http://chineseinput.net/에서 pinyin(병음)방식으로 중국어를 변환할 수 있습니다.
변환된 중국어를 복사하여 사용하시면 됩니다.
( Youngmin Yoon ),( Hyumwoo Kim ),( Sunae Han ),( Hyungnam Kim ),( Donghyun Kim ),( Ran Hong ),( Hyunlee Kim ),( Jonghoon Chung ),( Byungchul Shin ) 대한내과학회 2014 대한내과학회 추계학술대회 Vol.2014 No.1
Acute tubular necrosis (ATN) is a syndrome of intrinsic renal injury secondary to ischemic or toxic causes without parenchymal damages and usually non-oliguira. A 20- year old man presented with acute anuric renal failure preceded by 2 days of watery diarrhea. He had been anuria for 36hr with intravenous fiuid therapy. Oliguria persisted for 10 days and he required hemodialysis support for 6 days before renal recovery. He denied the use of any regular medication and any intravenous drug use. Renal biopsy revealed severe ATN. Histopathologic findings were marked desquamation of proximal tubular epithelial cells with intact distal tubules and normal glomeruli. We report an unusual case of ATN with anuria and clinically severe features.
Kim, Youngmin,Lee, Daewon,Kwon, Yonghyun,Kim, Tae-Wan,Kim, Kyoungsoo,Kim, Hyung Ju Elsevier 2019 Journal of Electroanalytical Chemistry Vol.838 No.-
<P><B>Abstract</B></P> <P>Here we report an efficient catalyst design strategy to develop high performance Pt-based electrocatalysts for oxygen reduction reaction (ORR). Finely-dispersed Pt nanoclusters supported on microporous graphene-like 3D carbon (Pt/MGTC) having a Pt size of <I>ca.</I> 1.3nm were synthesized by zeolite template-based carbon synthesis and subsequent Pt impregnation. The Pt/MGTC catalyst demonstrated about 2 times higher ORR activity than that of commercial Pt/C. In addition, the Pt/MGTC showed relatively stable ORR performance, maintaining an activity higher than that of Pt/C. This performance enhancement of electrocatalytic ORR on Pt/MGTC was attributed to the significant increase of Pt active sites and the efficient charge transport in Pt/MGTC.</P> <P><B>Highlights</B></P> <P> <UL> <LI> Highly-dispersed Pt nanoclusters supported on microporous graphene-like 3D carbon (Pt/MGTC) were synthesized. </LI> <LI> The Pt/MGTC led to improved catalytic performances for electrochemical oxygen reduction reaction. </LI> <LI> This performance enhancement was attributed to many Pt active sites and efficient charge transport in Pt/MGTC. </LI> </UL> </P>
Kim, Tae Wu,Yang, Cheolhee,Kim, Youngmin,Kim, Jong Goo,Kim, Jeongho,Jung, Yang Ouk,Jun, Sunhong,Lee, Sang Jin,Park, Sungjun,Kosheleva, Irina,Henning, Robert,van Thor, Jasper J.,Ihee, Hyotcherl The Royal Society of Chemistry 2016 Physical chemistry chemical physics Vol.18 No.13
<P>Real-time probing of structural transitions of a photoactive protein is challenging owing to the lack of a universal time-resolved technique that can probe the changes in both global conformation and light-absorbing chromophores of the protein. In this work, we combine time-resolved X-ray solution scattering (TRXSS) and transient absorption (TA) spectroscopy to investigate how the global conformational changes involved in the photoinduced signal transduction of photoactive yellow protein (PYP) is temporally and spatially related to the local structural change around the light-absorbing chromophore. In particular, we examine the role of internal proton transfer in developing a signaling state of PYP by employing its E46Q mutant (E46Q-PYP), where the internal proton transfer is inhibited by the replacement of a proton donor. The comparison of TRXSS and TA spectroscopy data directly reveals that the global conformational change of the protein, which is probed by TRXSS, is temporally delayed by tens of microseconds from the local structural change of the chromophore, which is probed by TA spectroscopy. The molecular shape of the signaling state reconstructed from the TRXSS curves directly visualizes the three-dimensional conformations of protein intermediates and reveals that the smaller structural change in E46Q-PYP than in wild-type PYP suggested by previous studies is manifested in terms of much smaller protrusion, confirming that the signaling state of E46Q-PYP is only partially developed compared with that of wildtype PYP. This finding provides direct evidence of how the environmental change in the vicinity of the chromophore alters the conformational change of the entire protein matrix.</P>
