Search Results - "Rajadhyaksha, Anjali M."

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    From Gene to Behavior: L-Type Calcium Channel Mechanisms Underlying Neuropsychiatric Symptoms by Kabir, Zeeba D., Martínez-Rivera, Arlene, Rajadhyaksha, Anjali M.

    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 by Inan, Melis, Zhao, Mingrui, Manuszak, Monica, Karakaya, Cansu, Rajadhyaksha, Anjali, Pickel, Virginia M, Schwartz, Theodore H, Goldstein, Peter A, Manfredi, Giovanni

    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 by Lin, Ying, Afshar, Shiva, Rajadhyaksha, Anjali M, Potash, James B, Han, Shizhong

    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 by Baker, Madelyn R., Lee, Andrew S., Rajadhyaksha, Anjali M.

    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 by Knouse, Melissa C, McGrath, Anna G, Deutschmann, Andre U, Rich, Matthew T, Zallar, Lia J, Rajadhyaksha, Anjali M, Briand, Lisa A

    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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    Markers of Celiac Disease and Gluten Sensitivity in Children with Autism by Lau, Nga M, Green, Peter H R, Taylor, Annette K, Hellberg, Dan, Ajamian, Mary, Tan, Caroline Z, Kosofsky, Barry E, Higgins, Joseph J, Rajadhyaksha, Anjali M, Alaedini, Armin

    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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    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 by Del Prete, Dolores, Rice, Richard C., Rajadhyaksha, Anjali M., D'Adamio, Luciano

    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 by Rajadhyaksha, Anjali M., Elemento, Olivier, Puffenberger, Erik G., Schierberl, Kathryn C., Xiang, Jenny Z., Putorti, Maria L., Berciano, José, Poulin, Chantal, Brais, Bernard, Michaelides, Michel, Weleber, Richard G., Higgins, Joseph J.

    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 by Sridharan, Preethy S, Lu, Yuan, Rice, Richard C, Pieper, Andrew A, Rajadhyaksha, Anjali M

    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 by Bavley, Charlotte C., Fischer, Delaney K., Rizzo, Bryant K., Rajadhyaksha, Anjali M.

    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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    Scn2a severe hypomorphic mutation decreases excitatory synaptic input and causes autism-associated behaviors by Wang, Hong-Gang, Bavley, Charlotte C, Li, Anfei, Jones, Rebecca M, Hackett, Jonathan, Bayleyen, Yared, Lee, Francis S, Rajadhyaksha, Anjali M, Pitt, Geoffrey S

    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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