-
1
-
-
0024424270
-
Identification of the cystic fibrosis gene: Cloning and characterization of complementary DNA
-
published erratum appears in Science 245:1437, 1989
-
1. RIORDAN JR, ROMMENS JM, KFREM B, ALON N, ROZMAHFL R, GRZELCZAK Z, ZIELENSKI J, LOK S, PLAVSIC N, CHOU JL: Identification of the cystic fibrosis gene: Cloning and characterization of complementary DNA. Science 245:1066-1073, 1989 [published erratum appears in Science 245:1437, 1989]
-
(1989)
Science
, vol.245
, pp. 1066-1073
-
-
Riordan, J.R.1
Rommens, J.M.2
Kfrem, B.3
Alon, N.4
Rozmahfl, R.5
Grzelczak, Z.6
Zielenski, J.7
Lok, S.8
Plavsic, N.9
Chou, J.L.10
-
2
-
-
0032957204
-
Biosynthesis and degradation of CFTR
-
2. KOPITO RR: Biosynthesis and degradation of CFTR. Physiol Rev 79(Suppl):S167-S173, 1999
-
(1999)
Physiol Rev
, vol.79
, Issue.SUPPL.
-
-
Kopito, R.R.1
-
3
-
-
0026325533
-
Altered chloride ion channel kinetics associated with the delta f508 cystic fibrosis mutation
-
3. DALEMANS W, BARBRY P, CHAMPIGNY G, JALLAT S, DOTI K, DREYER D, CRYSTAL RG, PAVIRANI A, LECOCQ JP, LAZDUNSKI M: Altered chloride ion channel kinetics associated with the delta F508 cystic fibrosis mutation [see comments]. Nature 354:526-528, 1991
-
(1991)
Nature
, vol.354
, pp. 526-528
-
-
Dalemans, W.1
Barbry, P.2
Champigny, G.3
Jallat, S.4
Doti, K.5
Dreyer, D.6
Crystal, R.G.7
Pavirani, A.8
Lecocq, J.P.9
Lazdunski, M.10
-
4
-
-
0028977988
-
Mutant (delta F508) cystic fibrosis transmembrane conductance regulator Cl channel is functional when retained in endoplasmic reticulum of mammalian cells
-
4. PASYK EA, FOSKETI JK: Mutant (delta F508) cystic fibrosis transmembrane conductance regulator Cl channel is functional when retained in endoplasmic reticulum of mammalian cells. J Biol Chem 270:12347-12350, 1995
-
(1995)
J Biol Chem
, vol.270
, pp. 12347-12350
-
-
Pasyk, E.A.1
Fosketi, J.K.2
-
5
-
-
0029899053
-
Delta F508-CFTR channels: Kinetics, activation by forskolin, and potentiation by xanthines
-
5. HAWS CM, NEPOMUCENO IB, KROUSE ME, WAKELFE H, LAW T, XIA Y, NGUYEN H, WINE JJ: Delta F508-CFTR channels: Kinetics, activation by forskolin, and potentiation by xanthines. Am J Physiol 270:C1544-C1555, 1996
-
(1996)
Am J Physiol
, vol.270
-
-
Haws, C.M.1
Nepomuceno, I.B.2
Krouse, M.E.3
Wakelfe, H.4
Law, T.5
Xia, Y.6
Nguyen, H.7
Wine, J.J.8
-
6
-
-
0027483610
-
The cystic fibrosis mutation (delta F508) does not influence the chloride channel activity of CFTR
-
6. LI C, RAMJEESINGH M, REYES E, JENSEN T, CHANG X, ROMMENS JM, BEAR CE: The cystic fibrosis mutation (delta F508) does not influence the chloride channel activity of CFTR. Nat Genet 3:311-316, 1993
-
(1993)
Nat Genet
, vol.3
, pp. 311-316
-
-
Li, C.1
Ramjeesingh, M.2
Reyes, E.3
Jensen, T.4
Chang, X.5
Rommens, J.M.6
Bear, C.E.7
-
7
-
-
0028896289
-
