Nature Search

Superfluidity in Neutron Stars

GORDON BAYM
CHRISTOPHER PETHICK
DAVID PINES
Research15 Nov 1969
Nature

Volume: 224, P: 673-674
Electrical Conductivity of Neutron Star Matter

GORDON BAYM
CHRISTOPHER PETHICK
DAVID PINES
Research15 Nov 1969
Nature

Volume: 224, P: 674-675
Bioinformatics analysis of homologies between pathogen antigens, autoantigens and the CFTR cystic fibrosis protein: A role for immunoadsorption therapy?

Christopher Carter
ResearchOpen Access02 Dec 2010
Nature Precedings

P: 1
A changepoint approach to automated estimation of soil moisture drydown parameters from time series data

Mengyi Gong
Jessica Davies
John N. Quinton
ResearchOpen Access02 Dec 2025
Scientific Reports

Volume: 15, P: 1-14
Whole-genome sequencing of patients with rare diseases in a national health system

Whole-genome sequencing and phenotype data sharing are introduced in a national health system to streamline diagnosis and to discover coding and non-coding variants that cause rare diseases.

Ernest Turro
William J. Astle
Willem H. Ouwehand
Research24 Jun 2020
Nature

Volume: 583, P: 96-102
Ancient Plasmodium genomes shed light on the history of human malaria

Genomic analysis of Plasmodium DNA from 36 ancient individuals provides insight into the global distribution and spread of malaria-causing species during around 5,500 years of human history.

Megan Michel
Eirini Skourtanioti
Johannes Krause
ResearchOpen Access12 Jun 2024
Nature

Volume: 631, P: 125-133
Climate and landscape drivers of a mosquito-borne pathogen in an iconic game bird in the eastern and upper midwestern USA

Melanie R. Kunkel
James A. Martin
Nicole M. Nemeth
ResearchOpen Access26 Sept 2025
Scientific Reports

Volume: 15, P: 1-12
Mutations in HFE2 cause iron overload in chromosome 1q–linked juvenile hemochromatosis

George Papanikolaou
Mark E Samuels
Y Paul Goldberg
Research30 Nov 2003
Nature Genetics

Volume: 36, P: 77-82
Senataxin, the ortholog of a yeast RNA helicase, is mutant in ataxia-ocular apraxia 2

Maria-Céu Moreira
Sandra Klur
Michel Koenig
Research08 Feb 2004
Nature Genetics

Volume: 36, P: 225-227
Tracking multiple components of a nuclear wavepacket in photoexcited Cu(I)-phenanthroline complex using ultrafast X-ray spectroscopy

Nonadiabatic excited state processes involve mixing of electronic and nuclear wavefunctions, which are difficult to disentangle. Here the authors explore by time-resolved X-ray absorption near edge structure the wavepacket dynamics of a copper(I)-phenanthroline complex, resolving different vibrational modes.

Tetsuo Katayama
Thomas Northey
Thomas J. Penfold
ResearchOpen Access09 Aug 2019
Nature Communications

Volume: 10, P: 1-8
The contribution of X-linked coding variation to severe developmental disorders

Developmental disorders (DDs) are more prevalent in males, thought to be due to X-linked genetic variation. Here, the authors investigate the burden of X-linked coding variants in 11,044 DD patients, showing that this contributes to ~6% of both male and female cases and therefore does not solely explain male bias in DDs.

Hilary C. Martin
Eugene J. Gardner
Matthew E. Hurles
ResearchOpen Access27 Jan 2021
Nature Communications

Volume: 12, P: 1-13
Evidence for 28 genetic disorders discovered by combining healthcare and research data

By integrating healthcare and exome-sequencing data from parent–offspring trios of patients with developmental disorders, 28 genes that had not previously been associated with developmental disorders were identified.

