-
1
-
-
0024423668
-
Identification of the cystic fibrosis gene: Genetic analysis
-
Kerem, B., et al. 1989. Identification of the cystic fibrosis gene: genetic analysis. Science. 245:1073-1080.
-
(1989)
Science
, vol.245
, pp. 1073-1080
-
-
Kerem, B.1
-
2
-
-
0025241696
-
The relation between genotype and phenotype in cystic fibrosis - analysis of the most common mutation (delta F508)
-
Kerem, E., et al. 1990. The relation between genotype and phenotype in cystic fibrosis - analysis of the most common mutation (delta F508). N. Engl. J. Med. 323:1517-1522.
-
(1990)
N. Engl. J. Med
, vol.323
, pp. 1517-1522
-
-
Kerem, E.1
-
3
-
-
0026734588
-
Genetic determination of exocrine pancreatic function in cystic fibrosis
-
Kristidis, P., et al. 1992. Genetic determination of exocrine pancreatic function in cystic fibrosis. Am. J. Hum. Genet. 50:1178-1184.
-
(1992)
Am. J. Hum. Genet
, vol.50
, pp. 1178-1184
-
-
Kristidis, P.1
-
4
-
-
34248346723
-
Heritability of lung disease severity in cystic fibrosis
-
Vanscoy, L.L., et al. 2007. Heritability of lung disease severity in cystic fibrosis. Am. J. Respir. Crit. Care Med. 175:1036-1043.
-
(2007)
Am. J. Respir. Crit. Care Med
, vol.175
, pp. 1036-1043
-
-
Vanscoy, L.L.1
-
5
-
-
33749328098
-
Relative contribution of genetic and nongenetic modifiers to intestinal obstruction in cystic fibrosis
-
Blackman, S.M., et al. 2006. Relative contribution of genetic and nongenetic modifiers to intestinal obstruction in cystic fibrosis. Gastroenterology. 131:1030-1039.
-
(2006)
Gastroenterology
, vol.131
, pp. 1030-1039
-
-
Blackman, S.M.1
-
6
-
-
33751113932
-
Genetic and physiologic correlates of longitudinal immunoreactive trypsinogen decline in infants with cystic fibrosis identified through newborn screening
-
Sontag, M.K., et al. 2006. Genetic and physiologic correlates of longitudinal immunoreactive trypsinogen decline in infants with cystic fibrosis identified through newborn screening. J. Pediatr. 149:650-657.
-
(2006)
J. Pediatr
, vol.149
, pp. 650-657
-
-
Sontag, M.K.1
-
7
-
-
25844491194
-
Genetic modifiers of lung disease in cystic fibrosis
-
Drumm, M.L., et al. 2005. Genetic modifiers of lung disease in cystic fibrosis. N. Engl. J. Med. 353:1443-1453.
-
(2005)
N. Engl. J. Med
, vol.353
, pp. 1443-1453
-
-
Drumm, M.L.1
-
8
-
-
33750454431
-
Disease modifying genes in cystic fibrosis: Therapeutic option or one-way road?
-
Buscher, R., and Grasemann, H. 2006. Disease modifying genes in cystic fibrosis: therapeutic option or one-way road? Naunyn. Schmiedebergs Arch. Pharmacol. 374:65-77.
-
(2006)
Naunyn. Schmiedebergs Arch. Pharmacol
, vol.374
, pp. 65-77
-
-
Buscher, R.1
Grasemann, H.2
-
9
-
-
40549083327
-
Complex two-gene modulation of lung disease severity in children with cys tic fibrosis
-
Dorfman, R., et al. 2008. Complex two-gene modulation of lung disease severity in children with cys tic fibrosis. J. Clin. Invest. 118:1040-1049.
-
(2008)
J. Clin. Invest
, vol.118
, pp. 1040-1049
-
-
Dorfman, R.1
-
10
-
-
0032695668
-
Association of mannose-binding lectin gene heterogeneity with severity of lung disease and survival in cystic fibrosis
-
Garred, P., et al. 1999. Association of mannose-binding lectin gene heterogeneity with severity of lung disease and survival in cystic fibrosis. J. Clin. Invest. 104:431-437.
-
(1999)
J. Clin. Invest
, vol.104
, pp. 431-437
-
-
Garred, P.1
-
11
-
-
34447530328
-
Risk factors for rate of decline in forced expiratory volume in one second in children and adolescents with cystic fibrosis
-
Konstan, M.W., et al. 2007. Risk factors for rate of decline in forced expiratory volume in one second in children and adolescents with cystic fibrosis. J. Pediatr. 151:134-139.
-
(2007)
J. Pediatr
, vol.151
, pp. 134-139
-
-
Konstan, M.W.1
-
12
-
-
0030995361
-
Antibiotic treatment of initial colonization with Pseudomonas aeruginosa postpones chronic infection and prevents deterioration of pulmonary function in cystic fibrosis
-
Frederiksen, B., Koch, C., and Hoiby, N. 1997. Antibiotic treatment of initial colonization with Pseudomonas aeruginosa postpones chronic infection and prevents deterioration of pulmonary function in cystic fibrosis. Pediatr. Pulmonol. 23:330-335.
-
(1997)
Pediatr. Pulmonol
, vol.23
, pp. 330-335
-
-
Frederiksen, B.1
Koch, C.2
Hoiby, N.3
-
13
-
-
34548286919
-
Detection of cystic fibrosis transmembrane conductance regulator activity in early-phase clinical trials
-
Rowe, S.M., Accurso, F., and Clancy, J.P. 2007. Detection of cystic fibrosis transmembrane conductance regulator activity in early-phase clinical trials. Proc. Am. Thorac. Soc. 4:387-398.
-
(2007)
Proc. Am. Thorac. Soc
, vol.4
, pp. 387-398
-
-
Rowe, S.M.1
Accurso, F.2
Clancy, J.P.3
-
14
-
-
34147103990
-
Variants in mannose-binding lectin and tumor necrosis factor {alpha} affect survival in cystic fibrosis
-
Buranawuti, K., et al. 2006. Variants in mannose-binding lectin and tumor necrosis factor {alpha} affect survival in cystic fibrosis. J. Med. Genet. 44:209-214.
-
(2006)
J. Med. Genet
, vol.44
, pp. 209-214
-
-
Buranawuti, K.1
-
15
-
-
33749246730
-
Mutations of TGFbeta signaling molecules in human disease
-
Harradine, K.A., and Akhurst, R.J. 2006. Mutations of TGFbeta signaling molecules in human disease. Ann. Med. 38:403-414.
-
(2006)
Ann. Med
, vol.38
, pp. 403-414
-
-
Harradine, K.A.1
Akhurst, R.J.2
-
16
-
-
34548273107
-
Advancing outcome measures for the new era of drug development in cystic fibrosis
-
Mayer-Hamblett, N., Ramsey, B.W., and Kronmal, R.A. 2007. Advancing outcome measures for the new era of drug development in cystic fibrosis. Proc. Am. Thorac. Soc. 4:370-377.
-
(2007)
Proc. Am. Thorac. Soc
, vol.4
, pp. 370-377
-
-
Mayer-Hamblett, N.1
Ramsey, B.W.2
Kronmal, R.A.3
-
17
-
-
17744372496
-
Early diagnosis of cystic fibrosis through neonatal screening prevents severe malnutrition and improves long-term growth
-
Farrell, P.M., et al. 2001. Early diagnosis of cystic fibrosis through neonatal screening prevents severe malnutrition and improves long-term growth. Pediatrics. 107:1-13.
-
(2001)
Pediatrics
, vol.107
, pp. 1-13
-
-
Farrell, P.M.1
|