Differential expression of ORCC and CFTR induced by low temperature in CF airway epithelial cells
-
Cell Physiol 37
-
7. EGAN ME, SCHWEIBERT EM, GUGGINO WB: Differential expression of ORCC and CFTR induced by low temperature in CF airway epithelial cells. Am J Physiol 268(Cell Physiol 37):C243-C251, 1995
-
(1995)
Am J Physiol
, vol.268
-
-
Egan, M.E.1
Schweibert, E.M.2
Guggino, W.B.3
-
8
-
-
0030896451
-
Correcting temperature-sensitive protein folding defects
-
8. BROWN CR, HONG-BROWN LQ, WELCH WJ: Correcting temperature-sensitive protein folding defects. J Clin Invest 99:1432-1444, 1997
-
(1997)
J Clin Invest
, vol.99
, pp. 1432-1444
-
-
Brown, C.R.1
Hong-Brown, L.Q.2
Welch, W.J.3
-
9
-
-
0028858161
-
Multiple proteolytic systems, including the proteasome, contribute to CFTR processing
-
9. JENSEN TJ, LOO MA, PIND S, WILLIAMS DB, GOLDBERG AL, RIORDAN JR: Multiple proteolytic systems, including the proteasome, contribute to CFTR processing. Cell 83:129-135, 1995
-
(1995)
Cell
, vol.83
, pp. 129-135
-
-
Jensen, T.J.1
Loo, M.A.2
Pind, S.3
Williams, D.B.4
Goldberg, A.L.5
Riordan, J.R.6
-
10
-
-
0028006681
-
Intracellular turnover of cystic fibrosis transmembrane conductance regulator. Inefficient processing and rapid degradation of wild-type and mutant proteins
-
10. WARD CL, KOPITO RR: Intracellular turnover of cystic fibrosis transmembrane conductance regulator. Inefficient processing and rapid degradation of wild-type and mutant proteins. J Biol Chem 269:25710-25718, 1994
-
(1994)
J Biol Chem
, vol.269
, pp. 25710-25718
-
-
Ward, C.L.1
Kopito, R.R.2
-
11
-
-
0028840915
-
Degradation of CFTR by the ubiquitin-proteasome pathway
-
11. WARD CL, OMURA S, KOPITO RR: Degradation of CFTR by the ubiquitin-proteasome pathway. Cell 83:121-127, 1995
-
(1995)
Cell
, vol.83
, pp. 121-127
-
-
Ward, C.L.1
Omura, S.2
Kopito, R.R.3
-
12
-
-
0026781952
-
Processing of mutant cystic fibrosis transmembrane conductance regulator is temperature-sensitive
-
12. DENNING GM, ANDERSON MP, AMARA JF, MARSHALL J, SMITH AE, WELSH MJ: Processing of mutant cystic fibrosis transmembrane conductance regulator is temperature-sensitive [see comments]. Nature 358:761-764, 1992
-
(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
-
13
-
-
0027524866
-
The cystic fibrosis transmembrane conductance regulator. Overexpression, purification, and characterization of wild type and delta F508 mutant forms of the first nucleotide binding fold in fusion with the maltose-binding protein
-
13. KO YH, THOMAS PJ, DELANNOY MR, PEDERSEN PL: The cystic fibrosis transmembrane conductance regulator. Overexpression, purification, and characterization of wild type and delta F508 mutant forms of the first nucleotide binding fold in fusion with the maltose-binding protein. J Biol Chem 268:24330-24338, 1993
-
(1993)
J Biol Chem
, vol.268
, pp. 24330-24338
-
-
Ko, Y.H.1
Thomas, P.J.2
