Nature Search

Phylogeny and palaeobiogeography of hadrosaurian dinosaurs

M. K. BRETT-SURMAN
Research01 Feb 1979
Nature

Volume: 277, P: 560-562
Epikeratophakia for keratoconus

Brett L Halliday
Research01 Jul 1990
Eye

Volume: 4, P: 531-534
A mouse model for mitochondrial myopathy and cardiomyopathy resulting from a deficiency in the heart/muscle isoform of the adenine nucleotide translocator

Brett H. Graham
Katrina G. Waymire
Douglas C. Wallace
Research01 Jul 1997
Nature Genetics

Volume: 16, P: 226-234
Joint, multifaceted genomic analysis enables diagnosis of diverse, ultra-rare monogenic presentations

Using well-calibrated statistical methods the authors jointly analyze Undiagnosed Diseases Network genomes, identifying known and novel disease genes. Software is publicly available to support future cross-cohort rare disease discovery efforts.

Shilpa Nadimpalli Kobren
Mikhail A. Moldovan
Shamil R. Sunyaev
ResearchOpen Access07 Aug 2025
Nature Communications

Volume: 16, P: 1-19
Erratum: MCUR1 is an essential component of mitochondrial Ca²⁺ uptake that regulates cellular metabolism

Karthik Mallilankaraman
César Cárdenas
Muniswamy Madesh
Amendments and Corrections24 Dec 2012
Nature Cell Biology

Volume: 15, P: 123
Correction: Corrigenda: MCUR1 is an essential component of mitochondrial Ca²⁺ uptake that regulates cellular metabolism

Karthik Mallilankaraman
César Cárdenas
Muniswamy Madesh
Amendments and Corrections30 Jun 2015
Nature Cell Biology

Volume: 17, P: 953
Determinants of maternal adherence to child vaccination in jordan: A cross-sectional study

Wafa’a F. Ta’an
Rand A. Al-rashdan
Tareq L. Mukattash
ResearchOpen Access20 Oct 2024
Scientific Reports

Volume: 14, P: 1-8
Systematic generation of high-resolution deletion coverage of the Drosophila melanogaster genome

Annette L Parks
Kevin R Cook
Helen L Francis-Lang
Research22 Feb 2004
Nature Genetics

Volume: 36, P: 288-292
Biallelic loss-of-function variants in WDR11 are associated with microcephaly and intellectual disability

Natja Haag
Ene-Choo Tan
Cordula Knopp
ResearchOpen Access20 Aug 2021
European Journal of Human Genetics

Volume: 29, P: 1663-1668
Space radiation damage rescued by inhibition of key spaceflight associated miRNAs

In space radiation-exposed cells, targeting specific microRNAs with antagomirs can reduce cardiovascular damage and improve cellular function. Here the authors describe a reduction in inflammation and DNA double-strand break activity within these cells upon antagomir treatment.

J. Tyson McDonald
JangKeun Kim
Afshin Beheshti
ResearchOpen Access11 Jun 2024
Nature Communications

Volume: 15, P: 1-23
Barriers and drivers of positive COVID-19 vaccination behaviours among healthcare workers in Europe and Central Asia: a qualitative cross-country synthesis

Cath Jackson
Sian Smith
Brett Craig
ResearchOpen Access08 Dec 2023
Humanities and Social Sciences Communications

Volume: 10, P: 1-15
Mitofusin 1 and 2 regulation of mitochondrial DNA content is a critical determinant of glucose homeostasis

Sidarala et al. examine the importance of the mitochondrial structural proteins, Mitofusins 1 and 2 (Mfn1/2), in diabetes. They find that Mfn1/2 control blood glucose by preserving mitochondrial DNA content, rather than mitochondrial structure.

Vaibhav Sidarala
Jie Zhu
Scott A. Soleimanpour
ResearchOpen Access29 Apr 2022
Nature Communications

Volume: 13, P: 1-16
A control oriented strategy of disruption prediction to avoid the configuration collapse of tokamak reactors

Confining plasma and managing disruptions in tokamak devices is a challenge. Here the authors demonstrate a method predicting and possibly preventing disruptions and macroscopic instabilities in tokamak plasma using data from JET.

Andrea Murari
Riccardo Rossi
Michela Gelfusa
ResearchOpen Access18 Mar 2024
Nature Communications

Volume: 15, P: 1-19
Differential clock comparisons with a multiplexed optical lattice clock

Multiple ultracold ensembles of strontium atoms are trapped in the same optical lattice, realizing a multiplexed optical clock where precision measurements can benefit from having all atoms share the same trapping light and clock laser.

