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Glutamate mediated signaling in the pathophysiology of autism spectrum disorders

Pharmacology, biochemistry and behavior, 2012-02, Vol.100 (4), p.841-849

2012

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Analysis of association between components of the folate metabolic pathway and autism spectrum disorder in eastern Indian subjects

Molecular biology reports, 2022-02, Vol.49 (2), p.1281-1293

2022

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Components of the folate metabolic pathway and ADHD core traits: an exploration in eastern Indian probands

Journal of human genetics, 2017-07, Vol.62 (7), p.687-695

2017

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Quercetin Improves Behavioral Deficiencies, Restores Astrocytes and Microglia, and Reduces Serotonin Metabolism in 3‐Nitropropionic Acid‐Induced Rat Model of Huntington's Disease

CNS neuroscience & therapeutics, 2014-01, Vol.20 (1), p.10-19

2014

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Association of Dopamine Transporter Gene with Heroin Dependence in an Indian Subpopulation from Manipur

Journal of molecular neuroscience, 2021, Vol.71 (1), p.122-136

2021

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Gender-Specific Effect of 5-HT and 5-HIAA on Threshold Level of Behavioral Symptoms and Sex-Bias in Prevalence of Autism Spectrum Disorder

Frontiers in neuroscience, 2020-01, Vol.13, p.1375-1375

2020

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Attention deficit-hyperactivity disorder suffers from mitochondrial dysfunction

BBA clinical, 2016-12, Vol.6, p.153-158

2016

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Pilot study indicate role of preferentially transmitted monoamine oxidase gene variants in behavioral problems of male ADHD probands

BMC medical genetics, 2017-10, Vol.18 (1), p.109-109, Article 109

2017

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Huntington’s disease: the coming of age

Journal of genetics, 2018-07, Vol.97 (3), p.649-664

2018

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Efficacy of defensins as neutralizing agents against the deadly SARS-CoV-2

Journal of biomolecular structure & dynamics, 2023-05, Vol.41 (7), p.2911-2925

2023

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Reelin gene polymorphisms in the Indian population: A possible paternal 5′UTR-CGG-repeat-allele effect on autism

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2007-01, Vol.144B (1), p.106-112

2007

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Genetic effect of monoamine oxidase B (MAOB) gene on ASD associated behavior phenotypes

Canadian Journal of Biotechnology, 2017-10, Vol.1 (Special Issue), p.77-77

2017

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Autistic traits and components of the folate metabolic system: an explorative analysis in the eastern Indian ASD subjects

Nutritional neuroscience, 2020-11, Vol.23 (11), p.860-867

2020

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Serotonin mediated immunoregulation and neural functions: Complicity in the aetiology of autism spectrum disorders

Neuroscience and biobehavioral reviews, 2015-08, Vol.55, p.413-431

2015

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Purification and characterization of a serine protease (CESP) from mature coconut endosperm

BMC research notes, 2009-05, Vol.2 (1), p.81-81

2009

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Genetic variants of the folate metabolic system and mild hyperhomocysteinemia may affect ADHD associated behavioral problems

Progress in neuro-psychopharmacology & biological psychiatry, 2018-06, Vol.84 (Pt A), p.1-10

2018

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A single nucleotide polymorphism in OPRM1(rs483481) and risk for heroin use disorder

Journal of addictive diseases, 2020-02, Vol.38 (2), p.214-222

2020

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SLC6A4 markers modulate platelet 5-HT level and specific behaviors of autism: A study from an Indian population

Progress in neuro-psychopharmacology & biological psychiatry, 2015-01, Vol.56, p.196-206

2015

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Genetic association and gene–gene interaction analyses suggest likely involvement of ITGB3 and TPH2 with autism spectrum disorder (ASD) in the Indian population

Progress in neuro-psychopharmacology & biological psychiatry, 2013-08, Vol.45, p.131-143

2013

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Genetic variants of MAOB affect serotonin level and specific behavioral attributes to increase autism spectrum disorder (ASD) susceptibility in males