Delannoy, M.R.3
Pedersen, P.L.4
-
14
-
-
0032524048
-
Defective aquaporin-2 trafficking in nephrogenic diabetes insipidus and correction by chemical chaperones
-
14. TAMARAPPOO BK, VERKMAN AS: Defective aquaporin-2 trafficking in nephrogenic diabetes insipidus and correction by chemical chaperones. J Clin Invest 101:2257-2267, 1999
-
(1999)
J Clin Invest
, vol.101
, pp. 2257-2267
-
-
Tamarappoo, B.K.1
Verkman, A.S.2
-
15
-
-
0031425079
-
Strategies for correcting the delta F508 CFTR protein-folding defect
-
15. BROWN CR, HONG-BROWN LQ, WELCH WJ: Strategies for correcting the delta F508 CFTR protein-folding defect. J Bioenerg Biomembr 29:491-502, 1997
-
(1997)
J Bioenerg Biomembr
, vol.29
, pp. 491-502
-
-
Brown, C.R.1
Hong-Brown, L.Q.2
Welch, W.J.3
-
16
-
-
0017886958
-
Sodium butyrate inhibits histone deacetylation in cultured cells
-
16. CANDIDO EP, REEVES R, DAVIE JR: Sodium butyrate inhibits histone deacetylation in cultured cells. Cell 14:105-113, 1978
-
(1978)
Cell
, vol.14
, pp. 105-113
-
-
Candido, E.P.1
Reeves, R.2
Davie, J.R.3
-
17
-
-
0027546872
-
Cystic fibrosis gene and protein expression during fetal lung development
-
17. MCGRATH SA, BASU A, ZEITLIN PL: Cystic fibrosis gene and protein expression during fetal lung development. Am J Respir Cell Mol Biol 8:201-208, 1993
-
(1993)
Am J Respir Cell Mol Biol
, vol.8
, pp. 201-208
-
-
McGrath, S.A.1
Basu, A.2
Zeitlin, P.L.3
-
18
-
-
0025883051
-
Expression of the cystic fibrosis gene in human development
-
18. HARRIS A, CHALKLEY G, GOODMAN S, COLEMAN L: Expression of the cystic fibrosis gene in human development. Development 113:305-310, 1991
-
(1991)
Development
, vol.113
, pp. 305-310
-
-
Harris, A.1
Chalkley, G.2
Goodman, S.3
Coleman, L.4
-
19
-
-
0028944377
-
Functional activation of the cystic fibrosis trafficking mutant delta F508-CFTR by overexpression
-
19. CHENG SH, FANG SL, ZABNER J, MARSHALL J, PIRAINO S, SCHIAVI SC, JEFFERSON DM, WELSH MJ, SMITH AE: Functional activation of the cystic fibrosis trafficking mutant delta F508-CFTR by overexpression. Am J Physiol 268:L615-L624, 1995
-
(1995)
Am J Physiol
, vol.268
-
-
Cheng, S.H.1
Fang, S.L.2
Zabner, J.3
Marshall, J.4
Piraino, S.5
Schiavi, S.C.6
Jefferson, D.M.7
Welsh, M.J.8
Smith, A.E.9
-
20
-
-
0030809817
-
In vitro pharmacologic restoration of CFTR-mediated chloride transport with sodium 4-phenylbutyrate in cystic fibrosis epithelial cells containing delta F508-CFTR
-
20. RUBENSTEIN RC, EGAN ME, ZEITLIN PL: In vitro pharmacologic restoration of CFTR-mediated chloride transport with sodium 4-phenylbutyrate in cystic fibrosis epithelial cells containing delta F508-CFTR. J Clin Invest 100:2457-2465, 1997
-
(1997)
J Clin Invest
, vol.100
, pp. 2457-2465
-
-
Rubenstein, R.C.1
Egan, M.E.2
Zeitlin, P.L.3
-
21
-
-
0027488993
-
