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Tailoring of hole eigenenergies in strained GaAsP/AlGaAs single quantum wells grown by atmospheric pressure organometallic chemical vapor deposition

Applied physics letters, 1988-12, Vol.53 (25), p.2501-2503

1988

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Exciton photoluminescence linewidths in very narrow AlGaAs/GaAs and GaAs/InGaAs quantum wells

Journal of applied physics, 1988-12, Vol.64 (11), p.6562-6564

1988

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Reversal of light- and heavy-hole valence bands in strained GaAsP/AlGaAs quantum wells

Surface science, 1990-04, Vol.228 (1), p.314-317

1990

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Pseudomorphic GaAs/InGaAs single quantum wells by atmospheric pressure organometallic chemical vapor deposition

Applied physics letters, 1988-01, Vol.52 (4), p.293-295

1988

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AlGaAs/GaAs quantum wells with high carrier confinement and luminescence efficiencies by organometallic chemical vapor deposition

Journal of applied physics, 1987-07, Vol.62 (1), p.120-125

1987

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Critical thickness of GaAs/InGaAs and AlGaAs/GaAsP strained quantum wells grown by organometallic chemical vapor deposition

Journal of electronic materials, 1990-09, Vol.19 (9), p.967-974

1990

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Effects of polyimide passivation on the photoluminescence of high-purity epitaxial GaAs

Journal of applied physics, 1988-02, Vol.63 (3), p.962-964

1988

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Photoluminescence characteristics of selectively grown GaAs and AlGaAs/GaAs quantum wells

Journal of applied physics, 1987-09, Vol.62 (6), p.2466-2469

1987

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Effects of growth interruption on the optical properties of AIGaAs/GaAs and GaAs/InGaAs quantum wells grown by atmospheric pressure organometallic chemical vapor deposition

Journal of electronic materials, 1991-02, Vol.20 (2), p.197-201

1991

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Photoluminescence study of heterostructures and interfaces

Hsu, Jung-Kuei

1989

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Discovery of M Protease Inhibitors Encoded by SARS-CoV-2

Antimicrobial agents and chemotherapy, 2020-08, Vol.64 (9)

2020

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Adsorption of CO2 onto amine-grafted mesoporous silicas

Separation and purification technology, 2009-11, Vol.70 (1), p.87-95

2009

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Critical Thickness of GaAs/InGaAs and AlGaAs/GaAsP Quantum Wells Grown by Atmospheric Pressure OMCVD

MRS proceedings, 1989, Vol.160, Article 141

1989

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Indoor localization and navigation using smartphone sensory data

Annals of operations research, 2018-06, Vol.265 (2), p.187-204

2018

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Suppression of Stat3 activity sensitizes gefitinib-resistant non small cell lung cancer cells

Biochemical pharmacology, 2011-06, Vol.81 (11), p.1263-1270

2011

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The Escherichia coli proton-translocating ATPase: Studies of the role of uncI and the stoichiometry ofc subunit

Hsu, Debbie Kuei-Jung Wang

1990

Volltextzugriff (PDF)

Evaluation of the antitumor effects of BPR1J-340, a potent and selective FLT3 inhibitor, alone or in combination with an HDAC inhibitor, vorinostat, in AML cancer

PloS one, 2014-01, Vol.9 (1), p.e83160

2014

Volltextzugriff (PDF)

Inhibition of enterovirus 71 replication and the viral 3D polymerase by aurintricarboxylic acid

Journal of antimicrobial chemotherapy, 2010-04, Vol.65 (4), p.676-683

2010

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Identification of a Multitargeted Tyrosine Kinase Inhibitor for the Treatment of Gastrointestinal Stromal Tumors and Acute Myeloid Leukemia

Journal of medicinal chemistry, 2019-12, Vol.62 (24), p.11135-11150

2019

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Development of a Humanized Antibody Targeting Extracellular HSP90α to Suppress Endothelial-Mesenchymal Transition-Enhanced Tumor Growth of Pancreatic Adenocarcinoma Cells

