Zobrazeno 1 - 10
of 58
pro vyhledávání: '"Manuel H Taft"'
Autor:
Johannes N Greve, Anja Marquardt, Robin Heiringhoff, Theresia Reindl, Claudia Thiel, Nataliya Di Donato, Manuel H Taft, Dietmar J Manstein
Publikováno v:
eLife, Vol 12 (2024)
Various heterozygous cytoskeletal γ-actin mutations have been shown to cause Baraitser–Winter cerebrofrontofacial syndrome, non-syndromic hearing loss, or isolated eye coloboma. Here, we report the biochemical characterization of human cytoskeleta
Externí odkaz:
https://doaj.org/article/321319569cd148a5aa5e8707afca94db
Autor:
Rasmus D Wollenberg, Søren S Donau, Manuel H Taft, Zoltan Balázs, Sven Giese, Claudia Thiel, Jens L Sørensen, Thorbjørn T Nielsen, Henriette Giese, Dietmar J Manstein, Reinhard Wimmer, Teis E Sondergaard
Publikováno v:
PLoS ONE, Vol 15, Iss 6, p e0235568 (2020)
Filamentous fungi belonging to the genus Fusarium are notorious plant-pathogens that infect, damage and contaminate a wide variety of important crops. Phenamacril is the first member of a novel class of single-site acting cyanoacrylate fungicides whi
Externí odkaz:
https://doaj.org/article/cdef8469221e44b98270913f548467c7
Autor:
Aleksandra Shcherbakova, Matthias Preller, Manuel H Taft, Jordi Pujols, Salvador Ventura, Birgit Tiemann, Falk FR Buettner, Hans Bakker
Publikováno v:
eLife, Vol 8 (2019)
Previous studies demonstrated importance of C-mannosylation for efficient protein secretion. To study its impact on protein folding and stability, we analyzed both C-mannosylated and non-C-mannosylated thrombospondin type 1 repeats (TSRs) of netrin r
Externí odkaz:
https://doaj.org/article/573919a03a124259935a6d4050ce1cfe
Autor:
Michael B Radke, Manuel H Taft, Britta Stapel, Denise Hilfiker-Kleiner, Matthias Preller, Dietmar J Manstein
Publikováno v:
eLife, Vol 3 (2014)
The small molecule EMD 57033 has been shown to stimulate the actomyosin ATPase activity and contractility of myofilaments. Here, we show that EMD 57033 binds to an allosteric pocket in the myosin motor domain. EMD 57033-binding protects myosin agains
Externí odkaz:
https://doaj.org/article/1c2b6f50130d4670973519e640507c6e
Autor:
Mirco Müller, Ralph P Diensthuber, Igor Chizhov, Peter Claus, Sarah M Heissler, Matthias Preller, Manuel H Taft, Dietmar J Manstein
Publikováno v:
PLoS ONE, Vol 8, Iss 7, p e70636 (2013)
Despite their near sequence identity, actin isoforms cannot completely replace each other in vivo and show marked differences in their tissue-specific and subcellular localization. Little is known about isoform-specific differences in their interacti
Externí odkaz:
https://doaj.org/article/0bc98f18476241ca8c1beb72883b3d93
Autor:
Theresia Reindl, Sven Giese, Johannes N. Greve, Patrick Y. Reinke, Igor Chizhov, Sharissa L. Latham, Daniel P. Mulvihill, Manuel H. Taft, Dietmar J. Manstein
Publikováno v:
iScience, Vol 25, Iss 7, Pp 104484- (2022)
Summary: The effects of N-terminal acetylation of the high molecular weight tropomyosin isoforms Tpm1.6 and Tpm2.1 and the low molecular weight isoforms Tpm1.12, Tpm3.1, and Tpm4.2 on the actin affinity and the thermal stability of actin-tropomyosin
Externí odkaz:
https://doaj.org/article/556ba07f2f664300a1a80037d71c6760
Autor:
Johannes N. Greve, Frederic V. Schwäbe, Thomas Pokrant, Jan Faix, Nataliya Di Donato, Manuel H. Taft, Dietmar J. Manstein
Publikováno v:
European Journal of Cell Biology, Vol 101, Iss 2, Pp 151216- (2022)
Heterozygous dominant mutations in the ubiquitously produced cytoskeletal β–actin isoform lead to a broad range of human disease phenotypes, which are currently classified as three distinct clinical entities termed Baraitser-Winter–Cerebrofronto
Externí odkaz:
https://doaj.org/article/f4cd10b5d3b14de5b63c994899b160c7
Autor:
Marc R. Reboll, Stefanie Klede, Manuel H. Taft, Chen-Leng Cai, Loren J. Field, Kory J. Lavine, Andrew L. Koenig, Jenni Fleischauer, Johann Meyer, Axel Schambach, Hans W. Niessen, Maike Kosanke, Joop van den Heuvel, Andreas Pich, Johann Bauersachs, Xuekun Wu, Linqun Zheng, Yong Wang, Mortimer Korf-Klingebiel, Felix Polten, Kai C. Wollert
Publikováno v:
Reboll, M R, Klede, S, Taft, M H, Cai, C-L, Field, L J, Lavine, K J, Koenig, A L, Fleischauer, J, Meyer, J, Schambach, A, Niessen, H W, Kosanke, M, van den Heuvel, J, Pich, A, Bauersachs, J, Wu, X, Zheng, L, Wang, Y, Korf-Klingebiel, M, Polten, F & Wollert, K C 2022, ' Meteorin-like promotes heart repair through endothelial KIT receptor tyrosine kinase ', Science, vol. 376, no. 6599, pp. 1343-1347 . https://doi.org/10.1126/science.abn3027
Science, 376(6599), 1343-1347. American Association for the Advancement of Science
Science, 376(6599), 1343-1347. American Association for the Advancement of Science
Effective tissue repair after myocardial infarction entails a vigorous angiogenic response, guided by incompletely defined immune cell–endothelial cell interactions. We identify the monocyte- and macrophage-derived cytokine METRNL (meteorin-like) a
Autor:
Dan Cojoc, Irene Pertici, Pasquale Bianco, Vincenzo Lombardi, Lorenzo Bongini, Giulio Bianchi, Dietmar J. Manstein, Manuel H. Taft
Publikováno v:
The Journal of Physiology. 599:1815-1831
KEY POINTS A nanomachine made of an ensemble of seven heavy-meromyosin (HMM) fragments of muscle myosin interacting with an actin filament is able to mimic the half-sarcomere generating steady force and constant-velocity shortening. To preserve Ca2+
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 11949, p 11949 (2021)
International Journal of Molecular Sciences
Volume 22
Issue 21
International Journal of Molecular Sciences
Volume 22
Issue 21
Mutations in the gene encoding cardiac myosin-binding protein-C (MyBPC), a thick filament assembly protein that stabilizes sarcomeric structure and regulates cardiac function, are a common cause for the development of hypertrophic cardiomyopathy. Abo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fbc175285ef91ebb0ccf796916385c6e