- Phylogenetically interrelated ETS genes, ETV1, ERM and E1A-F locate on different chromosomes
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Jeon IS, Shapiro DN
- KMID: 1038161
- J Korean Med Sci.
- 1998 Aug;13(4):355-360.
- doi: 10.3346/jkms.1998.13.4.355
ETV1, ERM and E1A-F are members of the multigene ETS domain containing a class of transcription factors, first identified in the genome of the avian retrovirus E26. Based upon... -
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- Loss of Heterozygosity on Chromosomes 3p,8p,9p and 17p in the Progression of Squamous Cell Carcinoma of the Larynx
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Yoo WJ, Cho SH, Lee YS, Park GS, Kim MS, Kim BK, Park WS, Lee JY, Kang CS
- KMID: 1786810
- J Korean Med Sci.
- 2004 Jun;19(3):345-351.
- doi: 10.3346/jkms.2004.19.3.345
Previous molecular genetic studies of laryngeal squamous cell carcinoma (SCC)have shown certain chromosomal regions with recurring alterations. But studies of sequential molecular alterations and genetic progression model of laryngeal SCC... -
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- First Case of Diffuse Large B-Cell Lymphoma Subtype of Monomorphic Post-Transplant Lymphoproliferative Disorder With 3q27 Translocation
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Kim H, Kim IS, Lee EY, Shin DH, Cho SH
- KMID: 2373562
- Ann Lab Med.
- 2016 Jul;36(4):380-383.
- doi: 10.3343/alm.2016.36.4.380
No abstract available. -
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- Spectra of Chromosomal Aberrations in 325 Leukemia Patients and Implications for the Development of New Molecular Detection Systems
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Choi HJ, Kim HR, Shin MG, Kook H, Kim HJ, Shin JH, Suh SP, Ryang DW
- KMID: 1094259
- J Korean Med Sci.
- 2011 Jul;26(7):886-892.
- doi: 10.3346/jkms.2011.26.7.886
This study investigated the spectrum of chromosomal abnormalities in 325 leukemia patients and developed optimal profiles of leukemic fusion genes for multiplex RT-PCR. We prospectively analyzed blood and bone marrow... -
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- Loss of Heterozygosity on Chromosome 3p, 9p, 17p in Oral & Oropharyngeal Squamous Cell Carcinoma
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Lee SH, Kim MS, Sun DI, Song CJ, Cho SH
- KMID: 2274729
- Korean J Otolaryngol-Head Neck Surg.
- 2000 Jul;43(7):746-750.
BACKGROUND AND OBJECTIVES: Patients of oral and oropharyngeal squamous cell carcinoma in the comparable stage have diverse clinical courses and responses to similar treatment. Understanding the genetic alterations that occur... -
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- A case of partial trisomy 3p syndrome with rare clinical manifestations
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Han DH, Chang JY, Lee WI, Bae CW
- KMID: 2284317
- Korean J Pediatr.
- 2012 Mar;55(3):107-110.
- doi: 10.3345/kjp.2012.55.3.107
Partial trisomy 3p results from either unbalanced translocation or de novo duplication. Common clinical features consist of dysmorphic facial features, congenital heart defects, psychomotor and mental retardation, abnormal muscle tone,... -
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- Detection of RUNX1-MECOM Fusion Gene and t(3;21) in a Very Elderly Patient Having Acute Myeloid Leukemia with Myelodysplasia-Related Changes
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Yang JJ, Cho SY, Suh JT, Lee HJ, Lee WI, Yoon HJ, Baek SK, Park TS
- KMID: 1387352
- Ann Lab Med.
- 2012 Sep;32(5):362-365.
- doi: 10.3343/alm.2012.32.5.362
An 87-yr-old woman was diagnosed with AML with myelodysplasia-related changes (AML-MRC). The initial complete blood count showed Hb level of 5.9 g/dL, platelet counts of 27x10(9)/L, and white blood cell... -
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- A Case of 3p Partial Trisomy
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Park JE, Kim IS, Song MY, Kim ER, Moon SY, Oh SK
- KMID: 2208244
- J Korean Pediatr Soc.
- 1996 Jun;39(6):873-879.
3p partial trisomy is a rare chromosomal anomaly. We experienced a case of 3p partial trisomy in a male neonate. It was diagnosed by clinical and chromosoaml study. He had... -
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- Analysis of Loss of Heterozygosity on the Chromosome 3, 4, 5 and 11 in Uterine Cervical Carcinomas
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Nam JH, Jung JJ, Choi C
- KMID: 2172444
- Chonnam Med J.
- 2000 Dec;36(4):349-356.
Infection of cervical epithelial cells with specific human papilloma virus subtypes appears to be necessary etiological factors for most cervical carcinomas, but yet additional genetic changes such as activation of... -
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- Genome-wide scan of granular corneal dystrophy, type II: confirmation of chromosome 5q31 and identification of new co-segregated loci on chromosome 3q26.3
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Lee EJ, Kim KJ, Kim HN, Bok J, Jung SC, Kim EK, Lee JY, Kim HL
- KMID: 1015458
- Exp Mol Med.
- 2011 Jul;43(7):393-400.
- doi: 10.3858/emm.2011.43.7.043
Granular corneal dystrophy, type II (CGD2; Avellino corneal dystrophy) is the most common corneal dystrophy among Koreans, but its pathophysiology is still poorly understood. Many reports showed that even though... -
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- A Case of Addition of Chromosome 3 associated with Multiple Anomalies
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Suh MA, Lee HJ, Park HJ, Lee KH, Lee GH, Choi EJ, Kim JK, Chung HL, Seo ES, Kim WT
- KMID: 1750724
- J Korean Soc Neonatol.
