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American Journal of Human Genetics|June 11, 2013
De novo mutations in the genome organizer CTCF cause intellectual disabilityAnne Gregor, Martin Oti, Evelyn N Kouwenhoven, et al.Cell Host & Microbe|July 25, 2023
A single-nucleotide polymorphism in Helicobacter pylori promotes gastric cancer developmentIrshad Sharafutdinov, Nicole Tegtmeyer, Bodo Linz, et al.Molecular & Cellular Proteomics : MCP|June 28, 2014
Proteomic analysis of the multimeric nuclear egress complex of human cytomegalovirusJens Milbradt, Alexandra Kraut, Corina Hutterer, et al.Cell Reports|September 16, 2020
Toll-like Receptor 5 Activation by the CagY Repeat Domains of Helicobacter pyloriNicole Tegtmeyer, Matthias Neddermann, Judith Lind, et al.Human Mutation|October 18, 2014
MAP4-dependent regulation of microtubule formation affects centrosome, cilia, and Golgi architecture as a central mechanism in growth regulationDiana Zahnleiter, Nadine N Hauer, Kristin Kessler, et al.American Journal of Human Genetics|March 5, 2017
Hypomorphic Pathogenic Variants in TAF13 Are Associated with Autosomal-Recessive Intellectual Disability and MicrocephalyHasan Tawamie, Igor Martianov, Natalie Wohlfahrt, et al.Annals of Neurology|September 8, 2022
De Novo Missense Variants in SLC32A1 Cause a Developmental and Epileptic Encephalopathy Due to Impaired GABAergic NeurotransmissionKonrad Platzer, Heinrich Sticht, Caleb Bupp, et al.Journal of Medical Genetics|April 10, 2017
Confirmation of mutations in PROSC as a novel cause of vitamin B -dependent epilepsyBarbara Plecko, Markus Zweier, Anaïs Begemann, et al.Journal of Cell Science|November 9, 2014
DAPK-HSF1 interaction as a positive-feedback mechanism stimulating TNF-induced apoptosis in colorectal cancer cellsNatalya Benderska, Jelena Ivanovska, Tilman T Rau, et al.Journal of Medicinal Chemistry|November 8, 2021
N-Terminus to Arginine Side-Chain Cyclization of Linear Peptidic Neuropeptide Y Y4 Receptor Ligands Results in Picomolar Binding ConstantsAdam Konieczny, Marcus Conrad, Fabian J Ertl, et al.Pageof 31