Research ArticleLung Disease

Pulmonary transplantation of macrophage progenitors as effective and long-lasting therapy for hereditary pulmonary alveolar proteinosis

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Science Translational Medicine  20 Aug 2014:
Vol. 6, Issue 250, pp. 250ra113
DOI: 10.1126/scitranslmed.3009750

Article Information

vol. 6 no. 250 250ra113

PubMed: 
Print ISSN: 
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History: 
  • Received for publication June 10, 2014
  • Accepted for publication August 1, 2014
  • .

Author Information

  1. Christine Happle1,2,*,
  2. Nico Lachmann3,4,*,
  3. Jelena Škuljec1,
  4. Martin Wetzke1,
  5. Mania Ackermann3,4,
  6. Sebastian Brennig3,4,
  7. Adele Mucci3,4,
  8. Adan Chari Jirmo1,2,
  9. Stephanie Groos5,
  10. Anja Mirenska1,
  11. Christina Hennig1,2,
  12. Thomas Rodt6,
  13. Jens P. Bankstahl7,
  14. Nicolaus Schwerk1,2,
  15. Thomas Moritz3,4, and
  16. Gesine Hansen1,2,
  1. 1Department of Pediatric Pneumology, Allergology and Neonatology, Hannover Medical School, 30625 Hannover, Germany.
  2. 2Biomedical Research in Endstage and Obstructive Lung Disease Hannover (BREATH), Member of the German Center for Lung Research (DZL), 30625 Hannover, Germany.
  3. 3Reprogramming and Gene Therapy Group, REBIRTH Cluster-of Excellence, Hannover Medical School, 30625 Hannover, Germany.
  4. 4Institute of Experimental Hematology, Hannover Medical School, 30625 Hannover, Germany.
  5. 5Institute of Cell Biology in the Center of Anatomy, Hannover Medical School, 30625 Hannover, Germany.
  6. 6Department of Diagnostic and Interventional Radiology, Hannover Medical School, 30625 Hannover, Germany.
  7. 7Institute for Preclinical Molecular Imaging, Hannover Medical School, 30625 Hannover, Germany.
  1. Corresponding author. E-mail: hansen.gesine{at}mh-hannover.de
    • * These authors contributed equally to this work.

    • These authors contributed equally to this work.

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