Xin Zheng
Jonathan Dolde
Shimon Kolkowitz
Research16 Feb 2022
Nature

Volume: 602, P: 425-430
Efficient generation of energetic ions in multi-ion plasmas by radio-frequency heating

Triggering and sustaining fusion reactions — with the goal of overall energy production — in a tokamak plasma requires efficient heating. Radio-frequency heating of a three-ion plasma is now experimentally shown to be a potentially viable technique.

Ye. O. Kazakov
J. Ongena
I. Zychor
Research19 Jun 2017
Nature Physics

Volume: 13, P: 973-978
IRGM1, a guardian of mitochondrial DAMP–mediated autoinflammation

IRGM1 is recognized as a master regulator of type I interferon responses against pathogens, while also protecting against autoimmune diseases. It has now been shown that IRGM1 controls autoinflammatory responses by modulating mitophagy flux.

Brett A. Kaufman
Ana L. Mora
News & Views05 Feb 2021
Nature Immunology

Volume: 22, P: 272-273
Enhanced performance in fusion plasmas through turbulence suppression by megaelectronvolt ions

Experiments at the Joint European Torus tokamak show improved thermal ion confinement in the presence of highly energetic ions and Alfvénic instabilities in the plasma.

S. Mazzi
J. Garcia
I. Zychor
Research30 Jun 2022
Nature Physics

Volume: 18, P: 776-782
OxPhos defects cause hypermetabolism and reduce lifespan in cells and in patients with mitochondrial diseases

A meta-analysis of 17 cohorts of mitochondrial disease patients reveals that OxPhos defects are associated with signs of hypermetabolism. Experiments in patient-derived fibroblast show that mitochondrial OxPhos defects trigger hypermetabolism in a cell-autonomous manner and this is linked to accelerated telomere shortening and epigenetic aging.

Gabriel Sturm
Kalpita R. Karan
Martin Picard
ResearchOpen Access12 Jan 2023
Communications Biology

Volume: 6, P: 1-22
Mutation in TACO1, encoding a translational activator of COX I, results in cytochrome c oxidase deficiency and late-onset Leigh syndrome

Eric Shoubridge and colleagues report the identification of a mutation in the CCDC44 gene that is causal in a Leigh syndrome pedigree. The CCDC44 gene product, TACO1, is involved in mitochondrial translation and is the first specific mitochondrial translational activator identified in mammals.

Woranontee Weraarpachai
Hana Antonicka
Eric A Shoubridge
Research07 Jun 2009
Nature Genetics

Volume: 41, P: 833-837
MCUR1 is an essential component of mitochondrial Ca²⁺ uptake that regulates cellular metabolism

The mitochondrial calcium uniporter (MCU) mediates calcium uptake by mitochondria and thus regulates cellular bioenergetics, but how MCU activity is modulated is not fully understood. Madesh, Foskett and colleagues report that the integral mitochondrial membrane protein MCUR1 (mitochondrial calcium uniporter regulator 1) binds to the MCU and promotes MCU-dependent calcium uptake to control ATP production and autophagy.

Karthik Mallilankaraman
César Cárdenas
Muniswamy Madesh
Research25 Nov 2012
Nature Cell Biology

Volume: 14, P: 1336-1343
Observation of the rare B_s⁰ →µ⁺µ⁻ decay from the combined analysis of CMS and LHCb data

Combined analysis of proton-proton collision data from the Large Hadron Collider at CERN by the CMS and LHCb collaborations leads to the observation of the extremely rare decay of the strange B meson into muons; the result is compatible with the standard model of particle physics, and does not show any signs of new physics, such as supersymmetry.

V. Khachatryan
A.M. Sirunyan
E. Pesen
ResearchOpen Access13 May 2015
Nature

Volume: 522, P: 68-72
HnRNPA2 is a novel histone acetyltransferase that mediates mitochondrial stress-induced nuclear gene expression

Manti Guha
Satish Srinivasan
Narayan G Avadhani
ResearchOpen Access06 Dec 2016
Cell Discovery

Volume: 2, P: 1-16
Small molecule-mediated allosteric activation of the base excision repair enzyme 8-oxoguanine DNA glycosylase and its impact on mitochondrial function

Gaochao Tian
Steven R. Katchur
William L. Rumsey
ResearchOpen Access29 Aug 2022
Scientific Reports

Volume: 12, P: 1-18
Functional characterization of variants of unknown significance in a spinocerebellar ataxia patient using an unsupervised machine learning pipeline

Siddharth Nath
Nicholas S. Caron
Ray Truant
ResearchOpen Access14 Apr 2022
Human Genome Variation

Volume: 9, P: 1-12
Correction to: HnRNPA2 is a novel histone acetyltransferase that mediates mitochondrial stress-induced nuclear gene expression

Manti Guha
Satish Srinivasan
Narayan G Avadhani
Amendments and CorrectionsOpen Access14 May 2019
Cell Discovery

Volume: 5, P: 1
Disruption prediction with artificial intelligence techniques in tokamak plasmas

Tokamak plasmas are prone to sudden collapses that terminate the nuclear fusion reactions. This perspective discusses the prediction of these so-called disruptions with artificial intelligence techniques.

