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Molecular dynamics of the human RhD and RhAG blood group proteins.
Published in:
Frontiers in Chemistry, 2024, p. 01, doi. 10.3389/fchem.2024.1360392
By:
- Floch, Aline;
- Galochkina, Tatiana;
- Pirenne, France;
- Tournamille, Christophe;
- de Brevern, Alexandre G.;
- Lixue Cheng;
- Slipchenko, Lyudmila
Publication type:
Article
3D analysis of CROMER (DAF) and a new antigen CRAG.
Published in:
Blood Transfusion (17232007), 2022, v. 20, n. 6, p. 483, doi. 10.2450/2022.0285-21
By:
- Floch, Aline;
- Vege, Sunitha;
- Kim Hue-Roye;
- Hamilton, Jan R.;
- Williams, Lance A.;
- Choate, Jacquelyn;
- Lomas-Francis, Christine;
- Westhoff, Connie M.
Publication type:
Article
Genotyping in Sickle Cell Disease Patients: The French Strategy.
Published in:
Transfusion Medicine & Hemotherapy, 2018, v. 45, n. 4, p. 264, doi. 10.1159/000490858
By:
- Floch, aline;
- Tournamille, Christophe;
- Chami, Btissam;
- Pirenne, France
Publication type:
Article
Red blood cell alloimmunisation in sickle cell disease patients in the Democratic Republic of the Congo.
Published in:
Transfusion Medicine, 2023, v. 33, n. 2, p. 137, doi. 10.1111/tme.12939
By:
- Kambale‐Kombi, Paul;
- Djang'eing'a, Roland Marini;
- Alworong'a Opara, Jean‐Pierre;
- Minon, Jean‐Marc;
- Sepulchre, Edith;
- Bours, Vincent;
- Floch, Aline;
- Pirenne, France;
- Tshilumba, Charles Kayembe;
- Batina‐Agasa, Salomon
Publication type:
Article
Two novel variants that disrupt the RHCE start codon with varying effect on RhCE antigen expression.
Published in:
Transfusion, 2023, v. 63, n. 4, p. E12, doi. 10.1111/trf.17256
By:
- Vege, Sunitha;
- Floch, Aline;
- Burgos, Anna;
- Tahiri, Toufik;
- Kirkegaard, Julie;
- Dupont, Megan;
- Ochoa‐Garay, Gorka;
- Lomas‐Francis, Christine;
- Westhoff, Connie M.
Publication type:
Article
A novel high‐prevalence antigen in the Lutheran system, LUGA (LU24), and an updated, full‐length 3D BCAM model.
Published in:
Transfusion, 2023, v. 63, n. 4, p. 798, doi. 10.1111/trf.17262
By:
- Floch, Aline;
- Lomas‐Francis, Christine;
- Vege, Sunitha;
- Brennan, Steven;
- Shakarian, Gayane;
- de Brevern, Alexandre G.;
- Westhoff, Connie M.
Publication type:
Article
Two new Scianna variants causing loss of high prevalence antigens: ERMAP model and 3D analysis of the antigens.
Published in:
Transfusion, 2023, v. 63, n. 1, p. 230, doi. 10.1111/trf.17182
By:
- Floch, Aline;
- Lomas‐Francis, Christine;
- Vege, Sunitha;
- Burgos, Anna;
- Hoffman, Roser;
- Cusick, Robin;
- de Brevern, Alexandre G.;
- Westhoff, Connie M.
Publication type:
Article
Four novel ABO*AW alleles associated with weak antigen expression.
Published in:
Transfusion, 2022, v. 62, n. 12, p. E76, doi. 10.1111/trf.17167
By:
- Tahiri, Toufik;
- Vege, Sunitha;
- Floch, Aline;
- Lomas‐Francis, Christine;
- Ochoa‐Garay, Gorka;
- Westhoff, Connie M.
Publication type:
Article
A novel RHCE*Ce710A allele (p.237Asp) in a Japanese patient with weak expression of C and no detectable e.
Published in:
2022
By:
- Barrault, Aurélie;
- Floch, Aline;
- Pirenne, France;
- Tournamille, Christophe
Publication type:
journal article
Novel RHD allele with c.333C>G change predicted to encode p.Phe111Leu.
Published in:
2022
By:
- Alluin, Gauthier;
- Durieux‐Roussel, Elisabeth;
- Fayoux, Pierre;
- Pirenne, France;
- Tournamille, Christophe;
- Floch, Aline;
- Durieux-Roussel, Elisabeth
Publication type:
journal article
First report of a null allele on a GYPB*s background: GYPB*s(37 + 4_8delAGTGA).
Published in:
Transfusion, 2022, v. 62, n. 5, p. E24, doi. 10.1111/trf.16874
By:
- Thonier, Vincent Louis;
- Floch, Aline;
- Babinet, Jérome;
- Pirenne, France;
- Vege, Sunitha;
- Tournamille, Christophe;
- Westhoff, Connie M.;
- Peyrard, Thierry
Publication type:
Article
An intron c.149‐2632T>A change in RHD is associated with aberrant transcription and very weak D phenotype.
Published in:
Transfusion, 2022, v. 62, n. 2, p. E14, doi. 10.1111/trf.16774
By:
- Floch, Aline;
- Vege, Sunitha;
- Berardi, Philip;
- Hannon, Judith;
- Ochoa‐Garay, Gorka;
- Lomas‐Francis, Christine;
- Westhoff, Connie M.
Publication type:
Article
Five novel silenced KEL*02 alleles.
Published in:
Transfusion, 2021, v. 61, n. 11, p. E77, doi. 10.1111/trf.16681
By:
- Floch, Aline;
- Velliquette, Randall W.;
- Vege, Sunitha;
- Burgos, Anna;
- Thomas, Rebecca;
- Lomas‐Francis, Christine;
- Westhoff, Connie M.
Publication type:
Article
Five novel FY null alleles associated with typing discrepancies.
Published in:
Transfusion, 2021, v. 61, n. 11, p. E80, doi. 10.1111/trf.16676
By:
- Vege, Sunitha;
- Floch, Aline;
- Lomas‐Frances, Christine;
- Clarke, Gwen;
- Westhoff, Connie M.
Publication type:
Article
Three new XK alleles; two associated with a McLeod RBC phenotype.
Published in:
Transfusion, 2021, v. 61, n. 10, p. E69, doi. 10.1111/trf.16650
By:
- Floch, Aline;
- Lomas‐Francis, Christine;
- Vege, Sunitha;
- Westhoff, Connie M.
Publication type:
Article
A novel P1PK allele in two Bangladeshi sisters with a history of spontaneous abortion: A4GALT*02N(951C).
Published in:
Transfusion, 2021, v. 61, n. 10, p. E71, doi. 10.1111/trf.16649
By:
- Floch, Aline;
- Lomas‐Francis, Christine;
- Vege, Sunitha;
- Chai, Jamie;
- Cai, Connie;
- Westhoff, Connie M.
Publication type:
Article
An insertion/deletion polymorphism in the KLF1 gene resulting in an In(Lu) phenotype.
Published in:
Transfusion, 2021, v. 61, n. 10, p. E73, doi. 10.1111/trf.16648
By:
- Floch, Aline;
- Vege, Sunitha;
- Burgos, Anna;
- Kuchma, Sharon;
- Bell, Mollie;
- Lomas‐Francis, Christine;
- Westhoff, Connie M.
Publication type:
Article
RHCE*01 48G>C, 366del allele with silenced RHCE*ce expression.
Published in:
2021
By:
- Barrault, Aurélie;
- Floch, Aline;
- Devaux, Laurent;
- Gaillard, Kévin;
- Muralitharan, Vintuya;
- Pirenne, France;
- Tournamille, Christophe
Publication type:
journal article
Insights into anti‐D formation in carriers of RhD variants through studies of 3D intraprotein interactions.
Published in:
Transfusion, 2021, v. 61, n. 4, p. 1286, doi. 10.1111/trf.16301
By:
- Floch, Aline;
- Pirenne, France;
- Barrault, Aurélie;
- Chami, Btissam;
- Toly‐Ndour, Cécile;
- Tournamille, Christophe;
- Brevern, Alexandre G.
Publication type:
Article
Alloimmunization risk associated with amino acid 223 substitution in the RhD protein: analysis in the light of molecular modeling.
Published in:
2018
By:
- Brevern, Alexandre G.;
- Floch, Aline;
- Barrault, Aurélie;
- Martret, Jennifer;
- Bodivit, Gwellaouen;
- Djoudi, Rachid;
- Pirenne, France;
- Tournamille, Christophe;
- de Brevern, Alexandre G
Publication type:
journal article
High immunogenicity of red blood cell antigens restricted to the population of African descent in a cohort of sickle cell disease patients.
Published in:
2018
By:
- Floch, Aline;
- Gien, Dominique;
- Tournamille, Christophe;
- Chami, Btissam;
- Habibi, Anoosha;
- Galactéros, Frédéric;
- Bierling, Philippe;
- Djoudi, Rachid;
- Pondarré, Corinne;
- Peyrard, Thierry;
- Pirenne, France
Publication type:
journal article
Molecular characterization of 13 new RHD alleles.
Published in:
2017
By:
- Floch, Aline;
- Barrault, Aurelie;
- De Brevern, Alexandre G.;
- Martret, Jennifer;
- Gaillard, Kevin;
- Devaux, Laurent;
- Chami, Btissam;
- Bierling, Philippe;
- Pirenne, France;
- Tournamille, Christophe
Publication type:
journal article

