Lista de obras - X. Long Zheng - Dominio Público Uruguay

A novel association of acquired ADAMTS13 inhibitor and acute dengue virus infection

artículo científico publicado en 2009

A team player: the disintegrin domain of ADAMTS13

scientific article published on 01 May 2009

AAV-mediated expression of an ADAMTS13 variant prevents shigatoxin-induced thrombotic thrombocytopenic purpura ⬇️

artículo científico publicado el 20 de marzo de 2013

ADAMTS13 and TTP

artículo científico publicado en 2002

ADAMTS13 and von Willebrand factor in thrombotic thrombocytopenic purpura

artículo científico publicado en 2015

ADAMTS13 and von Willebrand factor interactions

artículo científico publicado en 2015

ADAMTS13 autoantibodies cloned from patients with acquired thrombotic thrombocytopenic purpura: 1. Structural and functional characterization in vitro

artículo científico publicado en 2016

ADAMTS13 autoantibodies cloned from patients with acquired thrombotic thrombocytopenic purpura: 2. Pathogenicity in an animal model

artículo científico publicado en 2016

ADAMTS13 meets MR, then what? ⬇️

artículo científico publicado el 19 de abril de 2012

ADAMTS13 test and/or PLASMIC clinical score in management of acquired thrombotic thrombocytopenic purpura: a cost-effective analysis.

artículo científico publicado en 2017

ADAMTS13 testing: why bother?

artículo científico publicado en 2010

ADAMTS13, TTP and Beyond

artículo científico publicado en 2013

ADAMTS13, lucky to have a hydrophobic pocket

artículo científico publicado en 2015

Acquired autoimmune thrombotic thrombocytopenic purpura in a case of severe haemophilia A.

artículo científico publicado en 2016

Activation of Thrombin-activable Fibrinolysis Inhibitor Requires Epidermal Growth Factor-like Domain 3 of Thrombomodulin and Is Inhibited Competitively by Protein C ⬇️

artículo científico publicado el 15 de mayo de 1998

Amino acid residues Arg(659), Arg(660), and Tyr(661) in the spacer domain of ADAMTS13 are critical for cleavage of von Willebrand factor.

artículo científico publicado en 2010

An evaluation of cyclosporine alone for the treatment of early recurrences of thombotic thrombocytopenic purpura

artículo científico publicado en 2006

Analysis of morphology of platelet aggregates formed on collagen under laminar blood flow

artículo científico publicado en 2010

Anti-ADAMTS13 IgG autoantibodies present in healthy individuals share linear epitopes with those in patients with thrombotic thrombocytopenic purpura.

artículo científico publicado en 2014

Antigen and substrate withdrawal in the management of autoimmune thrombotic disorders.

artículo científico publicado en 2012

Apical sorting of bovine enteropeptidase does not involve detergent-resistant association with sphingolipid-cholesterol rafts.

artículo científico publicado en 1999

Apolipoprotein B100/Low-Density Lipoprotein Regulates Proteolysis and Functions of von Willebrand Factor under Arterial Shear

scientific article published on 07 September 2019

Arsenic trioxide induces apoptosis in B-cell chronic lymphocytic leukemic cells through down-regulation of survivin via the p53-dependent signaling pathway.

artículo científico publicado en 2013

Binding of platelet glycoprotein Ibalpha to von Willebrand factor domain A1 stimulates the cleavage of the adjacent domain A2 by ADAMTS13.

artículo científico publicado en 2004

Biochemistry and physiological functions of ADAMTS7 metalloprotease

scientific article published on January 2013

Bovine proenteropeptidase is activated by trypsin, and the specificity of enteropeptidase depends on the heavy chain

artículo científico publicado en 1997

Carboxyl terminus of ADAMTS13 directly inhibits platelet aggregation and ultra large von Willebrand factor string formation under flow in a free-thiol-dependent manner

artículo científico publicado en 2013

Cleavage of the ADAMTS13 Propeptide Is Not Required for Protease Activity

artículo científico publicado en 2003

Cleavage of von Willebrand factor requires the spacer domain of the metalloprotease ADAMTS13.

artículo científico publicado en 2003

Compromised shear-dependent cleavage of type 2N von Willebrand factor variants by ADAMTS13 in the presence of factor VIII.

artículo científico publicado en 2013

Conformational quiescence of ADAMTS-13 prevents proteolytic promiscuity: comment.

