- Selenoprotein S Suppression Enhances the Late Stage Differentiation of Proerythrocytes Via SIRT1
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Yang HY, Chung KJ, Park HR, Han SJ, Lee SR, Chay KO, Kim IY, Park BJ, Lee TH
- KMID: 1457118
- Int J Oral Biol.
- 2010 Jun;35(2):61-67.
Selenoprotein S (SelS) is widely expressed in diverse tissues where it localizes in the plasma membrane and endoplasmic reticulum. We studied the potential function of SelS in erythrocyte differentiation using... -
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- A Case of Pregnant Woman with beta-Thalassemia in Korean
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Ryu A
- KMID: 2404862
- Soonchunhyang Med Sci.
- 2017 Dec;23(2):143-145.
- doi: 10.0000/sms.2017.23.2.143
Thalassemia is hereditary disease characterized by impaired production of the normal globin peptide. Beta-thalassemia, a common disorder in Central Africa, the Middle East, and Southeast Asia, has been rarely reported... -
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- Beta-Thalassemia Minor Is Associated with IgA Nephropathy
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Kang JH, Park BR, Kim KS, Kim DY, Huh HJ, Chae SL, Shin SJ
- KMID: 1781318
- Ann Lab Med.
- 2013 Mar;33(2):153-155.
- doi: 10.3343/alm.2013.33.2.153
No abstract available. -
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- A Case of Familial beta-thalassemia Minor
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Kim SH, Han BK, Kim HT, Lee KH, Hwang CH, Cho MK, Choi KR
- KMID: 2208313
- J Korean Pediatr Soc.
- 1995 Apr;38(4):557-560.
Thalassemias are a diverse group of inherited anemias that are characterized by defective synthesis of one or more globin chains. The thalassemias are classified according to the globin chain or... -
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- Clinical Characteristics of Pediatric Thalassemia in Korea: A Single Institute Experience
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Hong CR, Kang HJ, Lee JW, Kim H, Kim NH, Park KD, Park JD, Seong MW, Park SS, Shin HY, Ahn HS
- KMID: 1777663
- J Korean Med Sci.
- 2013 Nov;28(11):1645-1649.
- doi: 10.3346/jkms.2013.28.11.1645
Few literatures have elaborated on the clinical characteristics of children with thalassemia from low-prevalence areas. A retrospective analysis was conducted on children genetically confirmed with thalassemia at Seoul National University... -
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- In vivo Mapping of the Cis-acting Element Responsible for Spatial Regulation of the EphA8 Gene Expression in Mesencephalon
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Kim J, Park S
- KMID: 1564264
- Korean J Anat.
- 2005 Apr;38(2):125-131.
This study was aimed to map the 1 kb cis-acting DNA of ephA8 gene, which regulates the spatial and temporal expression in the anterior mesencephalon. It was demonstrated that the... -
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- Three Cases of beta-thalassemia in Children with HBB Gene Mutation
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Kang EY, Lee HJ, Choi SI, Park EH, Kim SY, Hwang PH
- KMID: 2279917
- Clin Pediatr Hematol Oncol.
- 2007 Oct;14(2):192-197.
Beta thalassemia is an inherited anemia characterized by decreased or absent synthesis of beta globin chain and known to be uncommon in Korea, but is recently reported more frequently in... -
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- A Case of beta Thalassemia Intermedia Due to Hemoglobin Cagliari (beta 60 Val - >Glu)
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Park ES, Han HY, Lim JY, Park SS, Kim SY
- KMID: 2252134
- Korean J Hematol.
- 2009 Sep;44(3):153-156.
- doi: 10.5045/kjh.2009.44.3.153
Beta Thalassemia is a very rare disease in Korea. Only14 mutations have been reported in South Korea to date. This is the first case of beta thalassemia intermedia due to... -
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- A Novel-Thalassemic Mutation, Codons 89/90-TG, Found in Two Korean Families
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Lee YJ, Park SS, Kim J, Joo SI, Park S, Choi JW, Kim SK, Han KS, Kim JQ, Kim EC, Park MH, Cho HI
- KMID: 2089673
- Korean J Clin Pathol.
- 2001 Apr;21(2):160-163.
We describe a novel-thalassemia mutation, the deletion of TG at codons 89/90 of the globin gene, found in two unrelated Korean families. Their hematological findings varied, but some patients showed... -
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- A case of vaginal delivery in beta-thalassemia minor pregnant woman
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Shim HJ, Cho EK, Jeon HJ, Lee MR, Kim YS, Bae DH, Kim HJ
- KMID: 2274054
- Korean J Obstet Gynecol.
- 2011 Jul;54(7):381-385.
- doi: 10.5468/KJOG.2011.54.7.381
The thalassemias are a group of autosomal recessive genetic disorders of hemoglobin synthesis. The thalassemias are classified into two main varieties, alpha- and beta-, depending on which of the adult... -
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- beta-Thalassemia Mutation, IVS-II-1 G-->A Found in Koreans Uniquely Linked to the Silent Mutation C-->T at Codon 91 of the beta-Globin Gene
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Lee YJ, Paik NH, Park SS, Kim JY, Joo SI, Kim JQ, Han KS, Kim EC, Park MH, Cho HI
- KMID: 2135505
- J Clin Pathol Qual Control.
