-
2
-
-
79953288433
-
Development and applications of single-cell transcriptome analysis
-
Tang F, Lao K, Surani MA, (2011) Development and applications of single-cell transcriptome analysis. Nat Methods 8: S6-11.
-
(2011)
Nat Methods
, vol.8
, pp. 6-11
-
-
Tang, F.1
Lao, K.2
Surani, M.A.3
-
3
-
-
0024453308
-
Identification of the cystic fibrosis gene: chromosome walking and jumping
-
Rommens JM, Iannuzzi MC, Kerem B, Drumm ML, Melmer G, 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
Iannuzzi, M.C.2
Kerem, B.3
Drumm, M.L.4
Melmer, G.5
-
4
-
-
0024423668
-
Identification of the cystic fibrosis gene: genetic analysis
-
Kerem B, Rommens JM, Buchanan JA, Markiewicz D, Cox TK, 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
Rommens, J.M.2
Buchanan, J.A.3
Markiewicz, D.4
Cox, T.K.5
-
5
-
-
0024424270
-
Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA
-
Riordan JR, Rommens JM, Kerem B, Alon N, Rozmahel 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
Rommens, J.M.2
Kerem, B.3
Alon, N.4
Rozmahel, R.5
-
6
-
-
0037460729
-
Cystic fibrosis
-
Ratjen F, Doring G, (2003) Cystic fibrosis. Lancet 361: 681-689.
-
(2003)
Lancet
, vol.361
, pp. 681-689
-
-
Ratjen, F.1
Doring, G.2
-
7
-
-
0028858161
-
Multiple proteolytic systems, including the proteasome, contribute to CFTR processing
-
0092-8674(95)90241-4 [pii]
-
Jensen TJ, Loo MA, Pind S, Williams DB, Goldberg AL, et al. (1995) Multiple proteolytic systems, including the proteasome, contribute to CFTR processing. Cell 83: 129-135 0092-8674(95)90241-4 [pii].
-
(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
-
8
-
-
0028840915
-
Degradation of CFTR by the ubiquitin-proteasome pathway
-
0092-8674(95)90240-6 [pii]
-
Ward CL, Omura S, Kopito RR, (1995) Degradation of CFTR by the ubiquitin-proteasome pathway. Cell 83: 121-127 0092-8674(95)90240-6 [pii].
-
(1995)
Cell
, vol.83
, pp. 121-127
-
-
Ward, C.L.1
Omura, S.2
Kopito, R.R.3
-
9
-
-
0032588980
-
DeltaF508 CFTR protein expression in tissues from patients with cystic fibrosis
-
doi: 10.1172/JCI5731
-
Kalin N, Claass A, Sommer M, Puchelle E, Tummler B, (1999) DeltaF508 CFTR protein expression in tissues from patients with cystic fibrosis. J Clin Invest 103: 1379-1389 doi:10.1172/JCI5731.
-
(1999)
J Clin Invest
, vol.103
, pp. 1379-1389
-
-
Kalin, N.1
Claass, A.2
Sommer, M.3
Puchelle, E.4
Tummler, B.5
-
10
-
-
0033918281
-
Cystic fibrosis F508del patients have apically localized CFTR in a reduced number of airway cells
-
Penque D, Mendes F, Beck S, Farinha C, Pacheco P, et al. (2000) Cystic fibrosis F508del patients have apically localized CFTR in a reduced number of airway cells. Lab Invest 80: 857-868.
-
(2000)
Lab Invest
, vol.80
, pp. 857-868
-
-
Penque, D.1
Mendes, F.2
Beck, S.3
Farinha, C.4
Pacheco, P.5
-
11
-
-
79961074064
-
Is CFTR-delF508 really absent from the apical membrane of the airway epithelium?
-
doi:10.1371/journal.pone.0023226;PONE-D-11-05617 [pii]
-
Borthwick LA, Botha P, Verdon B, Brodlie MJ, Gardner A, et al. (2011) Is CFTR-delF508 really absent from the apical membrane of the airway epithelium? PLoS One 6 doi:10.1371/journal.pone.0023226;PONE-D-11-05617 [pii].
-
(2011)
PLoS One
, vol.6
-
-
Borthwick, L.A.1
Botha, P.2
Verdon, B.3
Brodlie, M.J.4
Gardner, A.5
-
12
-
-
18244377969
-
Characterization of wild-type and deltaF508 cystic fibrosis transmembrane regulator in human respiratory epithelia
-
E04-11-1010 [pii];doi: 10.1091/mbc.E04-11-1010
-
Kreda SM, Mall M, Mengos A, Rochelle L, Yankaskas J, et al. (2005) Characterization of wild-type and deltaF508 cystic fibrosis transmembrane regulator in human respiratory epithelia. Mol Biol Cell 16: 2154-2167 E04-11-1010 [pii];doi:10.1091/mbc.E04-11-1010.
