-
1
-
-
0024453308
-
Identification of the cystic fibrosis gene: Chromosome walking and jumping
-
Rommens JM, Iannuzzi MC, Kerem B, et al. Identification of the cystic fibrosis gene: chromosome walking and jumping. Science 1989;245:1059-65.
-
(1989)
Science
, vol.245
, pp. 1059-1065
-
-
Rommens, J.M.1
Iannuzzi, M.C.2
Kerem, B.3
-
2
-
-
0024424270
-
Identification of the cystic fibrosis gene: Cloning and characterization of complementary DNA
-
Riordan JR, Rommens JM, Kerem B, et al. Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA. Science 1989;245:1066-73.
-
(1989)
Science
, vol.245
, pp. 1066-1073
-
-
Riordan, J.R.1
Rommens, J.M.2
Kerem, B.3
-
3
-
-
0024423668
-
Identification of the cystic fibrosis gene: Genetic analysis
-
Kerem B, Rommens JM, Buchanan JA, et al. Identification of the cystic fibrosis gene: genetic analysis. Science 1989;245:1073-80.
-
(1989)
Science
, vol.245
, pp. 1073-1080
-
-
Kerem, B.1
Rommens, J.M.2
Buchanan, J.A.3
-
4
-
-
0025937887
-
Biochemical and molecular genetics of cystic fibrosis
-
Tsui LC, Buchwald M. Biochemical and molecular genetics of cystic fibrosis [review]. Adv Hum Genet 1991; 20:153-266, 311-2.
-
(1991)
Adv Hum Genet
, vol.20
, pp. 153-266
-
-
Tsui, L.C.1
Buchwald, M.2
-
5
-
-
0026532895
-
Purification and functional reconstitution of the cystic fibrosis transmembrane regulator (CFTR)
-
Bear CE, Li C, Kartner N, et al. Purification and functional reconstitution of the cystic fibrosis transmembrane regulator (CFTR). Cell 1992;68:809-18.
-
(1992)
Cell
, vol.68
, pp. 809-818
-
-
Bear, C.E.1
Li, C.2
Kartner, N.3
-
6
-
-
0000026508
-
Cystic fibrosis
-
Scriver CR, Beaudet AL, Sly WS,Valle D, editors. New York: McGraw-Hill
-
Welsh MJ, Tsui L-C, Boat TF, Beaudet AL. Cystic fibrosis. In: Scriver CR, Beaudet AL, Sly WS,Valle D, editors. The metabolic basis of inherited disease. 7th ed. New York: McGraw-Hill, 1994:3799-876.
-
(1994)
The Metabolic Basis of Inherited Disease. 7th Ed.
, pp. 3799-3876
-
-
Welsh, M.J.1
Tsui, L.-C.2
Boat, T.F.3
Beaudet, A.L.4
-
7
-
-
0023629643
-
Pathological confirmation of cystic fibrosis in the fetus following prenatal diagnosis
-
Ornoy, A, Arnos J, Katznelson D, Granat M, Caspi B, Chemke J. Pathological confirmation of cystic fibrosis in the fetus following prenatal diagnosis. Am J Med Genet 1987;28:935-47.
-
(1987)
Am J Med Genet
, vol.28
, pp. 935-947
-
-
Ornoy, A.1
Arnos, J.2
Katznelson, D.3
Granat, M.4
Caspi, B.5
Chemke, J.6
-
8
-
-
0016417460
-
Pathology of cystic fibrosis. Review of the literature and comparison with 146 autopsied cases
-
Oppenheimer EH, Esterly JR. Pathology of cystic fibrosis. Review of the literature and comparison with 146 autopsied cases. Perspect Pediatr Pathol 1975; 2:241-78.
