- Sonographic inner layer of the stomach : mucosal layer or interphase?
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Lim JH, Jeong YM, Ko YT
- KMID: 1692139
- J Korean Soc Med Ultrasound.
- 1993 May;12(1):38-45.
No abstract available. -
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- Detection of chromosome aberrations in interphase nuclei using fluorescence in situ hybridization technique
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Song HG, Choi SO, Kang IB
- KMID: 2157508
- J Korean Med Sci.
- 1993 Aug;8(4):257-261.
- doi: 10.3346/jkms.1993.8.4.257
We report here several experiences of interphase cytogenetics, using fluorescence in situ hybridization (FISH) technique, for the detection of chromosome aberrations. FISH, using alpha satellite specific probes of 18, X,... -
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- Detection of IgH and Cyclin D1 gene Rearrangement with Interphase FISH in Multiple Myeloma
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Huh JW, Ahn JY, Lee JH, Im SA, Seong CM, Chung WS
- KMID: 2082779
- Korean J Lab Med.
- 2002 Oct;22(5):367-371.
BACKGROUND: The t(11;14)(q13;q32) is known to be one of the most frequent chromosomal abnor-malities found in multiple myeloma (MM). However, studies on t(11;14) in MM have been problemat-ic due to... -
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- Interphase cytogenetics of non-Hodgkin's lymphoma using non-fluorescent in situ hybridization in paraffin embedded tissue
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Choi YJ, Han K, Lee W, Kang CS, Kim BK, Kim SM, Shim SI
- KMID: 644998
- J Korean Med Sci.
- 1996 Oct;11(5):402-408.
- doi: 10.3346/jkms.1996.11.5.402
Paraffin-embedded tissue samples from 30 cases of non-Hodgkin's lymphoma(NHL) and 10 of reactive hyperplasia, were processed for interphase cytogenetic chromosomal study. We performed non-fluorescent in situ hybridization(NFISH) using the enzymatic... -
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- Dysregulation of Telomere Lengths and Telomerase Activity in Myelodysplastic Syndrome
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Park HS, Choi J, See CJ, Kim JA, Park SN, Im K, Kim SM, Lee DS, Hwang SM
- KMID: 2369744
- Ann Lab Med.
- 2017 May;37(3):195-203.
- doi: 10.3343/alm.2017.37.3.195
BACKGROUND: Telomere shortening is thought to be involved in the pathophysiology of myeloid malignancies, but telomere lengths (TL) during interphase and metaphase in hematopoietic malignancies have not been analyzed. We... -
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- Variant Philadelphia Chromosome Identified by Interphase Fluorescence In Situ Hybridization (FISH) without Evidence on G-banded Karyotyping and Metaphase FISH
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Kim MK, Mun YC, Seong CM, Chung WS, Huh J
- KMID: 1781680
- Korean J Lab Med.
- 2010 Dec;30(6):711-717.
- doi: 10.3343/kjlm.2010.30.6.711
A variant Philadelphia chromosome (Ph) is generated from translocation of one or more partner chromosomes in addition to chromosomes 9 and 22. We have described the cases of 2 patients... -
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- Comparison between Conventional Cytogenetics and Interphase Fluorescence in situ Hybridization (FISH) for Patients with Multiple Myeloma
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Kim SH, Kim JH, Lee DM, Lee S, Oh SY, Kwon HC, Kim KE, Han JY, Kim HJ
- KMID: 2252168
- Korean J Hematol.
- 2009 Mar;44(1):14-21.
- doi: 10.5045/kjh.2009.44.1.14
BACKGROUND: For patients with multiple myeloma (MM), different strategies are used to detect chromosomal abnormalities (CA). There have been a few studies that have directly compared FISH with conventional cytogenetics... -
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- Chromosome Analysis in Clinical Samples by Chromosome Diagnostic System Using Fluorescence in Situ Hybridization
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Moon SY, Pang MG, Oh SK, Ryu BY, Hwang D, Jung BJ, Choe J, Sohn C, Chang JK, Kim JW, Kim SH, Choi YM
- KMID: 2235766
- Korean J Fertil Steril.
- 1997 Dec;24(3):335-340.
Fluorescence in situ hybridization (FISH) techniques allow the enumeration of chromosome abnormalities and from a great potential for many clinical applications. In order to produce quantitative and reproducible results, expensive... -
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- Anaplastic Large Cell Lymphoma with Massive Eosinophilia and Complex Karyotype Initially Misdiagnosed as Chronic Eosinophilic Leukemia
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So MK, Park S, Cho MS, Mun YC, Huh J
- KMID: 2407563
- Lab Med Online.
- 2018 Apr;8(2):56-61.
- doi: 10.3343/lmo.2018.8.2.56
We report a patient with massive eosinophilia and a complex karyotype that was initially misdiagnosed as chronic eosinophilic leukemia (CEL), but later diagnosed as anaplastic large cell lymphoma (ALCL) masked... -
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- Study on the Detection of Chromosome X, Y Using in situ PCR
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Kim YJ
- KMID: 1925233
- Korean J Obstet Gynecol.
- 1997 Nov;40(11):2568-2572.
Untill now, classical karyotyping remains the most reliable and conclusive method, but sometimes very rapid and sensitive method for the detection of chromosomal abnormality is needed. The primed in situ... -
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- Amniotic Fluid Interphase Fluorescence in situ Hybridization (FISH) for Detection of Aneuploidy;Experiences in 130 Prenatal Cases
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Lim HJ, Kim YJ, Yang JH, Kim EJ, Choi JS, Jung SH, Ahn HK, Han JY, Kim MY, Choi KH, Kim JM, Kim YM, Park SY, Ryu HM
- KMID: 1127246
- J Korean Med Sci.
