1.Corrigendum: Characterizing affinity epitopes between prion protein and beta-amyloid using an epitope mapping immunoassay.
Mino KANG ; Su Yeon KIM ; Seong Soo A AN ; Young Ran JU
Experimental & Molecular Medicine 2014;46(5):e96-
Due to an author error the National Research Foundation of Korea Grant Number was incorrectly listed in the original online publication of this article.
2.Modification of Immune Response by Cold Stress in Mice.
Young Min PARK ; Yang Hyo OH ; Young Ran SEONG ; Jung Cheol LEE ; Seol Hyang BAEK
Korean Journal of Immunology 1997;19(4):437-446
No abstract available.
Animals
;
Interleukin-2
;
Mice*
3.Chromosomal analysis of abortus chorionic villi in case of recurrent spontaneous abortions.
Hye Ran HWANG ; Seong Sook SEO ; Shin Young LEE ; Jung Hye KIM ; Sook Ja PARK
Korean Journal of Obstetrics and Gynecology 1993;36(12):3897-3904
No abstract available.
Abortion, Spontaneous*
;
Chorion*
;
Chorionic Villi*
;
Female
;
Humans
;
Pregnancy
4.A Case of Prader-Willi Syndrome with Diabetes Mellitus.
Hee Ran CHOI ; Eun Ha CHOI ; Seong Hee JANG ; Young Min AHN
Journal of the Korean Pediatric Society 1994;37(4):565-572
Prader-Willi syndrome is characterized by infantile hypotonia, mental retardation, hyperhagia, hypogonadism and obesity. Approximately 60% of all PLW syndrome show an interstitial deletion of chromosome 15, 37% have apparently normal chromosome, and 3.6% have a variety of other abnormalities involving chromosome 15. Diabetes mellitus has been considered a component of PLW syndrome and the incidence is about 7%. We experienced a 17-year-old female who revealed mental retardation, hypogonadism, obesity, and non-insulin dependent type DM, compatible with Prader-Willi syndrome.
Adolescent
;
Chromosomes, Human, Pair 15
;
Diabetes Mellitus*
;
Female
;
Humans
;
Hypogonadism
;
Incidence
;
Intellectual Disability
;
Muscle Hypotonia
;
Obesity
;
Prader-Willi Syndrome*
5.A Clinical Study on Urinary Tract Infection in Infants and Children.
Yoo Hwa CHA ; Hee Ran CHOI ; Seong Hee JONG ; Young Min AHN
Journal of the Korean Pediatric Society 1994;37(11):1488-1499
This is a report of clinical study on the 63 patients of symptomatic urinary tract infection who were hospitalized at the Department of Pediatrics in Kangnam General Hospital during the period between the May of 1989 and the September of 1992. The observation results were as follows: 1) The frequency of urinary tract infection (UTI) was the highest in children under the age of one year (66.7%). 35 patients were male, while the other 28 were female. The ratio of male and female patients was 1.25:1. 2) Fever was observed in most of the cases. Systemic nonspecific manifestation was predominant in the infancy and early childhood, whereas local symptom of UTI was predominant in the late childhood. Among the 35 male patients, 32 cases were phimoses. As for the other 3 cases, Phimoses were not identified. 3) E. coli had the most frequency (65.3%), followed by Klebsiella, Enterobacter, Pseudomonas in descending order. 4) In the vitro antimicrobial susceptibility test, Gram negative organisms such as E. coli Klebsiella, Enterobacter were sensitive to cefotaxime, amikacin, and ampicillin/sulbactam. Meanwhile, Gram positive organisms such as Staphylococcus, Enterococcus were sensitive to vancomycin and cephradine. 5) The renal ultrasonography test was performed for 59 patients, 13 cases of whom showed abnormal findings. 6 cases out of the 13 abnormal patients had hydronephrosis. 6) DMSA renal scan was performed for 40 patients within 2 months of an acute pyelonephritic attack. Signs of pyelonephritic change were found in 18 patients. DMSA scan was repeated 4~12 months later in 4 of these patients. This showed renal cortical scarring in all patients. 7) Voiding cystourethrographic findings in 38 patients showed vesicoureteral reflux in 13 patients. 8) We performed urine culture again after 48 hours from the beginning of therapy and 85.5% of the cases became sterile. 9) The recurrent percentage of UTI was 23.8% with the ratio of 1:1.5 between male and female. Most of the patients were clildren under the age of one year. 10) Operations were made on two cases showing the increase of reflux during the follow-up of unilateral Grade ll and Grade 3 reflux, respectively. Operations were also performed on other two cases with bilateral Grade IV reflux. All the cases were good after the operations. In the meantime, as for another two cases having the right reflux of Grade lland the bilateral reflux of Grade lll, the refluxes were able to be reduced by prophylaxis only, in the course of following up.
Amikacin
;
Cefotaxime
;
Cephradine
;
Child*
;
Cicatrix
;
Enterobacter
;
Enterococcus
;
Female
;
Fever
;
Follow-Up Studies
;
Hospitals, General
;
Humans
;
Hydronephrosis
;
Infant*
;
Klebsiella
;
Male
;
Pediatrics
;
Phimosis
;
Pseudomonas
;
Staphylococcus
;
Succimer
;
Ultrasonography
;
Urinary Tract Infections*
;
Urinary Tract*
;
Vancomycin
;
Vesico-Ureteral Reflux
6.Retroperitoneal Mucinous Tumor: Report of two Cases.
