Asian Science Citation Index is committed to provide an authoritative, trusted and significant information by the coverage of the most important and influential journals to meet the needs of the global scientific community.  
ASCI Database
308-Lasani Town,
Sargodha Road,
Faisalabad, Pakistan
Fax: +92-41-8815544
Contact Via Web
Suggest a Journal
 
Articles by M. Yu
Total Records ( 2 ) for M. Yu
  H.H. Zhang , M. Yu , G.Y. Li , T.T. Zhang , K.Y. Wang , J.B. Zhao and F.H. Yang
  The objective of this study was to examine whether growth performance, nutrient digestion and N-balance of growing minks were affected by different dietary protein levels from good protein feed resource. Eighty young male minks were allotted to five treatment groups (P36, P32, P28, P24 and P20) provided with diets containing approximately 36, 32, 28, 24 and 20% protein in Dry Matter (DM), respectively. From July to middle September the Body Weight (BW) was lower in group P20 than other groups (p<0.05). No significant difference of dietary protein on minks’ BW and average daily gain (ADG) between groups P36 and P32 (p>0.05). The performance and digestibility of DM, Crude Protein (CP) and Crude Fat (CF) were similar when the dietary protein level decreased from P36 to P32 (p>0.05). N intake, urinary N excretion and Blood Urinary Nitrogen (BUN) increased linearly with increasing dietary protein level (p<0.05). No significant difference was found of serum Total Protein (TP) among all groups (p>0.05). Considering of all the factors, when minks fed good protein resource the level of dietary protein should be about 32% of DM (29.78% of ME) of diet could meet the requirement of growing minks. Furthermore, the urinary N could decrease 6.06% in growing period of minks.
  M. Yu , Z.Y. Ning , Z.X. Cao , R.S. Li , C.L. Huang and G.H. Zhang
  In the present study, researchers describe a rescue system for duck hepatitis virus-1 using T7 RNA polymerase. This strain can not induce typical cytopathic effect in BHK-21 cells. First, there is used the vitro transcripts to infect BHK-21 cells. Then the infected cell supernatant were inoculated into chicken embryos to rescue the virus and the cDNA clone was engineered to contain one silent nucleotide change to create a BssHII site to distinguish from the parental virus. The rescued virus was able to result in embryonic death and have similar infection with parental virus in chicken embryos indicating that the cDNA clones were replication competent. It is proposed that this rescue system may benefit the investigation on viral virulence determinants and molecular virology of DHV-1 virus.
 
 
 
Copyright   |   Desclaimer   |    Privacy Policy   |   Browsers   |   Accessibility