artículo científico publicado en 2017

Current status in diagnosis and treatment of hereditary thrombotic thrombocytopenic purpura.

artículo científico publicado en 2014

DNase, ADAMTS13, and iPAD4: good for the heart.

artículo científico publicado en 2014

Effect of plasma exchange on plasma ADAMTS13 metalloprotease activity, inhibitor level, and clinical outcome in patients with idiopathic and nonidiopathic thrombotic thrombocytopenic purpura.

artículo científico publicado en 2004

Effect of protein C inhibitor (PCI) on in vitro fertilization

artículo científico publicado en 1996

Endometrial hyperplasia and apoptosis following neonatal diethylstilbestrol exposure and subsequent estrogen stimulation in both host and transplanted hamster uteri

scientific article published on 01 May 1997

Enteropeptidase, a type II transmembrane serine protease.

artículo científico publicado en 2009

Essential domains of a disintegrin and metalloprotease with thrombospondin type 1 repeats-13 metalloprotease required for modulation of arterial thrombosis.

artículo científico

Exome Sequencing Identifies Abnormalities in Glycosylation and ANKRD36C in Patients with Immune-Mediated Thrombotic Thrombocytopenic Purpura

artículo científico publicado en 2020

Exploiting the kinetic interplay between GPIbα-VWF binding interfaces to regulate hemostasis and thrombosis

artículo científico publicado en 2014

Expression of ADAMTS13 in Normal and Abnormal Placentae and Its Potential Role in Angiogenesis and Placenta Development.

artículo científico publicado en 2017

Factor VIII binding affects the mechanical unraveling of the A2 domain of von Willebrand factor

artículo científico publicado en 2020

Gain-of-function ADAMTS13 variants that are resistant to autoantibodies against ADAMTS13 in patients with acquired thrombotic thrombocytopenic purpura.

artículo científico publicado en 2012

Genetic ablation of Adamts13 gene dramatically accelerates the formation of early atherosclerosis in a murine model.

artículo científico publicado en 2012

Good practice statements (GPS) for the clinical care of patients with thrombotic thrombocytopenic purpura

scientific article published on 04 August 2020

High-resolution epitope mapping by HX MS reveals the pathogenic mechanism and a possible therapy for autoimmune TTP syndrome.

artículo científico publicado en 2015

Human neutrophil peptides and complement factor Bb in pathogenesis of acquired thrombotic thrombocytopenic purpura

artículo científico publicado en 2016

Human neutrophil peptides inhibit cleavage of von Willebrand factor by ADAMTS13: a potential link of inflammation to TTP.

artículo científico publicado en 2016

ISTH guidelines for the diagnosis of thrombotic thrombocytopenic purpura

scientific article published on 17 July 2020

ISTH guidelines for treatment of thrombotic thrombocytopenic purpura

scientific article published on 15 July 2020

Identification of cysteine thiol-based linkages in ADAMTS13 in support of a non-proteolytic regulation of von Willebrand factor

scientific article published on 03 September 2019

Incomplete embryonic lethality and fatal neonatal hemorrhage caused by prothrombin deficiency in mice

artículo científico publicado en 1998

Inhibition of acrosin by protein C inhibitor and localization of protein C inhibitor to spermatozoa ⬇️

artículo científico publicado el 1 de agosto de 1994

Interlaboratory agreement in the monitoring of unfractionated heparin using the anti-factor Xa-correlated activated partial thromboplastin time.

artículo científico publicado en 2008

Knockout of Adamts7, a novel coronary artery disease locus in humans, reduces atherosclerosis in mice

artículo científico publicado en 2015

Leukocyte proteases cleave von Willebrand factor at or near the ADAMTS13 cleavage site

artículo científico publicado en 2009

Light Chain of Factor VIII Is Sufficient for Accelerating Cleavage of von Willebrand Factor by ADAMTS13 Metalloprotease ⬇️

artículo científico publicado el 21 de septiembre de 2012

Longitudinal assessments of plasma ADAMTS13 biomarkers predict recurrence of immune thrombotic thrombocytopenic purpura

scientific article published on 01 December 2019

Low Plasma ADAMTS13 Activity Is Associated with Coagulopathy, Endothelial Cell Damage and Mortality after Severe Paediatric Trauma.