The common variant of cystic fibrosis transmembrane conductance regulator is recognised by hsp70 and degraded in a pre-golgi nonlysosomal compartment
-
21. YANG Y, JANICH S, COHN JA, WILSON JM: The common variant of cystic fibrosis transmembrane conductance regulator is recognised by hsp70 and degraded in a pre-Golgi nonlysosomal compartment. Proc Natl Acad Sci USA 90:9480-9484, 1993
-
(1993)
Proc Natl Acad Sci USA
, vol.90
, pp. 9480-9484
-
-
Yang, Y.1
Janich, S.2
Cohn, J.A.3
Wilson, J.M.4
-
22
-
-
0028232167
-
Participation of the endoplasmic reticulum chaperone calnexin (p88, IP90) in the biogenesis of the cystic fibrosis transmembrane conductance regulator
-
22. PIND 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 269:12784-12788, 1994
-
(1994)
J Biol Chem
, vol.269
, pp. 12784-12788
-
-
Pind, S.1
Riordan, J.R.2
Williams, D.B.3
-
23
-
-
0030798979
-
The molecular chaperone hsc70 assists the in vitro folding of the N-terminal nucleotide-binding domain of the cystic fibrosis transmembrane conductance regulator
-
23. STRICKLAND E, QU BH, MILLEN L, THOMAS PJ: The molecular chaperone hsc70 assists the in vitro folding of the N-terminal nucleotide-binding domain of the cystic fibrosis transmembrane conductance regulator. J Biol Chem 272:25421-25424, 1997
-
(1997)
J Biol Chem
, vol.272
, pp. 25421-25424
-
-
Strickland, E.1
Qu, B.H.2
Millen, L.3
Thomas, P.J.4
-
24
-
-
0033559258
-
The Hdf-2/Hsc70 chaperone pair facilitates early steps in CFTR biogenesis
-
24. MEACHAM GC, LU Z, KING S, SORSCHER E, TOUSSON A, D'AMORE-BRUNO M: The Hdf-2/Hsc70 chaperone pair facilitates early steps in CFTR biogenesis. EMBO J 18:1492-1505, 1999
-
(1999)
EMBO J
, vol.18
, pp. 1492-1505
-
-
Meacham, G.C.1
Lu, Z.2
King, S.3
Sorscher, E.4
Tousson, A.5
D'Amore-Bruno, M.6
-
25
-
-
0031889082
-
A pilot clinical trial of sodium 4-phenylbutyrate (buphenyl) in delta F508-homozygous cystic fibrosis patients: Evidence of restoration of nasal epithelial CFTR function
-
25. RUBENSTEIN RC, ZEITLIN PL: A pilot clinical trial of sodium 4-phenylbutyrate (Buphenyl) in delta F508-homozygous cystic fibrosis patients: Evidence of restoration of nasal epithelial CFTR function. Am J Resp Crit Care Med 157:484-490, 1998
-
(1998)
Am J Resp Crit Care Med
, vol.157
, pp. 484-490
-
-
Rubenstein, R.C.1
Zeitlin, P.L.2
-
26
-
-
0028870221
-
Oral sodium phenylbutyrate therapy in homozygous beta thalassemia: A clinical trial
-
26. COLLINS AF, PEARSON HA, GIARDINA P, MCDONAGH KT, BRUSILOW SW, DOVER GJ: Oral sodium phenylbutyrate therapy in homozygous beta thalassemia: A clinical trial. Blood 85:43-49, 1995
-
(1995)
Blood
, vol.85
, pp. 43-49
-
-
Collins, A.F.1
Pearson, H.A.2
Giardina, P.3
McDonagh, K.T.4
Brusilow, S.W.5
Dover, G.J.6
-
27
-
-
0029032965
-
Extended therapy with intravenous arginine butyrate in patients with beta-hemoglobinopathies
-
