Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Anna M. Kamińska"'
Autor:
Biruta Kierdaszuk, Magdalena Kaliszewska, Joanna Rusecka, Joanna Kosińska, Ewa Bartnik, Katarzyna Tońska, Anna M. Kamińska, Anna Kostera-Pruszczyk
Publikováno v:
Genes, Vol 12, Iss 1, p 54 (2020)
Mitochondrial encephalomyopathies comprise a group of heterogeneous disorders resulting from impaired oxidative phosphorylation (OxPhos). Among a variety of symptoms progressive external ophthalmoplegia (PEO) seems to be the most common. The aim of t
Externí odkaz:
https://doaj.org/article/c07ae59449ed42d19d0bcf8a6beff3da
Publikováno v:
Aktualności Neurologiczne, Vol 13, Iss 4, Pp 275-278 (2013)
Tętnica Percherona jest rzadkim wariantem anatomicznym unaczynienia, w którym przyśrodkowe części obu wzgórz i przyśrodkowa część śródmózgowia zaopatrywane są przez odgałęzienia pojedynczego naczynia krwionośnego odchodzącego od j
Externí odkaz:
https://doaj.org/article/7250614398cf45ee9e1d4bdb6618040a
Autor:
Justyna, Karolczak, Serge, Weis, Elisabeth, Ehler, Biruta, Kierdaszuk, Mariusz, Berdyński, Cezary, Zekanowski, Anna M, Kamińska, Maria Jolanta, Rędowicz
Publikováno v:
Anatomical record (Hoboken, N.J. : 2007). 297(9)
Myosin VI (MVI) is a unique unconventional myosin translocating, unlike other myosins, towards the minus end of actin filaments. It is involved in numerous cellular processes such as endocytosis, intracellular trafficking, cell migration, and transcr
Publikováno v:
Surface and Interface Analysis. 22:346-349
The application of ellipsometry to study the SiO x /Si system subjected to hydrostatic pressures up to 1.8 GPa at temperatures up to 1280 o C is described. The theoretical model of defects as the spherical disturbances of material has been assumed. T
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