| Year |
Citation |
Score |
| 2011 |
Burch LH. MUC5B promoter polymorphism and pulmonary fibrosis. The New England Journal of Medicine. 365: 178; author reply 17. PMID 21751916 DOI: 10.1056/Nejmc1105707 |
0.322 |
|
| 2009 |
Taylor-Cousar JL, Zariwala MA, Burch LH, Pace RG, Drumm ML, Calloway H, Fan H, Weston BW, Wright FA, Knowles MR. Histo-blood group gene polymorphisms as potential genetic modifiers of infection and cystic fibrosis lung disease severity. Plos One. 4: e4270. PMID 19169360 DOI: 10.1371/Journal.Pone.0004270 |
0.369 |
|
| 2006 |
Burch LH, Picher M. E-NTPDases in human airways: Regulation and relevance for chronic lung diseases. Purinergic Signalling. 2: 399-408. PMID 18404479 DOI: 10.1007/s11302-006-9001-7 |
0.332 |
|
| 2005 |
Highsmith WE, Friedman KJ, Burch LH, Spock A, Silverman LM, Boucher RC, Knowles MR. A CFTR mutation (D1152H) in a family with mild lung disease and normal sweat chlorides. Clinical Genetics. 68: 88-90. PMID 15952991 DOI: 10.1111/J.1399-0004.2005.00459.X |
0.433 |
|
| 2004 |
Voynow JA, Fischer BM, Malarkey DE, Burch LH, Wong T, Longphre M, Ho SB, Foster WM. Neutrophil elastase induces mucus cell metaplasia in mouse lung. American Journal of Physiology. Lung Cellular and Molecular Physiology. 287: L1293-302. PMID 15273079 DOI: 10.1152/Ajplung.00140.2004 |
0.398 |
|
| 2004 |
Picher M, Burch LH, Boucher RC. Metabolism of P2 receptor agonists in human airways: implications for mucociliary clearance and cystic fibrosis. The Journal of Biological Chemistry. 279: 20234-41. PMID 14993227 DOI: 10.1074/Jbc.M400305200 |
0.546 |
|
| 2004 |
Gray T, Coakley R, Hirsh A, Thornton D, Kirkham S, Koo JS, Burch L, Boucher R, Nettesheim P. Regulation of MUC5AC mucin secretion and airway surface liquid metabolism by IL-1beta in human bronchial epithelia. American Journal of Physiology. Lung Cellular and Molecular Physiology. 286: L320-30. PMID 14527933 DOI: 10.1152/Ajplung.00440.2002 |
0.452 |
|
| 2003 |
Picher M, Burch LH, Hirsh AJ, Spychala J, Boucher RC. Ecto 5'-nucleotidase and nonspecific alkaline phosphatase. Two AMP-hydrolyzing ectoenzymes with distinct roles in human airways. The Journal of Biological Chemistry. 278: 13468-79. PMID 12560324 DOI: 10.1074/Jbc.M300569200 |
0.496 |
|
| 1997 |
Highsmith WE, Burch LH, Zhou Z, Olsen JC, Strong TV, Smith T, Friedman KJ, Silverman LM, Boucher RC, Collins FS, Knowles MR. Identification of a splice site mutation (2789 +5 G > A) associated with small amounts of normal CFTR mRNA and mild cystic fibrosis. Human Mutation. 9: 332-8. PMID 9101293 DOI: 10.1002/(Sici)1098-1004(1997)9:4<332::Aid-Humu5>3.0.Co;2-7 |
0.488 |
|
| 1995 |
Burch LH, Talbot CR, Knowles MR, Canessa CM, Rossier BC, Boucher RC. Relative expression of the human epithelial Na+ channel subunits in normal and cystic fibrosis airways. The American Journal of Physiology. 269: C511-8. PMID 7653534 DOI: 10.1152/Ajpcell.1995.269.2.C511 |
0.508 |
|
| 1994 |
Parr CE, Sullivan DM, Paradiso AM, Lazarowski ER, Burch LH, Olsen JC, Erb L, Weisman GA, Boucher RC, Turner JT. Cloning and expression of a human P2U nucleotide receptor, a target for cystic fibrosis pharmacotherapy. Proceedings of the National Academy of Sciences of the United States of America. 91: 3275-9. PMID 8159738 DOI: 10.1073/Pnas.91.8.3275 |
0.525 |
|
| 1994 |
Parr CE, Sullivan DM, Paradiso AM, Lazarowski ER, Burch LH, Olsen JC, Erb L, Weisman GA, Boucher RC, Turner JT. Cloning and expression of a human P2U nucleotide receptor, a target for cystic fibrosis pharmacotherapy. Proceedings of the National Academy of Sciences of the United States of America. 91: 13067. PMID 7809171 DOI: 10.1073/Pnas.91.26.13067 |
0.498 |
|
| 1994 |
Highsmith WE, Burch LH, Zhou Z, Olsen JC, Boat TE, Spock A, Gorvoy JD, Quittel L, Friedman KJ, Silverman LM. A novel mutation in the cystic fibrosis gene in patients with pulmonary disease but normal sweat chloride concentrations. The New England Journal of Medicine. 331: 974-80. PMID 7521937 DOI: 10.1056/Nejm199410133311503 |
0.415 |
|
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