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Adriana P Rebelo

Showing results (1-10 of 38) with videos related to

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Journal of Inherited Metabolic Disease|May 5, 2011
Mitochondrial DNA transcription regulation and nucleoid organizationAdriana P Rebelo, Lloye M Dillon, Carlos T Moraes
Nucleic Acids Research|September 11, 2009
In vivo methylation of mtDNA reveals the dynamics of protein-mtDNA interactionsAdriana P Rebelo, Sion L Williams, Carlos T Moraes
IUBMB Life|January 27, 2012
The role of PGC-1 coactivators in aging skeletal muscle and heartLloye M Dillon, Adriana P Rebelo, Carlos T Moraes
Experimental Neurology|June 24, 2018
The human motor neuron axonal transcriptome is enriched for transcripts related to mitochondrial function and microtubule-based axonal transportRenata Maciel, Dana M Bis, Adriana P Rebelo, et al.
Nature Communications|July 13, 2023
Deep structured learning for variant prioritization in Mendelian diseasesMatt C Danzi, Maike F Dohrn, Sarah Fazal, et al.
Journal of the Peripheral Nervous System : JPNS|May 28, 2014
Characterization of the mitofusin 2 R94W mutation in a knock-in mouse modelAlleene V Strickland, Adriana P Rebelo, Fan Zhang, et al.
Journal of the Peripheral Nervous System : JPNS|March 8, 2019
POLG mutations presenting as Charcot-Marie-Tooth diseaseJade Phillips, Steve Courel, Adriana P Rebelo, et al.
Clinical Genetics|November 10, 2019
Hereditary spastic paraplegia is a novel phenotype for germline de novo ATP1A1 mutationFabrizia Stregapede, Lorena Travaglini, Adriana P Rebelo, et al.
Neurology. Genetics|December 12, 2018
Identification of a new SYT2 variant validates an unusual distal motor neuropathy phenotypeNataly I Montes-Chinea, Zhuo Guan, Marcella Coutts, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|July 10, 2024
Loss of Fic causes progressive neurodegeneration in a Drosophila model of hereditary spastic paraplegiaAmanda G Lobato, Natalie Ortiz-Vega, Tijana Canic, et al.
Pageof 4

Showing results (1-10 of 38) with videos related to

Sort By:
Pageof 4
Journal of Inherited Metabolic Disease|May 5, 2011
Mitochondrial DNA transcription regulation and nucleoid organizationAdriana P Rebelo, Lloye M Dillon, Carlos T Moraes
Nucleic Acids Research|September 11, 2009
In vivo methylation of mtDNA reveals the dynamics of protein-mtDNA interactionsAdriana P Rebelo, Sion L Williams, Carlos T Moraes
IUBMB Life|January 27, 2012
The role of PGC-1 coactivators in aging skeletal muscle and heartLloye M Dillon, Adriana P Rebelo, Carlos T Moraes
Experimental Neurology|June 24, 2018
The human motor neuron axonal transcriptome is enriched for transcripts related to mitochondrial function and microtubule-based axonal transportRenata Maciel, Dana M Bis, Adriana P Rebelo, et al.
Nature Communications|July 13, 2023
Deep structured learning for variant prioritization in Mendelian diseasesMatt C Danzi, Maike F Dohrn, Sarah Fazal, et al.
Journal of the Peripheral Nervous System : JPNS|May 28, 2014
Characterization of the mitofusin 2 R94W mutation in a knock-in mouse modelAlleene V Strickland, Adriana P Rebelo, Fan Zhang, et al.
Journal of the Peripheral Nervous System : JPNS|March 8, 2019
POLG mutations presenting as Charcot-Marie-Tooth diseaseJade Phillips, Steve Courel, Adriana P Rebelo, et al.
Clinical Genetics|November 10, 2019
Hereditary spastic paraplegia is a novel phenotype for germline de novo ATP1A1 mutationFabrizia Stregapede, Lorena Travaglini, Adriana P Rebelo, et al.
Neurology. Genetics|December 12, 2018
Identification of a new SYT2 variant validates an unusual distal motor neuropathy phenotypeNataly I Montes-Chinea, Zhuo Guan, Marcella Coutts, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|July 10, 2024
Loss of Fic causes progressive neurodegeneration in a Drosophila model of hereditary spastic paraplegiaAmanda G Lobato, Natalie Ortiz-Vega, Tijana Canic, et al.
Pageof 4