BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

1378 related articles for article (PubMed ID: 11875262)

  • 21. Episomal expression of wild-type CFTR corrects cAMP-dependent chloride transport in respiratory epithelial cells.
    Lei DC; Kunzelmann K; Koslowsky T; Yezzi MJ; Escobar LC; Xu Z; Ellison AR; Rommens JM; Tsui L-C ; Tykocinski M; Gruenert DC
    Gene Ther; 1996 May; 3(5):427-36. PubMed ID: 9156804
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Iontophoretic beta-adrenergic stimulation of human sweat glands: possible assay for cystic fibrosis transmembrane conductance regulator activity in vivo.
    Shamsuddin AK; Reddy MM; Quinton PM
    Exp Physiol; 2008 Aug; 93(8):969-81. PubMed ID: 18441335
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Modulation of cystic fibrosis transmembrane conductance regulator gene - expression by elevation of intracellular cyclic AMP.
    Bargon J; Loitsch S; Dauletbaev N; von Mallinckrodt C; Buhl R
    Eur J Med Res; 1998 May; 3(5):256-62. PubMed ID: 9580572
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Assessment of CFTR function in rectal biopsies for the diagnosis of cystic fibrosis.
    Mall M; Hirtz S; Gonska T; Kunzelmann K
    J Cyst Fibros; 2004 Aug; 3 Suppl 2():165-9. PubMed ID: 15463952
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Bicarbonate conductance and pH regulatory capability of cystic fibrosis transmembrane conductance regulator.
    Poulsen JH; Fischer H; Illek B; Machen TE
    Proc Natl Acad Sci U S A; 1994 Jun; 91(12):5340-4. PubMed ID: 7515498
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Independence of apical Cl-/HCO3- exchange and anion conductance in duodenal HCO3- secretion.
    Spiegel S; Phillipper M; Rossmann H; Riederer B; Gregor M; Seidler U
    Am J Physiol Gastrointest Liver Physiol; 2003 Nov; 285(5):G887-97. PubMed ID: 12842823
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Cystic fibrosis transmembrane conductance regulator and H+ permeability in regulation of Golgi pH.
    Machen TE; Chandy G; Wu M; Grabe M; Moore HP
    JOP; 2001 Jul; 2(4 Suppl):229-36. PubMed ID: 11875264
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Cl- absorption across the thick ascending limb is not altered in cystic fibrosis mice. A role for a pseudo-CFTR Cl- channel.
    Marvão P; De Jesus Ferreira MC; Bailly C; Paulais M; Bens M; Guinamard R; Moreau R; Vandewalle A; Teulon J
    J Clin Invest; 1998 Dec; 102(11):1986-93. PubMed ID: 9835624
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Stable knockdown of CFTR establishes a role for the channel in P2Y receptor-stimulated anion secretion.
    Palmer ML; Lee SY; Carlson D; Fahrenkrug S; O'Grady SM
    J Cell Physiol; 2006 Mar; 206(3):759-70. PubMed ID: 16245306
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Bicarbonate secretion in the murine gallbladder--lessons for the treatment of cystic fibrosis.
    Cuthbert AW
    JOP; 2001 Jul; 2(4 Suppl):257-62. PubMed ID: 11875268
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Aberrant CFTR-dependent HCO3- transport in mutations associated with cystic fibrosis.
    Choi JY; Muallem D; Kiselyov K; Lee MG; Thomas PJ; Muallem S
    Nature; 2001 Mar; 410(6824):94-7. PubMed ID: 11242048
    [TBL] [Abstract][Full Text] [Related]  

  • 32. cAMP stimulation of HCO3- secretion across airway epithelia.
    Welsh MJ; Smith JJ
    JOP; 2001 Jul; 2(4 Suppl):291-3. PubMed ID: 11875274
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Critical role of CFTR in uterine bicarbonate secretion and the fertilizing capacity of sperm.
    Chan HC; Shi QX; Zhou CX; Wang XF; Xu WM; Chen WY; Chen AJ; Ni Y; Yuan YY
    Mol Cell Endocrinol; 2006 May; 250(1-2):106-13. PubMed ID: 16414184
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Diversity of the basic defect of homozygous CFTR mutation genotypes in humans.
    Stanke F; Ballmann M; Bronsveld I; Dörk T; Gallati S; Laabs U; Derichs N; Ritzka M; Posselt HG; Harms HK; Griese M; Blau H; Mastella G; Bijman J; Veeze H; Tümmler B
    J Med Genet; 2008 Jan; 45(1):47-54. PubMed ID: 18178635
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Cystic fibrosis transmembrane conductance regulator (CFTR)-mediated residual chloride secretion does not protect against early chronic Pseudomonas aeruginosa infection in F508del homozygous cystic fibrosis patients.
    Derichs N; Mekus F; Bronsveld I; Bijman J; Veeze HJ; von der Hardt H; Tummler B; Ballmann M
    Pediatr Res; 2004 Jan; 55(1):69-75. PubMed ID: 14605249
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Partial correction of endogenous DeltaF508 CFTR in human cystic fibrosis airway epithelia by spliceosome-mediated RNA trans-splicing.
    Liu X; Jiang Q; Mansfield SG; Puttaraju M; Zhang Y; Zhou W; Cohn JA; Garcia-Blanco MA; Mitchell LG; Engelhardt JF
    Nat Biotechnol; 2002 Jan; 20(1):47-52. PubMed ID: 11753361
    [TBL] [Abstract][Full Text] [Related]  

  • 37. The CF-CIRC study: a French collaborative study to assess the accuracy of cystic fibrosis diagnosis in neonatal screening.
    Sermet-Gaudelus I; Roussel D; Bui S; Deneuville E; Huet F; Reix P; Bellon G; Lenoir G; Edelman A
    BMC Pediatr; 2006 Oct; 6():25. PubMed ID: 17018149
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Macromolecular complexes of cystic fibrosis transmembrane conductance regulator and its interacting partners.
    Li C; Naren AP
    Pharmacol Ther; 2005 Nov; 108(2):208-23. PubMed ID: 15936089
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Intestinal bicarbonate secretion in cystic fibrosis mice.
    Clarke LL; Stien X; Walker NM
    JOP; 2001 Jul; 2(4 Suppl):263-7. PubMed ID: 11875269
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Cystic fibrosis transmembrane conductance regulator currents in guinea pig pancreatic duct cells: inhibition by bicarbonate ions.
    O'Reilly CM; Winpenny JP; Argent BE; Gray MA
    Gastroenterology; 2000 Jun; 118(6):1187-96. PubMed ID: 10833494
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 69.