artículo científico publicado en 2018

Management of chronic myeloid leukemia in the setting of pregnancy: when is leukocytapheresis appropriate? A case report and review of the literature.

artículo científico publicado en 2017

Multiple domains of ADAMTS13 are targeted by autoantibodies against ADAMTS13 in patients with acquired idiopathic thrombotic thrombocytopenic purpura

artículo científico publicado en 2010

Murine systemic thrombophilia and hemolytic uremic syndrome from a factor H point mutation.

artículo científico publicado en 2017

Mutations in Coagulation Factor VIII Are Associated with More Favorable Outcome in Patients with Cutaneous Melanoma

artículo científico publicado en 2017

Neonatal diethylstilbestrol treatment alters the estrogen-regulated expression of both cell proliferation and apoptosis-related proto-oncogenes (c-jun, c-fos, c-myc, bax, bcl-2, and bcl-x) in the hamster uterus

scientific article published on 01 April 1997

Novel factor VIII variants with a modified furin cleavage site improve the efficacy of gene therapy for hemophilia A.

scientific article published on 17 October 2016

Novel recombinant glycosylphosphatidylinositol (GPI)-anchored ADAMTS13 and variants for assessment of anti-ADAMTS13 autoantibodies in patients with thrombotic thrombocytopenic purpura ⬇️

artículo científico publicado el 8 de septiembre de 2011

Plasma ADAMTS13 activity and von Willebrand factor antigen and activity in patients with subarachnoid haemorrhage.

artículo científico publicado en 2017

Plasma levels of S100A8/A9, histone/DNA complexes, and cell-free DNA predict adverse outcomes of immune thrombotic thrombocytopenic purpura

artículo científico publicado en 2020

Plasma levels of complement activation fragments C3b and sC5b-9 significantly increased in patients with thrombotic microangiopathy after allogeneic stem cell transplantation

artículo científico publicado en 2017

Platelet transactivation by monocytes promotes thrombosis in heparin-induced thrombocytopenia

artículo científico publicado en 2015

Platelet-delivered ADAMTS13 inhibits arterial thrombosis and prevents thrombotic thrombocytopenic purpura in murine models.

artículo científico publicado en 2015

Protein C inhibitor (PCI)

artículo científico publicado en 1996

Structure of murine enterokinase (enteropeptidase) and expression in small intestine during development ⬇️

artículo científico publicado el 1 de febrero de 1998

Synergistic effects of ADAMTS13 deficiency and complement activation in pathogenesis of thrombotic microangiopathy

scientific article published on 13 August 2019

The proximal carboxyl-terminal domains of ADAMTS13 determine substrate specificity and are all required for cleavage of von Willebrand factor.

artículo científico publicado en 2005

Thromboelastography of patients after fontan compared with healthy children.

artículo científico publicado en 2009

Thrombotic Thrombocytopenic Purpura: Pathogenesis, Diagnosis, and Potential Novel Therapeutics

artículo científico publicado en 2017

Ticlopidine-, clopidogrel-, and prasugrel-associated thrombotic thrombocytopenic purpura: a 20-year review from the Southern Network on Adverse Reactions (SONAR).

artículo científico publicado en 2012

Ticlopidine-associated ADAMTS13 activity deficient thrombotic thrombocytopenic purpura in 22 persons in Japan: a report from the Southern Network on Adverse Reactions (SONAR).

artículo científico publicado en 2013

Unconjugated bilirubin inhibits proteolytic cleavage of von Willebrand factor by ADAMTS13 protease.

artículo científico publicado en 2015

Understanding thrombotic microangiopathies in children

artículo científico publicado en 2018

[Research advances on ADAM28 expression and ADAM28-mediated tumor metastasis]

artículo científico publicado en 2014

von Willebrand factor cleaved from endothelial cells by ADAMTS13 remains ultralarge in size.

artículo científico publicado en 2009

Lista de obras de X. Long Zheng

A novel association of acquired ADAMTS13 inhibitor and acute dengue virus infection

A team player: the disintegrin domain of ADAMTS13

AAV-mediated expression of an ADAMTS13 variant prevents shigatoxin-induced thrombotic thrombocytopenic purpura ⬇️

ADAMTS13 and TTP

ADAMTS13 and von Willebrand factor in thrombotic thrombocytopenic purpura

ADAMTS13 and von Willebrand factor interactions

ADAMTS13 autoantibodies cloned from patients with acquired thrombotic thrombocytopenic purpura: 1. Structural and functional characterization in vitro

ADAMTS13 autoantibodies cloned from patients with acquired thrombotic thrombocytopenic purpura: 2. Pathogenicity in an animal model

ADAMTS13 meets MR, then what? ⬇️

ADAMTS13 test and/or PLASMIC clinical score in management of acquired thrombotic thrombocytopenic purpura: a cost-effective analysis.

