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이효종,Lee, Hyo-Jong,Yu, Du Ruo 한국정보처리학회 2011 정보처리학회논문지B Vol.18 No.6
디지털 형태로 저장된 의료정보가 네트워크를 통하여 제약 없이 전송될 수 있게 되면서, 환자의 개인정보 관리는 의료 업계에서 중요한 주제로 부각되었다. 현재 두뇌 영상의 의료정보를 보호하는 방법은 환자의 신원을 은닉시키기 위하여 얼굴을 절삭하는 것이다. 그러나 절삭 과정에서 간혹 중요한 두뇌 조직부가 함께 절단되어 탈면 두뇌 영상은 의료 용도로 활용될 수 없게 손상을 입게 된다. 실린더 모양의 마스크를 덧붙임으로써 두뇌 영상의 중요한 모든 정보를 유지하면서 환자의 신원 정보를 은닉시키는 직접적인 방법을 제안하였다. 제안하는 두뇌 영상의 무손실 변경 방법은 중요한 영상정보가 손상되지 않음을 확인하였다. 또한 마스크로 입혀진 두뇌영상의 신원을 확인할 수 없는 사실도 증명되었다. Patients' privacy protection is a heated issue in medical business, as medical information in digital format transmit everywhere through networks without any limitation. A current protection method for brain images is to deface from the brain image for patient's privacy. However, the defacing process often removes important brain voxels so that the defaced brain image is damaged for medical analysis. An ad-hoc method is proposed to conceal patient's identification by adding cylindrical mask, while the brain keep all important brain voxels. The proposed lossless deformation of brain image is verified not to loose any important voxels. Futhermore, the masked brain image is proved not to be recognized by others.
Ninjurin1: a Potential Adhesion Molecule and Its Role in Inflammation and Tissue Remodeling
이효종,안범주,Min Wook Shin,최정현,김규원 한국분자세포생물학회 2010 Molecules and cells Vol.29 No.3
Nerve injury induced protein 1, Ninj1 (Ninjurin1) is a cell surface protein that is induced by nerve injury and pro-motes axonal growth in the peripheral nervous system. However, the function of Ninj1 in the vascular system and central nervous system (CNS) is incompletely understood. Here we review recent studies that have shed further light on the role and regulation of Ninj1 in vascular remodeling and inflammation. Increasing evidence suggests that Ninj1 mediates cell communication and enhances the entry, migration, and activity of leukocytes such as monocytes and macrophages in developmental processes and in-flammatory responses. Moreover, our recent studies show that Ninj1 regulates close interaction between leukocytes and vascular endothelial cells in vascular remodeling and inflamed CNS. Additionally, Ninj1 enhances the apoptosis-inducing activity of leukocytes and is cleaved by MMPs, resulting in loss of adhesion during tissue remodeling. The collective data described here show that Ninj1 is re-quired for the entry, adhesion, activation, and movement of leukocytes during tissue remodeling and might be a potential therapeutic target to regulate the adhesion and trafficking of leukocytes in inflammation and leukocyte-mediated diseases such as multiple sclerosis, diabetic retinopathy, and neuropathy.
이효종,박승익,최태진,Lee, Hyojong,Park, Seung-Ik,Choi, Taejin 대한자원환경지질학회 2019 자원환경지질 Vol.52 No.5
Deposition of the Daedong Supergroup has been considered to be related with the Triassic Songrim and Jurassic Daebo orogenies. The Chungnam Basin fills is an important sedimentary succession to understand the geological evolution of the Early to Middle Mesozoic Korean Peninsula. Previous paleontological and paleomagnetic studies have suggested the Late Triassic to Early Jurassic sedimentation of the Chungnam Basin fills. However, the orogenic model of the basin development has remained controversial because recently reported zircon U-Pb isotopic ages are not harmonious with the previous studies. This paper aims to review the stratigraphy, depositional age, and composition of the Chungnam Basin fills, together with test of the basin development models. 대동누층군은 삼첩기 송림조산운동과 쥬라기 대보조산운동으로 대표되는 두 차례의 광역적인 중생대 지각변형과 관련하여 퇴적되었다. 한반도 남부의 대동누층군을 대표하는 충남분지 충전물은 전기-중기 중생대의 한반도 지질진화사를 이해하는데 있어 매우 중요한 연구 대상이다. 식물화석 및 고지자기를 기반으로 한 과거 연구들은 충남분지 충전물의 퇴적시기가 대체로 후기 삼첩기로부터 전기 쥬라기 사이에 해당하는 것으로 해석하였다. 그러나 저어콘 U-Pb 연대측정 결과에 기반한 퇴적시기가 기존의 해석과 불일치함에 따라 충남분지의 발달과 조산운동과의 관계에 대한 논쟁의 여지가 있어 왔다. 본 논문은 충남분지 충전물의 퇴적시기, 층서, 조성에 대한 최근까지의 연구결과를 다루면서, 분지발달 모델이 갖는 문제점을 함께 고찰하였다.
