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dc.contributor.authorMahesh, R.-
dc.date.accessioned2023-11-24T10:31:35Z-
dc.date.available2023-11-24T10:31:35Z-
dc.date.issued2017-02-
dc.identifier.urihttps://molpharm.aspetjournals.org/content/91/2/123.abstract-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/13268-
dc.description.abstractDynamin is a GTPase that plays a vital role in clathrin-dependent endocytosis and other vesicular trafficking processes by acting as a pair of molecular scissors for newly formed vesicles originating from the plasma membrane. Dynamins and related proteins are important components for the cleavage of clathrin-coated vesicles, phagosomes, and mitochondria. These proteins help in organelle division, viral resistance, and mitochondrial fusion/fission. Dysfunction and mutations in dynamin have been implicated in the pathophysiology of various disorders, such as Alzheimer’s disease, Parkinson’s disease, Huntington’s disease, Charcot-Marie-Tooth disease, heart failure, schizophrenia, epilepsy, cancer, dominant optic atrophy, osteoporosis, and Down’s syndrome. This review is an attempt to illustrate the dynamin-related mechanisms involved in the above-mentioned disorders and to help medicinal chemists to design novel dynamin ligands, which could be useful in the treatment of dynamin-related disorders.en_US
dc.language.isoenen_US
dc.publisherAmerican Society for Pharmacology and Experimental Therapeuticsen_US
dc.subjectPharmacyen_US
dc.subjectGTPaseen_US
dc.subjectMitochondrial fusion/fissionen_US
dc.subjectAlzheimer’s diseaseen_US
dc.subjectParkinson’s diseaseen_US
dc.titleDynamin Functions and Ligands: Classical Mechanisms Behinden_US
dc.typeArticleen_US
Appears in Collections:Department of Pharmacy

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