The Freud-1/CC2D1A family: Transcriptional regulators implicated in mental retardation
Author:
Publisher
Wiley
Subject
Cellular and Molecular Neuroscience
Reference46 articles.
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1. CC2D1A causes ciliopathy, intellectual disability, heterotaxy, renal dysplasia, and abnormal CSF flow;Life Science Alliance;2024-08-21
2. CaMKIV-Mediated Phosphorylation Inactivates Freud-1/CC2D1A Repression for Calcium-Dependent 5-HT1A Receptor Gene Induction;International Journal of Molecular Sciences;2024-06-04
3. Using Drosophila melanogaster to Analyse the Human Paralogs of the ESCRT-III Core Component Shrub/CHMP4/Snf7 and Its Interactions with Members of the LGD/CC2D1 Family;International Journal of Molecular Sciences;2022-07-06
4. Genetic Background Underlying 5-HT1A Receptor Functioning Affects the Response to Fluoxetine;International Journal of Molecular Sciences;2020-11-20
5. Investigation of the Brain Serotonin System Plasticity Using the Recombinant Mouse Lines Carring 1473G–Allele of Tryptophan Hydroxylase-2 Gene and Differing by the Distal Fragment of Chromosome 13 Containing 5-HT1A Receptor Gene;Neurochemical Journal;2020-10
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