There have been published manuscripts which fully suggest that there may be a topographic variance of contact sensitivity in experimental animals such as guinea pigs, hamsters and mice, probably due to a large extent to the topographic difference of Langerhans cell population and to a little extent to impact on the induction site. This assay was done to establish the possibility of involvement of a certain topographic variance in contact sensitivity reaction. Three different anatomical sites were chosen for the induction in three groups of five guinea pigs: the conventional site of the nuchal region, and the sacral aod. ahdominal skin regions. For the elicitation, two different concentrations of DNCB were applied on three sites along both sides of the spine in the back. The contact sensitivity reaction elicited by DNCB in the group of the nuchal abdominal skin induction was definitely stronger at the site closer to the nuchal region than that found at sites closer to the sacral regior. but all animals of the group sensitized on the sacral region showed comparatively uniform reaction. Zvidently, contact sensitivity reaction is influenced mainly by topographic variance hut shows a litte difference depending upon induction sites.
Animals ; Cricetinae ; Dermatitis, Contact* ; Dinitrochlorobenzene ; Guinea Pigs* ; Guinea* ; Mice ; Sacrococcygeal Region ; Skin ; Spine

34,073 prospective transfusion candidates sera, among 127,087 hospitalized patients in Hanyang University Medical Center between Jan. 1989 and Dec. 1993, were analyzed for detection of red cell irregular antibodies screening and identification. This study revealed investigation of the distribution and the characteristics of irregular antibodies. Tube method was performed including saline room temperature, saline 37 and antiglobuline phase. The following results were obtained. 1. Of 127,087 inpatients, prospective blood transfusion candidates were 34,078, 26.8%. 2. 151 cases out of 34,078 sera was positive irregular antibody, 0.443 %. 3. Frequency of irregular antibodies were 15 cases(0.044 %) of anti-Lea, 14 cases(0.041%) of anti-Leb, 14 cases(0.041%) of anti-P1, 8 cases(0.0234%) of anti-IH and 8 cases(0.0234 %) of anti-E in order. 4. Undetectable cold antibody was 39 cases(0.1145%), warm antibody, 27 cases(0.0792 %). 5. It is required that various testing method for the safty transfusion.
Academic Medical Centers ; Antibodies* ; Blood Transfusion ; Humans ; Inpatients ; Mass Screening

No Abstract Available.
Thyroid Diseases* ; Thyroid Gland*

No abstract available.
Primary Health Care* ; Smoke* ; Smoking*

No abstract available.
Anemia, Aplastic*

Anti-rat lymphocyte rabbit serum was prepared with lymphoid tissue of rat spleen. Prednisolone, Imuran and this antiserum were used to prolong the survival of full-thickness sliin homograft in albino rats. The results were as follows. l. Administratio of tle anti-rat lymphocyte rabbit serum in a dose of 0. 3cc for 2 days before grafting and 0. 3cc every 3 days until rejection resulted in prolongation of the, urvival of the grafts. (Mean, 15.3 days) 2. Administration of preInisolone to the recipients in a dose of 2mg/kg/day from 7 days Iielore grafting to the time of rejection resulted in prolongation of survival of the, rafts. (Mean, 8.4 days) 3. Adminitration of Imuran to the reciipients in a dose of 5mg/kg/day from 7 day defore gvafting to the time cif rejection resulted in prolongation of the survival of ther afts. (Mean,14.6 days)
Allografts* ; Animals ; Azathioprine ; Immunosuppressive Agents* ; Lymphocytes ; Lymphoid Tissue ; Prednisolone ; Rats* ; Skin* ; Spleen ; Transplants

OBJECTIVE: Among various methods developed to quantitatively explore electroencephalograms (EEG), we focused on a wavelet method that was known to yield robust results under nonstationary conditions. The aim of this study was thus to introduce the wavelet method and demonstrate its potential use in clinical sleep studies. METHOD: This study involved artificial EEG specifically designed to validate the wavelet method. The method was performed to obtain time-dependent spectral power and phase angles of the signal. Synchrony of multichannel EEG was analyzed by an order parameter of the instantaneous phase. The standard methods, such as Fourier transformation and coherence, were also performed and compared with the wavelet method. The method was further validated with clinical EEG and ERP samples available as pilot studies at academic sleep centers. RESULT: The time-frequency plot and phase synchrony level obtained by the wavelet method clearly showed dynamic changes in the EEG waveforms artificially fabricated. When applied to clinical samples, the method successfully detected changes in spectral power across the sleep onset period and identified differences between the target and background ERP. CONCLUSION: Our results suggest that the wavelet method could be an alternative and/or complementary tool to the conventional Fourier method in quantifying and identifying EEG and ERP biomarkers robustly, especially when the signals were nonstationary in a short time scale (1-100 seconds).
Biomarkers ; Electroencephalography ; Fourier Analysis ; Pilot Projects

No abstract available.
Genetics* ; Hyperaldosteronism*

No abstract available.
Pulmonary Disease, Chronic Obstructive*

No abstract available.
Malaria*