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Research on high instantaneous power droplet generator by using super-hydrophobic electrode

IOP conference series. Earth and environmental science, 2021-05, Vol.781 (4), p.42050

2021

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Discovery of TAK-981, a First-in-Class Inhibitor of SUMO-Activating Enzyme for the Treatment of Cancer

Journal of medicinal chemistry, 2021-03, Vol.64 (5), p.2501-2520

2021

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Comparison of Several Molecular Docking Programs: Pose Prediction and Virtual Screening Accuracy

Journal of Chemical Information and Modeling, 2009-06, Vol.49 (6), p.1455-1474

2009

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The China Alzheimer Report 2022

General Psychiatry, 2022-02, Vol.35 (1), p.e100751-e100751

2022

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Genetic variations in the retrograde endocannabinoid signaling pathway in Chinese patients with major depressive disorder

Frontiers in neurology, 2023-04, Vol.14, p.1153509-1153509

2023

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Clinical manifestations and imaging and pathological features of giant cell angioblastoma: Report of four cases and literature review

Frontiers in surgery, 2023-01, Vol.9, p.1062309-1062309

2023

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Analysis of axial scanning range and magnification variation in wide‐field microscope for measurement using an electrically tunable lens

Microscopy research and technique, 2019-02, Vol.82 (2), p.101-113

2019

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Development of an Efficient Manufacturing Process for E2212 toward Rapid Clinical Introduction

Organic process research & development, 2019-04, Vol.23 (4), p.603-613

2019

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Anthropogenic CH4 Emissions in the Yangtze River Delta Based on A “Top-Down” Method

Atmosphere, 2019-04, Vol.10 (4), p.185

2019

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Single Line-to-ground Fault Location and Information Modeling Based on the Interaction between Intelligent Distribution Equipment

Journal of Electrical Engineering & Technology, 2018, 13(5), , pp.1807-1813

2018

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Determining the Isotopic Composition of Surface Water Vapor Flux From High‐Frequency Observations Using Flux‐Gradient and Keeling Plot Methods

Earth and space science (Hoboken, N.J.), 2021-03, Vol.8 (3), p.n/a

2021

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Discovery of Potent and Selective Inhibitors of the Mammalian Target of Rapamycin (mTOR) Kinase

Journal of medicinal chemistry, 2009-11, Vol.52 (22), p.7081-7089

2009

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Multifunctional Nanostructure RAP‐RL Rescues Alzheimer's Cognitive Deficits through Remodeling the Neurovascular Unit

Advanced science, 2021-01, Vol.8 (2), p.2001918-n/a

2021

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Discovery of Dibenzo[c,f][2,7]naphthyridines as Potent and Selective 3-Phosphoinositide-Dependent Kinase-1 Inhibitors

Journal of medicinal chemistry, 2007-11, Vol.50 (23), p.5547-5549

2007

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LncRNA-SNHG1 contributes to gastric cancer cell proliferation by regulating DNMT1

Biochemical and biophysical research communications, 2017-09, Vol.491 (4), p.926-931

2017

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Preparation and application of a partially degradable gel in mass spectrometry-based proteomic analysis

Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 2011-10, Vol.879 (28), p.2957-2962

2011

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Discovery of the catechol structural moiety as a Stat3 SH2 domain inhibitor by virtual screening

Bioorganic & medicinal chemistry, 2008-09, Vol.18 (18), p.4988-4992

2008

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B-Raf kinase inhibitors: Hit enrichment through scaffold hopping

Bioorganic & medicinal chemistry letters, 2010-04, Vol.20 (8), p.2431-2434

2010

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Arginine methyltransferase PRMT3 promote tumorigenesis through regulating c-MYC stabilization in colorectal cancer

Gene, 2021-07, Vol.791, p.145718-145718, Article 145718

2021

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Small molecule inhibitors of HIV RT Ribonuclease H

Bioorganic & medicinal chemistry letters, 2010, Vol.20 (1), p.398-402

2010

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Discovery of highly potent and selective type I B-Raf kinase inhibitors

Bioorganic & medicinal chemistry letters, 2009-12, Vol.19 (23), p.6571-6574

2009

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Structure-based design of isoindoline-1,3-diones and 2,3-dihydrophthalazine-1,4-diones as novel B-Raf inhibitors

Bioorganic & medicinal chemistry letters, 2011-12, Vol.21 (23), p.6941-6944

2011

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Design and SAR of macrocyclic Hsp90 inhibitors with increased metabolic stability and potent cell-proliferation activity

Bioorganic & medicinal chemistry letters, 2011-04, Vol.21 (8), p.2278-2282

2011

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Macrocyclic lactams as potent Hsp90 inhibitors with excellent tumor exposure and extended biomarker activity

Bioorganic & medicinal chemistry letters, 2011-06, Vol.21 (11), p.3411-3416

2011

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Non-hinge-binding pyrazolo[1,5- a]pyrimidines as potent B-Raf kinase inhibitors

Bioorganic & medicinal chemistry letters, 2009-12, Vol.19 (23), p.6519-6523

2009

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Research on high instantaneous power droplet generator by using super-hydrophobic electrode

Discovery of TAK-981, a First-in-Class Inhibitor of SUMO-Activating Enzyme for the Treatment of Cancer

Comparison of Several Molecular Docking Programs: Pose Prediction and Virtual Screening Accuracy

The China Alzheimer Report 2022

Genetic variations in the retrograde endocannabinoid signaling pathway in Chinese patients with major depressive disorder

Clinical manifestations and imaging and pathological features of giant cell angioblastoma: Report of four cases and literature review

Analysis of axial scanning range and magnification variation in wide‐field microscope for measurement using an electrically tunable lens

Development of an Efficient Manufacturing Process for E2212 toward Rapid Clinical Introduction

Anthropogenic CH4 Emissions in the Yangtze River Delta Based on A “Top-Down” Method

Single Line-to-ground Fault Location and Information Modeling Based on the Interaction between Intelligent Distribution Equipment

Determining the Isotopic Composition of Surface Water Vapor Flux From High‐Frequency Observations Using Flux‐Gradient and Keeling Plot Methods

Discovery of Potent and Selective Inhibitors of the Mammalian Target of Rapamycin (mTOR) Kinase

Multifunctional Nanostructure RAP‐RL Rescues Alzheimer's Cognitive Deficits through Remodeling the Neurovascular Unit

Discovery of Dibenzo[c,f][2,7]naphthyridines as Potent and Selective 3-Phosphoinositide-Dependent Kinase-1 Inhibitors

LncRNA-SNHG1 contributes to gastric cancer cell proliferation by regulating DNMT1

Preparation and application of a partially degradable gel in mass spectrometry-based proteomic analysis

Discovery of the catechol structural moiety as a Stat3 SH2 domain inhibitor by virtual screening

B-Raf kinase inhibitors: Hit enrichment through scaffold hopping

Arginine methyltransferase PRMT3 promote tumorigenesis through regulating c-MYC stabilization in colorectal cancer

Small molecule inhibitors of HIV RT Ribonuclease H

Discovery of highly potent and selective type I B-Raf kinase inhibitors

Structure-based design of isoindoline-1,3-diones and 2,3-dihydrophthalazine-1,4-diones as novel B-Raf inhibitors

Design and SAR of macrocyclic Hsp90 inhibitors with increased metabolic stability and potent cell-proliferation activity

Macrocyclic lactams as potent Hsp90 inhibitors with excellent tumor exposure and extended biomarker activity

Non-hinge-binding pyrazolo[1,5- a]pyrimidines as potent B-Raf kinase inhibitors

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