OxInflammation in Rett Syndrome

نویسندگان

چکیده

Molecular motion of carbocyanine fluorophores DOCI, DODCI and DTDCI were studied in AOT/n-heptane microemulsions containing added polar solvents: water, methanol or acetonitrile. The response varied remarkably depending on the nature fluorophore solvent. When amount solvent was low, molecular mobility invariably retarded, due to a combination electrostatic hydrophobic forces that induce guest cling AOT molecules host reverse micelle. However, at high amounts these interactions diminished considerably, causing increase up different extents.

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منابع مشابه

[Rett syndrome].

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Rett Syndrome

Rett syndrome is an X-linked neurological disorder that is a leading cause of mental retardation among females. The progression of the disease consists of normal neonatal development followed by a regression period during which neurodevelopmental signs such as mental retardation and decline of motor abilities start to appear. The developmental progress of Rett patients is within normal range fo...

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Rett syndrome (RTT) is a post-natal neurological disorder that represents the second most common cause for mental retardation. The presence of cold hands and feet, and blue, a feature frequently observed in these patients, is one of the non-neurological phenotypes that characterizes RTT, up to now not well explained. We have performed videocapillaroscopy in subjects affected by Rett syndrome. W...

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Epilepsy in Rett syndrome--lessons from the Rett networked database.

OBJECTIVE Rett syndrome is an X-linked dominant neurodevelopmental disorder caused by mutations in the MECP2 gene, and characterized by cognitive and communicative regression, loss of hand use, and midline hand stereotypies. Epilepsy is a core symptom, but literature is controversial regarding genotype-phenotype correlation. Analysis of data from a large cohort should overcome this shortcoming....

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ژورنال

عنوان ژورنال: Free Radical Biology and Medicine

سال: 2021

ISSN: ['1873-4596', '0891-5849']

DOI: https://doi.org/10.1016/j.freeradbiomed.2021.08.027