Search

Your search keyword '"Peyrard, Thierry"' showing total 417 results
Start Over Author "Peyrard, Thierry"
417 results on '"Peyrard, Thierry"'

1. DNA Reference Reagents for Genotyping RH Variants

Author

Arnoni, Carine Prisco, Latini, Flavia, da Silva, Flavia Sant’Anna, Vendrame, Tatiane Aparecida, Hyland, Catherine, Millard, Glenda, Liew, Yew-Wah, Teramura, Gayle, Harris, Samantha, Nakaya Fletcher, Shelley, Peyrard, Thierry, Poyot, Thomas, Martin-Blanc, Stephanie, Ochoa, Gorka, Westhoff, Connie, Vege, Sunitha, Denomme, Gregory A., Stef, Marianne A., Castilho, Lilian, dos Santos, Tamires Delfino, Piefer, Cindy, Bensing, Kathleen, Schanen, Michael, Scholz, Sabine, König, Sabrina, Bein, Gregor, Roeder, Lida, Sachs, Ulrich J., Wittig, Michael, Steiert, Tim A., Franke, Andre, Henny, Christine, Tani, Yoshihiko, Tanaka, Mitsunobu, Flegel, Willy A., Srivastava, Kshitij, Conceicao, Michelle, Resto, Claribel, Gannett, Michael Sel, Doescher, Andrea, Bub, Carolina Bonet, Aravechia, Maria Giselda, Costa, Thiago Henrique, Sirianni, Marilia Fernandes Mascarenhas, Santos, Leandro Dinalli, Sippert, Emilia, Volkova, Evgeniya, Rippee-Brooks, Meagan, Lee, Christine, Araojo, Richardae, Illoh, Orieji, Liu, Zhugong, and Rios, Maria

Published
2024
Full Text
View/download PDF

2. Prise en charge transfusionnelle et suivi immunohématologique après allogreffe de cellules souches hématopoïétiques : recommandations de la Société francophone de greffe de moelle et de thérapie cellulaire (SFGM-TC)

Author

Xhaard, Aliénor, Bouton, Muriel, Delugin, Laurence, Giraud, Christine, Guyon, Alizée, Giroux-Lathuile, Claudine, Hajjout, Khadija, Nicolas, Pascal, Peyrard, Thierry, Ratie, Vanessa, Boisnard, Anne, Capelle, Lucie, Godin, Sandrine, Traineau, Richard, Yacoub-Agha, Ibrahim, and Leprêtre, Anne-Claire

Published
2024
Full Text
View/download PDF

4. DNA Reference Reagents for Genotyping RH Variants

Author

Sippert, Emilia, primary, Volkova, Evgeniya, additional, Rippee-Brooks, Meagan, additional, Denomme, Gregory A., additional, Flegel, Willy A., additional, Lee, Christine, additional, Araojo, Richardae, additional, Illoh, Orieji, additional, Liu, Zhugong, additional, Rios, Maria, additional, Arnoni, Carine Prisco, additional, Latini, Flavia, additional, da Silva, Flavia Sant’Anna, additional, Vendrame, Tatiane Aparecida, additional, Hyland, Catherine, additional, Millard, Glenda, additional, Liew, Yew-Wah, additional, Teramura, Gayle, additional, Harris, Samantha, additional, Nakaya Fletcher, Shelley, additional, Peyrard, Thierry, additional, Poyot, Thomas, additional, Martin-Blanc, Stephanie, additional, Ochoa, Gorka, additional, Westhoff, Connie, additional, Vege, Sunitha, additional, Stef, Marianne A., additional, Castilho, Lilian, additional, dos Santos, Tamires Delfino, additional, Piefer, Cindy, additional, Bensing, Kathleen, additional, Schanen, Michael, additional, Scholz, Sabine, additional, König, Sabrina, additional, Bein, Gregor, additional, Roeder, Lida, additional, Sachs, Ulrich J., additional, Wittig, Michael, additional, Steiert, Tim A., additional, Franke, Andre, additional, Henny, Christine, additional, Tani, Yoshihiko, additional, Tanaka, Mitsunobu, additional, Srivastava, Kshitij, additional, Conceicao, Michelle, additional, Resto, Claribel, additional, Gannett, Michael Sel, additional, Doescher, Andrea, additional, Bub, Carolina Bonet, additional, Aravechia, Maria Giselda, additional, Costa, Thiago Henrique, additional, Sirianni, Marilia Fernandes Mascarenhas, additional, and Santos, Leandro Dinalli, additional

