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Isabel Rivera

Showing results (31-40 of 58) with videos related to

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Biochimie|February 15, 2021
Structural and functional impact of clinically relevant E1α variants causing pyruvate dehydrogenase complex deficiencyHana Pavlu-Pereira, Diana Lousa, Catarina S Tomé, et al.
Plos Biology|July 26, 2021
IVEN: A quantitative tool to describe 3D cell position and neighbourhood reveals architectural changes in FGF4-treated preimplantation embryosJessica E Forsyth, Ali H Al-Anbaki, Roberto de la Fuente, et al.
Clinical Chemistry|July 26, 2003
Increased homocysteine and S-adenosylhomocysteine concentrations and DNA hypomethylation in vascular diseaseRita Castro, Isabel Rivera, Eduard A Struys, et al.
European Journal of Human Genetics : EJHG|July 24, 2014
Functional correction by antisense therapy of a splicing mutation in the GALT geneAna I Coelho, Sílvia Lourenço, Matilde Trabuco, et al.
Data in Brief|September 23, 2016
Data supporting the co-expression of PDHA1 gene and of its paralogue PDHA2 in somatic cells of a familyAna Pinheiro, Maria João Silva, Hana Pavlu-Pereira, et al.
Gene|June 26, 2016
Complex genetic findings in a female patient with pyruvate dehydrogenase complex deficiency: Null mutations in the PDHX gene associated with unusual expression of the testis-specific PDHA2 gene in her somatic cellsAna Pinheiro, Maria João Silva, Hana Pavlu-Pereira, et al.
Cell and Tissue Banking|December 23, 2023
Characterization of cornea donors at a tissue center in the city of Medellin, ColombiaJuan Camilo Cadavid Usuga, María Isabel Maya Naranjo, Sara Mesa Mesa, et al.
Journal of Molecular Medicine (Berlin, Germany)|June 25, 2005
Intracellular S-adenosylhomocysteine increased levels are associated with DNA hypomethylation in HUVECRita Castro, Isabel Rivera, Carla Martins, et al.
Atherosclerosis|April 10, 2012
Asymmetric dimethylarginine in adults with cystathionine β-synthase deficiencyMonica S Rocha, Tom Teerlink, Mirian C H Janssen, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|December 19, 2017
Molecular basis and clinical presentation of classic galactosemia in a Croatian populationDanijela Petković Ramadža, Vladimir Sarnavka, Jurica Vuković, et al.
Pageof 6

Showing results (31-40 of 58) with videos related to

Sort By:
Pageof 6
Biochimie|February 15, 2021
Structural and functional impact of clinically relevant E1α variants causing pyruvate dehydrogenase complex deficiencyHana Pavlu-Pereira, Diana Lousa, Catarina S Tomé, et al.
Plos Biology|July 26, 2021
IVEN: A quantitative tool to describe 3D cell position and neighbourhood reveals architectural changes in FGF4-treated preimplantation embryosJessica E Forsyth, Ali H Al-Anbaki, Roberto de la Fuente, et al.
Clinical Chemistry|July 26, 2003
Increased homocysteine and S-adenosylhomocysteine concentrations and DNA hypomethylation in vascular diseaseRita Castro, Isabel Rivera, Eduard A Struys, et al.
European Journal of Human Genetics : EJHG|July 24, 2014
Functional correction by antisense therapy of a splicing mutation in the GALT geneAna I Coelho, Sílvia Lourenço, Matilde Trabuco, et al.
Data in Brief|September 23, 2016
Data supporting the co-expression of PDHA1 gene and of its paralogue PDHA2 in somatic cells of a familyAna Pinheiro, Maria João Silva, Hana Pavlu-Pereira, et al.
Gene|June 26, 2016
Complex genetic findings in a female patient with pyruvate dehydrogenase complex deficiency: Null mutations in the PDHX gene associated with unusual expression of the testis-specific PDHA2 gene in her somatic cellsAna Pinheiro, Maria João Silva, Hana Pavlu-Pereira, et al.
Cell and Tissue Banking|December 23, 2023
Characterization of cornea donors at a tissue center in the city of Medellin, ColombiaJuan Camilo Cadavid Usuga, María Isabel Maya Naranjo, Sara Mesa Mesa, et al.
Journal of Molecular Medicine (Berlin, Germany)|June 25, 2005
Intracellular S-adenosylhomocysteine increased levels are associated with DNA hypomethylation in HUVECRita Castro, Isabel Rivera, Carla Martins, et al.
Atherosclerosis|April 10, 2012
Asymmetric dimethylarginine in adults with cystathionine β-synthase deficiencyMonica S Rocha, Tom Teerlink, Mirian C H Janssen, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|December 19, 2017
Molecular basis and clinical presentation of classic galactosemia in a Croatian populationDanijela Petković Ramadža, Vladimir Sarnavka, Jurica Vuković, et al.
Pageof 6