Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Maureen E. Sherer"'
Autor:
Jie Hu, Svetlana A. Yatsenko, Urvashi Surti, Zhishuo Ou, Maureen E. Sherer, Jane Casey, Erika Friehling, Susanne M. Gollin, Heather A. Bakos, Kathleen Vitullo
Publikováno v:
Cytogenetic and Genome Research. 150:242-252
We present a comprehensive comparison of PAX5,IKZF1, and CDKN2A/B abnormalities in 21 B-cell precursor acute lymphoblastic leukemia (B-ALL) patients studied by aCGH and gene-specific FISH assays. In our cohort of B-ALL patients, alterations of IKZF1,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::90a544317c7aae459c3e6820a221f949
https://doi.org/10.1159/000456572
https://doi.org/10.1159/000456572
Autor:
Fiona E. Craig, Robert L. Redner, Maureen E. Sherer, S Shekhter-Levin, Lydia Contis, Carol Evans
Publikováno v:
Leukemia. 20:376-379
A novel t(3;17)(p25;q21) variant translocation of acute promyelocytic leukemia with rearrangement of the RARA locus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d13b133f81703b7da50a56845dae38cc
https://doi.org/10.1038/sj.leu.2404062
https://doi.org/10.1038/sj.leu.2404062
Publikováno v:
Human Pathology. 34:1212-1215
Two translocations involving the MALT1 gene have been described in extranodal marginal zone B-cell lymphomas of MALT type. A t(11;18)(q21;q21) involving API2 and MALT1 occurs in a subset of MALT lymphomas but with only rare exception is absent in dif
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::25f6f399ea8b493e750df405e80b4813
https://doi.org/10.1016/j.humpath.2003.08.007
https://doi.org/10.1016/j.humpath.2003.08.007
Publikováno v:
Cancer Genetics and Cytogenetics. 143:154-159
Cytogenetic studies provide important information for the diagnosis and classification of malignant lymphomas that in some cases also has prognostic significance. Furthermore, the investigation of isolated novel cytogenetic findings in malignant lymp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::44e0706810a2cf19413475ae7d380b1a
https://doi.org/10.1016/s0165-4608(02)00857-9
https://doi.org/10.1016/s0165-4608(02)00857-9
Autor:
Silloo B. Kapadia, Steven H. Swerdlow, Maureen E. Sherer, Niel Wald, Sofia Shekhter-Levin, W.Victoria Li, Susanne M. Gollin, Edward D. Ball
Publikováno v:
Cancer Genetics and Cytogenetics. 103:124-129
We present the case of a 40-year-old man with aggressive systemic mast cell disease. The patient had a predominant near-haploid clone in his bone marrow cells, detected by cytogenetic analysis performed at the time of diagnosis. The similarities betw
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da3e595534170e42a6a3d767a75fe6be
https://doi.org/10.1016/s0165-4608(97)00386-5
https://doi.org/10.1016/s0165-4608(97)00386-5
Autor:
Susanne M. Gollin, Maureen E. Sherer, Elana J. Bloom, Niel Wald, Sofia Shekhter-Levin, Steven H. Swerdlow
Publikováno v:
Cancer Genetics and Cytogenetics. 95:190-197
Two years after a bone marrow transplant (BMT) from his haploidentical mother, a 28-year-old male with a history of acute lymphoblastic leukemia (ALI.) developed myelodysplastic syndrome (MDS) with monosomy 7 in his female bone marrow cells. Follow-u
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0129906c585ae26c318a191f223de65d
https://doi.org/10.1016/s0165-4608(96)00263-4
https://doi.org/10.1016/s0165-4608(96)00263-4
Publikováno v:
Cancer Genetics and Cytogenetics. 86:107-115
Tetraploidy and near-tetraploidy are observed infrequently in hematologic malignancies, most commonly seen in cases of childhood acute lymphoblastic leukemia, and are associated with large blast size. Four cases of adult acute myelogenous leukemia (A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb5d3a623761cf3e6b0919220682a7dd
https://doi.org/10.1016/0165-4608(95)00184-0
https://doi.org/10.1016/0165-4608(95)00184-0
Autor:
Niel Wald, Susanne M. Gollin, Lila Penchansky, Sofia Shekhter-Levin, Michael R. Wollman, Maureen E. Sherer
Publikováno v:
Cancer Genetics and Cytogenetics. 84:99-104
Cytogenetic analysis of bone marrow cells revealed an abnormal clone with monosomy 7 and trisomy 21 in a 12-year-old child with Kostmann disease (KD). The patient presented with anemia, thrombocytopenia, and splenomegaly after 5 years of treatment wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7317be00689d6b8010459e8739783e16
https://doi.org/10.1016/0165-4608(95)00095-x
https://doi.org/10.1016/0165-4608(95)00095-x
Publikováno v:
Cancer genetics and cytogenetics. 143(2)
Cytogenetic studies provide important information for the diagnosis and classification of malignant lymphomas that in some cases also has prognostic significance. Furthermore, the investigation of isolated novel cytogenetic findings in malignant lymp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8da63f629751c00b7a75129683eddd50
https://pubmed.ncbi.nlm.nih.gov/12781450
https://pubmed.ncbi.nlm.nih.gov/12781450
Autor:
Raj Rolston, Sofia Shekhter-Levin, Karen E. Weck, Maureen E. Sherer, Jean M. Tersak, Kathleen Cumbie
Publikováno v:
Cancer genetics and cytogenetics. 134(1)
We present the case of a 15-year-old female with acute promyelocytic leukemia and a new variant chromosome rearrangement identified as ins(15;17)(q22;q12q21) by conventional cytogenetic analysis. This finding was confirmed by fluorescence in situ hyb
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::602dd9659ce185c805a368df7fb0968a
https://pubmed.ncbi.nlm.nih.gov/11996797
https://pubmed.ncbi.nlm.nih.gov/11996797