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An overview of molecular basis of iron metabolism regulation and the associated pathologies

Biochimica et biophysica acta, 2015-07, Vol.1852 (7), p.1347-1359

2015

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From Stress to Sick(le) and Back Again–Oxidative/Antioxidant Mechanisms, Genetic Modulation, and Cerebrovascular Disease in Children with Sickle Cell Anemia

Antioxidants, 2023-11, Vol.12 (11), p.1977

2023

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Editing an α-globin enhancer in primary human hematopoietic stem cells as a treatment for β-thalassemia

Nature communications, 2017-09, Vol.8 (1), p.424-11, Article 424

2017

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The role of ICT in enhancing the autonomy of higher education students: Teachers’ insights

Education policy analysis archives, 2019-06, Vol.27

2019

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Prevalence Rate of Thalassemia Carriers among Individuals with Microcytosis or Hypochromia in Portugal

Acta medica portuguesa, 2023-07, Vol.36 (7-8), p.467-474

2023

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Apresentação - Dossiê História das Mulheres, Gênero e Interseccionalidades

Revista Eletrônica História em Reflexão, 2020-10, Vol.14 (28), p.4-5

2020

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Differential HFE gene expression is regulated by alternative splicing in human tissues

PloS one, 2011-03, Vol.6 (3), p.e17542-e17542

2011

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Decrease in APP and CP mRNA expression supports impairment of iron export in Alzheimer's disease patients

Biochimica et biophysica acta. Molecular basis of disease, 2015-10, Vol.1852 (10), p.2116-2122

2015

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Formação inicial de professores: análise da evasão em cursos de Pedagogia no Instituto Federal de São Paulo

Revista Principia, 2022-12, Vol.59 (4), p.1137-1157

2022

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Alternative polyadenylation and nonsense-mediated decay coordinately regulate the human HFE mRNA levels

PloS one, 2012-04, Vol.7 (4), p.e35461-e35461

2012

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Nonsense Mutations in Close Proximity to the Initiation Codon Fail to Trigger Full Nonsense-mediated mRNA Decay

The Journal of biological chemistry, 2004-07, Vol.279 (31), p.32170-32180

2004

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Pocket Pulse Oximetry Versus Standard Pulse Oximetry: Accuracy and Precision

Chest, 2014-03, Vol.145 (3), p.549A-1-549A-2

2014

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O papel das TIC no estímulo à autonomia dos estudantes do ensino superior: Visão dos professores

Education policy analysis archives, 2019-06, Vol.27, p.74

2019

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Evaluation of an RBD-nucleocapsid fusion protein as a booster candidate for COVID-19 vaccine

iScience, 2024-07, Vol.27 (7), p.110177, Article 110177

2024

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Ancestry of the major long-range regulatory site of the α-globin genes in the Portuguese population with the common 3.7 kb α-thalassemia deletion

Molecular biology reports, 2024-12, Vol.51 (1), p.612-612, Article 612

2024

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CRISPR Genome Editing and the Study of Chagas Disease

Genome Editing in Biomedical Sciences, 2023, Vol.1429, p.111-125

2023

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VCAM1, HMOX1 and NOS3 differential endothelial expression may impact sickle cell anemia vasculopathy

Blood cells, molecules, & diseases, 2022-03, Vol.93, p.102639-102639, Article 102639

2022

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The canonical UPF1-dependent nonsense-mediated mRNA decay is inhibited in transcripts carrying a short open reading frame independent of sequence context

RNA (Cambridge), 2006-12, Vol.12 (12), p.2160-2170

2006

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TP53 Pathogenic Variants in Early-Onset Breast Cancer Patients Fulfilling Hereditary Breast and Ovary Cancer and Li-Fraumeni-like Syndromes

Biomolecules (Basel, Switzerland), 2022-04, Vol.12 (5), p.640

2022

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Characterization of a cohort of Angolan children with sickle cell anemia treated with hydroxyurea

Blood cells, molecules, & diseases, 2024-03, Vol.105, p.102822-102822, Article 102822

