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468701 to 468800 most common queries
List represents a sample of symptoms, diseases, and other queries. Updated weekly.
Mechanism of eosinophilia. I. Factors affecting the eosinophil response of rats to Trichinella spiralis.
Role of IL-4, IL-13, and STAT6 in inflammation-induced hypercontractility of murine smooth muscle cells.
Intestinal nematode infection ameliorates experimental colitis in mice.
Induction of Ia antigen in rat epidermal cells and gut epithelium by immunological stimuli.
Sjogren's Syndrome, vitamin b12 deficiency, malaise
Absence of intestinal mast cell response in congenitally athymic mice during Trichinella spiralis infection.
A macrophage protein, Ym1, transiently expressed during inflammation is a novel mammalian lectin.
A critical role for IL-13 in resistance to intestinal nematode infection.
Heparin is essential for the storage of specific granule proteases in mast cells.
Delayed expulsion of the nematode Trichinella spiralis in mice lacking the mucosal mast cell-specific granule chymase, mouse mast cell protease-1.
Mechanism of eosinophilia. II. Role of the lymphocyte.
Histologic variants of papillary and follicular carcinomas associated with anaplastic spindle and giant cell carcinomas of the thyroid: an analysis of rhabdoid and thyroglobulin inclusions.
Giant cell ependymoma of the thoracic spine: pathology case report.
GIANT CELL CARCINOMA OF LUNG.
Atypical exocrine and endocrine pancreatic tumors (anaplastic, small cell, and giant cell types): CT and pathologic features in 14 patients.
Two cases of breast carcinoma with osteoclastic giant cells: are the osteoclastic giant cells pro-tumoural differentiation of macrophages?
Supratentorial giant cell ependymoma.
Loss of imprinting of PEG1/MEST in lung cancer cell lines.
Effective asymmetry in gap junctional intercellular communication between populations of human normal lung fibroblasts and lung carcinoma cells.
Antisense Tiam1 down-regulates the invasiveness of 95D cells in vitro.
Anaplastic giant cell carcinoma of the thyroid gland: treatment and survival over a 25-year period.
Activation of MMP-2 by human GCT23 giant cell tumour cells induced by osteopontin, bone sialoprotein and GRGDSP peptides is RGD and cell shape change dependent.
Sarcomatoid carcinoma of the lung: a clinicopathologic study of 37 cases.
Giant cell carcinoma of the lung; report of 5 cases.
Pleomorphic (spindle/giant cell) carcinoma of the lung. A clinicopathologic correlation of 78 cases.
Microvesicle-associated tissue factor and Trousseau's syndrome.
Overexpression of axin downregulates TCF-4 and inhibits the development of lung cancer.
Anaplastic carcinoma of the thyroid: a 24-year experience.
Interleukin-34 is expressed by giant cell tumours of bone and plays a key role in RANKL-induced osteoclastogenesis.
Comparison of EGFR and K-RAS gene status between primary tumours and corresponding metastases in NSCLC.
Expression of E-cadherin, beta-catenin and p120ctn in the pulmonary sclerosing hemangioma.
Expression and significance of stem cell markers in pulmonary sclerosing haemangioma.
Determination of clonal status of pulmonary sclerosing hemangioma with X-chromosome inactivation mosaicism and polymorphism of phosphoglycerate kinase and androgen receptor genes.
Bilateral multiple pulmonary sclerosing hemangioma.
A pulmonary sclerosing hemagioma with an increasing uptake on PET.
[Diagnosis and therapeutics of 24 cases of pulmonary sclerosing hemangioma].
Recurrence of pulmonary sclerosing hemangioma.
Sjogren's Syndrome, vitamin b12 deficiency
Pulmonary sclerosing hemangioma with pulmonary metastasis.
Pulmonary sclerosing hemangioma with metastasis to the mediastinal lymph node.
Gene expression and clonality analysis of the androgen receptor and phosphoglycerate kinase genes in polygonal cells and cuboidal cells in so-called pulmonary sclerosing hemangioma.
Pulmonary sclerosing hemangioma presenting as solitary pulmonary nodule: dynamic CT findings and histopathologic comparisons.
Frozen section diagnoses of small pulmonary nodules: accuracy and clinical implications.
[Small sclerosing hemangioma combined with primary lung cancer; report of a case].
Pulmonary sclerosing hemangioma presenting with dense spindle stroma cells: a potential diagnostic pitfall.
Loss of heterozygosity patterns of sclerosing hemangioma of the lung and bronchioloalveolar carcinoma indicate a similar molecular pathogenesis.
Sclerosing hemangioma of the lung.
Sclerosing hemangioma of the lung: a benign tumour with potential for malignancy?
From the Archives of the AFIP: pulmonary veno-occlusive disease and pulmonary capillary hemangiomatosis.
Clinicopathological analysis of pulmonary sclerosing hemangioma.
