Zobrazeno 1 - 10
of 17
pro vyhledávání: '"E. W. Fleischman"'
Autor:
E. W. Fleischman, O. I. Sokova, A. V. Popa, O. P. Kirichenko, L. N. Konstantinova, N. F. Metelkova
Publikováno v:
Онкогематология, Vol 0, Iss 4, Pp 12-16 (2022)
Peculiar age distribution of clinically significant recurring chromosome abnormalities was found as a result of investigation of526AML patients (249 children and 277 adults). Thus t(8;21) was more frequently detected in age from 2 to 10 years, t(15;1
Externí odkaz:
https://doaj.org/article/2b1d2cbd3e564918afd3ec6dd7efdea7
Publikováno v:
Онкогематология, Vol 11, Iss 1, Pp 14-23 (2016)
In this review we present current state of cytogenetic and molecular genetic diagnostics of various aberrations in infant acute leukemias together with our own experience in this field. A complex characteristic of acute leukemias was performed for bo
Externí odkaz:
https://doaj.org/article/dd9578b3cb124bc99aef1222f0903321
Deletion of theAlu-VpA/MycL1 (1p34.3) locus is a negative prognostic sign in human colorectal cancer
Publikováno v:
Molecular Biology. 34:337-344
We examined deletions of the short arm of chromosome 1 and aberrations of the microsatellite locusAlu-VpA/MycL1 (1p34.3) in human primary colorectal adenocarcinomas. Cytogenetically discernible deletions in 1p were found in 45% (14/31) of informative
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d59aba1132920fac0b0d4d13b4cdeb2e
https://doi.org/10.1007/bf02759663
https://doi.org/10.1007/bf02759663
Autor:
E W, Fleischman, S, Reshmi, M A, Frenkel, W I, Konovalova, G P, Guleva, O E, Kulagina, L N, Konstantinova, N N, Tupitsyn, J D, Rowley
Publikováno v:
Genes, chromosomescancer. 24(2)
We describe a patient with acute myeloblastic leukemia (AML-M0) whose cells had a t(2;11)(p21;q23). Fluorescence in situ hybridization analysis with a probe for MLL showed that it was split, hybridizing to both the derivative 2 and 11 chromosomes. Ni
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9cc864c31f54f0f629b0cdad15196144
https://pubmed.ncbi.nlm.nih.gov/9885982
https://pubmed.ncbi.nlm.nih.gov/9885982
Publikováno v:
Human genetics. 86(5)
The data of the chromosome abnormalities in 15 colorectal tumors are presented. Rearrangements of the short arm of chromosome 17, leading to deletions of this arm or its part were noted in 12 tumors; in 2 other cases, one of the homologs of pair 17 w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::853d4e34f4488c68d22f70eb59b04fba
https://pubmed.ncbi.nlm.nih.gov/2016090
https://pubmed.ncbi.nlm.nih.gov/2016090
Autor:
G. P. Puchkova, E. W. Fleischman, E. L. Prigogina, S. A. Balakirev, N. A. Zakhartchenko, M. A. Volkova, M. A. Frenkel, L. N. Konstantinova
Publikováno v:
Human Genetics. 58:285-293
Results of chromosome studies of blood and bone marrow cells from 101 patients with Ph1 positive chronic myeloid leukemia (CML) confirm the assumptions that clinical and morphologic manifestations of the disease correlate with karyotype peculiarities
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc1c595996fba2e583591d93b0ba91d3
https://doi.org/10.1007/bf00294925
https://doi.org/10.1007/bf00294925
Publikováno v:
Human Genetics. 50:101-104
Two male patients with myeloproliferative disorders (osteomyelosclerosis in one and CML in the other) were found to have a chromosomal marker 20q- in blood cells (unstimulated short time cultures). Marked erythropoietic disturbances were not revealed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75f915dcf698bc211b4ab2167ab99e54
https://doi.org/10.1007/bf00295596
https://doi.org/10.1007/bf00295596
Autor:
S. A. Balakirev, S A Majakova, E. W. Fleischman, I. S. Peterson, O. E. Kulagina, N V Khvatova, G. P. Puchkova, M. A. Frenkel, E. L. Prigogina
Publikováno v:
Human Genetics. 53:5-16
The karyotype of leukemic cells of 78 acute leukemia patients (37 ANLL, 34ALL, and 7 of unknown type) was studied by means of G-banding. Chromosomal abnormalities were found in 50 patients (72%). Chromosomes 8,21,5,7,11, and 19 were preferentially in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e9e079c41194e0cc83e73c0274297363
https://doi.org/10.1007/bf00289443
https://doi.org/10.1007/bf00289443
Autor:
E. L. Prigogina, E. W. Fleischman
Publikováno v:
Human Genetics. 35:269-279
Karyotypes of 30 malignant lymphomas were studied with the aid of G-banding. Frequent occurrence of rearranged chromosomes 14 and 11 was noted. In several tumors, identical acrocentric markers, appearing after translocation of the long arm of chromos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::530e8771c3869f05fa36bf05e04b6076
https://doi.org/10.1007/bf00446620
https://doi.org/10.1007/bf00446620
Autor:
E. W. Fleischman, E. L. Prigogina
Publikováno v:
Human Genetics. 30:113-119
The study of chromosome banding pattern of leukaemic cells in 15 patients with CML revealed t(9;22) in all cases. Similar additional chromosome abnormalities were observed in the terminal stage of the disease in 5 of 9 patients with aneuploid cell li
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b70f533fa8ab7c742500c8ed8a5a336
https://doi.org/10.1007/bf00291943
https://doi.org/10.1007/bf00291943