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Role and Mechanism of the Interaction of BCR-ABL with E3 Ligase c-CBL in Targeting Therapy of Chronic Myelogenous Leukemia

Zhongguo shi yan xue ye xue za zhi, 2017-02, Vol.25 (1), p.42

2017

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Multimodal imaging and clinical characteristics of bone lesions in POEMS syndrome

International journal of clinical and experimental medicine, 2015-01, Vol.8 (5), p.7467-7476

2015

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Gene therapy for hemophilia B

Zhōnghuá xuèyèxué zázhì, 2013-09, Vol.34 (9), p.809-811

2013

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Myr-RKEFAK Peptide Selectively Regulates Outside-in Signaling Transduction-related Functions in Human Platelets

Zhongguo shi yan xue ye xue za zhi, 2015-06, Vol.23 (3), p.761

2015

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Effect of the Integrin β3 Cytoplasmic NITY Motif on α II bβ3-Mediated Cell Functions in CHO Cell Model

Zhongguo shi yan xue ye xue za zhi, 2015-06, Vol.23 (3), p.768

2015

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Research progress on the effect of shear stress on thrombosis

Zhōnghuá xīnxuèguănbìng zázhì, 2013-10, Vol.41 (10), p.893

2013

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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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A single E726Q mutation in the membrane proximal α-helix of integrin β3 subunit induces membrane blebbing by disrupting the membrane-actin cortex interaction

Zhongguo shi yan xue ye xue za zhi, 2011-12, Vol.19 (6), p.1450

2011

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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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Two novel mutations in one pedigree with hereditary Factor VII deficiency

Zhōnghuá xuèyèxué zázhì, 2011-03, Vol.32 (3), p.158-162

2011

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Study of signal transduction mediated by integrin alphaIIbbeta3 using a dominant negative model

Zhongguo shi yan xue ye xue za zhi, 2009-08, Vol.17 (4), p.1026

2009

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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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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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Two new mutations of AT gene in type I inherited antithrombin deficiency.

Zhōnghuá xuèyèxué zázhì, 2010-03, Vol.31 (3), p.145-148

2010

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Analysis of clinical features and genotype in three Chinese pedigrees with Glanzmann thrombasthenia

Zhōnghuá xuèyèxué zázhì, 2008-03, Vol.29 (3), p.149-153

2008

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The application of thrombin generation tests to warfarin anticoagulation monitoring

Zhōnghuá xuèyèxué zázhì, 2008-03, Vol.29 (3), p.168

2008

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Establishment of urokinase receptor gene antisense RNA transfer system and its application in leukemia research

Zhongguo shi yan xue ye xue za zhi, 2003-12, Vol.11 (6), p.591

2003

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Lymphadenopathy in POEMS syndrome: a correlation between clinical features and imaging findings

International journal of clinical and experimental pathology, 2020, Vol.13 (1), p.21-25

2020

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4,5,6-Tri-O-acetyl-2,3-di-S-ethyl-2,3-dithio-d-allose diethyl dithio-acetal

Acta crystallographica. Section E, Structure reports online, 2009-05, Vol.65 (Pt 6), p.o1227-o1227

2009

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Role and Mechanism of the Interaction of BCR-ABL with E3 Ligase c-CBL in Targeting Therapy of Chronic Myelogenous Leukemia

Multimodal imaging and clinical characteristics of bone lesions in POEMS syndrome

Gene therapy for hemophilia B

Myr-RKEFAK Peptide Selectively Regulates Outside-in Signaling Transduction-related Functions in Human Platelets

Effect of the Integrin β3 Cytoplasmic NITY Motif on α II bβ3-Mediated Cell Functions in CHO Cell Model

Research progress on the effect of shear stress on thrombosis

The binding mechanisms of F VIII Trp1707Ser mutation-associated inhibitor

A single E726Q mutation in the membrane proximal α-helix of integrin β3 subunit induces membrane blebbing by disrupting the membrane-actin cortex interaction

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

Two novel mutations in one pedigree with hereditary Factor VII deficiency

Study of signal transduction mediated by integrin alphaIIbbeta3 using a dominant negative model

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

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

Two new mutations of AT gene in type I inherited antithrombin deficiency.

Analysis of clinical features and genotype in three Chinese pedigrees with Glanzmann thrombasthenia

The application of thrombin generation tests to warfarin anticoagulation monitoring

Establishment of urokinase receptor gene antisense RNA transfer system and its application in leukemia research

Lymphadenopathy in POEMS syndrome: a correlation between clinical features and imaging findings

4,5,6-Tri-O-acetyl-2,3-di-S-ethyl-2,3-dithio-d-allose diethyl dithio-acetal

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