• Korean Journal of Acupuncture
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• 제28권3호
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• pp.85-98
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• 2011

Objectives : The aim of this thesis is to examine the effect of acupuncture treatment at the GB37 on normal humans by using the power spectral analysis of the EEG. Methods : EEG (Electroencephalogram) power spectrum exhibits site-specific and state-related differences in specific frequency bands. In this thesis, the power spectrum was measured by the complexity. the 32 channels EEG study was carried out in the 13 subjects (12 males ; age=22.58 years old, 1 females ; 22 years old). Results : In the ${\alpha}$ (alpha) band, the power values at F7, F3, F4, F8, FTC2, C4, T4, CP1, CP2, TCP2, TT2, Pz, P4, Po1, Po2, O1, Oz, O2 channels (p<0.05) during the GB37-acupoint treatment were significantly changed. And in many channels were decreased. In the ${\beta}$ (beta) band, the power values at Cz, C4, T4, Tcp1, T6, Po1, O1, Oz, O2 channels (p<0.05) during the GB37-acupoint treatment were significantly changed. And in many channels were decreased. In the ${\delta}$(delta) band, the power values at Fp1, TT2 channels (p<0.05) during the GB37-acupoint treatment were significantly changed. And in many channels were decreased. In the $\theta$ (theta) band, the power values at Fp1, F8, FTC2, Pz channels (p<0.05) during the GB37-acupoint treatment were significantly changed. And in many channels were decreased. Conclusions : This results suggest that the acupuncture treatment at the GB37 significantly mostly change the power spectrum value on the alpha (18 channels), beta (9 channels) bands.

• Asian Pacific Journal of Cancer Prevention
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• 제13권12호
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• pp.6269-6272
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• 2012

We conducted a case-control study to determine the association between several potential SNPs of excision repair cross complementing group 5 (XPG) and gastric cancer susceptibility, and roles of XPG polymorphisms in combination with H.pylori infection in determining risk of gastric cancer. In our study, we collected 337 newly diagnosed gastric cancer cases and 347 health controls. Three SNPs of XPG, rs2296147T>C, rs2094258C>T and rs873601G>A, were genotyped using the Taqman real-time PCR method with a 7900 HT sequence detector system. H. pylori infection was diagnosed by ELISA. By multivariate logistic regression analysis, the rs2296147 CC genotype was associated with a decreased risk of gastric cancer (OR=0.52, 95% CI=0.27-0.97), and rs2094258 TT was associated with elevated risk (OR=2.13, 95% CI=1.22-3.35). Positive H.pylori individuals with rs2094258 TT genotypes demonstrated increased risk of gastric cancer (OR=2.13, 95% CI=1.22-3.35), while rs2296147 CC was associated with lower risk among patients with negative H.pylori (OR=0.45, 95%CI=0.22-0.89). Our findings suggested that XPG polymorphisms might contribute to risk of gastric cancer among Chinese populations, but the effect needs to be further validated by larger sample size studies.

• Asian Pacific Journal of Cancer Prevention
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• 제13권5호
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• pp.1799-1802
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• 2012

Objective: We aimed to analyze the association between excision repair cross-complementing rodent repair deficiency complementation group 1 (XRCC1) and ovarian cancer risk. Methods: We performed a hospital-based case-control study with 155 cases and 313 controls in China. All Chinese cases with newly diagnosed primary ovarian cancer between May 2005 to May 2010 in our hospital were invited to participate within 2 months of diagnosis. Controls were randomly selected from people who requested general health examinations in the same hospital during the same period. SNPs in EXCC1, ERCC1 C8092A and ERCC1 T19007C, were analyzed by PCR-RFLP method. Results: We observed a non-significantly increased risk of ovarian cancer among individuals with ERCC1 8092TT compared with those with the 8092CC genotype (adjusted OR=1.55, 95% CI%=0.74-2.97). Moreover, 19007TT genotype carriers also showed a non-significant increased risk of ovarian cancer over those with the 19007CC genotype (adjusted OR=1.78, 95% CI%=0.91-3.64). Conclusion: Our firstly investigation of links between polymorphisms in the ERCC1 gene and the risk of ovarian cancer in Chinese population demonstrated no significant association. Further large sample studies in Chinese populations are needed.