- 2001 Dec;23(2):277-280.
The mutation spectrum of beta-thalassemia in the Korean population is heterogeneous and quite different from the highly prevalent areas. We found four families with beta-thalassemia due to IVS-II-1, G-->A mutation... -
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- A Clinical Study on Hereditary Hemoglobinopathy: a Single Institute Experience
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Shin JS, Lee MJ, Jung HJ, Park JE
- KMID: 2279834
- Clin Pediatr Hematol Oncol.
- 2014 Apr;21(1):9-15.
BACKGROUND: Hemoglobinopathy is inherited anemia characterized by abnormal structure of one of the globin chains of the hemoglobin molecule and has been known to be rare in Korea. However, hemoglobinopathy... -
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- A Familial Case of beta-Thalassemia Minor due to a Point Mutation (G-->A) at Position 1 in the Second Intervening Sequence
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Choi JH, Lee KH, Kim ST, Choi YM, Park SS, Cho HI
- KMID: 2143389
- Korean J Hematol.
- 1997 Aug;32(2):306-311.
The thalassemias are congenital disorders in which globin chains are present in decreased amount or absent. Beta-thalassemia, a quite common disorder in Central Africa, the Middle East, and Southeast Asia,... -
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- A Korean Family with Thalassemia Intermedia due to Co-inheritance of Triplicated alpha-Globin Genes (alphaalpha/alphaalphaalphaanti3.7) and beta-Thalassemia Trait (IVSII-1 G -> A)
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Han JY, Kim TG, Kim KH, Kim IH, Lee EY, Cho GJ, Ren ZR, Huang SZ, Zeng YT, Rodgers GP
- KMID: 2083384
- Korean J Hematol.
- 1999 May;34(2):338-343.
We report a Korean family in which the interaction of a triplicated alpha-globin locus and a heterozygous beta-thalassemia gives rise to a clinical phenotype of thalassemia intermedia. The propositus, a... -
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- A Family Case of Hb Queens[ 34 (B15)Leu-->Arg]
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Jeon DS, Choi GJ, Chun HJ, Kim JR, Lee YJ, Park SS, Cho HI, Hattori Y, Ohba Y
- KMID: 2083359
- Korean J Hematol.
- 1997 May;32(1):112-118.
A 36-year-old pregnant woman with gestational diabetes mellitus and anemia was found to have an abnormal Hb (comprising 18.7%) in the automated midget low pressure cation- exchange chromatography (DiaSTATTM, Bio-Rad,... -
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- A Case of Dominantly Inherited beta Thalassemia Due to Hb Dieppe
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Choi YK, Lee HJ, Park WI, Lee KJ, Kang SH, Kim JY, Park SS
- KMID: 2335642
- J Korean Pediatr Soc.
- 2002 May;45(5):659-663.
beta thalassemias are usually transmitted as autosomal recessive traits. However, some dominant forms of beta thalassemia have been identified in individuals who have inherited a single copy of an abnormal... -
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- Development of Mutation Scanning Method for the Molecular Diagnosis of beta-thalassemia using Dideoxy Fingerprinting (ddF)
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Joo SI, Park SS
- KMID: 1963108
- J Clin Pathol Qual Control.
- 2001 Jun;23(1):193-199.
BACKGROUND: beta-Thalassaemia is the most common single-gene disorders due to the mutations of the beta-globin gene. Because beta-thalassemic mutations are scattered throughout the beta-globin gene, mutation scanning technique may be... -
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- HPV Genotyping in Squamous Cell Carcinoma of Upper Aerodigestive Tract
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Kim Y, Jeong EH, Min BW, Kim SS, Choi YD, Jung WJ, Nam JH, Park CS
- KMID: 2277556
- Korean J Pathol.
- 2010 Oct;44(5):483-487.
BACKGROUND: Smoking and alcohol consumption are the main risk factors for squamous cell carcinoma of the upper aerodigestive tract (SCCUAT). However, human papillomavirus (HPV) has been etiologically linked with tonsillar... -
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- Treatment and Management of Late Complications in Hereditary Hemolytic Anemia
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Chueh HW
- KMID: 2168902
- Clin Pediatr Hematol Oncol.
- 2016 Apr;23(1):1-7.
- doi: 10.15264/cpho.2016.23.1.1
Hereditary hemolytic anemia is a very heterogeneous disorder in which abnormalities of red blood cell structural protein, globin protein, or enzyme defect lead to shortened life span. There has been... -
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- Cryptic Plasmid Amplification of Chlamydia trachomatis at a Korean Health Center for Female Commercial Sex Workers
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Lee G, Sohng I
- KMID: 2294213
- Korean J Urol.
- 2006 Jan;47(1):37-41.
- doi: 10.4111/kju.2006.47.1.37
PURPOSE: Chlamydia trachomatis infection is the most common bacterial sexually transmitted disease. It is generally accepted that female commercial sex workers (FCSWs) are at an increased risk of incurring sexually... -
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