- Characterization of microsatellite markers covering chromosome 1 in the Korean and Japanese populations
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Lee YJ, Park SB
- KMID: 2400563
- Korean J Orthod.
- 2004 Dec;34(6):537-543.
Microsatellite markers are considered to be very promising genetic markers for genetic linkage analysis. The majority of the markers are as informative as in Caucasians but there are significant ethnic... -
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- Genetic linkage analysis in FAP/GS using DNA probe EF5.4(D5135)
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Kim HJ, Kim YK, Dong SH, Kim BH, Lee JI, Chang YW, Choi YK, Lee KH
- KMID: 1698313
- Korean J Med.
- 1993 Sep;45(3):361-368.
No abstract available. -
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- Recent advances in genetic studies of stuttering
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Kang C
- KMID: 2055585
- J Genet Med.
- 2015 Jun;12(1):19-24.
- doi: 10.5734/JGM.2015.12.1.19
Speech and language are uniquely human-specific traits, which contributed to humans becoming the predominant species on earth. Disruptions in the human speech and language function may result in diverse disorders.... -
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- Statistical Algorithm in Genetic Linkage Based on Haplotypes
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Kim J, Kang DR, Lee YK, Shin SM, Suh I, Nam CM
- KMID: 2283776
- J Prev Med Public Health.
- 2004 Nov;37(4):366-372.
OBJECTIVES: This study was conducted to propose a new transmission/disequilibrium test (TDT) to test the linkage between genetic markers and diseasesusceptibility genes based on haplotypes. Simulation studies were performed to... -
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- Genome-wide linkage analysis for ocular and nasal anthropometric traits in a Mongolian population
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Im SW, Kim HJ, Lee MK, Yi JH, Jargal G, Sung J, Cho SI, Kim JI
- KMID: 1115263
- Exp Mol Med.
- 2010 Dec;42(12):799-804.
- doi: 10.3858/emm.2010.42.12.080
Anthropometric traits for eyes and nose are complex quantitative traits influenced by genetic and environmental factors. To date, there have been few reports on the contribution of genetic influence to... -
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- Identification of a genetic locus on chromosome 4q34-35 for type 2 diabetes with overweight
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Park MH, Kwak SH, Kim KJ, Go MJ, Lee HJ, Kim KS, Hwang JY, Kimm K, Cho YM, Lee HK, Park KS, Lee JY
- KMID: 2154226
- Exp Mol Med.
- 2013 Feb;45(2):e7.
The incidence of type 2 diabetes is rising rapidly because of an increase in the incidence of being overweight and obesity. Identification of genetic determinants for complex diseases, such as... -
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- Class 1 Integron Carriage in Extended-spectrum beta-lactamase-producing K. pneumoniae
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Kim J
- KMID: 1963266
- J Bacteriol Virol.
- 2004 Sep;34(3):181-189.
Many antibiotic resistance genes found in gram-negative clinical isolates are a part of a gene cassette inserted into an integron. Incidence of the integron carriage in extended-spectrum beta-lactamases (ESBLs)-producing clinical... -
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- A genetic linkage study of Wilson disease in Korean families
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Kim JW, Kim SI, Seo JK
- KMID: 2208579
- J Korean Pediatr Soc.
- 1993 Nov;36(11):1596-1612.
Wilson disease gene (WND) locus is presumed to be located in chromosome 13q. There are studies on the clinical heterogeneities and variations between ethnic groups in Europe, North America, and... -
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- Molecular Application in Psychiatry
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Choi IG
- KMID: 1899244
- J Korean Soc Biol Psychiatry.
- 2000 Nov;7(2):115-122.
The development of molecular biology has brought many changes in psychiatry. Molecular biology makes us possible to know the cause of mental disorders that provide the way to prevent the... -
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- Severe acute alcoholic hepatitis and liver transplant: A never-ending mournful story
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Obed A, Bashir A, Stern S, Jarrad A
- KMID: 2433298
- Clin Mol Hepatol.
- 2018 Dec;24(4):358-366.
- doi: 10.3350/cmh.2018.0044
Severe acute alcoholic liver disease (SAAH) unresponsive to medical therapy shows one-year-mortality rates of up to 90%. Most transplant centers request six months of alcohol abstinence prior to transplantation, the... -
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- Child and Adolescent Onset Obsessive Compulsive Disorder
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Kim BN
- KMID: 1996822
- Korean J Psychopharmacol.
