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P Rebelo

Showing results (31-40 of 64) with videos related to

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Journal of Biotechnology|January 28, 2016
Adaptable stirred-tank culture strategies for large scale production of multicellular spheroid-based tumor cell modelsVítor E Santo, Marta F Estrada, Sofia P Rebelo, et al.
Biomaterials|February 25, 2018
3D-3-culture: A tool to unveil macrophage plasticity in the tumour microenvironmentSofia P Rebelo, Catarina Pinto, Tatiana R Martins, et al.
Annals of Clinical and Translational Neurology|March 20, 2024
Recurrent ATP1A1 variant Gly903Arg causes developmental delay, intellectual disability, and autismMaike F Dohrn, Guney Bademci, Adriana P Rebelo, et al.
Pulmonology|June 5, 2019
Embracing digital technology in chronic respiratory care: Surveying patients access and confidenceC Jácome, F Marques, C Paixão, et al.
SLAS Discovery : Advancing Life Sciences R & D|March 23, 2024
Aldehyde Dehydrogenase 2 (ALDH2): A novel sorafenib target in hepatocellular carcinoma unraveled by the proteome-wide cellular thermal shift assayInês C Ferreira, Estefania Torrejón, Bernardo Abecasis, et al.
JCI Insight|April 4, 2023
Sorbitol reduction via govorestat ameliorates synaptic dysfunction and neurodegeneration in sorbitol dehydrogenase deficiencyYi Zhu, Amanda G Lobato, Adriana P Rebelo, et al.
Brain : a Journal of Neurology|January 20, 2018
SCO2 mutations cause early-onset axonal Charcot-Marie-Tooth disease associated with cellular copper deficiencyAdriana P Rebelo, Dimah Saade, Claudia V Pereira, et al.
Neurology|May 9, 2014
Motor protein mutations cause a new form of hereditary spastic paraplegiaAndrés Caballero Oteyza, Esra Battaloğlu, Levent Ocek, et al.
Journal of the Neurological Sciences|June 5, 2021
Rare mutations in ATL3, SPTLC2 and SCN9A explaining hereditary sensory neuropathy and congenital insensitivity to pain in a Brazilian cohortVivian Pedigone Cintra, Maike F Dohrn, Pedro José Tomaselli, et al.
Biomaterials|December 10, 2015
Modelling the tumour microenvironment in long-term microencapsulated 3D co-cultures recapitulates phenotypic features of disease progressionMarta F Estrada, Sofia P Rebelo, Emma J Davies, et al.
Pageof 7

Showing results (31-40 of 64) with videos related to

Sort By:
Pageof 7
Journal of Biotechnology|January 28, 2016
Adaptable stirred-tank culture strategies for large scale production of multicellular spheroid-based tumor cell modelsVítor E Santo, Marta F Estrada, Sofia P Rebelo, et al.
Biomaterials|February 25, 2018
3D-3-culture: A tool to unveil macrophage plasticity in the tumour microenvironmentSofia P Rebelo, Catarina Pinto, Tatiana R Martins, et al.
Annals of Clinical and Translational Neurology|March 20, 2024
Recurrent ATP1A1 variant Gly903Arg causes developmental delay, intellectual disability, and autismMaike F Dohrn, Guney Bademci, Adriana P Rebelo, et al.
Pulmonology|June 5, 2019
Embracing digital technology in chronic respiratory care: Surveying patients access and confidenceC Jácome, F Marques, C Paixão, et al.
SLAS Discovery : Advancing Life Sciences R & D|March 23, 2024
Aldehyde Dehydrogenase 2 (ALDH2): A novel sorafenib target in hepatocellular carcinoma unraveled by the proteome-wide cellular thermal shift assayInês C Ferreira, Estefania Torrejón, Bernardo Abecasis, et al.
JCI Insight|April 4, 2023
Sorbitol reduction via govorestat ameliorates synaptic dysfunction and neurodegeneration in sorbitol dehydrogenase deficiencyYi Zhu, Amanda G Lobato, Adriana P Rebelo, et al.
Brain : a Journal of Neurology|January 20, 2018
SCO2 mutations cause early-onset axonal Charcot-Marie-Tooth disease associated with cellular copper deficiencyAdriana P Rebelo, Dimah Saade, Claudia V Pereira, et al.
Neurology|May 9, 2014
Motor protein mutations cause a new form of hereditary spastic paraplegiaAndrés Caballero Oteyza, Esra Battaloğlu, Levent Ocek, et al.
Journal of the Neurological Sciences|June 5, 2021
Rare mutations in ATL3, SPTLC2 and SCN9A explaining hereditary sensory neuropathy and congenital insensitivity to pain in a Brazilian cohortVivian Pedigone Cintra, Maike F Dohrn, Pedro José Tomaselli, et al.
Biomaterials|December 10, 2015
Modelling the tumour microenvironment in long-term microencapsulated 3D co-cultures recapitulates phenotypic features of disease progressionMarta F Estrada, Sofia P Rebelo, Emma J Davies, et al.
Pageof 7