Kết quả tìm kiếm - Jean‐Michel Dupont

  • Đang hiển thị 1 - 7 kết quả của 7
Tinh chỉnh kết quả
  1. 1
    In vitro proliferation and differentiation of erythroid progenitors from patients with myelodysplastic syndromes: evidence for Fas-dependent apoptosis

    In vitro proliferation and differentiation of erythroid progenitors from patients with myelodysplastic syndromes: evidence for Fas-dependent apoptosis Bằng Yann-Érick Claessens, Didier Bouscary, Jean‐Michel Dupont, Françoise Picard, J Melle, Sylvie Gisselbrecht, Catherine Lacombe, François Dreyfus, Patrick Mayeux, Michaëla Fontenay

    Được phát hành 2002
    lấy văn bản lấy văn bản
    Artigo
    Lưu vào danh sách
    Đã lưu trong:
  2. 2
    Specific epigenetic alterations of IGF2-H19 locus in spermatozoa from infertile men

    Specific epigenetic alterations of IGF2-H19 locus in spermatozoa from infertile men Bằng Céline Chalas Boissonnas, Hafida El abdalaoui, Virginie Haelewyn, Patricia Fauque, Jean‐Michel Dupont, Marta Gut, Daniel Vaiman, Pierre Jouannet, Jörg Tost, Hélène Jammes

    Được phát hành 2009
    lấy văn bản lấy văn bản
    Artigo
    Lưu vào danh sách
    Đã lưu trong:
  3. 3
    Could Digital PCR Be an Alternative as a Non-Invasive Prenatal Test for Trisomy 21: A Proof of Concept Study

    Could Digital PCR Be an Alternative as a Non-Invasive Prenatal Test for Trisomy 21: A Proof of Concept Study Bằng Laïla El Khattabi, Christelle Rouillac-Le Sciellour, Dominique Le Tessier, Armelle Luscan, Audrey Coustier, Raphaël Porcher, Rakia Bhouri, Juliette Nectoux, Valérie Serazin, Thibaut Quibel, Laurent Mandelbrot, Vassilis Tsatsaris, François Vialard, Jean‐Michel Dupont

    Được phát hành 2016
    lấy văn bản lấy văn bản
    Artigo
    Lưu vào danh sách
    Đã lưu trong:
  4. 4
    IFN-α and CD46 stimulation are associated with active lupus and skew natural T regulatory cell differentiation to type 1 regulatory T (Tr1) cells

    IFN-α and CD46 stimulation are associated with active lupus and skew natural T regulatory cell differentiation to type 1 regulatory T (Tr1) cells Bằng Hélène Le Buanec, Marie‐Lise Gougeon, Alexis Mathian, Pierre Lebon, Jean‐Michel Dupont, Gabriel Peltre, Patrice Hémon, michel schmid, B Bizzini, Thomas Künding, Arsène Burny, Armand Bensussan, Zahir Amoura, Robert C. Gallo, Daniel Zagury

    Được phát hành 2011
    lấy văn bản
    Artigo
    Lưu vào danh sách
    Đã lưu trong:
  5. 5
    Optical genome mapping enables constitutional chromosomal aberration detection

    Optical genome mapping enables constitutional chromosomal aberration detection Bằng Tuomo Mantere, Kornelia Neveling, Céline Pebrel‐Richard, Marion Benoist, Guillaume van der Zande, Ellen Kater‐Baats, Imane Baatout, Ronald van Beek, Tony Yammine, Michiel Oorsprong, Faten Hsoumi, Daniel Olde-Weghuis, Wed Majdali, Susan Vermeulen, Marc Pauper, Aziza Lebbar, Marian Stevens‐Kroef, Damien Sanlaville, Jean‐Michel Dupont, Dominique Smeets, Alexander Hoischen, Caroline Schluth–Bolard, Laïla El Khattabi

    Được phát hành 2021
    lấy văn bản
    Artigo
    Lưu vào danh sách
    Đã lưu trong:
  6. 6
    Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome

    Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome Bằng Catherine Dodé, Jacqueline Levilliers, Jean‐Michel Dupont, Anne De Paepe, Nathalie Le Dû, Nadia Soussi‐Yanicostas, Roney S. Coimbra, Sedigheh Delmaghani, Sylvie Compain-Nouaille, Françoise Baverel, Christophe Pécheux, Dominique Le Tessier, Corinne Cruaud, Marc Delpech, Frank Speleman, Stefan Vermeulen, Andrea Amalfitano, Y. Bachelot, Philippe Bouchard, Sylvie Cabrol, Jean‐Claude Carel, Henriette Delemarre-van de Waal, B. Goulet-Salmon, Marie‐Laure Kottler, Odile Richard, Franco Sánchez‐Franco, Robert Saura, Jacques Young, Christine Petit, Jean‐Pierre Hardelin

    Được phát hành 2003
    lấy văn bản lấy văn bản
    Artigo
    Lưu vào danh sách
    Đã lưu trong:
  7. 7
    Whole genome paired-end sequencing elucidates functional and phenotypic consequences of balanced chromosomal rearrangement in patients with developmental disorders

    Whole genome paired-end sequencing elucidates functional and phenotypic consequences of balanced chromosomal rearrangement in patients with developmental disorders Bằng Caroline Schluth–Bolard, Flavie Diguet, Nicolas Chatron, Pierre‐Antoine Rollat‐Farnier, Claire Bardel, Alexandra Afenjar, Florence Amblard, Jeanne Amiel, Sophie Blesson, Patrick Callier, Yline Capri, Patrick Collignon, Marie‐Pierre Cordier, Christine Coubes, Bénédicte Demeer, Annabelle Chaussenot, Florence Démurger, Françoise Devillard, Martine Doco‐Fenzy, Céline Dupont, Jean‐Michel Dupont, Sophie Dupuis‐Girod, Laurence Faivre, Brigitte Gilbert‐Dussardier, Anne‐Marie Guerrot, Marine Houlier, Bertrand Isidor, Sylvie Jaillard, Géraldine Joly‐Helas, Valérie Kremer, Didier Lacombe, Cédric Le Caignec, Aziza Lebbar, Marine Lebrun, Gaëtan Lesca, James Lespinasse, Jonathan Lévy, Valérie Malan, Michèle Mathieu‐Dramard, Julie Masson, Alice Masurel‐Paulet, Cyril Mignot, Chantal Missirian, Fanny Morice‐Picard, Sébastien Moutton, Gwenaël Nadeau, Céline Pebrel‐Richard, Sylvie Odent, Véronique Paquis‐Flucklinger, Laurent Pasquier, Nicole Philip, Morgane Plutino, Linda Pons, Marie‐France Portnoï, Fabienne Prieur, Jacques Puechberty, Audrey Putoux, Marlène Rio, Caroline Rooryck, Massimiliano Rossi, Catherine Sarret, Véronique Satre, Jean‐Pierre Siffroi, Marianne Till, Renaud Touraine, Annick Toutain, Jérôme Toutain, Stéphanie Valence, Alain Verloès, Sandra Whalen, Patrick Edery, Anne‐Claude Tabet, Damien Sanlaville

    Được phát hành 2019
    lấy văn bản lấy văn bản
    Artigo
    Lưu vào danh sách
    Đã lưu trong:

Công cụ tìm kiếm: