Carla Andreia Fidalgo Teixeira
AuthID: R-000-KZH
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TITLE: Impairment of autophagy by TTR V30M aggregates: in vivo reversal by TUDCA and curcumin
AUTHORS: Teixeira, CA; Almeida, MD ; Saraiva, MJ ;
PUBLISHED: 2016, SOURCE: CLINICAL SCIENCE, VOLUME: 130, ISSUE: 18
AUTHORS: Teixeira, CA; Almeida, MD ; Saraiva, MJ ;
PUBLISHED: 2016, SOURCE: CLINICAL SCIENCE, VOLUME: 130, ISSUE: 18
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TITLE: Early axonal loss accompanied by impaired endocytosis, abnormal axonal transport, and decreased microtubule stability occur in the model of Krabbe's disease Full Text
AUTHORS: Carla Andreia Teixeira; Catarina Oliveira Miranda; Vera Filipe Sousa; Telma Emanuela Santos; Ana Rita Malheiro; Melani Solomon; Gustavo H Maegawa; Pedro Brites; Monica Mendes Sousa ;
PUBLISHED: 2014, SOURCE: NEUROBIOLOGY OF DISEASE, VOLUME: 66
AUTHORS: Carla Andreia Teixeira; Catarina Oliveira Miranda; Vera Filipe Sousa; Telma Emanuela Santos; Ana Rita Malheiro; Melani Solomon; Gustavo H Maegawa; Pedro Brites; Monica Mendes Sousa ;
PUBLISHED: 2014, SOURCE: NEUROBIOLOGY OF DISEASE, VOLUME: 66
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TITLE: CNS Axons Globally Increase Axonal Transport after Peripheral Conditioning
AUTHORS: Fernando M Mar; Anabel R Simoes; Sergio Leite; Marlene M Morgado; Telma E Santos; Ines S Rodrigo; Carla A Teixeira; Thomas Misgeld; Monica M Sousa ;
PUBLISHED: 2014, SOURCE: JOURNAL OF NEUROSCIENCE, VOLUME: 34, ISSUE: 17
AUTHORS: Fernando M Mar; Anabel R Simoes; Sergio Leite; Marlene M Morgado; Telma E Santos; Ines S Rodrigo; Carla A Teixeira; Thomas Misgeld; Monica M Sousa ;
PUBLISHED: 2014, SOURCE: JOURNAL OF NEUROSCIENCE, VOLUME: 34, ISSUE: 17
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TITLE: Advances and Pitfalls of Cell Therapy in Metabolic Leukodystrophies
AUTHORS: Catarina Oliveira Miranda; Pedro Brites ; Monica Mendes Sousa ; Carla Andreia Teixeira;
PUBLISHED: 2013, SOURCE: CELL TRANSPLANTATION, VOLUME: 22, ISSUE: 2
AUTHORS: Catarina Oliveira Miranda; Pedro Brites ; Monica Mendes Sousa ; Carla Andreia Teixeira;
PUBLISHED: 2013, SOURCE: CELL TRANSPLANTATION, VOLUME: 22, ISSUE: 2
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TITLE: Systemic Delivery of Bone Marrow-Derived Mesenchymal Stromal Cells Diminishes Neuropathology in a Mouse Model of Krabbe's Disease Full Text
AUTHORS: Catarina Oliveira Miranda; Carla Andreia Teixeira; Marcia Almeida Liz ; Vera Filipe Sousa; Filipa Franquinho; Giancarlo Forte; Paolo Di Nardo; Perpetua Pinto Do O ; Monica Mendes Sousa ;
PUBLISHED: 2011, SOURCE: STEM CELLS, VOLUME: 29, ISSUE: 11
AUTHORS: Catarina Oliveira Miranda; Carla Andreia Teixeira; Marcia Almeida Liz ; Vera Filipe Sousa; Filipa Franquinho; Giancarlo Forte; Paolo Di Nardo; Perpetua Pinto Do O ; Monica Mendes Sousa ;
PUBLISHED: 2011, SOURCE: STEM CELLS, VOLUME: 29, ISSUE: 11
