Search Results - "Rajadhyaksha, Anjali M."
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From Gene to Behavior: L-Type Calcium Channel Mechanisms Underlying Neuropsychiatric Symptoms
Published in Neurotherapeutics (01-07-2017)“…The L-type calcium channels (LTCCs) Ca v 1.2 and Ca v 1.3, encoded by the CACNA1C and CACNA1D genes, respectively, are important regulators of calcium influx…”
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Energy deficit in parvalbumin neurons leads to circuit dysfunction, impaired sensory gating and social disability
Published in Neurobiology of disease (01-09-2016)“…Abstract Parvalbumin-expressing, fast spiking interneurons have high-energy demands, which make them particularly susceptible to energy impairment. Recent…”
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A Machine Learning Approach to Predicting Autism Risk Genes: Validation of Known Genes and Discovery of New Candidates
Published in Frontiers in genetics (10-09-2020)“…Autism spectrum disorder (ASD) is a complex neurodevelopmental condition with a strong genetic basis. The role of mutations in ASD has been well established,…”
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L-type calcium channels and neuropsychiatric diseases: Insights into genetic risk variant-associated genomic regulation and impact on brain development
Published in Channels (Austin, Tex.) (31-12-2023)“…Recent human genetic studies have linked a variety of genetic variants in the CACNA1C and CACNA1D genes to neuropsychiatric and neurodevelopmental disorders…”
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Sex differences in the medial prefrontal cortical glutamate system
Published in Biology of sex differences (08-11-2022)“…Dysregulation in the prefrontal cortex underlies a variety of psychiatric illnesses, including substance use disorder, depression, and anxiety. Despite the…”
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Regulation of social interaction in mice by a frontostriatal circuit modulated by established hierarchical relationships
Published in Nature communications (29-04-2023)“…Social hierarchies exert a powerful influence on behavior, but the neurobiological mechanisms that detect and regulate hierarchical interactions are not well…”
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Markers of Celiac Disease and Gluten Sensitivity in Children with Autism
Published in PloS one (18-06-2013)“…Gastrointestinal symptoms are a common feature in children with autism, drawing attention to a potential association with celiac disease or gluten sensitivity…”
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Rescue of Learning and Memory Deficits in the Human Nonsyndromic Intellectual Disability Cereblon Knock-Out Mouse Model by Targeting the AMP-Activated Protein Kinase-mTORC1 Translational Pathway
Published in The Journal of neuroscience (14-03-2018)“…A homozygous nonsense mutation in the cereblon ( ) gene results in autosomal recessive, nonsyndromic intellectual disability that is devoid of other phenotypic…”
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Extinction of Contextual Cocaine Memories Requires Cav1.2 within D1R-Expressing Cells and Recruits Hippocampal Cav1.2-Dependent Signaling Mechanisms
Published in The Journal of neuroscience (06-12-2017)“…Exposure to cocaine-associated contextual cues contributes significantly to relapse. Extinction of these contextual associations, which involves a new form of…”
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Contribution of D1R-expressing neurons of the dorsal dentate gyrus and Cav1.2 channels in extinction of cocaine conditioned place preference
Published in Neuropsychopharmacology (New York, N.Y.) (01-08-2020)“…Cocaine-associated contextual cues can trigger relapse behavior by recruiting the hippocampus. Extinction of cocaine-associated contextual memories can reduce…”
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Ligand-mediated protein degradation reveals functional conservation among sequence variants of the CUL4-type E3 ligase substrate receptor cereblon
Published in The Journal of biological chemistry (20-04-2018)“…Upon binding to thalidomide and other immunomodulatory drugs, the E3 ligase substrate receptor cereblon (CRBN) promotes proteosomal destruction by engaging the…”
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Sensory-Derived Glutamate Regulates Presynaptic Inhibitory Terminals in Mouse Spinal Cord
Published in Neuron (Cambridge, Mass.) (15-06-2016)“…Circuit function in the CNS relies on the balanced interplay of excitatory and inhibitory synaptic signaling. How neuronal activity influences synaptic…”
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Forebrain elimination of cacna1c mediates anxiety-like behavior in mice
Published in Molecular psychiatry (01-11-2012)Get full text
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Amyloid Precursor Protein (APP) May Act as a Substrate and a Recognition Unit for CRL4CRBN and Stub1 E3 Ligases Facilitating Ubiquitination of Proteins Involved in Presynaptic Functions and Neurodegeneration
Published in The Journal of biological chemistry (12-08-2016)“…The amyloid precursor protein (APP), whose mutations cause Alzheimer disease, plays an important in vivo role and facilitates transmitter release. Because the…”
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Mutations in FLVCR1 Cause Posterior Column Ataxia and Retinitis Pigmentosa
Published in American journal of human genetics (12-11-2010)“…The study of inherited retinal diseases has advanced our knowledge of the cellular and molecular mechanisms involved in sensory neural signaling. Dysfunction…”
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Loss of Cav1.2 channels impairs hippocampal theta burst stimulation-induced long-term potentiation
Published in Channels (Austin, Tex.) (01-01-2020)“…CACNA1 C, which codes for the Ca 1.2 isoform of L-type Ca channels (LTCCs), is a prominent risk gene in neuropsychiatric and neurodegenerative conditions. A…”
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Cav1.2 channels mediate persistent chronic stress-induced behavioral deficits that are associated with prefrontal cortex activation of the p25/Cdk5-glucocorticoid receptor pathway
Published in Neurobiology of stress (01-12-2017)“…Chronic stress is known to precipitate and exacerbate neuropsychiatric symptoms, and exposure to stress is particularly pathological in individuals with…”
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Cocaine- and stress-primed reinstatement of drug-associated memories elicit differential behavioral and frontostriatal circuit activity patterns via recruitment of L-type Ca2+ channels
Published in Molecular psychiatry (09-09-2019)“…Cocaine-associated memories are critical drivers of relapse in cocaine-dependent individuals that can be evoked by exposure to cocaine or stress. Whether these…”
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Correction: D-cycloserine improves synaptic transmission in an animal mode of Rett syndrome
Published in PloS one (2018)“…[This corrects the article DOI: 10.1371/journal.pone.0183026.]…”
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Scn2a severe hypomorphic mutation decreases excitatory synaptic input and causes autism-associated behaviors
Published in JCI insight (09-08-2021)“…SCN2A, encoding the neuronal voltage-gated Na+ channel NaV1.2, is one of the most commonly affected loci linked to autism spectrum disorders (ASDs). Most…”
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