Red blood cells (RBCs) are biocompatible carriers that can be employed to deliver different
bioactive substances. In the past few decades, many strategies have been developed to …

Complex circuitry connecting the basal ganglia, cerebellum, and cerebral cortex is involved
in producing coordinated movements of the eyes and limbs. Malfunction of any part of this …

ATM (ataxia-telangiectasia mutated) is a PI3K-like kinase best known for its role in the DNA
damage response (DDR), especially after double-strand breaks. Mutations in the ATM gene …

Senescence phenotypes and mitochondrial dysfunction are implicated in aging and in
premature aging diseases, including ataxia telangiectasia (A‐T). Loss of mitochondrial …

Erythrocyte drug encapsulation is one of the most promising therapeutic alternative
approaches for the administration of toxic or rapidly cleared drugs. Drug-loaded erythrocytes …

Ataxia-telangiectasia (AT) is an autosomal recessive multi-system disorder caused by
mutation in the ataxia-telangiectasia mutated gene (ATM). ATM is a large serine/threonine …

Abstract Introduction Ataxia–Telangiectasia (AT) syndrome is an autosomal recessive
neurodegenerative disorder characterized by cerebellar ataxia, oculocutaneous …

The Leishmaniases are a group of parasitic diseases caused by protozoa of the Leishmania
genus affecting both humans and other vertebrates. Leishmania is an intracellular pathogen …

Ataxia telangiectasia (AT) is an autosomal recessive multisystem genetic disorder caused by
a mutation in the ATM gene encoding for the ATM protein. AT systemic manifestations …

Ataxia telangiectasia (A‐T) is a rare incurable neurodegenerative disease caused by
biallelic mutations in the gene for ataxia‐telangiectasia mutated (ATM). The lack of a …