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TITLE: CLN2/TPP1 deficiency: The novel mutation IVS7-10A>G causes intron retention and is associated with a mild disease phenotype Full Text
AUTHORS: Bessa, C; Teixeira, CA; Dias, A; Alves, M; Rocha, S; Lacerda, L; Loureiro, L; Guimaraes, A; Ribeiro, MG;
PUBLISHED: 2008, SOURCE: MOLECULAR GENETICS AND METABOLISM, VOLUME: 93, ISSUE: 1
AUTHORS: Bessa, C; Teixeira, CA; Dias, A; Alves, M; Rocha, S; Lacerda, L; Loureiro, L; Guimaraes, A; Ribeiro, MG;
PUBLISHED: 2008, SOURCE: MOLECULAR GENETICS AND METABOLISM, VOLUME: 93, ISSUE: 1
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TITLE: Two novel CLN5 mutations in a Portuguese patient with vLINCL: Insights into molecular mechanisms of CLN5 deficiency Full Text
AUTHORS: Bessa, C; Teixeira, CAF; Mangas, M; Dias, A; Sa C S Miranda ; Guimaraes, A; Ferreira, JC; Canas, N; Cabral, P; Ribeiro, MG;
PUBLISHED: 2006, SOURCE: MOLECULAR GENETICS AND METABOLISM, VOLUME: 89, ISSUE: 3
AUTHORS: Bessa, C; Teixeira, CAF; Mangas, M; Dias, A; Sa C S Miranda ; Guimaraes, A; Ferreira, JC; Canas, N; Cabral, P; Ribeiro, MG;
PUBLISHED: 2006, SOURCE: MOLECULAR GENETICS AND METABOLISM, VOLUME: 89, ISSUE: 3
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TITLE: Gene expression profiling in vLINCL CLN6-deficient fibroblasts: Insights into pathobiology Full Text
AUTHORS: Teixeira, CAF; Lin, S; Mangas, M; Quinta, R; Bessa, CJP; Ferreira, C; Sa C S Miranda ; Boustany, RMN; Ribeiro, MG;
PUBLISHED: 2006, SOURCE: BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, VOLUME: 1762, ISSUE: 7
AUTHORS: Teixeira, CAF; Lin, S; Mangas, M; Quinta, R; Bessa, CJP; Ferreira, C; Sa C S Miranda ; Boustany, RMN; Ribeiro, MG;
PUBLISHED: 2006, SOURCE: BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, VOLUME: 1762, ISSUE: 7
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TITLE: Novel mutations in the CLN6 gene causing a variant late infantile neuronal ceroid lipofuscinosis Full Text
AUTHORS: Teixeira, CA; Espinola, J; Huo, L; Kohlschutter, J; Sawin, DAP; Minassian, B; Bessa, CJP ; Guimaraes, A; Stephan, DA; Miranda, MCS ; MacDonald, ME; Ribeiro, MG; Boustany, RMN;
PUBLISHED: 2003, SOURCE: HUMAN MUTATION, VOLUME: 21, ISSUE: 5
AUTHORS: Teixeira, CA; Espinola, J; Huo, L; Kohlschutter, J; Sawin, DAP; Minassian, B; Bessa, CJP ; Guimaraes, A; Stephan, DA; Miranda, MCS ; MacDonald, ME; Ribeiro, MG; Boustany, RMN;
PUBLISHED: 2003, SOURCE: HUMAN MUTATION, VOLUME: 21, ISSUE: 5
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TITLE: Retrovirus-mediated transfer and expression of beta-hexosaminidase alpha-chain cDNA in human fibroblasts from G(M2)-gangliosidosis B1 variant
AUTHORS: Teixeira, CA; Sena Esteves, M; Lopes, L; Miranda, MCS ; Ribeiro, MG;
PUBLISHED: 2001, SOURCE: HUMAN GENE THERAPY, VOLUME: 12, ISSUE: 14
AUTHORS: Teixeira, CA; Sena Esteves, M; Lopes, L; Miranda, MCS ; Ribeiro, MG;
PUBLISHED: 2001, SOURCE: HUMAN GENE THERAPY, VOLUME: 12, ISSUE: 14
