-
1
-
-
0029024314
-
Cloning of the β cell high-affinity sulfonylurea receptor: A regulator of insulin secretion
-
Aguilar-Bryan, L., Nichols, C.G., Wechsler, S.W., Clement, J.P.,IV, Boyd, A.E.,III, Gonzalez, G., Herrera-Sosa, H., Nguy, K., Bryan, J. and Nelson, D.A. (1995) Cloning of the β cell high-affinity sulfonylurea receptor: a regulator of insulin secretion. Science, 268, 423-26.
-
(1995)
Science
, vol.268
, pp. 423-426
-
-
Aguilar-Bryan, L.1
Nichols, C.G.2
Wechsler, S.W.3
Clement IV, J.P.4
Boyd III, A.E.5
Gonzalez, G.6
Herrera-Sosa, H.7
Nguy, K.8
Bryan, J.9
Nelson, D.A.10
-
2
-
-
0025931429
-
Nucleoside triphosphates are required to open the CFTR chloride channel
-
Anderson, M.P., Berger, H.A., Rich, D.P., Gregory, R.J., Smith, A.E. and Welsh, M.J. (1991a) Nucleoside triphosphates are required to open the CFTR chloride channel. Cell, 67, 775-784.
-
(1991)
Cell
, vol.67
, pp. 775-784
-
-
Anderson, M.P.1
Berger, H.A.2
Rich, D.P.3
Gregory, R.J.4
Smith, A.E.5
Welsh, M.J.6
-
3
-
-
0025868103
-
Demonstration that CFTR is a chloride channel by alteration of its anion selectivity
-
Anderson, M.P, Gregory, R.J., Thompson, S., Souza, D.W., Paul, S., Mulligan, R.C., Smith, A.E. and Welsh, M.J. (1991b) Demonstration that CFTR is a chloride channel by alteration of its anion selectivity. Science, 253, 202-205.
-
(1991)
Science
, vol.253
, pp. 202-205
-
-
Anderson, M.P.1
Gregory, R.J.2
Thompson, S.3
Souza, D.W.4
Paul, S.5
Mulligan, R.C.6
Smith, A.E.7
Welsh, M.J.8
-
5
-
-
0026532895
-
Purification and functional reconstitution of the cystic fibrosis transmembrane conductance regulator (CFTR)
-
Bear, C.E., Li, C., Kartner, N., Bridges, R.J., Jensen, T.J., Ramjeesingh, M. and Riordan, J.R. (1992) Purification and functional reconstitution of the cystic fibrosis transmembrane conductance regulator (CFTR). Cell, 68, 809-818.
-
(1992)
Cell
, vol.68
, pp. 809-818
-
-
Bear, C.E.1
Li, C.2
Kartner, N.3
Bridges, R.J.4
Jensen, T.J.5
Ramjeesingh, M.6
Riordan, J.R.7
-
6
-
-
0029861046
-
Cystic fibrosis transmembrane conductance regulator activation stimulates endosome fusion in vivo
-
Biwersi, J., Emans, N. and Verkman, A.S. (1996) Cystic fibrosis transmembrane conductance regulator activation stimulates endosome fusion in vivo. Proc. Natl Acad. Sci. USA, 93, 12484-12489.
-
(1996)
Proc. Natl Acad. Sci. USA
, vol.93
, pp. 12484-12489
-
-
Biwersi, J.1
Emans, N.2
Verkman, A.S.3
-
7
-
-
0028322331
-
Biochemical and biophysical identification of cystic fibrosis transmembrane conductance regulator chloride channels as components of endocytic clathrin-coated vesicles
-
Bradbury, N.A., Cohn, J.A., Venglarik, C.J. and Bridges, R.J. (1994) Biochemical and biophysical identification of cystic fibrosis transmembrane conductance regulator chloride channels as components of endocytic clathrin-coated vesicles. J. Biol. Chem., 269, 8296-8302.