-
(2005)
Mol Biol Cell
, vol.16
, pp. 2154-2167
-
-
Kreda, S.M.1
Mall, M.2
Mengos, A.3
Rochelle, L.4
Yankaskas, J.5
-
13
-
-
34347224756
-
No detectable improvements in cystic fibrosis transmembrane conductance regulator by nasal aminoglycosides in patients with cystic fibrosis with stop mutations
-
Clancy JP, Rowe SM, Bebok Z, Aitken ML, Gibson R, et al. (2007) No detectable improvements in cystic fibrosis transmembrane conductance regulator by nasal aminoglycosides in patients with cystic fibrosis with stop mutations. Am J Respir Cell Mol Biol 37: 57-66.
-
(2007)
Am J Respir Cell Mol Biol
, vol.37
, pp. 57-66
-
-
Clancy, J.P.1
Rowe, S.M.2
Bebok, Z.3
Aitken, M.L.4
Gibson, R.5
-
14
-
-
0019809960
-
Increased bioelectric potential difference across respiratory epithelia in cystic fibrosis
-
doi: 10.1056/NEJM198112173052502
-
Knowles M, Gatzy J, Boucher R, (1981) Increased bioelectric potential difference across respiratory epithelia in cystic fibrosis. N Engl J Med 305: 1489-1495 doi:10.1056/NEJM198112173052502.
-
(1981)
N Engl J Med
, vol.305
, pp. 1489-1495
-
-
Knowles, M.1
Gatzy, J.2
Boucher, R.3
-
15
-
-
0035190296
-
Localisation of wild-type and DeltaF508-CFTR in nasal epithelial cells
-
Dormer RL, McNeilly CM, Morris MR, Pereira MM, Doull IJ, et al. (2001) Localisation of wild-type and DeltaF508-CFTR in nasal epithelial cells. Pflugers Arch 443 (Suppl 1): S117-S120.
-
(2001)
Pflugers Arch
, vol.443
, Issue.SUPPL. 1
-
-
Dormer, R.L.1
McNeilly, C.M.2
Morris, M.R.3
Pereira, M.M.4
Doull, I.J.5
-
16
-
-
19944385576
-
Assessment of CFTR localisation in native airway epithelial cells obtained by nasal brushing
-
S156919930400061X [pii];doi: 10.1016/j.jcf.2004.05.009
-
Harris CM, Mendes F, Dragomir A, Doull IJ, Carvalho-Oliveira I, et al. (2004) Assessment of CFTR localisation in native airway epithelial cells obtained by nasal brushing. J Cyst Fibros 3 (Suppl 2) 43-48. S156919930400061X [pii];doi:10.1016/j.jcf.2004.05.009.
-
(2004)
J Cyst Fibros
, vol.3
, Issue.SUPPL. 2
, pp. 43-48
-
-
Harris, C.M.1
Mendes, F.2
Dragomir, A.3
Doull, I.J.4
Carvalho-Oliveira, I.5
-
17
-
-
0742322867
-
CFTR localization in native airway cells and cell lines expressing wild-type or F508del-CFTR by a panel of different antibodies
-
Carvalho-Oliveira I, Efthymiadou A, Malho R, Nogueira P, Tzetis M, et al. (2004) CFTR localization in native airway cells and cell lines expressing wild-type or F508del-CFTR by a panel of different antibodies. J Histochem Cytochem 52: 193-203.
-
(2004)
J Histochem Cytochem
, vol.52
, pp. 193-203
-
-
Carvalho-Oliveira, I.1
Efthymiadou, A.2
Malho, R.3
Nogueira, P.4
Tzetis, M.5
-
18
-
-
0026907529
-
Mislocalization of delta F508 CFTR in cystic fibrosis sweat gland
-
doi:10.1038/ng0892-321
-
Kartner N, Augustinas O, Jensen TJ, Naismith AL, Riordan JR, (1992) Mislocalization of delta F508 CFTR in cystic fibrosis sweat gland. Nat Genet 1: 321-327 doi:10.1038/ng0892-321.
-
(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
-
19
-
-
0029082368
-
CFTR and differentiation markers expression in non-CF and delta F 508 homozygous CF nasal epithelium
-
doi:10.1172/JCI118199
-
Dupuit F, Kalin N, Brezillon S, Hinnrasky J, Tummler B, et al. (1995) CFTR and differentiation markers expression in non-CF and delta F 508 homozygous CF nasal epithelium. J Clin Invest 96: 1601-1611 doi:10.1172/JCI118199.
-
(1995)
J Clin Invest
, vol.96
, pp. 1601-1611
-
-
Dupuit, F.1
Kalin, N.2
Brezillon, S.3
Hinnrasky, J.4
Tummler, B.5
-
20
-
-
49049089612
-
The DeltaF508-CFTR mutation results in increased biofilm formation by Pseudomonas aeruginosa by increasing iron availability
-
00391.2007 [pii];doi: 10.1152/ajplung.00391.2007
-
Moreau-Marquis S, Bomberger JM, Anderson GG, Swiatecka-Urban A, Ye S, et al. (2008) The DeltaF508-CFTR mutation results in increased biofilm formation by Pseudomonas aeruginosa by increasing iron availability. Am J Physiol Lung Cell Mol Physiol 295: L25-L37 00391.2007 [pii];doi:10.1152/ajplung.00391.2007.