Published
2024
Full Text
View/download PDF

14. Chronic Granulomatous Disease with the McLeod Phenotype: a French National Retrospective Case Series

Author

Lhomme, Faustine, Peyrard, Thierry, Babinet, Jérôme, Abou-Chahla, Wadih, Durieu, Isabelle, Moshous, Despina, Neven, Bénédicte, Rohrlich, Pierre-Simon, Albinni, Souha, Amiranoff, Denise, Dumont, Marie-Dominique, Lortholary, Olivier, Héritier, Sébastien, Marguet, Christophe, Suarez, Felipe, Fischer, Alain, Blanche, Stéphane, Hermine, Olivier, and Mahlaoui, Nizar

Published
2020
Full Text
View/download PDF

18. Prise en charge transfusionnelle et suivi immunohématologique après allogreffe de cellules souches hématopoïétiques : recommandations de la Société francophone de greffe de moelle et de thérapie cellulaire (SFGM-TC)

Author

Xhaard, Aliénor, primary, Bouton, Muriel, additional, Delugin, Laurence, additional, Giraud, Christine, additional, Guyon, Alizée, additional, Giroux-Lathuile, Claudine, additional, Hajjout, Khadija, additional, Nicolas, Pascal, additional, Peyrard, Thierry, additional, Ratie, Vanessa, additional, Boisnard, Anne, additional, Capelle, Lucie, additional, Godin, Sandrine, additional, Traineau, Richard, additional, Yacoub-Agha, Ibrahim, additional, and Leprêtre, Anne-Claire, additional

Published
2023
Full Text
View/download PDF

19. Molecular and structural characterization of a novel high‐prevalence antigen of the Augustine blood group system

Author

Vrignaud, Cédric, primary, Mikdar, Mahmoud, additional, Duval, Romain, additional, Reininger, Luc, additional, Damaraju, Vijaya L., additional, Sawyer, Michael, additional, Colin, Yves, additional, Le Van Kim, Caroline, additional, Gelly, Jean‐Christophe, additional, Etchebest, Catherine, additional, Peyrard, Thierry, additional, and Azouzi, Slim, additional

Published
2023
Full Text
View/download PDF

22. Lack of the human choline transporter‐like protein SLC44A2 causes hearing impairment and a rare red blood phenotype

Author

Koehl, Bérengère, primary, Vrignaud, Cédric, additional, Mikdar, Mahmoud, additional, Nair, Thankam S, additional, Yang, Lucy, additional, Landry, Seyve, additional, Laiguillon, Guy, additional, Giroux‐Lathuile, Claudine, additional, Anselme‐Martin, Sophie, additional, El Kenz, Hanane, additional, Hermine, Olivier, additional, Mohandas, Narla, additional, Cartron, Jean Pierre, additional, Colin, Yves, additional, Detante, Olivier, additional, Marlu, Raphaël, additional, Le Van Kim, Caroline, additional, Carey, Thomas E, additional, Azouzi, Slim, additional, and Peyrard, Thierry, additional

Published
2023
Full Text
View/download PDF

23. Erythrocyte type 1 equilibrative nucleoside transporter expression in sickle cell disease and sickle cell trait

Author

Koehl, Bérengère, primary, Claude, Livia, additional, Reminy, Karen, additional, Tarer, Vanessa, additional, Baccini, Véronique, additional, Romana, Marc, additional, Colin‐Aronovicz, Yves, additional, Damaraju, Vijaya L., additional, Sawyer, Michael, additional, Peyrard, Thierry, additional, Etienne‐Julan, Maryse, additional, Le Van Kim, Caroline, additional, Azouzi, Slim, additional, and Reininger, Luc, additional

