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532501 to 532600 most common queries
List represents a sample of symptoms, diseases, and other queries. Updated weekly.
Inflammatory responses induced by the filarial nematode Brugia malayi are mediated by lipopolysaccharide-like activity from endosymbiotic Wolbachia bacteria.
Alternatively activated macrophages induced by nematode infection inhibit proliferation via cell-to-cell contact.
A blueprint for success: integration of neglected tropical disease control programmes.
Specific cellular immune unresponsiveness in human filariasis.
The secretome of the filarial parasite, Brugia malayi: proteomic profile of adult excretory-secretory products.
Effect of yearly mass drug administration with diethylcarbamazine and albendazole on bancroftian filariasis in Egypt: a comprehensive assessment.
The Innovative Vector Control Consortium: improved control of mosquito-borne diseases.
Tetracycline therapy targets intracellular bacteria in the filarial nematode Litomosoides sigmodontis and results in filarial infertility.
Wolbachia bacterial endosymbionts of filarial nematodes.
Macrophages in chronic type 2 inflammation have a novel phenotype characterized by the abundant expression of Ym1 and Fizz1 that can be partly replicated in vitro.
Removal of regulatory T cell activity reverses hyporesponsiveness and leads to filarial parasite clearance in vivo.
Anopheles gambiae complex and disease transmission in Africa.
Alternative activation is an innate response to injury that requires CD4+ T cells to be sustained during chronic infection.
Local macrophage proliferation, rather than recruitment from the blood, is a signature of TH2 inflammation.
Draft genome of the filarial nematode parasite Brugia malayi.
Hepatic CB1 receptor is required for development of diet-induced steatosis, dyslipidemia, and insulin and leptin resistance in mice.
Expert panel on integrated guidelines for cardiovascular health and risk reduction in children and adolescents: summary report.
Mouse models for atherosclerosis and pharmaceutical modifiers.
Platelet CD36 links hyperlipidemia, oxidant stress and a prothrombotic phenotype.
Gene expression changes in foam cells and the role of chemokine receptor CCR7 during atherosclerosis regression in ApoE-deficient mice.
Feasibility of treating prehypertension with an angiotensin-receptor blocker.
2009 Canadian Cardiovascular Society/Canadian guidelines for the diagnosis and treatment of dyslipidemia and prevention of cardiovascular disease in the adult - 2009 recommendations.
Hepatic insulin resistance is sufficient to produce dyslipidemia and susceptibility to atherosclerosis.
ESC/EAS Guidelines for the management of dyslipidaemias: the Task Force for the management of dyslipidaemias of the European Society of Cardiology (ESC) and the European Atherosclerosis Society (EAS).
Functionally defective high-density lipoprotein: a new therapeutic target at the crossroads of dyslipidemia, inflammation, and atherosclerosis.
Effects of medical therapies on retinopathy progression in type 2 diabetes.
Lipid screening and cardiovascular health in childhood.
Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia.
Effects of rimonabant on metabolic risk factors in overweight patients with dyslipidemia.
Class of antiretroviral drugs and the risk of myocardial infarction.
Osama Abdallah Atta
Effects of long-term fenofibrate therapy on cardiovascular events in 9795 people with type 2 diabetes mellitus (the FIELD study): randomised controlled trial.
Dietary flour supplementation decreases post-menopausal hot flushes: effect of soy and wheat.
The mechanism of facial flushes in the carcinoid syndrome.
The nicotinic acid receptor GPR109A (HM74A or PUMA-G) as a new therapeutic target.
Paroxysmal extreme pain disorder (previously familial rectal pain syndrome).
Release of markedly increased quantities of prostaglandin D2 in vivo in humans following the administration of nicotinic acid.
Nicotinic acid-induced flushing is mediated by activation of epidermal langerhans cells.
Genetic polymorphisms of alcohol and aldehyde dehydrogenases and glutathione S-transferase M1 and drinking, smoking, and diet in Japanese men with esophageal squamous cell carcinoma.
Antagonism of the prostaglandin D2 receptor 1 suppresses nicotinic acid-induced vasodilation in mice and humans.
Nicotinic acid- and monomethyl fumarate-induced flushing involves GPR109A expressed by keratinocytes and COX-2-dependent prostanoid formation in mice.
Degrees of alcohol intoxication in 117 hospitalized cases.
Infliximab induction therapy for patients with severe plaque-type psoriasis: a randomized, double-blind, placebo-controlled trial.
Activation of G protein-coupled receptor 43 in adipocytes leads to inhibition of lipolysis and suppression of plasma free fatty acids.
Mechanism of action of niacin.
Release of vasoactive peptides in the extracerebral circulation of humans and the cat during activation of the trigeminovascular system.
