Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

Advertisement

Nature

View all journals
Search
Log in

nature
search

Search

Advanced search

Filter By:

Journal Check one or more journals to show results from those journals only.

Scientific Reports (44)
Nature (42)
Nature Communications (29)
Nature Genetics (27)
Oncogene (22)

Choose more journals

Article type Check one or more article types to show results from those article types only.

Research (264)
Reviews (13)
Amendments and Corrections (8)
News & Views (6)
Correspondence (3)
Special Features (2)
Comments & Opinion (1)
News (1)

Subject Check one or more subjects to show results from those subjects only.

Biochemistry
Biological techniques
Biomarkers
Biotechnology
Cancer
Cell biology
Chemical biology
Computational biology and bioinformatics
Diseases
Drug discovery
Environmental sciences
Evolution
Genetics
Health care
Immunology
Medical research
Microbiology
Molecular biology
Neuroscience
Physics

Date Choose a date option to show results from those dates only.

Today
Last 7 days
Last 30 days
Last 12 months
Last 2 years
Last 5 years

Custom date range

Clear all filters

Sort by:

Relevance

Date published (new to old)

Date published (old to new)

Showing 1–50 of 298 results

Advanced filters: Author: C Tsui Clear advanced filters

Bradykinesia induced by pallidal neurostimulation in dystonia: clinical risk factors and anatomical mapping

Florian Lange
Diego L. Guarin
Martin M. Reich
ResearchOpen Access23 Oct 2025
npj Parkinson's Disease

Volume: 11, P: 1-12
Detection of over 98% cystic fibrosis mutations in a Celtic population

C. Férec
M.P. Audrezet
C. Verlingue
Research01 Jun 1992
Nature Genetics

Volume: 1, P: 188-191
A polymorphic DNA marker linked to cystic fibrosis is located on chromosome 7

Robert G. Knowlton
Odile Cohen-Haguenauer
Helen Donis-Keller
Research28 Nov 1985
Nature

Volume: 318, P: 380-382
Anticoagulation to prevent ischemic stroke and neurocognitive impairment in atrial fibrillation: the BRAIN-AF randomized clinical trial

In a multicenter, randomized trial of patients with atrial fibrillation and a low risk of thromboembolic events, treatment with the anticoagulant rivaroxaban showed no benefit in reducing cognitive decline, stroke or transient ischemic attack when compared to placebo.

Léna Rivard
Paul Khairy
William Liang
ResearchOpen Access07 Jan 2026
Nature Medicine

Volume: 32, P: 297-305
The Taiwan Precision Medicine Initiative provides a cohort for large-scale studies

The Taiwan Precision Medicine Initiative (TPMI) has built a cohort of more than half a million individuals with Han Chinese ancestry, providing a rich resource of genetic and medical data for this group.

Hsin-Chou Yang
Pui-Yan Kwok
Jer-Yuarn Wu
ResearchOpen Access15 Oct 2025
Nature

Volume: 648, P: 117-127
The origin of the major cystic fibrosis mutation (ΔF508) in European populations

N. Morral
J. Bertranpetit
L. Kadasi
Research01 Jun 1994
Nature Genetics

Volume: 7, P: 169-175
Publisher Correction: Anticoagulation to prevent ischemic stroke and neurocognitive impairment in atrial fibrillation: the BRAIN-AF randomized clinical trial

Léna Rivard
Paul Khairy
William Liang
Amendments and CorrectionsOpen Access04 Feb 2026
Nature Medicine

Volume: 32, P: 767
Population-specific polygenic risk scores for people of Han Chinese ancestry

The Taiwan Precision Medicine Initiative recruited and genotyped more than half a million Taiwanese participants, almost all of Han Chinese ancestry, and performed comprehensive genomic analyses and developed polygenic risk score prediction models for numerous health conditions.

Hung-Hsin Chen
Chien-Hsiun Chen
Cathy S. J. Fann
ResearchOpen Access15 Oct 2025
Nature

Volume: 648, P: 128-137
Responses of a Fern Apex to Gibberellic Acid, Kinetin and α-Naphthaleneacetic Acid

C. W. WARDLAW
G. C. MITRA
Research08 Feb 1958
Nature

Volume: 181, P: 400-401
The murine Xe169 gene escapes X–inactivation like its human homologue

Jingshi Wu
Eduardo C. Salido
Larry J. Shapiro
Research01 Aug 1994
Nature Genetics

Volume: 7, P: 491-496
Lymph nodes fuel KLF2-dependent effector CD8⁺ T cell differentiation during chronic infection and checkpoint blockade

Here the authors show a function for lymph nodes in the maintenance of effector T cell differentiation and function during chronic infection and checkpoint blockade, identifying a spatial component in the regulation of exhausted T cell fitness.