-
(1994)
J. Biol. Chem.
, vol.269
, pp. 8296-8302
-
-
Bradbury, N.A.1
Cohn, J.A.2
Venglarik, C.J.3
Bridges, R.J.4
-
8
-
-
0027255319
-
5'-Adenylylimidodiphosphate does not activate CFTR chloride channels in cell-free patches of membrane
-
Carson, M.R. and Welsh, M.J. (1993) 5'-Adenylylimidodiphosphate does not activate CFTR chloride channels in cell-free patches of membrane. Am. J. Physiol., 265, L27-L32.
-
(1993)
Am. J. Physiol.
, vol.265
-
-
Carson, M.R.1
Welsh, M.J.2
-
9
-
-
0028906612
-
The two nucleotide- Binding domains of cystic fibrosis transmembrane conductance regulator (CFTR) have distinct functions in controlling channel activity
-
Carson, M.R., Travis, S.M. and Welsh, M.J. (1995) The two nucleotide- binding domains of cystic fibrosis transmembrane conductance regulator (CFTR) have distinct functions in controlling channel activity. J. Biol. Chem., 270, 1711-1717.
-
(1995)
J. Biol. Chem.
, vol.270
, pp. 1711-1717
-
-
Carson, M.R.1
Travis, S.M.2
Welsh, M.J.3
-
10
-
-
0025987020
-
Phosphorylation of the R domain by cAMP- Dependent protein kinase regulates the CFTR chloride channel
-
Cheng, S.H., Rich, D.P., Marshall, J., Gregory, R.J., Welsh, M.J. and Smith, A.E. (1991) Phosphorylation of the R domain by cAMP- dependent protein kinase regulates the CFTR chloride channel. Cell, 66, 1027-1036.
-
(1991)
Cell
, vol.66
, pp. 1027-1036
-
-
Cheng, S.H.1
Rich, D.P.2
Marshall, J.3
Gregory, R.J.4
Welsh, M.J.5
Smith, A.E.6
-
11
-
-
0030051032
-
Identification of cystic fibrosis transmembrane conductance regulator channel-lining residues in and flanking the M6 membrane-spanning segment
-
Cheung, M. and Akabas, M.H. (1996) Identification of cystic fibrosis transmembrane conductance regulator channel-lining residues in and flanking the M6 membrane-spanning segment. Biophys. J., 70, 2688-2695.
-
(1996)
Biophys. J.
, vol.70
, pp. 2688-2695
-
-
Cheung, M.1
Akabas, M.H.2
-
12
-
-
0027218689
-
Biochemistry of multidrug resistance mediated by the multidrug transporter
-
Gottesman, M.M. and Pastan, I. (1993) Biochemistry of multidrug resistance mediated by the multidrug transporter. Annu. Rev. Biochem., 62, 385-27.
-
(1993)
Annu. Rev. Biochem.
, vol.62
, pp. 385-427
-
-
Gottesman, M.M.1
Pastan, I.2
-
13
-
-
0030989580
-
CFTR-independent ATP release from epithelial cells triggered by mechanical stimuli
-
Grygorczyk, R. and Hanrahan, J.W. (1997) CFTR-independent ATP release from epithelial cells triggered by mechanical stimuli. Am. J. Physiol., 272, C1058-C1066.
-
(1997)
Am. J. Physiol.
, vol.272
-
-
Grygorczyk, R.1
Hanrahan, J.W.2
-
14
-
-
0029882509
-
CFTR channels expressed in CHO cells do not have detectable ATP conductance
-
Grygorczyk, R., Tabcharani, J.A. and Hanrahan, J.W. (1996) CFTR channels expressed in CHO cells do not have detectable ATP conductance. J. Membr. Biol., 151, 139-148.
-
(1996)
J. Membr. Biol.
, vol.151
, pp. 139-148
-
-
Grygorczyk, R.1
Tabcharani, J.A.2
Hanrahan, J.W.3
-
15
-
-
0028070453
-
Effects of pyrophosphate and nucleotide analogs suggest a role for ATP hydrolysis in cystic fibrosis transmembrane regulator channel gating
-
Gunderson, K.L. and Kopito, R.R. (1994) Effects of pyrophosphate and nucleotide analogs suggest a role for ATP hydrolysis in cystic fibrosis transmembrane regulator channel gating. J. Biol. Chem., 269, 19349-19353.
