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Methods in Molecular Biology (Clifton, N.J.)|June 25, 2011
Cell-based reporter assay to analyze activation of Nod1 and Nod2Birte Zurek, Harald Bielig, Thomas A Kufer
Innate Immunity|February 12, 2011
Mutational analysis of human NOD1 and NOD2 NACHT domains reveals different modes of activationBirte Zurek, Martina Proell, Roland N Wagner, et al.
Plos One|July 26, 2012
TRIM27 negatively regulates NOD2 by ubiquitination and proteasomal degradationBirte Zurek, Ida Schoultz, Andreas Neerincx, et al.
Plos Pathogens|September 5, 2014
The cofilin phosphatase slingshot homolog 1 (SSH1) links NOD1 signaling to actin remodelingHarald Bielig, Katja Lautz, Peter R Braun, et al.
Orphanet Journal of Rare Diseases|August 14, 2020
A guide to writing systematic reviews of rare disease treatments to generate FAIR-compliant datasets: building a TreatabolomeAntonio Atalaia, Rachel Thompson, Alberto Corvo, et al.
European Journal of Human Genetics : EJHG|June 2, 2021
Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseasesBirte Zurek, Kornelia Ellwanger, Lisenka E L M Vissers, et al.
Gigascience|September 20, 2024
An interconnected data infrastructure to support large-scale rare disease researchLennart F Johansson, Steve Laurie, Dylan Spalding, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 22, 2023
A Solve-RD ClinVar-based reanalysis of 1522 index cases from ERN-ITHACA reveals common pitfalls and misinterpretations in exome sequencingAnne-Sophie Denommé-Pichon, Leslie Matalonga, Elke de Boer, et al.
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