Zobrazeno 1 - 3
of 3
pro vyhledávání: '"R. L. Anisimov"'
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:
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
Publikováno v:
Applied Biochemistry and Microbiology. 53:770-774
Two previously obtained, full-size, fully human antibodies that reversibly bind the active form of an enzyme belonging to the subtype EC 3.2.1, which is used for substitutive enzymatic therapy in lysosomal storage diseases, have been characterized by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::490b3859e8d741c6ccdb408da4f83b80
https://doi.org/10.1134/s0003683817070055
https://doi.org/10.1134/s0003683817070055