Lista de obras - Thierry Peyrard - Dominio Público Uruguay

A functional AQP1 allele producing a Co(a-b-) phenotype revises and extends the Colton blood group system.

artículo científico publicado en 2010

A new AQP1 null allele identified in a Gypsy woman who developed an anti‐CO3 during her first pregnancy ⬇️

artículo científico publicado el 20 de febrero de 2012

A novel GYPB-A-B hybrid gene responsible for Ss and MN typing discrepancies.

artículo científico publicado en 2015

A review of the Colton blood group system.

artículo científico publicado en 2010

ABCB6 is dispensable for erythropoiesis and specifies the new blood group system Langereis

artículo científico publicado en 2012

Acute hemolytic transfusion reaction associated with anti-Mta : case report and review of the literature

scientific article published on 10 September 2019

Alloanti-c/ce in a c+ceAR/Ce patient suggests that the rare RHCE ceAR allele (ceAR) encodes a partial c antigen.

artículo científico publicado en 2009

Analysis of RhCE variants among 806 individuals in France: considerations for transfusion safety, with emphasis on patients with sickle cell disease ⬇️

artículo científico publicado el 16 de diciembre de 2010

Analysis of complement receptor type 1 expression on red blood cells in negative phenotypes of the Knops blood group system, according to CR1 gene allotype polymorphisms.

artículo científico publicado en 2010

Anti-D investigations in individuals expressing weak D Type 1 or weak D Type 2: allo- or autoantibodies?

artículo científico publicado en 2011

Anti-HI can cause a severe delayed hemolytic transfusion reaction with hyperhemolysis in sickle cell disease patients

artículo científico publicado en 2016

Anti-HrB and anti-hrb revisited

artículo científico publicado en 2009

Anti‐U‐like as an alloantibody in S−s−U− and S−s−U+var black people ⬇️

artículo científico publicado el 31 de agosto de 2011

Band 3 phosphorylation induces irreversible alterations of stored red blood cells.

artículo científico publicado en 2018

Banking of pluripotent adult stem cells as an unlimited source for red blood cell production: potential applications for alloimmunized patients and rare blood challenges.

artículo científico publicado en 2011

CORS (CROM20): A new high-prevalence antigen in the Cromer blood group system

artículo científico publicado en 2020

Characterization of a new human monoclonal antibody directed against the Vel antigen.

artículo científico publicado en 2015

Difficulties of the care of public antigen alloimmunization

artículo científico publicado en 2016

Disruption of SMIM1 causes the Vel- blood type.

artículo científico publicado en 2013

Donors with a rare pheno (geno) type

artículo científico publicado en 2008

Enhanced calreticulin expression in red cells of polycythemia vera patients harboring the JAK2V617F mutation.

artículo científico publicado en 2017

Family study of a Swiss patient uncovered a novel genetic basis for the S-s-U+(var) phenotype.

artículo científico publicado en 2014

Fatal hemolytic disease of the fetus and newborn associated with anti-Jr.

artículo científico publicado en 2008

Gene conversion events between GYPB and GYPE abolish expression of the S and s blood group antigens

artículo científico publicado en 2015

Genetic background of the rare Yus and Gerbich blood group phenotypes: homologous regions of the GYPC gene contribute to deletion alleles.

artículo científico publicado en 2017

High immunogenicity of red blood cell antigens restricted to the population of African descent in a cohort of sickle cell disease patients

scientific article published on 29 April 2018

Identification of the Molecular and Genetic Basis of PX2, a Glycosphingolipid Blood Group Antigen Lacking on Globoside-deficient Erythrocytes.

artículo científico publicado en 2015

Impact of hydroxycarbamide and interferon-α on red cell adhesion and membrane protein expression in polycythemia vera.

artículo científico publicado en 2018

Lack of the human choline transporter‐like protein <scp>SLC44A2</scp> causes hearing impairment and a rare red blood phenotype

artículo científico publicado en 2023

Lack of the nucleoside transporter ENT1 results in the Augustine-null blood type and ectopic mineralization

artículo científico publicado en 2015

Large deletions involving the regulatory upstream regions of A4GALT give rise to principally novel P1PK-null alleles.

