ゲノム研究所の将来を計画する.

Same author

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

bioRxiv : the preprint server for biology·2026

Same author

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

Same author

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

Nature communications·2026

Same author

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

Same author

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

bioRxiv : the preprint server for biology·2025

Same author

Pangenome discovery of missing autism variants.

medRxiv : the preprint server for health sciences·2025

Same journal

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

Science (New York, N.Y.)·2026

Same journal

Local signals, systemic decline.

Science (New York, N.Y.)·2026

Same journal

The mechanics of liver regeneration.

Science (New York, N.Y.)·2026

Same journal

Computing in a memory with physics.

Science (New York, N.Y.)·2026

Same journal

Retraction.

Science (New York, N.Y.)·2026

Same journal

Making time.

Science (New York, N.Y.)·2026

関連する実験動画

ゲノム研究所の将来を計画する.

関連する概念動画

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.

関連する実験動画

ゲノム研究所の将来を計画する.

関連する概念動画

関連記事

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.