-
(1994)
J. Biol. Chem.
, vol.269
, pp. 19349-19353
-
-
Gunderson, K.L.1
Kopito, R.R.2
-
16
-
-
0029117303
-
Conformational states of CFTR associated with channel gating: The role of ATP binding and hydrolysis
-
Gunderson, K.L. and Kopito, R.R. (1995) Conformational states of CFTR associated with channel gating: the role of ATP binding and hydrolysis. Cell 82, 231-239.
-
(1995)
Cell
, vol.82
, pp. 231-239
-
-
Gunderson, K.L.1
Kopito, R.R.2
-
17
-
-
0028876622
-
Protein kinase C-raediated phosphorylation of the human multidrug resistance P-glycoprotein regulates cell volume-activated chloride channels
-
Hardy, S.P., Goodfellow, H.R., Valverde, M.A., Gill, D.R., Sepulveda, F.V. and Higgins, C.F. (1995) Protein kinase C-raediated phosphorylation of the human multidrug resistance P-glycoprotein regulates cell volume-activated chloride channels. EMBO J., 14, 68-75.
-
(1995)
EMBO J.
, vol.14
, pp. 68-75
-
-
Hardy, S.P.1
Goodfellow, H.R.2
Valverde, M.A.3
Gill, D.R.4
Sepulveda, F.V.5
Higgins, C.F.6
-
18
-
-
0027051076
-
A multifunctional aqueous channel formed by CFTR
-
Hasegawa, H., Skach, W., Baker, O., Calayag, M.C., Lingappa, V. and Verkman, A.S. (1992) A multifunctional aqueous channel formed by CFTR. Science. 258, 1477-1479.
-
(1992)
Science.
, vol.258
, pp. 1477-1479
-
-
Hasegawa, H.1
Skach, W.2
Baker, O.3
Calayag, M.C.4
Lingappa, V.5
Verkman, A.S.6
-
19
-
-
0026621245
-
ABC transporters: From microorganisms to man
-
Higgins, C.F. (1992) ABC transporters: from microorganisms to man. Annu. Rev. Cell Biol., 8, 67-113.
-
(1992)
Annu. Rev. Cell Biol.
, vol.8
, pp. 67-113
-
-
Higgins, C.F.1
-
20
-
-
0028340159
-
Regulation of the gating of cystic fibrosis transmembrane conductance regulator Cl channels by phosphorylation and ATP hydrolysis
-
Hwang, T.-C., Nagel, G., Nairn, A.C. and Gadsby, D.C. (1994) Regulation of the gating of cystic fibrosis transmembrane conductance regulator Cl channels by phosphorylation and ATP hydrolysis. Proc. NatlAcad. Sci, USA, 91, 4698-4702.
-
(1994)
Proc. NatlAcad. Sci, USA
, vol.91
, pp. 4698-4702
-
-
Hwang, T.-C.1
Nagel, G.2
Nairn, A.C.3
Gadsby, D.C.4
-
21
-
-
0029785898
-
Apical and basolateral ATP stimulates tracheal epithelial chloride secretion via multiple purinergic receptors
-
Hwang, T.-H., Schwiebert, E.M. and Guggino, W.B. (1996) Apical and basolateral ATP stimulates tracheal epithelial chloride secretion via multiple purinergic receptors. Am. J. Physiol., 270, C1611-C1623.
-
(1996)
Am. J. Physiol.
, vol.270
-
-
Hwang, T.-H.1
Schwiebert, E.M.2
Guggino, W.B.3
-
22
-
-
0028972501
-
KATP:: An inward rectifier subunit plus the sulfonylurea receptor
-
KATP:: an inward rectifier subunit plus the sulfonylurea receptor. Science, 270, 1166-1170.
-
(1995)
Science
, vol.270
, pp. 1166-1170
-
-
Inagaki, N.1
Gonoi, T.2
Clement IV, J.P.3
Namba, N.4
Inazawa, J.5
Gonzalez, G.6
Aguilar-Bryan, L.7
Seino, S.8
Bryan, J.9
-
23
-
-
0030668944
-
Block by MOPS reveals a conformational change in the CFTR pore produced by ATP hydrolysis
-
Ishihara, H. and Welsh, M.J. (1997) Block by MOPS reveals a conformational change in the CFTR pore produced by ATP hydrolysis. Am. J. Physiol., 273, C1278-C1289.
