Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Paulina Dabrowska-Schlepp"'
Autor:
Todor Tschongov, Swagata Konwar, Andreas Busch, Christian Sievert, Andrea Hartmann, Marina Noris, Sara Gastoldi, Sistiana Aiello, Andreas Schaaf, Jens Panse, Peter F. Zipfel, Paulina Dabrowska-Schlepp, Karsten Häffner
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
Most drugs that target the complement system are designed to inhibit the complement pathway at either the proximal or terminal levels. The use of a natural complement regulator such as factor H (FH) could provide a superior treatment option by restor
Externí odkaz:
https://doaj.org/article/316e4e983cf84c93b83284c77b9c1ed8
Autor:
Paulina Dabrowska‐Schlepp, Andreas Busch, Jin‐Song Shen, Rachel Y. Cheong, Lone Bruhn Madsen, Daniel Mascher, Raphael Schiffmann, Andreas Schaaf
Publikováno v:
JIMD Reports, Vol 64, Iss 6, Pp 460-467 (2023)
Abstract Fabry disease (FD, OMIM 301500) is a rare X‐linked inherited lysosomal storage disorder associated with reduced activities of α‐galactosidase A (aGal, EC 3.2.1.22). The current standard of care for FD is based on enzyme replacement ther
Externí odkaz:
https://doaj.org/article/022e2d6d730d4b30aa55b3a684353bb0
Autor:
Stefan Hintze, Paulina Dabrowska‐Schlepp, Birgit Berg, Alexandra Graupner, Andreas Busch, Andreas Schaaf, Benedikt Schoser, Peter Meinke
Publikováno v:
JIMD Reports, Vol 59, Iss 1, Pp 81-89 (2021)
Abstract Pompe disease, an autosomal recessive lysosomal storage disorder, is caused by deficiency of lysosomal acid alpha‐glucosidase (GAA). On cellular level, there is lysosomal‐bound and free accumulation of glycogen and subsequent damage of o
Externí odkaz:
https://doaj.org/article/dfbde15b891c4aceaca56cb293eb26fe
Autor:
Stefan Hintze, Paulina Dabrowska‐Schlepp, Birgit Berg, Alexandra Graupner, Andreas Busch, Andreas Schaaf, Benedikt Schoser, Peter Meinke
Publikováno v:
JIMD Reports
JIMD Reports, Vol 59, Iss 1, Pp 81-89 (2021)
JIMD Reports, Vol 59, Iss 1, Pp 81-89 (2021)
Pompe disease, an autosomal recessive lysosomal storage disorder, is caused by deficiency of lysosomal acid alpha‐glucosidase (GAA). On cellular level, there is lysosomal‐bound and free accumulation of glycogen and subsequent damage of organelles
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::a246e25715308b723d73e65e775f4df7
http://europepmc.org/articles/PMC8100399
http://europepmc.org/articles/PMC8100399
Autor:
Andreas Schaaf, Nicola Krieghoff, Birgit Berg, Benedikt Schoser, Paulina Dabrowska-Schlepp, Peter Meinke, Stefan Hintze, S Limmer, Andreas Busch
Publikováno v:
International Journal of Molecular Sciences
International Journal of Molecular Sciences, Vol 21, Iss 2642, p 2642 (2020)
Volume 21
Issue 7
International Journal of Molecular Sciences, Vol 21, Iss 2642, p 2642 (2020)
Volume 21
Issue 7
Pompe disease is an autosomal recessive lysosomal storage disorder (LSD) caused by deficiency of lysosomal acid alpha-glucosidase (GAA). The result of the GAA deficiency is a ubiquitous lysosomal and non-lysosomal accumulation of glycogen. The most a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66583a6aa40dfb31db698578ce4d3cf3
https://pubmed.ncbi.nlm.nih.gov/32290314
https://pubmed.ncbi.nlm.nih.gov/32290314
Autor:
Thomas Frischmuth, Holger Niederkrüger, Paulina Dabrowska-Schlepp, Andreas Schaaf, Andreas Busch, Jin-Song Shen, Taniqua S. Day, Xingli Meng, Raphael Schiffmann, Benjamin Fode, Chun I. Yu, Shuyuan Chen, Sabrina Forni
Publikováno v:
Journal of Inherited Metabolic Disease
Enzyme replacement therapy (ERT) is an effective treatment for several lysosomal storage disorders (LSDs). Intravenously infused enzymes are taken up by tissues through either the mannose 6-phosphate receptor (M6PR) or the mannose receptor (MR). It i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f18d45e2504efdde5a11c9025c40da49
https://doi.org/10.1007/s10545-015-9886-9
https://doi.org/10.1007/s10545-015-9886-9
Autor:
Nicola Krieghoff, Thomas Frischmuth, J.H. Koch, Karsten Haeffner, Stefan Michelfelder, Lennard L. Bohlender, Juliana Parsons, Todor Tschogonov, Andreas Busch, Ralf Reski, Eva L. Decker, Andreas Schaaf, Paulina Dabrowska-Schlepp
Publikováno v:
Molecular Immunology. 102:209
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8b0a995486a1b50c29289a2557c37527
https://doi.org/10.1016/j.molimm.2018.06.203
https://doi.org/10.1016/j.molimm.2018.06.203
Publikováno v:
Industrial Scale Suspension Culture of Living Cells
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::addb6829d3dcc1c5f2d372ad6f59c22a
https://doi.org/10.1002/9783527683321.ch08
https://doi.org/10.1002/9783527683321.ch08
