Zobrazeno 1 - 10
of 39
pro vyhledávání: '"Michael C. Stankewich"'
Publikováno v:
Frontiers in Neuroscience, Vol 18 (2024)
IntroductionDeletion or mutation of members of the spectrin gene family contributes to many neurologic and neuropsychiatric disorders. While each spectrinopathy may generate distinct neuropathology, the study of βΙ spectrin’s role (Sptb) in the b
Externí odkaz:
https://doaj.org/article/dcdd540b693d4558a9a56092b22dbb64
Autor:
Arkadiusz Miazek, Michał Zalas, Joanna Skrzymowska, Bryan A. Bogin, Krzysztof Grzymajło, Tomasz M. Goszczynski, Zachary A. Levine, Jon S. Morrow, Michael C. Stankewich
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-18 (2021)
Abstract The neuronal membrane-associated periodic spectrin skeleton (MPS) contributes to neuronal development, remodeling, and organization. Post-translational modifications impinge on spectrin, the major component of the MPS, but their role remains
Externí odkaz:
https://doaj.org/article/40927af2976845f3a475e0d8a41ea927
Autor:
Arkadiusz Miazek, Michał Zalas, Joanna Skrzymowska, Bryan A. Bogin, Krzysztof Grzymajło, Tomasz M. Goszczynski, Zachary A. Levine, Jon S. Morrow, Michael C. Stankewich
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-3 (2021)
An amendment to this paper has been published and can be accessed via a link at the top of the paper.
Externí odkaz:
https://doaj.org/article/7310f47208a44e3d8d357a0f49fac737
Autor:
Krzysztof Grzymajło, Zachary A. Levine, Jon S. Morrow, Michael C. Stankewich, Bryan A. Bogin, Joanna Skrzymowska, Arkadiusz Miazek, Michał Zalas, Tomasz M. Goszczyński
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-18 (2021)
Scientific Reports
Scientific Reports
The neuronal membrane-associated periodic spectrin skeleton (MPS) contributes to neuronal development, remodeling, and organization. Post-translational modifications impinge on spectrin, the major component of the MPS, but their role remains poorly u
Autor:
Tomasz M. Goszczyński, Bryan A. Bogin, Joanna Skrzymowska, Michał Zalas, Arkadiusz Miazek, Michael C. Stankewich, Krzysztof Grzymajło, Zachary A. Levine, Jon S. Morrow
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-3 (2021)
An amendment to this paper has been published and can be accessed via a link at the top of the paper.
Publikováno v:
PLoS ONE, Vol 11, Iss 1, p e0142687 (2016)
The kidney displays specialized regions devoted to filtration, selective reabsorption, and electrolyte and metabolite trafficking. The polarized membrane pumps, channels, and transporters responsible for these functions have been exhaustively studied
Externí odkaz:
https://doaj.org/article/3e8af5d7324b4de7af587ef1551070be
Autor:
Michael C. Stankewich, Jon S. Morrow
Publikováno v:
Journal of Experimental Neurology. 2
Experimental and hereditary defects in the ubiquitous scaffolding proteins of the spectrin gene family cause an array of neuropathologies. Most recognized are ataxias caused by missense, deletions, or truncations in the SPTBN2 gene that encodes beta
Autor:
Jon S, Morrow, Michael C, Stankewich
Publikováno v:
Journal of experimental neurology
Experimental and hereditary defects in the ubiquitous scaffolding proteins of the spectrin gene family cause an array of neuropathologies. Most recognized are ataxias caused by missense, deletions, or truncations in the SPTBN2 gene that encodes beta
Autor:
Jessica Becker, Julia Bay, Deepa Ajit, Sheryl S. Moy, Katja Kloth, Michael T. Zimmermann, Pilar Cacheiro, Ingrid M.B.H. van de Laar, Richard H. van Jaarsveld, Queenie K-G Tan, Adriana S. Beltran, Allyn McConkie-Rosell, Keith A. Breau, Laura Schultz-Rogers, Deike Weiss, Damaris N Lorenzo, Marie T. McDonald, Robert Jech, Paul R. Mark, Erin Torti, Richard E. Person, Benjamin Cogné, Renske Oegema, Eva H. Brilstra, Robert Stratton, Koen L.I. van Gassen, Reginald James Edwards, Rebecca C. Spillmann, Michael C. Stankewich, Amy Kritzer, Liset Falcon Rodriguez, Parul Jayakar, Joseph T. Shieh, Margot A. Cousin, Elizabeth A. Normand, Jennifer L. Kemppainen, Jennifer MacKenzie, Hartmut Engels, Marjon van Slegtenhorst, Evangeline Kurtz-Nelson, Tianyun Wang, Yue Si, Damian Smedley, Bertrand Isidor, Blake A Creighton, Vimla Aggarwal, Michael Zech, Alvaro A. Beltran, Stefan Aretz, Brenda Temple, Simone Afriyie, Sarah E McKeown, Louise Bier, Tatjana Bierhals, Grace Yoon, Juliane Winkelmann, Swarnendu Tripathi, Brendan C. Lanpher, Amy Blevins, Pavel N. Pichurin, Eric W. Klee, Kathryn M. Harper, Cecilia Fairley, Lauren Gunderson, Ingo Helbig, Sruthi Dontu, Kirsten Cremer, Raphael Bernier, Helen V. Firth, Gretchen Parsons, Lorena J. Munoz, Evan E. Eichler, Alison S May, Grazia M.S. Mancini
Publikováno v:
Nature Genetics, 53(7), 1006-1021. Nature Publishing Group
Nature genetics
Nat. Genet. 53, 1006-1021 (2021)
Nature genetics
Nat. Genet. 53, 1006-1021 (2021)
SPTBN1 encodes βII-spectrin, the ubiquitously expressed β-spectrin that forms micrometer-scale networks associated with plasma membranes. Mice deficient in neuronal βII-spectrin have defects in cortical organization, developmental delay and behavi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4874221589b63cb383656f262aebe07d
https://pure.eur.nl/en/publications/2512cc47-cfda-403d-a937-3ee0a59e175a
https://pure.eur.nl/en/publications/2512cc47-cfda-403d-a937-3ee0a59e175a
Autor:
Michael C. Stankewich, Jun-Ping Bai, Paul R. Stabach, Saaim Khan, Winston J.T. Tan, Alexei Surguchev, Lei Song, Jon S. Morrow, Joseph Santos-Sacchi, Dhasakumar S. Navaratnam
Publikováno v:
Hearing Research. 423:108564
Reports have proposed a putative role for βV spectrin in outer hair cells (OHCs) of the cochlea. In an ongoing investigation of the role of the cytoskeleton in electromotility, we tested mice with a targeted exon deletion of βV spectrin (Spnb5), an