neuronal nuclei News Research Articles

This is a genetic map of chromosome 15q11-q13 region. This chromosome is associated with Prader-Willi syndrome.

·June 26, 2013·3 min read

Symptoms of Prader-Willi Syndrome Associated with Interference in Circadian, Metabolic Genes

Prader-Willi syndrome, a genetic disorder characterized by an insatiable appetite, is associated with the loss of non-coding RNAs; resulting in dysregulation of the circadian and metabolic genes.

neuronal nuclei

Symptoms of Prader-Willi Syndrome Associated with Interference in Circadian, Metabolic Genes

AI Detects Early Epilepsy Signs in EEG Data

Printing Monolithic Electronic Skins That Emulate Brain Chemistry

True Brain Multitasking Is Possible

Study Reverses Structural Autism Deficits in Brain Cells

Symptoms of Prader-Willi Syndrome Associated with Interference in Circadian, Metabolic Genes

AI Detects Early Epilepsy Signs in EEG Data

Printing Monolithic Electronic Skins That Emulate Brain Chemistry

True Brain Multitasking Is Possible

Study Reverses Structural Autism Deficits in Brain Cells

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