Search Results - "Deshpande, Prasannakumar"
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Regulators of proteostasis are translationally repressed in fibroblasts from patients with sporadic and LRRK2-G2019S Parkinson’s disease
Published in NPJ Parkinson's Disease (06-02-2023)“…Deficits in protein synthesis are associated with Parkinson’s disease (PD). However, it is not known which proteins are affected or if there are synthesis…”
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KIF5C S176 Phosphorylation Regulates Microtubule Binding and Transport Efficiency in Mammalian Neurons
Published in Frontiers in cellular neuroscience (15-03-2016)“…Increased phosphorylation of the KIF5 anterograde motor is associated with impaired axonal transport and neurodegeneration, but paradoxically also with normal…”
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JNK1 controls dendritic field size in L2/3 and L5 of the motor cortex, constrains soma size, and influences fine motor coordination
Published in Frontiers in cellular neuroscience (12-09-2014)“…Genetic anomalies on the JNK pathway confer susceptibility to autism spectrum disorders, schizophrenia, and intellectual disability. The mechanism whereby a…”
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Chondroitin Sulfate‐Coated Heteroduplex‐Molecular Spherical Nucleic Acids
Published in Chembiochem : a European journal of chemical biology (15-11-2024)“…Molecular Spherical Nucleic Acids (MSNAs) are atomically uniform dendritic nanostructures and potential delivery vehicles for oligonucleotides. The radial…”
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Protein synthesis is suppressed in sporadic and familial Parkinson’s disease by LRRK2
Published in The FASEB journal (01-11-2020)“…Gain of function LRRK2‐G2019S is the most frequent mutation found in familial and sporadic Parkinson's disease. It is expected therefore that understanding the…”
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Synthesis of Azide-Modified Chondroitin Sulfate Precursors: Substrates for “Click”- Conjugation with Fluorescent Labels and Oligonucleotides
Published in Bioconjugate chemistry (18-07-2018)“…Azidopropyl-modified precursors of chondroitin sulfate (CS) tetrasaccharides have been synthesized, which, after facile conversion to final CS structures, may…”
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Expanding the Molecular and Clinical Phenotype of Patients With De Novo Variants in KIF5C : A Six Patient Case Series
Published in American journal of medical genetics. Part A (06-11-2024)“…ABSTRACT Heterozygous de novo loss of function variants in the motor domain of KIF5C are associated with a neurodevelopmental disorder characterized by…”
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