نتایج جستجو برای: cytogenetic aberrations

تعداد نتایج: 27335  

2013
Carolina B Belli

Myelodysplastic Syndromes (MDS) are a heterogeneous group of hematologic diseases characterized by refractory cytopenia(s) and variable risk of leukemic progression. Cytogenetic analysis is important in day-to-day clinical practice helping to define subgroups of MDS patients who share similarities in the course of the disease. There are recurring aberrations affecting chromosomes 5, 7, 8, and 2...

Journal: :international journal of fertility and sterility 0
saeedeh ghazaey fatemeh keify farzaneh mirzaei masumeh maleki semiramis tootian mitra ahadian

background: cytogenetic study of reproductive wastage is an important aspect in determining the genetic background of early embryogenesis. approximately 15 to 20% of all pregnancies in humans are terminated as recurrent spontaneous abortions (rsas). the aim of this study was to detect chromosome abnormalities in couples with rsas and to compare our results with those reported previously. materi...

Journal: :Environmental Health Perspectives 2001
Z Smerhovsky K Landa P Rössner M Brabec Z Zudova N Hola Z Pokorna J Mareckova D Hurychova

We used cytogenetic analysis to carry out a cohort study in which the major objective was to test the association between frequency of chromosomal aberrations and subsequent risk of cancer. In spite of the extensive use of the cytogenetic analysis of human peripheral blood lymphocytes in biomonitoring of exposure to various mutagens and carcinogens on an ecologic level, the long-term effects of...

Journal: :Blood 1992
A Cuneo J L Michaux A Ferrant L Van Hove A Bosly M Stul P Dal Cin E Vandenberghe J J Cassiman M Negrini

Cytogenetic, biomolecular, and clinicopathologic features were retrospectively studied in 34 adult patients with acute myelogenous leukemia expressing one or more of the following lymphoid-associated markers (LMs): CD7, CD2, CD10, CD19, CD22, TdT. Six patients showed 11q23 rearrangements (group I); three patients had the classic Ph chromosome (group II); 15 patients had aberrations of the myelo...

2006
Chandrika Sreekantaiah Stanley P. L. Leong Constantine P. Karakousis Daniel L. McGee William D. Rappaport Hugo V. Villar David Neal Susan Fleming Albert Wankel Peter N. Herrington Richard Carmona Avery A. Sandberg

Cytogenetic analysis of short-term cultures was carried out on 109 lipomas from 92 patients. Clonal chromosomal abnormalities were pres ent in 50% of the tumors analyzed. Based on the results, three main Cytogenetic groups were identified and included: (a) tumors with normal karyotypes, (b) tumors with abnormalities involving region ql3-15 on chromosome 12, and (c) tumors with other clonal aber...

Journal: :Cancer research 1991
C Sreekantaiah S P Leong C P Karakousis D L McGee W D Rappaport H V Villar D Neal S Fleming A Wankel P N Herrington

Cytogenetic analysis of short-term cultures was carried out on 109 lipomas from 92 patients. Clonal chromosomal abnormalities were present in 50% of the tumors analyzed. Based on the results, three main cytogenetic groups were identified and included: (a) tumors with normal karyotypes, (b) tumors with abnormalities involving region q13-15 on chromosome 12, and (c) tumors with other clonal aberr...

Journal: :Blood 2010
Marta Salido Cristina Baró David Oscier Kostas Stamatopoulos Judith Dierlamm Estela Matutes Alexandra Traverse-Glehen Francoise Berger Pascale Felman Catherine Thieblemont Stefan Gesk Anastasia Athanasiadou Zadie Davis Anne Gardiner Fuensanta Milla Ana Ferrer Manuela Mollejo Maria José Calasanz Lourdes Florensa Blanca Espinet Elisa Luño Iwona Wlodarska Gregor Verhoef Marta García-Granero Antonio Salar Theodora Papadaki Sergio Serrano Miguel A Piris Francesc Solé

We conducted a retrospective collaborative study to cytogenetically characterize splenic marginal zone lymphoma (SMZL) and ascertain the prognostic value of chromosomal aberrations. Of 330 cases, 72% displayed an aberrant karyotype, 53% were complex, and 29% had a single aberration. The predominant aberrations were gains of 3/3q and 12q, deletions of 7q and 6q and translocations involving 8q/1q...

Journal: :European journal of medical genetics 2006
I Feenstra J Fang D A Koolen A Siezen C Evans R M Winter M M Lees M Riegel B B A de Vries C M A Van Ravenswaaij A Schinzel

During recent years a considerable improvement in diagnostic techniques has enabled cytogeneticists to find more and smaller chromosomal aberrations. However, accurate clinical knowledge about rare chromosome disorders is frequently lacking, mostly due to a significant decline in publishable cases. On the other hand, there is an increasing demand from parents and physicians for reliable informa...

2014
Bo-Ram Kim Jae-Lim Choi Ji-Eun Kim Kwang-Sook Woo Kyeong-Hee Kim Jeong-Man Kim Sung-Hyun Kim Jin-Yeong Han

BACKGROUND Specific cytogenetic aberrations detected by conventional karyotyping or FISH play a major role in the diagnosis, prognosis, and treatment of patients with acute leukemia. The FISH technique enhances the capacity of conventional karyotyping to detect subtle chromosomal aberrations. Multiprobe FISH assay (Cytocell, UK) can hybridize multiple probes to a single slide, thereby increasin...

Journal: :Haematologica 2010
Theo D Kim Seval Türkmen Michaela Schwarz Gökben Koca Hendrik Nogai Christiane Bommer Bernd Dörken Peter Daniel Philipp le Coutre

BACKGROUND Additional chromosomal aberrations in Philadelphia chromosome-positive chronic myeloid leukemia are non-random and strongly associated with disease progression, but their prognostic impact and effect on treatment response is not clear. Point mutations in the BCR-ABL kinase domain are probably the most common mechanisms of imatinib resistance. DESIGN AND METHODS We assessed the infl...

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