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Performance Study of Black Shale Modified Soil for Road Use Based on Eshelby–Mori–Tanaka Theory

Applied sciences, 2024-02, Vol.14 (4), p.1636

2024

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Mechanistic Study of Uba5 Enzyme and the Ufm1 Conjugation Pathway

The Journal of biological chemistry, 2014-08, Vol.289 (33), p.22648-22658

2014

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Mechanism of the Very Efficient Quenching of Tryptophan Fluorescence in Human γD- and γS-Crystallins: The γ-Crystallin Fold May Have Evolved To Protect Tryptophan Residues from Ultraviolet Photodamage

Biochemistry (Easton), 2009-05, Vol.48 (17), p.3708-3716

2009

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Mechanism of the Efficient Tryptophan Fluorescence Quenching in Human γD-Crystallin Studied by Time-Resolved Fluorescence

Biochemistry (Easton), 2008-10, Vol.47 (40), p.10705-10721

2008

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Mechanism of the Highly Efficient Quenching of Tryptophan Fluorescence in Human γD-Crystallin

Biochemistry (Easton), 2006-09, Vol.45 (38), p.11552-11563

2006

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Covalently linked HslU hexamers support a probabilistic mechanism that links ATP hydrolysis to protein unfolding and translocation

The Journal of biological chemistry, 2017-04, Vol.292 (14), p.5695-5704

2017

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Femtosecond Fluorescence Spectra of Tryptophan in Human γ-Crystallin Mutants: Site-Dependent Ultrafast Quenching

Journal of the American Chemical Society, 2009-11, Vol.131 (46), p.16751-16757

2009

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An ultrasensitive assay format for detecting ULK1 inhibition by monitoring the phosphorylation status of Atg13

Analytical biochemistry, 2016-09, Vol.509, p.73-78

2016

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The γ-Crystallin Fold May Have Evolved To Protect Conserved Tryptophan Residues From UV Radiation Damage Through Efficient Quenching

Biophysical journal, 2009-02, Vol.96 (3), p.47a-47a

2009

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Contributions of Tyrosine Residues to the Stability of Human γD-Crystallin

Biophysical journal, 2009-02, Vol.96 (3), p.332a-332a

2009

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Copper ions inactivate S-adenosylhomocysteine hydrolase

Chinese science bulletin, 2002-07, Vol.47 (14), p.1176-1179

2002

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Proteasome inhibitors bortezomib and carfilzomib used for the treatment of multiple myeloma do not inhibit the serine protease HtrA2/OmiElectronic supplementary information (ESI) available. See DOI: 10.1039/c6tx00220j

2016-10

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Proteasome inhibitors bortezomib and carfilzomib used for the treatment of multiple myeloma do not inhibit the serine protease HtrA2/Omi† †Electronic supplementary information (ESI) available. See DOI: 10.1039/c6tx00220j

Toxicology research (Cambridge), 2016-08, Vol.5 (6), p.1619-1628

2016

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Proteasome inhibitors bortezomib and carfilzomib used for the treatment of multiple myeloma do not inhibit the serine protease HtrA2/Omi

Toxicology research (Cambridge), 2016-01, Vol.5 (6), p.1619-1628

2016

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Copper Ions Inhibit S-Adenosylhomocysteine Hydrolase by Causing Dissociation of NAD+ Cofactor

Biochemistry (Easton), 2007-10, Vol.46 (41), p.11451-11458

2007

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Mechanism of the highly efficient quenching of tryptophan fluorescence in human gammaD-crystallin

Biochemistry (Easton), 2006-09, Vol.45 (38), p.11552-11563

2006

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Mechanism of the efficient quenching of tryptophan fluorescence in human gamma crystallin

Chen, Jiejin

2008

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Binding of Cu 2+ to S-adenosyl- l-homocysteine hydrolase

Journal of inorganic biochemistry, 2004, Vol.98 (6), p.977-983

2004

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Mechanism of the efficient tryptophan fluorescence quenching in human gammaD-crystallin studied by time-resolved fluorescence

