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Publisher Correction: COVID-19 vaccine BNT162b1 elicits human antibody and T_H1 T cell responses

Ugur Sahin
Alexander Muik
Özlem Türeci
Amendments and Corrections19 Jan 2021
Nature

Volume: 590, P: E17
Author Correction: BNT162b2 vaccine induces neutralizing antibodies and poly-specific T cells in humans

Uğur Şahin
Alexander Muik
Özlem Türeci
Amendments and Corrections16 Jul 2025
Nature

Volume: 643, P: E27
Antibody resistance of SARS-CoV-2 variants B.1.351 and B.1.1.7

The SARS-CoV-2 variant B.1.1.7 can be neutralized by convalescent sera or sera from vaccinated individuals, whereas the B.1.351 variant is resistant to neutralization by these sera and by several monoclonal antibodies that are in clinical use.

Pengfei Wang
Manoj S. Nair
David D. Ho
Research08 Mar 2021
Nature

Volume: 593, P: 130-135
Author Correction: Responses to acute infection with SARS-CoV-2 in the lungs of rhesus macaques, baboons and marmosets

Dhiraj Kumar Singh
Bindu Singh
Deepak Kaushal
Amendments and Corrections18 Jan 2021
Nature Microbiology

Volume: 6, P: 413
COVID-19 vaccine BNT162b1 elicits human antibody and T_H1 T cell responses

In a phase I/II dose-escalation clinical trial, the mRNA COVID-19 vaccine BNT162b1 elicits specific T cell and antibody responses that suggest it has protective potential.

Ugur Sahin
Alexander Muik
Özlem Türeci
Research30 Sept 2020
Nature

Volume: 586, P: 594-599
BNT162b2 vaccine induces neutralizing antibodies and poly-specific T cells in humans

In a phase-I/II trial in healthy adults, the BNT162b2 vaccine induces neutralizing antibodies and poly-specific T cells against SARS-CoV-2 epitopes that are conserved in a wide range of currently circulating variants.

Ugur Sahin
Alexander Muik
Özlem Türeci
Research27 May 2021
Nature

Volume: 595, P: 572-577
Responses to acute infection with SARS-CoV-2 in the lungs of rhesus macaques, baboons and marmosets

Acute respiratory distress in macaques and baboons recapitulates COVID-19 disease progression in humans, making them suitable as models to test vaccines and therapies.

Dhiraj Kumar Singh
Bindu Singh
Deepak Kaushal
Research18 Dec 2020
Nature Microbiology

Volume: 6, P: 73-86
Genetic risk factors for COVID-19 and influenza are largely distinct

Genome-wide analyses identify variants in B3GALT5 and ST6GAL1 associated with influenza susceptibility. Knockdown of ST6GAL1 in cell culture reduces influenza infectivity, likely by interfering with the glycoprotein modifications required for viral entry.

Jack A. Kosmicki
Anthony Marcketta
Manuel A. R. Ferreira
ResearchOpen Access05 Aug 2024
Nature Genetics

Volume: 56, P: 1592-1596
Fbxw7α- and GSK3-mediated degradation of p100 is a pro-survival mechanism in multiple myeloma

The SCF ubiquitin ligase subunit Fbxw7 is a tumour suppressor that is mutated in many cancers. Pagano and colleagues now show that in multiple myeloma, Fbxw7α instead functions as a pro-survival factor by activating the NF-κB pathway through the ubiquitin-mediated degradation of p100, an NF-κB pathway inhibitor.

Luca Busino
Scott E. Millman
Michele Pagano
Research04 Mar 2012
Nature Cell Biology

Volume: 14, P: 375-385
Potent Rifampicin derivatives can clear MRSA infections at single low doses when concomitantly dosed with Vancomycin

Thomas Nittoli
Anna Brotcke Zumsteg
William Olson
ResearchOpen Access23 Oct 2023
The Journal of Antibiotics

Volume: 77, P: 57-65
Evolutionary trajectory of SARS-CoV-2 genome shifts during widespread vaccination and emergence of Omicron variant

Kaitlyn Gayvert
Sheldon McKay
Gurinder S. Atwal
ResearchOpen Access14 Nov 2023
npj Viruses

Volume: 1, P: 1-10
A novel bispecific antibody platform to direct complement activity for efficient lysis of target cells

Jonathan W. Cruz
Ermelinda Damko
Brinda C. Prasad
ResearchOpen Access19 Aug 2019
Scientific Reports

Volume: 9, P: 1-16
Population-scale analysis of common and rare genetic variation associated with hearing loss in adults

A GWAS and exome-wide association study meta-analysis identifies 53 loci affecting hearing loss risk from over half a million individuals across five cohorts. Rare variants in Mendelian hearing loss genes contribute to hearing loss risk in adults.

Kavita Praveen
Lee Dobbyn
Giovanni Coppola
ResearchOpen Access03 Jun 2022
Communications Biology

Volume: 5, P: 1-12

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