-
(2008)
Am J Physiol Lung Cell Mol Physiol
, vol.295
-
-
Moreau-Marquis, S.1
Bomberger, J.M.2
Anderson, G.G.3
Swiatecka-Urban, A.4
Ye, S.5
-
21
-
-
33845739839
-
Domain interdependence in the biosynthetic assembly of CFTR
-
S0022-2836(06)01511-7 [pii];doi:10.1016/j.jmb.2006.10.086
-
Cui L, Aleksandrov L, Chang XB, Hou YX, He L, et al. (2007) Domain interdependence in the biosynthetic assembly of CFTR. J Mol Biol 365: 981-994 S0022-2836(06)01511-7 [pii];doi:10.1016/j.jmb.2006.10.086.
-
(2007)
J Mol Biol
, vol.365
, pp. 981-994
-
-
Cui, L.1
Aleksandrov, L.2
Chang, X.B.3
Hou, Y.X.4
He, L.5
-
22
-
-
2542480784
-
Endocytic trafficking routes of wild type and DeltaF508 cystic fibrosis transmembrane conductance regulator
-
doi:10.1091/mbc.E04-03-0176;E04-03-0176 [pii]
-
Gentzsch M, Chang XB, Cui L, Wu Y, Ozols VV, et al. (2004) Endocytic trafficking routes of wild type and DeltaF508 cystic fibrosis transmembrane conductance regulator. Mol Biol Cell 15: 2684-2696 doi:10.1091/mbc.E04-03-0176;E04-03-0176 [pii].
-
(2004)
Mol Biol Cell
, vol.15
, pp. 2684-2696
-
-
Gentzsch, M.1
Chang, X.B.2
Cui, L.3
Wu, Y.4
Ozols, V.V.5
-
23
-
-
55549094466
-
Multiple membrane-cytoplasmic domain contacts in the cystic fibrosis transmembrane conductance regulator (CFTR) mediate regulation of channel gating
-
M803894200 [pii];doi:10.1074/jbc.M803894200
-
He L, Aleksandrov AA, Serohijos AW, Hegedus T, Aleksandrov LA, et al. (2008) Multiple membrane-cytoplasmic domain contacts in the cystic fibrosis transmembrane conductance regulator (CFTR) mediate regulation of channel gating. J Biol Chem 283: 26383-26390 M803894200 [pii];doi:10.1074/jbc.M803894200.
-
(2008)
J Biol Chem
, vol.283
, pp. 26383-26390
-
-
He, L.1
Aleksandrov, A.A.2
Serohijos, A.W.3
Hegedus, T.4
Aleksandrov, L.A.5
-
24
-
-
0347361558
-
The DeltaF508 mutation results in loss of CFTR function and mature protein in native human colon
-
S0016508503017177 [pii]
-
Mall M, Kreda SM, Mengos A, Jensen TJ, Hirtz S, et al. (2004) The DeltaF508 mutation results in loss of CFTR function and mature protein in native human colon. Gastroenterology 126: 32-41 S0016508503017177 [pii].
-
(2004)
Gastroenterology
, vol.126
, pp. 32-41
-
-
Mall, M.1
Kreda, S.M.2
Mengos, A.3
Jensen, T.J.4
Hirtz, S.5
-
25
-
-
0001000969
-
Quantative detection of CFTR mRNA in gene transfer studies in human, murine, and simian respiratory tissues in vitro and in vivo
-
Nicolis E, Melotti P, Tamanini A, Lusky M, Pavarini A, et al. (1999) Quantative detection of CFTR mRNA in gene transfer studies in human, murine, and simian respiratory tissues in vitro and in vivo. Gene Therapy & Molecular Biology 4: 221-232.
-
(1999)
Gene Therapy & Molecular Biology
, vol.4
, pp. 221-232
-
-
Nicolis, E.1
Melotti, P.2
Tamanini, A.3
Lusky, M.4
Pavarini, A.5
-
26
-
-
70449730684
-
Regulation of myelopoiesis through syntenin-mediated modulation of IL-5 receptor output
-
Beekman JM, Verhagen LP, Geijsen N, Coffer PJ, (2009) Regulation of myelopoiesis through syntenin-mediated modulation of IL-5 receptor output. Blood 114: 3917-3927.
-
(2009)
Blood
, vol.114
, pp. 3917-3927
-
-
Beekman, J.M.1
Verhagen, L.P.2
Geijsen, N.3
Coffer, P.J.4
-
27
-
-
4043133804
-
Modulation of FcgammaRI (CD64) ligand binding by blocking peptides of periplakin
-
doi:10.1074/jbc.M401018200;M401018200 [pii]
-
Beekman JM, Bakema JE, van der Linden J, Tops B, Hinten M, et al. (2004) Modulation of FcgammaRI (CD64) ligand binding by blocking peptides of periplakin. J Biol Chem 279: 33875-33881 doi:10.1074/jbc.M401018200;M401018200 [pii].
-
(2004)
J Biol Chem
, vol.279
, pp. 33875-33881
-
-
Beekman, J.M.1
Bakema, J.E.2
van der Linden, J.3
Tops, B.4
Hinten, M.5
|