artículo científico publicado en 2014

Live Brucella spp. fail to induce tumor necrosis factor alpha excretion upon infection of U937-derived phagocytes.

artículo científico publicado en 1994

Management of a pregnant woman with anti-holley alloantibody

artículo científico publicado en 2015

Management of the blood supply for a Jk(a-b-) patient with an anti-Jk3 in preparation for an urgent heart transplant: An illustrative example of a successful international cooperation

artículo científico publicado en 2018

Null alleles of ABCG2 encoding the breast cancer resistance protein define the new blood group system Junior

artículo científico publicado en 2012

Prevalence and risk factors for red blood cell alloimmunization in 175 children with sickle cell disease in a French university hospital reference centre

artículo científico publicado en 2017

Proof of principle for transfusion of in vitro-generated red blood cells.

artículo científico publicado en 2011

RHDDOL1 and RHDDOL2 encode a partial D antigen and are in cis with the rare RHCE*ceBI allele in people of African descent

artículo científico publicado en 2012

Severe autoimmune hemolytic anemia in a liver transplanted child

artículo científico publicado en 2008

Severe hemolytic disease of the fetus and the newborn associated with anti-Vw (Vw)

artículo científico publicado en 2010

Short duplication within the RHCE gene associated with an in cis deleted RHD causing a Rhnull amorph phenotype in an immunized pregnant woman with anti-Rh29.

artículo científico publicado en 2014

Structural Basis for the ABO Blood-Group Dependence of Plasmodium falciparum Rosetting

artículo científico publicado en 2012

The French national rare blood program

artículo científico publicado en 2016

The Gerbich blood group system: old knowledge, new importance.

artículo científico publicado en 2018

The LAN blood group system:a review

artículo científico

The Vel blood group system: a review

artículo científico publicado en 2017

The rare blood groups: a public health challenge

artículo científico publicado en 2008

Transfusion of rare cryopreserved red blood cell units stored at -80 degrees C: the French experience.

artículo científico publicado en 2009

Transfusion-associated hazards: A revisit of their presentation

artículo científico publicado en 2018

Weak A phenotypes associated with novel ABO alleles carrying the A2-related 1061C deletion and various missense substitutions.

artículo científico publicado en 2010

[A KEL*02mod allele responsible for an apparent maternity exclusion]

artículo científico publicado en 2013

[Genotyping of blood group systems at the CNRGS. I: FY, JK, MNS systems]

scientific article published on 21 April 2009

[Quality control of labile blood products. Why and howto properly take a specimen? Labile Blood Products Group of the French Blood Transfusion Society]

scientific article published on 01 December 1999

[Transfusion safety, time for a new partnership between stake-holders]

artículo científico publicado en 2006

Lista de obras de Thierry Peyrard

A functional AQP1 allele producing a Co(a-b-) phenotype revises and extends the Colton blood group system.

A new AQP1 null allele identified in a Gypsy woman who developed an anti‐CO3 during her first pregnancy ⬇️

A novel GYPB-A-B hybrid gene responsible for Ss and MN typing discrepancies.

A review of the Colton blood group system.

ABCB6 is dispensable for erythropoiesis and specifies the new blood group system Langereis

Acute hemolytic transfusion reaction associated with anti-Mta : case report and review of the literature

Alloanti-c/ce in a c+ceAR/Ce patient suggests that the rare RHCE ceAR allele (ceAR) encodes a partial c antigen.

Analysis of RhCE variants among 806 individuals in France: considerations for transfusion safety, with emphasis on patients with sickle cell disease ⬇️

Analysis of complement receptor type 1 expression on red blood cells in negative phenotypes of the Knops blood group system, according to CR1 gene allotype polymorphisms.

Anti-D investigations in individuals expressing weak D Type 1 or weak D Type 2: allo- or autoantibodies?

