-
1
-
-
0002925782
-
Ontogenic processes in nephron epithelia: Structure, enzymes, and function
-
edited by D. W. Seldin and G. Giebisch. New York: Raven
-
Aperia, A., and G. Celsi. Ontogenic processes in nephron epithelia: structure, enzymes, and function. In: The Kidney: Physiology and Pathophysiology, edited by D. W. Seldin and G. Giebisch. New York: Raven, 1992, p. 803-828.
-
(1992)
The Kidney: Physiology and Pathophysiology
, pp. 803-828
-
-
Aperia, A.1
Celsi, G.2
-
2
-
-
0026523829
-
Cystic fibrosis: Molecular biology and therapeutic implications
-
Collins, F. S. Cystic fibrosis: molecular biology and therapeutic implications. Science Wash. DC 256: 774-779,1992.
-
(1992)
Science Wash. DC
, vol.256
, pp. 774-779
-
-
Collins, F.S.1
-
3
-
-
0025942250
-
Immunocytochemical localization of the cystic fibrosis gene product CFTR
-
Crawford, L, P. C. Maloney, P. L. Zeitlin, W. B. Guggino, S. C. Hyde, H. Turley, K. C. Gatter, A. Harris, and C. F. Higgins. Immunocytochemical localization of the cystic fibrosis gene product CFTR. Proc. Natl. Acad. Sei. USA 88: 9262-9266, 1991.
-
(1991)
Proc. Natl. Acad. Sei. USA
, vol.88
, pp. 9262-9266
-
-
Crawford, L.1
Maloney, P.C.2
Zeitlin, P.L.3
Guggino, W.B.4
Hyde, S.C.5
Turley, H.6
Gatter, K.C.7
Harris, A.8
Higgins, C.F.9
-
4
-
-
0028032866
-
Abnormal subcellular localization of mutated CFTR protein in a cystic fibrosis epithelial cell line
-
Demolombe, S., I. Baro, M. Laurent, A.-S. Hongre, A. Pavirani, and D. Escande. Abnormal subcellular localization of mutated CFTR protein in a cystic fibrosis epithelial cell line. Ear. J. CellBiol. 65: 214-219,1994.
-
(1994)
Ear. J. CellBiol.
, vol.65
, pp. 214-219
-
-
Demolombe, S.1
Baro, I.2
Laurent, M.3
Hongre, A.-S.4
Pavirani, A.5
Escande, D.6
-
5
-
-
0026781952
-
Processing of mutant cystic fibrosis transmembrane conductance regulator is temperaturesensitive
-
Denning, G. M., M. P. Anderson, J. F. Amara, J. Marshall, A. E. Smith, and M. J. Welsh. Processing of mutant cystic fibrosis transmembrane conductance regulator is temperaturesensitive. Nature Land. 358: 761-764.
-
Nature Land.
, 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
-
6
-
-
0029761139
-
Expression of aquaporins-1 and -2 during nephrogenesis and in autosomal dominant polycystic kidney disease
-
(Renal Fluid Electrolyte Physiol. 40)
-
Devuyst, O., C. R. Burrow, B. L. Smith, P. Agre, M. A. Knepper, and P. D. Wilson. Expression of aquaporins-1 and -2 during nephrogenesis and in autosomal dominant polycystic kidney disease. Am. J. Physiol. 271 (Renal Fluid Electrolyte Physiol. 40): F169-F183, 1996.
-
(1996)
Am. J. Physiol.
, vol.271
-
-
Devuyst, O.1
Burrow, C.R.2
Smith, B.L.3
Agre, P.4
Knepper, M.A.5
Wilson, P.D.6
-
7
-
-
9544245976
-
Postnatal development of the kidney
-
edited by M. A. Holliday, T. M. Barratt, and E. D. Avner. Baltimore, MD: Williams & Wilkins
-
Evan, A. P. Postnatal development of the kidney. In: Pédiatrie Nephrology, edited by M. A. Holliday, T. M. Barratt, and E. D. Avner. Baltimore, MD: Williams & Wilkins, 1994, p. 40-61.
-
(1994)
Pédiatrie Nephrology
, pp. 40-61
-
-
Evan, A.P.1
-
8
-
-
0025114509
-
Expression and characterization of the cystic fibrosis transmembrane conductance regulator
-
Gregory, R. J., S. H. Cheng, D. P. Rich, J. Marshall, S. Paul, K. Hehir, L. Ostedgaard, K. W. Klinger, M. J. Welsh, and A. E. Smith. Expression and characterization of the cystic fibrosis transmembrane conductance regulator. Nature Land. 347: 382-386,1990.
