Erythrocyte membrane ATP binding cassette (ABC) proteins: MRP1 and CFTR as well as CD39 (ecto-apyrase) involved in RBC ATP transport and elevated blood plasma ATP of cystic fibrosis.
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P. Okunieff | A. Hartov | A. Sartorelli | D. Jefferson | E. Demidenko | S. Robson | P. Okunieff | G. Rappa | A. Lorico | H. Parker | S. Grubman | E. Abraham | A. Salikhova | J. Kahn | R. J. Kim | J. Efird | H. Parker | K. M. Sterling | J. Thakar | N. Johnston | H. B. Huffman | M. A. Crockett | W. Boyle | E. Demidenko | J. Efird | Heather B. Huffman | Molly A. Crockett | William E. Boyle | Julia Kahn
[1] R. Boucher,et al. Constitutive Release of ATP and Evidence for Major Contribution of Ecto-nucleotide Pyrophosphatase and Nucleoside Diphosphokinase to Extracellular Nucleotide Concentrations* , 2000, The Journal of Biological Chemistry.
[2] H. Cantiello,et al. Increased circulating levels of plasma ATP in cystic fibrosis patients. , 2000, Clinical Physiology.
[3] M. Kool,et al. A family of drug transporters: the multidrug resistance-associated proteins. , 2000, Journal of the National Cancer Institute.
[4] J. Aleu,et al. ATP Crossing the Cell Plasma Membrane Generates an Ionic Current in Xenopus Oocytes* , 2000, The Journal of Biological Chemistry.
[5] H. Cantiello,et al. cAMP activates an ATP-permeable pathway in neonatal rat cardiac myocytes. , 2000, American journal of physiology. Cell physiology.
[6] I. Pastan,et al. Drug selection of MDR1-transduced hematopoietic cells ex vivo increases transgene expression and chemoresistance in reconstituted bone marrow in mice , 2000, Gene Therapy.
[7] D D Breimer,et al. Multidrug resistance protein 1 protects the choroid plexus epithelium and contributes to the blood-cerebrospinal fluid barrier. , 2000, The Journal of clinical investigation.
[8] Patricia D. Christie,et al. Targeted disruption of cd39/ATP diphosphohydrolase results in disordered hemostasis and thromboregulation , 1999, Nature Medicine.
[9] A. Sartorelli,et al. New insights into the biology and pharmacology of the multidrug resistance protein (MRP) from gene knockout models. , 1999, Biochemical pharmacology.
[10] H. M. Bender,et al. Role of blood‐brain barrier P‐glycoprotein in limiting brain accumulation and sedative side‐effects of asimadoline, a peripherally acting analgaesic drug , 1999, British journal of pharmacology.
[11] I. Pastan,et al. Contribution to substrate specificity and transport of nonconserved residues in transmembrane domain 12 of human P-glycoprotein. , 1998, Biochemistry.
[12] S. Cole,et al. Characterization of vincristine transport by the M(r) 190,000 multidrug resistance protein (MRP): evidence for cotransport with reduced glutathione. , 1998, Cancer research.
[13] Sreenivas Devidas,et al. Cystic Fibrosis Transmembrane Conductance Regulator–associated ATP Release Is Controlled by a Chloride Sensor , 1998, The Journal of cell biology.
[14] S. Cole,et al. Multidrug resistance mediated by the ATP‐binding cassette transporter protein MRP , 1998, BioEssays : news and reviews in molecular, cellular and developmental biology.
[15] M. L. Ellsworth,et al. Deformation-induced ATP release from red blood cells requires CFTR activity. , 1998, American journal of physiology. Heart and circulatory physiology.
[16] D. Hipfner,et al. Epitope mapping of monoclonal antibodies specific for the 190-kDa multidrug resistance protein (MRP). , 1998, British Journal of Cancer.
[17] G. Guidotti,et al. The Transmembrane Domains of Ectoapyrase (CD39) Affect Its Enzymatic Activity and Quaternary Structure* , 1998, The Journal of Biological Chemistry.
