Zobrazeno 1 - 10
of 55
pro vyhledávání: '"Birgit Hoffmann"'
Publikováno v:
FEBS Open Bio, Vol 14, Iss 4, Pp 626-642 (2024)
Proteins achieve their biological functions in cells by cooperation in protein complexes. In this study, we employed fluorescence lifetime imaging microscopy (FLIM)‐based Förster resonance energy transfer (FRET) measurements to investigate protein
Externí odkaz:
https://doaj.org/article/2dbc77c3822943059cfd9ac8fc8a30d4
Autor:
Mukhran Khundadze, Federico Ribaudo, Adeela Hussain, Jan Rosentreter, Sandor Nietzsche, Melanie Thelen, Dominic Winter, Birgit Hoffmann, Muhammad Awais Afzal, Tanja Hermann, Cecilia de Heus, Eva-Maria Piskor, Christian Kosan, Patricia Franzka, Lisa von Kleist, Tobias Stauber, Judith Klumperman, Markus Damme, Tassula Proikas-Cezanne, Christian A. Hübner
Publikováno v:
Neurobiology of Disease, Vol 127, Iss , Pp 419-431 (2019)
Hereditary spastic paraplegia is a spastic gait disorder that arises from degeneration of corticospinal axons. The subtype SPG48 is associated with mutations in the zeta subunit of the adaptor protein complex five (AP5). AP5 function and the pathophy
Externí odkaz:
https://doaj.org/article/c5d0d4197e294f66a8340361edbe5c4c
Autor:
Rita-Eva Varga, Mukhran Khundadze, Markus Damme, Sandor Nietzsche, Birgit Hoffmann, Tobias Stauber, Nicole Koch, J Christopher Hennings, Patricia Franzka, Antje K Huebner, Michael M Kessels, Christoph Biskup, Thomas J Jentsch, Britta Qualmann, Thomas Braulke, Ingo Kurth, Christian Beetz, Christian A Hübner
Publikováno v:
PLoS Genetics, Vol 11, Iss 8, p e1005454 (2015)
Hereditary spastic paraplegia (HSP) is characterized by a dying back degeneration of corticospinal axons which leads to progressive weakness and spasticity of the legs. SPG11 is the most common autosomal-recessive form of HSPs and is caused by mutati
Externí odkaz:
https://doaj.org/article/1fa6a82e141e4992ad336808f0f0fef5
Publikováno v:
Journal of Photochemistry and Photobiology A: Chemistry. 442:114798