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n-CdS_(0.46)Se_(0.54)/p-Cu_92-x)S_(0.46)Se_(0.54) 이종접합 태양전지의 제작과 그 특성에 관한 연구
유상하,최승평,이상열,홍광준,서상석,김혜숙,전승룡,윤은희,문종대,신영진,정태수,신현길,김택성,유기수 全北大學校 基礎科學硏究所 1994 基礎科學 Vol.16 No.-
승화방법에 의해 CdS_0.46Se_0.54 단결정을 성장하여 결정구조를 조사하고, Van der Pauw 방법으로 Hall effect를 측정하여 carrier density의 온도 의존성과 mobility의 온도 의존성을 조사하였다. 성장된 CdS_0.46Se_0.54 단결정을 치환반응하여 n-CdS_0.46Se_0.54/p-Cu_2-xS_0.46Se_0.54 이종접합 태양전지를 제작하였다. Spectral response, 전류-전압특성 및 전력변환 효율을 조사하여 그 결과로부터 개방전압은 0.48V, 단락 전류 밀도는 21mA/㎠, fill factor와 전력변환효율은 각각 0.75와 9.5%를 얻었다. CdS_0.46Se_0.54 single crystal was grown by a sublimation method. The crystal structure and the temperature dependence of carrier density and mobility of CdS_0.46Se_0.54 single crystal were studied. Heterojunction solar cells on n-CdS_0.46Se_0.54/p-Cu_2-xS_0.46Se_0.54 were fabricated by the substitution reaction. The spectral response, the J-U characteristics and the conversion efficiency of the n-CdS_0.46Se_0.54/p-Cu_2-xS_0.46Se_0.54 heterojunction solar cells were studied. The open-cricuit voltage, short-circuit density, fill factor and conversion efficiency of n-CdS_0.46Se_0.54/p-Cu_2-xS_0.46Se_0.54 heterojunction solar cells under 80mW/㎠ illumination were found to be 0.48V, 21mA/㎠, 0.75 and 9.5%, respectively.
Studies on the function of murine DNA polymerase β using transgenic Drosophila
Ha, Hye Yeong,Yoon, Dae Kyoung,Lee, Won Ho,An. Hye Suck,Yoo, Mi Ae 부산대학교 유전공학연구소 1993 분자생물학 연구보 Vol.9 No.-
DNA polymerase β는 DNA 대사의 여러 측면에 관여할 것으로 알려져 있지만, in vivo에서의 정확한 기능은 아직 완전히 밝혀져 있지 않다. DNA actin 5C유전자의 promotor에 rat DNA polymerase β cDNA를 연결시킨 chimeric 유전자를 도입한 transgenic Drosophila를 이용하여 개체 수준에서 DNA polymerase β의 기능을 조사하고자 하였다. Southern analysis와 p[w : polβ]의 transmission 양상의 조사를 통해, 각 transformant line에 한 개의 p[w : polβ]element가 삽입되었음을 밝혔다. MMC, MMS와 UV에 의한 killing에 대한 감수성을 transgenic strain과 비교하였다. 또한, MMC와 MMS에 의해 유발된 mitotic recombination에 대한 감수성을 transgenic strain과 host strain에서 비교하였다. 본 연구 결과에서, transgenic Drosophila에서 발현된 rat DNA polymerase β는 적어도 mitotic recombination의 생성과정에는 관여하는 것으로 나타났다. DNA polymerase β has been implicated in the several aspects of DNA metabolism, but its precise role in vivo remains to be fifined. The biological function of DNA polymerase β in the whole organism was examined using the transgenic Drosophila bearing chimeric gene consisting of a promoter region of Drosophila actin 5C gene and rat DNA polymerase β cDNA. Southern analysis of genomic DNA of transgenic flies and the pattern of transmission of p[w : polβ]indicated that a single copy of p[w : polβ] was integrated in each transformant line. The sen sitivity of transgenic strain to killing after treatment of MMC, MMS and UV were compared with that of host strain. The sensitivity of transformant strain to mitotic recombination induced by MMC or MMS were also compared with host strain. The present results showed that rat DNA polymerase β expressed in the transgenic flies role at least in the generation process of mitotic recombination.