The alcohol flushing response: an unrecognized risk factor for esophageal cancer from alcohol consumption.
beta-Arrestin1 mediates nicotinic acid-induced flushing, but not its antilipolytic effect, in mice.
Treatment of the malignant carcinoid syndrome. Evaluation of a long-acting somatostatin analogue.
Associations of ADH and ALDH2 gene variation with self report alcohol reactions, consumption and dependence: an integrated analysis.
Nicotinic acid: the broad-spectrum lipid drug. A 50th anniversary review.
Hot flashes: epidemiology and physiology.
Pathogenesis of cerebral white matter injury of prematurity.
Detection of 98% of DMD/BMD gene deletions by polymerase chain reaction.
A fetal systemic inflammatory response is followed by the spontaneous onset of preterm parturition.
The transcriptional control of hematopoiesis.
Review and meta-analysis of the epidemiology of congenital cytomegalovirus (CMV) infection.
Chorioamnionitis and early lung inflammation in infants in whom bronchopulmonary dysplasia develops.
Origins of chromosome translocations in childhood leukaemia.
Viral myocarditis. A review.
Behavioral and neural consequences of prenatal exposure to nicotine.
Prenatal stress, glucocorticoids and the programming of the brain.
The Danish National Birth Cohort--its background, structure and aim.
Neurobiology of periventricular leukomalacia in the premature infant.
The role of inflammation and infection in preterm birth.
Ineffective erythropoiesis in Stat5a(-/-)5b(-/-) mice due to decreased survival of early erythroblasts.
Bacteroides fragilis: a possible cause of acute diarrheal disease in newborn lambs.
The non-O157 shiga-toxigenic (verocytotoxigenic) Escherichia coli; under-rated pathogens.
A new class of anthelmintics effective against drug-resistant nematodes.
The exceptionally small size of the scrapie agent.
Mutations in the genes for oocyte-derived growth factors GDF9 and BMP15 are associated with both increased ovulation rate and sterility in Cambridge and Belclare sheep (Ovis aries).
The Rift Valley fever epizootic in Egypt 1977-78. 1. Description of the epizzotic and virological studies.
Ex vivo propagation of infectious sheep scrapie agent in heterologous epithelial cells expressing ovine prion protein.
Taxon K, a complex within the Burkholderia cepacia complex, comprises at least two novel species, Burkholderia contaminans sp. nov. and Burkholderia lata sp. nov.
Genetic diversity of Campylobacter jejuni isolates from farm animals and the farm environment.
Cryptosporidiosis in animals and humans.
The pathology and pathogenesis of paratuberculosis in ruminants and other species.
Large offspring syndrome in cattle and sheep.
Slow virus replication: the role of macrophages in the persistence and expression of visna viruses of sheep and goats.
Further observations on Escherichia coli enterotoxins with particular regard to those produced by atypical piglet strains and by calf and lamb strains: the transmissible nature of these enterotoxins and of a K antigen possessed by calf and lamb strains.
A summary of mutations in the UV-sensitive disorders: xeroderma pigmentosum, Cockayne syndrome, and trichothiodystrophy.
The hairless gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor.
Bone morphogenetic proteins and their antagonists in skin and hair follicle biology.
A mouse model for the basal transcription/DNA repair syndrome trichothiodystrophy.
Xeroderma pigmentosum and trichothiodystrophy are associated with different mutations in the XPD (ERCC2) repair/transcription gene.
Human keratin diseases: the increasing spectrum of disease and subtlety of the phenotype-genotype correlation.
Coordinated activation of Wnt in epithelial and melanocyte stem cells initiates pigmented hair regeneration.
Mutations in the XPD helicase gene result in XP and TTD phenotypes, preventing interaction between XPD and the p44 subunit of TFIIH.
Squamous cell carcinomas and increased apoptosis in skin with inhibited Rel/nuclear factor-kappaB signaling.
Basal transcription defect discriminates between xeroderma pigmentosum and trichothiodystrophy in XPD patients.
Remodeling of myocyte gap junctions in arrhythmogenic right ventricular cardiomyopathy due to a deletion in plakoglobin (Naxos disease).
The hair follicle as a dynamic miniorgan.
Expression of DeltaNLef1 in mouse epidermis results in differentiation of hair follicles into squamous epidermal cysts and formation of skin tumours.
The xeroderma pigmentosum group D (XPD) gene: one gene, two functions, three diseases.
A sex-linked recessive disorder with retardation of growth, peculiar hair, and focal cerebral and cerebellar degeneration.
Intermediate filament proteins and their associated diseases.
Premature aging in mice deficient in DNA repair and transcription.