Progress in neuro-psychopharmacology & biological psychiatry, 2016-11, Vol.71, p.123-136

2016

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Glutamate mediated signaling in the pathophysiology of autism spectrum disorders: Glutamate Receptors

Pharmacology, biochemistry and behavior, 2012, Vol.100 (4), p.841-849

2012

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Mitochondrial functional alterations in relation to pathophysiology of Huntington's disease

Journal of bioenergetics and biomembranes, 2010-06, Vol.42 (3), p.217-226

2010

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Sexual dimorphic effect in the genetic association of monoamine oxidase A (MAOA) markers with autism spectrum disorder

Progress in neuro-psychopharmacology & biological psychiatry, 2014-04, Vol.50, p.11-20

2014

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Mitochondrial NAD⁺-linked State 3 respiration and complex-I activity are compromised in the cerebral cortex of 3-nitropropionic acid-induced rat model of Huntington's disease

Journal of neurochemistry, 2008, Vol.104 (2), p.420-434

2008

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Genetic analysis of reelin gene ( RELN) SNPs: No association with autism spectrum disorder in the Indian population

Neuroscience letters, 2008-08, Vol.441 (1), p.56-60

2008

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Glutamate mediated signaling in the pathophysiology of autism spectrum disorders

Analysis of association between components of the folate metabolic pathway and autism spectrum disorder in eastern Indian subjects

Components of the folate metabolic pathway and ADHD core traits: an exploration in eastern Indian probands

Quercetin Improves Behavioral Deficiencies, Restores Astrocytes and Microglia, and Reduces Serotonin Metabolism in 3‐Nitropropionic Acid‐Induced Rat Model of Huntington's Disease

Association of Dopamine Transporter Gene with Heroin Dependence in an Indian Subpopulation from Manipur

Gender-Specific Effect of 5-HT and 5-HIAA on Threshold Level of Behavioral Symptoms and Sex-Bias in Prevalence of Autism Spectrum Disorder

Attention deficit-hyperactivity disorder suffers from mitochondrial dysfunction

Pilot study indicate role of preferentially transmitted monoamine oxidase gene variants in behavioral problems of male ADHD probands

Huntington’s disease: the coming of age

Efficacy of defensins as neutralizing agents against the deadly SARS-CoV-2

Reelin gene polymorphisms in the Indian population: A possible paternal 5′UTR-CGG-repeat-allele effect on autism

Genetic effect of monoamine oxidase B (MAOB) gene on ASD associated behavior phenotypes

Autistic traits and components of the folate metabolic system: an explorative analysis in the eastern Indian ASD subjects

Serotonin mediated immunoregulation and neural functions: Complicity in the aetiology of autism spectrum disorders

Purification and characterization of a serine protease (CESP) from mature coconut endosperm

Genetic variants of the folate metabolic system and mild hyperhomocysteinemia may affect ADHD associated behavioral problems

A single nucleotide polymorphism in OPRM1(rs483481) and risk for heroin use disorder

SLC6A4 markers modulate platelet 5-HT level and specific behaviors of autism: A study from an Indian population

Genetic association and gene–gene interaction analyses suggest likely involvement of ITGB3 and TPH2 with autism spectrum disorder (ASD) in the Indian population

Genetic variants of MAOB affect serotonin level and specific behavioral attributes to increase autism spectrum disorder (ASD) susceptibility in males

Glutamate mediated signaling in the pathophysiology of autism spectrum disorders: Glutamate Receptors

Mitochondrial functional alterations in relation to pathophysiology of Huntington's disease

Sexual dimorphic effect in the genetic association of monoamine oxidase A (MAOA) markers with autism spectrum disorder

Mitochondrial NAD⁺-linked State 3 respiration and complex-I activity are compromised in the cerebral cortex of 3-nitropropionic acid-induced rat model of Huntington's disease

Genetic analysis of reelin gene ( RELN) SNPs: No association with autism spectrum disorder in the Indian population

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