Nature Search

CRISPR/Cas9-engineering of Kell null erythrocytes to unveil host targeted irresistible antimalarial

This study highlights Kell, a zinc endopeptidase, as a key host-factor in P. falciparum invasion and demonstrates that its inhibition by Thiorphan and Racecadotril exerts potent antimalarial effects, supporting a host-targeted- therapy approach.

Geeta Kumari
Pragya Gupta
Shailja Singh
ResearchOpen Access11 May 2025
Communications Biology

Volume: 8, P: 1-14
Catalytic generation of N₂O₃ by the concerted nitrite reductase and anhydrase activity of hemoglobin

Swati Basu
Rozalina Grubina
Daniel B Kim-Shapiro
Research04 Nov 2007
Nature Chemical Biology

Volume: 3, P: 785-794
Optimizing cultivation practices to enhance growth and yield of Indian mustard

Akshita Sharma
Vandna Chhabra
Ali Salem
ResearchOpen Access03 Apr 2025
Scientific Reports

Volume: 15, P: 1-10
A second update on mapping the human genetic architecture of COVID-19

Masahiro Kanai
Shea J. Andrews
Matthew Solomonson
ResearchOpen Access06 Sept 2023
Nature

Volume: 621, P: E7-E26
Correction: Blood RNA analysis can increase clinical diagnostic rate and resolve variants of uncertain significance

Htoo A. Wai
Jenny Lord
L. Archer
Amendments and CorrectionsOpen Access01 Apr 2020
Genetics in Medicine

Volume: 22, P: 1129
Reply to 'Nitrite–methemoglobin inadequate for hypoxic vasodilation'

Bradley I. Goetz
Pamela Wang
Daniel B. Kim-Shapiro
Correspondence01 Jun 2009
Nature Chemical Biology

Volume: 5, P: 367
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
RGO/WO₃ hierarchical architectures for improved H₂S sensing and highly efficient solar-driving photo-degradation of RhB dye

Swati S. Mehta
Digambar Y. Nadargi
Sharad S. Suryavanshi
ResearchOpen Access03 Mar 2021
Scientific Reports

Volume: 11, P: 1-17
Guided internet-delivered cognitive-behaviour therapy for persons with spinal cord injury: a feasibility trial

Swati Mehta
Heather Hadjistavropoulos
Blake F. Dear
Research09 Jan 2020
Spinal Cord

Volume: 58, P: 544-552
Blood RNA analysis can increase clinical diagnostic rate and resolve variants of uncertain significance

Htoo A. Wai
Jenny Lord
L. Archer
ResearchOpen Access03 Mar 2020
Genetics in Medicine

Volume: 22, P: 1005-1014
A student and staff collaborative audit exploring the food and drinks available from a dental teaching hospital outlet

Amar S. V. K. Mohindra
Joshua Goh Hua Jie
Vanessa Muirhead
Research08 Jan 2021
British Dental Journal

Volume: 230, P: 32-38
Goat lung surfactant for treatment of respiratory distress syndrome among preterm neonates: a multi-site randomized non-inferiority trial

Kajal Jain
Sushma Nangia
Ramesh Agarwal
ResearchOpen Access04 Sept 2019
Journal of Perinatology

Volume: 39, P: 3-12
A novel natural product inspired scaffold with robust neurotrophic, neurogenic and neuroprotective action

Sumana Chakravarty
Swati Maitra
Arvind Kumar
ResearchOpen Access21 Sept 2015
Scientific Reports

Volume: 5, P: 1-11
Effect of residue and weed management practices on weed flora, yield, energetics, carbon footprint, economics and soil quality of zero tillage wheat

R. Puniya
B. R. Bazaya
Swati Mehta
ResearchOpen Access07 Nov 2023
Scientific Reports

Volume: 13, P: 1-15
A 2-oxa-spiro[5.4]decane scaffold displays neurotrophic, neurogenic and anti-neuroinflammatory activities with high potential for development as a versatile CNS therapeutic

Pranav Chintamani Joshi
Ramesh Samineni
Sumana Chakravarty
ResearchOpen Access04 May 2017
Scientific Reports

Volume: 7, P: 1-13
The CanPain SCI clinical practice guidelines for rehabilitation management of neuropathic pain after spinal cord injury: 2021 update

Eldon Loh
Magdalena Mirkowski
Swati Mehta
ResearchOpen Access05 Feb 2022
Spinal Cord

Volume: 60, P: 548-566
Mycobacterium tuberculosis Inhibits RAB7 Recruitment to Selectively Modulate Autophagy Flux in Macrophages

Pallavi Chandra
Swapnil Ghanwat
Dhiraj Kumar
ResearchOpen Access06 Nov 2015
Scientific Reports

Volume: 5, P: 1-10
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
Effectiveness of transcranial direct current stimulation for the management of neuropathic pain after spinal cord injury: a meta-analysis

S Mehta
A McIntyre
E Loh
Reviews21 Jul 2015
Spinal Cord

Volume: 53, P: 780-785

Search

CRISPR/Cas9-engineering of Kell null erythrocytes to unveil host targeted irresistible antimalarial

Catalytic generation of N₂O₃ by the concerted nitrite reductase and anhydrase activity of hemoglobin

Optimizing cultivation practices to enhance growth and yield of Indian mustard

A second update on mapping the human genetic architecture of COVID-19

Correction: Blood RNA analysis can increase clinical diagnostic rate and resolve variants of uncertain significance

Reply to 'Nitrite–methemoglobin inadequate for hypoxic vasodilation'

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

RGO/WO₃ hierarchical architectures for improved H₂S sensing and highly efficient solar-driving photo-degradation of RhB dye

Guided internet-delivered cognitive-behaviour therapy for persons with spinal cord injury: a feasibility trial

Blood RNA analysis can increase clinical diagnostic rate and resolve variants of uncertain significance

A student and staff collaborative audit exploring the food and drinks available from a dental teaching hospital outlet

Goat lung surfactant for treatment of respiratory distress syndrome among preterm neonates: a multi-site randomized non-inferiority trial

A novel natural product inspired scaffold with robust neurotrophic, neurogenic and neuroprotective action

Effect of residue and weed management practices on weed flora, yield, energetics, carbon footprint, economics and soil quality of zero tillage wheat

A 2-oxa-spiro[5.4]decane scaffold displays neurotrophic, neurogenic and anti-neuroinflammatory activities with high potential for development as a versatile CNS therapeutic

The CanPain SCI clinical practice guidelines for rehabilitation management of neuropathic pain after spinal cord injury: 2021 update

Mycobacterium tuberculosis Inhibits RAB7 Recruitment to Selectively Modulate Autophagy Flux in Macrophages

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

Effectiveness of transcranial direct current stimulation for the management of neuropathic pain after spinal cord injury: a meta-analysis

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