Oscillating per-cision

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Physiological brain clearance architecture revealed by neuronal protein tracing.

Cell·2026

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A mouse circadian proteome atlas.

Molecular cell·2026

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Unsaturated fat alters clock phosphorylation to align rhythms to the season in mice.

Science (New York, N.Y.)·2025

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<i>CACNA1D</i> is a circadian gene and causes familial advanced sleep phase.

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

Same author

The SIK3-N783Y mutation is associated with the human natural short sleep trait.

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

Same author

The ZFHX3 GGC Repeat Expansion Underlying Spinocerebellar Ataxia Type 4 has a Common Ancestral Founder.

Movement disorders : official journal of the Movement Disorder Society·2024

Same journal

The human claustrum supports cognitive networks for externally and internally driven task demands.

PLoS biology·2026

Same journal

Unusual decay: Recombination loss leads to splicing errors in green algae.

PLoS biology·2026

Same journal

Angptl5 restricts primitive hematopoiesis by promoting retinoic acid signaling in zebrafish.

PLoS biology·2026

Same journal

Engineered bipaternal mice reveal the consequences of life without a maternal genomic contribution.

PLoS biology·2026

Same journal

Multiple adhesion molecules act together in oligodendrocyte-mediated axonal selection and myelin formation.

PLoS biology·2026

Same journal

Splicing deficiency is driven by genomic erosion in non-recombining algal mating-type chromosomes.

PLoS biology·2026

Related Experiment Videos

Oscillating per-cision

Related Concept Videos

Physiological brain clearance architecture revealed by neuronal protein tracing.

A mouse circadian proteome atlas.

Unsaturated fat alters clock phosphorylation to align rhythms to the season in mice.

<i>CACNA1D</i> is a circadian gene and causes familial advanced sleep phase.

The SIK3-N783Y mutation is associated with the human natural short sleep trait.

The ZFHX3 GGC Repeat Expansion Underlying Spinocerebellar Ataxia Type 4 has a Common Ancestral Founder.

The human claustrum supports cognitive networks for externally and internally driven task demands.

Unusual decay: Recombination loss leads to splicing errors in green algae.

Angptl5 restricts primitive hematopoiesis by promoting retinoic acid signaling in zebrafish.

Engineered bipaternal mice reveal the consequences of life without a maternal genomic contribution.

Multiple adhesion molecules act together in oligodendrocyte-mediated axonal selection and myelin formation.

Splicing deficiency is driven by genomic erosion in non-recombining algal mating-type chromosomes.

Related Experiment Videos

Oscillating per-cision

Related Concept Videos

Related Articles

Physiological brain clearance architecture revealed by neuronal protein tracing.

A mouse circadian proteome atlas.

Unsaturated fat alters clock phosphorylation to align rhythms to the season in mice.

<i>CACNA1D</i> is a circadian gene and causes familial advanced sleep phase.

The SIK3-N783Y mutation is associated with the human natural short sleep trait.

The ZFHX3 GGC Repeat Expansion Underlying Spinocerebellar Ataxia Type 4 has a Common Ancestral Founder.

The human claustrum supports cognitive networks for externally and internally driven task demands.

Unusual decay: Recombination loss leads to splicing errors in green algae.

Angptl5 restricts primitive hematopoiesis by promoting retinoic acid signaling in zebrafish.

Engineered bipaternal mice reveal the consequences of life without a maternal genomic contribution.

Multiple adhesion molecules act together in oligodendrocyte-mediated axonal selection and myelin formation.

Splicing deficiency is driven by genomic erosion in non-recombining algal mating-type chromosomes.