Lista de obras - Dominique Meyer - Dominio Público Uruguay

A Taq I polymorphism in the 5' region of the von Willebrand factor (vWF) gene

artículo científico publicado en 1988

A monoclonal antibody (B724) to von Willebrand factor recognizing an epitope within the A1 disulphide loop (Cys509-Cys695) discriminates between type 2A and type 2B von Willebrand disease

artículo científico publicado en 1995

A novel case of compound heterozygosity with "Normandy"/type I von Willebrand disease (vWD). Direct demonstration of the segregation of one allele with a defective expression at the mRNA level causing type I vWD.

artículo científico

A simple and efficient method for isolating high molecular weight DNA from mammalian sperm

artículo científico publicado en 1988

Abnormal von Willebrand factor in bleeding angiodysplasias of the digestive tract

artículo científico publicado en 2001

Acquired von Willebrand syndrome: data from an international registry.

artículo científico publicado en 2000

Analysis of von Willebrand factor mRNA from the lung of pigs with severe von Willebrand disease by using a human cDNA probe

artículo científico publicado en 1988

Aplastic anemia presenting as spontaneous orbital hemorrhage

artículo científico publicado en 2008

Assessment of the expression of candidate human plasma membrane phospholipid scramblase in Scott syndrome cells

artículo científico publicado en 1999

Carbon monoxide exposure in the urban environment: an insidious foe for the heart?

artículo científico publicado en 2012

Carbon monoxide pollution impairs myocardial perfusion reserve: implication of coronary endothelial dysfunction.

artículo científico publicado en 2011

Characterization of recombinant von Willebrand factors mutated on cysteine 509 or 695.

artículo científico publicado en 1996

Comparison of FRETS-VWF73 to full-length VWF as a substrate for ADAMTS13 activity measurement in human plasma samples

artículo científico publicado en 2006

Comparison of the 5'-flanking sequences of the human and bovine von Willebrand factor-encoding genes reveals alternation of highly homologous domains with species-specific Alu-type repeats

artículo científico publicado en 1995

Comparison of the primary structure of the functional domains of human and porcine von Willebrand factor that mediate platelet adhesion

artículo científico publicado el 31 de enero de 1992

Cyclic adenosine monophosphate-dependent mechanisms induce von Willebrand factor expression in the Dami megakaryoblastic cell line.

artículo científico publicado en 1995

Estimation of the von Willebrand factor-cleaving protease in plasma using monoclonal antibodies to vWF.

artículo científico publicado en 1999

Ets transcription factors bind and transactivate the core promoter of the von Willebrand factor gene.

artículo científico publicado en 1997

Evidence that a secondary binding and protecting site for factor VIII on von Willebrand factor is highly unlikely

artículo científico publicado en 1992

Exercise-induced cardioprotection: a role for eNOS uncoupling and NO metabolites.

artículo científico publicado en 2013

Expression of two type 2N von Willebrand disease mutations identified in exon 18 of von Willebrand factor gene

artículo científico publicado en 2004

Factor VIII and IX Variants. Relationship between Haemophilia BM and Haemophilia B+ ⬇️

artículo científico publicado el 1 de septiembre de 1971

Functional characterization of bovine von Willebrand factor gene promoter in bovine endothelial cells demonstrates species-specific properties.

artículo científico publicado en 1997

Generation of von Willebrand factor epitope libraries expressed in E. coli

artículo científico publicado en 2002

Heterogeneity of von Willebrand's disease: study of 40 Iranian cases

artículo científico publicado el 1 de septiembre de 1977

Identification of a CpG mutation in the coagulation factor-IX gene by analysis of amplified DNA sequences

artículo científico publicado en 1988

Identification of the regulatory elements of the human von Willebrand factor for binding to platelet GPIb. Importance of structural integrity of the regions flanked by the CYS1272-CYS1458 disulfide bond

artículo científico publicado en 2002

Identification of type 1 von Willebrand disease patients with reduced von Willebrand factor survival by assay of the VWF propeptide in the European study: molecular and clinical markers for the diagnosis and management of type 1 VWD (MCMDM-1VWD).

artículo científico publicado en 2008

Impaired megakaryocytopoiesis in type 2B von Willebrand disease with severe thrombocytopenia

artículo científico publicado en 2006

Influence of high ionic strength buffers on factor VIII/von Willebrand factor from different species ⬇️

artículo científico publicado el 1 de septiembre de 1978

Influence of mutations and size of multimers in type II von Willebrand disease upon the function of von Willebrand factor.