Corrosion Behavior of Electroless Nickel/Immersion Gold Plating by Interfacial Morphology
이효종,이동준,허석환,김치성,신한균 대한금속·재료학회 2015 ELECTRONIC MATERIALS LETTERS Vol.11 No.4
Pad discoloration is caused by Ni corrosion during electroless nickel immersion gold (ENIG) treatment, and here it was investigated by SEM, XPS and cross-sectional EDS analysis. Interestingly, we found that the corrosion occurred at two different sites. For relatively thinner Ni layers, the Ni corrosion occurred at the nodule boundary, whereas thicker Ni deposits caused pit corrosions. The electroless Ni had an amorphous structure and had isotropic surface energy. In other words, the domain boundary energy between two Ni nodules did not change during Ni growth. However, the intersection angle of the two surfaces gradually increases during film growth, and the cusp stress between the two nodules also decreases gradually during Ni growth. Hence, the corrosion mode changed from nodule boundary corrosion to pit corrosion. Promoting Ni nucleation as well as increasing the Ni thickness is expected to suppress the pad discoloration by reducing the nodule boundary corrosion.
제대혈 유래 중간엽줄기세포에서 HLA의 발현과 Mixed Lymphocyte Reaction
이효종,강선영,박세진,이승용,이희천,고필옥,박지권,백원영,연성찬 한국임상수의학회 2011 한국임상수의학회지 Vol.28 No.4
In recent years, the mesenchymal stem cells (MSC) derived from various tissues have been widely tested for developing cell therapies, tissue repair and transplantation. Although there has been much interest in the immunomodulatory properties of MSC and their immunologic reactions following autologous, allogeneic and xenogenic transplantation of MSC in vivo, up to date, the expression of immunogenic markers, such as class I and II human leukocyte antigens (HLA), after differentiation of human umbilical cord blood (hUCB)-derived MSC has been poorly investigated and require extensive in vitro and in vivo testing. In this experiment, the expression of the HLA-ABC and HLA-DR on hUCB-derived MSC have been tested by immunocytochemical staining. The undifferentiated MSC were moderately stained for HLA-ABC but very weakly for HLA-DR. In order to investigate the inhibitory effect of allogeneic lymphocytes on proliferation of MSC, the MSC were cultured in the presence or absence of peripheral allogeneic lymphocytes stimulated with concanavalin A. The allogeneic lymphocytes did not significantly inhibit MSC proliferation. We conclude that hUCB-MSC expressed moderately class I HLA antigen while almost negatively class II HLA antigen. The MSC have an immunomodulatory effect which can suppress the allogeneic response of lymphocytes. These in vitro data suggest that allogeneic MSC derived from cord blood can be useful candidate for allogeneic cell therapy and transplantation without a major risk of rejection.
반복핵이식에 의한 복제동물 생산에 관한 연구 2. 토끼에서 공핵배의 세포주기 조절에 의한 제2세대 복제배의 생산효율 개선
이효종,전병균,박충생,최상용,윤창현,강대진 韓國受精卵移植學會 1995 한국동물생명공학회지 Vol.10 No.1
large scale production of cloned embryos requires the technology of multiple generation nuclear transplantation(NT) using NT embryos as the subsequent donor nuclei. The purposes of this study were producing the second generation cloned rabbit embryos, and also to determine the electrofusion rate and in vitro developmental potential comparatively in the cloned embryos of the first and second NT generation. The embryos of 16-cell stage were collected from the mated does by flushing oviducts with Dulbecco's phosphate buffered saline(D-PBS) containing 10% fetal calf serum(FCS) at 47 hours after hCG injection In the first generation NT, the nuclear donor embryos were synchronized in the phase of Gi /S transition of 32-cell stage. The first generation NT embryos which were developed to 8-cell were synchronized in Gi /S transition phase of the following 16-cell stage and used as donor nuclei for second generation Synchronization of the cell cycle of blastomeres was induced, first, using an inhibitor of microtuble polymerization, colcemid for 10 hours to arrest blastomeres in M phase, and secondly, using a DNA synthesis inhibitor, aphidicolin for 1.5 to 2 hours to arrest them in Gi /S transition boundary. The recipient cytoplasms were obtained by removing the nucleus and the first polar body from the oocytes collected at 14 hours after hCG injection. The separated donor blastomeres were injected into the enucleated recipient oocytes by micromanipulation and were electrofused by electrical stimulation of three pulses for 60 sec at 1.25 kV /cm in 0.28 M rnannitol solution The fused oocytes were co-cultured with a monolayer of rabbit oviductal epithelial cells in M-199 solution containing 10% FCS for 120 hours at 39 in a 5% incubator. Following in vitro culture of the first and second generation cloned embryos to blastocyst stage, they were stained with Hoechst 33342 dye for counting the number of blastomeres by fluorescence microscopy. The results obtained were summarized as follows: 1. The electrofusion rate was found to be similar as 79.4 and 91.5% in the first and second generation NT rabbit embryos, respectively. 2. The in vitro developmental potential to blastocyst stage of the second generation NT embryos (23.3%) was found significantly(p<0.05) lower, compared with that of the first generation NT embryos (56.8%). 3. The mean blastomeres counts of embryos developed to blastosyst stage following in vitro culture for 120 hours and also their daily cell cycles during the culture period were decreased significantly (p<0.05) to 104.3 cells and 1.33 cylces in the second NT generation, compoared with 210.4 cells and 1.54 cycles in the first NT generation, respectively.
