- 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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- 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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- Marker Chromosomes in Korean Patients: Incidence, Identification and Diagnostic Approach
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Woo HY, Cho HJ, Kong SY, Kim HJ, Jeon HB, Kim EC, Park H, Kim YJ, Kim SH
- KMID: 1086730
- J Korean Med Sci.
- 2003 Dec;18(6):773-778.
- doi: 10.3346/jkms.2003.18.6.773
The identification of marker chromosomes is important for genetic counseling. However, the origin or composition can rarely be defined with conventional cytogenetic technique alone. In this study, we investigated the... -
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- Non-Synteny Regions in the Human Genome
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Lee K, Kim S
- KMID: 2166483
- Genomics Inform.
- 2010 Jun;8(2):86-89.
Closely related species share large genomic segments called syntenic regions, where the genomic elements such as genes are arranged co-linearly among the species. While synteny is an important criteria in... -
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- A Case with Balanced Chromosome Rearrangement Involving Chromosomes 9, 14, and 13 in a Woman with Recurrent Abortion
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Kim SK, Kim HJ, Yang YH, Kim IK, Bai SW, Kim JY, Park KH, Cho DJ, Song CH
- KMID: 720632
- Yonsei Med J.
- 2001 Jun;42(3):345-348.
- doi: 10.3349/ymj.2001.42.3.345
A phenotypically normal couple was referred for cytogenetic evaluation due to three consecutive first-trimester spontaneous abortions. Chromosomal analysis from peripheral blood was performed according to standard cytogenetic methods using G-banding... -
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- A Case of Ring Chromosome 14 Syndrome Presenting with Intractable Epilepsy
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Kim MJ, Yu HJ, Lee J, Lee M
- KMID: 2008771
- J Korean Epilepsy Soc.
- 2012 Jun;16(1):33-36.
Ring chromosome 14 syndrome is a rare cytogenetic disorder characterized by typical facial appearance, developmental delay, and intractable epilepsy. There have been about 50 reported cases in the world and... -
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- A Case of 21-Monosomy with Holoprosencephaly(Semilobar Type)
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Lee SY, Cho SM
- KMID: 1606978
- J Korean Pediatr Soc.
- 2003 Aug;46(8):831-835.
Holoprosencephaly of unknown definite causes, has been associated with several chromosome abnormalities involving the autosomes and the sex chromosomes. The most commonly reported associations include dup(3p), del(7q), deletions of chromosome... -
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- Periodic Explosive Expansion of Human Retroelements Associated with the Evolution of the Hominoid Primate
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Kim TM, Hong SJ, Rhyu MG
- KMID: 1733474
- J Korean Med Sci.
- 2004 Apr;19(2):177-185.
- doi: 10.3346/jkms.2004.19.2.177
Five retroelement families, L1 and L2 (long interspersed nuclear element, LINE), Alu and MIR (short interspersed nuclear element, SINE), and LTR (long terminal repeat), comprise almost half of the human... -
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- Genentics in Rheumatoid Arthritis
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Lee HS
- KMID: 2168057
- Hanyang Med Rev.
- 2005 May;25(2):13-20.
The understanding of genetic factors contributed to the susceptibility or severity of rheumatoid arthritis (RA) might give new insights into the pathways involved in disease pathogenesis and lead to the... -
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- Identification of marker chromosomes by reverse painting fluorescence in situ hybridization and comparative genomic hybridization
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Kang JK, Cho YH, Kyhm JH, Shin ES, Hoh JK, Chung SR
- KMID: 2272680
- Korean J Obstet Gynecol.
- 2005 Sep;48(9):2125-2139.
OBJECTIVE: Although marker chromosome is defined as an abnormal chromosome in which no part can be identified, derivative chromosomes with structural abnormalities of unknown origin are also called as marker... -
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- A case of prenatally diagnosed Non-15, Non-22 marker chromosome
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Song SR, Song JH, Song JH, Jung YW, Lee SS, Kim MH
- KMID: 2272554
- Korean J Obstet Gynecol.
- 2005 Feb;48(2):480-483.
Midtrimester genetic amniocentesis is an important diagnostic tool in prenatal genetic diagnosis and counseling. We can identify karyotypes with metaphase chromosome analysis of cultured amniocytes. Marker chromosomes are defined as... -
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- Prenatal detection of de novo inversion of chromosome 9 with duplicated heterochromatic region and postnatal follow-up
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Kim JJ, Rhee HS, Chung YT, Park SY, Choi SK
- KMID: 755041
- Exp Mol Med.
- 1999 Sep;31(3):134-136.
We report the first de novo case of a heterochromatic duplication on the long arm of the chromosome 9, which then was pericentrically inverted at p11q13. This condition was detected prenatally and... -
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- Genomic Features of Retroelements and Implications for Human Disease
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Kim HS
- KMID: 2284672
- Genomics Inform.
- 2005 Dec;3(4):133-141.
Most of the endogenous retroviral genes integrated into the primate genome after the split of New World monkeys in the Oligocene era, approximately 33 million years ago. Because they can... -
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- A Cytogenetic Analysis of Abortus with Spontaneous Abortion
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Hwang SM, Kwon KH, Yoon KA, Oh SK
- KMID: 2244892
- J Genet Med.
- 2009 Jun;6(1):62-66.
PURPOSE: Chromosomal abnormalities of abortuses have been used to investigate common etiologies of spontaneous abortion, but the frequencies and types of spontaneous abortions have demonstrated considerable variation among different countries... -
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- Computational Analysis of Neighboring Genes on Arabidopsis thaliana Chromosomes 4 and 5: Their Genomic Association as Functional Subunits
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Goh SH, Kim TH, Kim JH, Nam DG, Choi D, Hur CG
- KMID: 1973994
- Genomics Inform.
- 2003 Sep;1(1):40-49.
The genes related to specific events or pathways in bacteria are frequently localized proximate to the genome of their neighbors, as with the structures known as operon, but eukaryotic genes... -
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- B-cell Acute Lymphoblastic Leukemia With t(9;22)(q34;q11) Translocation and Clonal Divergence Through ider(22) Chromosome and t(13;17)(q14;q25) Translocation
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Meza-Espinoza JP, Romo Martinez EJ, Aguilar Lopez L, Picos Cardenas VJ, Magana Torres MT, Gonzalez Garcia JR
- KMID: 2373523
- Ann Lab Med.
- 2016 Mar;36(2):185-187.
- doi: 10.3343/alm.2016.36.2.185
No abstract available. -
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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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- Concepts of Genomic Variant Research
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Kim SY, Kim TH
- KMID: 1455839
- J Korean Orthop Res Soc.
- 2010 Jun;13(1):7-15.
Genetic variation occurs on many different scales, ranging from gross alteration in human chromosomes to single nucleotide changes. Approximately 99.5% of the human genome sequence is identical among humans. The... -
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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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- Giant Invasive Sacral Schwannoma Showing Chromosomal Numerical Aberrations [-14,+18,+22]
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Kanamori M, Yasuda T, Hori T, Suzuki K
- KMID: 2270437
- Asian Spine J.
- 2013 Sep;7(3):227-231.
- doi: 10.4184/asj.2013.7.3.227
Here, we report on a rare case of a giant invasive sacral schwannoma. The patient was a 58-year-old woman who had a 6-year history of non-specific buttock pain. Histological investigation... -
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