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Institution

Seoul National University

EducationSeoul, South Korea
About: Seoul National University is a education organization based out in Seoul, South Korea. It is known for research contribution in the topics: Population & Catalysis. The organization has 65879 authors who have published 138759 publications receiving 3715170 citations. The organization is also known as: SNU & Seoul-dae.
Topics: Population, Catalysis, Thin film, Gene, Cancer


Papers
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Journal ArticleDOI
TL;DR: Among patients with advanced breast cancer and a germline BRCA1/2 mutation, single‐agent talazoparib provided a significant benefit over standard chemotherapy with respect to progression‐free survival.
Abstract: Background The poly(adenosine diphosphate–ribose) inhibitor talazoparib has shown antitumor activity in patients with advanced breast cancer and germline mutations in BRCA1 and BRCA2 (BRCA1/2). Methods We conducted a randomized, open-label, phase 3 trial in which patients with advanced breast cancer and a germline BRCA1/2 mutation were assigned, in a 2:1 ratio, to receive talazoparib (1 mg once daily) or standard single-agent therapy of the physician’s choice (capecitabine, eribulin, gemcitabine, or vinorelbine in continuous 21-day cycles). The primary end point was progression-free survival, which was assessed by blinded independent central review. Results Of the 431 patients who underwent randomization, 287 were assigned to receive talazoparib and 144 were assigned to receive standard therapy. Median progression-free survival was significantly longer in the talazoparib group than in the standard-therapy group (8.6 months vs. 5.6 months; hazard ratio for disease progression or death, 0.54; 95% c...

1,298 citations

Journal ArticleDOI
TL;DR: Ceritinib was highly active in patients with advanced, ALK-rearranged NSCLC, including those who had had disease progression during crizotinib treatment, regardless of the presence of resistance mutations in ALK.
Abstract: BackgroundNon–small-cell lung cancer (NSCLC) harboring the anaplastic lymphoma kinase gene (ALK) rearrangement is sensitive to the ALK inhibitor crizotinib, but resistance invariably develops. Ceritinib (LDK378) is a new ALK inhibitor that has shown greater antitumor potency than crizotinib in preclinical studies. MethodsIn this phase 1 study, we administered oral ceritinib in doses of 50 to 750 mg once daily to patients with advanced cancers harboring genetic alterations in ALK. In an expansion phase of the study, patients received the maximum tolerated dose. Patients were assessed to determine the safety, pharmacokinetic properties, and antitumor activity of ceritinib. Tumor biopsies were performed before ceritinib treatment to identify resistance mutations in ALK in a group of patients with NSCLC who had had disease progression during treatment with crizotinib. ResultsA total of 59 patients were enrolled in the dose-escalation phase. The maximum tolerated dose of ceritinib was 750 mg once daily; dose-l...

1,297 citations

Journal ArticleDOI
Suyong Choi1, S. L. Olsen, Kazuo Abe, T. Abe  +172 moreInstitutions (46)
TL;DR: In this article, a narrow charmonium-like state produced in the exclusive decay process B+/--->K+/-pi(+)pi(-)J/psi has been observed, which has a mass of 3872.0+/-0.6(stat)+/- 0.5(syst) MeV.
Abstract: We report the observation of a narrow charmoniumlike state produced in the exclusive decay process B+/--->K+/-pi(+)pi(-)J/psi. This state, which decays into pi(+)pi(-)J/psi, has a mass of 3872.0+/-0.6(stat)+/-0.5(syst) MeV, a value that is very near the M(D0)+M(D(*0)) mass threshold. The results are based on an analysis of 152M B-Bmacr; events collected at the Upsilon(4S) resonance in the Belle detector at the KEKB collider. The signal has a statistical significance that is in excess of 10sigma.

1,294 citations

Journal ArticleDOI
TL;DR: This review focuses on the various types of chitosan derivatives and their use in various tissue engineering applications namely, skin, bone, cartilage, liver, nerve and blood vessel.

1,278 citations

Journal ArticleDOI
TL;DR: In this paper, a high-work-function, low-sheet-resistance graphene anode was used to improve the luminous efficiency of organic light-emitting diodes (OLEDs).
Abstract: Although graphene films have a strong potential to replace indium tin oxide anodes in organic light-emitting diodes (OLEDs), to date, the luminous efficiency of OLEDs with graphene anodes has been limited by a lack of efficient methods to improve the low work function and reduce the sheet resistance of graphene films to the levels required for electrodes1,2,3,4. Here, we fabricate flexible OLEDs by modifying the graphene anode to have a high work function and low sheet resistance, and thus achieve extremely high luminous efficiencies (37.2 lm W–1 in fluorescent OLEDs, 102.7 lm W–1 in phosphorescent OLEDs), which are significantly higher than those of optimized devices with an indium tin oxide anode (24.1 lm W–1 in fluorescent OLEDs, 85.6 lm W–1 in phosphorescent OLEDs). We also fabricate flexible white OLED lighting devices using the graphene anode. These results demonstrate the great potential of graphene anodes for use in a wide variety of high-performance flexible organic optoelectronics. By replacing conventional indium tin oxide (ITO) anodes with high-work-function, low-sheet-resistance graphene anodes, researchers demonstrate flexible fluorescent organic LEDs with extremely high luminous efficiencies of 37.2 lm W–1 for fluorescent devices and 102.7 lm W–1 for phosphorescent devices. These values are significantly higher than those of optimized organic LEDs based on ITO anodes.

1,273 citations


Authors

Showing all 66324 results

NameH-indexPapersCitations
Hyun-Chul Kim1764076183227
Adi F. Gazdar157776104116
Alfred L. Goldberg15647488296
Yongsun Kim1562588145619
David J. Mooney15669594172
Roberto Romero1511516108321
Jongmin Lee1502257134772
Byung-Sik Hong1461557105696
Inkyu Park1441767109433
Teruki Kamon1422034115633
John L. Hopper140122986392
Ali Khademhosseini14088776430
Taeghwan Hyeon13956375814
Suyong Choi135149597053
Intae Yu134137289870
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
2023241
2022768
20218,297
20208,368
20198,175
20187,617