반복핵이식에 의한 복제동물 생산에 관한 연구 1 : 토끼 수핵난자의 전기자극에 의한 활성화
이효종,최민철,최상용,박충생,윤창현,강대진 韓國受精卵移植學會 1993 한국동물생명공학회지 Vol.8 No.2
The present study was undertaken to determine the optimal condition for parthenogenetic activation of rabbit oocytes by electric stimulation in vitro in an attempt to develop nuclear transplantation techniques for cloning mammalian embryos and animals. Freshly ovulated oocytes were collected from superovulated rabbits from 13 to 26 hrs. after hCG injection. The cumulus-free oocytes were activated parthenogetically by repeated stimuli of square direct electric pulses in O.3M mannitol solution. After applying electric stimulations of different voltages, pulse durations and pulse times, all of the oocytes were cultured in TCM-199 with 10% FCS for 96 hours in a 5% incubator, and their developmental potential in vitro was examined. The higher activation rate (68.9%) was achieved at the voltage of 2.0kv/cm, the pulse duration of 60 sec and three pulse times and the activation rate of 100% was achieved at the pulse duration of 100 and 200 sec, the voltage of 1.5kv/cm and three pulse times. Although the higher rates of activation of oocytes were achieved at 100 and 200 sec, none of them developed to blastocyst in vitro. The oocytes collected 18~20 hours post hCG injection showed the highest rate of activation and development to blastocyst in vitro than the oocytes collected 13~15 or 25~26 hours post hCG injection. Therefore, it can be suggested that the application of electric stimulation of 2.0kv/cm, 60 sec and three pulse times to the oocytes collected at 18~20 hours post hCG injection would be more beneficial for the parthenogenetic activation of oocytes in rabbits.
반복핵이식에 의한 복제동물 생산에 관한 연구 II. 토끼에서 공핵배의 세포주기 조절에 의한 제2세대 복제배의 생산효율 개선
이효종,전병균,박충생,최상용,윤창현,강대진 사단법인 한국동물생명공학회 1995 한국동물생명공학회지 Vol.10 No.1
large scale production of cloned embryos requires the technology of multiple generation nuclear transplantation(NT) using NT embryos as the subsequent donor nuclei. The purposes of this study were producing the second generation cloned rabbit embryos, and also to determine the electrofusion rate and in vitro developmental potential comparatively in the cloned embryos of the first and second NT generation. The embryos of 16-cell stage were collected from the mated does by flushing oviducts with Dulbecco's phosphate buffered saline(D-PBS) containing 10% fetal calf serum(FCS) at 47 hours after hCG injection In the first generation NT, the nuclear donor embryos were synchronized in the phase of Gi /S transition of 32-cell stage. The first generation NT embryos which were developed to 8-cell were synchronized in Gi /S transition phase of the following 16-cell stage and used as donor nuclei for second generation Synchronization of the cell cycle of blastomeres was induced, first, using an inhibitor of microtuble polymerization, colcemid for 10 hours to arrest blastomeres in M phase, and secondly, using a DNA synthesis inhibitor, aphidicolin for 1.5 to 2 hours to arrest them in Gi /S transition boundary. The recipient cytoplasms were obtained by removing the nucleus and the first polar body from the oocytes collected at 14 hours after hCG injection. The separated donor blastomeres were injected into the enucleated recipient oocytes by micromanipulation and were electrofused by electrical stimulation of three pulses for 60 $\mu$sec at 1.25 kV /cm in 0.28 M rnannitol solution The fused oocytes were co-cultured with a monolayer of rabbit oviductal epithelial cells in M-199 solution containing 10% FCS for 120 hours at 39$^{\circ}C$ in a 5% $CO_2$ incubator. Following in vitro culture of the first and second generation cloned embryos to blastocyst stage, they were stained with Hoechst 33342 dye for counting the number of blastomeres by fluorescence microscopy. The results obtained were summarized as follows: 1. The electrofusion rate was found to be similar as 79.4 and 91.5% in the first and second generation NT rabbit embryos, respectively. 2. The in vitro developmental potential to blastocyst stage of the second generation NT embryos (23.3%) was found significantly(p<0.05) lower, compared with that of the first generation NT embryos (56.8%). 3. The mean blastomeres counts of embryos developed to blastosyst stage following in vitro culture for 120 hours and also their daily cell cycles during the culture period were decreased significantly (p<0.05) to 104.3 cells and 1.33 cylces in the second NT generation, compoared with 210.4 cells and 1.54 cycles in the first NT generation, respectively.