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470101 to 470200 most common queries
List represents a sample of symptoms, diseases, and other queries. Updated weekly.
Oropharyngeal aspiration of a silica suspension produces a superior model of silicosis in the mouse when compared to intratracheal instillation.
Treatment by human recombinant soluble TNF receptor of pulmonary fibrosis induced by bleomycin or silica in mice.
Silica-stimulated monocytes release fibroblast proliferation factors identical to interleukin 1. A potential role for interleukin 1 in the pathogenesis of silicosis.
EXPERIMENTAL EMPHYSEMA: ITS PRODUCTION WITH PAPAIN IN NORMAL AND SILICOTIC RATS.
Reactive oxygen species (ROS) and reactive nitrogen species (RNS) generation by silica in inflammation and fibrosis.
The Nalp3 inflammasome is essential for the development of silicosis.
An examination of the cytotoxic effects of silica on macrophages.
Silica crystals and aluminum salts activate the NALP3 inflammasome through phagosomal destabilization.
muscas and general weakness in arms and chest, facial muscle weakness, weakness, fatigue, muscle weakness, pain, anemia, leukopenia, vitamin b12 decreased
Influence of MHC class II in susceptibility to beryllium sensitization and chronic beryllium disease.
HLA-DP allele-specific T cell responses to beryllium account for DP-associated susceptibility to chronic beryllium disease.
Differential susceptibilities to chronic beryllium disease contributed by different Glu69 HLA-DPB1 and -DPA1 alleles.
Beryllium sensitization progresses to chronic beryllium disease: a longitudinal study of disease risk.
Machining risk of beryllium disease and sensitization with median exposures below 2 micrograms/m3.
Interaction of genetic and exposure factors in the prevalence of berylliosis.
Disease-specific changes in gammadelta T cell repertoire and function in patients with pulmonary tuberculosis.
Biased accumulation of T lymphocytes with "memory"-type CD45 leukocyte common antigen gene expression on the epithelial surface of the human lung.
Target organ localization of memory CD4(+) T cells in patients with chronic beryllium disease.
Crystal structure of HLA-DP2 and implications for chronic beryllium disease.
Beryllium presentation to CD4+ T cells underlies disease-susceptibility HLA-DP alleles in chronic beryllium disease.
Reexamination of the blood lymphocyte transformation test in the diagnosis of chronic beryllium disease.
Proliferative response of bronchoalveolar lymphocytes to beryllium. A test for chronic beryllium disease.
Pathologic and immunologic alterations in early stages of beryllium disease. Re-examination of disease definition and natural history.
Beryllium disease screening in the ceramics industry. Blood lymphocyte test performance and exposure-disease relations.
Skin as a route of exposure and sensitization in chronic beryllium disease.
Epidemiology of beryllium sensitization and disease in nuclear workers.
Chest Pain, Rectal Bleeding, Volvulus, rectal bleeding whenever i have a bowel movement, chest pain worse on breathing
HLA-DPB1 glutamate 69: a genetic marker of beryllium disease.
Inflammatory giant cells.
Hepatic granulomas induced by glucan. An ultrastructural and peroxidase-cytochemical study.
Central giant cell granulomas of the jaws regress with calcitonin therapy.
Trapping of misdirected dendritic cells in the granulomatous lesions of giant cell arteritis.
From the archives of AFIP. Imaging of giant cell tumor and giant cell reparative granuloma of bone: radiologic-pathologic correlation.
Janet M Pruckler
The multinucleate cells in giant cell granulomas of the jaw are osteoclasts.
Familial granulomatous synovitis, uveitis, and cranial neuropathies.
Noonan-like/multiple giant cell lesion syndrome.
Langhans giant cells from M. tuberculosis-induced human granulomas cannot mediate mycobacterial uptake.
Granulomatous reaction to Bruch's membrane in age-related macular degeneration.
Granulomatous inflammation--a review.
Defective bromosulfophthalein clearance in patients with constitutional hepatic dysfunction (Gilbert's syndrome).
Involvement of an organic anion transporter (canalicular multispecific organic anion transporter/multidrug resistance-associated protein 2) in gastrointestinal secretion of glutathione conjugates in rats.
Bilirubin and biliverdin protect rodents against diabetic nephropathy by downregulating NAD(P)H oxidase.
The degradation of haem by mammals and its excretion as conjugated bilirubin.
Constitutional hepatic dysfunction (Gilbert's syndrome). A new definition based on kinetic studies with unconjugated radiobilirubin.
Translational control of gene expression and disease.
Complete OATP1B1 and OATP1B3 deficiency causes human Rotor syndrome by interrupting conjugated bilirubin reuptake into the liver.
