Search Results - "Fleischer, Daniel T"

Structure, 5'-flanking sequence, and chromosome location of the human N-formyl peptide receptor gene. A single-copy gene comprised of two exons on chromosome 19q.13.3 that yields two distinct transcripts by alternative polyadenylation by Haviland, David L, Borel, Angela C, Fleischer, Daniel T, Haviland, Joie C, Wetsel, Rick A

“…The N-formyl peptide chemoattractant receptor (fMLF-R) is a cell-surface, G-protein-coupled glycoprotein that mediates the directed locomotion of neutrophils…”
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Deficiency of the murine fifth complement component (C5). A 2-base pair gene deletion in a 5'-exon by Wetsel, R A, Fleischer, D T, Haviland, D L

“…To ascertain the molecular mechanism that causes murine C5 deficiency, genomic and cDNA libraries were constructed from mouse liver DNA and mRNA employing the…”
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Inherited human complement C5 deficiency. Nonsense mutations in exons 1 (Gln1 to Stop) and 36 (Arg1458 to Stop) and compound heterozygosity in three African-American families by Wang, X, Fleischer, DT, Whitehead, WT, Haviland, DL, Rosenfeld, SI, Leddy, JP, Snyderman, R, Wetsel, RA

“…Hereditary C5 deficiency has been reported in several families of different ethnic backgrounds and from different geographic regions, but the molecular genetic…”
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Structure of the murine fifth complement component (C5) gene. A large, highly interrupted gene with a variant donor splice site and organizational homology with the third and fourth complement component genes by HAVILAND, D. L, HAVILAND, J. C, FLEISCHER, D. T, WETSEL, R. A

“…To understand fifth complement component (C5) gene regulation, splicing, and C5 protein deficiency at the molecular level, the organization of the murine C5…”
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Complete cDNA sequence of human complement pro-C5. Evidence of truncated transcripts derived from a single copy gene by Haviland, DL, Haviland, JC, Fleischer, DT, Hunt, A, Wetsel, RA

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