- Cytogenetic Analysis of Squamous Cell Carcinoma of the Lung
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Jo SJ
- KMID: 2030733
- Korean J Anat.
- 1997 Oct;30(5):567-574.
The cytogenetic study of 3 cases of squamous cell carcinoma of the lung was performed to identify chromosomal abnormalities. All tumor cells were hypodiploid state on the average. Specicfic chromosomal... -
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- A Family of Charcot-Marie-Tooth 1A Confirmed by Molecular Genetic Analysis
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Choi BO, Sunwoo IN, Lee JS, Bae JC
- KMID: 1659740
- J Korean Neurol Assoc.
- 1996 Dec;14(4):1023-1029.
Recently, thanks to the development of the molecular genetics which had made us understand the nature of some genetic disorders, the concept of the classification has changed. Charcoal-Marie-Tooth disease (CMT)... -
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- Neurobiology of Alzheimer's Disease
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Chung YC, Seo SW, Lee SH
- KMID: 2142160
- J Korean Soc Biol Psychiatry.
- 2001 Jun;8(1):62-70.
Alzheimer's disease(AD) is associated with a characteristic neuropathology. The major hallmarks of AD are senile plaques(SPs) and neurofibrillary tangles(NFTs). beta-amyloid protein(Abeta) is derived from the proteolysis of amyloid precursor protein(APP)... -
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- A Case of Adult B Lymphoblastic Leukemia with ider(9)(q10)t(9;22)(q34;q11.2) and der(19)t(1;19)(q23;p13.3)
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Jung SI, Cho HS, Lee CH, Jung BC
- KMID: 1781663
- Korean J Lab Med.
- 2010 Dec;30(6):585-590.
- doi: 10.3343/kjlm.2010.30.6.585
In B lymphoblastic leukemia/lymphoma (B-ALL/LBL), t(9;22)(q34;q11.2) and t(1;19)(q23;p13.3) are recurrent cytogenetic abnormalities. The concurrent occurrence of both abnormalities is very rare, and only 3 cases have been previously reported. Here,... -
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- Molecular Neurobiology of Alzheimer's Disease
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Kim YH, Rhee CG, Kim YK, Kim SS
- KMID: 2333738
- J Korean Geriatr Psychiatry.
- 1998 May;2(1):37-46.
Alzheimer's disease (AD), the most common dementia in the elderly, is associated with a characteristic neuropathology:extracellular neuritic plaques (NPs) and intraneuronal neurofibrillary tangles (NFTs). AD is diagnosed clinically on the... -
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- Abnormalities in Chromosomes 1q and 13 Independently Correlate With Factors of Poor Prognosis in Multiple Myeloma
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Kim M, Ju YS, Lee EJ, Kang HJ, Kim HS, Cho HC, Kim HJ, Kim JA, Lee DS, Lee YK
- KMID: 2373596
- Ann Lab Med.
- 2016 Nov;36(6):573-582.
- doi: 10.3343/alm.2016.36.6.573
BACKGROUND: We comprehensively profiled cytogenetic abnormalities in multiple myeloma (MM) and analyzed the relationship between cytogenetic abnormalities of undetermined prognostic significance and established prognostic factors. METHODS: The karyotype of 333 newly... -
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- A Novel Translocation t(1;5)(p32;q31) that Was Not Associated with the TAL1 Rearrangement in a Case of T Lymphoblastic Leukemia/Lymphoma
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Cho HS, Kim MK, Bae YK
- KMID: 1096970
- Korean J Lab Med.
- 2009 Jun;29(3):199-203.
- doi: 10.3343/kjlm.2009.29.3.199
Chromosome 1 band p32 (1p32) aberrations are common in T lymphoblastic leukemia/lymphoma (T-ALL/LBL). Two types of 1p32 aberrations include translocations with different partners and submicroscopic interstitial deletion. Both aberrations are... -
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- Three-way Translocation of MLL/MLLT3, t(1;9;11)(p34.2;p22;q23), in a Pediatric Case of Acute Myeloid Leukemia
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Jun KR, Lee JN, Park JA, Kim HR, Shin JH, Oh SH, Lee JY, Song SA
- KMID: 1094354
- Korean J Lab Med.
- 2011 Apr;31(2):127-129.
- doi: 10.3343/kjlm.2011.31.2.127
The chromosome band 11q23 is a common target region of chromosomal translocation in different types of leukemia, including infantile leukemia and therapy-related leukemia. The target gene at 11q23, MLL, is... -
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- Construction and Application of Painting Probe for Chromosome Band 1p36.1, 7q11, 7q32-34, 17q12-21
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Kim KH, Park SY, Jeon YH, Park SH
- KMID: 2075422
- Korean J Obstet Gynecol.
- 1998 Feb;41(2):433-440.
Chromosome microdissection has become a very powerful approach to generate chromosome band-specific library and painting probes for physical mapping or cytogenetic analysis. Here we have constructed the band-specific painting probes... -
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- A Rare der(Y)t(Y;1)(q12;q12) in a Patient with Essential Thrombocythemia
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Lim HH, Choi JL, Kim BR, Woo KS, Kim KH, Kim JM, Kim SH, Han JY
- KMID: 2308735
- Lab Med Online.
- 2016 Jul;6(3):183-186.