Characterization of the Vertical Position of the Trapped Charge in Charge-trap Flash Memory
Kim, Seunghyun,Kwon, Dae Woong,Lee, Sang-Ho,Park, Sang-Ku,Kim, Youngmin,Kim, Hyungmin,Kim, Young Goan,Cho, Seongjae,Park, Byung-Gook The Institute of Electronics and Information Engin 2017 Journal of semiconductor technology and science Vol.17 No.2
In this paper, the characterization of the vertical position of trapped charges in the charge-trap flash (CTF) memory is performed in the novel CTF memory cell with gate-all-around structure using technology computer-aided design (TCAD) simulation. In the CTF memories, injected charges are not stored in the conductive poly-crystalline silicon layer in the trapping layer such as silicon nitride. Thus, a reliable technique for exactly locating the trapped charges is required for making up an accurate macro-models for CTF memory cells. When a programming operation is performed initially, the injected charges are trapped near the interface between tunneling oxide and trapping nitride layers. However, as the program voltage gets higher and a larger threshold voltage shift is resulted, additional charges are trapped near the blocking oxide interface. Intrinsic properties of nitride including trap density and effective capture cross-sectional area substantially affect the position of charge centroid. By exactly locating the charge centroid from the charge distribution in programmed cells under various operation conditions, the relation between charge centroid and program operation condition is closely investigated.
Kim, Kyung Hwan,Muniyappan, Srinivasan,Oang, Key Young,Kim, Jong Goo,Nozawa, Shunsuke,Sato, Tokushi,Koshihara, Shin-ya,Henning, Robert,Kosheleva, Irina,Ki, Hosung,Kim, Youngmin,Kim, Tae Wu,Kim, Jeongh American Chemical Society 2012 JOURNAL OF THE AMERICAN CHEMICAL SOCIETY - Vol.134 No.16
<P/><P>Proteins serve as molecular machines in performing their biological functions, but the detailed structural transitions are difficult to observe in their native aqueous environments in real time. For example, despite extensive studies, the solution-phase structures of the intermediates along the allosteric pathways for the transitions between the relaxed (R) and tense (T) forms have been elusive. In this work, we employed picosecond X-ray solution scattering and novel structural analysis to track the details of the structural dynamics of wild-type homodimeric hemoglobin (HbI) from the clam <I>Scapharca inaequivalvis</I> and its F97Y mutant over a wide time range from 100 ps to 56.2 ms. From kinetic analysis of the measured time-resolved X-ray solution scattering data, we identified three structurally distinct intermediates (I<SUB>1</SUB>, I<SUB>2</SUB>, and I<SUB>3</SUB>) and their kinetic pathways common for both the wild type and the mutant. The data revealed that the singly liganded and unliganded forms of each intermediate share the same structure, providing direct evidence that the ligand photolysis of only a single subunit induces the same structural change as the complete photolysis of both subunits does. In addition, by applying novel structural analysis to the scattering data, we elucidated the detailed structural changes in the protein, including changes in the heme–heme distance, the quaternary rotation angle of subunits, and interfacial water gain/loss. The earliest, R-like I<SUB>1</SUB> intermediate is generated within 100 ps and transforms to the R-like I<SUB>2</SUB> intermediate with a