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Numerical and structural chromosomal abnormalities are common in hematological malignancies. Near-triploidy (58-80 chromosomes) is a numerical abnormality observed in 3% of adult cases of acute lymphoblastic leukemia. Near-triploidy is rare in myeloid lineage hematologic malignancies and compared to near-triploidy in lymphoid malignancies, neartriploidy in myeloid malignancies is associated with poor outcomes. Few studies on neartriploidy in myelodysplastic syndrome (MDS) have been reported, and the clinicopathologic significance of this condition is still unclear. Here, we report a novel case of MDS with near-triploidy and multiple structural chromosomal abnormalities: del(5q) combined with del(1p) and del(13q). These abnormalities were detected by cytogenetic analysis with array comparative genomic hybridization (CGH). Our results suggest that array CGH can be a useful tool for detecting chromosomal abnormalities in patients with MDS.

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기사명 저자명 페이지 원문 목차
Trueness assessment for serum glucose measurement using commercial systems through the preparation of commutable reference materials ChangYu Xia, Ou Liu, LanZhen Wang, GuoBing Xu pp.243-249

Influence of a regular, standardized meal on clinical chemistry analytes Gabriel Lima-Oliveira, Gian Luca Salvagno, Giuseppe Lippi, Matteo Gelati, Martina Montagnana, Elisa Danese, Geraldo Picheth, Gian Cesare Guidi pp.250-256

Evaluation of peptide nucleic acid probe-based real-time PCR for detection of Mycobacterium tuberculosis complex and nontuberculous mycobacteria in respiratory specimens Young Jin Choi, Hwi Jun Kim, Hee Bong Shin, Hae Seon Nam, Sang Han Lee, Joon Soo Park, Kwi Sung Park, Kyoung Ah Baek pp.257-263

Rapid diagnosis of tuberculosis and multidrug resistance using a MGIT 960 system Won-Jung Koh, Yousang Ko, Chang-Ki Kim, Kyung Sun Park, Nam Yong Lee pp.264-269

Characterization of carbapenemase genes in Enterobacteriaceae species exhibiting decreased susceptibility to carbapenems in a university hospital in Chongqing, China Yun Xia, Zhenzhen Liang, Xiaoyan Su, Ying Xiong pp.270-275

Erythrocyte binding preference of human pandemic influenza virus A and its effect on antibody response detection Jarika Makkoch, Slinporn Prachayangprecha, Sunchai Payungporn, Thaweesak Chieochansin, Thaweesak Songserm, Alongkorn Amonsin, Yong Poovorawan pp.276-282

Role of plasma exchange in ABO-incompatible kidney transplantation Soohun Yoo, Eun Young Lee, Kyu Ha Huh, Myoung Soo Kim, Yu Seun Kim, Hyun Ok Kim pp.283-288

MYC rearrangement involving a novel non-immunoglobulin chromosomal locus in precursor B-cell acute lymphoblastic leukemia Ja-Young Seo, Soo Hyun Lee, Hee-Jin Kim, Keon Hee Yoo, Hong Hoe Koo, Yong Gon Cho, Sam Im Choi, Sun-Hee Kim pp.289-293

A case of near-triploidy in myelodysplastic syndrome with del5q combined with del1p and del13q Bo-Ram Kim, Ji-Eun Kim, Kwang-Sook Woo, Kyeong-Hee Kim, Jeong-Man Kim, Suee Lee, Lisa G. Shaffer, Jin-Yeong Han pp.294-297

Lung infection caused by Mycobacterium riyadhense confused with Mycobacterium tuberculosis : the first case in Korea Jung-In Choi, Ji-Hun Lim, Sung-Ryul Kim, Seon Ho Lee, Jae-Sun Park, Kwang Won Seo, Jae Bum Jeon, Joseph Jeong pp.298-303