-
(1975)
Perspect Pediatr Pathol
, vol.2
, pp. 241-278
-
-
Oppenheimer, E.H.1
Esterly, J.R.2
-
9
-
-
0345344670
-
The reproductive system
-
Taussig L, editor. New York: Thieme Stratton
-
Brugman S, Taussig L. The reproductive system. In: Taussig L, editor. Cystic fibrosis. New York: Thieme Stratton, 1984:323-37.
-
(1984)
Cystic Fibrosis
, pp. 323-337
-
-
Brugman, S.1
Taussig, L.2
-
10
-
-
0014904731
-
Observations on cystic fibrosis of the pancreas. VI. The uterine cervix
-
Oppenheimer EH, Esterly JR. Observations on cystic fibrosis of the pancreas. VI. The uterine cervix. J Pediatr 1970;77:991-5.
-
(1970)
J Pediatr
, vol.77
, pp. 991-995
-
-
Oppenheimer, E.H.1
Esterly, J.R.2
-
11
-
-
0014597161
-
Observations on cystic fibrosis of the pancreas. V. Developmental changes in the male genital system
-
Oppenheimer EH, Esterly JR. Observations on cystic fibrosis of the pancreas. V. Developmental changes in the male genital system. J Pediatr 1969;75:806-11.
-
(1969)
J Pediatr
, vol.75
, pp. 806-811
-
-
Oppenheimer, E.H.1
Esterly, J.R.2
-
12
-
-
0029160442
-
CFTR expression and organ damage in cystic fibrosis
-
Tizzano EF, Buchwald M. CFTR expression and organ damage in cystic fibrosis. Ann Intern Med 1995; 123:305-8.
-
(1995)
Ann Intern Med
, vol.123
, pp. 305-308
-
-
Tizzano, E.F.1
Buchwald, M.2
-
13
-
-
0028418099
-
Regional expression of CFTR in developing human respiratory tissues
-
Tizzano E, O'Brodovich H, Chitayat D, Bénichou JC, Buchwald M. Regional expression of CFTR in developing human respiratory tissues. Am J Resp Cell Mol Biol 1994;10:355-62.
-
(1994)
Am J Resp Cell Mol Biol
, vol.10
, pp. 355-362
-
-
Tizzano, E.1
O'Brodovich, H.2
Chitayat, D.3
Bénichou, J.C.4
Buchwald, M.5
-
14
-
-
0028914085
-
Early pulmonary inflammation in infants with cystic fibrosis
-
Khan TZ, Wagener JS, Bost T, Martinez J, Accurso FJ, Riches DWH. Early pulmonary inflammation in infants with cystic fibrosis. Am J Resp Crit Care Med 1995;151:1075-82.
-
(1995)
Am J Resp Crit Care Med
, vol.151
, pp. 1075-1082
-
-
Khan, T.Z.1
Wagener, J.S.2
Bost, T.3
Martinez, J.4
Accurso, F.J.5
Riches, D.W.H.6
-
15
-
-
0028874306
-
Bronchoalveolar lavage findings in cystic fibrosis patients with stable, clinically mild lung disease suggest ongoing infection and inflammation
-
Konstan MW, Hilliard KA, Norvell TM, Berger M. Bronchoalveolar lavage findings in cystic fibrosis patients with stable, clinically mild lung disease suggest ongoing infection and inflammation. Am J Resp Crit Care Med 1995;151:448-54.
-
(1995)
Am J Resp Crit Care Med
, vol.151
, pp. 448-454
-
-
Konstan, M.W.1
Hilliard, K.A.2
Norvell, T.M.3
Berger, M.4
-
16
-
-
0023505801
-
Pancreatic and intestinal dysfunction in cystic fibrosis
-
Riordan JR, Buchwald M, editors. New York: Alan R. Liss
-
Forstner G, Kopelman H, Durie P, Corey M. Pancreatic and intestinal dysfunction in cystic fibrosis. In: Riordan JR, Buchwald M, editors. Genetics and epithelial cell dysfunction in cystic fibrosis. New York: Alan R. Liss, 1987:7-17.
