Coyne KE - Search Results

1

Short consensus repeat-3 domain of recombinant decay-accelerating factor is recognized by Escherichia coli recombinant Dr adhesin in a model of a cell-cell interaction.

Nowicki B, Hart A, Coyne KE, Lublin DM, Nowicki S. Nowicki B, et al. Among authors: coyne ke. J Exp Med. 1993 Dec 1;178(6):2115-21. doi: 10.1084/jem.178.6.2115. J Exp Med. 1993. PMID: 7504058 Free PMC article.

2

Phospholipid-anchored and transmembrane versions of either decay-accelerating factor or membrane cofactor protein show equal efficiency in protection from complement-mediated cell damage.

Lublin DM, Coyne KE. Lublin DM, et al. Among authors: coyne ke. J Exp Med. 1991 Jul 1;174(1):35-44. doi: 10.1084/jem.174.1.35. J Exp Med. 1991. PMID: 1711565 Free PMC article.

3

Mapping of epitopes, glycosylation sites, and complement regulatory domains in human decay accelerating factor.

Coyne KE, Hall SE, Thompson S, Arce MA, Kinoshita T, Fujita T, Anstee DJ, Rosse W, Lublin DM. Coyne KE, et al. J Immunol. 1992 Nov 1;149(9):2906-13. J Immunol. 1992. PMID: 1383332

4

Construction of synthetic signals for glycosyl-phosphatidylinositol anchor attachment. Analysis of amino acid sequence requirements for anchoring.

Coyne KE, Crisci A, Lublin DM. Coyne KE, et al. J Biol Chem. 1993 Mar 25;268(9):6689-93. J Biol Chem. 1993. PMID: 8454641 Free article.

5

Molecular cloning of RhD cDNA derived from a gene present in RhD-positive, but not RhD-negative individuals.

Arce MA, Thompson ES, Wagner S, Coyne KE, Ferdman BA, Lublin DM. Arce MA, et al. Among authors: coyne ke. Blood. 1993 Jul 15;82(2):651-5. Blood. 1993. PMID: 8329718 Free article.

6

N-methyl-D-aspartate treatment increases circulating adrenocorticotropin and luteinizing hormone in the rat.

Farah JM Jr, Rao TS, Mick SJ, Coyne KE, Iyengar S. Farah JM Jr, et al. Among authors: coyne ke. Endocrinology. 1991 Apr;128(4):1875-80. doi: 10.1210/endo-128-4-1875. Endocrinology. 1991. PMID: 1848504

7

T cell repertoire development in humans with SCID after nonablative allogeneic marrow transplantation.

Sarzotti M, Patel DD, Li X, Ozaki DA, Cao S, Langdon S, Parrott RE, Coyne K, Buckley RH. Sarzotti M, et al. J Immunol. 2003 Mar 1;170(5):2711-8. doi: 10.4049/jimmunol.170.5.2711. J Immunol. 2003. PMID: 12594301

8

Complete DiGeorge syndrome: development of rash, lymphadenopathy, and oligoclonal T cells in 5 cases.

Markert ML, Alexieff MJ, Li J, Sarzotti M, Ozaki DA, Devlin BH, Sempowski GD, Rhein ME, Szabolcs P, Hale LP, Buckley RH, Coyne KE, Rice HE, Mahaffey SM, Skinner MA. Markert ML, et al. Among authors: coyne ke. J Allergy Clin Immunol. 2004 Apr;113(4):734-41. doi: 10.1016/j.jaci.2004.01.766. J Allergy Clin Immunol. 2004. PMID: 15100681

9

Isolated sulfite oxidase deficiency: identification of 12 novel SUOX mutations in 10 patients.

Johnson JL, Coyne KE, Garrett RM, Zabot MT, Dorche C, Kisker C, Rajagopalan KV. Johnson JL, et al. Among authors: coyne ke. Hum Mutat. 2002 Jul;20(1):74. doi: 10.1002/humu.9038. Hum Mutat. 2002. PMID: 12112661

10

Molybdopterin synthase mutations in a mild case of molybdenum cofactor deficiency.

Johnson JL, Coyne KE, Rajagopalan KV, Van Hove JL, Mackay M, Pitt J, Boneh A. Johnson JL, et al. Among authors: coyne ke. Am J Med Genet. 2001 Nov 22;104(2):169-73. doi: 10.1002/1096-8628(20011122)104:2<169::aid-ajmg1603>3.0.co;2-8. Am J Med Genet. 2001. PMID: 11746050

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