Zobrazeno 1 - 10
of 224
pro vyhledávání: '"Nathenson, S. G."'
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 1978 Jun 01. 75(6), 2909-2913.
Externí odkaz:
https://www.jstor.org/stable/68354
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 1978 Jul 01. 75(7), 3390-3394.
Externí odkaz:
https://www.jstor.org/stable/68239
Autor:
Pontarotti, P. A., Mashimo, H., Zeff, R. A., Fisher, D. A., Hood, L., Mellor, A., Flavell, R. A., Nathenson, S. G.
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 1986 Mar . 83(6), 1782-1786.
Externí odkaz:
https://www.jstor.org/stable/26877
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 1974 Mar 01. 71(3), 648-652.
Externí odkaz:
https://www.jstor.org/stable/63698
Autor:
Serreze, David V., Johnson, Ellis A., Chapman, Harold D., Graser, Robert T., Marron, Michele P., DiLorenzo, Teresa P., Silveira, Pablo, Yoshimura, Yoshitaka, Nathenson, Stanley G., Joyce, Sebastian, Serreze, D V, Johnson, E A, Chapman, H D, Graser, R T, Marron, M P, DiLorenzo, T P, Silveira, P, Yoshimura, Y, Nathenson, S G, Joyce, S
Publikováno v:
Diabetes; Sep2001, Vol. 50 Issue 9, p1992-2000, 9p, 4 Charts, 6 Graphs
Publikováno v:
Annual Review of Biochemistry; Jul1981, Vol. 50 Issue 1, p1025-1052, 28p
Publikováno v:
Annual Review of Genetics; 1980, Vol. 14, p241-277, 37p
Publikováno v:
Annual Review of Immunology; Apr1986, Vol. 4 Issue 1, p471-502, 32p
Publikováno v:
Scopus-Elsevier
We have taken the approach of producing somatic cell variants with altered H-2 products to study the structural requirements for cell surface expression of class I histocompatibility molecules. H-2 antigen variants generated by chemical mutagenesis o
Autor:
Geliebter, J, Nathenson, S G
Publikováno v:
Molecular and Cellular Biology. 8:4342-4352
The mechanism that generates spontaneous mutants of the Kb histocompatibility gene was analyzed. Nucleotide sequence analysis of four mutant genes (Kbm3, Kbm4, Kbm10, and Kbm11) revealed that each mutant K gene contains clustered, multiple nucleotide