Absence of mutations in the HBsAg “a” determinant during REP 2139 therapy validates serum HBsAg reductions observed in the REP 102 protocol
Sign Up to like & getrecommendations! Published in 2017 at "Journal of Hepatology"
DOI: 10.1016/s0168-8278(17)30822-x
Abstract: CONTACT INFORMATION Mahtab et al., 2016. Safety and Efficacy of Nucleic Acid Polymers in Monotherapy and Combined with Immunotherapy in Treatment-Naïve Bangladeshi Patients with HBeAg+ Chronic Hepatitis B Infection. PLOS ONE 2016; 11: e156667 Martin… read more here.
Keywords: determinant rep; absence mutations; hbsag determinant; 2139 therapy ... See more keywords
Cystinuria in a 13-Month-Old Girl with Absence of Mutations in the SLC3A1 and SLC7A9 Genes
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DOI: 10.4103/ijn.ijn_46_18
Abstract: First, it is obvious that two major genes responsible for cystinuria have been identified: SLC3A1 (chromosome 2p21) encodes the heavy subunit rBAT of a renal b (0, +) transporter while SLC7A9 (chromosome 19q12) encodes its… read more here.
Keywords: absence mutations; month old; patients cystinuria; cystinuria month ... See more keywords