-
(1987)
Genetics and Epithelial Cell Dysfunction in Cystic Fibrosis
, pp. 7-17
-
-
Forstner, G.1
Kopelman, H.2
Durie, P.3
Corey, M.4
-
17
-
-
0026641782
-
The spectrum of cystic fibrosis mutations
-
Tsui L-C. The spectrum of cystic fibrosis mutations. Trends Genet 1992;8:392-8.
-
(1992)
Trends Genet
, vol.8
, pp. 392-398
-
-
Tsui, L.-C.1
-
18
-
-
0025787393
-
In vivo cell-specific expression of the cystic fibrosis transmembrane regulator
-
Trezise AEO, Buchwald M. In vivo cell-specific expression of the cystic fibrosis transmembrane regulator. Nature 1991;353:434-7.
-
(1991)
Nature
, vol.353
, pp. 434-437
-
-
Trezise, A.E.O.1
Buchwald, M.2
-
19
-
-
0027195534
-
Cell-specific localization of CFTR mRNA shows developmentally regulated expression in human fetal tissues
-
Tizzano EF, Chitayat D, Buchwald M. Cell-specific localization of CFTR mRNA shows developmentally regulated expression in human fetal tissues. Hum Mol Genet 1993;3:219-24.
-
(1993)
Hum Mol Genet
, vol.3
, pp. 219-224
-
-
Tizzano, E.F.1
Chitayat, D.2
Buchwald, M.3
-
20
-
-
0027207509
-
Expression of the cystic fibrosis gene in human foetal tissues
-
Trezise A, Chambers J, Wardle C, Gould S, Harris A. Expression of the cystic fibrosis gene in human foetal tissues. Hum Mol Genet 1993;2:213-8.
-
(1993)
Hum Mol Genet
, vol.2
, pp. 213-218
-
-
Trezise, A.1
Chambers, J.2
Wardle, C.3
Gould, S.4
Harris, A.5
-
21
-
-
0028356865
-
Differential cellular expression of CFTR in human reproductive tissues: Clues for the infertility in patients with cystic fibrosis
-
Tizzano EF, Silver MM, Chitayat D, Benichou JC, Buchwald M. Differential cellular expression of CFTR in human reproductive tissues: clues for the infertility in patients with cystic fibrosis. Am J Pathol 1994; 144:906-14.
-
(1994)
Am J Pathol
, vol.144
, pp. 906-914
-
-
Tizzano, E.F.1
Silver, M.M.2
Chitayat, D.3
Benichou, J.C.4
Buchwald, M.5
-
22
-
-
0027250106
-
Stimulation of the cystic fibrosis transmembrane regulator expression by estrogen in vivo
-
Rochwerger L, Buchwald M. Stimulation of the cystic fibrosis transmembrane regulator expression by estrogen in vivo. Endocrinology 1993;133:921-30.
-
(1993)
Endocrinology
, vol.133
, pp. 921-930
-
-
Rochwerger, L.1
Buchwald, M.2
-
23
-
-
24644445310
-
Cell cultures in CF research
-
Dodge JA, Brock DJH, Widdicombe JH, editors. Chichester, England: John Wiley and Sons
-
Rochwerger L, Buchwald M. Cell cultures in CF research. In: Dodge JA, Brock DJH, Widdicombe JH, editors. Current topics in cystic fibrosis. Vol 3. Chichester, England: John Wiley and Sons, 1996:1-37.
-
(1996)
Current Topics in Cystic Fibrosis
, vol.3
, pp. 1-37
-
-
Rochwerger, L.1
Buchwald, M.2
-
25
-
-
0027488993
-
The common variant of cystic fibrosis transmembrane conductance regulator is recognized by hsp70 and degraded in a pre-Golgi nonlysosomal compartment
-
Yang Y, Janich S, Cohn JA, Wilson JM. The common variant of cystic fibrosis transmembrane conductance regulator is recognized by hsp70 and degraded in a pre-Golgi nonlysosomal compartment. Proc Natl Acad Sci U S A 1993;90:9480-4.