artículo científico publicado en 1994

Moderate exercise prevents impaired Ca2+ handling in heart of CO-exposed rat: implication for sensitivity to ischemia-reperfusion

artículo científico publicado en 2010

Molecular genetics of type 2 von Willebrand disease

artículo científico publicado en 2002

Mutations C1157F and C1234W of von Willebrand factor cause intracellular retention with defective multimerization and secretion

artículo científico publicado en 2006

Oct-1 is involved in the transcriptional repression of the von willebrand factor gene promoter.

artículo científico publicado en 1998

Optimization of the transfection of human endothelial cells by electroporation

artículo científico publicado en 1994

Platelet membrane glycoproteins implicated in ristocetin-induced aggregation. Studies of the proteins on platelets from patients with Bernard-Soulier syndrome and von Willebrand's disease ⬇️

artículo científico publicado el 1 de enero de 1976

Primary structure of the factor VIII binding domain of human, porcine and rabbit von Willebrand factor

artículo científico publicado en 1993

Primary structure of the propeptide and factor VIII-binding domain of bovine von Willebrand factor

artículo científico publicado en 1997

Prognostic value of anti-ADAMTS 13 antibody features (Ig isotype, titer, and inhibitory effect) in a cohort of 35 adult French patients undergoing a first episode of thrombotic microangiopathy with undetectable ADAMTS 13 activity

artículo científico publicado en 2007

Requirement of prestimulated THP-1 monocytic cells for endothelial cell activation. Involvement of TNF alpha

artículo científico publicado en 1997

Scott syndrome: an inherited defect of the procoagulant activity of platelets

artículo científico publicado en 1997

Ser968Thr mutation within the A3 domain of von Willebrand factor (VWF) in two related patients leads to a defective binding of VWF to collagen

artículo científico publicado en 2001

Severe deficiency of the specific von Willebrand factor-cleaving protease (ADAMTS 13) activity in a subgroup of children with atypical hemolytic uremic syndrome

artículo científico publicado en 2003

Simulated urban carbon monoxide air pollution exacerbates rat heart ischemia-reperfusion injury

artículo científico publicado en 2010

Specific von Willebrand factor-cleaving protease in thrombotic microangiopathies: a study of 111 cases

artículo científico publicado en 2001

Ten candidate ADAMTS13 mutations in six French families with congenital thrombotic thrombocytopenic purpura (Upshaw-Schulman syndrome).

artículo científico publicado en 2004

The human gene for von Willebrand factor. Identification of repetitive Alu sequences 5' to the transcription initiation site

artículo científico publicado en 1988

The role of the 5'-flanking region in the cell-specific transcription of the human von Willebrand factor gene

artículo científico publicado en 1993

Thrombotic thrombocytopenic purpura and its diagnosis

artículo científico publicado en 2005

Thrombotic thrombocytopenic purpura associated with von Willebrand factor-cleaving protease (ADAMTS13) deficiency in children

artículo científico publicado en 2006

Thrombotic thrombocytopenic purpura with severe ADAMTS-13 deficiency in two patients with primary antiphospholipid syndrome

artículo científico publicado en 2004

Update on the pathophysiology and classification of von Willebrand disease: a report of the Subcommittee on von Willebrand Factor

artículo científico publicado en 2006

von Willebrand factor fragments.

scientific article published on January 1991

von Willebrand factor: structure and function

artículo científico publicado en 1991

Lista de obras de Dominique Meyer

A Taq I polymorphism in the 5' region of the von Willebrand factor (vWF) gene

A monoclonal antibody (B724) to von Willebrand factor recognizing an epitope within the A1 disulphide loop (Cys509-Cys695) discriminates between type 2A and type 2B von Willebrand disease

A novel case of compound heterozygosity with "Normandy"/type I von Willebrand disease (vWD). Direct demonstration of the segregation of one allele with a defective expression at the mRNA level causing type I vWD.

A simple and efficient method for isolating high molecular weight DNA from mammalian sperm

Abnormal von Willebrand factor in bleeding angiodysplasias of the digestive tract

Acquired von Willebrand syndrome: data from an international registry.

Analysis of von Willebrand factor mRNA from the lung of pigs with severe von Willebrand disease by using a human cDNA probe

Aplastic anemia presenting as spontaneous orbital hemorrhage

Assessment of the expression of candidate human plasma membrane phospholipid scramblase in Scott syndrome cells

Carbon monoxide exposure in the urban environment: an insidious foe for the heart?

Carbon monoxide pollution impairs myocardial perfusion reserve: implication of coronary endothelial dysfunction.

Characterization of recombinant von Willebrand factors mutated on cysteine 509 or 695.

