Zobrazeno 1 - 10
of 181
pro vyhledávání: '"Patricia Tippett"'
Publikováno v:
Acta Pathologica Microbiologica Scandinavica. 54:287-290
Publikováno v:
Biographical Memoirs of Fellows of the Royal Society. 49:461-473
Ruth Ann Sanger's scientific career was concerned with the delineation and mapping of human blood group genes by simple manual methods using, as tools, blood group antibodies and the agglutination reaction followed by statistical analysis of the resu
Publikováno v:
Immunohematology. 12:4-7
The blood group antigens Ch and Rg are polymorphisms of C4d. Antigen-positive red blood cells (RBCs) treated with proteases type as Ch-, Rg-. Although RBCs treated with sialidase may type Ch+ Rg+, they cannot be coated with C4 by the 10 percent sucro
Publikováno v:
Immunohematology. 12:154-159
Initial Rh phenotyping of a man with hemolytic anemia, his wife, and son appeared to exclude paternity. No exclusion was found in other blood groups or in the human leukocyte antigen (HLA) system; excluding Rh, the paternity index was 98.58 percent.
Autor:
Patricia Tippett, A. C. Petty
Publikováno v:
Vox Sanguinis. 69:231-235
The biochemical relationship between the red cell antigens Xg a and the MIC2 gene product, CD99 - previously designated the 12E7 antigen - has been examined by immunoblotting and immunoprecipitation analyses of the protein molecules bearing these ant
Autor:
Patricia Tippett
Publikováno v:
Immunological Investigations. 24:173-186
Blood group antigens have provided tools for investigation of the red cell surface and been very useful as genetic markers in family, population and forensic studies. Precise definition of phenotypes is very important. Application of MAIEA (monoclona
Autor:
Alison C. Petty, Patricia Tippett
Publikováno v:
Vox Sanguinis. 69:231-235
Autor:
Polly A. Weller, Nathan A. Ellis, James German, Tian Z. Ye, Peter N. Goodfellow, Patricia Tippett, Stephen G. Thomas, A. C. Petty, George Banting, Marion E. Reid
Publikováno v:
Nature Genetics. 8:285-290
We have identified the Xga antigen, encoded by the XG blood group gene, by employing rabbit polyclonal and mouse monoclonal antibodies raised against a peptide derived from the N-terminal domain of a candidate gene, referred to earlier as PBDX. In in