Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Maria Stumpf"'
Autor:
Qiuhong Xiong, Rong Feng, Sarah Fischer, Malte Karow, Maria Stumpf, Susanne Meßling, Leonie Nitz, Stefan Müller, Christoph S. Clemen, Ning Song, Ping Li, Changxin Wu, Ludwig Eichinger
Publikováno v:
Cells, Vol 12, Iss 11, p 1514 (2023)
Autophagy and the ubiquitin proteasome system are the two major processes for the clearance and recycling of proteins and organelles in eukaryotic cells. Evidence is accumulating that there is extensive crosstalk between the two pathways, but the und
Externí odkaz:
https://doaj.org/article/b91cdcd1cd9e420688ca1b8b2fca1838
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-11 (2017)
Abstract SUN1, a component of the LINC (Linker of Nucleoskeleton and Cytoskeleton) complex, functions in mammalian mRNA export through the NXF1-dependent pathway. It associates with mRNP complexes by direct interaction with NXF1. It also binds to the
Externí odkaz:
https://doaj.org/article/d2506abca7434767a8c176879e184827
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:
Lin Song, Ramesh Rijal, Malte Karow, Maria Stumpf, Oliver Hahn, Laura Park, Robert Insall, Rolf Schröder, Andreas Hofmann, Christoph S. Clemen, Ludwig Eichinger
Publikováno v:
Disease Models & Mechanisms, Vol 11, Iss 9 (2018)
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–
Externí odkaz:
https://doaj.org/article/54f9a4bb7553498e8ad73ddc9d0c69d8
Autor:
Khalid Arhzaouy, Karl-Heinz Strucksberg, Sze Man Tung, Karthikeyan Tangavelou, Maria Stumpf, Jan Faix, Rolf Schröder, Christoph S Clemen, Ludwig Eichinger
Publikováno v:
PLoS ONE, Vol 13, Iss 6, p e0199548 (2018)
[This corrects the article DOI: 10.1371/journal.pone.0046879.].
Externí odkaz:
https://doaj.org/article/e13e0b72d46a47fa983bf7ae37537566
Autor:
Khalid Arhzaouy, Karl-Heinz Strucksberg, Sze Man Tung, Karthikeyan Tangavelou, Maria Stumpf, Jan Faix, Rolf Schröder, Christoph S Clemen, Ludwig Eichinger
Publikováno v:
PLoS ONE, Vol 7, Iss 10, p e46879 (2012)
Heterozygous mutations in the human VCP (p97) gene cause autosomal-dominant IBMPFD (inclusion body myopathy with early onset Paget's disease of bone and frontotemporal dementia), ALS14 (amyotrophic lateral sclerosis with or without frontotemporal dem
Externí odkaz:
https://doaj.org/article/00e2734f67aa4a1e9cd1d84adfd4350e
Autor:
Newton Tavares Escocard de Oliveira, Faculdade de Ensino Superior de São Miguel do Iguaçu, Silvana Teixeira Carvalho, Cristine Regina Gregory, Liliana Santos, Luciane Maria Stumpf, Paulo Evaristo Rupolo, Paulo Levi de Oliveira Carvalho, Jansller Luiz Genova, Jhuliendri Bortoluzzi, Geraldyne Nunes Wendt
Publikováno v:
Semina: Ciências Agrárias; Vol. 43 No. 1 (2022); 367-380
Semina: Ciências Agrárias; v. 43 n. 1 (2022); 367-380
Semina. Ciências Agrárias
Universidade Estadual de Londrina (UEL)
instacron:UEL
Semina: Ciências Agrárias; v. 43 n. 1 (2022); 367-380
Semina. Ciências Agrárias
Universidade Estadual de Londrina (UEL)
instacron:UEL
This study was conducted to assess the effect of two types of drinkers on water intake (WI) and two types of toys on behavioural observations of piglets in the nursery phase. A total of 72 crossbred entire male piglets (Landrace × Large White, Agroc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::738ca9913c09ef9c0843e7a89beeaa05
https://ojs.uel.br/revistas/uel/index.php/semagrarias/article/view/44078
https://ojs.uel.br/revistas/uel/index.php/semagrarias/article/view/44078
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:
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:
Jaqueline Deckstein, Maria Stumpf, Marios Tsangarides, Kyriacos Yiannakou, Salil K. Sukumaran, Rolf Müller, Jennifer van Appeldorn, Ludwig Eichinger, Angelika A. Noegel, Tanja Y. Riyahi
Publikováno v:
Eukaryotic Cell. 14:41-54
Dictyostelium discoideum GPHR ( G olgi pH r egulator)/Gpr89 is a developmentally regulated transmembrane protein present on the endoplasmic reticulum (ER) and the Golgi apparatus. Transcript levels are low during growth and vary during development, r