Nature Search

Genome signature-based dissection of human gut metagenomes to extract subliminal viral sequences

Bacteriophages have a significant impact on microbial ecosystems, but additional tools are needed to assess viral communities. Ogilvie et al.present a new strategy to extract viral sequences from metagenomic data sets, and present new insights on their function in the gut ecosystem.

Lesley A. Ogilvie
Lucas D. Bowler
Brian V. Jones
ResearchOpen Access16 Sept 2013
Nature Communications

Volume: 4, P: 1-16
Selective suppression of IgE antibody responsiveness by maternal influence

ELLEN JARRETT
ELIZABETH HALL
Research01 Jul 1979
Nature

Volume: 280, P: 145-147
AIDS politics change rules

Elizabeth Schaefer
News17 Jan 1991
Nature

Volume: 349, P: 187
Mapping the adaptive landscape of Batesian mimicry using 3D-printed stimuli

Birds have an excellent ability to learn to discriminate harmless insects from those that they mimic on the basis of subtle differences in appearance.

Christopher H. Taylor
David James George Watson
Tom Reader
ResearchOpen Access02 Jul 2025
Nature

Volume: 644, P: 706-713
Modulation of oxygen production in Archaean oceans by episodes of Fe(II) toxicity

Earth’s initial oxygenation took several hundred million years. Experiments and geochemical modelling suggest that early photosynthetic marine microbes may have been repeatedly stressed by Fe(II) delivered by submarine volcanism.

Elizabeth D. Swanner
Aleksandra M. Mloszewska
Andreas Kappler
Research05 Jan 2015
Nature Geoscience

Volume: 8, P: 126-130
CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

Chromodomain Helicase DNA-binding (CHD) proteins have been implicated in neurodevelopmental processes. Here, the authors identify missense variants in CHD3 that disturb its chromatin remodeling activities and cause a neurodevelopmental disorder with macrocephaly and speech and language impairment.

Lot Snijders Blok
Justine Rousseau
Philippe M. Campeau
ResearchOpen Access05 Nov 2018
Nature Communications

Volume: 9, P: 1-12
Prevalence and architecture of de novo mutations in developmental disorders

Whole-exome analysis of individuals with developmental disorders shows that de novo mutations can equally cause loss or altered protein function, but that most mutations causing altered protein function have not yet been described.

Jeremy F. McRae
Stephen Clayton
Matthew E. Hurles
Research25 Jan 2017
Nature

Volume: 542, P: 433-438
Organotypic sinonasal airway culture systems are predictive of the mucociliary phenotype produced by bronchial airway epithelial cells

Juliette Delhove
Moayed Alawami
Eugene Roscioli
ResearchOpen Access10 Nov 2022
Scientific Reports

Volume: 12, P: 1-11
Evaluation of three commercial progesterone receptor assays in a single tamoxifen-treated breast cancer cohort

Elizabeth N Kornaga
Alexander C Klimowicz
Anthony M Magliocco
Research26 Aug 2016
Modern Pathology

Volume: 29, P: 1492-1500
Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

Lot Snijders Blok
Justine Rousseau
Philippe M. Campeau
Amendments and CorrectionsOpen Access15 Feb 2019
Nature Communications

Volume: 10, P: 1-4
Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

Lot Snijders Blok
Justine Rousseau
Philippe M. Campeau
Amendments and CorrectionsOpen Access02 May 2019
Nature Communications

Volume: 10, P: 1-4
A systematic comparison of three commercial estrogen receptor assays in a single clinical outcome breast cancer cohort

Elizabeth N Kornaga
Alexander C Klimowicz
Anthony M Magliocco
Research29 Apr 2016
Modern Pathology

Volume: 29, P: 799-809

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Genome signature-based dissection of human gut metagenomes to extract subliminal viral sequences

Selective suppression of IgE antibody responsiveness by maternal influence

AIDS politics change rules

Mapping the adaptive landscape of Batesian mimicry using 3D-printed stimuli

Modulation of oxygen production in Archaean oceans by episodes of Fe(II) toxicity

CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

Prevalence and architecture of de novo mutations in developmental disorders

Organotypic sinonasal airway culture systems are predictive of the mucociliary phenotype produced by bronchial airway epithelial cells

Evaluation of three commercial progesterone receptor assays in a single tamoxifen-treated breast cancer cohort

Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

A systematic comparison of three commercial estrogen receptor assays in a single clinical outcome breast cancer cohort

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