J. Vega
A. Murari
I. Zychor
Reviews06 Jun 2022
Nature Physics

Volume: 18, P: 741-750
Digital PCR methods improve detection sensitivity and measurement precision of low abundance mtDNA deletions

Frances R. Belmonte
James L. Martin
Brett A. Kaufman
ResearchOpen Access28 Apr 2016
Scientific Reports

Volume: 6, P: 1-11
Host methylation predicts SARS-CoV-2 infection and clinical outcome

Konigsberg et al. profile DNA methylation in blood samples from SARS-CoV-2 cases and controls. The authors use machine learning to classify infected vs. non-infected individuals and predict clinical outcomes related to disease severity.

Iain R. Konigsberg
Bret Barnes
Kathleen C. Barnes
ResearchOpen Access26 Oct 2021
Communications Medicine

Volume: 1, P: 1-10
A multi-omics longitudinal aging dataset in primary human fibroblasts with mitochondrial perturbations

Gabriel Sturm
Anna S. Monzel
Martin Picard
ResearchOpen Access03 Dec 2022
Scientific Data

Volume: 9, P: 1-19

Search

Phylogeny and palaeobiogeography of hadrosaurian dinosaurs

Epikeratophakia for keratoconus

A mouse model for mitochondrial myopathy and cardiomyopathy resulting from a deficiency in the heart/muscle isoform of the adenine nucleotide translocator

Joint, multifaceted genomic analysis enables diagnosis of diverse, ultra-rare monogenic presentations

Erratum: MCUR1 is an essential component of mitochondrial Ca²⁺ uptake that regulates cellular metabolism

Correction: Corrigenda: MCUR1 is an essential component of mitochondrial Ca²⁺ uptake that regulates cellular metabolism

Determinants of maternal adherence to child vaccination in jordan: A cross-sectional study

Systematic generation of high-resolution deletion coverage of the Drosophila melanogaster genome

Biallelic loss-of-function variants in WDR11 are associated with microcephaly and intellectual disability

Space radiation damage rescued by inhibition of key spaceflight associated miRNAs

Barriers and drivers of positive COVID-19 vaccination behaviours among healthcare workers in Europe and Central Asia: a qualitative cross-country synthesis

Mitofusin 1 and 2 regulation of mitochondrial DNA content is a critical determinant of glucose homeostasis

A control oriented strategy of disruption prediction to avoid the configuration collapse of tokamak reactors

Differential clock comparisons with a multiplexed optical lattice clock

Efficient generation of energetic ions in multi-ion plasmas by radio-frequency heating

IRGM1, a guardian of mitochondrial DAMP–mediated autoinflammation

Enhanced performance in fusion plasmas through turbulence suppression by megaelectronvolt ions

OxPhos defects cause hypermetabolism and reduce lifespan in cells and in patients with mitochondrial diseases

Mutation in TACO1, encoding a translational activator of COX I, results in cytochrome c oxidase deficiency and late-onset Leigh syndrome

MCUR1 is an essential component of mitochondrial Ca²⁺ uptake that regulates cellular metabolism

Observation of the rare B_s⁰ →µ⁺µ⁻ decay from the combined analysis of CMS and LHCb data

HnRNPA2 is a novel histone acetyltransferase that mediates mitochondrial stress-induced nuclear gene expression

Small molecule-mediated allosteric activation of the base excision repair enzyme 8-oxoguanine DNA glycosylase and its impact on mitochondrial function

Functional characterization of variants of unknown significance in a spinocerebellar ataxia patient using an unsupervised machine learning pipeline

Correction to: HnRNPA2 is a novel histone acetyltransferase that mediates mitochondrial stress-induced nuclear gene expression

Disruption prediction with artificial intelligence techniques in tokamak plasmas

Digital PCR methods improve detection sensitivity and measurement precision of low abundance mtDNA deletions

Host methylation predicts SARS-CoV-2 infection and clinical outcome

A multi-omics longitudinal aging dataset in primary human fibroblasts with mitochondrial perturbations

Search

Quick links

Search

Filter By:

Search

Quick links