Search Results - "GANDHI, Sonia"
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Crucial role of protein oligomerization in the pathogenesis of Alzheimer's and Parkinson's diseases
Published in The FEBS journal (01-10-2018)“…Misfolding and aggregation of the proteins amyloid‐β, tau and alpha‐synuclein is the predominant pathology underlying the neurodegenerative disorders,…”
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Mechanism of Oxidative Stress in Neurodegeneration
Published in Oxidative medicine and cellular longevity (01-01-2012)“…Biological tissues require oxygen to meet their energetic demands. However, the consumption of oxygen also results in the generation of free radicals that may…”
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Radiation-induced inflammatory cascade and its reverberating crosstalks as potential cause of post-radiotherapy second malignancies
Published in Cancer and metastasis reviews (01-06-2017)“…The disease-free survival following radiotherapy is often limited by the development of second/secondary cancers. This significant impediment to effective…”
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Preexisting and de novo humoral immunity to SARS-CoV-2 in humans
Published in Science (American Association for the Advancement of Science) (11-12-2020)“…Zoonotic introduction of novel coronaviruses may encounter preexisting immunity in humans. Using diverse assays for antibodies recognizing SARS-CoV-2 proteins,…”
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α-synuclein oligomers interact with ATP synthase and open the permeability transition pore in Parkinson’s disease
Published in Nature communications (12-06-2018)“…Protein aggregation causes α-synuclein to switch from its physiological role to a pathological toxic gain of function. Under physiological conditions,…”
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Alpha synuclein aggregation drives ferroptosis: an interplay of iron, calcium and lipid peroxidation
Published in Cell death and differentiation (01-10-2020)“…Protein aggregation and abnormal lipid homeostasis are both implicated in neurodegeneration through unknown mechanisms. Here we demonstrate that…”
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Monomeric Alpha-Synuclein Exerts a Physiological Role on Brain ATP Synthase
Published in The Journal of neuroscience (12-10-2016)“…Misfolded α-synuclein is a key factor in the pathogenesis of Parkinson's disease (PD). However, knowledge about a physiological role for the native, unfolded…”
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Picomolar concentrations of oligomeric alpha-synuclein sensitizes TLR4 to play an initiating role in Parkinson’s disease pathogenesis
Published in Acta neuropathologica (01-01-2019)“…Despite the wealth of genomic and transcriptomic data in Parkinson’s disease (PD), the initial molecular events are unknown. Using LD score regression…”
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SARS-CoV-2 S2-targeted vaccination elicits broadly neutralizing antibodies
Published in Science translational medicine (27-07-2022)“…Several variants of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) have emerged during the current coronavirus disease 2019 (COVID-19) pandemic…”
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Kinetic model of the aggregation of alpha-synuclein provides insights into prion-like spreading
Published in Proceedings of the National Academy of Sciences - PNAS (01-03-2016)“…The protein alpha-synuclein (αS) self-assembles into small oligomeric species and subsequently into amyloid fibrils that accumulate and proliferate during the…”
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PINK1-Associated Parkinson's Disease Is Caused by Neuronal Vulnerability to Calcium-Induced Cell Death
Published in Molecular cell (13-03-2009)“…Mutations in PINK1 cause autosomal recessive Parkinson's disease. PINK1 is a mitochondrial kinase of unknown function. We investigated calcium homeostasis and…”
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Dopamine Induces Ca2+ Signaling in Astrocytes through Reactive Oxygen Species Generated by Monoamine Oxidase
Published in The Journal of biological chemistry (06-08-2010)“…Dopamine is a neurotransmitter that plays a major role in a variety of brain functions, as well as in disorders such as Parkinson disease and schizophrenia. In…”
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PINK1 cleavage at position A103 by the mitochondrial protease PARL
Published in Human molecular genetics (01-03-2011)“…Mutations in PTEN-induced kinase 1 (PINK1) cause early onset autosomal recessive Parkinson's disease (PD). PINK1 is a 63 kDa protein kinase, which exerts a…”
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Mitochondrial dysfunction in Parkinsonian mesenchymal stem cells impairs differentiation
Published in Redox biology (01-04-2018)“…Sporadic cases account for 90–95% of all patients with Parkinson's Disease (PD). Atypical Parkinsonism comprises approximately 20% of all patients with…”
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Urinary metabolic modulation in human participants residing in Siachen: a 1H NMR metabolomics approach
Published in Scientific reports (31-05-2022)“…The main physiological challenge in high altitude environment is hypoxia which affects the aerobic metabolism reducing the energy supply. These changes may…”
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Progressive Motor Neuron Pathology and the Role of Astrocytes in a Human Stem Cell Model of VCP-Related ALS
Published in Cell reports (Cambridge) (30-05-2017)“…Motor neurons (MNs) and astrocytes (ACs) are implicated in the pathogenesis of amyotrophic lateral sclerosis (ALS), but their interaction and the sequence of…”
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Improved antioxidant activities of spice require enrichment of distinct yet closely-related metabolic pathways
Published in Heliyon (01-11-2023)“…Improved biosynthesis of commercially and pharmacologically relevant phytometabolites through genetic and metabolic engineering is a lucrative strategy for…”
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The mitochondrial protease HtrA2 is regulated by Parkinson's disease-associated kinase PINK1
Published in Nature cell biology (01-11-2007)“…In mice, targeted deletion of the serine protease HtrA2 (also known as Omi) causes mitochondrial dysfunction leading to a neurodegenerative disorder with…”
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Enhancing nucleotide metabolism protects against mitochondrial dysfunction and neurodegeneration in a PINK1 model of Parkinson’s disease
Published in Nature cell biology (01-02-2014)“…Mutations in PINK1 cause early-onset Parkinson’s disease (PD). Studies in Drosophila melanogaster have highlighted mitochondrial dysfunction on loss of Pink1…”
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Generation of TWO G51D SNCA missense mutation iPSC lines (CRICKi011-A, CRICKi012-A) from two individuals at risk of Parkinson’s disease
Published in Stem cell research (01-09-2023)“…Mutations or multiplications of the SNCA (Synuclein Alpha) gene cause rare autosomal dominant Parkinson’s disease (PD). The SNCA G51D missense mutation is…”
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