Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Björn Kowalewski"'
Autor:
Myungsik Yoo, Muntasir Khaled, Kurt M Gibbs, Jonghun Kim, Björn Kowalewski, Thomas Dierks, Melitta Schachner
Publikováno v:
PLoS ONE, Vol 8, Iss 3, p e57415 (2013)
Bacterial chondroitinase ABC (ChaseABC) has been used to remove the inhibitory chondroitin sulfate chains from chondroitin sulfate proteoglycans to improve regeneration after rodent spinal cord injury. We hypothesized that the mammalian enzyme arylsu
Externí odkaz:
https://doaj.org/article/bd932431640d4ec48403ad6dc1a7cafb
Publikováno v:
The Biochemical journal. 478(17)
The lysosomal degradation of heparan sulfate is mediated by the concerted action of nine different enzymes. Within this degradation pathway, Arylsulfatase G (ARSG) is critical for removing 3-O-sulfate from glucosamine, and mutations in ARSG are causa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d72fce27adc4dd215a66d904b498ee6c
https://pubmed.ncbi.nlm.nih.gov/34405855
https://pubmed.ncbi.nlm.nih.gov/34405855
Autor:
Ann Saada, Carlo Rivolta, Alexey Obolensky, Dror Sharon, Thomas Dierks, Netta Pollack, Tamar Ben-Yosef, Samer Khateb, Markus Damme, Nicola Bedoni, Eyal Banin, Menachem Gross, Björn Kowalewski
Publikováno v:
Genetics in medicine : official journal of the American College of Medical Genetics. 20(9)
Purpose: We aimed to identify the cause of disease in patients suffering from a distinctive, atypical form of Usher syndrome. Methods: Whole-exome and genome sequencing were performed in five patients from three families of Yemenite Jewish origin, su
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::458c0e69a3477eb97646a55ca3c9f4b1
https://pubmed.ncbi.nlm.nih.gov/29300381
https://pubmed.ncbi.nlm.nih.gov/29300381
Autor:
Markus Damme, Thomas Dierks, Katrin Kollmann, Thomas Reinheckel, Torben Lübke, Thomas Braulke, Björn Kowalewski
Publikováno v:
Journal of Biological Chemistry. 289:27992-28005
Arylsulfatase G (ARSG) is a recently identified lysosomal sulfatase that was shown to be responsible for the degradation of 3-O-sulfated N-sulfoglucosamine residues of heparan sulfate glycosaminoglycans. Deficiency of ARSG leads to a new type of muco
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::31b3cd949a4e1224fce4509deb6085a1
https://doi.org/10.1074/jbc.m114.584144
https://doi.org/10.1074/jbc.m114.584144
Autor:
Peter Heimann, Thomas Dierks, Markus Damme, Steven U. Walkley, Tomo Sawada, Theresa Ortkras, Björn Kowalewski, Renate Lüllmann-Rauch
Publikováno v:
Human molecular genetics. 24(7)
Deficiency of arylsulfatase G (ARSG) leads to a lysosomal storage disease in mice resembling biochemical and pathological features of the mucopolysaccharidoses and particularly features of mucopolysaccharidosis type III (Sanfilippo syndrome). Here we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae2e29a73b5ea4231239c69955858e47
https://pubmed.ncbi.nlm.nih.gov/25452429
https://pubmed.ncbi.nlm.nih.gov/25452429
Autor:
Jonghun Kim, Melitta Schachner, Myungsik Yoo, Thomas Dierks, Björn Kowalewski, Muntasir Khaled, Kurt M. Gibbs
Publikováno v:
PLoS ONE
PLoS ONE, Vol 8, Iss 3, p e57415 (2013)
PLoS ONE, Vol 8, Iss 3, p e57415 (2013)
Bacterial chondroitinase ABC (ChaseABC) has been used to remove the inhibitory chondroitin sulfate chains from chondroitin sulfate proteoglycans to improve regeneration after rodent spinal cord injury. We hypothesized that the mammalian enzyme arylsu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c5fb64c5bfb815747861e9bc88507a7
https://pubmed.ncbi.nlm.nih.gov/23520469
https://pubmed.ncbi.nlm.nih.gov/23520469
Autor:
Juliane Poppe, Ulrike Demmer, Eberhard Warkentin, Klaus Schneider, Björn Kowalewski, Thomas Dierks, Ulrich Ermler
Some N-2-fixing bacteria prolong the functionality of nitrogenase in molybdenum starvation by a special Mo storage protein (MoSto) that can store more than 100 Mo atoms. The presented 1.6 angstrom X-ray structure of MoSto from Azotobacter vinelandii
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e00936c8909b6f847ffa999ec24bfa3
https://pub.uni-bielefeld.de/record/2517966
https://pub.uni-bielefeld.de/record/2517966
Autor:
Rrenate Lüllmann-Rauch, Torben Lübke, Markus Damme, Michael Padva, Ina Kalus, Björn Kowalewski, Jeffrey D. Esko, William C. Lamanna, Roger Lawrence, Stijn Stroobants, Thomas Dierks, Marc-André Frese, Rudi D'Hooge
Publikováno v:
Proceedings of the National Academy of Sciences; Vol 109
Deficiency of glycosaminoglycan (GAG) degradation causes a subclass of lysosomal storage disorders called mucopolysaccharidoses (MPSs), many of which present with severe neuropathology. Critical steps in the degradation of the GAG heparan sulfate rem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35c13508a5eef73459b5c2a36e4dbd54
https://doi.org/10.1073/pnas.1202071109
https://doi.org/10.1073/pnas.1202071109
Autor:
Björn Kowalewski, Juliane Poppe, Thomas Dierks, Eberhard Warkentin, Klaus Schneider, Ulrike Demmer, Ulrich Ermler
Publikováno v:
Journal of the American Chemical Society. 135:3729-3729
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1fb220bbe1b843c84a4170ec6fe5b4d9
https://doi.org/10.1021/ja311281g
https://doi.org/10.1021/ja311281g