Mahmoud Kiaei
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Also affiliated: NewYork–Presbyterian Hospital (2004–2011); Cornell University (2002–2011); Konkuk University (2006); University of Arkansas Medical Center (2018–2023); Weill Cornell Medicine (2002–2013); Icahn School of Medicine at Mount Sinai (2004)
Research Areas
Biomedical Subjects
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Biography and Research Information
OverviewAI-generated summary
Mahmoud Kiaei's research focuses on understanding the molecular mechanisms underlying neurodegenerative diseases, particularly amyotrophic lateral sclerosis (ALS). His work utilizes a combination of computational and experimental approaches to investigate the structural and functional consequences of genetic mutations associated with ALS. This includes in silico studies to predict how mutations in proteins like profilin-1 and TUBA4A affect protein structure and interactions with potential therapeutic agents, such as riluzole and edaravone.
Kiaei also employs biochemical techniques, including hydrogen/deuterium exchange mass spectrometry, to detect structural and conformational changes in mutant proteins in vitro and in vivo. His research has explored the potential of RNA as a biomarker for ALS and investigated the aggregation of mutant profilin-1. Collaborations with researchers at the University of Arkansas for Medical Sciences and the University of Arkansas at Fayetteville contribute to his ongoing investigations. Kiaei's publication record includes studies on disease models, protein structure, and the development of therapeutic strategies for neurological disorders.
Metrics
- h-index: 33
- Publications: 56
- Citations: 4,949
Selected Publications
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A systematic review of emerging technologies to enhance the treatment of ovarian cancer (2023)
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In silico analysis of TUBA4A mutations in Amyotrophic Lateral Sclerosis to define mechanisms of microtubule disintegration (2023)
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Correction to: RNA as a Source of Biomarkers for Amyotrophic Lateral Sclerosis (2022)
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Detection of Structural and Conformational Changes in ALS-Causing Mutant Profilin1 With Hydrogen/Deuterium Exchange Mass Spectrometry and Bioinformatics Techniques (2021)
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RNA as a source of biomarkers for amyotrophic lateral sclerosis (2021)
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Mutant Profilin1 Aggregation in Amyotrophic Lateral Sclerosis: An in Vivo Biochemical Analysis (2021)
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In silico studies reveal structural deviations of mutant profilin-1 and interaction with riluzole and edaravone in amyotrophic lateral sclerosis (2021)
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Detection of structural and conformational changes in ALS-causing mutant profilin-1 with hydrogen/deuterium exchange mass spectrometry and bioinformatics techniques (2021)
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Changes in biophysical characteristics of PFN1 due to mutation causing amyotrophic lateral sclerosis (2018)
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RNA-Seq Analysis of Spinal Cord Tissues from hPFN1G118V Transgenic Mouse Model of ALS at Pre-symptomatic and End-Stages of Disease (2018)
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ALS-causing mutations in profilin-1 alter its conformational dynamics: A computational approach to explain propensity for aggregation (2018)
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Antisense-mediated reduction of EphA4 in the adult CNS does not improve the function of mice with amyotrophic lateral sclerosis (2018)
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Mutant Profilin1 transgenic mice recapitulate cardinal features of motor neuron disease (2016)
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Profilin1 biology and its mutation, actin(g) in disease (2016)
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A retrospective review of the progress in amyotrophic lateral sclerosis drug discovery over the last decade and a look at the latest strategies (2015)
Collaboration Network
Top Collaborators
- In silico analysis of TUBA4A mutations in Amyotrophic Lateral Sclerosis to define mechanisms of microtubule disintegration
- Detection of structural and conformational changes in ALS-causing mutant profilin-1 with hydrogen/deuterium exchange mass spectrometry and bioinformatics techniques
- RNA as a source of biomarkers for amyotrophic lateral sclerosis
- Detection of Structural and Conformational Changes in ALS-Causing Mutant Profilin1 With Hydrogen/Deuterium Exchange Mass Spectrometry and Bioinformatics Techniques
- A systematic review of emerging technologies to enhance the treatment of ovarian cancer
Showing 5 of 6 shared publications
- In silico studies reveal structural deviations of mutant profilin-1 and interaction with riluzole and edaravone in amyotrophic lateral sclerosis
- Changes in biophysical characteristics of PFN1 due to mutation causing amyotrophic lateral sclerosis
- Detection of structural and conformational changes in ALS-causing mutant profilin-1 with hydrogen/deuterium exchange mass spectrometry and bioinformatics techniques