-
(1993)
Proc Natl Acad Sci U S A
, vol.90
, pp. 9480-9484
-
-
Yang, Y.1
Janich, S.2
Cohn, J.A.3
Wilson, J.M.4
-
26
-
-
0028232167
-
Participation of the endoplasmic reticulum chaperone calnexin (p88, IP90) in the biogenesis of the cystic fibrosis transmembrane conductance regulator
-
Find S, Riordan JR, Williams DB. Participation of the endoplasmic reticulum chaperone calnexin (p88, IP90) in the biogenesis of the cystic fibrosis transmembrane conductance regulator. J Biol Chem 1994;269:12784-8.
-
(1994)
J Biol Chem
, vol.269
, pp. 12784-12788
-
-
Find, S.1
Riordan, J.R.2
Williams, D.B.3
-
27
-
-
0026781952
-
Processing of mutant cystic fibrosis transmembrane conductance regulator is temperature-sensitive
-
Denning GM, Anderson MP, Amara JF, Marshall J, Smith AE, Welsh MJ. Processing of mutant cystic fibrosis transmembrane conductance regulator is temperature-sensitive. Nature 1992;358:761-4.
-
(1992)
Nature
, vol.358
, pp. 761-764
-
-
Denning, G.M.1
Anderson, M.P.2
Amara, J.F.3
Marshall, J.4
Smith, A.E.5
Welsh, M.J.6
-
28
-
-
0025242929
-
Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosis
-
Cheng SH, Gregory RJ, Marshall J, et al. Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosis. Cell 1990; 63:827-34.
-
(1990)
Cell
, vol.63
, pp. 827-834
-
-
Cheng, S.H.1
Gregory, R.J.2
Marshall, J.3
-
29
-
-
0027162649
-
Molecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosis
-
Welsh MJ, Smith AE. Molecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosis. Cell 1993;73:1251-4.
-
(1993)
Cell
, vol.73
, pp. 1251-1254
-
-
Welsh, M.J.1
Smith, A.E.2
-
30
-
-
0027483610
-
The cystic fibrosis mutation (ΔF508) does not influence the chloride channel activity of CFTR
-
Li C, Ramjeesingh M, Reyes E, et al. The cystic fibrosis mutation (ΔF508) does not influence the chloride channel activity of CFTR. Nat Genet 1993;3:311-6.
-
(1993)
Nat Genet
, vol.3
, pp. 311-316
-
-
Li, C.1
Ramjeesingh, M.2
Reyes, E.3
-
31
-
-
0027380236
-
The ΔF508 mutation decreases the stability of cystic fibrosis transmembrane conductance regulator in the plasma membrane
-
Lukacs GL, Chang X-B, Bear C, et al. The ΔF508 mutation decreases the stability of cystic fibrosis transmembrane conductance regulator in the plasma membrane. J Biol Chem 1993;268:21592-8.
-
(1993)
J Biol Chem
, vol.268
, pp. 21592-21598
-
-
Lukacs, G.L.1
Chang, X.-B.2
Bear, C.3
-
32
-
-
0026687360
-
- secretion in colonic epithelial cells expressing high levels of cystic fibrosis transmembrane conductance regulator
-
- secretion in colonic epithelial cells expressing high levels of cystic fibrosis transmembrane conductance regulator. J Biol Chem 1993; 267:5575-83.
-
(1993)
J Biol Chem
, vol.267
, pp. 5575-5583
-
-
Morris, A.P.1
Cunningham, S.A.2
Benos, D.J.3
Frizzel, R.A.4
-
33
-
-
0027402791
-
Localization of the cystic fibrosis transmembrane regulator in adult human lung
-
Jacquot J, Puchelle E, Hinnrasky J, et al. Localization of the cystic fibrosis transmembrane regulator in adult human lung. Eur Respir J 1993;6:169-76.