[18] C. Haest,et al. Evidence for a role of the multidrug resistance protein (MRP) in the outward translocation of NBD-phospholipids in the erythrocyte membrane. , 1998, Biochimica et biophysica acta.
[19] A. Sokal,et al. Radiation inactivation suggests that human multidrug resistance-associated protein 1 occurs as a dimer in the human erythrocyte membrane. , 1998, Archives of biochemistry and biophysics.
[20] W. Watt,et al. Cystic Fibrosis Transmembrane Regulator-independent Release of ATP , 1998, The Journal of Biological Chemistry.
[21] H. Cantiello,et al. Electrodiffusional ATP movement through the cystic fibrosis transmembrane conductance regulator. , 1998, The American journal of physiology.
[22] R. Flavell,et al. Evidence that the multidrug resistance protein (MRP) functions as a co-transporter of glutathione and natural product toxins. , 1997, Cancer research.
[23] R. Flavell,et al. Disruption of the murine MRP (multidrug resistance protein) gene leads to increased sensitivity to etoposide (VP-16) and increased levels of glutathione. , 1997, Cancer research.
[24] M. Drumm,et al. In vivo activation of CFTR-dependent chloride transport in murine airway epithelium by CNP. , 1997, American journal of physiology. Lung cellular and molecular physiology.
[25] Jos H. Beijnen,et al. Increased sensitivity to anticancer drugs and decreased inflammatory response in mice lacking the multidrug resistance-associated protein , 1997, Nature Medicine.
[26] L. Tsui,et al. Incomplete rescue of cystic fibrosis transmembrane conductance regulator deficient mice by the human CFTR cDNA. , 1997, Human molecular genetics.
[27] A. Nies,et al. Regulation and translocation of ATP-dependent apical membrane proteins in rat liver. , 1997, The American journal of physiology.
[28] K. Kunjilwar,et al. Association and Stoichiometry of KATP Channel Subunits , 1997, Neuron.
[29] G. Bartosz,et al. Peroxynitrite inhibits glutathione S-conjugate transport. , 1997, Biochimica et biophysica acta.
[30] M. Pazzagli,et al. Diabetes mellitus and subjects' ageing: a study on the ATP content and ATP‐related enzyme activities in human erythrocytes , 1997, European journal of clinical investigation.
[31] H. Cantiello. Nucleotide Transport Through the Cystic Fibrosis Transmembrane Conductance Regulator , 1997, Bioscience reports.
[32] M. Drumm,et al. In vivo activation of the cystic fibrosis transmembrane conductance regulator mutant deltaF508 in murine nasal epithelium. , 1997, Proceedings of the National Academy of Sciences of the United States of America.
[33] P. Okunieff,et al. Cystic Fibrosis Transmembrane Conductance Regulator and Adenosine Triphosphate , 1997, Science.
[34] Z. Gatmaitan,et al. Ectonucleotidases, purine nucleoside transporter, and function of the bile canalicular plasma membrane of the hepatocyte , 1997, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[35] R. Flavell,et al. Double knockout of the MRP gene leads to increased drug sensitivity in vitro. , 1996, Cancer research.
[36] H. Cantiello,et al. Expression of Drosophila melanogaster P-glycoproteins is associated with ATP channel activity. , 1996, The American journal of physiology.
[37] D. Keppler,et al. Identification of the multidrug-resistance protein (MRP) as the glutathione-S-conjugate export pump of erythrocytes. , 1996, European journal of biochemistry.
[38] E. Schwiebert,et al. Apical and basolateral ATP stimulates tracheal epithelial chloride secretion via multiple purinergic receptors. , 1996, The American journal of physiology.
[39] C. Bear,et al. Purified Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Does Not Function as an ATP Channel (*) , 1996, The Journal of Biological Chemistry.
[40] P. Okunieff,et al. Cystic fibrosis hetero–and homozygosity is associated with inhibition of breast cancer growth , 1996, Nature Medicine.
