Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Mary J. Morrison"'
Publikováno v:
Cancer Genetics and Cytogenetics. 113:126-133
A case of acute myeloid leukemia (M2) with double minute chromosomes and complex karyotypic abnormalities was analyzed cytogenetically and molecularly. Comparative genomic hybridization (CGH) showed that the 8q24 region that contains the MYC oncogene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e8d8a38e65bffaab80af25c1d37b523f
https://doi.org/10.1016/s0165-4608(99)00018-7
https://doi.org/10.1016/s0165-4608(99)00018-7
Publikováno v:
Cancer Genetics and Cytogenetics. 112:144-148
We have characterized the double minute chromosomes in a case of acute myeloid leukemia (AML). Southern blot analysis showed that the C-MYC was amplified. Further analysis with probes located both 3' and 5' of MYC indicated that the amplicon was at l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34aa5c5b6bba90f15056a5abcd6d3fd7
https://doi.org/10.1016/s0165-4608(98)00260-x
https://doi.org/10.1016/s0165-4608(98)00260-x
Autor:
Mary J. Morrison, Peter E. Crossen
Publikováno v:
Mechanisms of Ageing and Development. 88:61-65
We studied the frequency of an Sst I polymorphism of the ETS-I oncogene in 122 elderly subjects (mean age 78.14 years) and 115 teenagers (mean age 16.9 years). No difference in the frequency of the three genotypes (C1C1, C1C2, C2C2) was found between
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e9f7cc54f59a6c10ade4afbc9c26c3da
https://doi.org/10.1016/0047-6374(96)01721-6
https://doi.org/10.1016/0047-6374(96)01721-6
Autor:
Peter E. Crossen, Mary J. Morrison
Publikováno v:
Leukemia Research. 23:251-253
We examined the methylation status of the third exon of the MYC oncogene in 39 patients with B-cell malignancies. DNA was digested with MspI plus EcoRI or HpaII plus EcoRI and hybridised with a probe specific for the third exon of MYC. Thirty four pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::361c630f9054514e5138f88c1ba48b9f
https://doi.org/10.1016/s0145-2126(98)00167-2
https://doi.org/10.1016/s0145-2126(98)00167-2
Autor:
Gabi U. Dachs, Sarah P. Gunningham, Mary J. Morrison, Margaret J. Currie, Margret C. M. Vissers
Publikováno v:
Free radical biologymedicine. 42(6)
Control of the transcription factor hypoxia inducible factor (HIF)-1 is mediated by hydroxylation by proline and asparagine hydroxylases. These enzymes require ascorbate for optimal activity, but little attention has been given to the effect of ascor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15c248642a25e739f8d9d189c59053fd
https://pubmed.ncbi.nlm.nih.gov/17320759
https://pubmed.ncbi.nlm.nih.gov/17320759
Publikováno v:
Genes, Chromosomes and Cancer. 8:60-62
The t(14;19) is a recurring translocation found in a small number of cases of chronic B-cell leukemia (CLL). We have cloned and sequenced the breakpoint in a patient with a t(14;19) and shown that the breakpoint on chromosome 14 occurred in the Cμ s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b805b169be35c39d7ac8ac3b21703b3
https://doi.org/10.1002/gcc.2870080110
https://doi.org/10.1002/gcc.2870080110
Publikováno v:
Cancer genetics and cytogenetics. 128(2)
Cytogenetic analysis of a patient with non-Hodgkin lymphoma revealed the following karyotype: 49,XXX,t(2;14)(q21;q32),+4,+8,del(13)(q14q21). Southern blot analysis with an Ig region probe showed non-productive rearrangements indicative of a transloca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f307dd3bd35f5653e4971215783d22e
https://pubmed.ncbi.nlm.nih.gov/11463452
https://pubmed.ncbi.nlm.nih.gov/11463452
Autor:
Peter E. Crossen, Mary J. Morrison
Publikováno v:
Leukemialymphoma. 31(5-6)
Analysis of the organisation of the Cmu-switch region of the immunoglobulin heavy chain locus in B-lymphocytes from 80 patients with chronic B-cell leukemia revealed 25 patients with abnormal rearrangements that could not be explained by the normal r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ee7b3b8d39ae0f5629ba46c85c38f52
https://pubmed.ncbi.nlm.nih.gov/9922046
https://pubmed.ncbi.nlm.nih.gov/9922046
Publikováno v:
Cancer genetics and cytogenetics. 79(1)
We studied the frequency of a SstI polymorphism of the Ets-1 oncogene in 100 patients with non-Hodgkin's lymphoma, 44 patients with Hodgkin's disease, 49 patients with chronic myeloid leukemia, and 100 controls. There was no difference in the genotyp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3abb61c6e8b280b72afcc2fe87e85c48
https://pubmed.ncbi.nlm.nih.gov/7850755
https://pubmed.ncbi.nlm.nih.gov/7850755
Publikováno v:
Human Genetics. 93
New HindIII, RsaI and TaqI restriction fragment length polymorphisms (RFLPs) within the haemopoietic cell kinase gene in chromosome band 20q11.2 are described. These RFLPs provide a useful marker for linkage analysis in proximal 20q.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac30e31f831149abd215db677fc7a9ec
https://doi.org/10.1007/bf00202836
https://doi.org/10.1007/bf00202836