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M. Flint Beal

NewYork–Presbyterian Hospital · US
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Area of research
Molecular Biology · Neurology
Research interest
Research interests include Coenzyme Q10 studies and effects, Advancements in Battery Materials, Parkinson's Disease Mechanisms and Treatments, and Mitochondrial Function and Pathology.
h-index
3
citations
767
works
4
NIH funding
primary concept
email

Recent publications

The role of mitochondrial dysfunction in Alzheimer's disease pathogenesis
Alzheimer s & Dementia 2022cited by 431position: lastdoi
Altered succinylation of mitochondrial proteins, APP and tau in Alzheimer’s disease
Nature Communications 2022cited by 108position: middledoi
Brain energy rescue: an emerging therapeutic concept for neurodegenerative disorders of ageing
Nature Reviews Drug Discovery 2020cited by 959position: middledoi
PGC-1α, Sirtuins and PARPs in Huntington’s Disease and Other Neurodegenerative Conditions: NAD+ to Rule Them All
Neurochemical Research 2019cited by 49position: lastdoi
Rewiring of Glutamine Metabolism Is a Bioenergetic Adaptation of Human Cells with Mitochondrial DNA Mutations
Cell Metabolism 2018cited by 205position: middledoi
Benfotiamine treatment activates the Nrf2/ARE pathway and is neuroprotective in a transgenic mouse model of tauopathy
UVaDOC UVaDOC University of Valladolid Documentary Repository (University of Valladolid) 2018cited by 89position: lastdoi
Aberrant regulation of the GSK‐3β/NRF2 axis unveils a novel therapy for adrenoleukodystrophy
EMBO Molecular Medicine 2018cited by 61position: middledoi
Mitochondrial dysfunction in Parkinson's disease
Journal of Neurochemistry 2016cited by 839position: lastdoi
Distinct Nrf2 Signaling Mechanisms of Fumaric Acid Esters and Their Role in Neuroprotection against 1-Methyl-4-Phenyl-1,2,3,6-Tetrahydropyridine-Induced Experimental Parkinson's-Like Disease
Journal of Neuroscience 2016cited by 206position: middledoi
Mutant Profilin1 transgenic mice recapitulate cardinal features of motor neuron disease
Human Molecular Genetics 2016cited by 88position: middledoi
Preferential PPAR-α activation reduces neuroinflammation, and blocks neurodegeneration<i>in vivo</i>
Human Molecular Genetics 2015cited by 103position: middledoi
A Randomized Clinical Trial of High-Dosage Coenzyme Q10 in Early Parkinson Disease
JAMA Neurology 2014cited by 389position: middledoi
Inosine to Increase Serum and Cerebrospinal Fluid Urate in Parkinson Disease
JAMA Neurology 2014cited by 239position: middledoi
Methylene blue upregulates Nrf2/ARE genes and prevents tau-related neurotoxicity
Human Molecular Genetics 2014cited by 157position: middledoi
Mitochondrial Diseases of the Brain
Free Radical Biology and Medicine 2013cited by 409position: lastdoi
PGC-1α, mitochondrial dysfunction, and Huntington's disease
Free Radical Biology and Medicine 2013cited by 212position: lastdoi
Nitration of Hsp90 induces cell death
Proceedings of the National Academy of Sciences 2013cited by 145position: middledoi
A role of mitochondrial complex II defects in genetic models of Huntington's disease expressing N-terminal fragments of mutant huntingtin
Human Molecular Genetics 2013cited by 110position: middledoi
Usefulness of Proton and Phosphorus MR Spectroscopic Imaging for Early Diagnosis of Parkinson's Disease
Journal of Neuroimaging 2013cited by 52position: middledoi
Mitochondrial Dysfunction in Neurodegenerative Diseases
Journal of Pharmacology and Experimental Therapeutics 2012cited by 803position: lastdoi
Impaired mitochondrial function in psychiatric disorders
Nature reviews. Neuroscience 2012cited by 475position: middledoi
Targeting Nrf2-Mediated Gene Transcription by Extremely Potent Synthetic Triterpenoids Attenuate Dopaminergic Neurotoxicity in the MPTP Mouse Model of Parkinson's Disease
Antioxidants and Redox Signaling 2012cited by 166position: middledoi
Neuroprotection by cyclodextrin in cell and mouse models of Alzheimer disease
The Journal of Experimental Medicine 2012cited by 156position: lastdoi
Mitochondria targeted therapeutic approaches in Parkinson's and Huntington's diseases
Molecular and Cellular Neuroscience 2012cited by 135position: lastdoi
Somatic mitochondrial DNA mutations in early parkinson and incidental lewy body disease
Annals of Neurology 2012cited by 126position: middledoi
Transducer of regulated CREB-binding proteins (TORCs) transcription and function is impaired in Huntington's disease
Human Molecular Genetics 2012cited by 65position: lastdoi

Grants

No grants ingested yet.

Frequent collaborators

Noel Y. Calingasan · MIND Research Institute7 papers (2012–2018)Bobby Thomas · University of California, Davis4 papers (2012–2018)Navneet Ammal Kaidery · University of California, Davis4 papers (2012–2018)Ashu Johri · Weill Cornell Medicine3 papers (2012–2013)Rajnish Kumar Chaturvedi · NewYork–Presbyterian Hospital3 papers (2012–2013) · 3 papers (2012–2018)Magali Dumont · Centre National de la Recherche Scientifique3 papers (2014–2018)Anatoly A. Starkov · Johnson University3 papers (2014–2018)Irina G. Gazaryan · Pace University3 papers (2012–2018)Mahmoud Kiaei · NewGen Therapeutics (United States)3 papers (2013–2016)Manuj Ahuja · Bristol-Myers Squibb (United States)2 papers (2016–2018)Shilpi Yadav · University of Arkansas for Medical Sciences2 papers (2015–2016)Cliona Stack · Cornell University2 papers (2014–2018)Aurora Pujol · Université Claude Bernard Lyon 12 papers (2014–2018)Meri Gerges · Cornell University2 papers (2014–2018)Lichuan Yang · Sichuan University2 papers (2012–2016) · 2 papers (2012–2018)Michael T. Lin · Cornell University2 papers (2012–2012)Shari Jainuddin · Cornell University2 papers (2014–2018)Abigail DeLoach · University of Arkansas for Medical Sciences2 papers (2015–2016)
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