-
1
-
-
47249140827
-
Congenital tracheal malformation in cystic fibrosis transmembrane conductance regulator-deficient mice
-
Bonvin E., Le Rouzic P., Bernaudin J.F., Cottart C.H., Vandebrouck C., Crie A., Leal T., Clement A., Bonora M. Congenital tracheal malformation in cystic fibrosis transmembrane conductance regulator-deficient mice. J. Physiol. 2008, 586:3231-3243.
-
(2008)
J. Physiol.
, vol.586
, pp. 3231-3243
-
-
Bonvin, E.1
Le Rouzic, P.2
Bernaudin, J.F.3
Cottart, C.H.4
Vandebrouck, C.5
Crie, A.6
Leal, T.7
Clement, A.8
Bonora, M.9
-
2
-
-
25444507445
-
The "Goldilocks effect" in cystic fibrosis: identification of a lung phenotype in the cftr knockout and heterozygous mouse
-
Cohen J.C., Lundblad L.K., Bates J.H., Levitzky M., Larson J.E. The "Goldilocks effect" in cystic fibrosis: identification of a lung phenotype in the cftr knockout and heterozygous mouse. BMC Genet. 2004, 5:21.
-
(2004)
BMC Genet.
, vol.5
, pp. 21
-
-
Cohen, J.C.1
Lundblad, L.K.2
Bates, J.H.3
Levitzky, M.4
Larson, J.E.5
-
3
-
-
0031438318
-
Lung disease in mice with cystic fibrosis
-
Kent G., Iles R., Bear C.E., Huan L.J., Griesenbach U., McKerlie C., Frndova H., Ackerley C., Gosselin D., Radzioch D., O'Brodovich H., Tsui L.C., Buchwald M., Tanswell A.K. Lung disease in mice with cystic fibrosis. J. Clin. Invest. 1997, 100:3060-3069.
-
(1997)
J. Clin. Invest.
, vol.100
, pp. 3060-3069
-
-
Kent, G.1
Iles, R.2
Bear, C.E.3
Huan, L.J.4
Griesenbach, U.5
McKerlie, C.6
Frndova, H.7
Ackerley, C.8
Gosselin, D.9
Radzioch, D.10
O'Brodovich, H.11
Tsui, L.C.12
Buchwald, M.13
Tanswell, A.K.14
-
4
-
-
2442718786
-
Increased airway epithelial Na+ absorption produces cystic fibrosis-like lung disease in mice
-
Mall M., Grubb B.R., Harkema J.R., O'Neal W.K., Boucher R.C. Increased airway epithelial Na+ absorption produces cystic fibrosis-like lung disease in mice. Nat. Med. 2004, 10:487-493.
-
(2004)
Nat. Med.
, vol.10
, pp. 487-493
-
-
Mall, M.1
Grubb, B.R.2
Harkema, J.R.3
O'Neal, W.K.4
Boucher, R.C.5
-
5
-
-
58449116969
-
Role of the amiloride-sensitive epithelial Na+ channel in the pathogenesis and as a therapeutic target for cystic fibrosis lung disease
-
Mall M.A. Role of the amiloride-sensitive epithelial Na+ channel in the pathogenesis and as a therapeutic target for cystic fibrosis lung disease. Exp. Physiol. 2009, 94:171-174.
-
(2009)
Exp. Physiol.
, vol.94
, pp. 171-174
-
-
Mall, M.A.1
-
6
-
-
41749115751
-
Development of chronic bronchitis and emphysema in beta-epithelial Na+ channel-overexpressing mice
-
Mall M.A., Harkema J.R., Trojanek J.B., Treis D., Livraghi A., Schubert S., Zhou Z., Kreda S.M., Tilley S.L., Hudson E.J., O'Neal W.K., Boucher R.C. Development of chronic bronchitis and emphysema in beta-epithelial Na+ channel-overexpressing mice. Am. J. Respir. Crit. Care Med. 2008, 177:730-742.
-
(2008)
Am. J. Respir. Crit. Care Med.
, vol.177
, pp. 730-742
-
-
Mall, M.A.1
Harkema, J.R.2
Trojanek, J.B.3
Treis, D.4
Livraghi, A.5
Schubert, S.6
Zhou, Z.7
Kreda, S.M.8
Tilley, S.L.9
Hudson, E.J.10
O'Neal, W.K.11
Boucher, R.C.12
-
7
-
-
70249118542
-
Tracheomalacia in adults with cystic fibrosis: determination of prevalence and severity with dynamic cine CT
-
McDermott S., Barry S.C., Judge E.E., Collins S., de Jong P.A., Tiddens H.A., McKone E.F., Gallagher C.C., Dodd J.D. Tracheomalacia in adults with cystic fibrosis: determination of prevalence and severity with dynamic cine CT. Radiology 2009, 252:577-586.
-
(2009)
Radiology
, vol.252
, pp. 577-586
-
-
McDermott, S.1
Barry, S.C.2
Judge, E.E.3
Collins, S.4
de Jong, P.A.5
Tiddens, H.A.6
McKone, E.F.7
Gallagher, C.C.8
Dodd, J.D.9
-
8
-
-
78349237748
-
Loss of cystic fibrosis transmembrane conductance regulator function produces abnormalities in tracheal development in neonatal pigs and young children
-
Meyerholz D.K., Stoltz D.A., Namati E., Ramachandran S., Pezzulo A.A., Smith A.R., Rector M.V., Suter M.J., Kao S., McLennan G., Tearney G.J., Zabner J., McCray P.B., Welsh M.J. Loss of cystic fibrosis transmembrane conductance regulator function produces abnormalities in tracheal development in neonatal pigs and young children. Am. J. Respir. Crit. Care Med. 2010, 182:1251-1261.
-
(2010)
Am. J. Respir. Crit. Care Med.
, vol.182
, pp. 1251-1261
-
-
Meyerholz, D.K.1
Stoltz, D.A.2
Namati, E.3
Ramachandran, S.4
Pezzulo, A.A.5
Smith, A.R.6
Rector, M.V.7
Suter, M.J.8
Kao, S.9
McLennan, G.10
Tearney, G.J.11
Zabner, J.12
McCray, P.B.13
Welsh, M.J.14
-
9
-
-
49049118639
-
The transmembrane protein TMEM16A is required for normal development of the murine trachea
-
Rock J.R., Futtner C.R., Harfe B.D. The transmembrane protein TMEM16A is required for normal development of the murine trachea. Dev. Biol. 2008, 321:141-149.
-
(2008)
Dev. Biol.
, vol.321
, pp. 141-149
-
-
Rock, J.R.1
Futtner, C.R.2
Harfe, B.D.3
-
10
-
-
66749182796
-
Inspiratory duty cycle responses to flow limitation predict nocturnal hypoventilation
-
Schneider H., Krishnan V., Pichard L.E., Patil S.P., Smith P.L., Schwartz A.R. Inspiratory duty cycle responses to flow limitation predict nocturnal hypoventilation. Eur. Respir. J. 2009, 33:1068-1076.
-
(2009)
Eur. Respir. J.
, vol.33
, pp. 1068-1076
-
-
Schneider, H.1
Krishnan, V.2
Pichard, L.E.3
Patil, S.P.4
Smith, P.L.5
Schwartz, A.R.6
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