Burch LH - Search Results

1

Histo-blood group gene polymorphisms as potential genetic modifiers of infection and cystic fibrosis lung disease severity.

Taylor-Cousar JL, Zariwala MA, Burch LH, Pace RG, Drumm ML, Calloway H, Fan H, Weston BW, Wright FA, Knowles MR; Gene Modifier Study Group. Taylor-Cousar JL, et al. Among authors: burch lh. PLoS One. 2009;4(1):e4270. doi: 10.1371/journal.pone.0004270. Epub 2009 Jan 26. PLoS One. 2009. PMID: 19169360 Free PMC article.

2

Relative expression of the human epithelial Na+ channel subunits in normal and cystic fibrosis airways.

Burch LH, Talbot CR, Knowles MR, Canessa CM, Rossier BC, Boucher RC. Burch LH, et al. Am J Physiol. 1995 Aug;269(2 Pt 1):C511-8. doi: 10.1152/ajpcell.1995.269.2.C511. Am J Physiol. 1995. PMID: 7653534

3

Identification of a splice site mutation (2789 +5 G > A) associated with small amounts of normal CFTR mRNA and mild cystic fibrosis.

Highsmith WE Jr, Burch LH, Zhou Z, Olsen JC, Strong TV, Smith T, Friedman KJ, Silverman LM, Boucher RC, Collins FS, Knowles MR. Highsmith WE Jr, et al. Among authors: burch lh. Hum Mutat. 1997;9(4):332-8. doi: 10.1002/(SICI)1098-1004(1997)9:4<332::AID-HUMU5>3.0.CO;2-7. Hum Mutat. 1997. PMID: 9101293

4

A CFTR mutation (D1152H) in a family with mild lung disease and normal sweat chlorides.

Highsmith WE Jr, Friedman KJ, Burch LH, Spock A, Silverman LM, Boucher RC, Knowles MR. Highsmith WE Jr, et al. Among authors: burch lh. Clin Genet. 2005 Jul;68(1):88-90. doi: 10.1111/j.1399-0004.2005.00459.x. Clin Genet. 2005. PMID: 15952991 No abstract available.

5

Finding fibrosis genes: the lung.

Burch LH, Schwartz DA. Burch LH, et al. Methods Mol Med. 2005;117:293-313. doi: 10.1385/1-59259-940-0:293. Methods Mol Med. 2005. PMID: 16118459

6

Plasminogen alleles influence susceptibility to invasive aspergillosis.

Zaas AK, Liao G, Chien JW, Weinberg C, Shore D, Giles SS, Marr KA, Usuka J, Burch LH, Perera L, Perfect JR, Peltz G, Schwartz DA. Zaas AK, et al. Among authors: burch lh. PLoS Genet. 2008 Jun 20;4(6):e1000101. doi: 10.1371/journal.pgen.1000101. PLoS Genet. 2008. PMID: 18566672 Free PMC article.

7

Clinical and pathologic features of familial interstitial pneumonia.

Steele MP, Speer MC, Loyd JE, Brown KK, Herron A, Slifer SH, Burch LH, Wahidi MM, Phillips JA 3rd, Sporn TA, McAdams HP, Schwarz MI, Schwartz DA. Steele MP, et al. Among authors: burch lh. Am J Respir Crit Care Med. 2005 Nov 1;172(9):1146-52. doi: 10.1164/rccm.200408-1104OC. Epub 2005 Aug 18. Am J Respir Crit Care Med. 2005. PMID: 16109978 Free PMC article.

8

A novel mutation in the cystic fibrosis gene in patients with pulmonary disease but normal sweat chloride concentrations.

Highsmith WE, Burch LH, Zhou Z, Olsen JC, Boat TE, Spock A, Gorvoy JD, Quittel L, Friedman KJ, Silverman LM, et al. Highsmith WE, et al. Among authors: burch lh. N Engl J Med. 1994 Oct 13;331(15):974-80. doi: 10.1056/NEJM199410133311503. N Engl J Med. 1994. PMID: 7521937 Free article.

9

Metabolism of P2 receptor agonists in human airways: implications for mucociliary clearance and cystic fibrosis.

Picher M, Burch LH, Boucher RC. Picher M, et al. Among authors: burch lh. J Biol Chem. 2004 May 7;279(19):20234-41. doi: 10.1074/jbc.M400305200. Epub 2004 Mar 1. J Biol Chem. 2004. PMID: 14993227 Free article.

10

Cloning and expression of a human P2U nucleotide receptor, a target for cystic fibrosis pharmacotherapy.

Parr CE, Sullivan DM, Paradiso AM, Lazarowski ER, Burch LH, Olsen JC, Erb L, Weisman GA, Boucher RC, Turner JT. Parr CE, et al. Among authors: burch lh. Proc Natl Acad Sci U S A. 1994 Apr 12;91(8):3275-9. doi: 10.1073/pnas.91.8.3275. Proc Natl Acad Sci U S A. 1994. PMID: 8159738 Free PMC article.

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