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Heteroleptic cuprous complexes of a diimine MePBO ligand and their structure influence on phosphorescent color: Syntheses, structure characterizations, properties and TD‐DFT calculations

Zeitschrift für anorganische und allgemeine Chemie (1950), 2021-10, Vol.647 (19), p.1896-1905

2021

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Structural, spectroscopic and DFT theoretical studies of phosphorescent CuIP2S‐containing cuprous complexes

Acta crystallographica. Section C, Crystal structure communications, 2021-07, Vol.77 (7), p.331-339

2021

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An ionic luminescent complex of europium(III) and its fluorescence sensing performance for amine VOCs

Journal of molecular structure, 2025-01, Vol.1319, p.139595, Article 139595

2025

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Structural, spectroscopic and DFT theoretical studies of phosphorescent CuIP 2 S-containing cuprous complexes

Acta crystallographica. Section C, Structural chemistry, 2021-07, Vol.77 (7), p.331-339

2021

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SIRT2 Promotes HBV Transcription and Replication by Targeting Transcription Factor p53 to Increase the Activities of HBV Enhancers and Promoters

Frontiers in microbiology, 2022-05, Vol.13, p.836446-836446

2022

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Palladium-Catalyzed Regio‑, Diastereo‑, and Enantioselective Allylation of Nitroalkanes with Monosubstituted Allylic Substrates

Journal of organic chemistry, 2013-07, Vol.78 (13), p.6503-6509

2013

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Hereditary protein C deficiency caused by compound heterozygous mutants in two independent Chinese families

Pathology, 2014-12, Vol.46 (7), p.630-635

2014

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Molecular basis of type I antithrombin deficiency in two women with recurrent venous thromboembolism in the first trimester of pregnancy

Blood cells, molecules, & diseases, 2012-04, Vol.48 (4), p.254-259

2012

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Correlation of Thrombosis and Prothrombotic State with Coagulation Factor V Gene Polymorphism and APCR. HHcy

Zhongguo shi yan xue ye xue za zhi, 2016-12, Vol.24 (6), p.1850

2016

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Dichlorido(ethanol-κO)[2-(1,3-thia-zol-4-yl-κN)-1H-benzimidazole-κN(3)]copper(II)

Acta crystallographica. Section E, Structure reports online, 2012-04, Vol.68 (Pt 4), p.m508-m508

2012

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MR Molecular Imaging of Thrombus: Development and Application of a Gd-based Novel Contrast Agent Targeting to P-selectin

Clinical and applied thrombosis/hemostasis, 2010-04, Vol.16 (2), p.177-183

2010

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The binding mechanisms of F VIII Trp1707Ser mutation-associated inhibitor

Zhōnghuá xuèyèxué zázhì, 2013-08, Vol.34 (8), p.691-695

2013

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The molecular mechanism of haemophilia B caused by the Arg327Ile novel mutation in FIX gene in vitro expression

Zhōnghuá xuèyèxué zázhì, 2012-08, Vol.33 (8), p.642-647

2012

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Functional study of abnormal fibrinogen caused by Arg275His mutation in fibrinogen γ chain

Zhōnghuá xuèyèxué zázhì, 2013-03, Vol.34 (3), p.190-194

2013

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Phenotype and genotype analysis of two Chinese pedigrees with type 3 von Willebrand diseases

Zhonghua yi xue yi chuan xue za zhi, 2012-10, Vol.29 (5), p.524

2012

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The phenotypic and genotypic diagnosis of three Chinese patients with von Willebrand disease

Chung-hua nei kʿo tsa chih, 2012-10, Vol.51 (10), p.788

2012

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Molecular analysis of a patient with hemophilia A caused by FVIII His99Arg mutation

Zhōnghuá xuèyèxué zázhì, 2011-09, Vol.32 (9), p.587-591

2011

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Genotype and function analyses of four inherited dysfibrinogenemia pedigree caused by Arg16 amino acid substitution in fibrinogen Aα chain

