Vitelline duct cyst or double yolk sac.

1989 ◽  
Vol 8 (9) ◽  
pp. 523-526 ◽  
Author(s):  
M Barzilai ◽  
E A Lyons ◽  
C S Levi ◽  
D J Lindsay
Keyword(s):  
Yolk Sac ◽  
1982 ◽  
Vol 110 (17) ◽  
pp. 407-408 ◽  
Author(s):  
A. Basher ◽  
E. Appleby
Keyword(s):  

Radiology ◽  
1964 ◽  
Vol 82 (3) ◽  
pp. 476-477 ◽  
Author(s):  
Arch. W. Templeton ◽  
Emil Shebesta
Keyword(s):  

2017 ◽  
Vol 4 (22) ◽  
pp. 1291-1293
Author(s):  
Lokesh Reddy C ◽  
Sumana Rao R ◽  
Venkat Ram Reddy K ◽  
Satyanarayana Moorthy R ,(Brig) ◽  
Satyanarayana Moorthy ◽  
...  

2010 ◽  
Vol 16 (3) ◽  
pp. 129-131 ◽  
Author(s):  
R. Jones ◽  
R. K. W. Smith ◽  
E. Mitchell ◽  
J. C. Patterson-Kane
Keyword(s):  

Author(s):  
William P. Jollie

A technique has been developed for visualizing antibody against horseradish peroxidase (HRP) in rat visceral yolk sac, the placental membrane across which passive immunity previously has been shown to be transferred from mother to young just prior to birth. Female rats were immunized by injecting both hind foot pads with 1 mg HRP emulsified in complete Freund's adjuvant. They were given a booster of 0.5mg HRP in 0.1 ml normal saline i.v. after one week, then bred and autopsied at selected stages of pregnancy, viz., 12, 1 7 and 22 days post coitum, receiving a second booster, injected as above, five days before autopsy. Yolk sacs were removed surgically and fixed immediately in 2% paraformaldehye, 1% glutaraldehye in 0.1 M phosphate buffer with 0.01% CaCl2 at pH 7.4, room temperature, for 3 hr, rinsed 3X in 0.1 M phosphate buffer plus 5% sucrose, then exposed to 1 mg HRP in 1 ml 0.1 M phosphate buffer at pH 7.4 for 1 hr. They were refixed in aldehydes, as above, for 1 5 min (to assure binding of antigen-antibody complex). Following buffer washes, the tissues were incubated in 3 mg diaminobenzidine tetrahydrochloride and 0.01% H2O2 in 0.05 M Tris-HCl buffer for 30 min. After brief buffer washes, they were postfixed in 2% OsO4. in phosphate buffer at pH 7.4, 4°C for 2 hr, dehydrated through a graded series of ethanols, and embedded in Durcupan. Thin sections were observed and photographed without contrast-enhancement with heavy metals. Cytochemical reaction product marked the site of HRP (i.e., antigen) which, in turn, was present only where it was bound with anti-HRP antibody.


2017 ◽  
Vol 23 ◽  
pp. 214
Author(s):  
Mohammad El-Rifai ◽  
Issra Jamal ◽  
Gaurav Bhalla ◽  
Naveen Kakumanu ◽  
Saleh Aldasouqi

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