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J.P. Clancy
Observed names:
J. Clancy,
J. P. Clancy
Institution:
Cystic Fibrosis Foundation
Observed institutions:
Cincinnati Children's Hospital Medical Center,
University of Alabama at Birmingham Hospital,
Johns Hopkins University,
Johns Hopkins Medicine,
Cystic Fibrosis Foundation,
University of Rochester Medicine,
University of Alabama at Birmingham,
University of Rochester
show all 8
OpenAlex ID:
A5113740607
Glucocorticoid treatment decreases muscarinic receptor expression in canine airway smooth muscle
1997
·
C. W. Emala
, J. Clancy
, et al.
·
American Journal of Physiology-Lung Cellular and Molecular Physiology
·
52
MgSO4 relaxes porcine airway smooth muscle by reducing Ca2+ entry
1996
·
D. Kumasaka
, K. S. Lindeman
, et al.
·
American Journal of Physiology-Lung Cellular and Molecular Physiology
·
22
Clinical evaluation of VX-809, a novel investigational oral F508del-CFTR corrector, in subjects with cystic fibrosis homozygous for the F508del–CFTR mutation
2010
·
J.P. Clancy
, G. Spencer-Green
·
Journal of Cystic Fibrosis
·
13
Parallel effects of VX-770 on transepithelial potential difference in vitro and in vivo
2010
·
S.M. Rowe
, J.P. Clancy
, et al.
·
Journal of Cystic Fibrosis
·
8
PDF
Genetic and Reproductive Knowledge Among Adolescents and Adults With Cystic Fibrosis
2008
·
Grace H. Houser
, Cheryl L. Holt
, et al.
·
CHEST Journal
·
8
PDF
Chronic carbachol pretreatment decreases adenylyl cyclase activity in airway smooth muscle
1997
·
G. Schears
, J. Clancy
, et al.
·
American Journal of Physiology-Lung Cellular and Molecular Physiology
·
7
EPS1.3 Safety, tolerability and early signs of efficacy with riociguat for the treatment of adult Phe508del homozygous cystic fibrosis patients: study design and rationale for the Rio-CF study
2017
·
N. Derichs
, J. Taylor-Cousar
, et al.
·
Journal of Cystic Fibrosis
·
5
PDF
WS7.3 Once-daily liposomal amikacin for inhalation is noninferior to twice-daily tobramycin inhalation solution in improving pulmonary function in cystic fibrosis patients with chronic infection due to Pseudomonas aeruginosa
2014
·
D. Bilton
, T. Pressler
, et al.
·
Journal of Cystic Fibrosis
·
5
PDF
Diagnosing cystic fibrosis in patients with non-diagnostic results: the case for intestinal current measurements
2010
·
J. P. Clancy
·
Thorax
·
4
PDF
Final results of a 14- and 28-day study of VX-770 in subjects with CF
2009
·
F.J. Accurso
, S.M. Rowe
, et al.
·
Journal of Cystic Fibrosis
·
4
PDF
112 Analysis of long-term use of liposomal amikacin for inhalation (LAI) in patients with cystic fibrosis (CF) who have chronic infection from Pseudomonas aeruginosa
2015
·
D. Bilton
, T. Pressler
, et al.
·
Journal of Cystic Fibrosis
·
3
PDF
Neutrophil Extracellular Trap Burden in CF and Disease Control BAL
2020
·
K.M. Hudock
, M. Imbrogno
, et al.
·
2
WS13.1 QR-010, an investigational RNA therapeutic, improves CFTR activity in cystic fibrosis subjects homozygous for the F508del mutation
2017
·
S. Rowe
, I. Sermet-Gaudelus
, et al.
·
Journal of Cystic Fibrosis
·
2
Cationic Liposomes for Gene Therapy Applications
1999
·
J.P. Clancy
, Eric S. Sorscher
·
2
P090 Treatment use among SIMPLIFY trial participants through 24 weeks of follow-up
2023
·
A.H. Gifford
, K. Odem-Davis
, et al.
·
Journal of Cystic Fibrosis
·
1
PDF
43: Monitoring and phenotyping rapid cystic fibrosis disease progression using community characteristics and environmental exposures
2021
·
A. Palipana
, E. Gecili
, et al.
·
Journal of Cystic Fibrosis
·
1
PDF
Improvement in ion transport biomarkers and spirometry with the investigational CFTR potentiator VX-770 in subjects with cystic fibrosis and the G551D-CFTR mutation
2010
·
S.M. Rowe
, F.J. Accurso
, et al.
·
Paediatric Respiratory Reviews
·
1
In vivo glucocorticoids decrease expression of muscarinic receptors in airway smooth muscle
1997
·
C.W. Emala
, J. Clancy
, et al.
·
Life Sciences
·
1
57: Secular drift in predictive accuracy of pulmonary exacerbations: A registry study
2021
·
Z. Wang
, G. Zhou
, et al.
·
Journal of Cystic Fibrosis
PDF
378: CF mouse airway smooth muscle in advanced age and allergic asthma
2021
·
E. Kramer
, K. Hudock
, et al.
·
Journal of Cystic Fibrosis
PDF
322: Communities of color provide insights about engagement barriers
2021
·
J. Hudson
, J. Green
, et al.
·
Journal of Cystic Fibrosis
PDF
34: Predicting declines in lung function with the U.S. CF registry: Impact of initiating highly effective modulator therapy
2021
·
G. Zhou
, Z. Wang
, et al.
·
Journal of Cystic Fibrosis
PDF
33: Hypertonic saline withdraw in CF patients while on ivacaftor: An analysis of the CF Foundation Patient Registry (CFFPR)
2021
·
B. Huang
, C. Chen
, et al.
·
Journal of Cystic Fibrosis
PDF
578: Serum biomarkers identified by proteomics and measured by commercially available assays associated with lung function during clinically stable states
2021
·
R. Szczesniak
, S. Heltshe
, et al.
·
Journal of Cystic Fibrosis
PDF
588: Insights into and input on genetic-based therapies and clinical trials by the cystic fibrosis community
2021
·
E. Aliaj
, J. Hudson
, et al.
·
Journal of Cystic Fibrosis
PDF
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Works count:
31
Citation count:
141
H-index:
6
I10-index:
3
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