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Nature Genetics|August 30, 2016
Mutations in SNORD118 cause the cerebral microangiopathy leukoencephalopathy with calcifications and cystsEmma M Jenkinson, Mathieu P Rodero, Paul R Kasher, et al.
Acta Crystallographica. Section F, Structural Biology and Crystallization Communications|October 15, 2010
The structure of Jann_2411 (DUF1470) from Jannaschia sp. at 1.45 Å resolution reveals a new fold (the ABATE domain) and suggests its possible role as a transcription regulatorConstantina Bakolitsa, Alex Bateman, Kevin K Jin, et al.
Database : the Journal of Biological Databases and Curation|August 12, 2022
A roadmap for the functional annotation of protein families: a community perspectiveValérie de Crécy-Lagard, Rocio Amorin de Hegedus, Cecilia Arighi, et al.
Medrxiv : the Preprint Server for Health Sciences|January 20, 2025
De novo and inherited dominant variants in U4 and U6 snRNAs cause retinitis pigmentosaMathieu Quinodoz, Kim Rodenburg, Zuzana Cvackova, et al.
Genetics|March 3, 2023
The Gene Ontology knowledgebase in 2023, Suzi A Aleksander, James Balhoff, et al.
Nature Genetics|January 9, 2026
De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosaMathieu Quinodoz, Kim Rodenburg, Zuzana Cvackova, et al.
Nature|November 13, 2007
Evolution of genes and genomes on the Drosophila phylogeny, Andrew G Clark, Michael B Eisen, et al.
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