Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Vasily D. Antonenkov"'
Autor:
Kaisa M. Kettunen, Riitta Karikoski, Riikka H. Hämäläinen, Teija T. Toivonen, Vasily D. Antonenkov, Natalia Kulesskaya, Vootele Voikar, Maarit Hölttä-Vuori, Elina Ikonen, Kirsi Sainio, Anu Jalanko, Susann Karlberg, Niklas Karlberg, Marita Lipsanen-Nyman, Jorma Toppari, Matti Jauhiainen, J. Kalervo Hiltunen, Hannu Jalanko, Anna-Elina Lehesjoki
Publikováno v:
Biology Open, Vol 5, Iss 5, Pp 584-595 (2016)
Mulibrey nanism (MUL) is a rare autosomal recessive multi-organ disorder characterized by severe prenatal-onset growth failure, infertility, cardiopathy, risk for tumors, fatty liver, and type 2 diabetes. MUL is caused by loss-of-function mutations i
Externí odkaz:
https://doaj.org/article/f8f2c0d5711c4276a5a02eaf172b5914
Autor:
Melisa Gualdron-López, Miia H Vapola, Ilkka J Miinalainen, J Kalervo Hiltunen, Paul A M Michels, Vasily D Antonenkov
Publikováno v:
PLoS ONE, Vol 7, Iss 4, p e34530 (2012)
BACKGROUND: Glycosomes are a specialized form of peroxisomes (microbodies) present in unicellular eukaryotes that belong to the Kinetoplastea order, such as Trypanosoma and Leishmania species, parasitic protists causing severe diseases of livestock a
Externí odkaz:
https://doaj.org/article/9e09543587d240ac804bb5bb9e4f4ff0
Autor:
Aare Rokka, Vasily D Antonenkov, Raija Soininen, Hanna L Immonen, Päivi L Pirilä, Ulrich Bergmann, Raija T Sormunen, Matti Weckström, Roland Benz, J Kalervo Hiltunen
Publikováno v:
PLoS ONE, Vol 4, Iss 4, p e5090 (2009)
BACKGROUND: Peroxisomal metabolic machinery requires a continuous flow of organic and inorganic solutes across peroxisomal membrane. Concerning small solutes, the molecular nature of their traffic has remained an enigma. METHODS/PRINCIPAL FINDINGS: I
Externí odkaz:
https://doaj.org/article/82fa9d2b847f4cfaab1892bbe76aabda
Autor:
Wolfgang Girzalsky, J. Kalervo Hiltunen, Sabrina Mindthoff, Vasily D. Antonenkov, Laura L. Steinfort, Silke Grunau, Ralf Erdmann
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1863(2):271-283
More than 30 proteins (Pex proteins) are known to participate in the biogenesis of peroxisomes-ubiquitous oxidative organelles involved in lipid and ROS metabolism. The Pex11 family of homologous proteins is responsible for division and proliferation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e3381a9443d030a82b25dd64bfb7ec01
Autor:
Anu Jalanko, Susann Karlberg, Niklas Karlberg, Matti Jauhiainen, J. Kalervo Hiltunen, Kirsi Sainio, Anna-Elina Lehesjoki, Riikka H. Hämäläinen, Teija T. Toivonen, Natalia Kulesskaya, Marita Lipsanen-Nyman, Vootele Voikar, Kaisa Kettunen, Jorma Toppari, Elina Ikonen, Hannu Jalanko, Maarit Hölttä-Vuori, Riitta Karikoski, Vasily D. Antonenkov
Publikováno v:
Biology Open, Vol 5, Iss 5, Pp 584-595 (2016)
Biology Open
Biology Open
Mulibrey nanism (MUL) is a rare autosomal recessive multi-organ disorder characterized by severe prenatal-onset growth failure, infertility, cardiopathy, risk for tumors, fatty liver, and type 2 diabetes. MUL is caused by loss-of-function mutations i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1814512b4b7d4d5a40d17faf07e1dd19
https://doi.org/10.1242/bio.016246
https://doi.org/10.1242/bio.016246
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1822:1374-1386
Peroxisomes perform a large variety of metabolic functions that require a constant flow of metabolites across the membranes of these organelles. Over the last few years it has become clear that the transport machinery of the peroxisomal membrane is a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b984654fba6d5394ce16b62bd58b6af9
https://doi.org/10.1016/j.bbadis.2011.12.011
https://doi.org/10.1016/j.bbadis.2011.12.011
Publikováno v:
Antioxidants & Redox Signaling. 13:525-537
Peroxisomes are multifunctional organelles with an important role in the generation and decomposition of reactive oxygen species (ROS). In this review, the ROS-producing enzymes, as well as the antioxidative defense system in mammalian peroxisomes, a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb164dd95d286d540011555d97c31dc1
https://doi.org/10.1089/ars.2009.2996
https://doi.org/10.1089/ars.2009.2996
Autor:
Sabrina Mindthoff, Vasily D. Antonenkov, Silke Grunau, Hanspeter Rottensteiner, Raija Sormunen, J. Kalervo Hiltunen, Ralf Erdmann
Publikováno v:
FEBS Journal. 276:1698-1708
Highly-purified peroxisomes from the yeast Saccharomyces cerevisiae grown on oleic acid were investigated for the presence of channel (pore)-forming proteins in the membrane of these organelles. Solubilized membrane proteins were reconstituted in pla
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e97c6181ad89b096a262c1a61d83f538
https://doi.org/10.1111/j.1742-4658.2009.06903.x
https://doi.org/10.1111/j.1742-4658.2009.06903.x
Autor:
J. Kalervo Hiltunen, Hans Weiher, Vasily D. Antonenkov, Thomas Kietzmann, Miia Vapola, Daniela Mennerich, Antti Isomursu
The human MPV17-related mitochondrial DNA depletion syndrome is an inherited autosomal recessive disease caused by mutations in the inner mitochondrial membrane protein MPV17. Although more than 30 MPV17 gene mutations were shown to be associated wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c3a5c7bc52cde1787f5bca7d6517bea5
https://europepmc.org/articles/PMC4447960/
https://europepmc.org/articles/PMC4447960/
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1763(12):1697-1706
The review is dedicated to recent progress in the study of peroxisomal membrane permeability to solutes which has been a matter of debate for more than 40 years. Apparently, the mammalian peroxisomal membrane is freely permeable to small solute molec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf253851d72341b621e223fb27b0374b