Nature Search

The POU domain is a bipartite DNA-binding structure

Richard A. Sturm
Winship Herr
Research08 Dec 1988
Nature

Volume: 336, P: 601-604
Systematic approach to the correction of intonation in wind instruments

Richard A. Smith
Geoffrey J. Daniell
Research26 Aug 1976
Nature

Volume: 262, P: 761-765
A prognostic neural epigenetic signature in high-grade glioma

A neural epigenetic signature detectable via plasma analyses is prognostic in patients with glioblastoma, resembling an oligodendrocyte-progenitor- and neuronal-progenitor-cell-like state and showing increased neuro-to-glioma synapse formation.

Richard Drexler
Robin Khatri
Franz L. Ricklefs
ResearchOpen Access17 May 2024
Nature Medicine

Volume: 30, P: 1622-1635
Publisher Correction: Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways

David L. Duffy
Gu Zhu
Nicholas G. Martin
Amendments and CorrectionsOpen Access14 Jan 2019
Nature Communications

Volume: 10, P: 1-3
Deformation of a weak subducted slab and variation of seismicity with depth

Winston C. Tao
Richard J. O'Connell
Research18 Feb 1993
Nature

Volume: 361, P: 626-628
Microtubule-associated protein 1C from brain is a two-headed cytosolic dynein

Richard B. Vallee
Joseph S. Wall
Howard S. Shpetner
Research07 Apr 1988
Nature

Volume: 332, P: 561-563
A protein from human placental nuclei binds preferentially to 5-methylcytosine-rich DNA

Lan-Hsiang Huang
Richard Wang
Melanie Ehrlich
Research15 Mar 1984
Nature

Volume: 308, P: 293-295
Individual single-wall carbon nanotubes as quantum wires

Sander J. Tans
Michel H. Devoret
Cees Dekker
Research03 Apr 1997
Nature

Volume: 386, P: 474-477
An optical atomic clock based on a highly charged ion

An optical atomic clock operating on a magnetic-dipole transition in a highly charged argon ion is shown to improve uncertainties for the absolute transition frequency and isotope shift by several orders of magnitude.

Steven A. King
Lukas J. Spieß
Piet O. Schmidt
Research02 Nov 2022
Nature

Volume: 611, P: 43-47
Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility

Meta-analysis of 36,760 cases and 375,188 controls identifies 54 loci associated with susceptibility to cutaneous melanoma. Further analysis combining nevus count and hair color GWAS results provide insights into the genetic architecture of melanoma.

Maria Teresa Landi
D. Timothy Bishop
Matthew H. Law
Research27 Apr 2020
Nature Genetics

Volume: 52, P: 494-504
Detailed study of a rare hyperluminous rotating disk in an Einstein ring 10 billion years ago

An extreme Einstein ring ~10,000 times as bright as the Milky Way in the infrared is studied with VLT/ERIS and ALMA, and the authors find that the lensed galaxy is a starburst with a fast-rotating disk, rather than being driven by a major merger.

Daizhong Liu
Natascha M. Förster Schreiber
Min S. Yun
ResearchOpen Access15 Jul 2024
Nature Astronomy

Volume: 8, P: 1181-1194
Correction: Corrigendum: Massive gene amplification drives paediatric hepatocellular carcinoma caused by bile salt export pump deficiency

Fabio Iannelli
Agnese Collino
Francesca D. Ciccarelli
Amendments and Corrections02 Jul 2015
Nature Communications

Volume: 6, P: 1
Enhancer hijacking activates GFI1 family oncogenes in medulloblastoma

Focusing on two ill-characterized subtypes of medulloblastoma (group 3 and group 4), this study identifies prevalent genomic structural variants that are restricted to these two subtypes and independently bring together coding regions of GFI1 family proto-oncogenes with active enhancer elements, leading to their mutually exclusive oncogenic activation.

Paul A. Northcott
Catherine Lee
Stefan M. Pfister
Research22 Jun 2014
Nature

Volume: 511, P: 428-434
What is leptin for, and does it act on the brain?

Richard J. Wurtman
Correspondence01 May 1996
Nature Medicine

Volume: 2, P: 492-493
Derived immune and ancestral pigmentation alleles in a 7,000-year-old Mesolithic European

A complete pre-agricultural European human genome from a ∼7,000-year-old Mesolithic skeleton suggests the existence of a common genomic signature across western and central Eurasia from the Upper Paleolithic to the Mesolithic, and ancestral alleles in several skin pigmentation genes suggest that the light skin of modern Europeans was not yet ubiquitous in Mesolithic times.

