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Carla P. Jones

Researcher at National Institutes of Health

Publications -  22
Citations -  1409

Carla P. Jones is an academic researcher from National Institutes of Health. The author has contributed to research in topics: Bone marrow & Progenitor cell. The author has an hindex of 15, co-authored 21 publications receiving 1255 citations. Previous affiliations of Carla P. Jones include Wellcome Trust Sanger Institute & Federal University of Rio de Janeiro.

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Differential Mobilization of Subsets of Progenitor Cells from the Bone Marrow

TL;DR: It is shown that distinct factors and mechanisms regulate the mobilization of endothelial (EPCs) and stromal progenitor cells (SPCs) and that differential mobilization of progenitors cell subsets is dependent upon the cytokine milieu that regulates cell retention and proliferation.
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IL-9 governs allergen-induced mast cell numbers in the lung and chronic remodeling of the airways.

TL;DR: The data suggest an important role for an IL-9-MC axis in the pathology associated with chronic asthma and demonstrate that an impact on this axis could lead to a reduction in chronic inflammation and improved lung function in patients with asthma.
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IL-25 drives remodelling in allergic airways disease induced by house dust mite

TL;DR: A wider role for IL-25 is delineated in mediating structural changes to the lung following allergen exposure and this work implicatesIL-25 as a novel therapeutic target for the treatment of airway remodelling in asthma.
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Activin A and TGF-β promote TH9 cell–mediated pulmonary allergic pathology

TL;DR: A distinct functional role for T(H)9 cells is identified and a novel pathway for their generation in vitro and in vivo is outlined, which promotes allergic responses resulting in enhanced pathology mediated by the specific recruitment and activation of mast cells in the lungs.
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Quantifying the contribution of recessive coding variation to developmental disorders.

TL;DR: The results suggest that recessive coding variants account for a small fraction of currently undiagnosed nonconsanguineous individuals, and that the role of noncoding variants, incomplete penetrance, and polygenic mechanisms need further exploration.