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Blood|August 11, 2020
Hereditary α tryptasemia is a valid genetic biomarker for severe mediator-related symptoms in mastocytosisGeorg Greiner, Bettina Sprinzl, Aleksandra Górska, et al.
Nature Communications|December 8, 2019
Muscleblind acts as a modifier of FUS toxicity by modulating stress granule dynamics and SMN localizationIan Casci, Karthik Krishnamurthy, Sukhleen Kour, et al.
Wiener Klinische Wochenschrift|July 15, 2018
Ludwig Boltzmann Cluster Oncology (LBC ONC): first 10 years and future perspectivesPeter Valent, Emir Hadzijusufovic, Thomas Grunt, et al.
Molecular Biosystems|October 6, 2015
Backbone circularization of Bacillus subtilis family 11 xylanase increases its thermostability and its resistance against aggregationMax C Waldhauer, Silvan N Schmitz, Constantin Ahlmann-Eltze, et al.
Microbial Cell (Graz, Austria)|March 31, 2017
Autophagy extends lifespan via vacuolar acidificationChristoph Ruckenstuhl, Christine Netzberger, Iryna Entfellner, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|April 26, 2025
Developing digital health technologies for frontotemporal degenerationNaomi Nevler, Debra Niehoff, Amanda M Gleixner, et al.
Nature Communications|June 13, 2022
NUP62 localizes to ALS/FTLD pathological assemblies and contributes to TDP-43 insolubilityAmanda M Gleixner, Brandie Morris Verdone, Charlton G Otte, et al.
Neuron|March 4, 2019
RNA Binding Antagonizes Neurotoxic Phase Transitions of TDP-43Jacob R Mann, Amanda M Gleixner, Jocelyn C Mauna, et al.
American Journal of Human Genetics|December 7, 2015
SLC39A8 Deficiency: A Disorder of Manganese Transport and GlycosylationJulien H Park, Max Hogrebe, Marianne Grüneberg, et al.
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