- 2007 Nov;14(2):237-242.
Chromosomal anomalies are associated with various congenital malformations and impaired development. The addition or duplication of chromosome 3 is a very rare chromosomal anomaly, in comparison to the deletion of... -
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- Identification of a Novel Deletion Region in 3q29 Microdeletion Syndrome by Oligonucleotide Array Comparative Genomic Hybridization
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Seo EJ, Jun KR, Yoo HW, Yoo HK, Lee JO
- KMID: 1096822
- Korean J Lab Med.
- 2010 Feb;30(1):70-75.
- doi: 10.3343/kjlm.2010.30.1.70
BACKGROUND: The 3q29 microdeletion syndrome is a genomic disorder characterized by mental retardation, developmental delay, microcephaly, and slight facial dysmorphism. In most cases, the microdeletion spans a 1.6-Mb region between... -
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- Clinical characterization of a Korean case with 3p25 deletion
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Lee HJ, Kim JH, Cho JH, Lee BH, Choi JH, Yoo HW
- KMID: 1737962
- J Genet Med.
- 2014 Jun;11(1):36-39.
- doi: 10.5734/JGM.2014.11.1.36
Chromosome 3 (3p) deletion syndrome is a rare genomic disorder caused by a deletion at the terminal end of the short arm of chromosome 3. The primary characteristics of the... -
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- A Case of t(3;3)(q21;q26.2) Associated with Severe Multilineage Dysplasia and Multi-drug Resistance in Blastic Crisis of Chronic Myelogenous Leukemia
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Lee SA, Lim J, Kim M, Kim Y, Han K
- KMID: 1781665
- Korean J Lab Med.
- 2010 Dec;30(6):595-599.
- doi: 10.3343/kjlm.2010.30.6.595
The t(3;3)(q21;q26.2) is known to be mainly observed in hematologic myeloid malignancies, as a form of 3q21q26 syndrome. Cytogenetic abnormalities of 3q21q26 syndrome result in RPN1-EVI1 fusion transcripts involving ecotropic... -
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- PCR-based Study on Loss of Heterozygosity at the Short Arm of Chromosome 3 in Renal Cell Carcinoma
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Yoon JH, Park YH, Kim IH
- KMID: 1991363
- Korean J Urol.
- 1996 Jul;37(7):730-738.
Loss of heterozygosity (LOH) at polymorphic loci on the short arm of chromosome 3 which has multiple recurrence genes was investigated in histopathologically proven 35 sporadic renal cell carcinoma (RCC)... -
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- A Case of Concomitant Inv(3)(q21q26) and Cryptic BCR/ABL1 Rearrangement in the Blast Crisis of Chronic Myeloid Leukemia
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Lee H, Cho C, Kwon MJ, Nam MH, Lee CK, Kim YK
- KMID: 2312184
- Lab Med Online.
- 2011 Jul;1(3):163-167.
Structural abnormalities of the long arm of chromosome 3 (3q) have been associated with elevated platelet count and hyperplasia of megakaryocytes with dysplasia in various hematological malignancies. Some cases of... -
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- Analysis of the Azoospermia Factor (AZF) Gene on Y Chromosome and Expression Pattern of DAZ Gene in Korean Infertile Men
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Lee HJ, Lee HS, Song GJ, Byun HK, Seo JT, Kim JH, Lee YS
- KMID: 1930557
- Korean J Fertil Steril.
- 1997 Apr;24(1):57-65.
Cytogenetic observations of loss of the distal portion of the Y chromosome long arm were found to be associated with disrupted spermatogenesis. The existence of a gene involved in the... -
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- Clinical Usefulness of Fluorescence In Situ Hybridization for the Detection of Bladder Cancer
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Kim MH, Choi EH, Kim JH, Kang SY, Chang SG, Yoo KH, Suh JT, Lee WI
- KMID: 2082801
- Korean J Lab Med.
- 2005 Jun;25(3):199-204.
BACKGROUND: Early detection of bladder cancer and its recurrence is the key to long term survival in patients. However, because of nonspecific symptoms, it is difficult to verify such assumption.... -
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- Molecular Genetic Investigation of Sporadic Renal Cell Carcinoma: Analysis of Allele Loss on Chromosome 3p
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Choi JH, Choi HY, Lee HR, Lee SW, Park KH, Lee KS, Kim DS, Chai SE
- KMID: 2290021
- Korean J Urol.
- 1998 Jan;39(1):23-29.
PURPOSE: Renal cell carcinoma has been characterized by an abnormality on the short arm of chromosome 3, which suggests the presence of a tumor suppressor gene at this location.... -
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- Hematologic and Clinical Features of 3q21q26 Syndrome: Extremely Poor Prognosis and Association with Central Diabetes Insipidus
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Chung HJ, Seo EJ, Kim KH, Jang S, Park CJ, Chi HS, Lee JH, Lee JH, Lee KH
- KMID: 1781473
- Korean J Lab Med.
- 2007 Apr;27(2):133-138.
- doi: 10.3343/kjlm.2007.27.2.133
BACKGROUND: 3q21q26 syndrome includes chromosomal abnormalities of inv(3)(q21q26), t(3;3) (q21;q26), and ins(3;3)(q26;q21q26). It causes hematological diseases by the leukemogenic mechanism that the enhancer of ribophorin I gene in 3q21... -
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