Published
2022
Full Text
View/download PDF

24. Genetic Evidence That Dimerization of Glycophorin a Is Critical for Red Cell Invasion By Plasmodium Falciparum but Not for the Binding of EBA-175

Author

Azouzi, Slim, primary, Mikdar, Mahmoud, additional, Hermand-Tournamille, Patricia, additional, More, Kunal, additional, Dechavanne, Sébastien, additional, Duval, Romain, additional, Thonier, Vincent, additional, Le Van Kim, Caroline, additional, Mouro-Chanteloup, Isabelle, additional, Bertrand, Olivier, additional, Chitnis, Chetan, additional, Peyrard, Thierry, additional, and Colin Aronovicz, Yves, additional

Published
2022
Full Text
View/download PDF

25. How to improve issuing, transfusion and follow-up of blood components in Southern and Eastern Mediterranean countries? A benchmark assessment

Author

Haddad, Antoine, primary, Abu-Helu, Rasmi, additional, Khadijetou, BA, additional, Bou Assi, Tarek, additional, Benajiba, Mohamed, additional, Slama, Hmida, additional, Elgemmezi, Tarek, additional, Chaïb, Mohamed, additional, Alqodah, Mohammad, additional, Hachem, Berthe, additional, Najjar, Osama, additional, Peyrard, Thierry, additional, and Garraud, Olivier, additional

Published
2022
Full Text
View/download PDF

27. International Society of Blood Transfusion Working Party on Red Cell Immunogenetics and Blood Group Terminology Report of Basel and three virtual business meetings: Update on blood group systems

Author

Gassner, Christoph, primary, Castilho, Lilian, additional, Chen, Qing, additional, Clausen, Frederik Banch, additional, Denomme, Gregory A., additional, Flegel, Willy A., additional, Gleadall, Nick, additional, Hellberg, Åsa, additional, Ji, Yanli, additional, Keller, Margaret A., additional, Lane, William J., additional, Ligthart, Peter, additional, Lomas‐Francis, Christine, additional, Nogues, Nuria, additional, Olsson, Martin L., additional, Peyrard, Thierry, additional, Storry, Jill R., additional, Tani, Yoshihiko, additional, Thornton, Nicole, additional, van der Schoot, Ellen, additional, Veldhuisen, Barbera, additional, Wagner, Franz, additional, Weinstock, Christof, additional, Wendel, Silvano, additional, Westhoff, Connie, additional, Yahalom, Vered, additional, and Hyland, Catherine A., additional

Published
2022
Full Text
View/download PDF

28. Identification of an Alu-mediated 5.7-kb deletion of the LU gene in a pregnant Moroccan woman with anti-Lu3

Author

Pedini, Pascal, Laget, Laurine, Izard, Caroline, Menanteau, Cécile, Beley, Sophie, Granier, Thomas, Picard, Christophe, Bailly, Pascal, Chiaroni, Jacques, Mazieres, Stéphane, Peyrard, Thierry, Silvy, Monique, Etablissement Français du Sang Provence-Alpes Côte-d'Azur et Corse (EFS), Anthropologie bio-culturelle, Droit, Ethique et Santé (ADES), Aix Marseille Université (AMU)-EFS ALPES MEDITERRANEE-Centre National de la Recherche Scientifique (CNRS), Etablissement Français du Sang Ile de France (EFS), Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-CHU Necker - Enfants Malades [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), Institut National de la Santé et de la Recherche Médicale (INSERM)-Hôpital Henry Mondor, Biologie Intégrée du Globule Rouge (BIGR (UMR_S_1134 / U1134)), and Institut National de la Transfusion Sanguine [Paris] (INTS)-Université de La Réunion (UR)-Institut National de la Santé et de la Recherche Médicale (INSERM)-CHU Pointe-à-Pitre/Abymes [Guadeloupe] -Université des Antilles (UA)-Université Paris Cité (UPCité)

