Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Maria J. Rȩdowicz"'
Autor:
Krzysztof M. Bernadzki, Marta Gawor, Marcin Pęziński, Paula Mazurek, Paweł Niewiadomski, Maria J. Rędowicz, Tomasz J. Prószyński
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-12 (2017)
Abstract Neuromuscular junctions (NMJs) are specialized synapses that connect motor neurons to skeletal muscle fibers and orchestrate proper signal transmission from the nervous system to muscles. The efficient formation and maintenance of the postsy
Externí odkaz:
https://doaj.org/article/a915312fded04c5d85d5331d3e7c5e38
Autor:
Severyn Myronovkij, Nazar Negrych, Tetyana Nehrych, Maria J. Redowicz, Serhiy Souchelnytskyi, Rostyslav Stoika, Yuriy Kit
Publikováno v:
Biochemistry and Biophysics Reports, Vol 5, Iss C, Pp 175-179 (2016)
We searched for protein markers present in blood serum of multiple sclerosis (MS), rheumatoid arthritis (RA) and systemic lupus erythematosus (SLE) patients in comparison to healthy human individuals. We used precipitation/extraction methods and MALD
Externí odkaz:
https://doaj.org/article/648d65866e46479a8538d0eae201f530
Autor:
Anna Macias, Jakub Piotr Fichna, Malgorzata Topolewska, Maria J. Rȩdowicz, Anna M. Kaminska, Anna Kostera-Pruszczyk
Publikováno v:
Frontiers in Neuroscience, Vol 15 (2021)
Limb–girdle muscular dystrophy type R1 (LGMDR1) is caused by mutations in CAPN3 and is the most common type of recessive LGMD. Even with the use of whole-exome sequencing (WES), only one mutant allele of CAPN3 is found in a significant number of LG
Externí odkaz:
https://doaj.org/article/337ad31ac4cd4a9d8166ab21a5852521
Autor:
Jakub Piotr Fichna, Maria J. Rȩdowicz, Anna Macias, Anna Kamińska, Anna Kostera-Pruszczyk, Malgorzata Topolewska
Publikováno v:
Frontiers in Neuroscience
Frontiers in Neuroscience, Vol 15 (2021)
Frontiers in Neuroscience, Vol 15 (2021)
Limb–girdle muscular dystrophy type R1 (LGMDR1) is caused by mutations in CAPN3 and is the most common type of recessive LGMD. Even with the use of whole-exome sequencing (WES), only one mutant allele of CAPN3 is found in a significant number of LG
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fa5601798bd9bd4fae17dcfe2ff390db
https://doi.org/10.3389/fnins.2021.692482
https://doi.org/10.3389/fnins.2021.692482
Publikováno v:
FEBS Letters. 243:30-32
Limited digestion of filamentous myosin with chymotrypsin at 0 degrees C in the absence of divalent cations generates two forms of subfragment 1 (S1), with heavy chains of 95 kDa and 98 kDa. The difference is at the C-terminal end of the chain. The 9
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3ce63732f1e89a7e794670b2de43a17c
https://doi.org/10.1016/0014-5793(89)81211-6
https://doi.org/10.1016/0014-5793(89)81211-6
Publikováno v:
European journal of biochemistry. 165(2)
Tryptic digestion patterns reveal a close similarity of the substructure of frog subfragment-1 (S1) to that established for rabbit S1. The 97-kDa heavy chain of chymotryptic S1 of frog myosin is preferentially cleaved into three fragments with appare
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::743f918edd1e80d88b89b87a834dffe4
https://pubmed.ncbi.nlm.nih.gov/2954820
https://pubmed.ncbi.nlm.nih.gov/2954820