Iñigo Olalde
Morten E. Allentoft
Carles Lalueza-Fox
Research26 Jan 2014
Nature

Volume: 507, P: 225-228
A DNA prism for high-speed continuous fractionation of large DNA molecules

Lotien Richard Huang
Jonas O. Tegenfeldt
Edward C. Cox
Research03 Sept 2002
Nature Biotechnology

Volume: 20, P: 1048-1051
COVID-19 tissue atlases reveal SARS-CoV-2 pathology and cellular targets

Single-cell analysis of lung, heart, kidney and liver autopsy samples shows the molecular and cellular changes and immune response resulting from severe COVID-19 infection.

Toni M. Delorey
Carly G. K. Ziegler
Aviv Regev
Research29 Apr 2021
Nature

Volume: 595, P: 107-113
Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways

Melanocytic nevus count is associated with melanoma risk. In this study, a meta-analysis of 11 nevus GWAS studies identifies novel SNPs in KITLG and 9q32, and bivariate analysis with melanoma GWAS meta-analysis reveals that most nevus genes affect melanoma risk, while melanoma risk loci do not alter the nevus count.

David L. Duffy
Gu Zhu
Nicholas G. Martin
ResearchOpen Access14 Nov 2018
Nature Communications

Volume: 9, P: 1-10
Massive gene amplification drives paediatric hepatocellular carcinoma caused by bile salt export pump deficiency

Hepatocellular carcinoma (HCC) is associated with chronic inflammation, but the genetic basis of the disease remains unclear. Here, the authors report that defects in hepatocyte biliary transporters and subsequent liver inflammation induce genomic alterations that promote HCC in human and mouse.

Fabio Iannelli
Agnese Collino
Francesca D. Ciccarelli
Research13 May 2014
Nature Communications

Volume: 5, P: 1-12
Dissecting the genomic complexity underlying medulloblastoma

Medulloblastoma is the most common brain tumour in children; using whole-genome sequencing of tumour samples the authors show that the clinically challenging Group 3 and 4 tumours can be tetraploid, and reveal the expression of the first medulloblastoma fusion genes identified.

David T. W. Jones
Natalie Jäger
Peter Lichter
ResearchOpen Access25 Jul 2012
Nature

Volume: 488, P: 100-105
Remission of human breast cancer xenografts on therapy with humanized monoclonal antibody to HER-2 receptor and DNA-reactive drugs

Richard J Pietras
Mark D Pegram
Dennis J Slamon
Research29 Oct 1998
Oncogene

Volume: 17, P: 2235-2249
The AIMe registry for artificial intelligence in biomedical research

We present the AIMe registry, a community-driven reporting platform for AI in biomedicine. It aims to enhance the accessibility, reproducibility and usability of biomedical AI models, and allows future revisions by the community.

Julian Matschinske
Nicolas Alcaraz
David B. Blumenthal
Comments & Opinion25 Aug 2021
Nature Methods

Volume: 18, P: 1128-1131
Haloaldehyde Polymers. VIII. Preparation and Polymerization of Dichlorofluoroacetaldehyde

Bunichiro Yamada
Richard W Campbell
O Vogl
Research01 Jan 1977
Polymer Journal

Volume: 9, P: 23-31
Interplay between particle trapping and heterogeneity in anomalous diffusion

Position dependent diffusion coefficients are often estimated indirectly through mean square displacement. The authors propose a diffusion model merging position-dependent coefficients and comb-like trapping mechanisms, revealing that particle trapping mitigates the impact of media heterogeneity and that thus caution is needed in experimental interpretations.

Haroldo V. Ribeiro
Angel A. Tateishi
Matjaž Perc
ResearchOpen Access08 Sept 2023
Communications Physics

Volume: 6, P: 1-11
Recurrent somatic alterations of FGFR1 and NTRK2 in pilocytic astrocytoma

Stefan Pfister and the ICGC PedBrain Tumor Project report whole-genome sequencing of 96 pilocytic astrocytomas. They identify recurrent activating mutations in FGFR1 and PTPN11 and novel NTRK2 fusion genes.

