Zobrazeno 1 - 10
of 367
pro vyhledávání: '"Formylglycine-generating enzyme"'
Autor:
Krüger, Tobias1, Weiland, Stefanie2, Falck, Georg3, Gerlach, Marcus1, Boschanski, Mareile2, Alam, Sarfaraz2, Müller, Kristian M.3 kristian.mueller@uni-bielefeld.de, Dierks, Thomas2 thomas.dierks@uni-bielefeld.de, Sewald, Norbert1 norbert.sewald@uni-bielefeld.de
Publikováno v:
Angewandte Chemie. 6/11/2018, Vol. 130 Issue 24, p7365-7369. 5p.
Autor:
Wieczorek, Andrew1, Chan, Clara K.1, Kovacic, Suzana1,2, Li, Cindy1, Dierks, Thomas3, Forde, Nancy R.1,2,4,5
Publikováno v:
Canadian Journal of Chemistry. 2018, Vol. 96 Issue 2, p204-211. 8p.
Autor:
York, Dona1, Baker, Jeanne2, Holder, Patrick G.2, Jones, Lesley C.2, Drake, Penelope M.2, Barfield, Robyn M.2, Bleck, Gregory T.1, Rabuka, David2 david.rabuka@catalent.com
Publikováno v:
BMC Biotechnology. 2/24/2016, Vol. 16, p1-11. 11p.
Autor:
Peng, Jianhe1, Alam, Sarfaraz1, Radhakrishnan, Karthikeyan1,2, Mariappan, Malaiyalam1, Rudolph, Markus Georg3, May, Caroline4, Dierks, Thomas2, Figura, Kurt1, Schmidt, Bernhard1
Publikováno v:
FEBS Journal. Sep2015, Vol. 282 Issue 17, p3262-3274. 13p.
Akademický článek
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Autor:
S. S. Timonova, K. A. Smolova, I. A. Kirik, M. S. Pantyushenko, R. L. Anisimov, R. A. Khamitov, A. A. Piskunov, V. N. Bade
Publikováno v:
Биопрепараты: Профилактика, диагностика, лечение, Vol 22, Iss 3, Pp 279-292 (2022)
Maroteaux—Lamy syndrome (mucopolysaccharidosis type VI) is an orphan genetic disease caused by mutations in the arylsulfatase B gene (ARSB), which encodes the lysosomal enzyme arylsulfatase B (ASB). The relevance of the study lies in the need of a
Externí odkaz:
https://doaj.org/article/0b30e05b6856405db940aee08bf4c2fd
Autor:
Schlotawa, Lars1, Radhakrishnan, Karthikeyan2, Baumgartner, Matthias3, Schmid, Regula4, Schmidt, Bernhard5, Dierks, Thomas6, Gärtner, Jutta1
Publikováno v:
European Journal of Human Genetics. Sep2013, Vol. 21 Issue 9, p1020-1023. 4p. 1 Color Photograph, 2 Charts.
Autor:
S. S. Timonova, K. A. Smolova, D. T. Zaripova, M. S. Pantyushenko, M. A. Koroleva, R. L. Anisimov, R. A. Khamitov, A. A. Piskunov, V. N. Bade
Publikováno v:
Биопрепараты: Профилактика, диагностика, лечение, Vol 22, Iss 1, Pp 80-93 (2022)
Mucopolysaccharidosis type VI (Maroteaux–Lamy syndrome) is an orphan genetic disease caused by deficiency of the lysosomal enzyme arylsulfatase B (ASB). The need to develop a highly productive cell line for the production of recombinant ASB, is beh
Externí odkaz:
https://doaj.org/article/58915adae86c4684bea3a680aa9abe9c
Autor:
Lars Schlotawa, Karolina Tyka, Matthias Kettwig, Rebecca C Ahrens‐Nicklas, Matthias Baud, Tea Berulava, Nicola Brunetti‐Pierri, Alyssa Gagne, Zackary M Herbst, Jean A Maguire, Jlenia Monfregola, Tonatiuh Pena, Karthikeyan Radhakrishnan, Sophie Schröder, Elisa A Waxman, Andrea Ballabio, Thomas Dierks, André Fischer, Deborah L French, Michael H Gelb, Jutta Gärtner
Publikováno v:
EMBO Molecular Medicine, Vol 15, Iss 3, Pp n/a-n/a (2023)
Abstract Multiple sulfatase deficiency (MSD, MIM #272200) results from pathogenic variants in the SUMF1 gene that impair proper function of the formylglycine‐generating enzyme (FGE). FGE is essential for the posttranslational activation of cellular
Externí odkaz:
https://doaj.org/article/b678e69f8129428e87e0aebc0aa61cd4
Autor:
Álvarez-Barcia, Sonia1, Kästner, Johannes1
Publikováno v:
European Physical Journal: Special Topics. Mar2019, Vol. 227 Issue 14, p1657-1664. 8p.