Ction (in both LTP and LTD) that may be linked to the behavioral defects displayed in fmr1 KO fish. Thus, this study suggests that zebrafish is valuable as a potential complementary vertebrate model for the study of the molecular pathogenesis of human fragile X syndrome.AcknowledgmentsFor providing the zebrafish knockout alleles-fmr1hu2787- we thank the Hubrecht laboratory and the Sanger CB-5083 chemical information Institute Zebrafish Mutation Resource (ZF-MODELS Integrated Project; contract number LSHGCT-2003-503496). We also thank Dr. Rob Willemsen for the kind gift of zebrafish FMR-1 antibody.Author ContributionsConceived and designed the experiments: YLY KTL. Performed the experiments: MCN. Analyzed the data: MCN. Contributed reagents/ materials/analysis tools: MCN. Wrote the paper: MCN YLY KTL.Behavior Synapse Features in Fragile X Syndrome
Co-infection with Hepatitis C (HCV) and HIV is common, and HIV accelerates hepatic disease progression due to HCV [1]. As a result, HCV has 
become a leading cause of death of people living with HIV in Western settings [2]. Successful HDAC-IN-3 treatment of HCV can improve hepatic fibrosis, reduce incidence of hepatocellular carcinoma, reduce mortality [3,4], and has the potential to reduce disease transmission [5]. However, a number of factors contribute to the limited access to treatment for most of those infected globally: a long duration of therapy with a relatively complex system of treatment delivery, high drug costs, high toxicity of treatment and, perhaps most importantly, relatively poor success rates for HCV treatment in HIV/HCV co-infection. A recent systematic review of clinical trials assessing HCV treatment outcomes in HIV co-infected patients reported that around 37 of patients achieve a sustained virological response(SVR) with pegylated interferon and ribavarin, with a lower success rate observed in patients infected with HCV genotypes 1 and 4 [6]. These outcomes are poorer than those seen in HIV negative patients [7]. Although clinical trials are appropriate for determining drug efficacy, outcomes may differ under programmatic conditions where adherence to treatment, patient and provider motivation and available resources may be limited [8]. We conducted a systematic review to assess the outcomes of HCV treatment in HIV co-infected patients in programmatic settings.Methods Search Strategy and Study SelectionOur systematic review was conducted in accordance with the criteria of the Preferred Reporting Items for Systematic Reviews and Meta-Analyses group [9]. Using 
a pre-defined protocol (File S1) Medline and EMBASE were systematically searched fromOutcomes of Patients Co-Infected with HCV and HIVinception to 05 May, 2012 using a compound search strategy. The initial title screen was conducted by one of us (AD) with full text articles reviewed in duplicate (AD, NF). The bibliographies of relevant articles were also hand searched for potentially relevant articles. Agreement on inclusion of final articles was made through consensus by the same reviewers. No language or geographical restriction was applied during the search, but only English language publications were included in the final review. All cohort studies that reported treatment outcomes for in HIVpositive patients chronically infected with HCV and initiating HCV treatment for the first time were reviewed. Studies were excluded if they reported outcomes among patients with selected co-morbidities other than HIV, such as haemophilic or transplant patients, and.Ction (in both LTP and LTD) that may be linked to the behavioral defects displayed in fmr1 KO fish. Thus, this study suggests that zebrafish is valuable as a potential complementary vertebrate model for the study of the molecular pathogenesis of human fragile X syndrome.AcknowledgmentsFor providing the zebrafish knockout alleles-fmr1hu2787- we thank the Hubrecht laboratory and the Sanger Institute Zebrafish Mutation Resource (ZF-MODELS Integrated Project; contract number LSHGCT-2003-503496). We also thank Dr. Rob Willemsen for the kind gift of zebrafish FMR-1 antibody.Author ContributionsConceived and designed the experiments: YLY KTL. Performed the experiments: MCN. Analyzed the data: MCN. Contributed reagents/ materials/analysis tools: MCN. Wrote the paper: MCN YLY KTL.Behavior Synapse Features in Fragile X Syndrome
Co-infection with Hepatitis C (HCV) and HIV is common, and HIV accelerates hepatic disease progression due to HCV [1]. As a result, HCV has become a leading cause of death of people living with HIV in Western settings [2]. Successful treatment of HCV can improve hepatic fibrosis, reduce incidence of hepatocellular carcinoma, reduce mortality [3,4], and has the potential to reduce disease transmission [5]. However, a number of factors contribute to the limited access to treatment for most of those infected globally: a long duration of therapy with a relatively complex system of treatment delivery, high drug costs, high toxicity of treatment and, perhaps most importantly, relatively poor success rates for HCV treatment in HIV/HCV co-infection. A recent systematic review of clinical trials assessing HCV treatment outcomes in HIV co-infected patients reported that around 37 of patients achieve a sustained virological response(SVR) with pegylated interferon and ribavarin, with a lower success rate observed in patients infected with HCV genotypes 1 and 4 [6]. These outcomes are poorer than those seen in HIV negative patients [7]. Although clinical trials are appropriate for determining drug efficacy, outcomes may differ under programmatic conditions where adherence to treatment, patient and provider motivation and available resources may be limited [8]. We conducted a systematic review to assess the outcomes of HCV treatment in HIV co-infected patients in programmatic settings.Methods Search Strategy and Study SelectionOur systematic review was conducted in accordance with the criteria of the Preferred Reporting Items for Systematic Reviews and Meta-Analyses group [9]. Using a pre-defined protocol (File S1) Medline and EMBASE were systematically searched fromOutcomes of Patients Co-Infected with HCV and HIVinception to 05 May, 2012 using a compound search strategy. The initial title screen was conducted by one of us (AD) with full text articles reviewed in duplicate (AD, NF). The bibliographies of relevant articles were also hand searched for potentially relevant articles. Agreement on inclusion of final articles was made through consensus by the same reviewers. No language or geographical restriction was applied during the search, but only English language publications were included in the final review. All cohort studies that reported treatment outcomes for in HIVpositive patients chronically infected with HCV and initiating HCV treatment for the first time were reviewed. Studies were excluded if they reported outcomes among patients with selected co-morbidities other than HIV, such as haemophilic or transplant patients, and.