Infantile convulsions and paroxysmal kinesigenic dyskinesia with 16p11.2 microdeletion.
Decreased sensitivity of 17p-deleted chronic lymphocytic leukemia cells to a small molecule BCL-2 antagonist ABT-737.
Chronic lymphocytic leukaemia with 17p deletion: a retrospective analysis of prognostic factors and therapy results.
Bicytopenia, Fever, Leukopenia, Menstrual Flooding, Recurrent Urinary Tract Infection
Resolving the breakpoints of the 17q21.31 microdeletion syndrome with next-generation sequencing.
Transmembrane activator and CAML interactor (TACI) haploinsufficiency results in B-cell dysfunction in patients with Smith-Magenis syndrome.
Molecular analysis of the Retinoic Acid Induced 1 gene (RAI1) in patients with suspected Smith-Magenis syndrome without the 17p11.2 deletion.
Parental somatic mosaicism is underrecognized and influences recurrence risk of genomic disorders.
Smith-Magenis syndrome results in disruption of CLOCK gene transcription and reveals an integral role for RAI1 in the maintenance of circadian rhythmicity.
Identification of two independent nucleosome-binding domains in the transcriptional co-activator SPBP.
Functional and cellular characterization of human Retinoic Acid Induced 1 (RAI1) mutations associated with Smith-Magenis Syndrome.
Cyclophosphamide, fludarabine, alemtuzumab, and rituximab as salvage therapy for heavily pretreated patients with chronic lymphocytic leukemia.
Frontline chemoimmunotherapy with fludarabine, cyclophosphamide, alemtuzumab, and rituximab for high-risk chronic lymphocytic leukemia.
A duplication CNV that conveys traits reciprocal to metabolic syndrome and protects against diet-induced obesity in mice and men.
Rai1 haploinsufficiency causes reduced Bdnf expression resulting in hyperphagia, obesity and altered fat distribution in mice and humans with no evidence of metabolic syndrome.
Mutations in KANSL1 cause the 17q21.31 microdeletion syndrome phenotype.
Mutations in the chromatin modifier gene KANSL1 cause the 17q21.31 microdeletion syndrome.
Mutations in TP53 are exclusively associated with del(17p) in multiple myeloma.
Administration of bortezomib before and after autologous stem cell transplantation improves outcome in multiple myeloma patients with deletion 17p.
Double dens invaginatus of molarized maxillary central incisors, premolarization of maxillary lateral incisors, multituberculism of the mandibular incisors, canines and first premolar, and sensorineural hearing loss.
Dens invaginatus: treatment choices.
Dens invaginatus. Part 2: clinical, radiographic features and management options.
Dens invaginatus type III: report of a case and 10-year radiographic follow-up.
The radicular variety of dens invaginatus.
Prevalence of dens invaginatus in Jordanian adults.
Nonrecognition and subsequent endodontic treatment of dens invaginatus.
Dens invaginatus in the maxillary lateral incisor: treatment of 3 cases.
Anatomical redesign for the treatment of dens invaginatus type III with open apexes: a literature review and case presentation.
A previously unreported association between Nance-Horan syndrome and spontaneous dental abscesses.
Mineral trioxide aggregate obturation: a review and case series.
Characteristics of incisor-premolar hypodontia in families.
A rare presentation of dens invaginatus in a mandibular lateral incisor occurring concurrently with bilateral maxillary dens invaginatus: case report and review of literature.
Dens invaginatus. Part 1: classification, prevalence and aetiology.
Biologically based treatment of immature permanent teeth with pulpal necrosis: a case series.
Dens invaginatus: aetiology, classification, prevalence, diagnosis, and treatment considerations.
Dens invaginatus (dilated composite odontome). I. Variations of the invagination process and associated anterior crown forms.
Progressive, generalized, apical idiopathic root resorption and hypercementosis.
Hypercementosis--an important clue to Paget disease of the maxilla.
Finite element analysis of equine incisor teeth. Part 2: investigation of stresses and strain energy densities in the periodontal ligament and surrounding bone during tooth movement.
Equine odontoclastic tooth resorption and hypercementosis.
Enlarged occlusal surfaces on first molars due to severe attrition and hypercementosis: examples from prehistoric coastal populations of Texas.
Enamel dysplasia with hamartomatous atypical follicular hyperplasia: review of the literature and report of a case.
Enamel dysplasia with hamartomatous atypical follicular hyperplasia (EDHFH) syndrome: suggested pathogenic mechanisms.
Early Pleistocene human mandible from Sima del Elefante (TE) cave site in Sierra de Atapuerca (Spain): a palaeopathological study.
Dental patient with acromegaly: a case report.
A contribution to the histological study of hypercementosis using metal staining.
Secondary retention of permanent molars: a histologic study.
Guanylin and functional coupling proteins in the human salivary glands and gland tumors : expression, cellular localization, and target membrane domains.
Osteomyelitis of the mandible associated with autosomal dominant osteopetrosis: a case report.