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Uirá S Melo

Showing results (1-10 of 7) with videos related to

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International Journal of Molecular Epidemiology and Genetics|March 6, 2014
Strategies for genetic study of hearing loss in the Brazilian northeastern regionUirá S Melo, Silvana Santos, Hannalice G Cavalcanti, et al.
Orphanet Journal of Rare Diseases|January 9, 2019
Loss-of-function mutation in inositol monophosphatase 1 (IMPA1) results in abnormal synchrony in resting-state EEGChristopher P Walker, Andre L S Pessoa, Thalita Figueiredo, et al.
HGG Advances|May 22, 2023
A complex structural variant near <i>SOX3</i> causes X-linked split-hand/foot malformationElke de Boer, Carlo Marcelis, Kornelia Neveling, et al.
Human Molecular Genetics|April 14, 2020
Different gene expression profiles in iPSC-derived motor neurons from ALS8 patients with variable clinical courses suggest mitigating pathways for neurodegenerationDanyllo Oliveira, David A Morales-Vicente, Murilo S Amaral, et al.
Cell|October 22, 2016
Progressive Loss of Function in a Limb Enhancer during Snake EvolutionEvgeny Z Kvon, Olga K Kamneva, Uirá S Melo, et al.
Human Molecular Genetics|September 20, 2015
Overexpression of KLC2 due to a homozygous deletion in the non-coding region causes SPOAN syndromeUirá S Melo, Lucia I Macedo-Souza, Thalita Figueiredo, et al.
American Journal of Human Genetics|October 6, 2020
Structural Variants Create New Topological-Associated Domains and Ectopic Retinal Enhancer-Gene Contact in Dominant Retinitis PigmentosaSuzanne E de Bruijn, Alessia Fiorentino, Daniele Ottaviani, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
International Journal of Molecular Epidemiology and Genetics|March 6, 2014
Strategies for genetic study of hearing loss in the Brazilian northeastern regionUirá S Melo, Silvana Santos, Hannalice G Cavalcanti, et al.
Orphanet Journal of Rare Diseases|January 9, 2019
Loss-of-function mutation in inositol monophosphatase 1 (IMPA1) results in abnormal synchrony in resting-state EEGChristopher P Walker, Andre L S Pessoa, Thalita Figueiredo, et al.
HGG Advances|May 22, 2023
A complex structural variant near <i>SOX3</i> causes X-linked split-hand/foot malformationElke de Boer, Carlo Marcelis, Kornelia Neveling, et al.
Human Molecular Genetics|April 14, 2020
Different gene expression profiles in iPSC-derived motor neurons from ALS8 patients with variable clinical courses suggest mitigating pathways for neurodegenerationDanyllo Oliveira, David A Morales-Vicente, Murilo S Amaral, et al.
Cell|October 22, 2016
Progressive Loss of Function in a Limb Enhancer during Snake EvolutionEvgeny Z Kvon, Olga K Kamneva, Uirá S Melo, et al.
Human Molecular Genetics|September 20, 2015
Overexpression of KLC2 due to a homozygous deletion in the non-coding region causes SPOAN syndromeUirá S Melo, Lucia I Macedo-Souza, Thalita Figueiredo, et al.
American Journal of Human Genetics|October 6, 2020
Structural Variants Create New Topological-Associated Domains and Ectopic Retinal Enhancer-Gene Contact in Dominant Retinitis PigmentosaSuzanne E de Bruijn, Alessia Fiorentino, Daniele Ottaviani, et al.
Pageof 1