scholarly journals Seeking genes responsible for developmental origins of health and disease from the fetal mouse liver following maternal food restriction

2014 ◽  
pp. n/a-n/a ◽  
Author(s):  
Tetsuo Ogawa ◽  
Junko Shibato ◽  
Randeep Rakwal ◽  
Tomomi Saito ◽  
Gaku Tamura ◽  
...  





1983 ◽  
Vol 140 (1) ◽  
pp. 15-28 ◽  
Author(s):  
KOICHI HIRATA ◽  
KOJI SHIRAMATSU ◽  
TOMOAKI USUI ◽  
YUTAKA YOSHIDA ◽  
AARON E. FREEMAN ◽  
...  


1969 ◽  
Vol 17 (7) ◽  
pp. 454-466 ◽  
Author(s):  
EDWARD ESSNER

The peroxidase activity of microbodies in fetal mouse liver was studied by light and electron microscopy. Two types of microbodies were present; a small population of bodies that lacked a nucleoid, predominant on the 16th day of gestation, and a larger population of nucleoid-bearing microbodies, predominant on the 19th day, in association with the rough endoplasmic reticulum from which they probably originate. Both types of bodies were visualized when incubated for peroxidase activity but were negative (19th day) for acid phosphatase activity. The findings suggest that the anucleoid- and nucleoid-bearing organelles together constitute the microbody population of the fetal liver.



1982 ◽  
Vol 12 (2) ◽  
pp. 179-186 ◽  
Author(s):  
Takahiro Okamoto ◽  
Akihisa Kanamaru ◽  
Hiroshi Hara ◽  
Kiyoyasu Nagai


1990 ◽  
Vol 48 (1) ◽  
pp. 27-37 ◽  
Author(s):  
Makoto Naito ◽  
Kiyoshi Takahashi ◽  
Shin-lchi Nishikawa


1985 ◽  
Vol 61 (2) ◽  
pp. 293-302 ◽  
Author(s):  
Susumu Sakata ◽  
Yasunori Enoki ◽  
Susumu Tomita ◽  
Hisaharu Kohzuki


2004 ◽  
Vol 13 (3) ◽  
pp. 171
Author(s):  
Cheng-Hao Jin ◽  
Yoshikazu Yonemitsu ◽  
Shigeyuki Nagata ◽  
Ri-ichiro Kohno ◽  
Norifumi Tsutsumi ◽  
...  


1981 ◽  
Vol 88 (1) ◽  
pp. 79 ◽  
Author(s):  
M. R. Reddy ◽  
J. E. Fuhr


Blood ◽  
1980 ◽  
Vol 55 (6) ◽  
pp. 955-959
Author(s):  
G de Klerk ◽  
RJ Vet ◽  
PC Rosengarten ◽  
R Goudsmit

The commercially available hemagglutination inhibition (HAI) assay kit for erythropoietin (ESF) was compared with the fetal mouse liver cell (FMLC) bioassay. No correlation was obtained ESF levels determined by both methods in a variety of pathologic sera. The HAI kit showed a great batch variability. Significant immunoreactivity was found in those fractions of a normal human serum and a human urinary ESF preparation that were not active in the FMLC bioassay. A very poor recovery of immunoreactivity was found when the international reference preparation for erythropoietin (second IRPE) was added to a normal human serum.



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