Zobrazeno 1 - 10
of 122
pro vyhledávání: '"Philippe, Lacan"'
Autor:
Philippe Joly, Caroline Schluth-Bolard, Philippe Lacan, Claire Barro, Serge Pissard, Audrey Labalme, Damien Sanlaville, Catherine Badens
Publikováno v:
Haematologica, Vol 98, Iss 1 (2013)
Externí odkaz:
https://doaj.org/article/34ef3a4b0fd4496986553d0ae4b600d9
Autor:
Philippe Joly, Philippe Lacan, Audrey Labalme, Elodie Bonhomme, Damien Sanlaville, Alain Francina
Publikováno v:
Haematologica, Vol 95, Iss 5 (2010)
Externí odkaz:
https://doaj.org/article/c30d5ace56324300a75980baa51d4e35
Publikováno v:
Hemoglobin. 39:147-151
Autor:
Rokhaya Ndiaye Diallo, Aynina Cisse, El Hadji Malick Ndour, Philomène Lopez Sall, Ibrahima Diagne, Louis Chillotti, Papa Madieye Gueye, Indou Deme Ly, Pape Amadou Diop, Philippe Connes, Philippe Lacan, Cyril Martin, Céline Renoux, Philippe Joly, Fatou Gueye Tall, Nicolas Veyrenche
Publikováno v:
Hemoglobin
Hemoglobin, Informa Healthcare, 2017, 41 (2), pp.89-95. ⟨10.1080/03630269.2017.1339610⟩
Hemoglobin, Informa Healthcare, 2017, 41 (2), pp.89-95. ⟨10.1080/03630269.2017.1339610⟩
Sickle cell disease is a genetic disorder with a large variability in the pattern and severity of clinical manifestations. Different genetic modulators have been identified but very few epidemiologic data are available on these modifier genes in Sene
Autor:
Vincent Pialoux, Daniella Cuzzubbo, Philippe Connes, Yves Bertrand, Nathalie Garnier, Kamila Kebaili, Philippe Joly, Céline Renoux, Cyril Martin, Giovanna Cannas, Philippe Lacan, Alexandra Gauthier, Marc Romana, Cecile Renard
Publikováno v:
European Journal of Haematology
European Journal of Haematology, Wiley, 2017, 98 (3), pp.296-301. ⟨10.1111/ejh.12838⟩
European Journal of Haematology, Wiley, 2017, 98 (3), pp.296-301. ⟨10.1111/ejh.12838⟩
OBJECTIVES Because of the increased hemolytic rate, a significant proportion of patients with sickle cell disease (SCD) are prone to develop cholelithiasis. The present study investigated the role of several genetic factors (UGT1A1 promoter (TA)n rep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3ed63a375778bebfebafd84860ce010c
https://hal-univ-lyon1.archives-ouvertes.fr/hal-01881697
https://hal-univ-lyon1.archives-ouvertes.fr/hal-01881697
Autor:
Philippe, Joly, Céline, Renoux, Philippe, Lacan, Yves, Bertrand, Giovanna, Cannas, Nathalie, Garnier, Daniella, Cuzzubbo, Kamila, Kebaïli, Cécile, Renard, Alexandra, Gauthier, Vincent, Pialoux, Cyril, Martin, Marc, Romana, Philippe, Connes
Publikováno v:
European journal of haematology. 98(3)
Because of the increased hemolytic rate, a significant proportion of patients with sickle cell disease (SCD) are prone to develop cholelithiasis. The present study investigated the role of several genetic factors (UGT1A1 promoter (TA)One hundred and
Autor:
Philippe Lacan, Aurélie Desbrée, Alain Francina, Caroline Garcia, Philippe Joly, Nicole Couprie
Publikováno v:
Hemoglobin. 37:80-84
We report two new variants of the δ-globin gene: Hb A(2)-Saint-Etienne [δ14(A11)Leu→Pro] and Hb A(2)-Marseille [δ22(B4)Ala→Lys]. The first variant has a low rate of expression, the second results from a double nucleotide mutation on the same c
Publikováno v:
Clinical Chemistry and Laboratory Medicine
Clinical Chemistry and Laboratory Medicine, De Gruyter, 2016, 54 (2), ⟨10.1515/cclm-2015-0577⟩
Clinical Chemistry and Laboratory Medicine, De Gruyter, 2016, 54 (2), ⟨10.1515/cclm-2015-0577⟩
International audience
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d5196df8e91ff909c0eb304328bbb21
https://hal.archives-ouvertes.fr/hal-02127551
https://hal.archives-ouvertes.fr/hal-02127551
Autor:
Philippe Lacan, Philippe Joly, Patricia Bignet, Amrathlal Rabbind Singh, C. Dumesnil, Estelle Cadet, Jacques Rochette, Jean-Pierre Vannier
Publikováno v:
Hemoglobin
Hemoglobin, Informa Healthcare, 2015, 40 (2), pp.108-112. ⟨10.3109/03630269.2015.1136640⟩
Hemoglobin, Informa Healthcare, 2015, 40 (2), pp.108-112. ⟨10.3109/03630269.2015.1136640⟩
We have identified a deletion of 125 bp (α-α(Δ125)) (NG_000006.1: g.37040_37164del) in the α-globin gene cluster in a Kabyle population. A combination of singlex and multiplex polymerase chain reaction (PCR)-based assays have been used to identif
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::69518b2078fec148662a62e60d3a888a
https://hal.archives-ouvertes.fr/hal-02377939
https://hal.archives-ouvertes.fr/hal-02377939
Publikováno v:
Annales de biologie clinique. 69:571-576
Le diagnostic du deficit en α-1 antitrypsine (A1AT) repose sur la focalisation isoelectrique des proteines seriques et sur la mesure de la concentration serique. Cependant, la focalisation isoelectrique est techniquement delicate et une concentratio