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Scientific Reports|March 16, 2019
Biallelic loss-of-function LACC1/FAMIN Mutations Presenting as Rheumatoid Factor-Negative Polyarticular Juvenile Idiopathic ArthritisRaquel Rabionet, Agustín Remesal, Anna Mensa-Vilaró, et al.
Molecular Cell|June 17, 2019
Spatial Chromosome Folding and Active Transcription Drive DNA Fragility and Formation of Oncogenic MLL TranslocationsHenrike Johanna Gothe, Britta Annika Maria Bouwman, Eduardo Gade Gusmao, et al.
Molecular Cell|May 1, 2018
HMGB2 Loss upon Senescence Entry Disrupts Genomic Organization and Induces CTCF Clustering across Cell TypesAnne Zirkel, Milos Nikolic, Konstantinos Sofiadis, et al.
Human Molecular Genetics|July 19, 2015
Missense mutations in TENM4, a regulator of axon guidance and central myelination, cause essential tremorHyun Hor, Ludmila Francescatto, Luca Bartesaghi, et al.
Journal of the American Society of Nephrology : JASN|August 19, 2022
Inflammation in Children with CKD Linked to Gut Dysbiosis and Metabolite ImbalanceJohannes Holle, Hendrik Bartolomaeus, Ulrike Löber, et al.
Epidemiology and Infection|August 1, 2022
Transmission of SARS-CoV-2 among children and staff in German daycare centresJulika Loss, Juliane Wurm, Gianni Varnaccia, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|June 24, 2022
Advancing Precision Vaccinology by Molecular and Genomic Surveillance of Severe Acute Respiratory Syndrome Coronavirus 2 in Germany, 2021Djin Ye Oh, Martin Hölzer, Sofia Paraskevopoulou, et al.
Briefings in Bioinformatics|November 4, 2020
Computational strategies to combat COVID-19: useful tools to accelerate SARS-CoV-2 and coronavirus researchFranziska Hufsky, Kevin Lamkiewicz, Alexandre Almeida, et al.
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