Planificación del futuro del instituto del genoma.

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A massively parallel reporter assay of MECP2 cis-regulatory elements reveals genetic candidates for male-biased autism.

bioRxiv : the preprint server for biology·2026

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Sod1 trisomy causes ENS developmental defects and susceptibility to Hirschsprung disease via neuronal Ret suppression and glial remodeling.

bioRxiv : the preprint server for biology·2026

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Using the linear references from the pangenome to discover missing autism variants.

Nature communications·2026

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Joint disruption of Ret and Ednrb transcription shifts cell fate trajectories in the enteric nervous system in Hirschsprung disease.

Proceedings of the National Academy of Sciences of the United States of America·2025

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Sex differences in the developing human cortex intersect with genetic risk of neurodevelopmental disorders.

bioRxiv : the preprint server for biology·2025

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Pangenome discovery of missing autism variants.

medRxiv : the preprint server for health sciences·2025

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Erratum for the Research Article "Detecting supramolecular organic nanoparticles during heat wave".

Science (New York, N.Y.)·2026

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Local signals, systemic decline.

Science (New York, N.Y.)·2026

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Science (New York, N.Y.)·2026

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Computing in a memory with physics.

Science (New York, N.Y.)·2026

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Retraction.

Science (New York, N.Y.)·2026

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Making time.

Science (New York, N.Y.)·2026

Videos de Experimentos Relacionados

Planificación del futuro del instituto del genoma.

Videos de Conceptos Relacionados

A massively parallel reporter assay of <i>MECP2</i> cis-regulatory elements reveals genetic candidates for male-biased autism.

<i>Sod1</i> trisomy causes ENS developmental defects and susceptibility to Hirschsprung disease via neuronal <i>Ret</i> suppression and glial remodeling.

Using the linear references from the pangenome to discover missing autism variants.

Joint disruption of <i>Ret</i> and <i>Ednrb</i> transcription shifts cell fate trajectories in the enteric nervous system in Hirschsprung disease.

Sex differences in the developing human cortex intersect with genetic risk of neurodevelopmental disorders.

Pangenome discovery of missing autism variants.

Erratum for the Research Article "Detecting supramolecular organic nanoparticles during heat wave".

Local signals, systemic decline.

The mechanics of liver regeneration.

Computing in a memory with physics.

Retraction.

Making time.

Videos de Experimentos Relacionados

Planificación del futuro del instituto del genoma.

Videos de Conceptos Relacionados

Artículos Relacionados

A massively parallel reporter assay of <i>MECP2</i> cis-regulatory elements reveals genetic candidates for male-biased autism.

<i>Sod1</i> trisomy causes ENS developmental defects and susceptibility to Hirschsprung disease via neuronal <i>Ret</i> suppression and glial remodeling.

Using the linear references from the pangenome to discover missing autism variants.

Joint disruption of <i>Ret</i> and <i>Ednrb</i> transcription shifts cell fate trajectories in the enteric nervous system in Hirschsprung disease.

Sex differences in the developing human cortex intersect with genetic risk of neurodevelopmental disorders.

Pangenome discovery of missing autism variants.

Erratum for the Research Article "Detecting supramolecular organic nanoparticles during heat wave".

Local signals, systemic decline.

The mechanics of liver regeneration.

Computing in a memory with physics.

Retraction.

Making time.