• 생명과학회지
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• 제31권12호
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• pp.1088-1093
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• 2021

제주마는 한국의 말 품종으로 제주도에서 오랜 기간 자생하여 왔다. 제주마의 기원은 몽골마에서 유래한 것으로 추정되었다. 그러나 최근 연구에서 제주마와 몽골 토종마를 비교 한 결과, 유전적으로 가까우나 제주마가 몽고마와 독립적으로 진화해 온 것으로 보고되었다. 제주마는 경주마로 이용되어 경주 능력이 주요한 경제 형질로 활용되고 있다. Myostatin (MSTN) 유전자는 다양한 포유류에서 골격근량에 영향을 미치는 것으로 연구되었다. Thoroughbred에서 MSTN 유전자 내 존재하는 변이가 경주 능력 및 스태미너에 영향을 미치는 것으로 알려져 있다. 우리는 제주마 1,433두를 포함하여 여러 말 품종의 MSTN 유전자내 변이 빈도를 비교하였다. MSTN 유전자의 g.66493737 변이 중 장거리 적성 유전자형(TT)의 경우 제주마에서 빈도가 0.826으로 한라마(0.285) 및 Thoroughbred (0.252)보다 높은 것으로 확인되었다. 또한 다른 연구를 참고하여 8종 말에서 g.66493737 빈도를 비교하였다. 그 결과, 경주마로 활용되는 품종은 CC형의 빈도가 높았으나, TT형의 빈도는 낮은 것으로 확인되었다. 반대로 승용마 및 역용마 등의 품종은 TT형의 빈도가 높은 것으로 확인되었다. 제주마의 경주 거리(400 m, 800 m, 900 m, 1,000 m, 1,110 m, 1,200 m)별로 유전자형과 도착 기록을 비교 분석했다. 그 결과 1,000 m 이하의 경주에서는 CT형이 TT형보다 더 빠른 도달 기록을 보였다. 그러나 1,110 m 이상의 경주에서는 거의 동일한 결과가 확인되었다. 본 연구에서는 제주마의 MSTN 유전자 변이가 경주 거리 적성과 관련이 있을 수 있음을 시사하였다. 이러한 결과는 추후 연구를 통해 제주마에서 경주 거리 적성 및 경주 능력과 연관된 마커 개발을 위한 자료로 활용이 가능할 것으로 사료된다.

• 한국식품과학회지
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• 제22권6호
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• pp.681-685
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• 1990

반응온도 $210^{\circ}C$, 수소압력 $0.3\;kg/cm^2$, 니켈촉매량 0.12%, 교반속도 280 rpm의 선택적 수소첨가조건에서 반응이 진행됨에 따른 면실유의 지방산 조성, 트란스산 및 이화학적인 특성의 변화를 연구하였다. 지방산 조성에 있어서는 팔미트산(16 : 0), 스테아르산(18 : 0)같은 포화지방산은 거의 변함이 없었고, 리놀레산(18 : 2), ($50.03%{\rightarrow}9.38%$)이 올레산(18 : 1) ($20.65%{\rightarrow}60.35%$)으로 전환되었으며, 특히 리놀레산 이성체 변화에서는 ct, tc, tt형의 변화보다는 cc형의 변화가 현저하였고, 올레산 이성체 변화에서는 t형 생성량은 현저하게 증가한데 비해 c형의 변화는 거의 없었다. 반면, 수소첨가됨에 따라 녹는점 및 고체지함량은 직선적으로 증가하였고 요드값은 직선적으로 감소하였다. 이들의 결과로부터 다음과 같은 직선회귀식을 구하였다. 녹는점과 요드값 : Y=1.59-2.36X(r=0.96, p<0.05), 고체지함량($at\;20^{\circ}C$)과 녹는점 : Y=2.81+2.01X(r=0.96, p<0.05), 고체지함량($at\;20^{\circ}C$)과 요드값 : Y=9.40-5.16X(r=-0.99, p<0.01), 고체지함량($at\;20^{\circ}C$)과 18 : 1 t : Y=6.25+8.48X(r=0.97, p<0.05).

