Zobrazeno 1 - 10
of 192
pro vyhledávání: '"Kuntz, I. D."'
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 1999 Aug . 96(18), 9997-10002.
Externí odkaz:
https://www.jstor.org/stable/48682
Autor:
DesJarlais, R. L., Seibel, G. L., Kuntz, I. D., Furth, P. S., Alvarez, J. C., DeCamp, D. L., Babé, L. M., Craik, C. S.
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 1990 Sep 01. 87(17), 6644-6648.
Externí odkaz:
https://www.jstor.org/stable/2355356
Publikováno v:
Science, 1986 Oct . 234(4774), 349-352.
Externí odkaz:
https://www.jstor.org/stable/1697767
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 1964 Mar . 51(3), 515-520.
Externí odkaz:
https://www.jstor.org/stable/72024
Publikováno v:
Science, 1969 Mar . 163(3873), 1329-1331.
Externí odkaz:
https://www.jstor.org/stable/1726393
Autor:
Ye, S M, Huang, Y D, Mullendorff, K, Dong, L M, Giedt, G, Meng, E C, Cohen, F E, Kuntz, I D, Weisgraber, Karl H, Mahley, R W
Publikováno v:
Ye, S M; Huang, Y D; Mullendorff, K; Dong, L M; Giedt, G; Meng, E C; et al.(2005). Apolipoprotein (apo) E4 enhances amyloid beta peptide production in cultured neuronal cells: ApoE structure as a potential therapeutic target. Proceedings of the National Academy of Sciences of the United States of America, 102(51), 18700-18705. UC San Francisco: Retrieved from: http://www.escholarship.org/uc/item/2tq6k7v4
Apolipoprotein (apo) E4 is a major risk factor for Alzheimer's disease, and many studies have suggested that apoE has isoform-specific effects on the deposition or clearance of amyloid beta (A beta) peptides. We examined the effects of apoE isoforms
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::331d595a6a0334f411e08b5d6f40559b
http://www.escholarship.org/uc/item/2tq6k7v4
http://www.escholarship.org/uc/item/2tq6k7v4
Autor:
Hurle, M. R., Eads, C. D., Pearlman, D. A., Seibel, G. L., Thomason, J., Kosen, P. A., Kollman, P., Anderson, S., Kuntz, I. D.
Structural perturbations due to a series of mutations at the 30-51 disulfide bond of bovine pancreatic trypsin inhibitor have been explored using NMR. The mutants replaced cysteines at positions 30 and 51 by alanine at position 51 and alanine, threon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a928eed46fc93a4e3e7363b41f3bdb49
https://europepmc.org/articles/PMC2142081/
https://europepmc.org/articles/PMC2142081/
Autor:
Oshiro, C. M., Kuntz, I. D.
Publikováno v:
Biopolymers; Jan1993, Vol. 33 Issue 1, p107-115, 9p
Publikováno v:
Biopolymers; Aug1991, Vol. 31 Issue 9, p1049-1064, 16p
Publikováno v:
Biopolymers; Jun1987, Vol. 26 Issue 6, p777-793, 17p