Meet ApplyKite Twin, the application assistant that learns with you

Meet your Twin, it learns with you

Your Twin learns with you

Launch week codes:30% off annual Pro20% off monthly Pro

Ends in00h00m00s

Luigi Donato

Ricercatori a tempo determinato

University of Messina

Research Interests

Explore related searches

Articles (20)

Collaborators (6)

Marcella Nebbioso

Docenti di ruolo di IIa fascia

Sapienza University of Rome

Magda Gharbiya

Rosalia d'Angelo

University of Messina

Alfredo Conti

University of Bologna

angela d'ascola

Professor of Biochemistry

University of Messina

Matthias Carl

Associate Professor

University of Trento

ApplyKite TwinLearns as you apply

Make your next move.

Prepare your application

Review drafts before you send them.

Luigi Donato

Research Interests

Explore related searches

Articles (20)

Collaborators (6)

Marcella Nebbioso

Magda Gharbiya

Rosalia d'Angelo

Alfredo Conti

angela d'ascola

Matthias Carl

Make your next move.

Luigi Donato

Research Interests

Explore related searches

Articles (20)

Oxidative Stress Signaling and Regenerative Responses in a Larval Zebrafish Model of Retinal Light Damage

Comprehensive transcriptomic analysis reveals canonical and novel pathways modulated by nanoceria in mammalian retinal degeneration

Association of aryl hydrocarbon receptor gene polymorphisms with hashimoto’s thyroiditis

Special Issue “Retinal Diseases and Macular Degeneration: Cell Biology and Molecular Genetics”

Circulating lncRNAs Remark Expression Profile of Cerebrovascular Malformation Endothelial Cells

Combined exome and RNA-seq analysis in patients with rare non-syndromic inherited brain arteriovenous malformation suggests a novel function for PTPN13 in arterial specification.

State of the Art on Inherited Retinal Dystrophies: Management and Molecular Genetics

QMR® and Patient Blood-Derived Secretome Modulate RPE microRNA Networks Under Oxidative Stress

Mechanotransduction in Development: A Focus on Angiogenesis

Decoding pediatric inherited retinal dystrophies: Bridging genetic complexity and clinical heterogeneity

Computational Evidence for Digenic Contribution of AIPL1 and BBS2 Rare Variants in Inherited Retinal Dystrophy

First report of PDCD10 somatic mutation in liver cavernous malformation

Multifaceted disruption of AMPA receptor signaling by CACNG8 variants: Integrated evidence from human genetics and molecular simulation

Efficacy of an experimental gaseous ozone-based sterilization method for clear aligners

From powerhouse to regulator: The role of mitoepigenetics in mitochondrion-related cellular functions and human diseases

Investigating G-quadruplex structures in RPGR gene: Implications for understanding X-linked retinal degeneration

Methylome analysis of endothelial cells suggests new insights on sporadic brain arteriovenous malformation

The genomic mosaic of mitochondrial dysfunction: Decoding nuclear and mitochondrial epigenetic contributions to maternally inherited diabetes and deafness pathogenesis

Bridging Retinal and Cerebral Neurodegeneration: A Focus on Crosslinks between Alzheimer–Perusini’s Disease and Retinal Dystrophies

Impaired Nuclear and Mitochondrial Cross-Talk Might Alter mtDNA Epigenetic Regulation in Maternally Inherited Diabetes- and Deafness-Affected Patients

Collaborators (6)

Marcella Nebbioso

Magda Gharbiya

Rosalia d'Angelo

Alfredo Conti

angela d'ascola

Matthias Carl

Make your next move.