Subjects
[SDV]Life Sciences [q-bio]
Abstract

International audience

Published
2022

29. Lack of the human choline transporter-like protein CTL2 causes hearing impairment and a rare red blood cell phenotype

Author

Koehl, Bérengère, primary, Vrignaud, Cédric, additional, Mikdar, Mahmoud, additional, Nair, Thankam S., additional, Yang, Lucy, additional, Laiguillon, Guy, additional, Anselme-Martin, Sophie, additional, Giroux-Lathuile, Claudine, additional, Kenz, Hanane El, additional, Hermine, Olivier, additional, Mohandas, Narla, additional, Cartron, Jean Pierre, additional, Colin, Yves, additional, Detante, Olivier, additional, Le Van Kim, Caroline, additional, Carey, Thomas E., additional, Azouzi, Slim, additional, and Peyrard, Thierry, additional

Published
2022
Full Text
View/download PDF

30. Recommendation for validation and quality assurance of non-invasive prenatal testing for foetal blood groups and implications for IVD risk classification according to EU regulations

Author

Clausen, Frederik Banch, Hellberg, Åsa, Bein, Gregor, Bugert, Peter, Schwartz, Dieter, Drnovsek, Tadeja Dovc, Finning, Kirstin, Guz, Katarzyna, Haimila, Katri, Henny, Christine, O'Brien, Helen, Orzinska, Agnieszka, Sørensen, Kirsten, Thorlacius, Steinunn, Wikman, Agneta, Denomme, Gregory Andrew, Flegel, Willy Albert, Gassner, Christoph, de Haas, Masja, Hyland, Catherine, Ji, Yanli, Lane, William J., Nogués, Núria, Olsson, Martin L., Peyrard, Thierry, van der Schoot, C. Ellen, Weinstock, Christof, Legler, Tobias, Clausen, Frederik Banch, Hellberg, Åsa, Bein, Gregor, Bugert, Peter, Schwartz, Dieter, Drnovsek, Tadeja Dovc, Finning, Kirstin, Guz, Katarzyna, Haimila, Katri, Henny, Christine, O'Brien, Helen, Orzinska, Agnieszka, Sørensen, Kirsten, Thorlacius, Steinunn, Wikman, Agneta, Denomme, Gregory Andrew, Flegel, Willy Albert, Gassner, Christoph, de Haas, Masja, Hyland, Catherine, Ji, Yanli, Lane, William J., Nogués, Núria, Olsson, Martin L., Peyrard, Thierry, van der Schoot, C. Ellen, Weinstock, Christof, and Legler, Tobias

Abstract

Background and Objectives: Non-invasive assays for predicting foetal blood group status in pregnancy serve as valuable clinical tools in the management of pregnancies at risk of detrimental consequences due to blood group antigen incompatibility. To secure clinical applicability, assays for non-invasive prenatal testing of foetal blood groups need to follow strict rules for validation and quality assurance. Here, we present a multi-national position paper with specific recommendations for validation and quality assurance for such assays and discuss their risk classification according to EU regulations. Materials and Methods: We reviewed the literature covering validation for in-vitro diagnostic (IVD) assays in general and for non-invasive foetal RHD genotyping in particular. Recommendations were based on the result of discussions between co-authors. Results: In relation to Annex VIII of the In-Vitro-Diagnostic Medical Device Regulation 2017/746 of the European Parliament and the Council, assays for non-invasive prenatal testing of foetal blood groups are risk class D devices. In our opinion, screening for targeted anti-D prophylaxis for non-immunized RhD negative women should be placed under risk class C. To ensure high quality of non-invasive foetal blood group assays within and beyond the European Union, we present specific recommendations for validation and quality assurance in terms of analytical detection limit, range and linearity, precision, robustness, pre-analytics and use of controls in routine testing. With respect to immunized women, different requirements for validation and IVD risk classification are discussed. Conclusion: These recommendations should be followed to ensure appropriate assay performance and applicability for clinical use of both commercial and in-house assays.

