Zobrazeno 1 - 10
of 19
pro vyhledávání: '"L. I. Krivov"'
Publikováno v:
Biomedical Engineering. 49:79-84
Hardware and software for measuring respiration rate in mice are described. The design is based on slightly modified source code of the QPULSECAPTURE project. The measuring device based on an 86x PC and a webcam enables measurements with absolute err
Publikováno v:
Bulletin of Experimental Biology and Medicine. 152:692-695
Differences in the pools of 10 cytokine were found in blood samples from the caudal vein of mice with normal and abnormal heart rhythm. Both groups were albino mice bred by us and differing from mdx albino mice by the absence of mutation in muscular
Publikováno v:
Biology Bulletin. 35:151-160
Responses of the skeletal muscle tissue and thymus to muscle injury (complete transection) and wound xenoplasty with the minced muscle tissue of newborn rats (tissue therapy) were studied in mdx mice aged 12–16 and 40–48 weeks. The muscle tissue
Publikováno v:
Meditsinskaia tekhnika. (2)
Autor:
R. A. Poltavtseva, V. N. Yarygin, V. I. Savchuk, Gennady T. Sukhikh, A. V. Revishchin, L. I. Krivov, A. B. Kuznetsov, L. I. Korochkin, M. A. Aleksandrova, V. F. Sitnikov, M. A. Stenina, D. A. Voevodin
Publikováno v:
Bulletin of Experimental Biology and Medicine. 136:88-92
Human embryonic myogenic precursors were transplanted into muscles of mdx mice with hereditary dystrophin-deficient muscular dystrophy. Transplantation induced the synthesis of human dystrophin. The number of dystrophin-positive fibers progressively
Publikováno v:
Bulletin of experimental biology and medicine. 155(3)
In mdx mice, mutation in the muscle protein dystrophin gene results in the development of chronic degeneration of the muscle tissue. We performed a comparative analysis of blood cytokine levels in mdx mice, classical black mice and mice with addition
Publikováno v:
Patologicheskaia fiziologiia i eksperimental'naia terapiia. (4)
Dystrophin is a protein linking the cytoskeleton to a complex of transmembrane proteins that interact with the extracellular matrix. The fragility of the cardiomyocyte cell membrane resulting from the lack of dystrophin is thought to cause an excessi
Autor:
Potapova Aa, Malakhova Ea, A. A. Poznanskaya, O. V. Buyuklinskaya, Korsova Tl, S. M. Yakushina, L. I. Krivov, Morozova Na
Publikováno v:
Bulletin of Experimental Biology and Medicine. 116:1514-1517
Autor:
S. A. Obrubov, M. A. Stenina, L. I. Krivov, V. N. Yarygin, N. V. Komarova, A. V. Polyakov, V. I. Savchuk
Publikováno v:
Bulletin of experimental biology and medicine. 147(5)
Genetic selection in a colony of mdx mice (suffering from X-chromosome-linked muscular dystrophy) resulted in generation of their new genetic variant. In this new variant, the genetic, biochemical, and histological markers of muscular dystrophy are c
Publikováno v:
Izvestiia Akademii nauk. Seriia biologicheskaia. (2)
Responses of the skeletal muscle tissue and thymus to muscle injury (complete transection) and wound xenoplasty with the minced muscle tissue of newborn rats (tissue therapy) were studied in mdx mice aged 12-16 and 40-48 weeks. The muscle tissue of m