The Use of Pluripotent Stem Cell for Personalized Cell Therapies against Neurological Disorders
Ha, Hye-Yeong,Jang, Si-Hyong,Jung, Ji-Won Hindawi Publishing Corporation 2011 Journal of biomedicine & biotechnology Vol.2011 No.-
<P>Although there are a number of weaknesses for clinical use, pluripotent stem cells are valuable sources for patient-specific cell therapies against various diseases. Backed-up by a huge number of basic researches, neuronal differentiation mechanism is well established and pluripotent stem cell therapies against neurological disorders are getting closer to clinical application. However, there are increasing needs for standardization of the sourcing pluripotent stem cells by establishing stem cell registries and banking. Global harmonization will accelerate practical use of personalized therapies using pluripotent stem cells.</P>
Ha, Hye-Yeong,Cho, Ik-Hyun,Lee, Kang-Woo,Lee, Ko-Woon,Song, Ji-Young,Kim, Kyoung-Shim,Yu, Young-Mi,Lee, Ja-Kyeong,Song, Jin-Sook,Yang, Sung-Don,Shin, Hee-Sup,Han, Pyung-Lim Elsevier 2005 Developmental Biology Vol.277 No.1
<P><B>Abstract</B></P><P>The JNK interacting protein, JSAP1, has been identified as a scaffold protein for mitogen-activated protein kinase (MAPK) signaling pathways and as a linker protein for the cargo transport along the axons. To investigate the physiological function of JSAP1 in vivo, we generated mice lacking JSAP1. The JSAP1 null mutation produced various developmental deficits in the brain, including an axon guidance defect of the corpus callosum, in which phospho-FAK and phospho-JNK were distributed at reduced levels. The axon guidance defect of the corpus callosum in the <I>jsap1</I><SUP><I>−/−</I></SUP> brain was correlated with the misplacement of glial sling cells, which reverted to their normal position after the transgenic expression of JNK interacting protein 1(JIP1). The transgenic JIP1 partially rescued the axon guidance defect of the corpus callosum and the anterior commissure of the <I>jsap1</I><SUP><I>−/−</I></SUP> brain. The JSAP1 null mutation impaired the normal distribution of the Ca<SUP>+2</SUP> regulating protein, calretinin, but not the synaptic vesicle marker, SNAP-25, along the axons of the thalamocortical tract. These results suggest that JSAP1 is required for the axon guidance of the telencephalic commissures and the distribution of cellular protein(s) along axons in vivo, and that the signaling network organized commonly by JIP1 and JSAP1 regulates the axon guidance in the developing brain.</P>
Lee, Hye Yeong,Lee, Hye-Lan,Yun, Yeomin,Kim, Jin-Su,Ha, Yoon,Yoon, Do Heum,Lee, Soo-Hong,Shin, Dong Ah Mary Ann Liebert 2015 Tissue engineering. Part A Vol.21 No.13
<P>Stem cells are a promising source of tissue engineering due to their differentiation potential. Today, direct transplantation of stem cells for cell therapy is commonly performed. However, in cases of nerve injury, direct transplantation of cells could lead to secondary nerve damage. Male Sprague-Dawley rats were randomized into four groups: the phosphate-buffered saline epineural transplantation (PBS-ENT) group, the PBS intraneural transplantation (PBS-INT) group, the human adipose-derived stem cells epineural transplantation (hASCs-ENT) group, and human adipose-derived stem cells intraneural transplantation (hASCs-INT) group. Transplantation was conducted 1 week later after inflicting a crush injury with subsequent observation for 5 weeks. To evaluate pain, each group was examined with regard to paw withdrawal latency and evoked potentials. The sciatic functional index (SFI) was calculated to estimate functional recovery. The sciatic nerve was also examined histologically. The hASCs-ENT group showed a more rapid paw withdrawal threshold and SFI recovery than the other groups (p<0.05). The hASCs-ENT group also showed shorter initial latencies in both somatosensory evoked potential (SSEP) and motor evoked potential (MEP) than the PBS-INT group (p<0.05). In addition, the N1 latency of the MEP and the N1 and P1 latencies of the SSEP were significantly shorter than those of the PBS-INT group (p<0.05). Histological examination revealed that the transplanted groups showed better neural recovery and remyelination than the groups injected with PBS. These results show that the transplantation of hASCs into the injured sciatic nerve improved mechanical allodynia and functional recovery as determined by the paw withdrawal test, SFI analysis, and electrophysiological studies. ENT is superior to INT in terms of invasiveness and better outcomes.</P>