Zobrazeno 1 - 10
of 15
pro vyhledávání: '"V. M. Pampukha"'
Autor:
O. V. Gorodna, T. I. Bevz, V. S. Berezenko, Y. G. Antypkin, L. A. Livshits, M. B. Dyba, V. I. Bulavenko, L. V. Moroz, A. M. Kucherenko, V. M. Pampukha
Publikováno v:
Cytology and Genetics. 53:300-306
Toll-like receptor 4 (encoded by TLR4 gene) has a variety of functions, including tissue homeostasis, regulation of cell death and survival via activation of signaling pathways which lead to interferon regulatory factor 3 (IRF-3) activation and type
Autor:
K. Yu. Romanchuk, A. M. Kucherenko, S. Yu. Chernushyn, L. A. Livshits, L. V. Moroz, I. A. Bobrova, V. M. Pampukha
Publikováno v:
Cytology and Genetics
The aim of this study was to examine association between IFNL4 gene ss469415590 and treatment efficiency in group of Ukrainian PEG-interferon/ribavirin-treated chronic hepatitis C patients. Study group consisted of 92 unrelated hepatitis C virus geno
Autor:
Halyna Makukh, I. O. Kiselyk, B. I. Tretiak, V. M. Pampukha, I. Ye. Haiboniuk, S. A. Kravchenko, M. I. Dats-Opoka
Publikováno v:
Bulletin of Problems Biology and Medicine. 2:91
Publikováno v:
Genes and Diseases, Vol 4, Iss 2, Pp 108-110 (2017)
Phenylketonuria (PKU) is an autosomal recessive metabolic disorder caused by deficiency of phenylalanine hydroxylase (PAH). The major molecular defects causing PKU are missense mutations of PAH gene. Large deletions of exon 5 (EX5del955 and EX5del423
Autor:
S. Yu. Lohush, I. V. Dubrovska, T. V. Nikitchina, N. V. Hryshchenko, O. O. Soloviov, P. F. Tatarskyy, G. M. Bychkova, A. M. Kucherenko, G. B. Livshyts, V. M. Pampukha, N. O. Afanasieva, N. O. Zymak-Zakutnia, S. A. Kravchenko, E. J. Patskun, L. A. Livshits
Publikováno v:
Cytology and Genetics; Vol 46
The results of clinical, genealogical, cytogenetic, and molecular genetic studies of 113 patients from 96 families with different forms of mental retardation from Ukraine are presented. This study was held as part of the CHERISH project of the Sevent
Publikováno v:
Biopolymers and Cell, Vol 30, Iss 5, Pp 400-402 (2014)
Aim. To determine genotype and allele disribution for the IFNL4 gene ss469415590 and examine it for linkage with the IL28B gene rs12979860 in Ukrainian population. Methods. The studied group consisted of 100 unrelated donors of Eastern European origi
Publikováno v:
Biopolymers and Cell. 24:231-237
Publikováno v:
Biopolymers and Cell. 24:60-68
Publikováno v:
Cytology and Genetics. 47:164-166
TGFBI gene mutations cause corneal stromal dystrophies of autosomal dominant inheritance. The most frequent complication of stromal dystrophies is recurrent corneal erosion with varying degree of accompanying inflammation. IL-1β, IL-6 and IL-8 are m
Publikováno v:
Biopolymers and Cell. 19:536-540