Published
2022

31. Erythrocyte type 1 equilibrative nucleoside transporter expression in sickle cell disease and sickle cell trait.

Author

Koehl, Bérengère, Claude, Livia, Reminy, Karen, Tarer, Vanessa, Baccini, Véronique, Romana, Marc, Colin‐Aronovicz, Yves, Damaraju, Vijaya L., Sawyer, Michael, Peyrard, Thierry, Etienne‐Julan, Maryse, Le Van Kim, Caroline, Azouzi, Slim, and Reininger, Luc

Subjects
SICKLE cell trait, SICKLE cell anemia, NUCLEOSIDE transport proteins, ERYTHROCYTES, FATIGUE (Physiology)
Abstract

Summary: Hypoxia‐mediated red blood cell (RBC) sickling is central to the pathophysiology of sickle cell disease (SCD). The signalling nucleoside adenosine is thought to play a significant role in this process. This study investigated expression of the erythrocyte type 1 equilibrative nucleoside transporter (ENT1), a key regulator of plasma adenosine, in adult patients with SCD and carriers of sickle cell trait (SCT). Relative quantitative expression analysis of erythrocyte ENT1 was carried out by Western blot and flow cytometry. Patients with SCD with steady state conditions, either with SS or SC genotype, untreated or under hydroxycarbamide (HC) treatment, exhibited a relatively high variability of erythrocyte ENT1, but with levels not significantly different from normal controls. Most strikingly, expression of erythrocyte ENT1 was found to be significantly decreased in patients with SCD undergoing painful vaso‐occlusive episode and, unexpectedly, also in healthy SCT carriers. Promoting hypoxia‐induced adenosine signalling, the reduced expression of erythrocyte ENT1 might contribute to the pathophysiology of SCD and to the susceptibility of SCT individuals to altitude hypoxia or exercise to exhaustion. [ABSTRACT FROM AUTHOR]

Published
2023
Full Text
View/download PDF

37. Emm : un nouveau système de groupe sanguin associé à des troubles neurodéveloppementaux

Author

Duval, Romain, primary, Nicolas, Gael, additional, Willemetz, Alexandra, additional, Murakami, Yoshiko, additional, Mikdar, Mahmoud, additional, Vrignaud, Cedric, additional, Megahed, Hisham, additional, Cartron, Jean-Pierre, additional, Masson, Cecile, additional, Wehbi, Samer, additional, Koehl, Bérengere, additional, Hully, Marie, additional, Siquier, Karine, additional, Chemlay, Nicole, additional, Rotig, Agnes, additional, Lyonnet, Stanislas, additional, Colin, Yves, additional, Barcia, Giulia, additional, Cantagrel, Vincent, additional, Le Van Kim, Caroline, additional, Hermine, Olivier, additional, Kinoshita, Taroh, additional, Peyrard, Thierry, additional, and Azouzi, Slim, additional

Published
2021
Full Text
View/download PDF

41. Physique des solitons

Author

Michel Peyrard, Thierry Dauxois and Michel Peyrard, Thierry Dauxois

Published
2004

42. The equilibrative nucleoside transporter ENT1 is critical for nucleotide homeostasis and optimal erythropoiesis

Author

Mikdar, Mahmoud, primary, González-Menéndez, Pedro, additional, Cai, Xiaoli, additional, Zhang, Yujin, additional, Serra, Marion, additional, Dembele, Abdoul K., additional, Boschat, Anne-Claire, additional, Sanquer, Sylvia, additional, Chhuon, Cerina, additional, Guerrera, Ida Chiara, additional, Sitbon, Marc, additional, Hermine, Olivier, additional, Colin, Yves, additional, Le Van Kim, Caroline, additional, Kinet, Sandrina, additional, Mohandas, Narla, additional, Xia, Yang, additional, Peyrard, Thierry, additional, Taylor, Naomi, additional, and Azouzi, Slim, additional

Published
2021
Full Text
View/download PDF

43. Recommendation for validation and quality assurance of non‐invasive prenatal testing for foetal blood groups and implications for IVD risk classification according to EU regulations

