• 제목/요약/키워드: Mel-B

검색결과 92건 처리시간 0.021초

PNCC와 robust Mel-log filter bank 특징을 결합한 조류 울음소리 분류 (Bird sounds classification by combining PNCC and robust Mel-log filter bank features)

  • 알자흐라 바디;고경득;고한석
    • 한국음향학회지
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    • 제38권1호
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    • pp.39-46
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    • 2019
  • 본 논문에서는 합성곱 신경망(Convolutional Neural Network, CNN) 구조를 이용하여 잡음 환경에서 음향신호를 분류할 때, 인식률을 높이는 결합 특징을 제안한다. 반면, Wiener filter를 이용한 강인한 log Mel-filter bank와 PNCCs(Power Normalized Cepstral Coefficients)는 CNN 구조의 입력으로 사용되는 2차원 특징을 형성하기 위해 추출됐다. 자연환경에서 43종의 조류 울음소리를 포함한 ebird 데이터베이스는 분류 실험을 위해 사용됐다. 잡음 환경에서 결합 특징의 성능을 평가하기 위해 ebird 데이터베이스를 3종류의 잡음을 이용하여 4개의 다른 SNR (Signal to Noise Ratio)(20 dB, 10 dB, 5 dB, 0 dB)로 합성했다. 결합 특징은 Wiener filter를 적용한 log-Mel filter bank, 적용하지 않은 log-Mel filter bank, 그리고 PNCC와 성능을 비교했다. 결합 특징은 잡음이 없는 환경에서 1.34 % 인식률 향상으로 다른 특징에 비해 높은 성능을 보였다. 추가적으로, 4단계 SNR의 잡음 환경에서 인식률은 shop 잡음 환경과 schoolyard 잡음 환경에서 각각 1.06 %, 0.65 % 향상했다.

Glycyrrhizin이 Mel/ret transgenic mice에서의 melanoma 세포의 apoptosis에 미치는 영향 (Effect of Glycyrrhizin on the Aoptosis of Melanoma Cells in Mel/ret Transgenic Mice)

  • 오찬호;염정열
    • KSBB Journal
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    • 제13권6호
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    • pp.718-723
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    • 1998
  • The effect of glycyrrhizin on melanoma cells was investigated. DNA fragmentation in cultured melanoma cells was promoted by the addition of glycyrrhizin in a dose dependent manner. Administration(i.m.) of glycyrrhizin to Mel/ret transgenic mice resulted in apoptosis induction, reduction of mitochondrial transmembrane potential in melanoma cells. Decreased B220+ B cells were recovered by the treatment of glycyrrhizin in splenocytes and mesenteric lymph node cells, while Thy-1+ T cells were not influenced. Results suggested that glycyrrhizin acted as an inducer of apoptosis of melanoma cells and an immuno-potentiator via recovered B lymphocyte population in Mel/ret transgenic mice.

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The Expression Pattern of Melatonin Receptor 1a Gene during Early Life Stages in the Nile tilapia (Oreochromis niloticus)

  • Jin, Ye Hwa;Park, Jin Woo;Kim, Jung-Hyun;Kwon, Joon Yeong
    • 한국발생생물학회지:발생과생식
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    • 제17권1호
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    • pp.45-53
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    • 2013
  • The action of melatonin within the body of animals is known to be mediated by melatonin receptors. Three different types of melatonin receptors have been identified so far in fish. However, which of these are specifically involved in puberty onset is not known in fish. We cloned and analyzed the sequence of melatonin receptor 1a (mel 1a) gene in Nile tilapia Oreochromis niloticus. In addition, we examined the tissue distribution of gene expressions for three types of receptors, mel 1a, 1b and lc and investigated which of them is involved in the onset of puberty by comparing their expression with that of gonadotropin-releasing hormone receptor I (GnRHr I) gene using quantitative real-time PCR from 1 week post hatch (wph) to 24 wph. The mel 1a gene of Nile tilapia consisted of two exons and one bulky intron between them. Mel 1a gene was found to be highly conserved gene showing high homology with the corresponding genes from different teleost. All three types of melatonin receptor genes were expressed in the brain, eyes and ovary in common. Expression of mel 1a gene was the most abundant and ubiquitous among 3 receptors in the brain, liver, gill, ovary, muscle, eye, heart, intestine, spleen and kidney. Mel 1b and mel 1c genes were, however, expressed in fewer tissues at low level. During the development post hatch, expressions of both mel 1a and GnRHr I genes significantly increased at 13 wph which was close to the putative timing of puberty onset in this species. These results suggest that among three types of receptors mel 1a is most likely associated with the action of melatonin in the onset of puberty in Nile tilapia.

