Natércia Maria da Silva Conceição
AuthID: R-000-DG3
1
TITLE: Regulation of human ZNF687, a gene associated with Paget's disease of bone
AUTHORS: Varela, Debora; Varela, Tatiana; Conceicao, Natercia; Cancela, M. Leonor;
PUBLISHED: 2023, SOURCE: INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, VOLUME: 154
AUTHORS: Varela, Debora; Varela, Tatiana; Conceicao, Natercia; Cancela, M. Leonor;
PUBLISHED: 2023, SOURCE: INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, VOLUME: 154
2
TITLE: mef2ca and mef2cb Double Mutant Zebrafish Show Altered Craniofacial Phenotype and Motor Behaviour
AUTHORS: Andreia Adrião; Sara Mariano; José Mariano; Paulo Gavaia; Leonor Cancela; Marta Vitorino; Natércia Conceição;
PUBLISHED: 2023, SOURCE: Biomolecules, VOLUME: 13, ISSUE: 5
AUTHORS: Andreia Adrião; Sara Mariano; José Mariano; Paulo Gavaia; Leonor Cancela; Marta Vitorino; Natércia Conceição;
PUBLISHED: 2023, SOURCE: Biomolecules, VOLUME: 13, ISSUE: 5
3
TITLE: Assessment of MGP gene expression in cancer and contribution to prognosis
AUTHORS: Caiado, Helena; Cancela, M. Leonor; Conceicao, Natercia;
PUBLISHED: 2023, SOURCE: BIOCHIMIE, VOLUME: 214
AUTHORS: Caiado, Helena; Cancela, M. Leonor; Conceicao, Natercia;
PUBLISHED: 2023, SOURCE: BIOCHIMIE, VOLUME: 214
4
TITLE: ZEBRAFISH MUTANT FOR CDKL5 MIMICS PHENOTYPES ASSOCIATED WITH HUMAN CDKL5 DEFICIENCY DISORDER Full Text
AUTHORS: Varela, Tatiana; Varela, Debora; Conceicao, Natercia; Cancela, M. Leonor;
PUBLISHED: 2023, SOURCE: 26th Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 102, ISSUE: 13
AUTHORS: Varela, Tatiana; Varela, Debora; Conceicao, Natercia; Cancela, M. Leonor;
PUBLISHED: 2023, SOURCE: 26th Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 102, ISSUE: 13
INDEXED IN: 
WOS
WOS5
TITLE: REGULATION OF ZNF687 DURING OSTEOBLAST DIFFERENTIATION Full Text
AUTHORS: Varela, Debora; Varela, Tatiana; Conceicao, Natercia; Cancela, M. Leonor;
PUBLISHED: 2023, SOURCE: 26th Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 102, ISSUE: 13
AUTHORS: Varela, Debora; Varela, Tatiana; Conceicao, Natercia; Cancela, M. Leonor;
PUBLISHED: 2023, SOURCE: 26th Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 102, ISSUE: 13
INDEXED IN: WOS
WOS6
TITLE: Cdkl5 mutant zebrafish shows skeletal and neuronal alterations mimicking human CDKL5 deficiency disorder Full Text
AUTHORS: Varela, Tatiana; Varela, Debora; Martins, Gil; Conceicao, Natercia; Cancela, M. Leonor;
PUBLISHED: 2022, SOURCE: SCIENTIFIC REPORTS, VOLUME: 12, ISSUE: 1
AUTHORS: Varela, Tatiana; Varela, Debora; Martins, Gil; Conceicao, Natercia; Cancela, M. Leonor;
PUBLISHED: 2022, SOURCE: SCIENTIFIC REPORTS, VOLUME: 12, ISSUE: 1
INDEXED IN: WOS
WOS7
TITLE: Zebrafish optineurin: genomic organization and transcription regulation
AUTHORS: Silva, Iris A. L.; Varela, Debora; Cancela, M. Leonor; Conceicao, Natercia;
PUBLISHED: 2022, SOURCE: GENOME, VOLUME: 65, ISSUE: 10
AUTHORS: Silva, Iris A. L.; Varela, Debora; Cancela, M. Leonor; Conceicao, Natercia;
PUBLISHED: 2022, SOURCE: GENOME, VOLUME: 65, ISSUE: 10
8
TITLE: Functional analysis of two novel TBX5 variants present in individuals with Holt-Oram syndrome with different clinical manifestations
AUTHORS: Varela, D; Varela, T; Conceicao, N; Ferreira, A; Marques, N; Silva, AP; Azevedo, P; Pereira, S; Camacho, A; de Jesus, I; Cancela, ML;
PUBLISHED: 2021, SOURCE: MOLECULAR GENETICS AND GENOMICS, VOLUME: 296, ISSUE: 4
AUTHORS: Varela, D; Varela, T; Conceicao, N; Ferreira, A; Marques, N; Silva, AP; Azevedo, P; Pereira, S; Camacho, A; de Jesus, I; Cancela, ML;
PUBLISHED: 2021, SOURCE: MOLECULAR GENETICS AND GENOMICS, VOLUME: 296, ISSUE: 4
9
TITLE: Identification of a novel mutation in MEF2C gene in an atypical patient with frontotemporal lobar degeneration Full Text
AUTHORS: Adriao, A; Santana, I; Ribeiro, C; Cancela, ML; Conceicao, N; Grazina, M;
PUBLISHED: 2021, SOURCE: NEUROLOGICAL SCIENCES
AUTHORS: Adriao, A; Santana, I; Ribeiro, C; Cancela, ML; Conceicao, N; Grazina, M;
PUBLISHED: 2021, SOURCE: NEUROLOGICAL SCIENCES
INDEXED IN: WOS
WOS10
TITLE: Identification of a novel mutation in MEF2C gene in an atypical patient with frontotemporal lobar degeneration
AUTHORS: Adrião, A; Santana, I; Ribeiro, C; Cancela, ML; Conceição, N; Grazina, M;
PUBLISHED: 2021, SOURCE: Neurological Sciences, VOLUME: 43, ISSUE: 1
AUTHORS: Adrião, A; Santana, I; Ribeiro, C; Cancela, ML; Conceição, N; Grazina, M;
PUBLISHED: 2021, SOURCE: Neurological Sciences, VOLUME: 43, ISSUE: 1