Comparison of FRETS-VWF73 to full-length VWF as a substrate for ADAMTS13 activity measurement in human plasma samples

Comparison of the 5'-flanking sequences of the human and bovine von Willebrand factor-encoding genes reveals alternation of highly homologous domains with species-specific Alu-type repeats

Comparison of the primary structure of the functional domains of human and porcine von Willebrand factor that mediate platelet adhesion

Cyclic adenosine monophosphate-dependent mechanisms induce von Willebrand factor expression in the Dami megakaryoblastic cell line.

Estimation of the von Willebrand factor-cleaving protease in plasma using monoclonal antibodies to vWF.

Ets transcription factors bind and transactivate the core promoter of the von Willebrand factor gene.

Evidence that a secondary binding and protecting site for factor VIII on von Willebrand factor is highly unlikely

Exercise-induced cardioprotection: a role for eNOS uncoupling and NO metabolites.

Expression of two type 2N von Willebrand disease mutations identified in exon 18 of von Willebrand factor gene

Factor VIII and IX Variants. Relationship between Haemophilia BM and Haemophilia B+ ⬇️

Functional characterization of bovine von Willebrand factor gene promoter in bovine endothelial cells demonstrates species-specific properties.

Generation of von Willebrand factor epitope libraries expressed in E. coli

Heterogeneity of von Willebrand's disease: study of 40 Iranian cases

Identification of a CpG mutation in the coagulation factor-IX gene by analysis of amplified DNA sequences

Identification of the regulatory elements of the human von Willebrand factor for binding to platelet GPIb. Importance of structural integrity of the regions flanked by the CYS1272-CYS1458 disulfide bond

Identification of type 1 von Willebrand disease patients with reduced von Willebrand factor survival by assay of the VWF propeptide in the European study: molecular and clinical markers for the diagnosis and management of type 1 VWD (MCMDM-1VWD).

Impaired megakaryocytopoiesis in type 2B von Willebrand disease with severe thrombocytopenia

Influence of high ionic strength buffers on factor VIII/von Willebrand factor from different species ⬇️

Influence of mutations and size of multimers in type II von Willebrand disease upon the function of von Willebrand factor.

Moderate exercise prevents impaired Ca2+ handling in heart of CO-exposed rat: implication for sensitivity to ischemia-reperfusion

Molecular genetics of type 2 von Willebrand disease

Mutations C1157F and C1234W of von Willebrand factor cause intracellular retention with defective multimerization and secretion

Oct-1 is involved in the transcriptional repression of the von willebrand factor gene promoter.

Optimization of the transfection of human endothelial cells by electroporation

Platelet membrane glycoproteins implicated in ristocetin-induced aggregation. Studies of the proteins on platelets from patients with Bernard-Soulier syndrome and von Willebrand's disease ⬇️

Primary structure of the factor VIII binding domain of human, porcine and rabbit von Willebrand factor

Primary structure of the propeptide and factor VIII-binding domain of bovine von Willebrand factor

Prognostic value of anti-ADAMTS 13 antibody features (Ig isotype, titer, and inhibitory effect) in a cohort of 35 adult French patients undergoing a first episode of thrombotic microangiopathy with undetectable ADAMTS 13 activity

Requirement of prestimulated THP-1 monocytic cells for endothelial cell activation. Involvement of TNF alpha

Scott syndrome: an inherited defect of the procoagulant activity of platelets

Ser968Thr mutation within the A3 domain of von Willebrand factor (VWF) in two related patients leads to a defective binding of VWF to collagen

Severe deficiency of the specific von Willebrand factor-cleaving protease (ADAMTS 13) activity in a subgroup of children with atypical hemolytic uremic syndrome

Simulated urban carbon monoxide air pollution exacerbates rat heart ischemia-reperfusion injury

Specific von Willebrand factor-cleaving protease in thrombotic microangiopathies: a study of 111 cases

Ten candidate ADAMTS13 mutations in six French families with congenital thrombotic thrombocytopenic purpura (Upshaw-Schulman syndrome).

The human gene for von Willebrand factor. Identification of repetitive Alu sequences 5' to the transcription initiation site

The role of the 5'-flanking region in the cell-specific transcription of the human von Willebrand factor gene

Thrombotic thrombocytopenic purpura and its diagnosis

Thrombotic thrombocytopenic purpura associated with von Willebrand factor-cleaving protease (ADAMTS13) deficiency in children

Thrombotic thrombocytopenic purpura with severe ADAMTS-13 deficiency in two patients with primary antiphospholipid syndrome

Update on the pathophysiology and classification of von Willebrand disease: a report of the Subcommittee on von Willebrand Factor

von Willebrand factor fragments.

von Willebrand factor: structure and function