Anaphylactic transfusion reaction in a patient with anhaptoglobinemia : the first case in Korea Hyunsoo Kim, Jonghyeon Choi, Kyoung Un Park, Hyon-Suk Kim, Yoo Hong Min, Moon Jung Kim, Hyun Ok Kim pp.304-306

Ring chromosome 5 in acute myeloid leukemia defined by whole-genome single nucleotide polymorphism array Jungwon Huh, Yeung Chul Mun, Wha Soon Chung, Chu Myong Seong pp.307-311

Identification of SLC26A3 mutations in a Korean patient with congenital chloride diarrhea Eun-Sil Lee, Ah Ra Cho, Chang-Seok Ki pp.312-315

Diagnostic Usefulness of Genomic Breakpoint Analysisof Various Gene Rearrangements in Acute Leukemias : A Perspective of Long Distance- or Long Distance Inverse-PCR-based Approaches John Jeongseok Yang, Rolf Marschalek, Claus Meyer, 박태성 pp.316-318

참고문헌 (21건) : 자료제공( 네이버학술정보 )

참고문헌 목록에 대한 테이블로 번호, 참고문헌, 국회도서관 소장유무로 구성되어 있습니다.
번호 참고문헌 국회도서관 소장유무
1 WHO classification of tumours of haematopoietic and lymphoid tissues in 2008: an overview. 네이버 미소장
2 Identification of novel cytogenetic markers with prognostic significance in a series of 968 patients with primary myelodysplastic syndromes. 네이버 미소장
3 Clinical and cytogenetic correlations in 63 patients with therapy-related myelodysplastic syndromes and acute nonlymphocytic leukemia: further evidence for characteristic abnormalities of chromosomes no. 5 and 7. 네이버 미소장
4 Unusual complex hyperdiploid karyotypes in myelodysplastic syndromes 네이버 미소장
5 Massive hyperdiploidy and tetraploidy in acute myelocytic leukemia and myelodysplastic syndrome 네이버 미소장
6 Leukemic transformation associated with massive hyperdiploidy in myelodysplastic syndrome (MDS) with der(1;7)(q10;p10): a novel case study. 네이버 미소장
7 Tetraploidy and 5q deletion in myelodysplastic syndrome: A case report 네이버 미소장
8 Hyperdiploid karyotype in a childhood MDS patient. 네이버 미소장
9 Polyploidy in myelodysplastic syndrome: a case report. 네이버 미소장
10 Myelodysplastic syndrome associated with hypotriploidy. 네이버 미소장
11 The impact of cytomorphology, cytogenetics, molecular genetics, and immunophenotyping in a comprehensive diagnostic workup of myelodysplastic syndromes. 네이버 미소장
12 Cytogenetic abnormalities in myelodysplastic syndrome: an overview. 네이버 미소장
13 Shaffer LG, Slovak MI, Campbell LJ, eds. An International System for Human Cytogenetic Nomenclature (ISCN). Basel: S, Karger, 2009:36-84. 미소장
14 Exploiting noise in array CGH data to improve detection of DNA copy number change 네이버 미소장
15 Near-triploidy and near-tetraploidy in hematological malignancies and mutation of the p53 gene. 네이버 미소장
16 Case of near triploidy with i(17)(q10) in blast crisis CML 네이버 미소장
17 A Case of Near-Triploidy in Chronic Myelogenous Leukemia 네이버 미소장
18 Impact of adjunct cytogenetic abnormalities for prognostic stratification in patients with myelodysplastic syndrome and deletion 5q. 네이버 미소장
19 Cytogenetic features of 5q deletion and 5q− syndrome in myelodysplastic syndrome in Korea; marker chromosomes proved to be chromosome 5 with interstitial deletion by fluorescence in situ hybridization 네이버 미소장
20 Analysis of myelodysplastic syndromes with complex karyotypes by high‐resolution comparative genomic hybridization and subtelomeric CGH array 네이버 미소장
21 Clonal heterogeneity in childhood myelodysplastic syndromes—Challenge for the detection of chromosomal imbalances by array‐CGH 네이버 미소장

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