Carlson Tsui
Leonie Heyden
Axel Kallies
Research15 Sept 2025
Nature Immunology

Volume: 26, P: 1752-1765
A mutation in CFTR produces different phenotypes depending on chromosomal background

S. Kiesewetter
M. Macek Jr.
G. R. Cutting
Research01 Nov 1993
Nature Genetics

Volume: 5, P: 274-278
Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephaly

E. Belloni
M. Muenke
S.W. Scherer
Research01 Nov 1996
Nature Genetics

Volume: 14, P: 353-356
IκBβ enhances the generation of the low-affinity NFκB/RelA homodimer

The NFκB signalling pathway is regulated through the formation of transcription factor dimers but mechanisms controlling their formation are poorly understood. Here, Tsui et al. report that IκBb is a positive regulator of Rel-NFκB dimer formation, using in vitro and in vivoexperiments and mathematical modelling.

Rachel Tsui
Jeffrey D. Kearns
Alexander Hoffmann
Research07 May 2015
Nature Communications

Volume: 6, P: 1-10
Genomic surveillance uncovers regional variation in HCV transmission networks in rural United States

This study explores the genetic structure of hepatitis C virus outbreaks in rural U.S communities affected by the opioid crisis. Analysis of intra-host viral populations from 692 participants reveals hidden transmission networks.

Damien C. Tully
David J. Bean
Todd M. Allen
ResearchOpen Access02 Dec 2025
Nature Communications

Volume: 17, P: 1-16
Clinical impact of pharmacogenetic risk variants in a large chinese cohort

Here the authors reveal a study of 486,956 Han Chinese individuals showing that most people with genetic variants affecting drug response do not have the predicted adverse events, highlighting the challenges of implementing pharmacogenetics in clinical practice.

Chun-Yu Wei
Ming-Shien Wen
Pui-Yan Kwok
ResearchOpen Access09 Jul 2025
Nature Communications

Volume: 16, P: 1-15
CRISPR screens and lectin microarrays identify high mannose N-glycan regulators

Glycan synthesis is regulated by the concerted activity of many genes. Here, Tsui et al. present a generalizable strategy utilizing CRISPR screens and lectin microarrays to identify and characterize regulators of glycosylation.

C. Kimberly Tsui
Nicholas Twells
Andrew Dillin
ResearchOpen Access18 Nov 2024
Nature Communications

Volume: 15, P: 1-13
Common origins of BRCA1 mutations in Canadian breast and ovarian cancer families

J. Simard
P. Tonin
S.A. Narod
Research01 Dec 1994
Nature Genetics

Volume: 8, P: 392-398
Delayed crystallization response-inspired waterborne polyurethane with high performance

Waterborne polyurethane elastomers eliminate the organic solvent emissions encountered in conventional polyurethane production. Here, a high strength and high toughness waterborne polyurethane elastomer was developed, where mechanical properties were enhanced via a delayed crystallisation response process.

Chenxi Huyan
Dong Liu
Liqun Zhang
ResearchOpen Access29 Oct 2025
Nature Communications

Volume: 16, P: 1-11
Mitochondrial Diseases in Men and Mice

Douglas C Wallace
Research01 Jan 2000
Genetics in Medicine

Volume: 2, P: 6
X-ray analysis of βB2-crystallin and evolution of oligomeric lens proteins

B. Bax
R. Lapatto
C. Slingsby
Research25 Oct 1990
Nature

Volume: 347, P: 776-780
The Drosophila claret segregation protein is a minus-end directed motor molecule

Richard A. Walker
Edward D. Salmon
Sharyn A. Endow
Research25 Oct 1990
Nature

Volume: 347, P: 780-782
Lymph-node-derived stem-like but not tumor-tissue-resident CD8⁺ T cells fuel anticancer immunity

Here the authors dissect the developmental and functional relationship between tumor-responsive cytotoxic T cells in the tumor versus the tumor-draining lymph nodes (tdLNs), finding that stem-like T_PEX cells dependent on MYB in the tdLNs are required for CD8⁺ T cell tumor infiltration and ICB responses.