Defective ATP-dependent bile canalicular transport of organic anions in mutant (TR-) rats with conjugated hyperbilirubinemia.
Considerations of the pathogenesis of neonatal hepatitis, biliary atresia and choledochal cyst--the concept of infantile obstructive cholangiopathy.
Hepatobiliary transport of glutathione and glutathione conjugate in rats with hereditary hyperbilirubinemia.
Recent advances in the separation and analysis of diazo-positive bile pigments.
Urinary D-glucaric-acid excretion as a test for hepatic enzyme induction in man.
Hepatocellular transplantation for metabolic deficiencies: decrease of plasms bilirubin in Gunn rats.
Hereditary chronic conjugated hyperbilirubinemia in mutant rats caused by defective hepatic anion transport.
Hepatic bilirubin udp-glucuronyl transferase activity in liver disease and gilbert's syndrome.
Chronic nonhemolytic unconjugated hyperbilirubinemia with glucuronyl transferase deficiency. Clinical, biochemical, pharmacologic and genetic evidence for heterogeneity.
Congenital jaundice in rats with a mutation in a multidrug resistance-associated protein gene.
The trachomatous trichiasis clamp: a surgical instrument designed to improve bilamellar tarsal rotation procedure outcomes.
Relationship between immediate post-operative appearance and 6-week operative outcome in trichiasis surgery.
Quality assurance in trichiasis surgery: a methodology.
Blindness-causing trachomatous trichiasis biomarkers sighted.
Why do people not attend for treatment for trachomatous trichiasis in Ethiopia? A study of barriers to surgery.
Trachoma prevalence in women living in rural northern India: rapid assessment findings.
New method for the correction of entropion with trichiasis by tarsotomy.
Definitions and standardization of a new grading scheme for eyelid contour abnormalities after trichiasis surgery.
In vivo confocal microscopy in scarring trachoma.
muscas and general weakness in arms and chest, facial muscle weakness, weakness, fatigue, muscle weakness, pain, anemia, leukopenia
Epilation for trachomatous trichiasis and the risk of corneal opacification.
A SIMPLE PROCEDURE FOR THE RELIEF OF TRICHIASIS AND ENTROPION OF THE UPPER LID.
Trachomatous trichiasis and its management in endemic countries.
Surgery versus epilation for the treatment of minor trichiasis in Ethiopia: a randomised controlled noninferiority trial.
Bacterial infection in scarring trachoma.
Genome-wide identification of Chlamydia trachomatis antigens associated with trachomatous trichiasis.
Clearing the backlog: trichiasis surgeon retention and productivity in northern Ethiopia.
Absorbable versus silk sutures for surgical treatment of trachomatous trichiasis in Ethiopia: a randomised controlled trial.
Conjunctival transcriptome in scarring trachoma.
FOXE3 plays a significant role in autosomal recessive microphthalmia.
The prevalence of eye disease in Leicester: a comparison of adults of Asian and European descent.
Cleft Palate, Glomerulonephritis, Polycystic Kidney Disease
Selective suture removal can reduce postkeratoplasty astigmatism.
Jagged 1 is necessary for normal mouse lens formation.
5-Fluorouracil and glaucoma filtering surgery. III. Intermediate follow-up of a pilot study.
Changing pattern of childhood blindness in Maharashtra, India.
Which is better? One or two? A randomized clinical trial of single-plate versus double-plate Molteno implantation for glaucomas in aphakia and pseudophakia.
Enhanced striatal cholinergic neuronal activity mediates L-DOPA-induced dyskinesia in parkinsonian mice.
A double-deletion mutation in the Pitx3 gene causes arrested lens development in aphakia mice.
Foxe view of lens development and disease.
Homozygous nonsense mutation in the FOXE3 gene as a cause of congenital primary aphakia in humans.
Deletion in the promoter region and altered expression of Pitx3 homeobox gene in aphakia mice.
Genetic mouse models of parkinsonism: strengths and limitations.
Impetigo, One Report of Brother and Sister from Non-Consanguineous Parents
Isolation of a new homeobox gene belonging to the Pitx/Rieg family: expression during lens development and mapping to the aphakia region on mouse chromosome 19.
Selective loss of dopaminergic neurons in the substantia nigra of Pitx3-deficient aphakia mice.
Early developmental failure of substantia nigra dopamine neurons in mice lacking the homeodomain gene Pitx3.
Pitx3 is required for development of substantia nigra dopaminergic neurons.
Pitx3 is required for motor activity and for survival of a subset of midbrain dopaminergic neurons.
Differences in the ability of human T-cell lymphotropic virus type 1 (HTLV-1) and HTLV-2 tax to inhibit p53 function.
HTLV-1 and associated adult T-cell leukemia/lymphoma.
Hew D T Torrance