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Genetics|June 21, 2005
Identification of a rat model for usher syndrome type 1B by N-ethyl-N-nitrosourea mutagenesis-driven forward geneticsBart M G Smits, Theo A Peters, Joram D Mul, et al.Human Molecular Genetics|February 26, 2011
Chromothripsis as a mechanism driving complex de novo structural rearrangements in the germlineWigard P Kloosterman, Victor Guryev, Mark van Roosmalen, et al.Cell Reports|May 7, 2020
Challenges in Establishing Pure Lung Cancer Organoids Limit Their Utility for Personalized MedicineKrijn K Dijkstra, Kim Monkhorst, Luuk J Schipper, et al.Nature Protocols|November 5, 2011
Multiplexed array-based and in-solution genomic enrichment for flexible and cost-effective targeted next-generation sequencingMagdalena Harakalova, Michal Mokry, Barbara Hrdlickova, et al.Nature Neuroscience|January 26, 2016
Epigenomic annotation of gene regulatory alterations during evolution of the primate brainMarit W Vermunt, Sander C Tan, Bas Castelijns, et al.Plos Biology|January 28, 2022
Efficient and error-free fluorescent gene tagging in human organoids without double-strand DNA cleavageYannik Bollen, Joris H Hageman, Petra van Leenen, et al.The Journal of Pathology|March 29, 2024
Polyketide synthase positive Escherichia coli one-time measurement in stool is not informative of colorectal cancer risk in a screening settingWillemijn de Klaver, Meike de Wit, Anne Bolijn, et al.Seminars in Cancer Biology|June 27, 2021
Clinical utility of whole-genome sequencing in precision oncologyRichard Rosenquist, Edwin Cuppen, Reinhard Buettner, et al.Nature Genetics|April 30, 2008
Distribution and functional impact of DNA copy number variation in the ratVictor Guryev, Kathrin Saar, Tatjana Adamovic, et al.Nature Biomedical Engineering|January 26, 2021
In vivo cytidine base editing of hepatocytes without detectable off-target mutations in RNA and DNALukas Villiger, Tanja Rothgangl, Dominik Witzigmann, et al.Pageof 34