Zobrazeno 1 - 10
of 26
pro vyhledávání: '"N M, Pleskach"'
Autor:
N N, Nikolsky, V M, Mikhelson, I M, Spivak, N M, Pleskach, V V, Prokofieva, Ya Yu, Komissarchik, A L, Yudin, Vladimir Davidovich, Zhestyanikov
Publikováno v:
Tsitologiia. 57(2)
Publikováno v:
Tsitologiia. 52(9)
We analyzed the effectiveness of wound healing in rats after application of the dermal equivalent (DE) based on fibrin with dermal fibroblasts. Histological studies of newly formed dermis biopsy samples selected during its recovery in the model wound
Publikováno v:
Tsitologiia. 50(10)
A case of adult progeria has been described. It has been suggested that this case is an atypical form of Werner syndrome with laminopathy--not WRN helicase-nuclease defect. During detailed studies of the patient's cells, epigenetic control and DNA da
Autor:
R I, Krutilina, A N, Smirnova, O S, Mudrak, M P, Svetlova, N M, Pleskach, S L, Oei, E M, Bradbury, A O, Zalensky, N V, Tomilin
Publikováno v:
Tsitologiia. 45(12)
Mammalian telomeres contain long tandem (TTAGGG)n repeats, which are protected by a complex of different proteins. Telomeric repeat-binding factors TRF1 and TRF2 play the key role in protection of telomeres through the formation of terminal loops (ca
Publikováno v:
Tsitologiia. 42(2)
XPA repair protein is absolutely needed for nucleotide excision repair (NER). It preferentially binds UV-irradiated DNA in vitro and possibly takes place in the recognition of pyrimidine dimers, the main type of UV-lesions in DNA. Using immunofluores
Autor:
L S, Barenfel'd, N V, Kalmykova, L F, Andreeva, N M, Pleskach, V V, Prokof'ev, V M, Mikhel'son
Publikováno v:
Tsitologiia. 41(11)
Some morphofunctional characters of fibroblasts in two genetic disorders--Cockayne syndrome (CS) and Basal cell naevus syndrome (BCNS) have been examined. The size of nucleus in BCN1SP line has been shown to be about 1.5 times less as well as the tot
Publikováno v:
Doklady Akademii nauk. 367(3)
Publikováno v:
Tsitologiia. 40(1)
The repair of gamma-ray-induced DNA single-strand breaks in transcribed (protooncogene c-myc) and non-transcribed (human satellite III) DNA of normal human fibroblasts and fibroblasts obtained from a patient with Cockayne's syndrome (CS) has been inv
Publikováno v:
Tsitologiia. 39(1)
Using DNA fiber autoradiography, DNA replication in cells of healthy donors and in those of patients with ataxia telangiectasia (AT) was estimated. A new fact has been demonstrated showing a decreased number of simultaneously operating in tandem grou
Publikováno v:
Tsitologiia. 38(8)
Complementation groups for xeroderma pigmentosum (XP) and Cockayne's syndrome (CS) cells have been first determined for patients encountered in the former Soviet Union. The determination was carried out using fusion of fibroblasts to be examined with