27. SHER GD, GINDER GD, LITTLE J, YANG S, DOVER GJ, OLIVIERI NF: Extended therapy with intravenous arginine butyrate in patients with beta-hemoglobinopathies [see comments]. N Engl J Med 332:1606-1610, 1995
-
(1995)
N Engl J Med
, vol.332
, pp. 1606-1610
-
-
Sher, G.D.1
Ginder, G.D.2
Little, J.3
Yang, S.4
Dover, G.J.5
Olivieri, N.F.6
-
28
-
-
0031730433
-
Gene redundancy and pharmacological gene therapy: Implications for X-linked adrenoleukodystrophy
-
28. KEMP S, WEI HM, LU JF, BRAITERMAN LT, MCGUINNESS MC, MOSER AB, WATKINS PA, SMITH KD: Gene redundancy and pharmacological gene therapy: Implications for X-linked adrenoleukodystrophy [see comments]. Nat Med 4:1261-1268, 1998
-
(1998)
Nat Med
, vol.4
, pp. 1261-1268
-
-
Kemp, S.1
Wei, H.M.2
Lu, J.F.3
Braiterman, L.T.4
McGuinness, M.C.5
Moser, A.B.6
Watkins, P.A.7
Smith, K.D.8
-
29
-
-
0001341465
-
Phenylbutyrate (PB) for refractory solid tumors: A phase I clinical and pharmacological evaluation
-
29. CARDUCCI M, BOWLING M, EISENBERGER M, SINIBALDI V, SIMONS J, CHEN T, NOE D, GROCHOW L, DONEHOWER R: Phenylbutyrate (PB) for refractory solid tumors: A phase I clinical and pharmacological evaluation. Proc AACR 39:506-506, 1998
-
(1998)
Proc AACR
, vol.39
, pp. 506-506
-
-
Carducci, M.1
Bowling, M.2
Eisenberger, M.3
Sinibaldi, V.4
Simons, J.5
Chen, T.6
Noe, D.7
Grochow, L.8
Donehower, R.9
-
30
-
-
0031853136
-
Partial restoration of cAMP-stimulaled CFTR chloride channel activity in DeltaF508 cells by deoxyspergualin
-
30. JIANG C, FANG SL, XIAO YF, O'CONNOR SP, NADLER SG, LEE DW, JEFFERSON DM, KAPLAN JM, SMITH AE, CHENG SH: Partial restoration of cAMP-stimulaled CFTR chloride channel activity in DeltaF508 cells by deoxyspergualin. Am J Physiol 275:C171-C178, 1998
-
(1998)
Am J Physiol
, vol.275
-
-
Jiang, C.1
Fang, S.L.2
Xiao, Y.F.3
O'Connor, S.P.4
Nadler, S.G.5
Lee, D.W.6
Jefferson, D.M.7
Kaplan, J.M.8
Smith, A.E.9
Cheng, S.H.10
-
31
-
-
0030943895
-
8-Cyclopentyl-1,3-dipropylxanthine and other xanthines differentially bind to the wild-type and delta F508 first nucleotide binding fold (NBF-1) domains of the cystic fibrosis transmembrane conductance regulator
-
31. COHEN BE, LEE G, JACOBSON KA, KIM YC, HUANG Z, SORSCHER EJ, POLLARD HB: 8-cyclopentyl-1,3-dipropylxanthine and other xanthines differentially bind to the wild-type and delta F508 first nucleotide binding fold (NBF-1) domains of the cystic fibrosis transmembrane conductance regulator. Biochemistry 36:6455-6461, 1997
-
(1997)
Biochemistry
, vol.36
, pp. 6455-6461
-
-
Cohen, B.E.1
Lee, G.2
Jacobson, K.A.3
Kim, Y.C.4
Huang, Z.5
Sorscher, E.J.6
Pollard, H.B.7
-
32
-
-
0028990824
-
A1 receptor antagonist 8-cyclopentyl-1,3-dipropylxanthine selectively activates chloride efflux from human epithelial and mouse fibroblast cell lines expressing the cystic fibrosis transmembrane regulator delta F508 mutation
-
