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Doyle, RL
Hertz, MI
Dunitz, JM
Loyd, JE
Stecenko, AA
Wong, RL
Chappell, KA
Brazelton, T
Kovarik, JM
Appeldingmanse, S
Dou, L
Smith, HT
Tudor, D
Morris, RE
Citation: Rl. Doyle et al., RAD in stable lung and heart/lung transplant recipients: Safety, tolerability, pharmacokinetics, and impact of cystic fibrosis, J HEART LUN, 20(3), 2001, pp. 330-339
Citation: Ts. Blackwell et al., Dysregulated NF-kappa B activation in cystic fibrosis: evidence for a primary inflammatory disorder, AM J P-LUNG, 281(1), 2001, pp. L69-L70
Authors:
Stecenko, AA
King, G
Torii, K
Breyer, RM
Dworski, R
Blackwell, TS
Christman, JW
Brigham, KL
Citation: Aa. Stecenko et al., Dysregulated cytokine production in human cystic fibrosis bronchial epithelial cells, INFLAMMATIO, 25(3), 2001, pp. 145-155
Authors:
Cruz-Gervis, RA
Stecenko, AA
Blackwell, TS
Sealy, L
Loyd, JE
King, G
Brigham, KL
Citation: Ra. Cruz-gervis et al., Regulation of CCAAT/enhancer-binding protein-beta is altered in primary lung fibroblasts obtained from patients with idiopathic pulmonary fibrosis, CHEST, 120(1), 2001, pp. 9S-9S
Authors:
Davenport, PW
Cruz, M
Stecenko, AA
Kifle, Y
Citation: Pw. Davenport et al., Respiratory-related evoked potentials in children with life-threatening asthma, AM J R CRIT, 161(6), 2000, pp. 1830-1835
Authors:
Venkatakrishnan, A
Stecenko, AA
King, G
Blackwell, TR
Brigham, KL
Christman, JW
Blackwell, TS
Citation: A. Venkatakrishnan et al., Exaggerated activation of nuclear factor-kappa B and altered I kappa B-beta processing in cystic fibrosis bronchial epithelial cells, AM J RESP C, 23(3), 2000, pp. 396-403
Authors:
Brigham, KL
Lane, KB
Meyrick, B
Stecenko, AA
Strack, S
Cannon, DR
Caudill, M
Canonico, AE
Citation: Kl. Brigham et al., Transfection of nasal mucosa with a normal alpha(1)-antitrypsin gene in alpha(1)-antitrypsin-deficient subjects: Comparison with protein therapy, HUM GENE TH, 11(7), 2000, pp. 1023-1032
Authors:
Peters, MT
Brigham, KL
King, GA
Meyrick, BO
Gao, X
Stecenko, AA
Citation: Mt. Peters et al., Optimization of cationic liposome-mediated gene transfer to human bronchial epithelial cells expressing wild-type or abnormal cystic fibrosis transmembrane conductance regulator (CFTR), EXP LUNG R, 25(3), 1999, pp. 183-197