Search filters

List of works by Rita M. Cabral

Anti-cancer precision theranostics: a focus on multifunctional gold nanoparticles

scientific article

Autosomal recessive gingival hyperplasia and dental anomalies caused by a 29-base pair duplication in the FAM20A gene

scientific article

Combination of chemotherapy and Au-nanoparticle photothermy in the visible light to tackle doxorubicin resistance in cancer cells

scientific article published in Scientific Reports

Copy number variations on chromosome 4q26-27 are associated with Cantu syndrome

scientific article published on January 2011

Genetic basis of alopecia areata: a roadmap for translational research

scientific article

Homozygous mutations in the 5' region of the JUP gene result in cutaneous disease but normal heart development in children

scientific article

Identification and characterization of DSPIa, a novel isoform of human desmoplakin

scientific article

Inflammatory skin and bowel disease linked to ADAM17 deletion

scientific article published in October 2011

Mutations in CSTA, encoding Cystatin A, underlie exfoliative ichthyosis and reveal a role for this protease inhibitor in cell-cell adhesion

scientific article

Novel compound heterozygous mutations in thedesmoplakingene cause hair shaft abnormalities and culminate in lethal cardiomyopathy

scientific article published on 01 June 2014

POxylated Dendrimer-Based Nano-in-Micro Dry Powder Formulations for Inhalation Chemotherapy

scientific article published on 25 July 2018

The DSPII splice variant is crucial for desmosome-mediated adhesion in HaCaT keratinocytes

scientific article

The genetics of alopecia areata: What's new and how will it help our patients?

article

Tumor Microenvironment Modulation via Gold Nanoparticles Targeting Malicious Exosomes: Implications for Cancer Diagnostics and Therapy

scientific article (publication date: 14 January 2017)

Unveiling the roots of monogenic genodermatoses: genotrichoses as a paradigm

scientific article published on 15 December 2011

Whole-exome sequencing in a single proband reveals a mutation in the CHST8 gene in autosomal recessive peeling skin syndrome

scientific article