Anti-HI can cause a severe delayed hemolytic transfusion reaction with hyperhemolysis in sickle cell disease patients

Anti-HrB and anti-hrb revisited

Anti‐U‐like as an alloantibody in S−s−U− and S−s−U+var black people ⬇️

Band 3 phosphorylation induces irreversible alterations of stored red blood cells.

Banking of pluripotent adult stem cells as an unlimited source for red blood cell production: potential applications for alloimmunized patients and rare blood challenges.

CORS (CROM20): A new high-prevalence antigen in the Cromer blood group system

Characterization of a new human monoclonal antibody directed against the Vel antigen.

Difficulties of the care of public antigen alloimmunization

Disruption of SMIM1 causes the Vel- blood type.

Donors with a rare pheno (geno) type

Enhanced calreticulin expression in red cells of polycythemia vera patients harboring the JAK2V617F mutation.

Family study of a Swiss patient uncovered a novel genetic basis for the S-s-U+(var) phenotype.

Fatal hemolytic disease of the fetus and newborn associated with anti-Jr.

Gene conversion events between GYPB and GYPE abolish expression of the S and s blood group antigens

Genetic background of the rare Yus and Gerbich blood group phenotypes: homologous regions of the GYPC gene contribute to deletion alleles.

High immunogenicity of red blood cell antigens restricted to the population of African descent in a cohort of sickle cell disease patients

Identification of the Molecular and Genetic Basis of PX2, a Glycosphingolipid Blood Group Antigen Lacking on Globoside-deficient Erythrocytes.

Impact of hydroxycarbamide and interferon-α on red cell adhesion and membrane protein expression in polycythemia vera.

Lack of the human choline transporter‐like protein <scp>SLC44A2</scp> causes hearing impairment and a rare red blood phenotype

Lack of the nucleoside transporter ENT1 results in the Augustine-null blood type and ectopic mineralization

Large deletions involving the regulatory upstream regions of A4GALT give rise to principally novel P1PK-null alleles.

Live Brucella spp. fail to induce tumor necrosis factor alpha excretion upon infection of U937-derived phagocytes.

Management of a pregnant woman with anti-holley alloantibody

Management of the blood supply for a Jk(a-b-) patient with an anti-Jk3 in preparation for an urgent heart transplant: An illustrative example of a successful international cooperation

Null alleles of ABCG2 encoding the breast cancer resistance protein define the new blood group system Junior

Prevalence and risk factors for red blood cell alloimmunization in 175 children with sickle cell disease in a French university hospital reference centre

Proof of principle for transfusion of in vitro-generated red blood cells.

RHD*DOL1 and RHD*DOL2 encode a partial D antigen and are in cis with the rare RHCE*ceBI allele in people of African descent

Severe autoimmune hemolytic anemia in a liver transplanted child

Severe hemolytic disease of the fetus and the newborn associated with anti-Vw (Vw)

Short duplication within the RHCE gene associated with an in cis deleted RHD causing a Rhnull amorph phenotype in an immunized pregnant woman with anti-Rh29.

Structural Basis for the ABO Blood-Group Dependence of Plasmodium falciparum Rosetting

The French national rare blood program

The Gerbich blood group system: old knowledge, new importance.

The LAN blood group system:a review

The Vel blood group system: a review

The rare blood groups: a public health challenge

Transfusion of rare cryopreserved red blood cell units stored at -80 degrees C: the French experience.

Transfusion-associated hazards: A revisit of their presentation

Weak A phenotypes associated with novel ABO alleles carrying the A2-related 1061C deletion and various missense substitutions.

[A KEL*02mod allele responsible for an apparent maternity exclusion]

[Genotyping of blood group systems at the CNRGS. I: FY, JK, MNS systems]

[Quality control of labile blood products. Why and howto properly take a specimen? Labile Blood Products Group of the French Blood Transfusion Society]

[Transfusion safety, time for a new partnership between stake-holders]

RHDDOL1 and RHDDOL2 encode a partial D antigen and are in cis with the rare RHCE*ceBI allele in people of African descent