Zobrazeno 1 - 10
of 11
pro vyhledávání: '"D H, Spathas"'
Autor:
Chiara Magnanini, E. Karayianni, G. M. Maniatis, V. Orphanos, Giuseppe Barbanti-Brodano, Massimo Negrini, D. H. Spathas, Cristina Morelli
Publikováno v:
Cytogenetic and Genome Research. 86:263-266
We present the transcription map of chromosome region 6q16→q21 by mapping fifteen known genes within this region. Five genes lay in the subregion containing a tumor suppressor gene, eight genes are located in the subregion harboring a senescence ge
Publikováno v:
Prenatal Diagnosis. 14:1061-1069
In this paper we describe the use of five-colour fluorescence in situ hybridization for prenatal diagnosis of aneuploidy using uncultured amniotic fluid cells. The analysis is based on ratio mixing of dual-labelled probes and digital imaging for the
Publikováno v:
Prenatal Diagnosis. 14:1049-1054
A prospective study was undertaken to evaluate the use of fluorescence in situ hybridization (FISH) for the detection of trisomy 21 in interphase nuclei of uncultured amniotic fluid cells. Five hundred cases were analysed in situ and classified as no
Autor:
V. Macheraki, N. Demopoulos, M. Kokkinaki, D. H. Spathas, G. Stephanou, N. Moschonas, V. Orphanos, G. M. Maniatis, S. Kamakari
Publikováno v:
Analytical Use of Fluorescent Probes in Oncology ISBN: 9781461376798
Deletions or loss of heterozygosity in certain regions of the long arms of human chromosomes 6 and 10 have been reported over the last few years in several types of malignancies; more specifically, region 6ql6.3-q21 is frequently deleted in patients
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e2c0c436b9fa8ca045d72c22dbb0a52b
https://doi.org/10.1007/978-1-4615-5845-3_45
https://doi.org/10.1007/978-1-4615-5845-3_45
Autor:
M, Mouratidou, D, Sotiropoulos, K, Deremitzaki, D H, Spathas, A V, Hoffbrand, H G, Prentice, K, Papanastasiou, S, Tsakanikas, P, Tsaftaridis, M, Stamatelou
Publikováno v:
Bone marrow transplantation. 12(1)
Donor cell leukemia after BMT has been documented in a small number of cases mainly by cytogenetic studies. We describe a case of leukemia relapse in a 16-year-old girl 1 year after BMT from her histocompatible brother. Relapse in donor cells was ini
Publikováno v:
Molecular biologymedicine. 7(5)
We have used a moderate repeat probe and a number of single copy DNA probes of varying sizes to compare different approaches to non-radioactive in situ hybridization. We have compared the ease and speed of the methods, the sensitivity, resolution, re
Publikováno v:
FEMS Microbiology Letters. 17:345-348
Publikováno v:
Human Genetics. 81:153-156
A gene for tRNAGlu has been assigned to human chromosome 1p36 by in situ hybridisation using a [3H]-labelled or biotinylated 2.4-kb (human) DNA fragment containing a tRNAGlu gene as a probe. With the biotinylated DNA probe a secondary statistically s
Publikováno v:
Journal of general microbiology. 128(3)
Summary: The uptake of putrescine, spermidine and spermine was studied in Aspergillus nidulans using 14C-labelled polyamines. Active transport systems, inhibited by azide and regulated by nitrogen availability, exist at least for putrescine and sperm
Publikováno v:
Journal of general microbiology. 129(6)
SUMMARY: A mutation designated spsA1 has been induced in the putrescine (puA2) auxotroph of Aspergillus nidulans which enables this mutant to grow on low concentrations of spermidine in place of putrescine. In addition, the spsA1 mutant, irrespective