Hematopoietic changes in NMRI mice after the intravenous and subcutaneous injection ofBordetella pertussis vaccine

1972 ◽  
Vol 28 (12) ◽  
pp. 1484-1486
Author(s):  
H. Finger ◽  
P. Emmerling ◽  
L. Plager
Keyword(s):  
Pertussis Vaccine ◽  
Subcutaneous Injection ◽  
Nmri Mice ◽  
Ofbordetella Pertussis

Ability ofBordetella pertussis vaccine to induce delayed-type hypersensitivity to DNA

1981 ◽  
Vol 92 (3) ◽  
pp. 1226-1228
Author(s):  
E. P. Moskalenko ◽  
S. I. Il'ina ◽  
V. V. Plavan ◽  
A. M. Poverennyi
Keyword(s):  
Pertussis Vaccine ◽  
Delayed Type Hypersensitivity ◽  
Ofbordetella Pertussis

Very Early Pertussis Vaccine Confers Protection

2007 ◽  
Vol 41 (10) ◽  
pp. 14
Author(s):  
PATRICE WENDLING
Keyword(s):  
Pertussis Vaccine

Pertussis Vaccine Urged for All Health Workers

2011 ◽  
Vol 10 (4) ◽  
pp. 48
Author(s):  
MIRIAM E. TUCKER
Keyword(s):  
Pertussis Vaccine ◽  
Health Workers

ACIP: Pertussis Vaccine For Adults 65 and Older

2012 ◽  
Vol 42 (4) ◽  
pp. 2
Author(s):  
MIRIAM E. TUCKER
Keyword(s):  
Pertussis Vaccine

A SUBCUTANEOUS INJECTION ASSAY FOR ANTI-ANDROGENS IN THE CHICK

1962 ◽  
Vol 41 (2) ◽  
pp. 268-273 ◽  
Author(s):  
Ralph I. Dorfman
Keyword(s):  
Dose Response ◽  
Subcutaneous Injection ◽  
Response Relationship ◽  
Dose Response Relationship

ABSTRACT The stimulating action of testosterone on the chick's comb can be inhibited by the subcutaneous injection of 0.1 mg of norethisterone or Ro 2-7239 (2-acetyl-7-oxo-1,2,3,4,4a,4b,5,6,7,9,10,10a-dodecahydrophenanthrene), 0.5 mg of cortisol or progesterone, and by 4.5 mg of Mer-25 (1-(p-2-diethylaminoethoxyphenyl)-1-phenyl-2-p-methoxyphenyl ethanol). No dose response relationship could be established. Norethisterone was the most active anti-androgen by this test.

THE THYMOLYTIC ACTIVITY OF 6- AND 9-HALOCORTICOIDS AND RELATED STEROIDS

1965 ◽  
Vol 49 (2) ◽  
pp. 262-270 ◽  
Author(s):  
Ralph I. Dorfman ◽  
P. G. Holton ◽  
Fred A. Kind
Keyword(s):  
Double Bond ◽  
Subcutaneous Injection ◽  
Fluocinolone Acetonide ◽  
Relative Potency ◽  
Subcutaneous Route ◽  
Adrenalectomized Rats

ABSTRACT Adrenalectomized rats were used for the determination of the relative potency of various 6- and 9-halo substituted corticoids administered subcutaneously or by gavage using thymus weightas the endpoint. By subcutaneous injection, fluocinolone acetonide was the most active corticoid at 700 times that of cortisol. This compound was also the most active corticoid by the gavage route and was judged to be 570 times as active as the standard cortisol. The introduction of the 16,17-acetonide and 16,17-acetone 21-acetate groups into 17α,21-dihydroxy-9α,11β-dichloropregna-1,4-diene-3,20-dione increased the activity by a factor of 42 and 100, respectively. The introduction of the δ1 double bond into 6α-fluoroprogesterone 16,17-acetonide caused an increase of 10-fold in thymolytic activity assessed by the subcutaneous route

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