Found: 22

Molecular dynamics of the human RhD and RhAG blood group proteins.

3D analysis of CROMER (DAF) and a new antigen CRAG.

Genotyping in Sickle Cell Disease Patients: The French Strategy.

Red blood cell alloimmunisation in sickle cell disease patients in the Democratic Republic of the Congo.

Two novel variants that disrupt the RHCE start codon with varying effect on RhCE antigen expression.

A novel high‐prevalence antigen in the Lutheran system, LUGA (LU24), and an updated, full‐length 3D BCAM model.

Two new Scianna variants causing loss of high prevalence antigens: ERMAP model and 3D analysis of the antigens.

Four novel ABO*AW alleles associated with weak antigen expression.

A novel RHCE*Ce710A allele (p.237Asp) in a Japanese patient with weak expression of C and no detectable e.

Novel RHD allele with c.333C>G change predicted to encode p.Phe111Leu.

First report of a null allele on a GYPBs background: GYPBs(37 + 4_8delAGTGA).

An intron c.149‐2632T>A change in RHD is associated with aberrant transcription and very weak D phenotype.

Five novel silenced KEL*02 alleles.

Five novel FY null alleles associated with typing discrepancies.

Three new XK alleles; two associated with a McLeod RBC phenotype.

A novel P1PK allele in two Bangladeshi sisters with a history of spontaneous abortion: A4GALT*02N(951C).

An insertion/deletion polymorphism in the KLF1 gene resulting in an In(Lu) phenotype.

RHCE01 48G>C, 366del allele with silenced RHCEce expression.

Insights into anti‐D formation in carriers of RhD variants through studies of 3D intraprotein interactions.

Alloimmunization risk associated with amino acid 223 substitution in the RhD protein: analysis in the light of molecular modeling.

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

Molecular characterization of 13 new RHD alleles.