[41] D. Keppler,et al. Absence of the canalicular isoform of the MRP gene–encoded conjugate export pump from the hepatocytes in Dubin‐Johnson syndrome , 1996, Hepatology.
[42] K. Gunderson,et al. Failure of the Cystic Fibrosis Transmembrane Conductance Regulator to Conduct ATP , 1996, Science.
[43] C. Ellis,et al. The erythrocyte as a regulator of vascular tone. , 1995, The American journal of physiology.
[44] J. Inazawa,et al. Reconstitution of IKATP: An Inward Rectifier Subunit Plus the Sulfonylurea Receptor , 1995, Science.
[45] C. Higgins,et al. The ABC of channel regulation , 1995, Cell.
[46] G. Cutting,et al. CFTR regulates outwardly rectifying chloride channels through an autocrine mechanism involving ATP , 1995, Cell.
[47] B. Koller,et al. A murine model of cystic fibrosis. , 1995, American journal of respiratory and critical care medicine.
[48] J. Whitsett,et al. Correction of lethal intestinal defect in a mouse model of cystic fibrosis by human CFTR. , 1994, Science.
[49] Matthew P. Anderson,et al. Dysfunction of CFTR bearing the ΔF508 mutation , 1993, Journal of Cell Science.
[50] M. Summan,et al. Raised adenine nucleotide concentrations in erythrocytes of patients with cystic fibrosis. , 1993, Biochemical Society transactions.
[51] M. Welsh,et al. Molecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosis , 1993, Cell.
[52] C. Higgins,et al. ABC transporters: from microorganisms to man. , 1992, Annual review of cell biology.
[53] H. A. Berger,et al. Chloride channels in the apical membrane of normal and cystic fibrosis airway and intestinal epithelia. , 1992, The American journal of physiology.
[54] J. Casey,et al. Enzymatic deglycosylation of human Band 3, the anion transport protein of the erythrocyte membrane. Effect on protein structure and transport properties. , 1992, The Journal of biological chemistry.
[55] J. Casey,et al. Structure and Function of the Band 3 Cl‐/HCO‐3 Transporter a , 1989, Annals of the New York Academy of Sciences.
[56] I. Fidler,et al. Distribution and fate of free and liposome-encapsulated [3H]nor-muramyl dipeptide and [3H]muramyl tripeptide phosphatidylethanolamine in mice. , 1985, Journal of immunology.
[57] C. Smith,et al. Relationships among purine nucleoside metabolism, adenosine triphosphate catabolism, and glycolysis in human erythrocytes. , 1979, Canadian journal of biochemistry.
[58] U. K. Laemmli,et al. Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4 , 1970, Nature.
[59] D. Benos,et al. CFTR is a conductance regulator as well as a chloride channel. , 1999, Physiological reviews.
[60] A. Schinkel. Pharmacological insights from P-glycoprotein knockout mice. , 1998, International journal of clinical pharmacology and therapeutics.
[61] K. Kunjilwar,et al. Toward understanding the assembly and structure of KATP channels. , 1998, Physiological reviews.
[62] I. Pastan,et al. Genetic analysis of the multidrug transporter. , 1995, Annual review of genetics.
[63] R. Arceci,et al. The multidrug resistance (mdr1) gene product functions as an ATP channel. , 1993, Proceedings of the National Academy of Sciences of the United States of America.
[64] M. Welsh,et al. Dysfunction of CFTR bearing the delta F508 mutation. , 1993, Journal of cell science. Supplement.
[65] T. Forrester,et al. Release of ATP from human erythrocytes in response to a brief period of hypoxia and hypercapnia. , 1992, Cardiovascular research.
[66] J. Casey,et al. Purification and characterization of band 3 protein. , 1989, Methods in enzymology.
[67] C. Smith,et al. Variation in erythrocyte purine metabolism among mouse strains. , 1983, Comparative biochemistry and physiology. B, Comparative biochemistry.