English (United Kingdom)

https://curated-unify.zendy.io/wp-json/zendy-region/v1/featured_content/oa?rat=en

https://curated-unify.zendy.io/wp-json/zendy-region/v1/highlighted_journal/

Global: Zendy Plus annual

Presents the access of premium content as premium feature

Premium Content

Presents the keyphrase highlighting as premium feature

Keyphrase Highlighting

Presents the summarisation as premium feature

Summarisation

Insights

Presents the pdf analysis as premium feature

PDF Analysis

Presents the zaia usage as premium feature

ZAIA

Global: Zendy Tools annual

Global: Zendy Free Plan

Global: Zendy Tools monthly

Global: Zendy Plus monthly

described by Naresh seems to be robust and correlation with plasmid control is also very good. The authors have chosen three areas, i.e. surface antigen, core and X region of HBV genome sequences, for amplifications. Presence of all three nucleotide sequences in the sample will make infection very likely. Infection of hepatitis B virus transmitted through blood and blood products is an important preventable complication.[2] In India, NAT testing has not been made compulsory in all blood banks as yet, but the data that have been emerging from some of the blood banks[3,4] clearly show Hepatitis B virus to be responsible for majority of seronegative but nucleic acid positive samples when Hepatitis B, Hepatitis C and HIV infections were tested from voluntary blood donors. Hepatitis C is also an important cause of transfusion transmitted liver infections in multi transformed hemophiliacs[5] and thalasseamic patients,[6] accounting for about 18–34% positivity in these patients.

Quantitation of HBV DNA; another modification of the test: Will it withstand the test of time?