W Ealding
Overview
Explore the profile of W Ealding including associated specialties, affiliations and a list of published articles.
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Articles
8
Citations
328
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0
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Recent Articles
1.
Woogen S, Ealding W, Elson C
J Immunol
. 1987 Dec;
139(11):3764-70.
PMID: 2824614
Cholera toxin is known to inhibit lymphocyte activation in vitro, an effect attributed to its ability to activate adenylate cyclase and increase intracellular cyclic adenosine monophosphate. In these studies the...
2.
Elson C, Ealding W
Eur J Immunol
. 1987 Mar;
17(3):425-8.
PMID: 3106062
In these experiments we examined the genetic control of the secretory IgA (sIgA) response to cholera toxin (CT) after CT feeding. Inbred, congenic and intra-H-2I region recombinant mouse strains were...
3.
Elson C, Woogen S, Gaspari M, Ealding W
Adv Exp Med Biol
. 1987 Jan;
216B:877-85.
PMID: 2892359
No abstract available.
4.
Elson C, Ealding W
J Immunol
. 1985 Aug;
135(2):930-2.
PMID: 3925014
This study was undertaken to determine whether previously noted differences in the immune response of inbred strains of mice to cholera toxin (CT) might be under immune response gene control....
5.
Elson C, Ealding W
J Immunol
. 1984 Dec;
133(6):2892-7.
PMID: 6491278
The feeding of protein antigens to mice results in a state of tolerance when feeding is followed by parenteral immunization. Cholera toxin (CT) is a protein that has been used...
6.
Elson C, Ealding W
J Immunol
. 1984 Jun;
132(6):2736-41.
PMID: 6233359
Cholera toxin (CT) has been found to be an extremely potent immunogen for mucosal IgA responses when administered via the intestine. This study has examined both mucosal and systemic immune...
7.
Elson C, Ealding W, Lefkowitz J
J Immunol Methods
. 1984 Feb;
67(1):101-8.
PMID: 6366063
Mouse intestinal secretions can be readily obtained without harm to the mice by administering a lavage solution to them intragastrically followed by pilocarpine intraperitoneally. These secretions are rich in proteases...
8.
Elson C, Weiserbs D, Ealding W, Machelski E
Ann N Y Acad Sci
. 1983 Jun;
409:230-7.
PMID: 6223564
No abstract available.