-
(1993)
Eur Respir J
, vol.6
, pp. 169-176
-
-
Jacquot, J.1
Puchelle, E.2
Hinnrasky, J.3
-
34
-
-
0026907529
-
Mislocalization of ΔF508 CFTR in the cystic fibrosis sweat gland
-
Kartner N, Augustinas O, Jensen TJ, Naismith AL, Riordan JR. Mislocalization of ΔF508 CFTR in the cystic fibrosis sweat gland. Nat Genet 1992;1:321-7.
-
(1992)
Nat Genet
, vol.1
, pp. 321-327
-
-
Kartner, N.1
Augustinas, O.2
Jensen, T.J.3
Naismith, A.L.4
Riordan, J.R.5
-
35
-
-
0026954365
-
Differential localization of the cystic fibrosis transmembrane conductance regulator in normal and cystic fibrosis airway epithelium
-
Puchelle E, Gaillard D, Ploton D, et al. Differential localization of the cystic fibrosis transmembrane conductance regulator in normal and cystic fibrosis airway epithelium. Am J Resp Cell Mol Biol 1992; 7:485-91.
-
(1992)
Am J Resp Cell Mol Biol
, vol.7
, pp. 485-491
-
-
Puchelle, E.1
Gaillard, D.2
Ploton, D.3
-
36
-
-
0026325533
-
Altered chloride ion channel kinetics associated with the ΔF508 cystic fibrosis mutation
-
Dalemans W, Barbry P, Champigny G, et al. Altered chloride ion channel kinetics associated with the ΔF508 cystic fibrosis mutation. Nature 1991;354: 526-8.
-
(1991)
Nature
, vol.354
, pp. 526-528
-
-
Dalemans, W.1
Barbry, P.2
Champigny, G.3
-
37
-
-
0026581842
-
Regulation of plasma membrane recycling by CFTR
-
Bradbury NA, Jilling T, Barta G, Sorscher EJ, Bridges RJ, Kirk KL. Regulation of plasma membrane recycling by CFTR. Science 1992;256:530-2.
-
(1992)
Science
, vol.256
, pp. 530-532
-
-
Bradbury, N.A.1
Jilling, T.2
Barta, G.3
Sorscher, E.J.4
Bridges, R.J.5
Kirk, K.L.6
-
38
-
-
0028977988
-
- channel is functional when retained in endoplasmic reticulum of mammalian cells
-
- channel is functional when retained in endoplasmic reticulum of mammalian cells. J Biol Chem 1995;270:12347-50.
-
(1995)
J Biol Chem
, vol.270
, pp. 12347-12350
-
-
Pasyk, E.A.1
Foskett, J.K.2
-
40
-
-
0026649122
-
An animal model for cystic fibrosis made by gene targeting
-
Snouwaert JN, Brigman KK, Latour AM, et al. An animal model for cystic fibrosis made by gene targeting. Science 1992;257:1083-8.
-
(1992)
Science
, vol.257
, pp. 1083-1088
-
-
Snouwaert, J.N.1
Brigman, K.K.2
Latour, A.M.3
-
41
-
-
84920208084
-
Cystic fibrosis mouse with intestinal obstruction
-
Colledge WH, Ratcliff R, Foster D, Williamson R, Evans MJ. Cystic fibrosis mouse with intestinal obstruction [letter]. Lancet 1992;340:680.
-
(1992)
Lancet
, vol.340
, pp. 680
-
-
Colledge, W.H.1
Ratcliff, R.2
Foster, D.3
Williamson, R.4
Evans, M.J.5
-
42
-
-
0027379757
-
A severe phenotype in mice with a duplication of exon 3 in the cystic fibrosis locus
-
O'Neal WK, Hasty P, McCray PB, et al. A severe phenotype in mice with a duplication of exon 3 in the cystic fibrosis locus. Hum Mol Genet 1993;2:1561-9.
