Airway microbiota across age and disease spectrum in cystic fibrosis von Zemanick, Edith T, Wagner, Brandie D, Robertson, Charles E, Ahrens, Richard C, Chmiel, James F, Clancy, John P, Gibson, Ronald L, Harris, William T, Kurland, Geoffrey, Laguna, Theresa A, McColley, Susanna A, McCoy, Karen, Retsch-Bogart, George, Sobush, Kurtis T, Zeitlin, Pamela L, Stevens, Mark J, Accurso, Frank J, Sagel, Scott D, Harris, J Kirk

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Myofibroblast differentiation and enhanced TGF-B signaling in cystic fibrosis lung disease von Harris, William T, Kelly, David R, Zhou, Yong, Wang, Dezhi, MacEwen, Mark, Macewen, Mark, Hagood, James S, Clancy, J P, Ambalavanan, Namasivayam, Sorscher, Eric J

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Flexible bronchoscopy findings and management impact in children with oropharyngeal dysphagia von Simpson, Ryne C., Ale, Guillermo Beltran, Harris, William T

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An open-label extension study of ivacaftor in children with CF and a CFTR gating mutation initiating treatment at age 2–5 years (KLIMB) von Rosenfeld, Margaret, Cunningham, Steve, Harris, William T., Lapey, Allen, Regelmann, Warren E., Sawicki, Gregory S., Southern, Kevin W., Chilvers, Mark, Higgins, Mark, Tian, Simon, Cooke, Jon, Davies, Jane C.

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MicroRNA-145 Antagonism Reverses TGF-β Inhibition of F508del CFTR Correction in Airway Epithelia von Lutful Kabir, Farruk, Ambalavanan, Namasivayam, Liu, Gang, Li, Peng, Solomon, George M, Lal, Charitharth V, Mazur, Marina, Halloran, Brian, Szul, Tomasz, Gerthoffer, William T, Rowe, Steven M, Harris, William T

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MicroRNA-145 Antagonism Reverses TGF-b Inhibition of F508del CFTR Correction in Airway Epithelia von Kabir, Farruk Lutful, Ambalavanan, Namasivayam, Liu, Gang, Li, Peng, Solomon, George M, Lal, Charitharth V, Mazur, Marina, Halloran, Brian, Szul, Tomasz, Gerthoffer, William T, Rowe, Steven M, Harris, William T

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Tobacco smoke exposure limits the therapeutic benefit of tezacaftor/ivacaftor in pediatric patients with cystic fibrosis von Baker, Elizabeth, Harris, William T., Rowe, Steven M., Rutland, Sarah B., Oates, Gabriela R.

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Reply to Finotti et al. : Enhancing the Expression of CFTR Using Antisense Molecules against MicroRNA miR-145-5p von Lutful Kabir, Farruk, Harris, William T

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Effect of Prenatal versus Postnatal Vitamin D Deficiency on Pulmonary Structure and Function in Mice von Saadoon, Ammar, Ambalavanan, Namasivayam, Zinn, Kurt, Ashraf, Ambika P, MacEwen, Mark, Nicola, Teodora, Fanucchi, Michelle V, Harris, William T

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Adherence to airway clearance therapy in pediatric cystic fibrosis: Socioeconomic factors and respiratory outcomes von Oates, Gabriela R., Stepanikova, Irena, Gamble, Stephanie, Gutierrez, Hector H., Harris, William T.

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Objective Versus Self-Reported Adherence to Airway Clearance Therapy in Cystic Fibrosis von Oates, Gabriela R, Stepanikova, Irena, Rowe, Steven M, Gamble, Stephanie, Gutierrez, Hector H, Harris, William T

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Tobacco smoke exposure and socioeconomic factors are independent predictors of pulmonary decline in pediatric cystic fibrosis von Oates, Gabriela R., Baker, Elizabeth, Rowe, Steven M., Gutierrez, Hector H., Schechter, Michael S., Morgan, Wayne, Harris, William T.

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Alterations in blood leukocytes of G551D-bearing cystic fibrosis patients undergoing treatment with ivacaftor von Bratcher, Preston E, Rowe, Steven M, Reeves, Ginger, Roberts, Tambra, Szul, Tomasz, Harris, William T, Tirouvanziam, Rabindra, Gaggar, Amit

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Tobacco smoke exposure in pediatric cystic fibrosis: A qualitative study of clinician and caregiver perspectives on smoking cessation von Oates, Gabriela R., Harris, William T., Gutierrez, Hector H., Mims, Cathy, Rutland, Sarah B., Ott, Corilyn, Niranjan, Soumya J., Scarinci, Isabel C., Walley, Susan C.

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Cessation of smoke exposure improves pediatric CF outcomes: Longitudinal analysis of CF Foundation Patient Registry data von Oates, Gabriela R., Baker, Elizabeth, Collaco, Joseph M., Rowe, Steven M., Rutland, Sarah B., Fowler, Christopher M., Harris, William T.

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Risk factors for acute kidney injury during aminoglycoside therapy in patients with cystic fibrosis von Downes, Kevin J., Patil, Neha R., Rao, Marepalli B., Koralkar, Rajesh, Harris, William T., Clancy, John P., Goldstein, Stuart L., Askenazi, David J.

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Risk stratification model to detect early pulmonary disease in infants with cystic fibrosis diagnosed by newborn screening von Britton, Lacrecia J., Oates, Gabriela R., Oster, Robert A., Self, Staci T., Troxler, Robert B., Hoover, Wynton C., Gutierrez, Hector H., Harris, William T.

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CFTR dysfunction increases endoglin and TGF‐β signaling in airway epithelia von Nicola, Teodora, Kabir, Farruk L., Coric, Tatjana, Wall, Stephanie B., Zhang, Weifeng, James, Masheika, MacEwen, Mark, Ren, Changchun, Halloran, Brian, Ambalavanan, Namasivayam, Harris, William T.

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Transforming growth factor-β1 in bronchoalveolar lavage fluid from children with cystic fibrosis von Harris, William T., Muhlebach, Marianne S., Oster, Robert A., Knowles, Michael R., Noah, Terry L.

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Transforming growth factor-beta(1) in bronchoalveolar lavage fluid from children with cystic fibrosis von Harris, William T, Muhlebach, Marianne S, Oster, Robert A, Knowles, Michael R, Noah, Terry L

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