J.-G. Park
서울대학교 의과학과 · 물리·천문학
J.-G. Park 교수의 연구실은 항암제의 임상적 효과와 약물 저항성 메커니즘을 중심으로 암 치료의 유효성을 규명하는 데 초점을 맞추고 있습니다. 특히 5-플루오로우라실(5-FU)과 리코바린(LV)의 상호작용이 대장암 세포주에서 미치는 세포독성 영향을 분석하며, 다약물내성(MDR1) 유전자 발현과의 연관성도 연구하고 있습니다. 또한, 고에너지 비탄성 중성자산란을 활용해 우라늄 기반 화합물(UrSi₂)과 Cerium 기반 합금(CeNiSn)의 자기 및 결정장 상태를 탐구하며, 이들의 전자 구조적 특성과 관련된 근본적인 물리 메커니즘을 규명하고 있습니다.
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Some widely used anticancer agents might be ineffective for treating hepatocellular carcinoma in clinical situations even when combined with reversing agents.
Reduced folates have been shown to increase the cytotoxicity of 5-fluorouracil (5-FU) by stabilizing the 5-fluoro-2'-deoxyuridine-5'-monophosphate-thymidylate synthase complex, thus increasing the block in the DNA synthetic pathway. Using an in vitro colorimetric [3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide] cytotoxicity assay, we tested the effects of 5-FU and 5-fluoro-2'-deoxyuridine (FdUrd) with and without leucovorin (LV) on a panel of 11 human colorectal carcinoma cell line
We compared the in vitro sensitivity patterns to cytotoxic drugs and expression of the multidrug resistance-associated MDR1 gene (also known as PGY1 gene) in four gastric carcinoma cell lines with those obtained in a panel of 11 colorectal carcinoma cell lines. In addition, we tested the effects of leucovorin on enhancement of fluorinated pyrimidine-induced cytotoxicity. We used a semiautomated tetrazolium dye assay [3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (tetrazolyl blue)]
We investigated dc and ac susceptibilities of ${\mathrm{Pr}}_{0.63}{\mathrm{Sr}}_{0.37}{\mathrm{MnO}}_{3}$ and ${\mathrm{Nd}}_{0.7}{\mathrm{Sr}}_{0.3}{\mathrm{MnO}}_{3}$ single crystals. Surprisingly, real components of the ac susceptibility of both samples are frequency dependent below ${T}_{C},$ indicating competition between ferromagnetic and antiferromagnetic interactions even in the ferromagnetic phase. We also found evidence of rare-earth moment ordering at low temperatures. Our ac suscept
We have investigated the magnetic excitations of ${\mathrm{URu}}_{2}{\mathrm{Si}}_{2}$ up to 800 meV using high energy inelastic neutron scattering. There is clear evidence of magnetic scattering in the energy range up to 200 meV. This scattering can be fitted to four broad peaks which we attribute to heavily damped crystal field excitations. We also observed the ${\mathrm{U}}^{4+}$ ${}^{3}{\stackrel{\ensuremath{\rightarrow}}{{\mathrm{H}}_{4}}}^{3}{\mathrm{F}}_{2}$ intermultiplet transition at 3
Chromosomal phase separation is involved in a broad spectrum of chromosome organization and functional processes. Nonetheless, the intricacy of this process has left its molecular mechanism unclear. Here, we introduce the principles governing phase separation and its connections to physiological roles in this context. Our primary focus is contrasting two phase separation mechanisms: self-association-induced phase separation (SIPS) and bridging-induced phase separation (BIPS). We provide a compre
We present inelastic-neutron-scattering results for single-crystal CeNiSn. Apart from phonon-related structures appearing mainly below 30 meV, we have observed clear indications of a crystal-field excitation centered around 40 meV. However, we cannot yet determine whether there is another crystal-field excitation at a lower energy because of the presence of strong phonon peaks. We have also made measurements to investigate the quasielastic response of CeNiSn. We discuss the current understanding
${\text{PrFe}}_{4}{\text{P}}_{12}$ exhibits a unique transition at 6.5 K with an order parameter whose nature is still controversial. In order to elucidate the origin of the transition, we have carried out inelastic neutron scattering experiments in a range of temperatures and magnetic fields. Our data reveal a different type of low-lying excitations centered at 1.5 and 3.5 meV in the ordered phase with an unusual $Q$ dependence. With increasing field or temperature, the well-defined excitations