Sharanya K. M. Wijesinghe
Lisa Rausch
Axel Kallies
Research29 Jul 2025
Nature Immunology

Volume: 26, P: 1367-1383
Complexity in a monogenic disease

Xavier Estivill
News & Views01 Apr 1996
Nature Genetics

Volume: 12, P: 348-350
Production of human clotting Factor IX without toxicity in mice after vascular delivery of a lentiviral vector

Lisa V. Tsui
Michael Kelly
James G. McArthur
Research01 Jan 2002
Nature Biotechnology

Volume: 20, P: 53-57
Molecular genetic approaches to the analysis of human ophthalmic disease

David N Cooper
Marcelle Jay
Barrie Jay
Research01 Nov 1987
Eye

Volume: 1, P: 699-721
Pigments in Trichophyton rubrum

P. D. MIER
Research25 May 1957
Nature

Volume: 179, P: 1084-1085
Alteration of Sulfation of Glycoconjugates, but Not Sulfate Transport and Intracellular Inorganic Sulfate Content in Cystic Fibrosis Airway Epithelial Cells

Nirupama K Mohapatra
Pi-Wan Cheng
Thomas F Boat
Research01 Jul 1995
Pediatric Research

Volume: 38, P: 42-48
NaCl enhances CD8⁺ T cell effector functions in cancer immunotherapy

Along with a back-to-back published paper from Zielisnki and co. in this issue of Nature Immunology, this paper shows that NaCl affects CD8⁺ T cell function by counteracting the exhaustion of these cells in the tumor microenvironment.

Caterina Scirgolea
Rosa Sottile
Enrico Lugli
Research28 Aug 2024
Nature Immunology

Volume: 25, P: 1845-1857
The facts on cystic fibrosis testing

DAVID J.H. BROCK
VERONICA VAN HEYNINGEN
Research16 Jan 1986
Nature

Volume: 319, P: 184
AAV9-mediated MYBPC3 gene therapy with optimized expression cassette enhances cardiac function and survival in MYBPC3 cardiomyopathy models

Loss-of-function mutations in Myosin Binding Protein C3, MYBPC3, are the most common genetic cause of hypertrophic cardiomyopathy. Here, the authors present an AAV9-based gene therapy system with an optimized expression cassette with minimal promoter and cis-regulatory elements that can ameliorate cardiac functions and prolong survival in a murine MYBPC3-deficient model.

Amara Greer-Short
Anna Greenwood
Laura M. Lombardi
ResearchOpen Access04 Mar 2025
Nature Communications

Volume: 16, P: 1-18
Quantized fractional Thouless pumping of solitons

Interactions between photons arise due to the presence of optical nonlinearities. In topological Thouless pumps, a sufficiently strong nonlinearity leads to soliton transport with a fractionally quantized plateau structure—reminiscent of transport in the fractional quantum Hall effect.

Marius Jürgensen
Sebabrata Mukherjee
Mikael C. Rechtsman
Research12 Jan 2023
Nature Physics

Volume: 19, P: 420-426
Photodissociation of particulate nitrate as a source of daytime tropospheric Cl₂

This study unravels an important daytime Cl₂ source in the extra-polar atmosphere and shows that photolysis of particle nitrate at high acidity produced unprecedented levels of Cl₂, boosting the oxidative power and air pollutants like O₃.

Xiang Peng
Tao Wang
Jianmin Chen
ResearchOpen Access17 Feb 2022
Nature Communications

Volume: 13, P: 1-10
Association of nucleophosmin/B23 with bladder cancer recurrence based on immunohistochemical assessment in clinical samples

Ke-hung Tsui
Horng-heng Juang
Benjamin Yat-ming Yung
Research01 Mar 2008
Acta Pharmacologica Sinica

Volume: 29, P: 364-370
Alteration of the N-Formyl-Methionyl-Leucyl- Phenylalanine-Induced Response in Cystic Fibrosis Neutrophils

Thierry Kemp
Angèle Schram-Doumont
Claude Szpirer
Research01 Jun 1986
Pediatric Research

Volume: 20, P: 520-526
Demonstration of Super-X divertor exhaust control for transient heat load management in compact fusion reactors

Managing power exhaust in fusion reactors is a key challenge, especially in compact designs for cost-effective commercial energy. This study shows how alternative divertor configurations improve exhaust control, enhance stability, absorb transients and enable independent plasma regulation.

B. Kool
K. Verhaegh
V. Zamkovska
ResearchOpen Access05 Sept 2025
Nature Energy

Volume: 10, P: 1116-1131
Mutations in the human Jagged1 gene are responsible for Alagille syndrome

Takaya Oda
Abdel G. Elkahloun
Settara C. Chandrasekharappa
Research01 Jul 1997
Nature Genetics

Volume: 16, P: 235-242
Multimodal sensor dataset from vehicle-mounted mobile mapping system for comprehensive urban scenes

Shengyu Lu
Sheng Bao
Daping Yang
ResearchOpen Access13 Aug 2025
Scientific Data

Volume: 12, P: 1-12
Non–invasive liposome–mediated gene delivery can correct the ion transport defect in cystic fibrosis mutant mice

E. W. F. W. Alton
P. G. Middleton
D. J. Porteous
Research01 Oct 1993
Nature Genetics

Volume: 5, P: 135-142
CFTR expression is regulated during both the cycle of the seminiferous epithelium and the oestrous cycle of rodents

