Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Galina Soboleva"'
Autor:
Galina Soboleva, Irina Nepoklonova
Publikováno v:
Russian veterinary journal. 2021:5-13
The present article addresses issues related to feline leptospirosis. The causative agent of the infection is reviewed, alongside its morphology and up-to-date taxonomic classification including the concepts of serogroup and serovar. The fact that le
Autor:
Oleg Verhovsky, A G Yuzhakov, Irina Nepoklonova, Galina Soboleva, Sergey A. Raev, Konstantin Alexeev, A D Zaberezhny, Trevor Drew, Alexsandr Kotelnikov, Vladimir Shevkoplyas, Boris Orkyankin, Andrey Kapustin, Linda J. Saif, Grebennikova Tv, Alexsandr Mishin, Alexey Laishevtcev, Evgeniy Nepoklonov, Anastasia N. Vlasova, Natalia Vlasova, Evgeniy Shemelkov, T. I. Aliper
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4868cffb547004e2054b021409131002
https://doi.org/10.31016/viev-2019-1
https://doi.org/10.31016/viev-2019-1
Autor:
Aleksey Nikolaevich Marchenko, Dmitry I Dudich, Igor Dudich, Elena Dudich, Olga Roslovtceva, Luidmila Khromikh, Elena Vladimirovna Morozkina, Lidia Nikolaevna Semenkova, Sergey Vladimirovich Benevolensky, Sergey Zatcepin, Galina Soboleva, Eduard Borisovich Tatulov
Publikováno v:
Protein Expression and Purification. 84:94-107
Alpha-fetoprotein (AFP) is a biological drug candidate of high medicinal potential in the treatment of autoimmune diseases, cancer, and regenerative medicine. Large-scale production of recombinant human alpha-fetoprotein (rhAFP) is desirable for stru
Publikováno v:
Journal of Cellular Physiology. 197:149-156
The tissue inhibitor of metalloproteinases-3 (TIMP3) is a multifunctional protein tightly associated with the extracellular matrix (ECM). A specific type of mutation in TIMP3 which results in potentially unpaired cysteine residues at the C-terminus o
Autor:
Bernhard H F, Weber, Biaoyang, Lin, Karen, White, Konrad, Kohler, Galina, Soboleva, Sabine, Herterich, Mathias W, Seeliger, Gesine B, Jaissle, Christian, Grimm, Charlotte, Reme, Andreas, Wenzel, Esther, Asan, Heinrich, Schrewe
Publikováno v:
Investigative ophthalmologyvisual science. 43(8)
Sorsby fundus dystrophy (SFD) is a rare, late-onset macular dystrophy caused by mutations in the tissue inhibitor of metalloproteinases-3 (TIMP3) gene. The known mutations introduce potentially unpaired cysteine residues in the C terminus of the prot
Publikováno v:
Journal of Cellular Physiology; Oct2003, Vol. 197 Issue 1, p149-156, 8p
Autor:
Weber, B. H. F., Lin, B., White, K., Kohler, K., Galina Soboleva, Herterich, S., Seeliger, M. W., Jaissle, G. B., Grimm, C., Reme, C., Wenzel, A., Asan, E., Schrewe, H.
Publikováno v:
Europe PubMed Central
Scopus-Elsevier
Scopus-Elsevier
purpose. Sorsby fundus dystrophy (SFD) is a rare, late-onset macular dystrophy caused by mutations in the tissue inhibitor of metalloproteinases-3 (TIMP3) gene. The known mutations introduce potentially unpaired cysteine residues in the C terminus of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1fe647e7d848757ae54622cff667393
http://europepmc.org/abstract/med/12147610
http://europepmc.org/abstract/med/12147610