- Mutant Profilin1 Aggregation in Amyotrophic Lateral Sclerosis: An in Vivo Biochemical Analysis
- Detection of Structural and Conformational Changes in ALS-Causing Mutant Profilin1 With Hydrogen/Deuterium Exchange Mass Spectrometry and Bioinformatics Techniques
- Alginate oligosaccharide protects against endoplasmic reticulum- and mitochondrial-mediated apoptotic cell death and oxidative stress
- Nrf2 and Nrf1 signaling and ER stress crosstalk: implication for proteasomal degradation and autophagy
- Interaction of 2-APB, dantrolene, and TDMT with IP3R and RyR modulates ER stress-induced programmed cell death I and II in neuron-like PC12 cells: an experimental and computational investigation
- P3‐302: Alginate oligosaccharide protects against H2O2 ‐induced endoplasmic reticulum‐ and mitochondrial‐mediated apoptotic cell death
- Changes in biophysical characteristics of PFN1 due to mutation causing amyotrophic lateral sclerosis
- Detection of structural and conformational changes in ALS-causing mutant profilin-1 with hydrogen/deuterium exchange mass spectrometry and bioinformatics techniques
- Mutant Profilin1 Aggregation in Amyotrophic Lateral Sclerosis: An in Vivo Biochemical Analysis
- Detection of Structural and Conformational Changes in ALS-Causing Mutant Profilin1 With Hydrogen/Deuterium Exchange Mass Spectrometry and Bioinformatics Techniques
- Changes in biophysical characteristics of PFN1 due to mutation causing amyotrophic lateral sclerosis
- Detection of structural and conformational changes in ALS-causing mutant profilin-1 with hydrogen/deuterium exchange mass spectrometry and bioinformatics techniques
- Mutant Profilin1 Aggregation in Amyotrophic Lateral Sclerosis: An in Vivo Biochemical Analysis
- Detection of Structural and Conformational Changes in ALS-Causing Mutant Profilin1 With Hydrogen/Deuterium Exchange Mass Spectrometry and Bioinformatics Techniques
- Profilin1 biology and its mutation, actin(g) in disease
- Mutant Profilin1 transgenic mice recapitulate cardinal features of motor neuron disease
- Molecular Dynamics Guided Design of Tocoflexol: A New Radioprotectant Tocotrienol with Enhanced Bioavailability
- Molecular Dynamics Guided Design of Tocoflexol: A New Radioprotectant Tocotrienol with Enhanced Bioavailability
- ALS-causing mutations in profilin-1 alter its conformational dynamics: A computational approach to explain propensity for aggregation
- In silico analysis of TUBA4A mutations in Amyotrophic Lateral Sclerosis to define mechanisms of microtubule disintegration
- Premature death of <scp>TDP</scp>‐43 (<scp>A</scp>315<scp>T</scp>) transgenic mice due to gastrointestinal complications prior to development of full neurological symptoms of amyotrophic lateral sclerosis
- Anticancer effect of calycopterin via PI3K/Akt and MAPK signaling pathways, ROS-mediated pathway and mitochondrial dysfunction in hepatoblastoma cancer (HepG2) cells
- Antioxidants and Anti-Inflammatory Drugs in the Treatment of Motor Neuron Disease
- Nrf2/ARE Signaling Pathway: Key Mediator in Oxidative Stress and Potential Therapeutic Target in ALS
- Neuroprotective effect of Nrf2/ARE activators, CDDO ethylamide and CDDO trifluoroethylamide, in a mouse model of amyotrophic lateral sclerosis
- Amyotrophic Lateral Sclerosis and Novel Therapeutic Strategies
- Profilin1 biology and its mutation, actin(g) in disease
- Mutant Profilin1 transgenic mice recapitulate cardinal features of motor neuron disease
- Antisense-mediated reduction of EphA4 in the adult CNS does not improve the function of mice with amyotrophic lateral sclerosis
- In silico studies reveal structural deviations of mutant profilin-1 and interaction with riluzole and edaravone in amyotrophic lateral sclerosis
- Detection of structural and conformational changes in ALS-causing mutant profilin-1 with hydrogen/deuterium exchange mass spectrometry and bioinformatics techniques
- Detection of Structural and Conformational Changes in ALS-Causing Mutant Profilin1 With Hydrogen/Deuterium Exchange Mass Spectrometry and Bioinformatics Techniques
- In silico studies reveal structural deviations of mutant profilin-1 and interaction with riluzole and edaravone in amyotrophic lateral sclerosis
- Detection of structural and conformational changes in ALS-causing mutant profilin-1 with hydrogen/deuterium exchange mass spectrometry and bioinformatics techniques
- Detection of Structural and Conformational Changes in ALS-Causing Mutant Profilin1 With Hydrogen/Deuterium Exchange Mass Spectrometry and Bioinformatics Techniques
- Mutant Profilin1 transgenic mice recapitulate cardinal features of motor neuron disease
- Molecular Dynamics Guided Design of Tocoflexol: A New Radioprotectant Tocotrienol with Enhanced Bioavailability
- Mutant Profilin1 transgenic mice recapitulate cardinal features of motor neuron disease
- A retrospective review of the progress in amyotrophic lateral sclerosis drug discovery over the last decade and a look at the latest strategies
- Alginate oligosaccharide protects against endoplasmic reticulum- and mitochondrial-mediated apoptotic cell death and oxidative stress
- P3‐302: Alginate oligosaccharide protects against H2O2 ‐induced endoplasmic reticulum‐ and mitochondrial‐mediated apoptotic cell death
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