Informacja

Drogi użytkowniku, aplikacja do prawidłowego działania wymaga obsługi JavaScript. Proszę włącz obsługę JavaScript w Twojej przeglądarce.

Wyszukujesz frazę "Zajaczek, S." wg kryterium: Autor


Wyświetlanie 1-5 z 5
Tytuł:
Increased constitutional chromosome sensitivity to bleomycin in patients with hereditary non-polyposis colorectal cancer [HNPCC]
Autorzy:
Kladny, J
Zajaczek, S
Lubinski, J
Powiązania:
https://bibliotekanauki.pl/articles/2047245.pdf
Data publikacji:
1996
Wydawca:
Polska Akademia Nauk. Czytelnia Czasopism PAN
Tematy:
chromosome sensitivity
lymphocyte
hereditary non-polyposis colorectal cancer
tumour
colorectal cancer
bleomycin
genotoxic effect
Opis:
It has been suggested that mutagen sensitivity is a constitutional factor which may be useful in identification of patients with an increased risk for the development of tumors. In this study, the chromosome sensitivity to bleomycin was measured according to Hsu in patients with hereditary non-polyposis colorectal cancer (HNPCC), sporadic colorectal cancer and in control persons with no tumor history in family. In vitro lymphocytes were exposed to bleomycin according to Hsu and chromosomal damage was quantified by scoring breaks of 100 cells. A significant difference (P < 0.01) in the mean number of breaks per cell (b/c) was found between HNPCC patients (0.59 ± 0.14; n = 12; mean age 55.4 yrs) and control individuals (0.35 ± 0.13: n = 12; mean age 55.8 yrs). In contrast, patients with sporadic colorectal cancer showed a mean b/c value of 0.43 ± 0.14 (n = 14; mean age 63.4 yrs) which was not significantly higher than that in control individuals for this group (0.42 ± 0.15; n = 14; mean age 63.1 yrs). Selenium protected lymphocytes of HNPCC patients against bleomycin activity in vitro.
Źródło:
Journal of Applied Genetics; 1996, 37, 4; 385-392
1234-1983
Pojawia się w:
Journal of Applied Genetics
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Constitutional chromosome instability in families with patients affected by sporadic non-hereditary retinoblastoma
Autorzy:
Zajaczek, S
Gorski, B.
Krzystolik, Z.
Lubinski, J.
Powiązania:
https://bibliotekanauki.pl/articles/2043598.pdf
Data publikacji:
1999
Wydawca:
Polska Akademia Nauk. Czytelnia Czasopism PAN
Tematy:
retinoblastoma
sporadic non-hereditary retinoblastoma
chromosome
patient
bleomycin test
Źródło:
Journal of Applied Genetics; 1999, 40, 4; 343-353
1234-1983
Pojawia się w:
Journal of Applied Genetics
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
The first Rb-1 gene promoter germ-line de novo mutation in patient with retinoblastoma
Autorzy:
Zajaczek, S
Jakubowska, A.
Kurzawski, G.
Krzystolik, Z.
Lubinski, J.
Powiązania:
https://bibliotekanauki.pl/articles/2043638.pdf
Data publikacji:
1999
Wydawca:
Polska Akademia Nauk. Czytelnia Czasopism PAN
Tematy:
retinoblastoma
genetics
patient
Rb-1 gene
de novo mutation
Źródło:
Journal of Applied Genetics; 1999, 40, 3; 241-247
1234-1983
Pojawia się w:
Journal of Applied Genetics
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Molecular analysis of a large novel constitutional deletion in a patient with sporadic unilateral retinoblastoma
Autorzy:
Zajaczek, S
Cragg, H.
Jakubowska, A.
Gorski, B.
Krzystolik, Z.
Cowell, J.K.
Lubinski, J.
Powiązania:
https://bibliotekanauki.pl/articles/2043635.pdf
Data publikacji:
1999
Wydawca:
Polska Akademia Nauk. Czytelnia Czasopism PAN
Tematy:
retinoblastoma
large deletion
patient
Rb-1 gene
constitutional mutation
peripheral blood lymphocyte
molecular analysis
sporadic unilateral retinoblastoma
DNA
cancer
Źródło:
Journal of Applied Genetics; 1999, 40, 3; 233-239
1234-1983
Pojawia się w:
Journal of Applied Genetics
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Relationship between DNA replication and DNA repair in human lymphocytes proliferating in vitro in the presence and in absence of mutagen
Autorzy:
Szyfter, K
Wiktorowicz, K.
Wielgosz, M.S.
Zajaczek, S.
Kujawski, M.
Jaloszynski, P.
Czub, M.
Markowska, J.
Powiązania:
https://bibliotekanauki.pl/articles/2048210.pdf
Data publikacji:
1995
Wydawca:
Polska Akademia Nauk. Czytelnia Czasopism PAN
Tematy:
genotoxicity
DNA replication
human lymphocyte
DNA repair
lymphocyte proliferation
mutagenesis
in vitro
Opis:
The effects of mutagens on DNA replication and DNA repair were studied in peripheral blood lymphocytes (PBL) obtained from 21 healthy subjects, 2 samples from healthy heterozygote of Xeroderma pigmentosum (XP) and 2 samples from patient with clinically recognised XP. Inter-individual variations were found in DNA replication and in the level of spontaneous DNA repair measured under standard culture condition. Exposure of human PBL proliferating in vitro to B(a)P was followed by a partial inhibition of replicative DNA synthesis in all subjects and by an induction of DNA repair in healthy subjects. In XP patients DNA repair synthesis remained at the level attributed to spontaneous DNA repair. The response to mutagen varied individually. Results were analysed statistically. It was established that the studied indices of DNA synthesis correlate well with each other. The highest correlation was found between the levels of spontaneous and B(a)P-induced DNA repair. It is concluded that the level of spontaneous DNA repair is predictive for an estimation of cells ability to repair DNA damage. Inter-individual variations in the inhibition of DNA replication and in DNA repair synthesis are also dependent on the type of mutagen as shown by effects of other mutagens. Different effects of mutagen exposure on the inhibition of DNA replicative synthesis and induction of DNA repair can be explained by genetically controlled differences in the activity of enzymes responsible for mutagen processing and lesion removal.
Źródło:
Journal of Applied Genetics; 1995, 36, 4; 379-388
1234-1983
Pojawia się w:
Journal of Applied Genetics
Dostawca treści:
Biblioteka Nauki
Artykuł
    Wyświetlanie 1-5 z 5

    Ta witryna wykorzystuje pliki cookies do przechowywania informacji na Twoim komputerze. Pliki cookies stosujemy w celu świadczenia usług na najwyższym poziomie, w tym w sposób dostosowany do indywidualnych potrzeb. Korzystanie z witryny bez zmiany ustawień dotyczących cookies oznacza, że będą one zamieszczane w Twoim komputerze. W każdym momencie możesz dokonać zmiany ustawień dotyczących cookies