-
(1993)
Hum Mol Genet
, vol.2
, pp. 1561-1569
-
-
O'Neal, W.K.1
Hasty, P.2
McCray, P.B.3
-
43
-
-
0026640380
-
Defective epithelial chloride transport in a gene-targeted mouse model of cystic fibrosis
-
Clarke LL, Grubb BR, Gabriel SE, Smithies O, Koller BH, Boucher RC. Defective epithelial chloride transport in a gene-targeted mouse model of cystic fibrosis. Science 1992;257:1125-8.
-
(1992)
Science
, vol.257
, pp. 1125-1128
-
-
Clarke, L.L.1
Grubb, B.R.2
Gabriel, S.E.3
Smithies, O.4
Koller, B.H.5
Boucher, R.C.6
-
44
-
-
0026730466
-
Cystic fibrosis in the mouse by targeted insertional mutagenesis
-
Comment in: Nature 1992;359:195
-
Dorin JR, Dickinson P, Alton EW, Smith SN, Geddes DM, Stevenson BJ, et al.: Cystic fibrosis in the mouse by targeted insertional mutagenesis. Nature 1992;359:211-5. Comment in: Nature 1992;359:195.
-
(1992)
Nature
, vol.359
, pp. 211-215
-
-
Dorin, J.R.1
Dickinson, P.2
Alton, E.W.3
Smith, S.N.4
Geddes, D.M.5
Stevenson, B.J.6
-
45
-
-
0028074301
-
Somatic gene therapy for cystic fibrosis
-
O'Neal WKO, Beaudet AL. Somatic gene therapy for cystic fibrosis. Hum Mol Genet 1994;3:1497-502.
-
(1994)
Hum Mol Genet
, vol.3
, pp. 1497-1502
-
-
O'Neal, W.K.O.1
Beaudet, A.L.2
-
46
-
-
0028170353
-
Correction of cAMP-stimulated fluid secretion in cystic fibrosis airway epithelia: Efficiency of adenovirus-mediated gene transfer in vitro
-
Zabner J, Couture LA, Smith AE, Welsh MJ. Correction of cAMP-stimulated fluid secretion in cystic fibrosis airway epithelia: efficiency of adenovirus-mediated gene transfer in vitro. Hum Gene Ther 1994;5:585-93.
-
(1994)
Hum Gene Ther
, vol.5
, pp. 585-593
-
-
Zabner, J.1
Couture, L.A.2
Smith, A.E.3
Welsh, M.J.4
-
47
-
-
0027377523
-
Adenovirus-mediated gene transfer transiently corrects the chloride transport defect in nasal epithelia of patients with cystic fibrosis
-
Zabner J, Couture LA, Gregory RJ, Graham SM, Smith AE, Welsh MJ. Adenovirus-mediated gene transfer transiently corrects the chloride transport defect in nasal epithelia of patients with cystic fibrosis, Cell 1993;75:207-16.
-
(1993)
Cell
, vol.75
, pp. 207-216
-
-
Zabner, J.1
Couture, L.A.2
Gregory, R.J.3
Graham, S.M.4
Smith, A.E.5
Welsh, M.J.6
-
48
-
-
0028124741
-
Gene transfer to freshly isolated human respiratory epithelial cells in vitro using a replication-deficient adenovirus containing the human cystic fibrosis transmembrane conductance regulator cDNA
-
Rosenfeld MA, Chu CS, Seth P, et al. Gene transfer to freshly isolated human respiratory epithelial cells in vitro using a replication-deficient adenovirus containing the human cystic fibrosis transmembrane conductance regulator cDNA. Hum Gene Ther 1994;5:331-42.
