Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Erik M Lehmkuhl"'
Autor:
Ernesto Manzo, Ileana Lorenzini, Dianne Barrameda, Abigail G O'Conner, Jordan M Barrows, Alexander Starr, Tina Kovalik, Benjamin E Rabichow, Erik M Lehmkuhl, Dakotah D Shreiner, Archi Joardar, Jean-Charles Liévens, Robert Bowser, Rita Sattler, Daniela C Zarnescu
Publikováno v:
eLife, Vol 8 (2019)
Amyotrophic Lateral Sclerosis (ALS), is a fatal neurodegenerative disorder, with TDP-43 inclusions as a major pathological hallmark. Using a Drosophila model of TDP-43 proteinopathy we found significant alterations in glucose metabolism including inc
Externí odkaz:
https://doaj.org/article/988f50fd13f5471a917861ca1a66e325
Autor:
Erik M. Lehmkuhl, Suvithanandhini Loganathan, Eric Alsop, Alexander D. Blythe, Tina Kovalik, Nicholas P. Mortimore, Dianne Barrameda, Chuol Kueth, Randall J. Eck, Bhavani B. Siddegowda, Archi Joardar, Hannah Ball, Maria E. Macias, Robert Bowser, Kendall Van Keuren-Jensen, Daniela C. Zarnescu
Publikováno v:
Acta Neuropathologica Communications, Vol 9, Iss 1, Pp 1-21 (2021)
Abstract Amyotrophic lateral sclerosis (ALS) is a genetically heterogeneous neurodegenerative disease in which 97% of patients exhibit cytoplasmic aggregates containing the RNA binding protein TDP-43. Using tagged ribosome affinity purifications in D
Externí odkaz:
https://doaj.org/article/bd7f212aa7f244239b10e60b869cabc4
Publikováno v:
Frontiers in Molecular Biosciences, Vol 6 (2020)
TAR DNA binding protein (TDP-43) is a nucleic acid binding protein associated with insoluble cytoplasmic aggregates in several neurodegenerative disorders, including 97% of the ALS cases. In healthy individuals, TDP-43 is primarily localized to the n
Externí odkaz:
https://doaj.org/article/5460281b79b840e6904568a600df6ecf
Autor:
Maria E. Macias, Robert Bowser, Daniela C. Zarnescu, Eric Alsop, Kendall Van Keuren-Jensen, Chuol Kueth, Randall J. Eck, Nicholas P. Mortimore, Suvithanandhini Loganathan, Tina Kovalik, Archi Joardar, Bhavani Bagevalu Siddegowda, Erik M. Lehmkuhl, Hannah Ball, Dianne Barrameda, Alexander D. Blythe
Publikováno v:
Acta Neuropathologica Communications
Acta Neuropathologica Communications, Vol 9, Iss 1, Pp 1-21 (2021)
Acta Neuropathologica Communications, Vol 9, Iss 1, Pp 1-21 (2021)
Amyotrophic lateral sclerosis (ALS) is a genetically heterogeneous neurodegenerative disease in which 97% of patients exhibit cytoplasmic aggregates containing the RNA binding protein TDP-43. Using tagged ribosome affinity purifications in Drosophila
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::308d3f8cd993e313215698fd92900912
https://doi.org/10.1101/2020.07.01.182360
https://doi.org/10.1101/2020.07.01.182360
Autor:
Abigail G. O’Conner, Dianne Barrameda, Benjamin E. Rabichow, Tina Kovalik, Jean-Charles Liévens, Ernesto Manzo, Jordan M. Barrows, Daniela C. Zarnescu, Rita Sattler, Ileana Lorenzini, Robert Bowser, Erik M. Lehmkuhl, Archi Joardar, Alexander Starr, Dakotah D. Shreiner
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3d28aab06fe1f9705a4ec92f05d31219
https://doi.org/10.7554/elife.45114.037
https://doi.org/10.7554/elife.45114.037