- Study of point mutation at codon 175 of p53 gene in breast carcinoma by PCR
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Kim YC, Kim CS, Kim SH, Mok YJ, Choi SY, Moon HY, Koo BH
- KMID: 1693957
- J Korean Surg Soc.
- 1993 Oct;45(4):465-470.
No abstract available. -
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- “p53 Polymorphism at Codon 72 and Breast Cancerâ€: Letter
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Afzaljavan F, Pasdar A
- KMID: 2375549
- J Cancer Prev.
- 2017 Mar;22(1):55-55.
- doi: 10.15430/JCP.2017.22.1.55
No abstract available. -
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- Codon Usage Bias of Human Cytomegalovirus Genes with Different Evolutionary Conservancy
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Kim YY, Lee CH
- KMID: 1502000
- J Bacteriol Virol.
- 2013 Dec;43(4):317-327.
- doi: 10.4167/jbv.2013.43.4.317
Human cytomegalovirus (HCMV) is a member of beta-herpesvirus and contains a double-stranded genome with longer than 230 Kbp. HCMV infection of human is mostly asymptomatic, but often causes fatal diseases... -
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- Comparative Analysis of Predicted Gene Expression among Crenarchaeal Genomes
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Das S, Chottopadhyay B, Sahoo S
- KMID: 2375583
- Genomics Inform.
- 2017 Mar;15(1):38-47.
- doi: 10.5808/GI.2017.15.1.38
Research into new methods for identifying highly expressed genes in anonymous genome sequences has been going on for more than 15 years. We presented here an alternative approach based on... -
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- Aflatoxin Related p53 Codon 249 Point Mutation in Korean Hepatocellular Carcinoma
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Wang HJ, Hong SW, Park YS, Kim WH, Kim MW
- KMID: 1928537
- Korean J Hepatobiliary Pancreat Surg.
- 1998 Feb;2(1):79-83.
PURPOSE: P53 point mutation, especially G to T transversion at codon 249, has been found in many cases of the aflatoxin-related hepatocellular carcinoma(HCC). This study was aimed to exam the... -
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- Association Study of the Relationship between Endometriosis and Polymorphism of p53 Codon 72
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Hur SE, Shim SS, Lee KS, Moon HS, Yu HK, Chung HW
- KMID: 1566328
- Korean J Fertil Steril.
- 2002 Dec;29(4):311-316.
OBJECTIVE: The present study was performed to evaluate the association of p53 codon 72 polymorphism and endometriosis. MATERIALS AND METHODS: We investigate 74 women who were operated for endometriosis and 93... -
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- Familial Creutzfeldt–Jakob Disease with a PRNP Mutation at Codon 180 Presented with Visual Hallucinations and Illusions
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Ryu DW, Hong YJ, Park JW, Lee SB, Kim SH, Kim Y, Seong MJ, Kim BS
- KMID: 2461051
- Dement Neurocogn Disord.
- 2019 Sep;18(3):105-107.
- doi: 10.12779/dnd.2019.18.3.105
No abstract available. -
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- Mutation Analysis of K-ras Codon 12 in Malignant Effusion
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Huh JW, Chi HS
- KMID: 2089550
- Korean J Clin Pathol.
- 1998 Sep;18(3):469-475.
BACKGROUND: Many studies suggest that point mutations of ras oncogene develop tumors. The advantages of body fluid analysis are easy accessibility and more simple procedure than tissue specimen. So, we... -
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- Mutations of the NF1 gene in Korean Neurofibromatosis type 1 patients
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Park KC, Choi HO, Han WS, Hwang JH, Kim KH, Chung JH, Eun HC
- KMID: 2163872
- Ann Dermatol.
- 2001 Jun;13(2):102-105.
- doi: 10.5021/ad.2001.13.2.102
BACKGROUND: Neurofibromatosis type 1 (NF1) is one of the most common inherited disorders and is characterized by abnormalities in multiple tissues derived from the neural crest. OBJECTIVES: We analyzed the presence... -
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- Codon Usage Patterns of Tyrosinase Genes in Clonorchis sinensis
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Bae YA
- KMID: 2379420
- Korean J Parasitol.
