Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Angeliki Ferti-Passantonopoulou"'
Publikováno v:
Cancer Genetics and Cytogenetics. 54:259-261
We present here 3 of 30 cases of large bowel cancer cytogenetically studied, with deletion of chromosome 5. One of them presented a terminal deletion and the other two an interstitial deletion of chromosome 5q. In all three cases the segment 5q12-22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34fc810515a42f141e497c91e29429af
https://doi.org/10.1016/0165-4608(91)90217-i
https://doi.org/10.1016/0165-4608(91)90217-i
Publikováno v:
Cancer Genetics and Cytogenetics. 50:165-167
A case of acute nonlymphocytic leukemia (M4) secondary to treatment for multiple myeloma is described. The patient presented a translocation t(1;3)(p36;q21) and monosomy 7.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7055232ba7137d790233348d7515835e
https://doi.org/10.1016/0165-4608(90)90251-5
https://doi.org/10.1016/0165-4608(90)90251-5
Autor:
John Dervenoulas, Angeliki Ferti-Passantonopoulou, Sotos Raptis, Anna D. Panani, Vasiliki Pappa
Publikováno v:
Cancer genetics and cytogenetics. 55(2)
We report 2 of 80 cases of myelodysplastic syndromes (MDS) cytogenetically studied, with involvement of chromosome 13. The first case had a t(6;13), and the second had a t(1;13). Abnormalities of chromosome 13 mainly involving loss of band 13q14 have
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e01b67f0d7574da0d777dd0a3ea7815
https://pubmed.ncbi.nlm.nih.gov/1933815
https://pubmed.ncbi.nlm.nih.gov/1933815
Publikováno v:
Cancer genetics and cytogenetics. 51(2)
Thirty cases of breast cancer were cytogenetically studied by G-banding using direct tumor preparations. Among them 20 cases exhibited abnormalities of the long and/or short arm of chromosome 11. Thus, 11q was involved in 16 cases and 11p in ten case
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d7cfba03ac78c72ea088507f329c9c6
https://pubmed.ncbi.nlm.nih.gov/1993303
https://pubmed.ncbi.nlm.nih.gov/1993303
Publikováno v:
Cancer Genetics and Cytogenetics. 11:227-232
Cytogenetic findings of a primary renal-cell carcinoma are reported. The chromosome number was near triploid and there was tetrasomy for the long arm of chromosomes #1 and #3. The following structural chromosomal abnormalities were identified by the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55d1cfad24b33466cf242c1fc54a151c
https://doi.org/10.1016/0165-4608(84)90118-3
https://doi.org/10.1016/0165-4608(84)90118-3
Publikováno v:
Cancer Genetics and Cytogenetics. 11:87-90
A case of malignant lymphoma with a partial duplication of the long arm of chromosome #1, as well as 14q+ and 11q+ marker chromosomes, is presented. The coincidence of this duplicated segment of chromosome #1 with others described in the literature s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::495dfcf8c081770f664d6eae9ac3eb5f
https://doi.org/10.1016/0165-4608(84)90101-8
https://doi.org/10.1016/0165-4608(84)90101-8
Autor:
Robert P. Huben, Avery A. Sandberg, George R. Prout, Paola Dal Cin, Angeliki Ferti-Passantonopoulou, Frederick P. Li, Jerome P. Richie, Janusz Limon
Publikováno v:
Cancer genetics and cytogenetics. 35(1)
Clonal chromosome abnormalities in short-term cultures were found in 18 of 51 nonfamilial renal cell carcinomas. The breakpoints on chromosome 3 in seven specimens clustered in region 3p11–3p24.2, confirming its importance in the genesis of renal c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c68b25dc86a47278d74be5bf12578db
https://pubmed.ncbi.nlm.nih.gov/3180007
https://pubmed.ncbi.nlm.nih.gov/3180007
Publikováno v:
Cancer genetics and cytogenetics. 21(4)
Cytogenetic analysis of a biopsy specimen taken during sigmoidoscopy from an adenocarcinoma of the large bowel revealed a hypodiploid karyotype with numerical and structural abnormalities identified as trisomy 7, t(3;12), t(1;17), interstitial deleti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1040cc85f51ffc4b9626545865a4709f
https://pubmed.ncbi.nlm.nih.gov/3456826
https://pubmed.ncbi.nlm.nih.gov/3456826
Publikováno v:
Cancer genetics and cytogenetics. 24(1)
Cytogenetic analysis was performed in five cases of intestinal type gastric carcinoma. Three cases were near-diploid and two others were near-triploid. The chromosomes involved were: #9 (four cases), #8 (three cases), #1, and #7 (two cases each). The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a18a89c6f3436b6ab64f8edc358c2190
https://pubmed.ncbi.nlm.nih.gov/3791173
https://pubmed.ncbi.nlm.nih.gov/3791173