-
(1994)
Hum Gene Ther
, vol.5
, pp. 331-342
-
-
Rosenfeld, M.A.1
Chu, C.S.2
Seth, P.3
-
49
-
-
0028168641
-
Administration of an adenovirus containing the human CFTR cDNA to the respiratory tract of individuals with cystic fibrosis
-
see comment Comment in: Nat Genet 1994;8;8-9
-
Crystal RG, McElvaney MA, Chu CS, Mastrangeli A, Hay JG, Rosenfeld MA, et al. Administration of an adenovirus containing the human CFTR cDNA to the respiratory tract of individuals with cystic fibrosis [see comment]. Nat Genet 1994;8:42-51 Comment in: Nat Genet 1994;8;8-9.
-
(1994)
Nat Genet
, vol.8
, pp. 42-51
-
-
Crystal, R.G.1
McElvaney, M.A.2
Chu, C.S.3
Mastrangeli, A.4
Hay, J.G.5
Rosenfeld, M.A.6
-
50
-
-
0027967986
-
Inefficient gene transfer by adenovirus vector to cystic fibrosis airway epithelia of mice and humans
-
Grubb BR, Pickles RJ, Ye H, et al. Inefficient gene transfer by adenovirus vector to cystic fibrosis airway epithelia of mice and humans. Nature 1994; 371:802-6.
-
(1994)
Nature
, vol.371
, pp. 802-806
-
-
Grubb, B.R.1
Pickles, R.J.2
Ye, H.3
-
51
-
-
0026933071
-
Prolonged transgene expression in rodent lung cells
-
Debs R, Pian M, Gaensler K, Clements J, Friend DS, Dobbs L. Prolonged transgene expression in rodent lung cells. Am J Respir Cell Mol Biol 1992;7:406-13.
-
(1992)
Am J Respir Cell Mol Biol
, vol.7
, pp. 406-413
-
-
Debs, R.1
Pian, M.2
Gaensler, K.3
Clements, J.4
Friend, D.S.5
Dobbs, L.6
-
52
-
-
0027475701
-
Correction of the ion transport defect in cystic fibrosis transgenic mice by gene therapy
-
Hyde SC, Gill DR, Higgins CF, et al. Correction of the ion transport defect in cystic fibrosis transgenic mice by gene therapy. Nature 1993;362:250-5.
-
(1993)
Nature
, vol.362
, pp. 250-255
-
-
Hyde, S.C.1
Gill, D.R.2
Higgins, C.F.3
-
53
-
-
0028670906
-
Gene therapy for cystic fibrosis using cationic liposome mediated gene transfer: A phase I trial of safety and efficacy in the nasal airway
-
Sorscher EJ, Logan JJ, Frizzell RA, et al. Gene therapy for cystic fibrosis using cationic liposome mediated gene transfer: a phase I trial of safety and efficacy in the nasal airway. Hum Gene Ther 1994;5:1259-77.
-
(1994)
Hum Gene Ther
, vol.5
, pp. 1259-1277
-
-
Sorscher, E.J.1
Logan, J.J.2
Frizzell, R.A.3
-
54
-
-
0002815131
-
Lung cell kinetics
-
L'Enfant C, Massaro D, editors. New York: Dekker
-
Evans MJ, Shami SG. Lung cell kinetics. In: L'Enfant C, Massaro D, editors. Lung cell biology. New York: Dekker, 1989:1-36.
-
(1989)
Lung Cell Biology
, pp. 1-36
-
-
Evans, M.J.1
Shami, S.G.2
-
55
-
-
0026336412
-
Reconstitution of tracheal grafts with a genetically modified epithelium
-
Engelhardt JF, Allen ED, Wilson JM. Reconstitution of tracheal grafts with a genetically modified epithelium. Proc Natl Acad Sci U S A. 1991;88:11192-6.
-
(1991)
Proc Natl Acad Sci U S A
, vol.88
, pp. 11192-11196
-
-
Engelhardt, J.F.1
Allen, E.D.2
Wilson, J.M.3
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