Zobrazeno 1 - 10 of 10 pro vyhledávání: '"E P, Nacheva"'
1
High-resolution analysis of acquired genomic imbalances in bone marrow samples from chronic myeloid leukemia patients by use of multiple short DNA probes
Autor: E. P. Nacheva, Patrick S. Tarpey, Alistair G. Reid
Publikováno v: Genes, Chromosomes and Cancer. 37:282-290
Chronic myeloid leukemia (CML) is a biphasic hematopoietic malignancy associated with a single cytogenetic aberration, the Philadelphia translocation t(9;22)(q34;q11), resulting in the BCR-ABL1 fusion oncogene. Molecular heterogeneity was recently de
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c07a684825e5201874d9c2332a4c485
https://doi.org/10.1002/gcc.10215
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3
The application of FISH techniques for physical mapping in the dog (Canis familiaris)
Autor: E. P. Nacheva, H. F. Dickens, Matthew M. Binns, N. G. Holmes, P. E. Fischer, Rachael Thomas
Publikováno v: Mammalian Genome. 7:37-41
The abundance of CA/GT repeats in the DNA of the dog (Canis familiaris) has established the importance of polymorphic microsatellites in the development of a low density map of the canine genome. The assignment of linkage groups of markers to chromos
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b3ee1a20765f15e53f714e42abd0c6a
https://doi.org/10.1007/s003359900009
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5
Genomic profile of chronic myelogenous leukemia: Imbalances associated with disease progression
Autor: Junia V. Melo, T. Holyoke, Colin Grace, Julie Howard, Diana Brazma, J. F. Apperley, E. P. Nacheva
Publikováno v: Genes, chromosomescancer. 46(11)
The expression of the chimeric BCR/ABL1 fusion gene resulting from t(9;22)(q34;q11) in chronic myelogenous leukemia (CML) is necessary for malignant transformation, but not sufficient to maintain disease progression. The appearance of various chromos
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::932bbbc932a288472f8d345ad5a28484
https://pubmed.ncbi.nlm.nih.gov/17696194
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6
Screening for specific chromosome involvement in hematological malignancies using a set of seven chromosome painting probes. An alternative approach for chromosome analysis using standard FISH instrumentation
Autor: E P, Nacheva, S, Gribble, K, Andrews, J, Wienberg, C D, Grace
Publikováno v: Cancer genetics and cytogenetics. 122(2)
We report the application of multi-color fluorescence in situ hydribidization (FISH) for bone marrow metaphase cell analysis of hematological malignancies using a sub-set of the human karyotype for chromosome painting. A combination of chromosome pro
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::9479622a9266ad555c95c628fdf4a2e5
https://pubmed.ncbi.nlm.nih.gov/11106813
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7
Cytogenetics of the chronic myeloid leukemia-derived cell line K562: karyotype clarification by multicolor fluorescence in situ hybridization, comparative genomic hybridization, and locus-specific fluorescence in situ hybridization
Autor: S M, Gribble, I, Roberts, C, Grace, K M, Andrews, A R, Green, E P, Nacheva
Publikováno v: Cancer genetics and cytogenetics. 118(1)
The transformation of chronic myeloid leukemia (CML) from a chronic phase to an acute phase is frequently accompanied by additional chromosome changes. Extensive chromosome G-banded studies have revealed the secondary changes are nonrandom and freque
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::699b4b1ebecb344ad0e1d054cc7495a3
https://pubmed.ncbi.nlm.nih.gov/10731582
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8
Molecular genetics and cytogenetics of myeloproliferative disorders
Autor: A J, Bench, E P, Nacheva, K M, Champion, A R, Green
Publikováno v: Bailliere's clinical haematology. 11(4)
The myeloproliferative disorders are believed to represent clonal malignancies resulting from transformation of a pluripotent stem cell. X-inactivation patterns of peripheral blood cells have been proposed as a useful diagnostic tool but this method
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::7f818a4aa46cc800658695955ab4905d
https://pubmed.ncbi.nlm.nih.gov/10640219
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10
Detection of chromosome 20q deletions in bone marrow metaphases but not peripheral blood granulocytes in patients with myeloproliferative disorders or myelodysplastic syndromes
Autor: F A, Asimakopoulos, T L, Holloway, E P, Nacheva, M A, Scott, P, Fenaux, A R, Green
Publikováno v: Blood. 87(4)
Myeloproliferative disorders and myelodysplastic syndromes arise in multipotent progenitors and may be associated with chromosomal deletions that can be detected in peripheral blood granulocytes. We present here seven patients with myeloproliferative
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::226c7121b7c8ffbdbd1429fbd0ecd774
https://pubmed.ncbi.nlm.nih.gov/8608248
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