- 2002 Oct;17(5):589-592.
- doi: 10.3346/jkms.2002.17.5.589
The major aneuploidies diagnosed prenatally involve the autosomes 13, 18, 21, and sex chromosomes X and Y. Fluorescence in situ hybridization (FISH) allows rapid analysis of chromosome copy number... -
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- The incidence of ABL Deletion on Derivative 9 Chromosome in Chronic Myelogenous Leukemia by Interphase Fluorescence In Situ Hybridization and its Association with Progression to Blast Crisis
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Jeong S, Lee DS, See CJ, Ko EK, Park S, Cho HI
- KMID: 2225972
- Korean J Clin Pathol.
- 2000 Dec;20(6):521-526.
BACKGROUND: Philadelphia(Ph) chromosome is found in about 95 percent of chronic myelogenous leukemia(CML) patients. Ph chromosome results from a reciprocal translocation between the long arms of chromosomes 9 and 22,... -
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- Prenatal Aneuploidy Detection in Uncultured Amniotic Fluid Interphase Cells by Fluorescence in situ Hybridization (FISH)
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Seol HW, Ko HJ, Song NH, Kim SR, Lee HJ, Oh SK, Park JS, Jun JK, Yoon BH, Syn HC, Moon SY
- KMID: 1864648
- Korean J Fertil Steril.
- 2003 Sep;30(3):223-232.
OBJECTIVE: The aim of the present study was to evaluate the clinical efficiency of fluorescent in situ hybridization (FISH) in the prenatal diagnosis of chromosomal aneuploidy. METHODS: We reviewed data of... -
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- Effects of Some Drugs and Toxins on Positive Rate of Y-Body in Leukocytes of Rabbits
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Yun NS, Lee HY
- KMID: 2060007
- Korean J Urol.
- 1976 Jun;17(2):77-94.
This study was carried out to investigate the response of interphase Y chromosome to some drugs and toxins by observing the rate of leukocytes showing Y-body in the peripheral blood.... -
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- Double Minutes Containing C-MYC oncogene with a Normal Karyotype in Acute Myelogenous Leukemia: A Case Report
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Kim HS, Cho HC, Moon Y, Nahm CH, Choi JW, Yi SG, Kim SH
- KMID: 2082793
- Korean J Lab Med.
- 2005 Jun;25(3):152-154.
We report a case of a female karyotype that was normal except for double minutes (dmin) in acute myeloid leukemia. Using fluorescence in situ hybridization, the amplification of C-MYC was... -
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- Detection of Mixed Chimerism after Sex-Mismatched Bone Marrow Transplantation Using Fluorescence in situ Hybridization: Engraftment and Follow-up Evaluation
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Ryang DW, Hong WP, Cho D, Lee JJ, Chung IJ, Cho MK, Kook H, Hwang TJ, Shin JH, Suh SP
- KMID: 2143370
- Korean J Hematol.
- 1999 Aug;34(3):461-470.
BACKGROUND: Interphase fluorescence in situ hybridization (FISH) analysis following sex-mismatched bone marrow transplantation (BMT) is a sensitive and quantitative method to better assess the engraftment state and mixed chimerism. METHODS:... -
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- A Case of Chronic Lymphocytic Leukemia with Trisomy 12 detected by Fluorescence in situ Hybridization (FISH)
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Cho D, Hong WP, Kim HJ, Ryang DW
- KMID: 1892644
- Korean J Clin Pathol.
- 1997 Oct;17(5):689-693.
We report a case of B-cell chronic lymphocytic leukemia (CLL) with trisomy 12 detected by FISH using chromosome 12 alpha-satellite Probe (Oncor , USA) in uncultured interphase cells. Chromosome studies... -
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- Adreno-Hepatic Fusion: A case report
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Yang KM, Park YN, Park CI
- KMID: 1725394
- Korean J Pathol.
- 1998 May;32(5):385-387.
Adreno-hepatic fusion is rare condition defined as adhesion of the liver and right adrenal cortex with close intermingling of the respective parenchyme. It is suggested to be an aging phenomenon,... -
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- Prenatal Diagnosis of the 22q11.2 Duplication Syndrome
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Lee MH, Park SY, Lee BY, Choi EY, Kim JW, Park JY, Lee YW, Oh AR, Lee SY, Yang JH, Ryu HM
- KMID: 1473823
- J Genet Med.
- 2009 Dec;6(2):175-178.
The 22q11.2 duplication syndrome is an extremely variable disorder with a phenotype ranging from normal to congenital defects and learning disabilities. Recently, the detection rate of 22q11.2 duplication has been... -
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- Molecular Cytogenetic Analysis of Gene Rearrangements in Childhood Acute Lymphoblastic Leukemia
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Woo HY, Kim DW, Park H, Seong KW, Koo HH, Kim SH
- KMID: 1781721
- J Korean Med Sci.
- 2005 Feb;20(1):36-41.
- doi: 10.3346/jkms.2005.20.1.36
The aims of this study were to estimate the incidences of BCR/ABL, MLL, TEL/AML1 rearrangements, and p16 deletions in childhood acute lymphoblastic leukemia (ALL), to identify new abnormalities, and to... -
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