Mario Zurita

Synphilin suppresses α-synuclein neurotoxicity in a Parkinson's disease Drosophila model.

The Drosophila melanogaster homologue of the Xeroderma pigmentosum D gene product is located in euchromatic regions and has a dynamic response to UV light-induced lesions in polytene chromosomes.

DNA repair and transcriptional effects of mutations in TFIIH in Drosophila development.

From noxiustoxin to scorpine and possible transgenic mosquitoes resistant to malaria.

A new peroxinectin-like gene preferentially expressed during oogenesis and early embryogenesis in Drosophila melanogaster.

Molecular characterization and developmental expression of the TFIIH factor p62 gene from Drosophila melanogaster: effects on the UV light sensitivity of a p62 mutant fly.

The transcriptional complexity of the TFIIH complex.

RNA polymerase II 140wimp mutant and mutations in the TFIIH subunit XPB differentially affect homeotic gene expression in Drosophila.

Oviduct contraction in Drosophila is modulated by a neural network that is both, octopaminergic and glutamatergic.

DNA repair and transcriptional deficiencies caused by mutations in the Drosophila p52 subunit of TFIIH generate developmental defects and chromosome fragility.

gammaTub23C interacts genetically with brahma chromatin-remodeling complexes in Drosophila melanogaster.

p8/TTDA overexpression enhances UV-irradiation resistance and suppresses TFIIH mutations in a Drosophila trichothiodystrophy model.

Drosophila p53 is required to increase the levels of the dKDM4B demethylase after UV-induced DNA damage to demethylate histone H3 lysine 9.

Open, repair and close again: chromatin dynamics and the response to UV-induced DNA damage.

Trafficking and chromatin dynamics of holocarboxylase synthetase during development of Drosophila melanogaster.

XNP/dATRX interacts with DREF in the chromatin to regulate gene expression.

Physical and functional interactions between Drosophila homologue of Swc6/p18Hamlet subunit of the SWR1/SRCAP chromatin-remodeling complex with the DNA repair/transcription factor TFIIH.

The basal transcription machinery as a target for cancer therapy.

Characterization of the Drosophila group ortholog to the amino-terminus of the alpha-thalassemia and mental retardation X-Linked (ATRX) vertebrate protein.

Analysis of Drosophila p8 and p52 mutants reveals distinct roles for the maintenance of TFIIH stability and male germ cell differentiation.

RhoA/ROCK pathway activity is essential for the correct localization of the germ plasm mRNAs in zebrafish embryos.

TFIIH: New Discoveries Regarding its Mechanisms and Impact on Cancer Treatment.

DREF plays multiple roles during Drosophila development.

dAdd1 and dXNP prevent genome instability by maintaining HP1a localization at Drosophila telomeres.

Heterochromatin Reduction Correlates with the Increase of the KDM4B and KDM6A Demethylases and the Expression of Pericentromeric DNA during the Acquisition of a Transformed Phenotype.

The Dmp8-Dmp18 bicistron messenger RNA enables unusual translation during cellular stress.

The role of the trithorax group TnaA isoforms in Hox gene expression, and in Drosophila late development.

as a Model Organism to Understand the Effects during Development of TFIIH-Related Human Diseases.

Novel tephritid-specific features revealed from cytological and transcriptomic analysis of Anastrepha ludens embryonic development.

Disruption of TFIIH activities generates a stress gene expression response and reveals possible new targets against cancer.

Insights into HP1a-Chromatin Interactions.