Eun Kyung KIM ; Seong Ran HONG ; Hy Sook KIM ; Young Hyeh KO ; Jung Dal LEE
Korean Journal of Pathology 1992;26(6):632-634
Primary retroperitoneal mucinous tumor is very rare. In the worldwide literature, only 14 cases have been reported. Herein, we report two cases of retroperitoneal mucinous tumor found at laparotomy. The patients were females, aged 24 and 21 years, respectively. They had bilateral normal ovaries. Histologically, one was mucinous cystadenoma and the other showed borderline histology. The connective tissue wall resembling ovarian stroma was noted in one case. The pathogenesis was discussed.
Female
;
Humans
7.Loss of Heterozygosity of p73, APC, and p53 in Hepatoblastoma.
Han Seong KIM ; Young Mi JUNG ; Mi Ran KIM ; Jung Young LEE ; Mi Sook LEE ; Ja June JANG
The Korean Journal of Hepatology 1999;5(1):43-49
BACKGROUND/AIMS: The status of tumor suppression gene can be assessed indirectly by analyzing the loss of heterozygosity. Hepatoblastoma is a malignant liver tumor in childhood. To find the molecular carcinogenetic mechanism of hepatoblastoma, loss of heterozygosity (LOH) of p73, APC and p53 was studied. MATERIALS AND METHODS: Hepatoblastoma tissues from thirty-three cases were collected by lobectomy or tumorectomy. On H- stained sections, normal and tumor cells were microdissected separately and LOH analysis was perfomed using 8 markers: six of p73, one of APC and one of p53. RESULTS: Number of cases showing at least one LOH in six p73 markers was four out of twenty- six (15.4%): each LOH frequencies in D1S160, D1S170, D1S199, D1S228, D1S243 and D1S253 were in order of 7.7%, 0%, 9.1%, 0%, 12.5% and 0%. LOH frequency of APC was 41.7% and that of p53 was 13.3%. CONCLUSION: Low LOH frequency of p73 related markers indicates that p73 gene may not be implicated in carcinogenesis of hepatoblastoma.
Carcinogenesis
;
Hepatoblastoma*
;
Liver
;
Loss of Heterozygosity*
8.Evaluation of blood transfusion practice in infant.
Seong Geun HONG ; Hyun Ok KIM ; Oh Hun KWON ; Ran NAMGUNG ; Dong Kwan HAN ; Kir Young KIM
Korean Journal of Blood Transfusion 1992;3(1):15-20
No abstract available.
Blood Transfusion*
;
Humans
;
Infant*
9.Characterizing affinity epitopes between prion protein and beta-amyloid using an epitope mapping immunoassay.
Mino KANG ; Su Yeon KIM ; Seong Soo A AN ; Young Ran JU
Experimental & Molecular Medicine 2013;45(8):e34-
Cellular prion protein, a membrane protein, is expressed in all mammals. Prion protein is also found in human blood as an anchorless protein, and this protein form is one of the many potential sources of misfolded prion protein replication during transmission. Many studies have suggested that beta-amyloid1-42 oligomer causes neurotoxicity associated with Alzheimer's disease, which is mediated by the prion protein that acts as a receptor and regulates the hippocampal potentiation. The prevention of the binding of these proteins has been proposed as a possible preventative treatment for Alzheimer's disease; therefore, a greater understanding of the binding hot-spots between the two molecules is necessary. In this study, the epitope mapping immunoassay was employed to characterize binding epitopes within the prion protein and complementary epitopes in beta-amyloid. Residues 23-39 and 93-119 in the prion protein were involved in binding to beta-amyloid1-40 and 1-42, and monomers of this protein interacted with prion protein residues 93-113 and 123-166. Furthermore, beta-amyloid antibodies against the C-terminus detected bound beta-amyloid1-42 at residues 23-40, 104-122 and 159-175. beta-Amyloid epitopes necessary for the interaction with prion protein were not determined. In conclusion, charged clusters and hydrophobic regions of the prion protein were involved in binding to beta-amyloid1-40 and 1-42. The 3D structure appears to be necessary for beta-amyloid to interact with prion protein. In the future, these binding sites may be utilized for 3D structure modeling, as well as for the pharmaceutical intervention of Alzheimer's disease.
Amyloid beta-Peptides/*metabolism
;
Electrophoresis
;
Enzyme-Linked Immunosorbent Assay
;
*Epitope Mapping
;
Epitopes/*metabolism
;
Humans
;
*Immunoassay
;
Prions/*metabolism
;
Protein Binding
;
Recombinant Proteins/metabolism
10.A Case of Synchronous Multiple Primary Cancers in Esophagus and Stomach with Mutiple Gastric Cancers.
Seong Ho CHOI ; Young Ran SEONG ; Tae Yeong LEE ; Jae Seuk PARK ; Mi Hye JEONG
Korean Journal of Gastrointestinal Endoscopy 1998;18(1):71-75
A case of synchronous multiple primary esophageal squamous cell carcinomas and multiple gastric adenocarcinomas is reported. The lesions were found on gastrofiberscopic examination for the evaluation of dysphagia and epigastric pain. The esophageal lesions were 2 ulceromfiltrating mass lesions at mid- and lower esophagus and 2 lesions were separated by normal mucosa. The main leiosn of stomach was an ulcerative one (Borrmanns type II) on lower body and the accessory lesion was an EGC IIc like lesion on antrum and 2 lesions were independent.
Adenocarcinoma
;
Carcinoma, Squamous Cell
;
Deglutition Disorders
;
Esophagus*
;
Mucous Membrane
;
Stomach Neoplasms*
;
Stomach*
;
Ulcer