-
(1997)
Am. J. Physiol.
, vol.273
-
-
Ishihara, H.1
Welsh, M.J.2
-
24
-
-
15844392129
-
Purified cystic fibrosis transmembrane conductance regulator (CFTR) does not function as an ATP channel
-
Li, C., Ramjeesingh, M. and Bear, C.E. (1996a) Purified cystic fibrosis transmembrane conductance regulator (CFTR) does not function as an ATP channel. J. Biol., Chem., 271, 11623-11626.
-
(1996)
J. Biol., Chem.
, vol.271
, pp. 11623-11626
-
-
Li, C.1
Ramjeesingh, M.2
Bear, C.E.3
-
25
-
-
0029904733
-
ATPase activity of the cystic fibrosis transmembrane conductance regulator
-
Li, C., Ramjeesingh, M., Wang, W., Garami, E., Hewryk, M., Lee, D., Rommens, J.M., Gally, K. and Bear, C.E. (1996b) ATPase activity of the cystic fibrosis transmembrane conductance regulator. J. Biol. Chem., 271, 28463-28468.
-
(1996)
J. Biol. Chem.
, vol.271
, pp. 28463-28468
-
-
Li, C.1
Ramjeesingh, M.2
Wang, W.3
Garami, E.4
Hewryk, M.5
Lee, D.6
Rommens, J.M.7
Gally, K.8
Bear, C.E.9
-
26
-
-
0029736743
-
Flickery block of single CFTR chloride channels by intracellular anions and osmolytes
-
Linsdell, P. and Hanrahan, J.W. (1996a) Flickery block of single CFTR chloride channels by intracellular anions and osmolytes. Am. J. Physiol., 271, C628-C634.
-
(1996)
Am. J. Physiol.
, vol.271
-
-
Linsdell, P.1
Hanrahan, J.W.2
-
27
-
-
0029861859
-
- channels expressed in a mammalian cell line and its regulation by a critical pore residue
-
- channels expressed in a mammalian cell line and its regulation by a critical pore residue. J. Physiol., 496, 687-693.
-
(1996)
J. Physiol.
, vol.496
, pp. 687-693
-
-
Linsdell, P.1
Hanrahan, J.W.2
-
28
-
-
0030885564
-
Permeability of wild-type and mutant cystic fibrosis transmembrane conductance regulator chloride channels to polyatomic anions
-
Linsdell, P., Tabcharani, J.A., Rommens, J.M., Hou, Y-X., Chang, X-B., Tsui, L-C., Riordan, J.R. and Hanrahan, J.W. (1997) Permeability of wild-type and mutant cystic fibrosis transmembrane conductance regulator chloride channels to polyatomic anions. J. Gen. Physiol., 110, 355-364.
-
(1997)
J. Gen. Physiol.
, vol.110
, pp. 355-364
-
-
Linsdell, P.1
Tabcharani, J.A.2
Rommens, J.M.3
Hou, Y.-X.4
Chang, X.-B.5
Tsui, L.-C.6
Riordan, J.R.7
Hanrahan, J.W.8
-
29
-
-
0028264035
-
Cystic fibrosis transmembrane conductance regulator mutations that disrupt nucleotide binding
-
Logan, J., Hiestand, D., Daram, P., Huang, Z., Muccio, D.D., Hartman, J., Haley, B., Cook, W.J. and Sorscher, E.J. (1994) Cystic fibrosis transmembrane conductance regulator mutations that disrupt nucleotide binding. J. Clin. Invest., 94, 228-236.
-
(1994)
J. Clin. Invest.
, vol.94
, pp. 228-236
-
-
Logan, J.1
Hiestand, D.2
Daram, P.3
Huang, Z.4
Muccio, D.D.5
Hartman, J.6
Haley, B.7
Cook, W.J.8
Sorscher, E.J.9
-
30
-
-
0029743660
-
Two physically distinct pores in the dimeric C1C-0 chloride channel
-
Ludewig, U., Pusch, M. and Jentsch, T.J. (1996) Two physically distinct pores in the dimeric C1C-0 chloride channel. Nature, 383, 340-343.
