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Showing 1–8 of 8 results
Advanced filters: Author: Pierre Dulac Clear advanced filters

  • This study identifies an altered chromatin conformation associated to a cardiac disorder observed in 7 independent families. A deletion of 2 diverging CTCF binding sites on 4q25 induces TAD fusion and leads to PITX2 expression dysregulation.

    • Manon Baudic
    • Hiroshige Murata
    • Julien Barc
    ResearchOpen Access
    Nature Communications
    Volume: 15, P: 1-15

  • The authors show that a gene expression switch operated by microRNAs regulates the control of puberty onset and adult fertility by the CNS by triggering increased hypothalamic Gnrh mRNA expression during the infantile period of postnatal development.

    • Andrea Messina
    • Fanny Langlet
    • Vincent Prevot
    Research
    Nature Neuroscience
    Volume: 19, P: 835-844

  • Mapping of the global potential of atmospheric water harvesting using solar energy shows that it could provide safely managed drinking water for a billion people worldwide based on climate suitability.

    • Jackson Lord
    • Ashley Thomas
    • Philipp H. Schmaelzle
    ResearchOpen Access
    Nature
    Volume: 598, P: 611-617

  • Neurological morbidity is common in children who have undergone convulsive status epilepticus (CSE), so a recent study evaluating the utility of MRI in determining the extent of brain lesions following CSE is welcome. How might imaging results from children with CSE influence diagnostic, prognostic, and therapeutic decisions?

    • Rima Nabbout
    • Olivier Dulac
    News & Views
    Nature Reviews Neurology
    Volume: 8, P: 243-244

  • Tuberous sclerosis complex (TSC) is a rare genetic condition characterized by epileptic seizures that start in infancy. Here, the authors show that these seizures are modulated by GluN2C-containing NMDA receptors in the cortex of a mouse model of TSC, and that suppressing their activity attenuates seizures.

    • N. Lozovaya
    • S. Gataullina
    • N. Burnashev
    ResearchOpen Access
    Nature Communications
    Volume: 5, P: 1-15

  • Genetically determined epilepsy with encephalopathy can develop early in life, often with prenatal onset, which makes diagnosis difficult. New molecular screening studies have identified causative mutations in patients with early-onset epilepsy with encephalopathy. What can we learn from the results of genetic screening in patients with this disorder?

    • Rima Nabbout
    • Olivier Dulac
    News & Views
    Nature Reviews Neurology
    Volume: 8, P: 129-130