What are the critical issues arising from the SADC trade integration process?

This policy brief is a shortened version of the following paper: Overview of Trade Relations in SADC: Some Empirical Observations by Paul Kalenga

Regional Trade Integration in Southern Africa: Critical Policy Issues

The aim of this paper is to highlight key issues arising from regional trade integration in the Southern African Development Community (SADC) as well as the concomitant policies required to facilitate the trade process. The paper highlights issues pertaining to distribution effects arising from integrating unequal partners and the need for open trade policies in order to realise potential positive spillovers

What are the major trends and determinants of foreign direct investment in SADC countries?

This policy brief is a shortened version of the following paper: Foreign Direct Investment in Sub-Saharan Africa by Paul Kalenga

Regional Trade Integration in Southern Africa: Critical Policy Issues

The aim of this paper is to highlight key issues arising from regional trade integration in the Southern African Development Community (SADC) as well as the concomitant policies required to facilitate the trade process. The paper highlights issues pertaining to distribution effects arising from integrating unequal partners and the need for open trade policies in order to realise potential positive spillovers. The main policy issues discussed are competition policies, standards and related technical regulations, rules of origin, macroeconomic policies, fiscal revenue implications, industrial strategies and the need for an appropriate institutional framework.South Africa: regional trade integration, distribution effects

Intrafamilial phenotype variability in nephrogenic diabetes insipidus.

X-Linked nephrogenic diabetes insipidus (NDI), which accounts for 90% of inherited cases of NDI, is caused by mutations in the AVPR2 gene that encodes the arginine vasopressin (AVP) receptor type 2 (V2R). The V2R mediates the antidiuretic action of AVP in principal cells of the collecting duct. To date, only three AVPR2 mutations (P322S, D85N, and G201D) have been associated with a mild NDI phenotype, and intrafamilial phenotype variability has not been reported in affected males. We describe a novel Belgian family with X-linked NDI caused by substitution of a histidine for an arginine at position 137 (R137H) of AVPR2. This mutation has been identified in two brothers and their mother. The R137H mutation results in a failure of V2R to stimulate adenylate cyclase and has been associated consistently with severe NDI and the inability to increase urinary osmolality to greater than plasma osmolality during water deprivation and/or infusion of 1-desamino-8-d-arginine vasopressin. Detailed examination of the two affected brothers showed the typical NDI phenotype in the 45-year-old proband, whereas a milder clinical phenotype associated with significant urinary concentrating ability during water deprivation was documented in the 33-year-old brother. Thus, in this family, the R137H mutation is associated with either a mild or severe NDI phenotype. Mechanisms that might account for these findings include genetic and/or environmental modifiers

Sequence Diversity of Tp1 and Tp2 Antigens and Population Genetic Analysis of Theileria parva in Unvaccinated Cattle in Zambia’s Chongwe and Chisamba Districts

East Coast Fever (ECF), caused by Theileria parva, is a major constraint to improved livestock keeping in east and central Africa, including Zambia. To understand the dynamics and determine the candidates for immunization in Zambia’s Chongwe and Chisamba districts, a combination of Tp1 and Tp2 gene sequencing and microsatellite analysis using nine markers was conducted from which an abundance of Muguga, Kiambu, Serengeti and Katete epitopes in the field samples was obtained. Phylogenetic analysis showed six (Tp1) and three (Tp2) clusters with an absence of geographical origin clustering. The majority of haplotypes were related to Muguga, Kiambu, Serengeti and Katete, and only a few were related to Chitongo. Both antigens showed purifying selection with an absence of positive selection sites. Furthermore, low to moderate genetic differentiation was observed among and within the populations, and when vaccine stocks were compared with field samples, Chongwe samples showed more similarity to Katete and less to Chitongo, while Chisamba samples showed similarity to both Katete and Chitongo and not to Muguga, Kiambu or Serengeti. We conclude that the use of Katete stock for immunization trials in both Chongwe and Chisamba districts might produce desirable protection against ECF