• Asian Pacific Journal of Cancer Prevention
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• 제15권18호
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• pp.7731-7735
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• 2014

Colorectal cancer (CRC) is the third most common cause of death due to cancer in the worldwide and the incidence is also increasing in Turkey. Our present aim was to investigate any association between germ-line methylenetetrahydrofolate reductase (MTHFR) C677T and A1298C polymorphisms and CRC risk in Turkey. A total of 86 CRC cases and 212 control individuals of the same ethnicity were included in the current study. Peripheral blood-DNA samples were used for genotyping by StripAssay technique, based on the reverse-hybridization principle and real-time PCR methods. Results were compared in Pearson Chi-square and multiple logistic regression models. The MTHFR 677TT (homozygous) genotype was found in 20.9% and the T allele frequency 4.2-fold increased in CRC when compared with the control group.The second SNP MTHFR 1298CC (homozygous) genotype was found in 14.0% and the C allele frequency 1.4-fold elevated in the CRC group. The current data suggest strong associations between both SNPs of germ-line MTHFR 677 C>T and 1298 A>C genotypes and CRC susceptibility in the Turkish population. Now the results need to be confirmed with a larger sample size.

• Asian Pacific Journal of Cancer Prevention
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• 제17권4호
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• pp.1903-1907
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• 2016

Background: Studies of effects of IL-1 polymorphisms, CYP2C19 genotype together with antibiotic resistance for H. pylori eradication are rare worldwide. The present study was designed to evaluate efficacy of 10-day sequential therapy (SQT) and 14-day standard triple therapy (STT) with four- times-daily dosing of amoxicillin for H. pylori eradication related to these important host and bacterial factors in Thailand. Materials and Methods: This prospective randomized study was performed during March 2015 to January 2016. H. pylori infected gastritis patients were randomized to receive 10-day sequential therapy and 14-day standard triple therapy. CYP2C19 genotyping, IL1 polymorphism (IL-1B and IL-1RN genotypes) and antibiotic susceptibility tests were performed in all patients. 13C-UBT was conducted to confirm H. pylori eradication at least 4 weeks after treatment. Results: A total of 100 patients (33 males and 67 females, mean age=51.1 years) were enrolled. Eradication rate by PP analysis was 97.9% (47/48) with the 10-day SQT regimen and 87.8% (43/49) with 14-day STT regimen (97.9% vs 87.8%; p-value=0.053). Antibiotic susceptibility testing demonstrated 45% resistance to metronidazole, 14.8% to clarithromycin, and 24.1% to levofloxacin. CYP2C19 genotyping revealed 44.9% RM, 49% IM and 6.1% PM. IL-1B and IL-1RN genotypes were demonstrated as 21.4% for CC, 48.1% for TC, 36.8% for TT, 72.7% for 1/1, and 21.2% for 1/2 genotypes, respectively. The 10-day SQT regimen provided 100% eradication in patients with clarithromycin or dual clarithromycin and levofloxacin H. pylori resistant strains. Moreover, the 10-day SQT regimen resulted in a 100% eradication rate in all patients with CYP2C19 genotype RM and almost type of IL-1B (TC and TT) and IL1-RN genotypes ( 1/2 and other). Conclusions: Treatment with 10-day sequential therapy is highly effective for H. pylori eradication regardless of the effects of clarithromycin resistance, dual clarithromycin and levofloxacin resistance, CYP2C19 genotype, IL-1B and IL1-RN genetic polymorphisms and can be used as effective first line therapy in Thailand.