Cloning and characterization of polyA- RNA transcripts encoded by activated B1-like retrotransposons in mouse erythroleukemia MEL cells exposed to methylation inhibitors

  • Tezias, Sotirios S.;Tsiftsoglou, Asterios S.;Amanatiadou, Elsa P.;Vizirianakis, Ioannis S.
    • BMB Reports
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    • 제45권2호
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    • pp.126-131
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    • 2012
  • We have previously identified a DNA silent region located downstream of the 3'-end of the ${\beta}^{major}$ globin gene (designated B1-559) that contains a B1 retrotransposon, consensus binding sites for erythroid specific transcription factors and shares the capacity to act as promoter in hematopoietic cells interacting with ${\beta}$-globin gene LCR sequences in vitro. In this study, we have cloned four new non-polyA RNA transcripts being detected upon blockade of murine erythroleukemia (MEL) cell differentiation to erythroid maturation by methylation inhibitors and demonstrated that two of them share high structural homology with sequences of B1 element found within the B1-559 region. Although it is not clear yet whether and how these RNAs interfere with induction of erythroid maturation, these data provide evidence for the first time showing that methylation inhibitors can activate silent repetitive DNA sequences in MEL cells and may have implications in cancer chemotherapy using demethylating drugs as antineoplastic agents.

Towards developing a diagnostic regimen for the treatment follow-up of Trypanosoma brucei gambiense

  • Mbati, Peter-A.;Hirumi, Kazuko;Inoue, Noboru;Situakibanza, Nanituma-H.;Hirumi, Hiroyuki
    • Parasites, Hosts and Diseases
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    • 제37권4호
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    • pp.289-292
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    • 1999
  • BALB/c mice infected with a high virulent strain of Trypanosoma brucei gambiense IL3707 were treated intraperitoneally (ip) with either Melarsoprol (Mel-B) or PSG(+) buffer as controls. The mice were subsequently monitored regularly for parasites by direct microscopic examination of their tail blood or buffy coat and by polymerase chain reaction (PCR). Mel-B was found to be an effective drug for treatment against T.b. gambiense because at the end of the first treatment schedule, all treated mice were negative for parasites even by PCR, while all the control animals were positive. Three of the five Mel-B treated mice, while parasitologically negative, were PCR positive between 53 and 80 days post infection (DPI), indicating that they still harbored an infection. All treated mice were subsequently negative for parasites even by PCR at 88 DPI. A combination of conventional microscopic examination and PCR offers a good prediction of cure following treatment of trypanosomosis.

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EFFICACY EVALUATION OF THE WHITENING COSMETICS USING MELANOGENESIS INHIBITION ASSAY COSMETICS IN B-16 MELANOMA CELL

  • S. J. Yang;S. J. Jang;Park, S. S.;J. Y. Jang;K. H. Son;Lee, J. P.;Lee, K. S.;M. Y. Heo;Kim, Y. O.
    • 대한화장품학회:학술대회논문집
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    • 대한화장품학회 2003년도 IFSCC Conference Proceeding Book II
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    • pp.544-544
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    • 2003
  • We investigated the inhibitory effect of whitening materials with growth factor or alone on melanomas derived from Human (B-16) and mouse (SK-MEL-31) using melanin content. Melanin content was determined by the absorbance value at 470nm per cells. we used the growth factors known as activators of Adenylate cyclase, Protein kinase C and tyrosine kinase pathway separately. In addition, we compared the action of UV-induced with non-biological growth factor with whitening materials in melanomas derived from Human and mouse. The results showed that the aspect of inhibitory effect of whitening materials on B16 and SK-MEL-31 was not different. And, the action of each growth factor involved in the differentiation and proliferation of melanoma on the inhibition of melanogenesis in B-16 and SK-MEL-31 using whitening agents showed no difference. Also, The action of UV -induced and non-biological growth factors didn't exhibit different pattern on the effect of whitening agent in B-16 and SK-MEL-31.

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Potent Influence of Exogenous Melatonin on In Vitro Oocyte Maturation in the Longchin Goby, Chaenogobius annularis

  • Dae Guen Kim;In Joon Hwang;Hea Ja Baek
    • 한국발생생물학회지:발생과생식
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    • 제27권3호
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    • pp.127-135
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    • 2023
  • Effects of changes in photoperiod on the reproductive events in fish are suggested to be mediated mainly via the action of melatonin (MEL). Changing levels of plasma MEL throughout the day and year are suggested to influence the hypothalamus-pituitary-gonadal axis in fish. Therefore, in this study, we aimed to investigate the effects of MEL on oocyte maturation and germinal vesicle breakdown (GVBD) in the marine fish, Chaenogobius annularis, in vitro. Oocytes at three different stages (pre-, mid-, and late-vitellogenesis) were incubated with (a) only MEL (5, 10, 50, 100, 500, and 1,000 pg/mL) and (b) 50 pg/mL of 17α,20β-dihydroxy-4-pregnen-3-one (17α20βP), maturation-inducing hormone (MIH) of this species, and MEL (4-h incubation before addition of MIH). Any single MEL treatment did not significantly induce GVBD. However, treatment with 50 pg/mL MEL or MIH significantly induced GVBD. These results suggest that preincubation with MEL accelerates the effect of MIH on longchin goby oocyte maturation.

