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Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 22, 2022
Missense mutation in ATXN2 gene (c.2860C > T) in an amyotrophic lateral sclerosis patient with aggressive disease phenotypeAndrea Ghezzi, Ilaria Martinelli, Serena Carra, et al.
The Journal of Biological Chemistry|September 23, 2010
Identification of the Drosophila ortholog of HSPB8: implication of HSPB8 loss of function in protein folding diseasesSerena Carra, Alessandra Boncoraglio, Bart Kanon, et al.
Elife|August 5, 2015
Promiscuous interactions and protein disaggregases determine the material state of stress-inducible RNP granulesSonja Kroschwald, Shovamayee Maharana, Daniel Mateju, et al.
Cell Stress & Chaperones|February 17, 2010
Abnormal interaction of motor neuropathy-associated mutant HspB8 (Hsp22) forms with the RNA helicase Ddx20 (gemin3)Xiankui Sun, Jean-Marc Fontaine, Adam D Hoppe, et al.
Oncotarget|January 7, 2017
The small heat shock protein B8 (HSPB8) modulates proliferation and migration of breast cancer cellsMargherita Piccolella, Valeria Crippa, Riccardo Cristofani, et al.
Biology Open|June 20, 2020
Filament formation by the translation factor eIF2B regulates protein synthesis in starved cellsElisabeth Nüske, Guendalina Marini, Doris Richter, et al.
Communications Biology|October 8, 2024
Chemical inhibition of the integrated stress response impairs the ubiquitin-proteasome systemShanshan Xu, Maria E Gierisch, Enrica Barchi, et al.
Elife|July 3, 2019
Proteome-wide signatures of function in highly diverged intrinsically disordered regionsTaraneh Zarin, Bob Strome, Alex N Nguyen Ba, et al.
Frontiers in Molecular Neuroscience|July 7, 2017
The Role of the Heat Shock Protein B8 (HSPB8) in Motoneuron DiseasesPaola Rusmini, Riccardo Cristofani, Mariarita Galbiati, et al.
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