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Epigenetics & Chromatin|August 2, 2016
Epigenetic dynamics of monocyte-to-macrophage differentiationStefan Wallner, Christopher Schröder, Elsa Leitão, et al.
Cell Systems|January 15, 2026
A combinatorial transcription factor screening platform for immune cell reprogrammingIlia Kurochkin, Abigail R Altman, Inês Caiado, et al.
The Journal of Experimental Medicine|November 10, 2019
Extensive dissemination and intraclonal maturation of HIV Env vaccine-induced B cell responsesGanesh E Phad, Pradeepa Pushparaj, Karen Tran, et al.
Genome Research|April 18, 2015
Characteristics of de novo structural changes in the human genomeWigard P Kloosterman, Laurent C Francioli, Fereydoun Hormozdiari, et al.
F1000Research|August 16, 2021
A strategy for building and using a human reference pangenomeBastien Llamas, Giuseppe Narzisi, Valerie Schneider, et al.
Orphanet Journal of Rare Diseases|July 25, 2013
Oto-facial syndrome and esophageal atresia, intellectual disability and zygomatic anomalies - expanding the phenotypes associated with EFTUD2 mutationsClaudia Voigt, André Mégarbané, Kornelia Neveling, et al.
Nature|March 23, 2018
Corrigendum: Cloche is a bHLH-PAS transcription factor that drives haemato-vascular specificationSven Reischauer, Oliver A Stone, Alethia Villasenor, et al.
European Journal of Human Genetics : EJHG|August 24, 2017
SweGen: a whole-genome data resource of genetic variability in a cross-section of the Swedish populationAdam Ameur, Johan Dahlberg, Pall Olason, et al.
Nature|July 15, 2016
Cloche is a bHLH-PAS transcription factor that drives haemato-vascular specificationSven Reischauer, Oliver A Stone, Alethia Villasenor, et al.
Nature|October 19, 2022
Semi-automated assembly of high-quality diploid human reference genomesErich D Jarvis, Giulio Formenti, Arang Rhie, et al.
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