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Qatar Foundation Annual Research Forum Volume 2010 Issue 1
- Conference date: 12-13 Dec 2010
- Location: Qatar National Convention Center (QNCC), Doha, Qatar
- Volume number: 2010
- Published: 13 December 2010
61 - 80 of 166 results
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Gender differences in body composition, inflammatory markers and risk of metabolic abnormalities in Arabs
Authors: Abdulaziz Farooq, Wade Knez, Asma Al Nuiami, Bengt Saltin, Vidya Mohamed-Ali and Justin GranthamAbstract Background: Metabolic syndrome may be a result of both increased and/or inappropriate fat accumulation. As a consequence of the obesity epidemic, which has particularly manifested amongst the populations of the Arabian Gulf, associated with increases in type 2 diabetes mellitus and cardiovascular diseases, metabolic syndrome is becoming an increasing problem. Recent studies from the Gulf region have Read More
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Novel poly (diol-co-tricarballylate) biodegradable elastomers. What makes them excellent carriers for controlled drug delivery and tissue engineering applications?
Authors: Husam Mohammed Younes and Mohamed ShakerAbstract In the past decade, biodegradable elastomeric polymers have gained considerable attention due to the renewed interest in their applications in the fields of biomedical tissue engineering and implantable drug delivery systems. Elastomers can be regarded as one of the best biomaterials for such applications because their mechanical properties can be manipulated in a manner that makes them as soft as bod Read More
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Factors influencing breast cancer screening practices among Arab women living in the State of Qatar
Abstract Breast cancer is frequently diagnosed in Arab women living in Qatar. Al Amal Hospital in Doha reported that 20% of cancer cases receiving treatment in 2007 involved the treatment of breast cancer among women. Early detection and treatment can reduce breast cancer morbidity and mortality rates significantly. However, Arab women are often diagnosed at advanced stages of breast cancer. Funded by the Qatar Natio Read More
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Screening for and cloning and molecular characterization of two new oligopeptidase B encoding genes
Authors: Fatma Baoumi Rashidi, Hatem El Shanti and Sayed GodaAbstract Oligopeptidase B (opdB, EC 3.4.21.83) is a member of the prolyl oligopeptidase family of serine peptidases and unrelated to the trypsin and subtilisin families. It is a potential processing enzyme of prokaryotes to produce biologically active products, being very specific for the basic amino acid pairs of polypeptides. Bacterial oligopeptidase B cleaves globular proteins, albeit in a highly restricted fashion. While most m Read More
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Potential role of inositol 1,4,5 - triphosphate receptors in the pathogenesis of hypertension
Authors: Abou Saleh Haissam, Shirley Haun, Nancy Rusch and Khaled MachacaAbstract Inositol 1,4,5-triphosphate receptors (IP3R) are tetrameric intracellular channels that mediate the release of Calcium (Ca2+) from sarcoplasmic reticulum (SR) into the cytosol in response to IP3 binding. Modulation of vascular smooth muscle cells (VSMC) contractility allows small arteries to regulate blood flow and determine peripheral vascular resistance and blood pressure levels. The level of contraction of VSMC Read More
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Molecular characterization and structure determination of human ADAMTSL4
Authors: Yasmin Walid Abu aqel, Abdulghani Kohilan, Hatem El Shanti and Sayed Kamel GodaAbstract The thrombospondin type 1 repeat (TSR) is an ancient extracellular protein domain that is commonly found in invertebrate and vertebrate proteins. The ADAMTSL4 protein, also known as TSRC1, belongs to the TSR superfamily and has multiple thrombospondin repeats, most of which are clustered at the C-terminus. It has been reported that some TSP1 domain-containing proteins, e.g. thrombospondin 1 and thrombos Read More
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The impact of interventions on HIV transmission among couples in sub-Saharan Africa
Authors: Hiam Chemaitelly and Laith Abu RaddadAbstract Background: In areas highly endemic with HIV, discordancy is prevalent among couples affected by HIV, where a substantial proportion of infected individuals are in stable sexual relationships with non-infected individuals. Designing a package of interventions to reduce HIV incidence among discordant partnerships is critical. We assessed quantitatively the impact of four interventions (antiretroviral therapy (ART), pre-e Read More
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Polymorphism in adiponectin receptor gene type 1 (ADIPOR1) in individuals with coronary artery disease with and without type 2 diabetes in the state of Qatar
More LessAbstract Background: Previous studies demonstrated polymorphisms of adiponectin receptor type1 (AdipoR1) as a strong determinant of coronary artery diseases (CAD) susceptibility in type 2 diabetes. The aim of the study is to investigate the associations of the genetic marker (SNP) no of AdipoR1 locus; rs10920531 with CAD in patients with and without type 2 diabetes in the population of Qatar. Methods: Blood was drawn f Read More
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The spectrum of Mediterranean fever (MEFV) mutations in an Arabic cohort
Abstract Autoinflammatory diseases are a group of disorders characterized by seemingly unprovoked inflammation in the absence of high-titer autoantibodies or antigen-specific T cells. Familial Mediterranean fever (FMF) is an autosomal recessive disorder and the archetypal autoinflammatory disease. It is characterized by recurrent self-limiting episodes of fever and painful polyserositis. FMF is prevalent in sp Read More
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Metal toxicity at the synapse: presynaptic, postsynaptic and long-term effects
Authors: Zena Basil Ghazala, Sanah Sadiq, Arnab Chowdhury and Dietrich BüsselbergAbstract Metal toxicity is a global health concern. We summarize the evidence for metal interactions with the nervous system with an emphasis on synaptic transmission. The appropriate functioning of synaptic transmission is crucial for the information transfer in any neural network. Presynaptically, metal ions modulate transmitter release through their interaction with neurotransmitter (NT) synthesis, fusion of synapti Read More
