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Items: 4

1.
A Single Point Mutation in the Gene Encoding Gb3/CD77 Synthase Causes a Rare Inherited Polyagglutination Syndrome
Anna Suchanowska, Radoslaw Kaczmarek, Maria Duk, Jolanta Lukasiewicz, Dorota Smolarek, Edyta Majorczyk, Ewa Jaskiewicz, Anna Laskowska, Kazimiera Wasniowska, Magdalena Grodecka, Elwira Lisowska, Marcin Czerwinski
J Biol Chem. 2012 Nov 2; 287(45): 38220–38230. Published online 2012 Sep 10. doi: 10.1074/jbc.M112.408286
Correction in:
J Biol Chem. 2013 Jan 4; 288(1): 294.
PMCID:
PMC3488091
AbstractArticlePDF–1.8M
2.
A linkage and physical map of chromosome 22, and some applications to gene mapping.
C Julier, G M Lathrop, A Reghis, M F Szajnert, J M Lalouel, J C Kaplan
Am J Hum Genet. 1988 Feb; 42(2): 297–308.
PMCID:
PMC1715259
SummaryPage BrowsePDF–2.1M
3.
Abnormalities in the glycosphingolipid content of human Pk and p erythrocytes.
D M Marcus, M Naiki, S K Kundu
Proc Natl Acad Sci U S A. 1976 Sep; 73(9): 3263–3267. doi: 10.1073/pnas.73.9.3263
PMCID:
PMC431001
SummaryPage BrowsePDF–1.1M
4.
P-antigen-recognizing fimbriae from human uropathogenic Escherichia coli strains.
T K Korhonen, V Väisänen, H Saxén, H Hultberg, S B Svenson
Infect Immun. 1982 Jul; 37(1): 286–291. doi: 10.1128/iai.37.1.286-291.1982
PMCID:
PMC347525
SummaryPage BrowsePDF–1.1M

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