32. GUAY-BRODER C, JACOBSON KA, BARNOY S, CABANTCHIK ZI, GUGGINO WB, ZEITLIN PL, TURNER RJ, VERGARA L, EIDELMAN O, POLLARD HB: A1 receptor antagonist 8-cyclopentyl-1,3-dipropylxanthine selectively activates chloride efflux from human epithelial and mouse fibroblast cell lines expressing the cystic fibrosis transmembrane regulator delta F508 mutation. Biochemistry 34:9079-9087, 1995
-
(1995)
Biochemistry
, vol.34
, pp. 9079-9087
-
-
Guay-Broder, C.1
Jacobson, K.A.2
Barnoy, S.3
Cabantchik, Z.I.4
Guggino, W.B.5
Zeitlin, P.L.6
Turner, R.J.7
Vergara, L.8
Eidelman, O.9
Pollard, H.B.10
-
33
-
-
0032489513
-
Direct activation of cystic fibrosis transmembrane conductance regulator channels by 8-cyclopentyl-1,3-dipropylxanthine (CPX) and 1,3-diallyl-8-cyclohexylzanthine (DAX)
-
33. ARISPE N, MA J, JACOBSON KA, POLLARD HB: Direct activation of cystic fibrosis transmembrane conductance regulator channels by 8-Cyclopentyl-1,3-dipropylxanthine (CPX) and 1,3-Diallyl-8-cyclohexylzanthine (DAX). J Biol Chem 273:5727-5734, 1997
-
(1997)
J Biol Chem
, vol.273
, pp. 5727-5734
-
-
Arispe, N.1
Ma, J.2
Jacobson, K.A.3
Pollard, H.B.4
-
34
-
-
0031747854
-
Regulation of CFTR by protein phosphatase 2B and protein kinase C
-
34. FISCHER H, ILLEK B, MACHEN TE: Regulation of CFTR by protein phosphatase 2B and protein kinase C. Pflügers Arch 436:175-181, 1998
-
(1998)
Pflügers Arch
, vol.436
, pp. 175-181
-
-
Fischer, H.1
Illek, B.2
Machen, T.E.3
-
35
-
-
0031723518
-
Cystic fibrosis transmembrane conductance regulator activation by cAMP-independent mechanisms
-
Cell Physiol
-
35. HE Z, RAMAN S, GUO Y, REENSTRA W: Cystic fibrosis transmembrane conductance regulator activation by cAMP-independent mechanisms. Am J Physiol 275(Cell Physiol):958-966, 1998
-
(1998)
Am J Physiol
, vol.275
, pp. 958-966
-
-
He, Z.1
Raman, S.2
Guo, Y.3
Reenstra, W.4
-
36
-
-
0030818110
-
Direct action of genistein on CFTR
-
36. WEINREICH F, WOOD PG, RIORDAN JR, NAGEL G: Direct action of genistein on CFTR. Pflügers Arch 434:484-491, 1997
-
(1997)
Pflügers Arch
, vol.434
, pp. 484-491
-
-
Weinreich, F.1
Wood, P.G.2
Riordan, J.R.3
Nagel, G.4
-
37
-
-
0031908477
-
Effects of the flavonoids quercetin and apigenin on hemostasis in healthy volunteers: Results from an in vitro and a dietary supplement study
-
37. JANSSEN K, MENSINK RP, COX FJ, HARRYVAN JL, HOVENIER R, HOLLMAN PC, KATAN MB: Effects of the flavonoids quercetin and apigenin on hemostasis in healthy volunteers: Results from an in vitro and a dietary supplement study. Am J Clin Nutr 67:255-262, 1998
-
(1998)
Am J Clin Nutr
, vol.67
, pp. 255-262
-
-
Janssen, K.1
Mensink, R.P.2
Cox, F.J.3
Harryvan, J.L.4
Hovenier, R.5
Hollman, P.C.6
Katan, M.B.7
-
38
-
-
0031763141
-
Flavonoids stimulate Cl conductance of human airway epithelium in vitro and in vivo
-
38. ILLEK B, FISCHER H: Flavonoids stimulate Cl conductance of human airway epithelium in vitro and in vivo. Am J Physiol 275:L902-L910, 1998