Ann E.O. Trezise
Carol C. Linder
Manual Buchwald
Research01 Feb 1993
Nature Genetics

Volume: 3, P: 157-164
A candidate for the cystic fibrosis locus isolated by selection for methylation-free islands

Xavier Estivill
Martin Farrall
Brandon J. Wainwright
Research01 Apr 1987
Nature

Volume: 326, P: 840-845
The Wilson disease gene is a putative copper transporting P–type ATPase similar to the Menkes gene

Peter C. Bull
Gordon R. Thomas
Diane Wilson Cox
Research01 Dec 1993
Nature Genetics

Volume: 5, P: 327-337
Disruption of seasonal influenza circulation and evolution during the 2009 H1N1 and COVID-19 pandemics in Southeastern Asia

East, South, and Southeast Asia are key regions in the dissemination of seasonal influenza viruses, but major perturbations (e.g., pandemics) may disrupt their role. Here, the authors demonstrate the impact of the 2009 H1N1 and COVID-19 pandemics on seasonal influenza circulation and evolution within Southeastern Asia.

Zhiyuan Chen
Joseph L.-H. Tsui
Hongjie Yu
ResearchOpen Access08 Jan 2025
Nature Communications

Volume: 16, P: 1-14
Polar Mapper: a computational tool for integrated visualization of protein interaction networks and mRNA expression data

Joana P. Gonçalves
Mário Grãos
Andre Valente
ResearchOpen Access15 Dec 2008
Nature Precedings

P: 1
Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS)

Lorraine A. Everett
Benjamin Glaser
Eric D. Green
Research01 Dec 1997
Nature Genetics

Volume: 17, P: 411-422
Identification of a 1300 kilobase deletion unit on chromosome 7q31.3 in invasive epithelial ovarian carcinomas

M I Edelson
S W Scherer
S C Mok
Research19 Jun 1997
Oncogene

Volume: 14, P: 2979-2984
Genomic epidemiology of SARS-CoV-2 under an elimination strategy in Hong Kong

Hong Kong has used an elimination strategy to control SARS-CoV-2 with stringent measures including traveller quarantine. Here, the authors show that the majority of community-acquired cases until January 2021 resulted from three importations, and that increased transmission followed prolonged periods of restrictions, likely due to adherence fatigue.

Haogao Gu
Ruopeng Xie
Leo L. M. Poon
ResearchOpen Access08 Feb 2022
Nature Communications

Volume: 13, P: 1-10
Enhanced specificity of clinical high-sensitivity tumor mutation profiling in cell-free DNA via paired normal sequencing using MSK-ACCESS

Liquid biopsies allow the non-invasive detection of somatic mutations from tumours. Here, the authors develop and test MSK-ACCESS, an NGS-based clinical assay for identifying low frequency mutations in 129 genes and describe how it benefits patients in the clinic.

A. Rose Brannon
Gowtham Jayakumaran
Ryma Benayed
ResearchOpen Access18 Jun 2021
Nature Communications

Volume: 12, P: 1-12
An intron in the 23S ribosomal RNA gene of the archaebacterium Desulfurococcus mobilis

Jørgen Kjems
Roger A. Garrett
Research19 Dec 1985
Nature

Volume: 318, P: 675-677
Germline and somatic mutations in the tyrosine kinase domain of the MET proto-oncogene in papillary renal carcinomas

Laura Schmidt
Fuh-Mei Duh
Berton Zbar
Research01 May 1997
Nature Genetics

Volume: 16, P: 68-73

Previous page
page 1
page 2
page 3
…
page 6
Next page

Search

Search articles by subject, keyword or author

Show results from

Advanced search

Quick links

Explore articles by subject
Find a job
Guide to authors
Editorial policies

Nature.com

nature.com sitemap

About Nature Portfolio

About us
Press releases
Press office
Contact us

Discover content

Journals A-Z
Articles by subject
protocols.io
Nature Index

Publishing policies

Nature portfolio policies
Open access

Author & Researcher services

Reprints & permissions
Research data
Language editing
Scientific editing
Nature Masterclasses
Research Solutions

Libraries & institutions

Librarian service & tools
Librarian portal
Open research
Recommend to library

Advertising & partnerships

Advertising
Partnerships & Services
Media kits
Branded content

Professional development

Nature Awards
Nature Careers
Nature Conferences

Regional websites

Nature Africa
Nature China
Nature India
Nature Japan
Nature Middle East

Privacy Policy
Use of cookies
Legal notice
Accessibility statement
Terms & Conditions
Your US state privacy rights

© 2026 Springer Nature Limited