Zhōnghuá xuèyèxué zázhì, 2012-06, Vol.33 (6), p.475-479

2012

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Molecular mechanisms of recurrent venous thrombosis in two pedigrees with type I antithrombin deficiency

Zhōnghuá xuèyèxué zázhì, 2011-12, Vol.32 (12), p.848-853

2011

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Analysis of phenotype and genotype in three Chinese pedigrees with inherited dysfibrinogenemia

Zhōnghuá xuèyèxué zázhì, 2011-03, Vol.32 (3), p.153-157

2011

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Hereditary protein C deficiency: a case report

Pathology, 2007-04, Vol.39 (2), p.290-291

2007

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Analysis of phenotype and genotype in four Chinese pedigrees with inherited coagulation factor V deficiency.

Zhōnghuá xuèyèxué zázhì, 2010-03, Vol.31 (3), p.149-153

2010

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Phenotype and genotype analysis of three Chinese pedigrees with von Willebrand disease

Zhōnghuá xuèyèxué zázhì, 2011-02, Vol.32 (2), p.99-102

2011

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Intron 1 and 22 inversions in factor VIII gene in patients with haemophilia A

Zhōnghuá xuèyèxué zázhì, 2009-03, Vol.30 (3), p.150-153

2009

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Investigation of the spectra of Sr2CeO4 due to charge transfer transition

Wuli xuebao, 2005-05, Vol.54 (5), p.2369

2005

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Heteroleptic cuprous complexes of a diimine MePBO ligand and their structure influence on phosphorescent color: Syntheses, structure characterizations, properties and TD‐DFT calculations

Structural, spectroscopic and DFT theoretical studies of phosphorescent CuIP2S‐containing cuprous complexes

An ionic luminescent complex of europium(III) and its fluorescence sensing performance for amine VOCs

Structural, spectroscopic and DFT theoretical studies of phosphorescent CuIP 2 S-containing cuprous complexes

SIRT2 Promotes HBV Transcription and Replication by Targeting Transcription Factor p53 to Increase the Activities of HBV Enhancers and Promoters

Palladium-Catalyzed Regio‑, Diastereo‑, and Enantioselective Allylation of Nitroalkanes with Monosubstituted Allylic Substrates

Hereditary protein C deficiency caused by compound heterozygous mutants in two independent Chinese families

Molecular basis of type I antithrombin deficiency in two women with recurrent venous thromboembolism in the first trimester of pregnancy

Correlation of Thrombosis and Prothrombotic State with Coagulation Factor V Gene Polymorphism and APCR. HHcy

Dichlorido(ethanol-κO)[2-(1,3-thia-zol-4-yl-κN)-1H-benzimidazole-κN(3)]copper(II)

MR Molecular Imaging of Thrombus: Development and Application of a Gd-based Novel Contrast Agent Targeting to P-selectin

The binding mechanisms of F VIII Trp1707Ser mutation-associated inhibitor

The molecular mechanism of haemophilia B caused by the Arg327Ile novel mutation in FIX gene in vitro expression

Functional study of abnormal fibrinogen caused by Arg275His mutation in fibrinogen γ chain

Phenotype and genotype analysis of two Chinese pedigrees with type 3 von Willebrand diseases

The phenotypic and genotypic diagnosis of three Chinese patients with von Willebrand disease

Molecular analysis of a patient with hemophilia A caused by FVIII His99Arg mutation

Genotype and function analyses of four inherited dysfibrinogenemia pedigree caused by Arg16 amino acid substitution in fibrinogen Aα chain

Molecular mechanisms of recurrent venous thrombosis in two pedigrees with type I antithrombin deficiency

Analysis of phenotype and genotype in three Chinese pedigrees with inherited dysfibrinogenemia

Hereditary protein C deficiency: a case report

Analysis of phenotype and genotype in four Chinese pedigrees with inherited coagulation factor V deficiency.

Phenotype and genotype analysis of three Chinese pedigrees with von Willebrand disease

Intron 1 and 22 inversions in factor VIII gene in patients with haemophilia A

Investigation of the spectra of Sr2CeO4 due to charge transfer transition

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