-
(1998)
Am J Physiol
, vol.275
-
-
Illek, B.1
Fischer, H.2
-
39
-
-
0030773897
-
Genistein potentiates wild-type and delta F508-CFTR channel activity
-
39. HWANG TC, WANG F, YANG IC, REENSTRA WW: Genistein potentiates wild-type and delta F508-CFTR channel activity. Am J Physiol 273:C988-C998, 1997
-
(1997)
Am J Physiol
, vol.273
-
-
Hwang, T.C.1
Wang, F.2
Yang, I.C.3
Reenstra, W.W.4
-
40
-
-
0031888308
-
Effect of IBMX and alkaline phosphatase inhibitors on Cl secretion in G551D cystic fibrosis mutant mice
-
40. SMITH SN, DELANEY SJ, DORIN JR, PARLEY R, GEDDES DM, PORTEOUS DJ, WAINWRIGHT BJ, ALTON EW: Effect of IBMX and alkaline phosphatase inhibitors on Cl secretion in G551D cystic fibrosis mutant mice. Am J Physiol 274:C492-C499, 1998
-
(1998)
Am J Physiol
, vol.274
-
-
Smith, S.N.1
Delaney, S.J.2
Dorin, J.R.3
Parley, R.4
Geddes, D.M.5
Porteous, D.J.6
Wainwright, B.J.7
Alton, E.W.8
-
41
-
-
0029994529
-
Aminoglycoside antibiotics restore CFTR function by overcoming premature stop mutations
-
41. HOWARD M, FRIZZELL RA, BEDWELL DM: Aminoglycoside antibiotics restore CFTR function by overcoming premature stop mutations [see comments]. Nat Med 2:467-469, 1996
-
(1996)
Nat Med
, vol.2
, pp. 467-469
-
-
Howard, M.1
Frizzell, R.A.2
Bedwell, D.M.3
-
42
-
-
0028299654
-
Similar levels of mRNA from the W1282X and the delta F508 cystic fibrosis alleles, in nasal epithelial cells
-
42. SHOSHANI T, KEREM E, SZEINBERG A, AUGARTEN A, YAHAV Y, COHEN D, RIVLIN J, TAL A, KEREM B: Similar levels of mRNA from the W1282X and the delta F508 cystic fibrosis alleles, in nasal epithelial cells. J Clin Invest 93:1502-1507, 1994
-
(1994)
J Clin Invest
, vol.93
, pp. 1502-1507
-
-
Shoshani, T.1
Kerem, E.2
Szeinberg, A.3
Augarten, A.4
Yahav, Y.5
Cohen, D.6
Rivlin, J.7
Tal, A.8
Kerem, B.9
-
43
-
-
0008548159
-
Aminoglycoside repair of premature translation termination mutations
-
43. BEDWELL DM, KAENJAK A, KEELING K, MANOUVAKHOVA M, ZSUZSA B, BENOS D, BUBIEN JK, SCHWIEBERT EM, CLANCY JP, RUIZ F, SORSCHER EJ: Aminoglycoside repair of premature translation termination mutations. Pediatric Pulmonol S 17:168-168, 1998
-
(1998)
Pediatric Pulmonol S
, vol.17
, pp. 168-168
-
-
Bedwell, D.M.1
Kaenjak, A.2
Keeling, K.3
Manouvakhova, M.4
Zsuzsa, B.5
Benos, D.6
Bubien, J.K.7
Schwiebert, E.M.8
Clancy, J.P.9
Ruiz, F.10
Sorscher, E.J.11
-
44
-
-
0347537540
-
Phosphodiesterase inhibitor-stimulated chloride secretion from gut and respiratory epithelia
-
44. DRUMM ML, STEAGALL WK, KELLEY TJ, MILGRAM LJ, KONSTAN MW: Phosphodiesterase inhibitor-stimulated chloride secretion from gut and respiratory epithelia. Pediatric Pulmonol S 17:168-169, 1998
-
(1998)
Pediatric Pulmonol S
, vol.17
, pp. 168-169
-
-
Drumm, M.L.1
Steagall, W.K.2
Kelley, T.J.3
Milgram, L.J.4
Konstan, M.W.5
|