-
(1996)
Nature
, vol.383
, pp. 340-343
-
-
Ludewig, U.1
Pusch, M.2
Jentsch, T.J.3
-
31
-
-
0030840713
-
Independent gating of single pores in CLC-0 chloride channels
-
Ludcwig, U., Pusch, M. and Jentsch, T.J., (1997) Independent gating of single pores in CLC-0 chloride channels. Biophys. J., 73, 789-797.
-
(1997)
Biophys. J.
, vol.73
, pp. 789-797
-
-
Ludcwig, U.1
Pusch, M.2
Jentsch, T.J.3
-
32
-
-
0027220707
-
- channel by two closely related arylaminobenzoates
-
- channel by two closely related arylaminobenzoates. J. Gen. Physiol., 102, 1-23.
-
(1993)
J. Gen. Physiol.
, vol.102
, pp. 1-23
-
-
McCarty, N.A.1
McDonough, S.2
Cohen, B.N.3
Riordan, J.R.4
Davidson, N.5
Lester, H.A.6
-
33
-
-
0028111941
-
Novel pore-lining residues in CFTR that govern permeation and openchannel block
-
McDonough, S., Davidson, N., Lester, H.A. and McCarty, N.A. (1994) Novel pore-lining residues in CFTR that govern permeation and openchannel block. Neuron, 13, 623-634.
-
(1994)
Neuron
, vol.13
, pp. 623-634
-
-
McDonough, S.1
Davidson, N.2
Lester, H.A.3
McCarty, N.A.4
-
34
-
-
0029661878
-
Homodimeric architecture of a CIC-type chloride ion channel
-
Middleton, R.E., Pheasant, D.J. and Miller, C. (1996) Homodimeric architecture of a CIC-type chloride ion channel. Nature, 383, 337-340.
-
(1996)
Nature
, vol.383
, pp. 337-340
-
-
Middleton, R.E.1
And, P.D.J.2
Miller, C.3
-
35
-
-
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., 270, 12347-12350.
-
(1995)
J. Biol., Chem.
, vol.270
, pp. 12347-12350
-
-
Pasyk, E.A.1
Foskett, J.K.2
-
36
-
-
0009682572
-
Cystic fibrosis transmembrane conductance regulater-associated ATP and adenosine 3′-phosphate 5′-phosphosulfate channels in endoplasmic reticulum and plasma membranes
-
Pasyk, E.A. and Foskett, J.K. (1997) Cystic fibrosis transmembrane conductance regulater-associated ATP and adenosine 3′-phosphate 5′-phosphosulfate channels in endoplasmic reticulum and plasma membranes. J. Biol. Chem., 272, 7746-7751.
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 7746-7751
-
-
Pasyk, E.A.1
Foskett, J.K.2
-
37
-
-
0030007316
-
Cellular ATP release by the cystic fibrosis transmembrane conductance regulator
-
Prat, A.G., Reisin, I.L., Ausiello, D.A. and Cantiello, H.F. (1996) Cellular ATP release by the cystic fibrosis transmembrane conductance regulator Am, J. Physiol., 270, C538-C545.
-
(1996)
Am, J. Physiol.
, vol.270
-
-
Prat, A.G.1
Reisin, I.L.2
Ausiello, D.A.3
Cantiello, H.F.4
-
38
-
-
0029998981
-
Failure of the cystic fibrosis transmembrane conductance regulator to conduct ATP
-
Reddy, M.M., Quinton, P.M., Haws, C., Wine, J.J., Grygorczyk, R., Tabcharani, J.A. Hanrahan, J.W., Gunderson, K.L. and Kopito, R.R. (1996) Failure of the cystic fibrosis transmembrane conductance regulator to conduct ATP. Science, 271, 1876-1879.
-
(1996)
Science
, vol.271
, pp. 1876-1879
-
-
Reddy, M.M.1
Quinton, P.M.2
Haws, C.3
Wine, J.J.4
Grygorczyk, R.5
Tabcharani, J.A.6
Hanrahan, J.W.7
Gunderson, K.L.8
Kopito, R.R.9
-
39
-
-
0027937589
-
The cystic fibrosis transmembrane conductance regulator is a dual ATP and chloride channel
-
Reisin, I.L., Prat, A.G., Abraham, E.H., Amara, J.F., Gregory, R.J., Ausiello, D.A. and Cantiello, H.F. (1994) The cystic fibrosis transmembrane conductance regulator is a dual ATP and chloride channel. J. Biol Chem., 269, 20584-20591.
