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Clinical Epigenetics|August 24, 2019
Deficiency and haploinsufficiency of histone macroH2A1.1 in mice recapitulate hematopoietic defects of human myelodysplastic syndromeOxana Bereshchenko, Oriana Lo Re, Fedor Nikulenkov, et al.
The EMBO Journal|November 22, 2021
Postnatal expression of the lysine methyltransferase SETD1B is essential for learning and the regulation of neuron-enriched genesAlexandra Michurina, M Sadman Sakib, Cemil Kerimoglu, et al.
The British Journal of General Practice : the Journal of the Royal College of General Practitioners|March 3, 2021
Associations with antibiotic prescribing for acute exacerbation of COPD in primary care: secondary analysis of a randomised controlled trialDavid Gillespie, Christopher C Butler, Janine Bates, et al.
Nature|June 17, 2011
A conditional knockout resource for the genome-wide study of mouse gene functionWilliam C Skarnes, Barry Rosen, Anthony P West, et al.
Nature Genetics|October 21, 2025
Complete genome assemblies of two mouse subspecies reveal structural diversity of telomeres and centromeresBailey A Francis, Landen Gozashti, Kevin Costello, et al.
Journal of Multimorbidity and Comorbidity|April 3, 2025
Capturing the human impact of living with multiple long-term conditions in routine electronic health records - lost in translation?Simon D S Fraser, Emilia Holland, Lynn Laidlaw, et al.
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