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January 1, 1997BloodOpen Access

Molecular Pathogenesis of Type I Congenital Plasminogen Deficiency: Expression of Recombinant Human Mutant Plasminogens in Mammalian Cells

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Authors

HAHiroyuki AzumaFujita Health University HospitalNMNobuaki MimaMSMitsuo Shirakawa

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Azuma et al. (1997) studied this question.

synapsesocial.com/papers/6a8386a13c50b6027c960886https://doi.org/10.1182/blood.v89.1.183
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Plasminogen: Purification from Human Plasma by Affinity Chromatography1970 · 2,145 citations
  2. 2Interaction of Hsp 70 with Newly Synthesized Proteins: Implications for Protein Folding and Assembly1990 · 1,308 citations
  3. 3Protein C deficiency Hong Kong 1 and 2: hereditary protein C deficiency caused by two mutant alleles, a 5-nucleotide deletion and a missense mutation1992 · 18 citations
  4. 4Binding of plasminogen to cultured human endothelial cells.1986 · 311 citations
  5. 5Plasminogen Tochigi: inactive plasmin resulting from replacement of alanine-600 by threonine in the active site.1982 · 94 citations