- Mutation of gyrA in Quinolone-Resistant Clinical Isolates of Escherichia coli
-
Seol SY, Lee YC, Chang HK
- KMID: 1943425
- J Korean Soc Microbiol.
- 1999 Apr;34(2):103-113.
To study the gyrA mutations of E. coli from clinical specimens, 410 strains were isolated from 1994 to 1997 in Kyungpook National Vniversity hospital. Antimicrobial susceptibility tests, PCR and sequencing... -
- CITED
-
- Close
- SHARE
-
- Close
- Cloning and Sequence Analysis of the Full-length cDNA of Coxsackievirus B3 Isolated in Korea
-
Chung YS, Kim KS, Park JK, Lee YS, Shin SY, Cheon DS, Jee Y, Kim MB, Na BK, Yoon JD, Lee KH, Song CY
- KMID: 1896564
- J Korean Soc Virol.
- 2000 Mar;30(1):71-81.
We have determined and analyzed the full-length cDNA sequence of a coxsackievirus B3 (CVB3) Korean isolate (CVB3-Korea/97) which has been known as a general human pathogen. The whole genome contains... -
- CITED
-
- Close
- SHARE
-
- Close
- Molecular characterization of a 13-amino acid deletion in VP1 (1D) protein and novel amino acid substitutions in 3D polymerase protein of foot and mouth disease virus subtype A/Iran87
-
Esmaelizad M, Jelokhani-Niaraki S, Hashemnejad K, Kamalzadeh M, Lotfi M
- KMID: 1365020
- J Vet Sci.
- 2011 Dec;12(4):363-371.
- doi: 10.4142/jvs.2011.12.4.363
The nucleotide sequence of the VP1 (1D) and partial 3D polymerase (3Dpol) coding regions of the foot and mouth disease virus (FMDV) vaccine strain A/Iran87, a highly passaged isolate (~150... -
- CITED
-
- Close
- SHARE
-
- Close
- Molecular characterization of two Bangladeshi infectious bursal disease virus isolates using the hypervariable sequence of VP2 as a genetic marker
-
Islam MT, Le TH, Rahman MM, Islam MA
- KMID: 2391999
- J Vet Sci.
- 2012 Dec;13(4):405-412.
Two Bangladeshi infectious bursal disease virus (IBDV) isolates collected in 2007, termed GB1 and GB3, were subjected to comparative sequencing and phylogenetic analyses. Sequence analysis of a 474-bp hypervariable region... -
- CITED
-
- Close
- SHARE
-
- Close
- Amino Acid Substitution Caused by Mutated rpoB Gene of Rifampin - Resistant Mycobacterium tuberculosis
-
Cho DT, Lee YC, Bang SH, Kim JM
- KMID: 2001260
- J Korean Soc Microbiol.
- 1997 Aug;32(4):389-399.
Mobility shifts in non-denatured gel electrophoresis of PCR-amplified Rif' region in each of fifteen different mutants of M. tuberculosis were discerned by single strand conformation polymorphism (SSCP) analysis. The findings... -
- CITED
-
- Close
- SHARE
-
- Close
- Point mutation and polymorphism in Duchenne/Becker muscular dystrophy (D/BMD) patients
-
Chaturvedi LS, Mukherjee , Srivastava S, Mittal RD, Mittal B
- KMID: 1457538
- Exp Mol Med.
- 2001 Dec;33(4):251-256.
Duchenne and Becker muscular dystrophies (D/BMD) are caused by mutations in the dystrophin gene. Two-thirds of patients have large intragenic deletions or duplications and the remaining one-third have point mutations,... -
- CITED
-
- Close
- SHARE
-
- Close
- Non-Type I Cystinuria Associated with Mental retardation and Ataxia in a Korean Boy with a New Missence Mutation(G173R) in the SLC7A9 Gene
-
Lee EH, Kim YH, Hwang JS, Kim SH
- KMID: 1713853
- J Korean Med Sci.
- 2010 Jan;25(1):172-175.
- doi: 10.3346/jkms.2010.25.1.172
Cystinuria is an inherited renal and intestinal disease characterized by defective amino acids reabsorption and cystine urolithiasis. It is unusually associated with neurologic symptoms. Mutations in two genes, SLC3A1 and... -
- CITED
-
- Close
- SHARE
-
- Close
- Molecular Epidemiology of Nalidixic Acid Resistance in Shigella sonnei Isolates
-
Seol SY, Do YK, Jeong YS, Kang HY, Lee JC, Lee YC, Cho DT, Jung TH
- KMID: 2168478
- J Bacteriol Virol.
- 2005 Mar;35(1):23-30.
Twenty-six nalidixic acid-resistant Shigella sonnei strains isolated from 1982 to 2001 and 56 nalidixic acid-resistant mutants induced by quinolone drugs from susceptible wild strains were analyzed by sequencing the gyrA... -
- CITED
-
- Close
- SHARE
-
- Close
- Substitutions in Penicillin-Binding Protein 1 in Amoxicillin-Resistant Helicobacter pylori Strains Isolated from Korean Patients
-
Kim BJ, Kim JG
- KMID: 1712324
- Gut Liver.
- 2013 Nov;7(6):655-660.
