Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Malte A. Karow"'
Autor:
Maria Stumpf, Rolf Müller, Berthold Gaßen, Regina Wehrstedt, Petra Fey, Malte A. Karow, Ludwig Eichinger, Gernot Glöckner, Angelika A. Noegel
Publikováno v:
Disease Models & Mechanisms, Vol 10, Iss 7, Pp 897-907 (2017)
Mutations in tripeptidyl peptidase 1 (TPP1) have been associated with late infantile neuronal ceroid lipofuscinosis (NCL), a neurodegenerative disorder. TPP1 is a lysosomal serine protease, which removes tripeptides from the N-terminus of proteins an
Externí odkaz:
https://doaj.org/article/a6e224ba147a4d4faf20a060ea74f3c8
Autor:
Megan Cross, Andreas Hofmann, Malte A. Karow, Jan Hendrik Straub, Christoph S. Clemen, Ludwig Eichinger
Publikováno v:
Biochemistry and Molecular Biology Education. 47:207-210
The Java software jBar consists of a graphical user interface that allows the user to customize and assemble an included script for R. The scripted R pipeline calculates means and standard errors/deviations for replicates of numerical bivariate data
Autor:
Malte A. Karow, Jana Riehl, Qiuhong Xiong, Roman Konertz, Prerana Wagle, Ludwig Eichinger, Christoph S. Clemen, Sarah Fischer, Ramesh Rijal, Susanne Meßling
Publikováno v:
Cells, Vol 9, Iss 1179, p 1179 (2020)
Cells
Volume 9
Issue 5
Cells
Volume 9
Issue 5
Macroautophagy, a highly conserved and complex intracellular degradative pathway, involves more than 20 core autophagy (ATG) proteins, among them the hexameric ATG12~5/16 complex, which is part of the essential ubiquitin-like conjugation systems in a
Autor:
Andreas Hofmann, Christoph S. Clemen, Laura Park, Lin Song, Oliver Hahn, Rolf Schröder, Malte A. Karow, Ludwig Eichinger, Ramesh Rijal, Maria Stumpf, Robert H. Insall
Publikováno v:
Disease Models & Mechanisms, Vol 11, Iss 9 (2018)
Disease Models & Mechanisms
Disease Models & Mechanisms
Hereditary spastic paraplegias (HSPs) are genetically diverse and clinically characterised by lower limb weakness and spasticity. The N471D and several other point mutations of human strumpellin (Str; also known as WASHC5), a member of the Wiskott–
Autor:
Andreas, Hofmann, Megan, Cross, Malte A, Karow, Jan H, Straub, Christoph S, Clemen, Ludwig, Eichinger
Publikováno v:
Biochemistry and molecular biology education : a bimonthly publication of the International Union of Biochemistry and Molecular Biology. 47(2)
The Java software jBar consists of a graphical user interface that allows the user to customize and assemble an included script for R. The scripted R pipeline calculates means and standard errors/deviations for replicates of numerical bivariate data
Publikováno v:
European journal of cell biology. 97(8)
Autophagy and the ubiquitin proteasome system are the two major cellular processes for protein and organelle recycling and clearance in eukaryotic cells. Evidence is accumulating that these two pathways are interrelated through adaptor proteins. Here
Autor:
Salil K. Sukumaran, Rolf Müller, Marija Marko, Malte A. Karow, Ludwig Eichinger, Angelika A. Noegel, Maria Stumpf, Regina Wehrstedt
Publikováno v:
Genes to cells : devoted to molecularcellular mechanisms. 23(10)
phr2AB is the regulatory subunit of the Dictyostelium discoideum phosphatase PP2A and is the ortholog of the human B55 regulatory subunit of PP2A. phr2AB was isolated as a binding partner of the centrosomal protein CEP161, an ortholog of mammalian CD
Autor:
Ludwig Eichinger, Regina Wehrstedt, Petra Fey, Gernot Glöckner, Berthold Gaßen, Rolf Müller, Maria Stumpf, Malte A. Karow, Angelika A. Noegel
Publikováno v:
Disease Models & Mechanisms, Vol 10, Iss 7, Pp 897-907 (2017)
Mutations in tripeptidyl peptidase 1 (TPP1) have been associated with late infantile neuronal ceroid lipofuscinosis (NCL2), a neurodegenerative disorder. TPP1 is a lysosomal serine protease, which removes tripeptides from the amino terminus of protei