ADAMTS13 testing: why bother?

ADAMTS13, TTP and Beyond

ADAMTS13, lucky to have a hydrophobic pocket

Acquired autoimmune thrombotic thrombocytopenic purpura in a case of severe haemophilia A.

Activation of Thrombin-activable Fibrinolysis Inhibitor Requires Epidermal Growth Factor-like Domain 3 of Thrombomodulin and Is Inhibited Competitively by Protein C ⬇️

Amino acid residues Arg(659), Arg(660), and Tyr(661) in the spacer domain of ADAMTS13 are critical for cleavage of von Willebrand factor.

An evaluation of cyclosporine alone for the treatment of early recurrences of thombotic thrombocytopenic purpura

Analysis of morphology of platelet aggregates formed on collagen under laminar blood flow

Anti-ADAMTS13 IgG autoantibodies present in healthy individuals share linear epitopes with those in patients with thrombotic thrombocytopenic purpura.

Antigen and substrate withdrawal in the management of autoimmune thrombotic disorders.

Apical sorting of bovine enteropeptidase does not involve detergent-resistant association with sphingolipid-cholesterol rafts.

Apolipoprotein B100/Low-Density Lipoprotein Regulates Proteolysis and Functions of von Willebrand Factor under Arterial Shear

Arsenic trioxide induces apoptosis in B-cell chronic lymphocytic leukemic cells through down-regulation of survivin via the p53-dependent signaling pathway.

Binding of platelet glycoprotein Ibalpha to von Willebrand factor domain A1 stimulates the cleavage of the adjacent domain A2 by ADAMTS13.

Biochemistry and physiological functions of ADAMTS7 metalloprotease

Bovine proenteropeptidase is activated by trypsin, and the specificity of enteropeptidase depends on the heavy chain

Carboxyl terminus of ADAMTS13 directly inhibits platelet aggregation and ultra large von Willebrand factor string formation under flow in a free-thiol-dependent manner

Cleavage of the ADAMTS13 Propeptide Is Not Required for Protease Activity

Cleavage of von Willebrand factor requires the spacer domain of the metalloprotease ADAMTS13.

Compromised shear-dependent cleavage of type 2N von Willebrand factor variants by ADAMTS13 in the presence of factor VIII.

Conformational quiescence of ADAMTS-13 prevents proteolytic promiscuity: comment.

Current status in diagnosis and treatment of hereditary thrombotic thrombocytopenic purpura.

DNase, ADAMTS13, and iPAD4: good for the heart.

Effect of plasma exchange on plasma ADAMTS13 metalloprotease activity, inhibitor level, and clinical outcome in patients with idiopathic and nonidiopathic thrombotic thrombocytopenic purpura.

Effect of protein C inhibitor (PCI) on in vitro fertilization

Endometrial hyperplasia and apoptosis following neonatal diethylstilbestrol exposure and subsequent estrogen stimulation in both host and transplanted hamster uteri

Enteropeptidase, a type II transmembrane serine protease.

Essential domains of a disintegrin and metalloprotease with thrombospondin type 1 repeats-13 metalloprotease required for modulation of arterial thrombosis.

Exome Sequencing Identifies Abnormalities in Glycosylation and ANKRD36C in Patients with Immune-Mediated Thrombotic Thrombocytopenic Purpura

Exploiting the kinetic interplay between GPIbα-VWF binding interfaces to regulate hemostasis and thrombosis

Expression of ADAMTS13 in Normal and Abnormal Placentae and Its Potential Role in Angiogenesis and Placenta Development.

Factor VIII binding affects the mechanical unraveling of the A2 domain of von Willebrand factor

Gain-of-function ADAMTS13 variants that are resistant to autoantibodies against ADAMTS13 in patients with acquired thrombotic thrombocytopenic purpura.

Genetic ablation of Adamts13 gene dramatically accelerates the formation of early atherosclerosis in a murine model.