-
(1990)
Nature Land.
, vol.347
, pp. 382-386
-
-
Gregory, R.J.1
Cheng, S.H.2
Rich, D.P.3
Marshall, J.4
Paul, S.5
Hehir, K.6
Ostedgaard, L.7
Klinger, K.W.8
Welsh, M.J.9
Smith, A.E.10
-
9
-
-
0024544576
-
Ductal epithelial cells cultured from human foetal epididymis and vas deferens: Relevance to sterility in cystic fibrosis
-
Harris, A., and L. Coleman. Ductal epithelial cells cultured from human foetal epididymis and vas deferens: relevance to sterility in cystic fibrosis. J. Cell Sei. 92: 687-690,1989.
-
(1989)
J. Cell Sei.
, vol.92
, pp. 687-690
-
-
Harris, A.1
Coleman, L.2
-
10
-
-
0025883051
-
Expression of the cystic fibrosis gene in human development
-
Harris, A., G. Chalkley, S. Goodman, and L. Coleman. 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
-
11
-
-
0030075382
-
Crystal-clear chloride channels
-
Hebert, S. C. Crystal-clear chloride channels. Nature Land. 379: 398-399,1996.
-
(1996)
Nature Land.
, vol.379
, pp. 398-399
-
-
Hebert, S.C.1
-
12
-
-
0028861577
-
Anion secretion by the inner medullary collecting duct. Evidence for involvement of the cystic fibrosis transmembrane conductance regulator
-
Husted, R. F., K. A. Volk, R. D. Sigmund, and J. B. Stokes. Anion secretion by the inner medullary collecting duct. Evidence for involvement of the cystic fibrosis transmembrane conductance regulator. J. Clin. Invest. 95: 644-650,1995.
-
(1995)
J. Clin. Invest.
, vol.95
, pp. 644-650
-
-
Husted, R.F.1
Volk, K.A.2
Sigmund, R.D.3
Stokes, J.B.4
-
13
-
-
0027402791
-
Localization of the cystic fibrosis transmembrane conductance regulator in airway secretory glands
-
Jacquot, J., E. Puchelle, J. Hinnrasky, C. Fuchey, C. Bettinger, C. Spilmont, N. Bonnet, A. Dieterle, D. Dreyer, A. Pavirani, and W. Dalemans. Localization of the cystic fibrosis transmembrane conductance regulator in airway secretory glands. Eur. Respir. J. 6: 169-176, 1993.
-
(1993)
Eur. Respir. J.
, vol.6
, pp. 169-176
-
-
Jacquot, J.1
Puchelle, E.2
Hinnrasky, J.3
Fuchey, C.4
Bettinger, C.5
Spilmont, C.6
Bonnet, N.7
Dieterle, A.8
Dreyer, D.9
Pavirani, A.10
Dalemans, W.11
-
14
-
-
0023772728
-
Purification of Na+,K+ -ATPase: Enzyme sources, preparative problems, and preparation from mammalian kidney
-
edited by S. Fleischer and B. Fleischer. San Diego, CA: Academic
-
Jorgensen, P. L. Purification of Na+,K+ -ATPase: enzyme sources, preparative problems, and preparation from mammalian kidney. In: Methods in Enzymology: Biomembranes, edited by S. Fleischer and B. Fleischer. San Diego, CA: Academic, 1988, p. 29-43.
-
(1988)
Methods in Enzymology: Biomembranes
, pp. 29-43
-
-
Jorgensen, P.L.1
-
15
-
-
0026593016
-
Assembly and function of the two ABC transporter proteins encoded in the human major histocompatibility complex
-
Kelly, A., S. H. Powis, L.-A. Kerr, I. Mockridge, T. Elliott, J. Bastin, B. Uchanska-Ziegler, A. Ziegler, J. Trowsdale, and A. Townsend. Assembly and function of the two ABC transporter proteins encoded in the human major histocompatibility complex. Nature Lond. 355: 641-646,1992.
-
(1992)
Nature Lond.
