1.A scanning electron microscopic study of the root resorption and repair in bicuspid intrusion.
Korean Journal of Orthodontics 1988;18(2):387-399
The purpose of this study was to investigate the root resorption and repair pattern of human teeth under intrusive orthodontic loadings of varying magnitude and duration. 50 gms, 100 gms, 200 gms of force applied to the 96 experimental teeth with duration of 2, 5, 7, 10 weeks, after removing the arch wire and retaining during 2 and 6 weeks, experimental teeth were extracted. Results were as follows: 1. The initial resorption site was visible in the apex within 2 weeks with 50 gms, 100 gms samples. 2. The sites of resorption increased markedly with duration of the force. 3. The 50 grams samples of the all duration reveal the shallow resorption and the 100 gms samples of the all duration except 2 weeks reveal the shallow and deep resorption sites. 4. After 7 weeks with 50 gms and 100 gms, cellular cementum repair accompanied the continuing resorption. 5. 2 and 6 weeks after removing the force with 200 gms, the same cellular cementum repair accompanied with 50 gms, 100 gms samples.
Bicuspid*
;
Dental Cementum
;
Humans
;
Root Resorption*
;
Tooth
2.Esophagus, Stomach & Intestine; A Case of Collagenous Colitis.
Jae Hong CHOI ; Byoung Ku NA ; Sang Woo OH ; Jee Hyun LEE ; Moo Sang JUNG ; Seun Mee PARK ; Sae Jin YOUN ; Bok Hee LEE ; Hwa Sook JUNG ; No Hyun SUNG
Korean Journal of Gastrointestinal Endoscopy 1997;17(1):79-84
The term ""collagenous colitis"" was coined by Lindstrom in 1976 to describe the patient with chronic watery diarrhea who had normal rectal mucosa by proctoscopy but who had a thick subepithelial collagenous deposit on biopsy, and now collagenous colitis is recognized as one of the more common causes of chronic diarrhea of obscure origin. But in this country only a few case has been reported. We have seen a 68-year-old man with chronic watery diarrhea with abdominal pain. Physical examination, laboratory and radiologic studies were no abnormal finding. Colonoscopy disclosed grossly normal mucosa through the entire colon but by histologic examination there are chronic inflammation in the lamina propria and thickened subepithelial collagen layer. Symptoms and pathologic findings of patient improved after treatment with sulfasalazine and prednisolone.
Abdominal Pain
;
Aged
;
Biopsy
;
Colitis, Collagenous*
;
Collagen*
;
Colon
;
Colonoscopy
;
Diarrhea
;
Esophagus*
;
Humans
;
Inflammation
;
Intestines*
;
Mucous Membrane
;
Numismatics
;
Physical Examination
;
Prednisolone
;
Proctoscopy
;
Stomach*
;
Sulfasalazine
3.No Association Between Single Nucleotide Polymorphisms in Distal-Less Homeobox-6 (DLX6) and Autism Spectrum Disorders (ASD) from the Korean Male Population.
Hyoun Geun KIM ; SeongSik WON ; Seung Ku LEE ; Min NAM ; Hee Jung BANG ; Hyun Jung PARK ; Jin Young YOON ; Kyung Sik CHOI ; Mee Sook HONG ; Joo Ho CHUNG ; Kyu Bum KWACK
Journal of the Korean Academy of Child and Adolescent Psychiatry 2010;21(1):17-22
OBJECTIVES: Autism spectrum disorder (ASD) is a neurodevelopmental disorder that is characterized by abnormalities of social functioning, communication and behavior. The association of the 7q21-34 region with ASD has been reported. The DLX6 gene, which is located at the 7q22 region, is one of the positional and functional candidate genes for ASD. We found that there is no association between DLX6 polymorphisms and ASD in the Korean male population. METHODS: We selected three single nucleotide polymorphisms (SNPs) that might be implicated in the change of the DLX6 gene expression. The genomic DNA was collected from the venous blood of 147 male controls and 179 male patients with ASD. The genotypes of the selected SNPs were determined using the Illumina GoldenGate assay, and the statistical analyses were performed using HapAnalyzer software and SAS Enterprise. RESULTS: We found no association of the three SNPs in the DLX6 gene with ASD in the Korean male population. CONCLUSION: Our study suggests that the three SNPs in the DLX6 gene are not associated with ASD, and we need to analyze the previously reported regions for their associations with ASD.
Autistic Disorder
;
Child
;
Autism Spectrum Disorder
;
DNA
;
Gene Expression
;
Genotype
;
Humans
;
Male
;
Phenothiazines
;
Polymorphism, Single Nucleotide