Good practice statements (GPS) for the clinical care of patients with thrombotic thrombocytopenic purpura

High-resolution epitope mapping by HX MS reveals the pathogenic mechanism and a possible therapy for autoimmune TTP syndrome.

Human neutrophil peptides and complement factor Bb in pathogenesis of acquired thrombotic thrombocytopenic purpura

Human neutrophil peptides inhibit cleavage of von Willebrand factor by ADAMTS13: a potential link of inflammation to TTP.

ISTH guidelines for the diagnosis of thrombotic thrombocytopenic purpura

ISTH guidelines for treatment of thrombotic thrombocytopenic purpura

Identification of cysteine thiol-based linkages in ADAMTS13 in support of a non-proteolytic regulation of von Willebrand factor

Incomplete embryonic lethality and fatal neonatal hemorrhage caused by prothrombin deficiency in mice

Inhibition of acrosin by protein C inhibitor and localization of protein C inhibitor to spermatozoa ⬇️

Interlaboratory agreement in the monitoring of unfractionated heparin using the anti-factor Xa-correlated activated partial thromboplastin time.

Knockout of Adamts7, a novel coronary artery disease locus in humans, reduces atherosclerosis in mice

Leukocyte proteases cleave von Willebrand factor at or near the ADAMTS13 cleavage site

Light Chain of Factor VIII Is Sufficient for Accelerating Cleavage of von Willebrand Factor by ADAMTS13 Metalloprotease ⬇️

Longitudinal assessments of plasma ADAMTS13 biomarkers predict recurrence of immune thrombotic thrombocytopenic purpura

Low Plasma ADAMTS13 Activity Is Associated with Coagulopathy, Endothelial Cell Damage and Mortality after Severe Paediatric Trauma.

Management of chronic myeloid leukemia in the setting of pregnancy: when is leukocytapheresis appropriate? A case report and review of the literature.

Multiple domains of ADAMTS13 are targeted by autoantibodies against ADAMTS13 in patients with acquired idiopathic thrombotic thrombocytopenic purpura

Murine systemic thrombophilia and hemolytic uremic syndrome from a factor H point mutation.

Mutations in Coagulation Factor VIII Are Associated with More Favorable Outcome in Patients with Cutaneous Melanoma

Neonatal diethylstilbestrol treatment alters the estrogen-regulated expression of both cell proliferation and apoptosis-related proto-oncogenes (c-jun, c-fos, c-myc, bax, bcl-2, and bcl-x) in the hamster uterus

Novel factor VIII variants with a modified furin cleavage site improve the efficacy of gene therapy for hemophilia A.

Novel recombinant glycosylphosphatidylinositol (GPI)-anchored ADAMTS13 and variants for assessment of anti-ADAMTS13 autoantibodies in patients with thrombotic thrombocytopenic purpura ⬇️

Plasma ADAMTS13 activity and von Willebrand factor antigen and activity in patients with subarachnoid haemorrhage.

Plasma levels of S100A8/A9, histone/DNA complexes, and cell-free DNA predict adverse outcomes of immune thrombotic thrombocytopenic purpura

Plasma levels of complement activation fragments C3b and sC5b-9 significantly increased in patients with thrombotic microangiopathy after allogeneic stem cell transplantation

Platelet transactivation by monocytes promotes thrombosis in heparin-induced thrombocytopenia

Platelet-delivered ADAMTS13 inhibits arterial thrombosis and prevents thrombotic thrombocytopenic purpura in murine models.

Protein C inhibitor (PCI)

Structure of murine enterokinase (enteropeptidase) and expression in small intestine during development ⬇️

Synergistic effects of ADAMTS13 deficiency and complement activation in pathogenesis of thrombotic microangiopathy

The proximal carboxyl-terminal domains of ADAMTS13 determine substrate specificity and are all required for cleavage of von Willebrand factor.

Thromboelastography of patients after fontan compared with healthy children.

Thrombotic Thrombocytopenic Purpura: Pathogenesis, Diagnosis, and Potential Novel Therapeutics

Ticlopidine-, clopidogrel-, and prasugrel-associated thrombotic thrombocytopenic purpura: a 20-year review from the Southern Network on Adverse Reactions (SONAR).

Ticlopidine-associated ADAMTS13 activity deficient thrombotic thrombocytopenic purpura in 22 persons in Japan: a report from the Southern Network on Adverse Reactions (SONAR).