D
Dallas M. Hyde
Researcher at California National Primate Research Center
Publications - 212
Citations - 9715
Dallas M. Hyde is an academic researcher from California National Primate Research Center. The author has contributed to research in topics: Lung & Bronchoalveolar lavage. The author has an hindex of 49, co-authored 212 publications receiving 9198 citations. Previous affiliations of Dallas M. Hyde include University of California, Davis.
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Journal ArticleDOI
An Official Research Policy Statement of the American Thoracic Society/European Respiratory Society: Standards for Quantitative Assessment of Lung Structure
TL;DR: The lung poses special challenges, some of which are outlined below and discussed in later sections: Heterogeneity of lung structure requires standardized preparation methods, and the practice of picking specific samples or sections often fails to account for regional heterogeneity, leading to biased conclusions with respect to the whole organ.
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Mild and moderate asthma is associated with airway goblet cell hyperplasia and abnormalities in mucin gene expression.
Claudia L. Ordoñez,Ramin Khashayar,Hofer Wong,Ron Ferrando,Reen Wu,Dallas M. Hyde,Jon A. Hotchkiss,Yifan Zhang,Alexander Novikov,Gregory Dolganov,John V. Fahy +10 more
TL;DR: It is concluded that even mild asthma is associated with goblet cell hyperplasia and increased stored mucin in the airway epithelium, whereas moderate asthma isassociated with increased stored bronchial mucin and secreted mucin.
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Hypoxia-induced pulmonary artery adventitial remodeling and neovascularization: contribution of progenitor cells.
Neil Davie,Joseph T. Crossno,Maria G. Frid,Stephen Hofmeister,John T. Reeves,Dallas M. Hyde,Todd C. Carpenter,Jacqueline A. Brunetti,Ian McNiece,Kurt R. Stenmark +9 more
TL;DR: It is suggested that the vasa vasorum and circulating progenitor cells could be involved in vessel wall thickening in the setting of hypoxia-induced PH.
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Lung morphometry: a new generation of tools and experiments for organ, tissue, cell, and molecular biology
TL;DR: The new tools of quantitative morphology are described and it is shown how they can be used to design new experiments for lung research.
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In vivo blockade of OX40 ligand inhibits thymic stromal lymphopoietin driven atopic inflammation
Dhaya Seshasayee,Wyne P. Lee,Meijuan Zhou,Jean Shu,Eric Suto,Juan Zhang,Laurie Diehl,Cary D. Austin,Y. Gloria Meng,Martha Tan,Sherron Bullens,Stefan Seeber,Maria E. Fuentes,Aran F. Labrijn,Yvo Graus,Lisa A. Miller,Edward S. Schelegle,Dallas M. Hyde,Lawren C. Wu,Sarah G. Hymowitz,Sarah G. Hymowitz,Flavius Martin +21 more
TL;DR: It is shown that OX40 ligand (OX40L) is a critical in vivo mediator of TSLP-mediated Th2 responses and presents a promising strategy for the treatment of allergic diseases associated with pathologic Th2 immune responses.