The neurotransmitter(s) that generate the inhibitory junctional potential (IJP) in the circular muscle of hamster distal colon and their mechanisms have not been elucidated. The aim of the present study, therefore, was to determine the contributing roles of the non-adrenergic, non-cholinergic (NANC) inhibitory transmitter(s) including nitric oxide (NO), adenosine 5′-triphosphate (ATP) and vasoactive intestinal polypeptide (VIP) in the generation of IJP in the hamster distal colon. For this purpose, the effects of the corresponding blockers of these putative NANC inhibitory mediators have been investigated using microelectrode technique. arabic 8 English 62
M. Draid(12-2006)

The coronavirus disease (COVID-19) pandemic has posed serious health and economic threats, particularly in developing countries. The presentation of the disease is highly variable and could be easily confused with other respiratory tract infections.1 In Africa, tuberculosis (TB) is one of the top causes of mortality and has a presentation conspicuously similar to the current severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. During the past coronavirus epidemics like SARS and Middle East respiratory syndrome-related coronavirus (MERSCoV), co-infections with TB had posed a major threat to the spread of the disease. Hence, the association between COVID-19 and TB cannot be ruled out, and more evidence should be gathered to increase our understanding of the dynamics of both diseases during the spread of the pandemic.2 Therefore, it is important to understand the distribution and aggregation degree of TB and COVID-19 and to follow up the spatial trends of both of them during the pandemic period. In this study, we aimed to analyze the spatiotemporal variation and the trends of TB and COVID-19 during the pandemic at the national and regional levels. This will provide more information and thus help implement proper strategies to combat the burden of the pandemic
Daw MA, Ahmed MO, ET AL.(11-2020)

Background Disruption of 11p15 imprinting results in two fetal growth disorders with opposite phenotypes: the Beckwith–Wiedemann (BWS; MIM 130650) and the Silver–Russell (SRS; MIM 180860) syndromes. DNA methylation defects account for 60% of BWS and SRS cases and, in most cases, occur without any identified mutation in a cis-acting regulatory sequence or a trans-acting factor. Methods We investigated whether 11p15 cis-acting sequence variants account for primary DNA methylation defects in patients with SRS and BWS with loss of DNA methylation at ICR1 and ICR2, respectively. Results We identified a 4.5 kb haplotype that, upon maternal transmission, is associated with a risk of ICR2 loss of DNA methylation in patients with BWS. This novel region is located within the second intron of the KCNQ1 gene, 170 kb upstream of the ICR2 imprinting centre and encompasses two CTCF binding sites. We showed that, within the 4.5 kb region, two SNPs (rs11823023 and rs179436) affect CTCF occupancy at DNA motifs flanking the CTCF 20 bp core motif. Conclusions This study shows that genetic variants confer a risk of DNA methylation defect with a parent-of-origin effect and highlights the crucial role of CTCF for the regulation of genomic imprinting of the CDKN1C/KCNQ1 domain. arabic 26 English 132
Julie Demars, Mansur Ennuri Moftah Shmela, Abdul Waheed Khan , Kai Syin Lee, Salah Azzi, Patrice Dehais, Irène Netchine, Sylvie Rossignol, Yves Le Bouc, Assam El-Osta, Christine Gicquel(7-2014)