BACKGROUND/AIMS: A worldwide increase in amoxicillin resistance in Helicobacter pylori is having an adverse effect on eradication therapy. In this study, we investigated the mechanism of the amoxicillin resistance of... -
- CITED
-
- Close
- SHARE
-
- Close
- First Case in Korea of Group B Streptococcus With Reduced Penicillin Susceptibility Harboring Amino Acid Substitutions in Penicillin-Binding Protein 2X
-
Yi A, Kim CK, Kimura K, Arakawa Y, Hur M, Yun YM, Moon HW
- KMID: 2438892
- Ann Lab Med.
- 2019 Jul;39(4):414-416.
- doi: 10.3343/alm.2019.39.4.414
No abstract available. -
- CITED
-
- Close
- SHARE
-
- Close
- Distribution of mec Regulator Genes in Methicillin - Resistant Staphylococci
-
Cho DT, Lim DG, Kim JM
- KMID: 1540522
- J Korean Soc Microbiol.
- 1997 Jun;32(3):275-284.
In order to understand the role of mec regulator genes in the evolution of methicillin-resistant S. aureus (MRSA), the distribution of the mec regulator genes among the 66 clinical isolates... -
- CITED
-
- Close
- SHARE
-
- Close
- In Silico Functional Assessment of Sequence Variations: Predicting Phenotypic Functions of Novel Variations
-
Won HH, Kim JW
- KMID: 2166416
- Genomics Inform.
- 2008 Dec;6(4):166-172.
A multitude of protein-coding sequence variations (CVs) in the human genome have been revealed as a result of major initiatives, including the Human Variome Project, the 1000 Genomes Project, and... -
- CITED
-
- Close
- SHARE
-
- Close
- Polymorphisms of TAP2 Gene in Schizophrenia
-
Song JM, Jun TY, Lee KU, Pae CU, Pyo CW
- KMID: 2340999
- J Korean Neuropsychiatr Assoc.
- 2004 May;43(3):277-282.
OBJECTIVES: The genes for transporters associated with antigen processing (TAP) are located near to HLA class II coding regions and related to antigen presentation. Therefore polymorphisms of TAP might alter... -
- CITED
-
- Close
- SHARE
-
- Close
- Complete androgen insensitivity syndrome due to androgen receptor gene mutation in the amino acid position 607 which bilateral testes situated in the normal ovary sites
-
Kim HJ, Ko DS, Lee JY, Hong SY, Shin JH, Park CH, Park EJ, Seo YS, Park WI
- KMID: 2272885
- Korean J Obstet Gynecol.
- 2006 Aug;49(8):1795-1802.
Androgen insensitivity syndrome (AIS) is a disorder of male sexual differentiation caused by mutations within the androgen receptor gene, represents a variety of phenotypes from females with 46,XY karyotype over... -
- CITED
-
- Close
- SHARE
-
- Close
- Efficacy and safety of sorafenib in patients with advanced hepatocellular carcinoma
-
Heo J
- KMID: 1381445
- Korean J Hepatol.
- 2009 Jun;15(2):227-230.
- doi: 10.3350/kjhep.2009.15.2.227
No abstract available. -
- CITED
-
- Close
- SHARE
-
- Close
- Mutation of p53 and p16 Tumor Suppressor Genes in Cancer and Precancerous Lesions of the Gallbladder
-
Yoon YB, Kim CY, Kim WH, Kim SW, Kim YT, Ryu JK, Lee WJ
- KMID: 2084961
- Korean J Gastroenterol.
- 1999 Sep;34(3):390-398.
BACKGROUND/AIMS: The purpose of this study was to analyze the frequencies of p53 and p16 gene mutations in gallbladder cancer and precancerous lesions such as dysplasia or adenoma. METHODS: Tissues... -
- CITED
-
- Close
- SHARE
-
- Close
- Haplotype analysis at R778L mutation of ATP7B gene in Korean patients with Wilson disease
-
Jin HS, Oh B
- KMID: 1374957
- Korean J Hepatol.
- 2009 Sep;15(3):295-298.
- doi: 10.3350/kjhep.2009.15.3.295
No abstract available. -
- CITED
-
- Close
- SHARE
-
- Close
- Genetic Variations of the KISS1R Gene in Korean Girls with Central Precocious Puberty
-
Oh YJ, Rhie YJ, Nam HK, Kim HR, Lee KH
- KMID: 2417592
- J Korean Med Sci.
- 2017 Jan;32(1):108-114.
- doi: 10.3346/jkms.2017.32.1.108
The timing of puberty onset varies greatly among individuals, and much of this variation is modulated by genetic factors. This study aimed to identify the kisspeptin receptor (KISS1R) gene variations... -
- CITED
-
- Close
- SHARE
-
- Close
- Hereditary Pancreatitis
-
Lee SK
- KMID: 772858
- Korean J Gastroenterol.
- 2005 Nov;46(5):358-367.
The first family of hereditary pancreatitis was described in 1952. The mode of inheritance is autosomal dominant trait with an 80% of penetrance rate. Although hereditary pancreatitis is rare, this... -
- CITED
-
- Close
- SHARE
-
- Close
- Conservation of matrix protein genes in rabies viruses circulating in South Korea since 1999
-
Lee YA, Kim HH, Yang DK, Cho IS
- KMID: 2401295
- Korean J Vet Res.
- 2017 Dec;57(4):249-252.
- doi: 10.14405/kjvr.2017.57.4.249
Rabies virus (RABV) causes a neurological disease in warm-blooded animals that is nearly always fatal. In this study, we analyzed the matrix (M) genes in 10 Korean street RABV strains... -
- CITED
-
- Close
- SHARE
-
- Close
