about
Autosomal recessive gingival hyperplasia and dental anomalies caused by a 29-base pair duplication in the FAM20A geneMutations in CSTA, encoding Cystatin A, underlie exfoliative ichthyosis and reveal a role for this protease inhibitor in cell-cell adhesionHomozygous mutations in the 5' region of the JUP gene result in cutaneous disease but normal heart development in childrenTumor Microenvironment Modulation via Gold Nanoparticles Targeting Malicious Exosomes: Implications for Cancer Diagnostics and TherapyGenetic basis of alopecia areata: a roadmap for translational research.Whole-exome sequencing in a single proband reveals a mutation in the CHST8 gene in autosomal recessive peeling skin syndrome.Copy number variations on chromosome 4q26-27 are associated with Cantu syndromeUnveiling the roots of monogenic genodermatoses: genotrichoses as a paradigm.Anti-cancer precision theranostics: a focus on multifunctional gold nanoparticles.The DSPII splice variant is crucial for desmosome-mediated adhesion in HaCaT keratinocytes.Identification and characterization of DSPIa, a novel isoform of human desmoplakin.Inflammatory skin and bowel disease linked to ADAM17 deletion.POxylated Dendrimer-Based Nano-in-Micro Dry Powder Formulations for Inhalation ChemotherapyCombination of chemotherapy and Au-nanoparticle photothermy in the visible light to tackle doxorubicin resistance in cancer cellsNovel compound heterozygous mutations in thedesmoplakingene cause hair shaft abnormalities and culminate in lethal cardiomyopathyThe genetics of alopecia areata: What's new and how will it help our patients?
P50
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P50
description
hulumtuese
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Rita M Cabral
@nl
Rita M Cabral
@sl
Rita M. Cabral
@en
Rita M. Cabral
@es
type
label
Rita M Cabral
@nl
Rita M Cabral
@sl
Rita M. Cabral
@en
Rita M. Cabral
@es
prefLabel
Rita M Cabral
@nl
Rita M Cabral
@sl
Rita M. Cabral
@en
Rita M. Cabral
@es
P106
P1153
36054503100
P21
P31
P496
0000-0003-2741-8100