time constant of 3.2 ± 0.2 ns. Subsequently, the late, T-like I<SUB>3</SUB> intermediate is formed via subunit rotation, a decrease in the heme–heme distance, and substantial gain of interfacial water and exhibits ligation-dependent formation kinetics with time constants of 730 ± 120 ns for the fully photolyzed form and 5.6 ± 0.8 μs for the partially photolyzed form. For the mutant, the overall kinetics are accelerated, and the formation of the T-like I<SUB>3</SUB> intermediate involves interfacial water loss (instead of water entry) and lacks the contraction of the heme–heme distance, thus underscoring the dramatic effect of the F97Y mutation. The ability to keep track of the detailed movements of the protein in aqueous solution in real time provides new insights into the protein structural dynamics.</P>
Kim, Hyeong Seok,Jang, Jin-Young,Han, Youngmin,Lee, Kyoung Bun,Joo, Ijin,Lee, Doo-Ho,Kim, Jae Ri,Kim, Hongbeom,Kwon, Wooil,Kim, Sun-Whe The Korean Surgical Society 2017 Annals of Surgical Treatment and Research(ASRT) Vol.93 No.4
<P><B>Purpose</B></P><P>Neoadjuvant treatment may provide improved survival outcomes for patients with borderline resectable pancreatic cancer (BRPC). The purpose of this study is to evaluate the clinical outcomes of neoadjuvant treatment and to identify prognostic factors.</P><P><B>Methods</B></P><P>Forty patients who met the National Comprehensive Cancer Network definition of BRPC and received neoadjuvant treatment followed by surgery between 2007 and 2015 were evaluated. Prospectively collected clinicopathological outcomes were analyzed retrospectively.</P><P><B>Results</B></P><P>The mean age was 61.7 years and the male-to-female ratio was 1.8:1. Twenty-six, 3, and 11 patients received gemcitabine-based chemotherapy, 5-fluorouracil, and FOLFIRINOX, respectively. The 2-year survival rate (2YSR) was 36.6% and the median overall survival (OS) was 20 months. Of the 40 patients, 34 patients underwent resection and the 2YSR was 41.2% while the 2YSR of patients who did not undergo resection was 16.7% (P = 0.011). The 2YSR was significantly higher in patients who had partial response compared to stable disease (60.6% <I>vs</I>. 24.3%, P = 0.038), in patients who did than did not show a CA 19-9 response after neoadjuvant treatment (40.5% <I>vs</I>. 0%, P = 0.039) and in patients who did than did not receive radiotherapy (50.8% <I>vs</I>. 25.3%, P = 0.036). Five patients had local recurrence and 17 patients had systemic recurrence with a median disease specific survival of 15 months.</P><P><B>Conclusion</B></P><P>Neoadjuvant treatment followed by resection is effective for BRPC. Pancreatectomy and neoadjuvant treatment response may affect survival. Effective systemic therapy is needed to improve long-term survival since systemic metastasis accounts for a high proportion of recurrence.</P>
Kim, Jong Guk,Kim, Youngmin,Noh, Yuseong,Lee, Seonhwa,Kim, Yoongon,Kim, Won Bae American Chemical Society 2018 ACS APPLIED MATERIALS & INTERFACES Vol.10 No.6
<P>In this paper, bifunctional catalysts consisting of perovskite LaCo0.8Fe0.2O3 nanowires (LCFO NWs) with reduced graphene oxide (rGO) sheets were prepared for use in lithiumoxygen (LiO2) battery cathodes. The prepared LCFO@rGO composite was explored as a cathode catalyst for LiO2 batteries, resulting in an outstanding discharge capacity (ca. 7088.2 mAh g(-1)) at the first cycle. Moreover, a high stability of the O-2-cathode with the LCFO@rGO catalyst was achieved over 56 cycles under the capacity limit of 500 mAh g(-1) with a rate of 200 mA g(-1), as compared to the Ketjenblack carbon and LCFO NWs. The enhanced electrochemical performance suggests that these hybrid composites of perovskite LCFO NWs with rGO nanosheets could be a perspective bifunctional catalyst for the cathode oxygen reduction and oxygen evolution reactions in the development of next-generation LiO2 battery cathodes.</P>