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Louise C. Pyle

Researcher at Children's Hospital of Philadelphia

Publications -  39
Citations -  1134

Louise C. Pyle is an academic researcher from Children's Hospital of Philadelphia. The author has contributed to research in topics: Medicine & Cystic fibrosis transmembrane conductance regulator. The author has an hindex of 16, co-authored 34 publications receiving 865 citations. Previous affiliations of Louise C. Pyle include National Institutes of Health & University of Alabama at Birmingham.

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Integrated Molecular Characterization of Testicular Germ Cell Tumors

TL;DR: High-dimensional analyses identified distinct molecular patterns that characterized the major recognized histologic subtypes of TGCT: seminoma, embryonal carcinoma, yolk sac tumor, and teratoma, and a subset of pure seminomas defined by KIT mutations, increased immune infiltration, globally demethylated DNA, and decreased KRAS copy number.
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ΔF508 CFTR processing correction and activity in polarized airway and non-airway cell monolayers

TL;DR: Treatment with non-specific inhibitors of phosphodiesterases or phosphatases did not restore DeltaF508 CFTR activation by forskolin in CFBE41o(-) cells, indicating that the Cl(-) transport defect in airway cells is distal to cAMP or its metabolism.
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Cloning and Characterization of HB2, a Candidate High Density Lipoprotein Receptor SEQUENCE HOMOLOGY WITH MEMBERS OF THE IMMUNOGLOBULIN SUPERFAMILY OF MEMBRANE PROTEINS

TL;DR: If the interaction between HDL and HB2 reduces the adhesion-induced inflammatory cellular events that characterize arterial wall injury, thereby achieving the protection associated with higher plasma levels of HDL, these findings may provide a clue to one mitigating effect of HDL in heart disease.
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Identification of human and mouse hematopoietic stem cell populations expressing high levels of mRNA encoding retrovirus receptors

TL;DR: HSC from frozen cord blood and cytokine-mobilized BM may be superior targets for amphotropic retrovirus transduction compared with HSC from untreated adult BM.