, Alexandre Reymond, Christophe Girardet, et al.
Plos One|November 23, 2013
Structural variation-associated expression changes are paralleled by chromatin architecture modificationsNele Gheldof, Robert M Witwicki, Eugenia Migliavacca, et al.
Nucleic Acids Research|April 6, 2005
Comparative gene finding in chicken indicates that we are closing in on the set of multi-exonic widely expressed human genesRobert Castelo, Alexandre Reymond, Carine Wyss, et al.
Genome Research|November 19, 2010
Copy number variation modifies expression time coursesEvelyne Chaignat, Emilie Aït Yahya-Graison, Charlotte N Henrichsen, et al.
American Journal of Medical Genetics. Part A|April 29, 2010
A t(7;12) balanced translocation with breakpoints overlapping those of the Williams-Beuren and 12q14 microdeletion syndromesStefania Gimelli, Jacqueline Chrast, Anwar Baban, et al.
Gene|May 31, 2020
A de novo 13q31.3 microduplication encompassing the miR-17 ~ 92 cluster results in features mirroring those associated with Feingold syndrome 2Evelina Siavrienė, Eglė Preikšaitienė, Živilė Maldžienė, et al.
Human Molecular Genetics|July 1, 2005
LKB1 interacts with and phosphorylates PTEN: a functional link between two proteins involved in cancer predisposing syndromesHamid Mehenni, Nathalie Lin-Marq, Karine Buchet-Poyau, et al.
Pageof 17