-
(1994)
J. Biol Chem.
, vol.269
, pp. 20584-20591
-
-
Reisin, I.L.1
Prat, A.G.2
Abraham, E.H.3
Amara, J.F.4
Gregory, R.J.5
Ausiello, D.A.6
Cantiello, H.F.7
-
40
-
-
0027171978
-
- channel by negative charge in the R domain
-
- channel by negative charge in the R domain. J. Biol. Chem., 268, 20259-20267.
-
(1993)
J. Biol. Chem.
, vol.268
, pp. 20259-20267
-
-
Rich, D.P.1
Berger, H.A.2
Cheng, S.H.3
Travis, S.M.4
Saxena, M.5
Smith, A.E.6
Welsh, M.J.7
-
41
-
-
0024424270
-
Identification of the cystic fibrosis gene: Cloning and characterization of complementary DNA
-
Riordan, J.R. et al. (1989) Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA. Science, 245, 1066-1073.
-
(1989)
Science
, vol.245
, pp. 1066-1073
-
-
Riordan, J.R.1
-
42
-
-
0024453308
-
Identification of the cystic fibrosis gene: Chromosome walking and jumping
-
Rommens, J.M. et al. (1989) Identification of the cystic fibrosis gene: chromosome walking and jumping. Science, 245, 1059-1065.
-
(1989)
Science
, vol.245
, pp. 1059-1065
-
-
Rommens, J.M.1
-
43
-
-
0028109264
-
Nucleotide-induced conformational changes of MalK, a bacterial ATP binding cassette transporter protein
-
Schneider, E., Wilken, S. and Schmid, R. (1994) Nucleotide-induced conformational changes of MalK, a bacterial ATP binding cassette transporter protein. J. Biol. Chem., 269, 20456-20461.
-
(1994)
J. Biol. Chem.
, vol.269
, pp. 20456-20461
-
-
Schneider, E.1
Wilken, S.2
Schmid, R.3
-
44
-
-
0029837055
-
Glibenclamide blockade of CFTR chloride channels
-
Schultz, B.D., DeRoos, A.D.G., Venglarik, C.J., Singh, A.K., Frizzell, R.A. and Bridges, R.J. (1996) Glibenclamide blockade of CFTR chloride channels. Am. J. Physiol., 271, L192-L200.
-
(1996)
Am. J. Physiol.
, vol.271
-
-
Schultz, B.D.1
Deroos, A.D.G.2
Venglarik, C.J.3
Singh, A.K.4
Frizzell, R.A.5
Bridges, R.J.6
-
45
-
-
0028980536
-
CFTR regulates outwardly rectifying chloride channels through an autocrine mechanism involving ATP
-
Schwiebert, E.M., Egan, M.E., Hwang, T.-H., Fulmer, S.B., Allen, S.S., Cutting, G.R. and Guggino, W.B. (1995) CFTR regulates outwardly rectifying chloride channels through an autocrine mechanism involving ATP. Cell, 81, 1063-1073.
-
(1995)
Cell
, vol.81
, pp. 1063-1073
-
-
Schwiebert, E.M.1
Egan, M.E.2
Hwang, T.-H.3
Fulmer, S.B.4
Allen, S.S.5
Cutting, G.R.6
Guggino, W.B.7
-
47
-
-
0030970422
-
Cystic fibrosis transmembrane conductance regulator inverts protein kinase A-mediated regulation of epithelial sodium channel single channel kinetics
-
Stutts, M.J., Rossier, B.C. and Boucher, R.C. (1997) Cystic fibrosis transmembrane conductance regulator inverts protein kinase A-mediated regulation of epithelial sodium channel single channel kinetics, J. Biol. Chem., 272, 14037-14040.
