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American Journal of Physical Anthropology|September 1, 1983
Alpha-1-antitrypsin-deficient phenotype is not maintained by segregation distortionB K Suarez, J A Pierce
The Journal of Laboratory and Clinical Medicine|December 1, 1979
Improved identification of antitrypsin phenotypes through isoelectric focusing with dithioerythritolJ A Pierce, B G Eradio
Journal of Pediatric Gastroenterology and Nutrition|May 10, 2001
Outcome of early hepatic portoenterostomy for biliary atresiaD Volpert, F White, M J Finegold, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 1985
Expression of the alpha 1-proteinase inhibitor gene in human monocytes and macrophagesD H Perlmutter, F S Cole, P Kilbridge, et al.
The Journal of Biological Chemistry|April 17, 1999
Disruption of disulfide bonds is responsible for impaired secretion in human complement factor H deficiencyB Z Schmidt, N L Fowler, T Hidvegi, et al.
Science (New York, N.Y.)|May 16, 1986
Regulation of class III major histocompatibility complex gene products by interleukin-1D H Perlmutter, G Goldberger, C A Dinarello, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1990
Identification of a serpin-enzyme complex receptor on human hepatoma cells and human monocytesD H Perlmutter, G I Glover, M Rivetna, et al.
The Journal of Biological Chemistry|October 5, 1990
Endocytosis and degradation of alpha 1-antitrypsin-protease complexes is mediated by the serpin-enzyme complex (SEC) receptorD H Perlmutter, G Joslin, P Nelson, et al.
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