Zobrazeno 1 - 10 of 11 pro vyhledávání: '"S A Schichman"'
1
Comparison of short tandem repeat and variable number tandem repeat genetic markers for quantitative determination of allogeneic bone marrow transplant engraftment
Autor: P Suess, P S Gray, S A Schichman, A M Vertino
Publikováno v: Bone Marrow Transplantation. 29:243-248
Variable number tandem repeats (VNTRs) were among the first genetic markers used to quantitate bone marrow transplant engraftment. The limitations of PCR-based VNTR markers in distinguishing some donor/recipient pairs has shown the need for additiona
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6cf2b189ade335dda70232dcee8db537
https://doi.org/10.1038/sj.bmt.1703360
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3
Chronic lymphocytic leukemia incidence is substantially higher than estimated from tumor registry data
Autor: C S, Zent, M J, Kyasa, R, Evans, S A, Schichman
Publikováno v: Cancer. 92(5)
Although chronic lymphocytic leukemia (CLL) often is described as the most common leukemia in the U.S. and Western Europe, to the authors' knowledge the true incidence of CLL in the U.S. is unknown. CLL incidence is estimated from tumor registry repo
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::cf7b8f5cda89d10cd4990e2168dd5191
https://pubmed.ncbi.nlm.nih.gov/11571749
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4
Use of HFE mutation analysis for hereditary hemochromatosis: the need for physician education in the translation of basic science to clinical practice
Autor: M, Kohli, S A, Schichman, L, Fink, C S, Zent
Publikováno v: Southern medical journal. 93(5)
Hereditary hemochromatosis (HH) is a common hereditary disorder of iron metabolism causing iron overload, organ failure, and malignancy. Preclinical diagnosis using HFE gene analysis followed by prophylactic phlebotomy can completely prevent the dise
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::61ca1556024b0298f986257ed5496696
https://pubmed.ncbi.nlm.nih.gov/10832943
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5
Partial tandem duplication of ALL1 as a recurrent molecular defect in acute myeloid leukemia with trisomy 11
Autor: M A, Caligiuri, M P, Strout, S A, Schichman, K, Mrózek, D C, Arthur, G P, Herzig, M R, Baer, C A, Schiffer, K, Heinonen, S, Knuutila, T, Nousiainen, T, Ruutu, A W, Block, P, Schulman, J, Pedersen-Bjergaard, C M, Croce, C D, Bloomfield
Publikováno v: Cancer research. 56(6)
Gains of a single chromosome are frequent cytogenic findings in human cancer, but no molecular rearrangement has been consistently associated with any trisomy. In acute myeloid leukemia (AML), trisomy 11 (+11) occurring as a sole abnormality is the t
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::32c6fc83fdbf9188e29bb862723df4a8
https://pubmed.ncbi.nlm.nih.gov/8640834
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8
ALL-1 tandem duplication in acute myeloid leukemia with a normal karyotype involves homologous recombination between Alu elements
Autor: S A, Schichman, M A, Caligiuri, M P, Strout, S L, Carter, Y, Gu, E, Canaani, C D, Bloomfield, C M, Croce
Publikováno v: Cancer research. 54(16)
Rearrangements of the ALL-1 gene by reciprocal translocations involving chromosome band 11q23 are frequently associated with human acute leukemia. We have previously reported the detection of ALL-1 gene rearrangements in adult patients with acute mye
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::189a43eb7f4c9f74f96e3ca1cb38b351
https://pubmed.ncbi.nlm.nih.gov/8044771
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9
Sequence analysis of the breakpoint cluster region in the ALL-1 gene involved in acute leukemia
Autor: Y, Gu, H, Alder, T, Nakamura, S A, Schichman, R, Prasad, O, Canaani, H, Saito, C M, Croce, E, Canaani
Publikováno v: Cancer research. 54(9)
DNA rearrangements caused by chromosome translocations between band 11q23 and various chromosomes can be detected by a single probe, B859, an 859-base pair complementary DNA fragment derived from the human ALL-1 gene. To try to understand why band 11
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::3a1bd28dd72960e9209a6267d0202de9
https://pubmed.ncbi.nlm.nih.gov/8162575
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10
Recurrent hairy cell leukemia presenting as a large mesenteric mass diagnosed by fine needle aspiration cytology. A case report
Autor: Y T, Kaw, R L, Artymyshyn, S A, Schichman, K E, Salhany
Publikováno v: Acta cytologica. 38(2)
A case of hairy cell leukemia (HCL) diagnosed by fine needle aspiration (FNA) biopsy performed under computed tomographic (CT) guidance is presented. The patient, who had a three-year history of HCL treated with splenectomy and interferon therapy, ha
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::9b12f150f798c604e48cf1fdefded7c6
https://pubmed.ncbi.nlm.nih.gov/8147223
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