- doi: 10.3343/lmo.2016.6.3.183
Among hematologic diseases, structural abnormalities of autosomal chromosomes are well-known, but cases involving the sex chromosomes are uncommon. Duplications of the long arm of chromosome 1 have been reported in... -
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- Partial Trisomy 1q41 Syndrome Delineated by Whole Genomic Array Comparative Genome Hybridization
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Shin YB, Nam SO, Seo EJ, Kim HH, Chang CL, Lee EY, Son HC, Hwang SH
- KMID: 1107538
- J Korean Med Sci.
- 2008 Dec;23(6):1097-1101.
- doi: 10.3346/jkms.2008.23.6.1097
Partial trisomy 1q syndrome is a rare chromosomal abnormality. We report on a male infant with 46,XY,der(11)t(1;11)(q41;p15.5) due to unbalanced segregation of the maternal reciprocal balanced translocation 46,XX,t(1;11)(q41;p15.5). The baby... -
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- The Optimization of Human Sperm Decondensation Procedure for Fluorescence in Situ Hybridization
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Pang MG
- KMID: 2235771
- Korean J Fertil Steril.
- 1997 Dec;24(3):369-375.
Studies were conducted to determine the efficiency of decondensation protocols. Sperm obtained from seven normal donors was immediately washed after liquefaction and then decondensed using the method of West or... -
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- Correlation of Chromosomal Aberrations with Prognostic Markers in Multiple Myeloma Patients- A Single Institution Study
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Lee JW, Lee JK, Hong YJ, Hong SI, Chang YH
- KMID: 1781574
- Korean J Lab Med.
- 2008 Dec;28(6):413-418.
- doi: 10.3343/kjlm.2008.28.6.413
BACKGROUND: Immunoglobulin heavy chain (IGH) gene rearrangement, 13q14 deletion and trisomy 1q are frequently observed in Korean patients with multiple myeloma. The purpose of our study was to analyze the... -
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- Alpha Internexin Expression Related with Molecular Characteristics in Adult Glioblastoma and Oligodendroglioma
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Suh JH, Park CK, Park SH
- KMID: 1786969
- J Korean Med Sci.
- 2013 Apr;28(4):593-601.
- doi: 10.3346/jkms.2013.28.4.593
Alpha-internexin (INA) is a proneuronal gene-encoding neurofilament interacting protein. INA is overexpressed mostly in oligodendroglial phenotype gliomas, is related to 1p/19q codeletion, and is a favorable prognostic marker. We studied... -
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- Analysis of Chromosome-specific Aneusomy in Breast Tumor by Using Fluorescence in Situ Hybridization
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Kang SS, Lee HK, Park BJ, Lee JH, Kim JM, Kim YM, Choi SK, Yoon SO, Lee SG
- KMID: 2004819
- J Korean Surg Soc.
- 2000 May;58(5):599-606.
PURPOSE: Several studies have used FISH (fluorescence in situ hybridization) to analyze aneuploids in various solid tumors. FISH, using chromosome-specific, alpha-stellite DNA probes, can be used to detect aneusomy in... -
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- Isochromosome 1q in Childhood Burkitt Lymphoma: The First Reported Case in Korea
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Rim JH, Kim HS, Shin S, Park SJ, Choi JR
- KMID: 2363276
- Ann Lab Med.
- 2015 Nov;35(6):663-665.
- doi: 10.3343/alm.2015.35.6.663
No abstract available. -
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- Short Stature Associated with Polymorphisms in Chromosome 1qh+, and 16qh+
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Kim KH, Lee SW, Kim MG, Kim DH, Kim HS
- KMID: 2321983
- J Korean Soc Pediatr Endocrinol.
- 2005 Jun;10(1):95-99.
Chromosomal polymorphism of constitutive heterochromatin regions of chromosome 1, 9, 16, and Y is a stable evolutionary feature that is thought to cause no phenotypic alterations. The presence of definite... -
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- Aberrant Chromosomal Alterations in Bizarre Parosteal Osteochondromatous Proliferation (Nora's Lesion) of Hand: A Case Report
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Kim KJ, Kim HY, Yang DS, Choy WS, Ihm CW
- KMID: 2106447
- J Korean Orthop Assoc.
- 2008 Apr;43(2):247-251.
- doi: 10.4055/jkoa.2008.43.2.247
Bizarre parosteal osteochondromatous proliferation is a disease similar to an osteochondroma that usually involves the metatarsal, metacarpal, proximal and middle phalanx. The symptoms are normally caused by the bone mass,... -
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- Linkage analysis between gene marker of chromosome 11q13 and total serum IgE level in sib - pairs with probands of asthmatic children
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Kim YK, Son JW, Cho SH, Lee MH, Koh YY, Min KU, Kim YY
- KMID: 2286138
- J Asthma Allergy Clin Immunol.
- 1998 Sep;18(3):473-482.
BACKGROUND: It is known that total serum IgE levels closely corrleate with prevaience of asthma regardless of atopic status. Although heredity is reported to be important in expression of total serum IgE... -
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- Chromosomal Alterations in Hepatocellular Carcinoma Cell Lines Detected by Comparative Genomic Hybridization
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Park SJ, Ha MJ, Kim HC, Kim HJ
- KMID: 2134351
- Cancer Res Treat.
- 2002 Jun;34(3):175-185.
PURPOSE: There have only been a few cytogenetic studies of hepatocellular carcinoma (HCC), and so far, no consistent specific chromosomal abnormalities have been described. Here, we have used comparative genomic... -
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