, vol.355
, pp. 641-646
-
-
Kelly, A.1
Powis, S.H.2
Kerr, L.-A.3
Mockridge, I.4
Elliott, T.5
Bastin, J.6
Uchanska-Ziegler, B.7
Ziegler, A.8
Trowsdale, J.9
Townsend, A.10
-
16
-
-
0027546872
-
Cystic fibrosis gene and protein expression during fetal lung development
-
McGrath, S.A., A. Basu, and P. L. Zeitlin. 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
-
17
-
-
0029846003
-
Both the wild type and a functional isoform of CFTR are expressed in kidney
-
Renal Fluid Electrolyte Physiol. 39
-
Morales, M. M., T. P. Carroll, T. Morita, E. M. Schwiebert, O. Devuyst, P. D. Wilson, A. G. Lopes, B. A. Stanton, H. C. Dietz, G. R, Cutting, and W. B. Guggino. Both the wild type and a functional isoform of CFTR are expressed in kidney. Am. J. Physiol. 270 (Renal Fluid Electrolyte Physiol. 39): F1038-F1048, 1996.
-
(1996)
Am. J. Physiol.
, vol.270
-
-
Morales, M.M.1
Carroll, T.P.2
Morita, T.3
Schwiebert, E.M.4
Devuyst, O.5
Wilson, P.D.6
Lopes, A.G.7
Stanton, B.A.8
Dietz, H.C.9
Cutting, G.R.10
Guggino, W.B.11
-
19
-
-
0027532282
-
Putative X-linked adrenoleukodystrophy gene shares unexpected homology with ABC transporters
-
Mosser, J., A.-M. Douar, C.-O. Sarde, P. Kioschis, R. Feil, H. Moser, A.-M. Poustka, J.-L. Mandel, and P. Aubourg. Putative X-linked adrenoleukodystrophy gene shares unexpected homology with ABC transporters. Nature Lond. 361: 726-730, 1993.
-
(1993)
Nature Lond.
, vol.361
, pp. 726-730
-
-
Mosser, J.1
Douar, A.-M.2
Sarde, C.-O.3
Kioschis, P.4
Feil, R.5
Moser, H.6
Poustka, A.-M.7
Mandel, J.-L.8
Aubourg, P.9
-
20
-
-
0023629643
-
Pathological confirmation of cystic fibrosis in the fetus following prenatal diagnosis
-
Ornoy, A., J. Arnos, D. Katznelson, M. Granat, B. Caspi, and J. Chemke. Pathological confirmation of cystic fibrosis in the fetus following prenatal diagnosis. Am. J. Med. Genet. 28: 935-947,1987.
-
(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
-
21
-
-
0026005544
-
Chloride channels on epithelial cells cultured from human fetal epididymis
-
Pollard, C. E., A. Harris, L. Coleman, and B. E. Argent. Chloride channels on epithelial cells cultured from human fetal epididymis. J. Membr. Biol. 124: 275-284,1991.
-
(1991)
J. Membr. Biol.
, vol.124
, pp. 275-284
-
-
Pollard, C.E.1
Harris, A.2
Coleman, L.3
Argent, B.E.4
-
22
-
-
0024424270
-
Identification of the cystic fibrosis gene: Cloning and characterization of complementary DNA
-
Riordan, J. R., J. M. Rommens, B. Kerem, N. Alon, R. Rozmahel, Z. Grzelczak, J. Zielenski, S. Lok, N. Plavsic, J.-L. Chou, M. L. Drunim, M. C. lannuzzi, F. S. Celling, and L.-C. Tsui. Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA. Science Wash. DC 245: 1066-1073,1989.
-
(1989)
Science Wash. DC
, vol.245
, pp. 1066-1073
-
-
Riordan, J.R.1
Rommens, J.M.2
Kerem, B.3
Alon, N.4
Rozmahel, R.5
Grzelczak, Z.6
Zielenski, J.7
Lok, S.8
Plavsic, N.9
Chou, J.-L.10
Drunim, M.L.11
Lannuzzi, M.C.12
Celling, F.S.13
Tsui, L.-C.14
-
23
-
-
0028980536
-
CFTR regulates outwardly rectifying chloride channels through an autocrine mechanism involving ATP
-
Schwiebert, E. M., M. E. Egan, T.-H. Hwang, S. B. Fulmer, S. S. Alien, G. R. Cutting, and W. B. Guggino. CFTR regulates outwardly rectifying chloride channels through an autocrine mechanism involving ATP. Cell 81: 1063-1073, 1995.