Author

Clausen, Frederik Banch, primary, Hellberg, Åsa, additional, Bein, Gregor, additional, Bugert, Peter, additional, Schwartz, Dieter, additional, Drnovsek, Tadeja Dovc, additional, Finning, Kirstin, additional, Guz, Katarzyna, additional, Haimila, Katri, additional, Henny, Christine, additional, O'Brien, Helen, additional, Orzinska, Agnieszka, additional, Sørensen, Kirsten, additional, Thorlacius, Steinunn, additional, Wikman, Agneta, additional, Denomme, Gregory Andrew, additional, Flegel, Willy Albert, additional, Gassner, Christoph, additional, de Haas, Masja, additional, Hyland, Catherine, additional, Ji, Yanli, additional, Lane, William J., additional, Nogués, Núria, additional, Olsson, Martin L., additional, Peyrard, Thierry, additional, van der Schoot, C. Ellen, additional, Weinstock, Christof, additional, and Legler, Tobias, additional

Published
2021
Full Text
View/download PDF

44. A dominant mutation in the gene encoding the erythroid transcription factor KLF1 causes a congenital dyserythropoietic anemia

Author

Arnaud, Lionel, Saison, Carole, Helias, Virginie, Lucien, Nicole, Steschenko, Dominique, Giarratana, Marie-Catherine, Prehu, Claude, Foliguet, Bernard, Montout, Lory, de Brevern, Alexandre G., Francina, Alain, Ripoche, Pierre, Fenneteau, Odile, Costa, Lydie Da, Peyrard, Thierry, Coghlan, Gail, Illum, Niels, Birgens, Henrik, Tamary, Hannah, Iolascon, Achille, Delaunay, Jean, Tchernia, Gil, and Cartron, Jean-Pierre

Subjects
Anemia -- Genetic aspects, Erythropoiesis -- Genetic aspects, Erythropoiesis -- Physiological aspects, Gene mutations -- Analysis, Transcription factors -- Analysis, Biological sciences
Abstract

A study was conducted to identify a missense mutation in the gene encoding erythroid transcription factor KLF1 which causes congenital dyserythropoietic anemia. The results obtained for the disease-causing mutation in KLF1 provides better insight into the critical role of KLF1 transcription factor during erythropoiesis in humans.

Published
2010

46. ABCG2 Is Overexpressed on Red Blood Cells in Ph-Negative Myeloproliferative Neoplasms and Potentiates Ruxolitinib-Induced Apoptosis

Author

Buks, Ralfs, primary, Brusson, Mégane, additional, Cochet, Sylvie, additional, Galochkina, Tatiana, additional, Cassinat, Bruno, additional, Nemazanyy, Ivan, additional, Peyrard, Thierry, additional, Kiladjian, Jean-Jacques, additional, de Brevern, Alexandre G., additional, Azouzi, Slim, additional, and El Nemer, Wassim, additional

Published
2021
Full Text
View/download PDF

47. Inherited glycosylphosphatidylinositol defects cause the rare Emm-negative blood phenotype and developmental disorders

Author

Duval, Romain, primary, Nicolas, Gaël, additional, Willemetz, Alexandra, additional, Murakami, Yoshiko, additional, Mikdar, Mahmoud, additional, Vrignaud, Cedric, additional, Megahed, Hisham, additional, Cartron, Jean-Pierre, additional, Masson, Cecile, additional, Wehbi, Samer, additional, Koehl, Bérengere, additional, Hully, Marie, additional, Siquier, Karine, additional, Chemlay, Nicole, additional, Rotig, Agnes, additional, Lyonnet, Stanislas, additional, Colin, Yves, additional, Barcia, Giulia, additional, Cantagrel, Vincent, additional, Le Van Kim, Caroline, additional, Hermine, Olivier, additional, Kinoshita, Taroh, additional, Peyrard, Thierry, additional, and Azouzi, Slim, additional

Published
2021
Full Text
View/download PDF

Catalog

Books, media, physical & digital resources
See catalog results