Search Results - "GANDHI, Sonia"

Refine Results
  1. 1

    Crucial role of protein oligomerization in the pathogenesis of Alzheimer's and Parkinson's diseases by Choi, Minee L., Gandhi, Sonia

    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,…”
    Get full text
    Journal Article
  2. 2

    Mechanism of Oxidative Stress in Neurodegeneration by Gandhi, Sonia, Abramov, Andrey Y.

    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…”
    Get full text
    Journal Article
  3. 3

    Radiation-induced inflammatory cascade and its reverberating crosstalks as potential cause of post-radiotherapy second malignancies by Gandhi, Sonia, Chandna, Sudhir

    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…”
    Get full text
    Journal Article
  4. 4
  5. 5
  6. 6
  7. 7

    Monomeric Alpha-Synuclein Exerts a Physiological Role on Brain ATP Synthase by Ludtmann, Marthe H R, Angelova, Plamena R, Ninkina, Natalia N, Gandhi, Sonia, Buchman, Vladimir L, Abramov, Andrey Y

    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…”
    Get full text
    Journal Article
  8. 8

    Picomolar concentrations of oligomeric alpha-synuclein sensitizes TLR4 to play an initiating role in Parkinson’s disease pathogenesis by Hughes, Craig D., Choi, Minee L., Ryten, Mina, Hopkins, Lee, Drews, Anna, Botía, Juan A., Iljina, Maria, Rodrigues, Margarida, Gagliano, Sarah A., Gandhi, Sonia, Bryant, Clare, Klenerman, David

    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…”
    Get full text
    Journal Article
  9. 9
  10. 10
  11. 11

    PINK1-Associated Parkinson's Disease Is Caused by Neuronal Vulnerability to Calcium-Induced Cell Death by Gandhi, Sonia, Wood-Kaczmar, Alison, Yao, Zhi, Plun-Favreau, Helene, Deas, Emma, Klupsch, Kristina, Downward, Julian, Latchman, David S., Tabrizi, Sarah J., Wood, Nicholas W., Duchen, Michael R., Abramov, Andrey Y.

    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…”
    Get full text
    Journal Article
  12. 12

    Dopamine Induces Ca2+ Signaling in Astrocytes through Reactive Oxygen Species Generated by Monoamine Oxidase by Vaarmann, Annika, Gandhi, Sonia, Abramov, Andrey Y.

    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…”
    Get full text
    Journal Article
  13. 13

    PINK1 cleavage at position A103 by the mitochondrial protease PARL by DEAS, Emma, PLUN-FAVREAU, Helene, ABRAMOV, Andrey Y, WOOD, Nicholas W, GANDHI, Sonia, DESMOND, Howard, KJAER, Svend, LOH, Samantha H. Y, RENTON, Alan E. M, HARVEY, Robert J, WHITWORTH, Alexander J, MARTINS, L. Miguel

    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…”
    Get full text
    Journal Article
  14. 14

    Mitochondrial dysfunction in Parkinsonian mesenchymal stem cells impairs differentiation by Angelova, Plamena R., Barilani, Mario, Lovejoy, Christopher, Dossena, Marta, Viganò, Mariele, Seresini, Agostino, Piga, Daniela, Gandhi, Sonia, Pezzoli, Gianni, Abramov, Andrey Y., Lazzari, Lorenza

    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…”
    Get full text
    Journal Article
  15. 15

    Urinary metabolic modulation in human participants residing in Siachen: a 1H NMR metabolomics approach by Gandhi, Sonia, Chinnadurai, Vijayakumar, Bhadra, Kuntal, Gupta, Isha, Kanwar, Ratnesh Singh

    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…”
    Get full text
    Journal Article
  16. 16
  17. 17

    Improved antioxidant activities of spice require enrichment of distinct yet closely-related metabolic pathways by Gandhi, Sonia, Saha, Manas Ranjan, Dey, Priyankar

    Published in Heliyon (01-11-2023)
    “…Improved biosynthesis of commercially and pharmacologically relevant phytometabolites through genetic and metabolic engineering is a lucrative strategy for…”
    Get full text
    Journal Article
  18. 18

    The mitochondrial protease HtrA2 is regulated by Parkinson's disease-associated kinase PINK1 by Martins, L. Miguel, Downward, Julian, Plun-Favreau, Hélène, Klupsch, Kristina, Moisoi, Nicoleta, Gandhi, Sonia, Kjaer, Svend, Frith, David, Harvey, Kirsten, Deas, Emma, Harvey, Robert J, McDonald, Neil, Wood, Nicholas W

    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…”
    Get full text
    Journal Article
  19. 19
  20. 20

    Generation of TWO G51D SNCA missense mutation iPSC lines (CRICKi011-A, CRICKi012-A) from two individuals at risk of Parkinson’s disease by Devito, Liani G., Zanjani, Zeinab Shadman, Evans, James R., Scardamaglia, Annarita, Houlden, Henry, Gandhi, Sonia, Healy, Lyn

    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…”
    Get full text
    Journal Article