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David Salgado

Showing results (31-40 of 56) with videos related to

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Human Mutation|September 8, 2016
Actionable Genes, Core Databases, and Locus-Specific DatabasesAmélie Pinard, Morgane Miltgen, Arnaud Blanchard, et al.
Elife|August 18, 2020
<i>Hox</i>-dependent coordination of mouse cardiac progenitor cell patterning and differentiationSonia Stefanovic, Brigitte Laforest, Jean-Pierre Desvignes, et al.
Haematologica|July 29, 2017
Exome sequencing identifies recurrent <i>BCOR</i> alterations and the absence of <i>KLF2</i>, <i>TNFAIP3</i> and <i>MYD88</i> mutations in splenic diffuse red pulp small B-cell lymphomaLaurent Jallades, Lucile Baseggio, Pierre Sujobert, et al.
Blood|July 8, 2015
A mutation in the Gardos channel is associated with hereditary xerocytosisRaphael Rapetti-Mauss, Caroline Lacoste, Véronique Picard, et al.
European Journal of Cancer (Oxford, England : 1990)|October 26, 2021
Standardisation of pathogenicity classification for somatic alterations in solid tumours and haematologic malignanciesFlorence Koeppel, Etienne Muller, Alexandre Harlé, et al.
Biomedicines|March 6, 2021
The lncRNA 44s2 Study Applicability to the Design of 45-55 Exon Skipping Therapeutic Strategy for DMDElena Gargaun, Sestina Falcone, Guilhem Solé, et al.
Nature Communications|April 28, 2019
Human pre-valvular endocardial cells derived from pluripotent stem cells recapitulate cardiac pathophysiological valvulogenesisTui Neri, Emilye Hiriart, Patrick P van Vliet, et al.
Physiological Genomics|October 12, 2020
Identification of a peripheral blood gene signature predicting aortic valve calcificationDonal MacGrogan, Beatriz Martínez-Poveda, Jean-Pierre Desvignes, et al.
Genome Research|July 22, 2010
The ANISEED database: digital representation, formalization, and elucidation of a chordate developmental programOlivier Tassy, Delphine Dauga, Fabrice Daian, et al.
BMC Bioinformatics|December 14, 2011
BioCreative III interactive task: an overviewCecilia N Arighi, Phoebe M Roberts, Shashank Agarwal, et al.
Pageof 6

Showing results (31-40 of 56) with videos related to

Sort By:
Pageof 6
Human Mutation|September 8, 2016
Actionable Genes, Core Databases, and Locus-Specific DatabasesAmélie Pinard, Morgane Miltgen, Arnaud Blanchard, et al.
Elife|August 18, 2020
<i>Hox</i>-dependent coordination of mouse cardiac progenitor cell patterning and differentiationSonia Stefanovic, Brigitte Laforest, Jean-Pierre Desvignes, et al.
Haematologica|July 29, 2017
Exome sequencing identifies recurrent <i>BCOR</i> alterations and the absence of <i>KLF2</i>, <i>TNFAIP3</i> and <i>MYD88</i> mutations in splenic diffuse red pulp small B-cell lymphomaLaurent Jallades, Lucile Baseggio, Pierre Sujobert, et al.
Blood|July 8, 2015
A mutation in the Gardos channel is associated with hereditary xerocytosisRaphael Rapetti-Mauss, Caroline Lacoste, Véronique Picard, et al.
European Journal of Cancer (Oxford, England : 1990)|October 26, 2021
Standardisation of pathogenicity classification for somatic alterations in solid tumours and haematologic malignanciesFlorence Koeppel, Etienne Muller, Alexandre Harlé, et al.
Biomedicines|March 6, 2021
The lncRNA 44s2 Study Applicability to the Design of 45-55 Exon Skipping Therapeutic Strategy for DMDElena Gargaun, Sestina Falcone, Guilhem Solé, et al.
Nature Communications|April 28, 2019
Human pre-valvular endocardial cells derived from pluripotent stem cells recapitulate cardiac pathophysiological valvulogenesisTui Neri, Emilye Hiriart, Patrick P van Vliet, et al.
Physiological Genomics|October 12, 2020
Identification of a peripheral blood gene signature predicting aortic valve calcificationDonal MacGrogan, Beatriz Martínez-Poveda, Jean-Pierre Desvignes, et al.
Genome Research|July 22, 2010
The ANISEED database: digital representation, formalization, and elucidation of a chordate developmental programOlivier Tassy, Delphine Dauga, Fabrice Daian, et al.
BMC Bioinformatics|December 14, 2011
BioCreative III interactive task: an overviewCecilia N Arighi, Phoebe M Roberts, Shashank Agarwal, et al.
Pageof 6