D T Fleischer

Deficiency of the murine fifth complement component (C5). A 2-base pair gene deletion in a 5'-exon.

Rick A. Wetsel, D T Fleischer, David L. Haviland · Journal of Biological Chemistry · 1990 · 199 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

Complete cDNA sequence of human complement pro-C5. Evidence of truncated transcripts derived from a single copy gene

David L. Haviland, Joie C. Haviland, D T Fleischer et al. · The Journal of Immunology · 1991 · 47 citations

Life Sciences, Genetics, Molecular Biology +12

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.

X Wang, D T Fleischer, William Whitehead et al. · The Journal of Immunology · 1995 · 44 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

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

David L. Haviland, Joie C. Haviland, D T Fleischer et al. · Journal of Biological Chemistry · 1991 · 39 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

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

David L. Haviland, Angela C. Borel, D T Fleischer et al. · Biochemistry · 1993 · 23 citations

Life Sciences, Biochemistry, Genetics +7