• Pediatric Gastroenterology, Hepatology & Nutrition
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• 제24권5호
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• pp.455-469
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• 2021

Purpose: The rs641738 C>T in membrane-bound O-acyltransferase domain-containing protein 7 (MBOAT7) is implicated, along with the rs738409 C>G polymorphism in patatin-like phospholipase domain-containing protein 3 (PNPLA3), in nonalcoholic fatty liver disease (NAFLD). The association of these polymorphisms and NAFLD are investigated in Hispanic children with obesity. Methods: Obese children with and without NAFLD were enrolled at a pediatric tertiary care health system and genotyped for MBOAT7 rs641738 C>T and PNPLA3 rs738409 C>G. NAFLD was characterized by the ultrasonographic presence of hepatic steatosis along with persistently elevated liver enzymes. Genetic variants and demographic and biochemical data were analyzed for the effects on NAFLD. Results: Among 126 enrolled subjects, 84 in the case group had NAFLD and 42 in the control group did not. The two groups had similar demographic distribution. NAFLD was associated with abnormal liver enzymes and elevated triglycerides and cholesterol (p<0.05). Children with NAFLD had higher percentage of PNPLA3 GG genotype at 70.2% versus 31.0% in non-NAFLD, and lower MBOAT7 TT genotype at 4.8% versus 16.7% in non-NAFLD (p<0.05). PNPLA3 rs738409 C>G had an additive effect in NAFLD; however, MBOAT7 rs641738 C>T had no effects alone or synergistically with PNPLA3 polymorphism. NAFLD risk increased 3.7-fold in subjects carrying PNPLA3 GG genotype and decreased in MBOAT7 TT genotype. Conclusion: In Hispanic children with obesity, PNPLA3 rs738409 C>G polymorphism increased the risk for NAFLD. The role of MBOAT7 rs641738 variant in NAFLD is less evident.

• Asian Pacific Journal of Cancer Prevention
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• 제17권3호
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• pp.1215-1219
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• 2016

Background: Worldwide, breast cancer is the most common cancer among women and is a leading cause of cancer death. In the present study, we investigated the NQO1 C609T genotypic and allelic distribution in north Indian breast cancer patients. Materials and Methods: The genotypic distribution of the NQ01 C609T polymorphism was assessed in 100 invasive ductal carcinoma (IDC) breast cancer patients and 100 healthy controls using allele specific PCR (AS-PCR). Results: A lower frequency of the CC genotype was found in breast cancer patients (24%) than in the controls. On the other hand, TT genotype frequency was also found to be higher in female healthy controls (32%) than the female breast cancer patients (20%). The frequencies of all three genotypes CC, CT, TT in patients were 24%, 56% and 20% and in healthy controls 50%, 22% and 32% respectively. We did not find any significant correlation between the NQO1 C609T polymorphism and age group, grading, menopausal status and distant metastasis. A less significant association was found between the NQ01 C609T polymorphism and the stage of breast cancer (X2=5.931, P=0.05). Conclusions: The present study shows a strong association between NQO1 C609T polymorphism with the breast cancer risk in the north Indian breast cancer patients so that possible use as a risk factor should be further expel.

• 한국진공학회지
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• 제6권2호
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• pp.122-128
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• 1997

본 연구는 건식 프로세스의 일종인 열증착법을 이용하여 PVDF유기박막을 제조하는 데 있다. 발열원과 기판간의 거리는 5cm로 하였고, 기판의 온도를 $30^{\circ}C$로 유지시키면서 반 응조의 진공도가 $2.0\times10^{-5}$Torr로 되었을 때 발열원의 온도를 6~$8^{\circ}C$/min로 상승시켜, 발열 원의 온도가 $270^{\circ}C$될 때 셔터(shutter)를 열고 증착을 개시하였다. 전계인가 강도의 증가에 따라 $\alpha$형 피크들인 $530\textrm{cm}^{-1},795\textrm{cm}^{-1},1182\textrm{cm}^{-1}$ 피크는 점점 작아지고 $\beta$형 피크 인 $510\textrm{cm}^{-1},1273\textrm{cm}^{-1}$ 피크가 증가함을 알 수 있었다. 전계인가강도 71.4kV/cm 이하에서는 $530\textrm{cm}^{-1}$ 피크가 $510\textrm{cm}^{-1}$피크의 강도보다 큰 것을 알 수 있는데 이는 $\beta$형 성분보다 $\alpha$형 성분이 필름의 특성을 지배함을 알 수 있었다. 이상의 결과로 전계인가 강도의 증가에 따라 PVDF 유기박막의 분자쇄는 $\alpha$형인 TGT 또는 TG'T에서 $\beta$형인 평면지그재그 TT형태로 변화함을 알 수 있다.