- 2003 Jun;14(2):119-128.
Obsessive compulsive disorder with child & adolescent onset (C-OCD) is not a rare disorder. Though OCD patients with prepubertal onset is scarce, the prevalence of OCD with postpubertal, adolescent onset... -
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- Combined Genome-Wide Linkage and Association Analyses of Fasting Glucose Level in Healthy Twins and Families of Korea
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Suh YJ, Kim S, Kim SH, Park J, Lim HA, Park HJ, Choi H, Ng D, Lee MK, Nam M
- KMID: 1786940
- J Korean Med Sci.
- 2013 Mar;28(3):415-423.
- doi: 10.3346/jkms.2013.28.3.415
This study was undertaken to identify genetic polymorphisms that are associated with the risk of an elevated fasting glucose (FG) level using genome-wide analyses. We explored a quantitative trait locus... -
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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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- Atopic Dermatitis
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Bieber T
- KMID: 2265381
- Ann Dermatol.
- 2010 May;22(2):125-137.
- doi: 10.5021/ad.2010.22.2.125
Atopic dermatitis (AD) is a chronic and relapsing disease affecting an increasing number of patients. Usually starting in early childhood, AD can be the initial step of the so-called atopic... -
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- Two Siblings of Non Salt Losing Congenital Adrenal Hyperplasia due to 21-hydroxylase Deficiency
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Lee SC, Suh BK, Lee BC
- KMID: 2208316
- J Korean Pediatr Soc.
- 1995 Apr;38(4):574-581.
Congenital adrenal hyperplasia in caused by a defect in the biosynthesis of cortisol as a result of deviciency in one of the essential enzymes, most commonly 21-hydroxylase and is an... -
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- A Case of Familial Hemiplegic Migraine
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Sa-Kong Y, Lee BH, Bae SN, Lee KW, Nam SO
- KMID: 2007409
- J Korean Child Neurol Soc.
- 2003 Nov;11(2):367-371.
Familial hemiplegic migraine(FHM) is an autosomal dominant subtype of migraine with aura, characterized by the occurrence of hemiplegia during the aura. Two subforms of FHM families exist; pure FHM in... -
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- Depression and suicide
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Jeon HJ
- KMID: 2190417
- J Korean Med Assoc.
- 2011 Apr;54(4):370-375.
- doi: 10.5124/jkma.2011.54.4.370
Suicide is the fourth leading cause of death in South Korea, which is the highest rate among the Organization for Economic Cooperation and Development member countries. The World Health Organization... -
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- Development and Molecular Characterization of Novel Polymorphic Genomic DNA SSR Markers in Lentinula edodes
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Moon S, Lee HY, Shim D, Kim M, Ka KH, Ryoo R, Ko HG, Koo CD, Chung JW, Ryu H
- KMID: 2385659
- Mycobiology.
- 2017 Jun;45(2):105-109.
- doi: 10.5941/MYCO.2017.45.2.105
Sixteen genomic DNA simple sequence repeat (SSR) markers of Lentinula edodes were developed from 205 SSR motifs present in 46.1-Mb long L. edodes genome sequences. The number of alleles ranged... -
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- Hashimoto's Thyroiditis and Papillary Thyroid Cancer
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Nam KH
- KMID: 2325292
- J Korean Thyroid Assoc.
- 2014 May;7(1):57-61.
The association of Hashimoto's thyroiditis (HT) with papillary thyroid cancer (PTC) has been still under debate. Some suggest that these two are positively correlated, whereas other studies report no relationship.... -
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- The tumor necrosis factor beta * 1 allele is linked significantly to HLA-DR8 in Koreans with atrophic autoimmune thyroiditis who are positive for thyrotropin receptor blocking antibody
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Chung JH, Cho BY, Lee HK, Kim TG, Han H, Koh CS
- KMID: 1422171
- J Korean Med Sci.
- 1994 Apr;9(2):155-161.
- doi: 10.3346/jkms.1994.9.2.155
The localization and functional characteristics of tumor necrosis factor(TNF) beta gene raise the possibility that it may be involved in the susceptibility to autoimmune thyroid diseases. To investigate whether a... -
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