Biochemistry (Easton), 2008-10, Vol.47 (40), p.10705-10721

2008

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Binding of Cu2+ to S-adenosyl-L-homocysteine hydrolase

Journal of inorganic biochemistry, 2004-06, Vol.98 (6), p.977-983

2004

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Copper ions inactivate S-adenosylhomocysteine hydrolase

Chinese science bulletin, 2002-07, Vol.47 (14), p.1176

CHEN, Jiejin

2002

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Copper ions inactivate S-ade-nosylhomocysteine hydrolase

科学通报(英文版), 2002, Vol.47 (14), p.1176-1179

2002

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An improved A algorithm for searching the minimum dose path in nuclear facilities

Progress in nuclear energy (New series), 2020-08, Vol.126, p.103394, Article 103394

2020

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Gastric gastrointestinal stromal tumours (2-5 cm): Correlation of CT features with malignancy and differential diagnosis

European journal of radiology, 2020-02, Vol.123, p.108783-108783, Article 108783

2020

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Design, Synthesis and Biological Evaluation of Multi-Target Anti-Cancer Agent PYR26

International journal of molecular sciences, 2023-04, Vol.24 (8), p.7131

2023

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Performance Study of Black Shale Modified Soil for Road Use Based on Eshelby–Mori–Tanaka Theory

Mechanistic Study of Uba5 Enzyme and the Ufm1 Conjugation Pathway

Mechanism of the Very Efficient Quenching of Tryptophan Fluorescence in Human γD- and γS-Crystallins: The γ-Crystallin Fold May Have Evolved To Protect Tryptophan Residues from Ultraviolet Photodamage

Mechanism of the Efficient Tryptophan Fluorescence Quenching in Human γD-Crystallin Studied by Time-Resolved Fluorescence

Mechanism of the Highly Efficient Quenching of Tryptophan Fluorescence in Human γD-Crystallin

Covalently linked HslU hexamers support a probabilistic mechanism that links ATP hydrolysis to protein unfolding and translocation

Femtosecond Fluorescence Spectra of Tryptophan in Human γ-Crystallin Mutants: Site-Dependent Ultrafast Quenching

An ultrasensitive assay format for detecting ULK1 inhibition by monitoring the phosphorylation status of Atg13

The γ-Crystallin Fold May Have Evolved To Protect Conserved Tryptophan Residues From UV Radiation Damage Through Efficient Quenching

Contributions of Tyrosine Residues to the Stability of Human γD-Crystallin

Copper ions inactivate S-adenosylhomocysteine hydrolase

Proteasome inhibitors bortezomib and carfilzomib used for the treatment of multiple myeloma do not inhibit the serine protease HtrA2/OmiElectronic supplementary information (ESI) available. See DOI: 10.1039/c6tx00220j

Proteasome inhibitors bortezomib and carfilzomib used for the treatment of multiple myeloma do not inhibit the serine protease HtrA2/Omi† †Electronic supplementary information (ESI) available. See DOI: 10.1039/c6tx00220j

Proteasome inhibitors bortezomib and carfilzomib used for the treatment of multiple myeloma do not inhibit the serine protease HtrA2/Omi

Copper Ions Inhibit S-Adenosylhomocysteine Hydrolase by Causing Dissociation of NAD+ Cofactor

Mechanism of the highly efficient quenching of tryptophan fluorescence in human gammaD-crystallin

Mechanism of the efficient quenching of tryptophan fluorescence in human gamma crystallin

Binding of Cu 2+ to S-adenosyl- l-homocysteine hydrolase

Mechanism of the efficient tryptophan fluorescence quenching in human gammaD-crystallin studied by time-resolved fluorescence

Binding of Cu2+ to S-adenosyl-L-homocysteine hydrolase

Copper ions inactivate S-adenosylhomocysteine hydrolase

Copper ions inactivate S-ade-nosylhomocysteine hydrolase

An improved A algorithm for searching the minimum dose path in nuclear facilities

Gastric gastrointestinal stromal tumours (2-5 cm): Correlation of CT features with malignancy and differential diagnosis

Design, Synthesis and Biological Evaluation of Multi-Target Anti-Cancer Agent PYR26

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