• Login
    View Item 
    •   Oxy Scholar Home
    • Bulletin of the Southern California Academy of Sciences
    • Bulletin of the Southern California Academy of Sciences
    • View Item
    •   Oxy Scholar Home
    • Bulletin of the Southern California Academy of Sciences
    • Bulletin of the Southern California Academy of Sciences
    • View Item
    JavaScript is disabled for your browser. Some features of this site may not work without it.

    Studies of the Blood of Ascidia nigra (Savigny) I. Total Blood Cell Counts, Differential Blood Cell Counts, and Hematocrit Values

    Thumbnail
    Subject
    blood; blood cell; Ascidia; differential; count; hematocrit; tunicate; solitary tunicate
    Author
    Vallee Jr., James A.
    Journal Title
    Scas: Bulletin of the Southern California Academy of Sciences
    Volume
    66
    Issue
    scas/vol66/iss1; 1
    Metadata
    Show full item record
    URI
    https://scholar.oxy.edu/handle/20.500.12711/10515
    Collections
    • Bulletin of the Southern California Academy of Sciences

    Related items

    Showing items related by title, author, creator and subject.

    • Synthesis of a Glycosylated DNA Fragment that Codes for a Truncated B-Domain of Human Blood Coagulation Factor VIII 

      Simpson, Samuel (2010-01-01)
      The focus of this summer?s project was to synthesize the DNA for a glycosylated version of the human coagulation Factor VIII protein using the same methods used to obtain the DNA for a non-glycosylated version, which ...
    • Construction of a pFast Plasmid-based Expression Vector for Expression and Purification of Human Blood Coagulation Factor VIII, the Causative Agent of Hemophilia A 

      Dornbush, Eliza (2011-01-01)
      Hemophilia A is an X-linked recessive genetic disorder caused by mutations in the gene coding for the Factor VIII (F8). Since the F8 protein is a vital component of the blood coagulation cascade, mutations in the F8 gene ...
    • Construction of a pFast Plasmid-based Expression Vector for Expression and Purification of Human Blood Coagulation Factor VIII, the Causative Agent of Hemophilia A 

      Minich, Hillary (2011-01-01)
      Hemophilia A is an X-linked recessive genetic disorder caused by mutations in the gene coding for the Factor VIII (F8). Since the F8 protein is a vital component of the blood coagulation cascade, mutations in the F8 gene ...

    Browse

    All of Oxy ScholarCommunities & CollectionsBy Issue DateAuthorsTitlesSubjectsJournal TitleJournal IssueThis CollectionBy Issue DateAuthorsTitlesSubjectsJournal TitleJournal Issue

    My Account

    LoginRegister

    DSpace software copyright © 2002-2021  DuraSpace
    Contact Us | Send Feedback
    DSpace Express is a service operated by 
    Atmire NV