Showing results (441-450 of 519) with videos related to
Sort By:
Pageof 52
Viruses|August 28, 2021
The Positive Rhinovirus/Enterovirus Detection and SARS-CoV-2 Persistence beyond the Acute Infection Phase: An Intra-Household Surveillance StudyPedro Brotons, Iolanda Jordan, Quique Bassat, et al.Nature Communications|June 12, 2021
E2F6 initiates stable epigenetic silencing of germline genes during embryonic developmentThomas Dahlet, Matthias Truss, Ute Frede, et al.Journal of Oral Microbiology|June 9, 2021
Citizen-science based study of the oral microbiome in Cystic fibrosis and matched controls reveals major differences in diversity and abundance of bacterial and fungal speciesJesse R Willis, Ester Saus, Susana Iraola-Guzmán, et al.Science Advances|March 7, 2025
Key role of Desulfobacteraceae in C/S cycles of marine sediments is based on congeneric catabolic-regulatory networksLars Wöhlbrand, Marvin Dörries, Roberto Siani, et al.Molecular Genetics and Metabolism|August 12, 2015
Key features and clinical variability of COG6-CDGDaisy Rymen, Julia Winter, Peter M Van Hasselt, et al.Kidney International|September 14, 2022
In vitro and in vivo evidence that the switch from calcineurin to mTOR inhibitors may be a strategy for immunosuppression in Epstein-Barr virus-associated post-transplant lymphoproliferative disorderConstantin J Thieme, Malissa Schulz, Patrizia Wehler, et al.American Journal of Human Genetics|October 2, 2012
Homeotic arm-to-leg transformation associated with genomic rearrangements at the PITX1 locusMalte Spielmann, Francesco Brancati, Peter M Krawitz, et al.Human Molecular Genetics|February 26, 2015
Molecular mechanism of CHRDL1-mediated X-linked megalocornea in humans and in Xenopus modelThorsten Pfirrmann, Denise Emmerich, Peter Ruokonen, et al.Genome Research|September 3, 2013
Distinct global shifts in genomic binding profiles of limb malformation-associated HOXD13 mutationsDaniel M Ibrahim, Peter Hansen, Christian Rödelsperger, et al.Blood|April 23, 2013
Whole-exome sequencing in adult ETP-ALL reveals a high rate of DNMT3A mutationsMartin Neumann, Sandra Heesch, Cornelia Schlee, et al.Pageof 52