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Proceedings of the National Academy of Sciences of the United States of America|October 1, 1985
The cellular defect in alpha 1-proteinase inhibitor (alpha 1-PI) deficiency is expressed in human monocytes and in Xenopus oocytes injected with human liver mRNAD H Perlmutter, R M Kay, F S Cole, et al.
Biochemistry|June 16, 1987
Complementary DNA and derived amino acid sequence of the alpha subunit of human complement protein C8: evidence for the existence of a separate alpha subunit messenger RNAA G Rao, O M Howard, S C Ng, et al.
The Journal of Allergy and Clinical Immunology|April 1, 1977
Delayed cold-induced urticaria: a dominantly inherited disorderN A Soter, N P Joshi, F J Twarog, et al.
The Journal of Biological Chemistry|June 25, 1985
Human serum amyloid P component. cDNA isolation, complete sequence of pre-serum amyloid P component, and localization of the gene to chromosome 1E C Mantzouranis, S B Dowton, A S Whitehead, et al.
The Journal of Clinical Investigation|April 1, 1994
A mutation in the surfactant protein B gene responsible for fatal neonatal respiratory disease in multiple kindredsL M Nogee, G Garnier, H C Dietz, et al.
The Journal of Pediatrics|September 1, 1994
Surfactant protein B deficiency: antenatal diagnosis and prospective treatment with surfactant replacementA Hamvas, F S Cole, D E deMello, et al.
The New England Journal of Medicine|July 4, 1985
The molecular basis for genetic deficiency of the second component of human complementF S Cole, A S Whitehead, H S Auerbach, et al.
The Journal of Laboratory and Clinical Medicine|October 1, 1987
Induction of mouse monocyte-macrophage replication by a mesangial cell-derived factorB S Ooi, E P MacCarthy, M A Weiss, et al.
The Journal of Biological Chemistry|March 8, 1996
Type II human complement C2 deficiency. Allele-specific amino acid substitutions (Ser189 --> Phe; Gly444 --> Arg) cause impaired C2 secretionR A Wetsel, J Kulics, M L Lokki, et al.
Biochemistry|June 4, 1985
Human serum amyloid A (SAA): biosynthesis and postsynthetic processing of preSAA and structural variants defined by complementary DNAJ D Sipe, H R Colten, G Goldberger, et al.
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