Joanna Kaplanis
Kaitlin E. Samocha
Kyle Retterer
Research14 Oct 2020
Nature

Volume: 586, P: 757-762
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
Effects of Repeated Nicotine Administration and Footshock Stress on Rat Mesoprefrontal Dopamine Systems: Evidence for Opioid Mechanisms

Tony P George
Christopher D Verrico
Robert H Roth
Research01 Jul 2000
Neuropsychopharmacology

Volume: 23, P: 79-88
Sensorimotor adaptation as a behavioural biomarker of early spinocerebellar ataxia type 6

Muriel T. N. Panouillères
Raed A. Joundi
Ned Jenkinson
ResearchOpen Access24 May 2017
Scientific Reports

Volume: 7, P: 1-12
High-resolution ¹³C metabolic flux analysis

Precise quantification of metabolic pathway fluxes is needed in many applications, e.g., microbiological engineering. The authors describe a GC–MS method for ¹³C metabolic flux analysis with data analysis using Metran software.

Christopher P. Long
Maciek R. Antoniewicz
Protocols30 Aug 2019
Nature Protocols

Volume: 14, P: 2856-2877
Author Correction: Sensorimotor adaptation as a behavioural biomarker of early spinocerebellar ataxia type 6

Muriel T. N. Panouillères
Raed A. Joundi
Ned Jenkinson
Amendments and CorrectionsOpen Access30 Apr 2018
Scientific Reports

Volume: 8, P: 1
Precise in vivo genome editing via single homology arm donor mediated intron-targeting gene integration for genetic disease correction

Keiichiro Suzuki
Mako Yamamoto
Juan Carlos Izpisua Belmonte
Research23 Aug 2019
Cell Research

Volume: 29, P: 804-819
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
Pleckstrin-2 is essential for erythropoiesis in β-thalassemic mice, reducing apoptosis and enhancing enucleation

Maria Feola et al., elucidate the compensatory role of pleckstrin-2 in ineffective erythropoiesis in β-thalassemic mice by reducing cofilin-mediated apoptosis and enhancing enucleation by activating RacGTPases. These findings could support future therapeutic interventions.

Maria Feola
Andrea Zamperone
Yelena Z. Ginzburg
ResearchOpen Access03 May 2021
Communications Biology

Volume: 4, P: 1-14

Search

Superfluidity in Neutron Stars

Electrical Conductivity of Neutron Star Matter

Bioinformatics analysis of homologies between pathogen antigens, autoantigens and the CFTR cystic fibrosis protein: A role for immunoadsorption therapy?

A changepoint approach to automated estimation of soil moisture drydown parameters from time series data

Whole-genome sequencing of patients with rare diseases in a national health system

Ancient Plasmodium genomes shed light on the history of human malaria

Climate and landscape drivers of a mosquito-borne pathogen in an iconic game bird in the eastern and upper midwestern USA

Mutations in HFE2 cause iron overload in chromosome 1q–linked juvenile hemochromatosis

Senataxin, the ortholog of a yeast RNA helicase, is mutant in ataxia-ocular apraxia 2

Tracking multiple components of a nuclear wavepacket in photoexcited Cu(I)-phenanthroline complex using ultrafast X-ray spectroscopy

The contribution of X-linked coding variation to severe developmental disorders

Evidence for 28 genetic disorders discovered by combining healthcare and research data

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

Effects of Repeated Nicotine Administration and Footshock Stress on Rat Mesoprefrontal Dopamine Systems: Evidence for Opioid Mechanisms

Sensorimotor adaptation as a behavioural biomarker of early spinocerebellar ataxia type 6

High-resolution ¹³C metabolic flux analysis

Author Correction: Sensorimotor adaptation as a behavioural biomarker of early spinocerebellar ataxia type 6

Precise in vivo genome editing via single homology arm donor mediated intron-targeting gene integration for genetic disease correction

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

Pleckstrin-2 is essential for erythropoiesis in β-thalassemic mice, reducing apoptosis and enhancing enucleation

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