2024

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Ruthenium(II)/Benzonitrile Complex Induces Cytotoxic Effect in Sarcoma-180 Cells by Caspase-Mediated and Tp53/p21-Mediated Apoptosis, with Moderate Brine Shrimp Toxicity

Biological trace element research, 2020-12, Vol.198 (2), p.669-680

2020

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cis-[RuCl(BzCN)(bipy)(dppe)]PF6 induces anti-angiogenesis and apoptosis by a mechanism of caspase-dependent involving DNA damage, PARP activation, and Tp53 induction in Ehrlich tumor cells

Chemico-biological interactions, 2017-12, Vol.278, p.101-113

2017

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Genetic modulation of anemia severity, hemolysis level, and hospitalization rate in Angolan children with Sickle Cell Anemia

Molecular biology reports, 2022-11, Vol.49 (11), p.10347-10356

2022

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The role of HFE mutations on iron metabolism in beta-thalassemia carriers

Journal of human genetics, 2004-12, Vol.49 (12), p.651-655

2004

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Early modification of sickle cell disease clinical course by UDP-glucuronosyltransferase 1A1 gene promoter polymorphism

Journal of human genetics, 2008-06, Vol.53 (6), p.524-528

2008

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An overview of molecular basis of iron metabolism regulation and the associated pathologies

From Stress to Sick(le) and Back Again–Oxidative/Antioxidant Mechanisms, Genetic Modulation, and Cerebrovascular Disease in Children with Sickle Cell Anemia

Editing an α-globin enhancer in primary human hematopoietic stem cells as a treatment for β-thalassemia

The role of ICT in enhancing the autonomy of higher education students: Teachers’ insights

Prevalence Rate of Thalassemia Carriers among Individuals with Microcytosis or Hypochromia in Portugal

Apresentação - Dossiê História das Mulheres, Gênero e Interseccionalidades

Differential HFE gene expression is regulated by alternative splicing in human tissues

Decrease in APP and CP mRNA expression supports impairment of iron export in Alzheimer's disease patients

Formação inicial de professores: análise da evasão em cursos de Pedagogia no Instituto Federal de São Paulo

Alternative polyadenylation and nonsense-mediated decay coordinately regulate the human HFE mRNA levels

Nonsense Mutations in Close Proximity to the Initiation Codon Fail to Trigger Full Nonsense-mediated mRNA Decay

Pocket Pulse Oximetry Versus Standard Pulse Oximetry: Accuracy and Precision

O papel das TIC no estímulo à autonomia dos estudantes do ensino superior: Visão dos professores

Evaluation of an RBD-nucleocapsid fusion protein as a booster candidate for COVID-19 vaccine

Ancestry of the major long-range regulatory site of the α-globin genes in the Portuguese population with the common 3.7 kb α-thalassemia deletion

CRISPR Genome Editing and the Study of Chagas Disease

VCAM1, HMOX1 and NOS3 differential endothelial expression may impact sickle cell anemia vasculopathy

The canonical UPF1-dependent nonsense-mediated mRNA decay is inhibited in transcripts carrying a short open reading frame independent of sequence context

TP53 Pathogenic Variants in Early-Onset Breast Cancer Patients Fulfilling Hereditary Breast and Ovary Cancer and Li-Fraumeni-like Syndromes

Characterization of a cohort of Angolan children with sickle cell anemia treated with hydroxyurea

Ruthenium(II)/Benzonitrile Complex Induces Cytotoxic Effect in Sarcoma-180 Cells by Caspase-Mediated and Tp53/p21-Mediated Apoptosis, with Moderate Brine Shrimp Toxicity

cis-[RuCl(BzCN)(bipy)(dppe)]PF6 induces anti-angiogenesis and apoptosis by a mechanism of caspase-dependent involving DNA damage, PARP activation, and Tp53 induction in Ehrlich tumor cells

Genetic modulation of anemia severity, hemolysis level, and hospitalization rate in Angolan children with Sickle Cell Anemia

The role of HFE mutations on iron metabolism in beta-thalassemia carriers

Early modification of sickle cell disease clinical course by UDP-glucuronosyltransferase 1A1 gene promoter polymorphism

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