Amaral, Margarida, 1958-
Amaral, Margarida D.
Amaral, Margarida D., 19..-....
VIAF ID: 171630201 ( Personal )
Permalink: http://viaf.org/viaf/171630201
Preferred Forms
- 100 1 _ ‡a Amaral, Margarida D.
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- 100 1 _ ‡a Amaral, Margarida D., ‡d 19..-....
- 100 1 _ ‡a Amaral, Margarida ‡d 1958-
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4xx's: Alternate Name Forms (4)
Works
Title | Sources |
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Analysis of CFTR mutants in epithelial cells-tissues and testing of CFTR-repairing therapies | |
Analysis of clonality, ploidy and peroxisome proliferator-activated receptor (PPAR) y expression in thyroid tumours | |
Anoctamin 1 - a member of a novel family of ion channels with extended functions and significance in disease | |
ASYN and Tau interaction new drug target for neurodegenerative diseases | |
Biologia como ideologia doutrina do ADN | |
Characterization of genomic sequences of the CFTR gene and analysis of the respective transcripts | |
Characterization of mRNA dysfunctional mechanisms associated with the genetic disease cystic fibosis | |
Characterization of the genetic structure of the azorean population | |
Control of the mediolateral specification of the presomitic mesoderm | |
Correction of the ion transport defect in cystic fibrosis by small molecules | |
Cystic fibrosis : diagnosis and protocols. volume 2, Methods and resources to understand cystic fibrosis | |
Functional characterization of Ion channels with a crucial role in cystic fibrosis regulation of epithelial Na+ channel (ENaC) and Ca2+ - activated CI- channels (CaCCs) in epithelial cells | |
Functional characterization of proteins interacting or modulating CFTR and ENaC traffic and activity | |
Funtional characterization of complexes regulating chloride and mucus transport and their significance in disease | |
Genetic screens in C. elegans for new modulators of protein homeostasis with relevance for conformational diseases | |
Genética molecular trabalhos práticos | |
Identification of modulators of polyglutamine folding and aggregation in C. elegans | |
Orphan CFTR mutations from disease mechanisms to novel therapeutic opportunities | |
Personalised therapies for all targeting alternative chloride channels in cystic fibrosis | |
Plasticity of neural crest-derived glial and melanocytic lineages reversal to stem cells and influence of the cytokine endothelin 3 | |
Production of a genomic CFTR construct inserted into a human artificial chromosome (HAC) and characterization of its expression | |
Protein profiles os cystic fibrosis nasal cells characterization of mutant and revertant forms of the CFTR protein | |
Regulating proteostasis by a chemical genetics approach | |
Restoration of cystic fibrosis transmembrane conductance regulator function to CF mutants by enhancing protein processing and channel activity | |
Role of CFTR in epithelial to mesenchymal transition (EMT) by funtional genomics | |
role of mRNA translation on nonsense-mediated decay inhibition of transcripts carrying a short open reading frame | |
Study of CFTR mutants and their processing properties structural implications | |
trad. Margarida Amaral | |
Transcriptomic analysis of the dendritic cell regulation by malaria production of fever mediators in the absence of maturation | |
Using a systems approach to identify the mechanism of action correctors |