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 14037-14040
-
-
Stutts, M.J.1
Rossier, B.C.2
Boucher, R.C.3
-
48
-
-
0024095589
-
Mutation of lysine-48 to arginine in the yeast RAD3 protein abolishes its ATPase and DNA helicase activities but not the ability to bind ATP
-
Sung, P., Higgins, D., Prakash, L. and Prakash, S. (1988) Mutation of lysine-48 to arginine in the yeast RAD3 protein abolishes its ATPase and DNA helicase activities but not the ability to bind ATP. EMBO J., 7, 3263-3269.
-
(1988)
EMBO J.
, vol.7
, pp. 3263-3269
-
-
Sung, P.1
Higgins, D.2
Prakash, L.3
Prakash, S.4
-
49
-
-
0027423190
-
Multi-ion pore behaviour in the CFTR chloride channel
-
Tabcharani, J.A., Rommens, J.M., Hou,Y.-X., Chang, X.-B., Tsui, L.-C., Riordan, J.R. and Hanrahan, J.W. (1993) Multi-ion pore behaviour in the CFTR chloride channel. Nature, 366, 79-82.
-
(1993)
Nature
, vol.366
, pp. 79-82
-
-
Tabcharani, J.A.1
Rommens, J.M.2
Hou, Y.-X.3
Chang, X.-B.4
Tsui, L.-C.5
Riordan, J.R.6
Hanrahan, J.W.7
-
50
-
-
0030964656
-
Halide permeation in wild-type and mutant cystic fibrosis transmembrane conductance regulator chloride channels
-
Tabcharani, J.A., Linsdell, P. and Hanrahan, J.W. (1997) Halide permeation in wild-type and mutant cystic fibrosis transmembrane conductance regulator chloride channels. J. Gen. Physiol., 110, 341-354.
-
(1997)
J. Gen. Physiol.
, vol.110
, pp. 341-354
-
-
Tabcharani, J.A.1
Linsdell, P.2
Hanrahan, J.W.3
-
51
-
-
0027179469
-
Interaction of nucleotides with membrane-associated cystic fibrosis transmembrane conductance regulator
-
Travis, S.M., Carson, M.R., Ries, D.R. and Welsh, M.J. (1993) Interaction of nucleotides with membrane-associated cystic fibrosis transmembrane conductance regulator. J. Biol. Chem., 268, 15336-15339.
-
(1993)
J. Biol. Chem.
, vol.268
, pp. 15336-15339
-
-
Travis, S.M.1
Carson, M.R.2
Ries, D.R.3
Welsh, M.J.4
-
52
-
-
0029954974
-
Autocrine signaling through ATP release represents a novel mechanism for cell volume regulation
-
Wang,Y., Roman, R., Lidofsky, S.D. and Fitz, J.G. (1996) Autocrine signaling through ATP release represents a novel mechanism for cell volume regulation. Proc. Natl Acad. Sci. USA, 93, 12020-12025.
-
(1996)
Proc. Natl Acad. Sci. USA
, vol.93
, pp. 12020-12025
-
-
Wang, Y.1
Roman, R.2
Lidofsky, S.D.3
Fitz, J.G.4
-
53
-
-
0027162649
-
Molecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosis
-
Welsh, M.J. and Smith, A.E. (1993) Molecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosis. Cell, 73, 1251-1254.
-
(1993)
Cell
, vol.73
, pp. 1251-1254
-
-
Welsh, M.J.1
Smith, A.E.2
-
54
-
-
0026763138
-
Cystic fibrosis transmembrane conductance regulator: A chloride channel with novel regulation
-
Welsh, M.J., Anderson, M.P, Rich, D.P., Berger, H.A., Denning, G.M., Ostedgaard, L.S., Sheppard, D.N., Cheng, S.H., Gregory, R.J. and Smith, A.E. (1992) Cystic fibrosis transmembrane conductance regulator: a chloride channel with novel regulation. Neuron, 8, 821-829.
-
(1992)
Neuron
, vol.8
, pp. 821-829
-
-
Welsh, M.J.1
Anderson, M.P.2
Rich, D.P.3
Berger, H.A.4
Denning, G.M.5
Ostedgaard, L.S.6
Sheppard, D.N.7
Cheng, S.H.8
Gregory, R.J.9
Smith, A.E.10
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