- 2017 Apr;55(2):175-183.
- doi: 10.3347/kjp.2017.55.2.175
Codon usage bias (CUB) is a unique property of genomes and has contributed to the better understanding of the molecular features and the evolution processes of particular gene. In this... -
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- Identification of mutagenic site of c-H-ras oncogene damaged by N-acetoxyacetylaminofluorene(AAAF)
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Oh SH, Kim KH, Lee SE, Yeh BI
- KMID: 1729587
- Yonsei Med J.
- 1991 Sep;32(3):207-214.
- doi: 10.3349/ymj.1991.32.3.207
A molecularly cloned human cellular H-ras (c-H-ras) oncogene(pbc N1 plasmid) was treated with N-acetoxyacetylaminofluorene (AAAF) in vitro and subcloned into E.coli. This was done to identify the mutational changes at... -
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- Point mutation at codon 12 of the c-Ha-ras gene in human gastric cancers.
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Koh EH, Chung HC, Lee KB, Han EK, Oh SH, Min JS, Choi EM, Youn JK, Kim BS
- KMID: 1421899
- J Korean Med Sci.
- 1992 Jun;7(2):110-115.
- doi: 10.3346/jkms.1992.7.2.110
The molecular mechanisms of the carcinogenic process of gastric cancer have not been fully understood yet. In order to know whether c-Ha-ras gene is being involved in the process... -
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- Characterization of the Repeat Sequences of Varicella-Zoster Virus
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Won YH, Kim JI, Kim YY, Lee CH
- KMID: 1737321
- J Bacteriol Virol.
- 2014 Dec;44(4):326-335.
- doi: 10.4167/jbv.2014.44.4.326
Varicella-zoster virus (VZV) is a causative agent for shingles and herpes zoster. The genomes of VZV contain five reiteration (R) sequences and an origin of replication (ORI) sequences composed of... -
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- Characteristics of the RET Oncogene Germline Mutations in Korean Medullary Thyroid Carcinoma: A Literature Review
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Sin DJ, Min JW, Chang MC
- KMID: 2375723
- Korean J Endocr Surg.
- 2010 Jun;10(2):93-98.
- doi: 10.16956/kjes.2010.10.2.93
PURPOSE: Germline mutation of the RET oncogene results in multiple endocrine neoplasia (MEN) types 2A and 2B and familial medullary thyroid cancer (FMTC). We reviewed the literature to determine the... -
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- The Relationship between Isoniazid Resistance and 463 CodonMutation of katG Gne in Mycobacterium Tuberculosis
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Park YK, Shim MS, Cho SH, Bai GH, Kim SJ
- KMID: 2317967
- Tuberc Respir Dis.
- 1996 Feb;43(1):8-13.
BACKGROUND: The 463 codon mutation of katG gene has been reported as an useful marker for the detection of isoniazid(INH) resistant strains of M. tuberculosis. This study aimed to elucidate... -
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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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- Gastric Cancer Susceptibility in the P53 Codon 72 Polymorphism
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Heo YJ, Cho HM, Chin HM, Kim W, Jeon HM
- KMID: 2325065
- J Korean Surg Soc.
- 2005 Jul;69(1):24-30.
Purpose: The P53 codon 72 polymorphism results in either arginine or proline, there are many studies to clear the relationship between P53 codon 72 genotypes and specific cancer risk and... -
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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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- Synonymous Codon Usage Controls Various Molecular Aspects
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Im EH, Choi SS
- KMID: 2404048
- Genomics Inform.
- 2017 Dec;15(4):123-127.
- doi: 10.5808/GI.2017.15.4.123
Synonymous sites are generally considered to be functionally neutral. However, there are recent contradictory findings suggesting that synonymous alleles might have functional roles in various molecular aspects. For instance, a... -
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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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