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Publication

Macrophage Migration Inhibitory Factor (MIF) Inhibition in a Murine Model of Bleomycin-Induced Pulmonary Fibrosis.

Sven Günther | Jennifer Bordenave | Thông Hua-Huy | Carole Nicco | Amélie Cumont | Raphaël Thuillet | Ly Tu | Timothée Quatremarre | Thomas Guilbert | Gaël Jalce | Frédéric Batteux | Marc Humbert | Laurent Savale | Christophe Guignabert | Anh-Tuan Dinh-Xuan
International journal of molecular sciences | 2018

Pulmonary hypertension (PH) is a common complication of idiopathic pulmonary fibrosis (IPF) that significantly contributes to morbidity and mortality. Macrophage migration inhibitory factor (MIF) is a critical factor in vascular remodeling of the pulmonary circulation.

Pubmed ID: 30567353

Research resources used in this publication

None found

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Antibodies used in this publication

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Associated grants

  • Agency: Agence Nationale de la Recherche,
    Id: ANR-16-CE17-0014
  • Agency: Fondation pour la Recherche Médicale,
    Id: DEQ20150331712
  • Agency: Agence Nationale de la Recherche,
    Id: ANR-10-LABX-0033
  • Agency: Chancellerie des Universités de Paris,
    Id: Legs Poix
  • Agency: Assistance publique-Hôpitaux de Paris,
    Id: DHU TORINO
  • Agency: Fondation pour la Recherche Médicale,
    Id: Allocation de Thèse (JB)

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C57BL/6J (tool)

RRID:IMSR_JAX:000664

Mus musculus with name C57BL/6J from IMSR.

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