Cells (Basel, Switzerland), 2024-07, Vol.13 (13), p.1146

2024

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Identification of a potent 5-phenyl-thiazol-2-ylamine-based inhibitor of FLT3 with activity against drug resistance-conferring point mutations

European journal of medicinal chemistry, 2015-07, Vol.100, p.151-161

2015

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Facile Identification of Dual FLT3-Aurora A Inhibitors: A Computer-Guided Drug Design Approach

ChemMedChem, 2014-05, Vol.9 (5), p.953-961

2014

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Discovery of 3-phenyl-1H-5-pyrazolylamine derivatives containing a urea pharmacophore as potent and efficacious inhibitors of FMS-like tyrosine kinase-3 (FLT3)

Bioorganic & medicinal chemistry, 2013-06, Vol.21 (11), p.2856-2867

2013

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Anemonin is a natural bioactive compound that can regulate tyrosinase-related proteins and mRNA in human melanocytes

Journal of dermatological science, 2008-02, Vol.49 (2), p.115-123

2008

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Tailoring of hole eigenenergies in strained GaAsP/AlGaAs single quantum wells grown by atmospheric pressure organometallic chemical vapor deposition

Exciton photoluminescence linewidths in very narrow AlGaAs/GaAs and GaAs/InGaAs quantum wells

Reversal of light- and heavy-hole valence bands in strained GaAsP/AlGaAs quantum wells

Pseudomorphic GaAs/InGaAs single quantum wells by atmospheric pressure organometallic chemical vapor deposition

AlGaAs/GaAs quantum wells with high carrier confinement and luminescence efficiencies by organometallic chemical vapor deposition

Critical thickness of GaAs/InGaAs and AlGaAs/GaAsP strained quantum wells grown by organometallic chemical vapor deposition

Effects of polyimide passivation on the photoluminescence of high-purity epitaxial GaAs

Photoluminescence characteristics of selectively grown GaAs and AlGaAs/GaAs quantum wells

Effects of growth interruption on the optical properties of AIGaAs/GaAs and GaAs/InGaAs quantum wells grown by atmospheric pressure organometallic chemical vapor deposition

Photoluminescence study of heterostructures and interfaces

Discovery of M Protease Inhibitors Encoded by SARS-CoV-2

Adsorption of CO2 onto amine-grafted mesoporous silicas

Critical Thickness of GaAs/InGaAs and AlGaAs/GaAsP Quantum Wells Grown by Atmospheric Pressure OMCVD

Indoor localization and navigation using smartphone sensory data

Suppression of Stat3 activity sensitizes gefitinib-resistant non small cell lung cancer cells

The Escherichia coli proton-translocating ATPase: Studies of the role of uncI and the stoichiometry ofc subunit

Evaluation of the antitumor effects of BPR1J-340, a potent and selective FLT3 inhibitor, alone or in combination with an HDAC inhibitor, vorinostat, in AML cancer

Inhibition of enterovirus 71 replication and the viral 3D polymerase by aurintricarboxylic acid

Discovery of BPR1K871, a quinazoline based, multi-kinase inhibitor for the treatment of AML and solid tumors: Rational design, synthesis, in vitro and in vivo evaluation

Identification of a Multitargeted Tyrosine Kinase Inhibitor for the Treatment of Gastrointestinal Stromal Tumors and Acute Myeloid Leukemia

Development of a Humanized Antibody Targeting Extracellular HSP90α to Suppress Endothelial-Mesenchymal Transition-Enhanced Tumor Growth of Pancreatic Adenocarcinoma Cells

Identification of a potent 5-phenyl-thiazol-2-ylamine-based inhibitor of FLT3 with activity against drug resistance-conferring point mutations

Facile Identification of Dual FLT3-Aurora A Inhibitors: A Computer-Guided Drug Design Approach

Discovery of 3-phenyl-1H-5-pyrazolylamine derivatives containing a urea pharmacophore as potent and efficacious inhibitors of FMS-like tyrosine kinase-3 (FLT3)

Anemonin is a natural bioactive compound that can regulate tyrosinase-related proteins and mRNA in human melanocytes

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