David T W Jones
Barbara Hutter
Stefan M Pfister
Research30 Jun 2013
Nature Genetics

Volume: 45, P: 927-932
Role of MC1R variants in uveal melanoma

N Hearle
J Humphreys
R S Houlston
ResearchOpen Access11 Nov 2003
British Journal of Cancer

Volume: 89, P: 1961-1965
Tumor biomechanics as a novel imaging biomarker to assess response to immunotherapy in a murine glioma model

Yannik Streibel
Michael O. Breckwoldt
Katharina Schregel
ResearchOpen Access06 Jul 2024
Scientific Reports

Volume: 14, P: 1-15
Comprehensive reanalysis for CNVs in ES data from unsolved rare disease cases results in new diagnoses

German Demidov
Burcu Yaldiz
Steven Laurie
ResearchOpen Access26 Oct 2024
npj Genomic Medicine

Volume: 9, P: 1-24
Elevated Dopamine D_2/3 Receptor Availability in Obese Individuals: A PET Imaging Study with [¹¹C](+)PHNO

Edward C Gaiser
Jean-Dominique Gallezot
David Matuskey
Research04 Jul 2016
Neuropsychopharmacology

Volume: 41, P: 3042-3050
Inheritance of a novel mutated allele of the OCA2 gene associated with high incidence of oculocutaneous albinism in a Polynesian community

Helene C Johanson
Wei Chen
Richard A Sturm
Research18 Dec 2009
Journal of Human Genetics

Volume: 55, P: 103-111
Early cessation of a randomised study in acute graft versus host disease: upfront mesenchymal stromal cells with corticosteroids versus corticosteroids alone

Duncan Purtill
Melita Cirillo
Marian Sturm
Correspondence27 May 2020
Bone Marrow Transplantation

Volume: 55, P: 2199-2201
Adaptation and validation of the ACMG/AMP variant classification framework for MYH7-associated inherited cardiomyopathies: recommendations by ClinGen’s Inherited Cardiomyopathy Expert Panel

Melissa A Kelly
Colleen Caleshu
Birgit Funke
ResearchOpen Access04 Jan 2018
Genetics in Medicine

Volume: 20, P: 351-359

Search

The POU domain is a bipartite DNA-binding structure

Systematic approach to the correction of intonation in wind instruments

A prognostic neural epigenetic signature in high-grade glioma

Publisher Correction: Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways

Deformation of a weak subducted slab and variation of seismicity with depth

Microtubule-associated protein 1C from brain is a two-headed cytosolic dynein

A protein from human placental nuclei binds preferentially to 5-methylcytosine-rich DNA

Individual single-wall carbon nanotubes as quantum wires

An optical atomic clock based on a highly charged ion

Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility

Detailed study of a rare hyperluminous rotating disk in an Einstein ring 10 billion years ago

Correction: Corrigendum: Massive gene amplification drives paediatric hepatocellular carcinoma caused by bile salt export pump deficiency

Enhancer hijacking activates GFI1 family oncogenes in medulloblastoma

What is leptin for, and does it act on the brain?

Derived immune and ancestral pigmentation alleles in a 7,000-year-old Mesolithic European

A DNA prism for high-speed continuous fractionation of large DNA molecules

COVID-19 tissue atlases reveal SARS-CoV-2 pathology and cellular targets

Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways

Massive gene amplification drives paediatric hepatocellular carcinoma caused by bile salt export pump deficiency

Dissecting the genomic complexity underlying medulloblastoma

Remission of human breast cancer xenografts on therapy with humanized monoclonal antibody to HER-2 receptor and DNA-reactive drugs

The AIMe registry for artificial intelligence in biomedical research

Haloaldehyde Polymers. VIII. Preparation and Polymerization of Dichlorofluoroacetaldehyde

Interplay between particle trapping and heterogeneity in anomalous diffusion

Recurrent somatic alterations of FGFR1 and NTRK2 in pilocytic astrocytoma

Role of MC1R variants in uveal melanoma

Tumor biomechanics as a novel imaging biomarker to assess response to immunotherapy in a murine glioma model

Comprehensive reanalysis for CNVs in ES data from unsolved rare disease cases results in new diagnoses

Elevated Dopamine D_2/3 Receptor Availability in Obese Individuals: A PET Imaging Study with [¹¹C](+)PHNO

Inheritance of a novel mutated allele of the OCA2 gene associated with high incidence of oculocutaneous albinism in a Polynesian community

Early cessation of a randomised study in acute graft versus host disease: upfront mesenchymal stromal cells with corticosteroids versus corticosteroids alone

Adaptation and validation of the ACMG/AMP variant classification framework for MYH7-associated inherited cardiomyopathies: recommendations by ClinGen’s Inherited Cardiomyopathy Expert Panel

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