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American Journal of Respiratory Cell and Molecular Biology|November 20, 2001
Germline mutations in an intermediate chain dynein cause primary ciliary dyskinesiaM Zariwala, P G Noone, A Sannuti, et al.American Journal of Respiratory and Critical Care Medicine|July 3, 1999
Effect of aerosolized uridine-5'-triphosphate on airway clearance with cough in patients with primary ciliary dyskinesiaP G Noone, W D Bennett, J A Regnis, et al.Human Gene Therapy|May 1, 1994
Gene therapy for cystic fibrosis using E1-deleted adenovirus: a phase I trial in the nasal cavity. The University of North Carolina at Chapel HillR C Boucher, M R Knowles, L G Johnson, et al.Diabetologia|July 9, 2009
A susceptibility gene for type 2 diabetes confers substantial risk for diabetes complicating cystic fibrosisS M Blackman, S Hsu, S E Ritter, et al.The Journal of Pediatrics|May 15, 1998
Uncertainty in the diagnosis of cystic fibrosis: possible role of in vivo nasal potential difference measurementsD C Wilson, L Ellis, J Zielenski, et al.Human Gene Therapy|February 24, 1998
A double-blind, placebo controlled, dose ranging study to evaluate the safety and biological efficacy of the lipid-DNA complex GR213487B in the nasal epithelium of adult patients with cystic fibrosisM R Knowles, P G Noone, K Hohneker, et al.FEBS Letters|June 7, 1993
Characterisation of a chimeric hD3/D2 dopamine receptor expressed in CHO cellsG McAllister, M R Knowles, S Patel, et al.The Journal of Clinical Investigation|November 20, 1997
Ion composition of airway surface liquid of patients with cystic fibrosis as compared with normal and disease-control subjectsM R Knowles, J M Robinson, R E Wood, et al.Clinical Radiology|December 2, 2014
Standardization and validation of a novel and simple method to assess lumbar dural sac sizeM L A Daniels, J R Lowe, P Roy, et al.Journal of Receptor and Signal Transduction Research|January 1, 1995
Functional coupling of human D2, D3, and D4 dopamine receptors in HEK293 cellsG McAllister, M R Knowles, S M Ward-Booth, et al.Pageof 10