-
(1995)
Cell
, vol.81
, pp. 1063-1073
-
-
Schwiebert, E.M.1
Egan, M.E.2
Hwang, T.-H.3
Fulmer, S.B.4
Alien, S.S.5
Cutting, G.R.6
Guggino, W.B.7
-
24
-
-
0005058328
-
CAMP-activated chloride channel on the basolateral membrane of renal proximal tubule
-
Segal, A. S., and E. L. Boulpaep. cAMP-activated chloride channel on the basolateral membrane of renal proximal tubule (Abstract). J. Am. Soc. Nephrol. 3: 819, 1992.
-
(1992)
J. Am. Soc. Nephrol.
, vol.3
, pp. 819
-
-
Segal, A.S.1
Boulpaep, E.L.2
-
25
-
-
0028982894
-
CFTR as a cAMPdependent regulator of sodium channels
-
Stutts, M. J., C. M. Canessa, J. C. Olsen, M. Hamrick, J. A. Cohn, B. C. Rossier, and R. C. Boucher. CFTR as a cAMPdependent regulator of sodium channels. Science Wash. DC 269: 847-850,1995.
-
(1995)
Science Wash. DC
, vol.269
, pp. 847-850
-
-
Stutts, M.J.1
Canessa, C.M.2
Olsen, J.C.3
Hamrick, M.4
Cohn, J.A.5
Rossier, B.C.6
Boucher, R.C.7
-
26
-
-
0027195534
-
Cell-specific localization of CFTR mRNAshows developmentally regulated expression in human fetal tissues
-
Tizzano, E. F., D. Chitayat, and M. Buchwald. Cell-specific localization of CFTR mRNAshows developmentally regulated expression in human fetal tissues. Hum. Mol. Genet. 2: 219-224,1993.
-
(1993)
Hum. Mol. Genet.
, vol.2
, pp. 219-224
-
-
Tizzano, E.F.1
Chitayat, D.2
Buchwald, M.3
-
27
-
-
0025787393
-
In vivo cell-specific expression of the cystic fibrosis transmembrane conductance regulator
-
Trezise, A. E. O., and M. Buchwald. In vivo cell-specific expression of the cystic fibrosis transmembrane conductance regulator. Nature Land. 353: 434-437, 1991.
-
(1991)
Nature Land.
, vol.353
, pp. 434-437
-
-
Trezise, A.E.O.1
Buchwald, M.2
-
28
-
-
0027207509
-
Expression of the cystic fibrosis gene in human foetal tissues
-
Trezise, A. E. O., J.A. Chambers, C. J. Wardle, S. Gould, and A. Harris. Expression of the cystic fibrosis gene in human foetal tissues. Hum. Mol. Genet. 2: 213-218, 1993.
-
(1993)
Hum. Mol. Genet.
, vol.2
, pp. 213-218
-
-
Trezise, A.E.O.1
Chambers, J.A.2
Wardle, C.J.3
Gould, S.4
Harris, A.5
-
29
-
-
0000026508
-
Cystic fibrosis
-
edited by C. R. Scriver, A. L. Beaudet, W. S. Sly and D. Valle. New York: McGraw-Hill
-
Welsh, M. J., L.-C. Tsui, T. F. Boat, and A. L. Beaudet. Cystic fibrosis. In: The Metabolic and Molecular Bases of Inherited Disease, edited by C. R. Scriver, A. L. Beaudet, W. S. Sly and D. Valle. New York: McGraw-Hill, 1995, p. 3799-3876.
-
(1995)
The Metabolic and Molecular Bases of Inherited Disease
, pp. 3799-3876
-
-
Welsh, M.J.1
Tsui, L.-C.2
Boat, T.F.3
Beaudet, A.L.4
-
30
-
-
0026595804
-
CFTR protein expression in primary and cultured epithelia
-
Zeitlin, P. L., I. Crawford, L. Lu, S. Woel, M. E. Cohen, M. Donowitz, M. H. Montrose, A. Hamosh, G. R. Cutting, D. Gruenert, R. Huganir, P. Maloney, and W. B. Guggino. CFTR protein expression in primary and cultured epithelia. Proc. Natl. Acad. Sei. USA 89: 344-347, 1992.
-
(1992)
Proc. Natl. Acad. Sei. USA
, vol.89
, pp. 344-347
-
-
Zeitlin, P.L.1
Crawford, I.2
Lu, L.3
Woel, S.4
Cohen, M.E.5
Donowitz, M.6
Montrose, M.H.7
Hamosh, A.8
Cutting, G.R.9
Gruenert, D.10
Huganir, R.11
Maloney, P.12
Guggino, W.B.13
|