흑색종세포주 SK-MEL-2에서 레티노이드에 의한 GD3합성효소(hST8Sia I)의 발현억제 (Suppression of Human GD3 Synthase (hST8Sia I) Expression Induced by Retinoic Acid in Human Melanoma SK-MEL-2 Cells)

  • 권화영;강남영;이영춘
    • 생명과학회지
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    • 제20권5호
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    • pp.655-661
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    • 2010
  • 흑색종세포주 SK-MEL-2에서 레티노이드에 의한 GD3합성효소(hST8Sia I)의 발현억제기작을 규명하게 위하여 hST8Sia I의 프로모터 활성을 조사해 본 결과 -1146에서 -646영역에서 레티노이드에 의한 활성억제를 나타내었다. 또한 부위특이적 변이와 ChIP분석은 -731에서 -722영역에 위치한 전사인자NF-kB 결합부위가 hST8Sia I의 레티노이드에 의한 활성억제에 중요하게 관여하고 있음을 나타내었다. 이러한 발현 억제는 PKC/ERK 신호전달경로를 통하여 일어난다는 것을 신호전달경로 저해제를 이용한 RT-PCR과 프로모터 활성조사에 의해 규명하였다.

이동형 배출가스 측정시스템(MEL)을 이용한 디젤 및 가솔린 차량에서 배출되는 입자상 물질 평가 (On-Road Investigation of PM Emissions of Passenger Vehicles Fuelled with Diesel and Gasoline Using Mobile Emission Laboratory)

  • 이석환;김홍석;박준혁;우세종
    • 대한기계학회논문집B
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    • 제36권7호
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    • pp.737-744
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    • 2012
  • 차량에 의한 대기오염을 실제 주행 조건에서 시간과 공간에 구애받지 않고 실시간으로 측정하기 위하여 이동형 배출가스 측정장치(MEL)가 제작되었다. 미니밴 차량에 CO, NOx, $CO_2$와 같은 배출가스 측정 장비와 입자의 수농도 및 입경별 개수농도 분포 측정을 위한 FMPS, CPC가 탑재되었다. 차량 전단에 장착되는 흡입 샘플링 포트를 사용하여 여러 종류의 차량 추적 실험을 수행하였다. 본 연구에서는 MEL의 상세 사양 및 이를 이용하여 디젤 및 가솔린 연료를 사용하는 승용차량들을 추적 실험한 결과를 나타내었다. 디젤 차량에서 배출되는 입자의 수농도는 가솔린 차량에서 배출되는 입자의 수농도보다 높았으며 다량의 극미세입자를 포함하고 있었다. 하지만, 직접분사식 가솔린 차량은 DPF가 장착된 디젤 차량에 비하여 50 nm 이상의 입경 영역에서 입자의 농도가 높은 경향을 보였다.

목단피의 세포독성 물질 (A Cytotoxic Compound from Moutan Cortex Radicis)

  • 주보연;김문일;최수라;명평근;성연희;송경식;배기환
    • 한국약용작물학회지
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    • 제12권3호
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    • pp.255-261
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    • 2004
  • 21 종의 생약 추출물을 선정하여 $5\;{\mu}g/ml$의 농도에서 SK-MEL-28 cell 에 대한 세포독성을 조사한 결과 목단피의 메탄올 추출물이 74.3%의 성장율을 보였다. 활성 물질을 찾기 위하여 목단피로부터 silica gel column chromatography를 실시하여 hexane 분획과 EtOAc 분획에서 충 5개의 화합물을 분리하였고 $mp,\;UV,\;IR,\;^1H-NMR,\;^{13}C-NMR$ 등 각종 물리, 화학적 data로부터 그 구조를 paeonol (1), benzoylpaeoniflorin (2), benzoic acid (3), 2,5-dihydroxy-4-methoxy-acetophenone (4), paeoniflorin (5)으로 동정하였다. 분리한 물질을 human 피부 암세포인 SK-MEL-28 세포주에 대하여 $10\;{\mu}g/ml$의 농도에서 SRB방법으로 세포독성을 측정한 결과 compound 4가 $ED_50$ 값이 $5.92\;{\mu}g/ml$로 가장 좋은 세포독성을 나타내었다. 이결과는 compound 4가 SK-MEL-28 melanoma 세포주에 대한 새로운 항암 후보 물질임을 제시한다.