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Analysis of cortical development in Lis1-GFP mice
Authors: Khawla Fuad Ali and Anamaria SudarovAbstract The Lis1 gene encodes a non-catalytic sub-unit of the platelet-activating factor acetyl hydrolase enzyme (PAFAH1B1). Increased PAFAH1B1 dosage in humans causes mild brain structural abnormalities, moderate to severe developmental delay and failure to thrive. To investigate the effects of Lis1 over expression on cortical development, we analyzed the brains of Lis1-GFP mice with 30% over expression in the Lis1 g Read More
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Regulation of store-operated channels by endoplasmic reticulum chaperons
Authors: Mashael Al-Shafai, Abdelilah Arredouani, Hamid Mesaeli, Nasrin Mesaeli and Khaled MachacaAbstract Calreticulin is a conserved Ca2+ binding chaperone protein that is localized to the lumen of the endoplasmic reticulum (ER). The protein is implicated in many cellular functions such as the regulation of intracellular Ca2+ homeostasis, the regulation of gene expression, the folding of the newly synthesized proteins, cell adhesion, cancer and auto-immunity. The role of calreticulin in Ca2+ homeostasis regulation through Ca Read More
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Tumor associated mesenchymal stem cells protect ovarian cancer cells from hyperthermia through CXCL12
Authors: Fadwa Ali, Arash Rafii, Raphael Lis and C TouboulAbstract Hyperthermic intraperitoneal chemotherapy (HIPEC) has shown promise in the treatment of ovarian carcinosis. Despite its efficiency for the treatment of peritoneal carcinosis from digestive tract neoplasia, it has failed to demonstrate significant benefit in ovarian cancers. It is therefore essential to understand the mechanism underlying the resistance to HIPEC in ovarian cancers. Mesenchymal Stem Cells (MSC) Read More
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Initial investigation of ubiquitination pathway in mammalian meiosis
Authors: Amna Mohammed Al-Khuzaei and Paula CohenAbstract The Cohen's lab research focuses mainly on the regulation of mammalian meiosis in mouse models, which include several induced mutants that have helped in broadening our knowledge of meiotic recombination and the gametogenesis. The lab also studies several DNA mismatch repair (MMR) proteins and their subsequent effects on meiotic recombination. Thus, our research serves two major purposes; Read More
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Gene identification in Mendelian forms of familial epilepsy
Authors: Hala Mint El Moctar, Mohamed El Dow, Yasser Al Saraj, Jamil Alami and Hatem El ShantiAbstract Epilepsy encompasses a heterogeneous group of recurrent seizure disorders affecting 1% of the world's population. Idiopathic generalized epilepsy accounts for 40% of all epilepsy disorders. Genetic factors contribute significantly to the etiology of idiopathic generalized epilepsies. Complex non-Mendelian forms of familial epilepsies comprise the majority of idiopathic generalized epilepsies, where susceptibility gene Read More
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Role of mesenchymal stem cells in enhancing ovarian cancer metastasis
Authors: Hamda Al-Thawadi, Rafael Lis, C Touboul, C Raynaud and Arash RafiiAbstract Cancer accounts for the death of thousands of people each year and brings pain and suffering to thousands more. Among cancers that specifically affect women, ovarian cancer has the highest fatality rate as 7 out of 10 women die within 5 years of surgery. As highlighted in numerous recent publications, the role of the microenvironment in the development and progression of cancer is critical, albeit not entir Read More
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Enhanced EGFR expression and function in calreticulin deficient cells
Authors: Amit Abraham, Hanin Abou Ayash, Hala Omar, Hamid Massaeli and Nasrin MesaeliAbstract Introduction: Calreticulin is a multi-functioning protein located in the endoplasmic reticulum. Several functions have been attributed to calreticulin including lectin-like chaperoning, regulation of gene expression, cell adhesion, auto-immunity and calcium homeostasis. As an endoplasmic reticulum chaperone calreticulin regulates the maturation and folding of several trans-membrane proteins. We hypothesiz Read More
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Label-free intrinsic imaging capillary zone electrophoresis analysis to detect homocysteine from blood serum for the detection of genetic metabolic disorders in new-born babies in Qatar
More LessAbstract Over 14,000 babies are born in Qatar each year, and it is the State's intention to provide each with a health screen at birth for the timely diagnosis of inborn errors of metabolism. And since the population is characterized by a high consanguinity (estimates vary between 25–70%) from first-cousin marriages, congenital and genetic disorders are responsible for a major proportion of infant mortality, morbidity, and handic Read More
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Calreticulin mediated control of polycystin-2 expression
Authors: Amit Abraham, Emine Turgut-Neary, Hala Omar, Hamid Massaeli and Nasrin MesaeliAbstract Polycystin-2 or transient receptor potential polycystic 2 (TRPP2) is a membrane glycoprotein that is encoded for by the gene pkd-2, which accounts for ˜15% of autosomal dominant polycystic kidney disease. TRPP2 is an independent non selective cation channel localized to either the plasma membrane or the endoplasmic reticulum (ER) that is involved in diverse cellular functions including control of cell cycle, cell wall Read More
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A new 3-dimensional model for ovarian cancer based on amniotic membrane
More LessAbstract Epithelial ovarian carcinoma (EOC) is the sixth most common malignancy in women and the leading cause of death from gynecological cancer in the world. One of the main differences between ovarian cancers and other neoplasm is burden of local extension. Hence the majority of mortality in ovarian cancer is due to extensive peritoneal disease, with a high rate of mortality and an overall survival rate ranging from Read More
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