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497301 to 497400 most common queries
List represents a sample of symptoms, diseases, and other queries. Updated weekly.
Peripheral CD4 T-cell depletion is not sufficient to prevent ischemic acute renal failure.
Delayed graft function in the kidney transplant.
Marked variation in the definition and diagnosis of delayed graft function: a systematic review.
The pathogenesis and treatment of chronic allograft nephropathy.
Th-17, monokines, collagen type V, and primary graft dysfunction in lung transplantation.
Association between delayed graft function and allograft and patient survival: a systematic review and meta-analysis.
De novo donor-specific antibody at the time of kidney transplant biopsy associates with microvascular pathology and late graft failure.
Machine perfusion or cold storage in deceased-donor kidney transplantation.
Kidney NGAL is a novel early marker of acute injury following transplantation.
Rabbit antithymocyte globulin versus basiliximab in renal transplantation.
Antibody-mediated microcirculation injury is the major cause of late kidney transplant failure.
IL-18 and urinary NGAL predict dialysis and graft recovery after kidney transplantation.
Urine NGAL and IL-18 are predictive biomarkers for delayed graft function following kidney transplantation.
Molecular genetics of Krabbe disease (globoid cell leukodystrophy): diagnostic and clinical implications.
Krabbe disease: psychosine-mediated activation of phospholipase A2 in oligodendrocyte cell death.
Identification of a molecular target of psychosine and its role in globoid cell formation.
Sphingolipid activator protein deficiency in a 16-week-old atypical Gaucher disease patient and his fetal sibling: biochemical signs of combined sphingolipidoses.
Prolonged survival and remyelination after hematopoietic cell transplantation in the twitcher mouse.
A mutation in the saposin A domain of the sphingolipid activator protein (prosaposin) gene results in a late-onset, chronic form of globoid cell leukodystrophy in the mouse.
Psychosine accumulates in membrane microdomains in the brain of krabbe patients, disrupting the raft architecture.
Autoimmune Hemolytic Anemia, Pneumocystis Carinii Pneumonia, Polyserositis
Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroids.
Central nervous system-directed AAV2/5-mediated gene therapy synergizes with bone marrow transplantation in the murine model of globoid-cell leukodystrophy.
Molecular cloning and expression of cDNA for murine galactocerebrosidase and mutation analysis of the twitcher mouse, a model of Krabbe's disease.
Prostaglandin D2-mediated microglia/astrocyte interaction enhances astrogliosis and demyelination in twitcher.
Identification of hematopoietic stem cell-specific miRNAs enables gene therapy of globoid cell leukodystrophy.
Donor-derived cells in the central nervous system of twitcher mice after bone marrow transplantation.
Krabbe disease: a galactosylsphingosine (psychosine) lipidosis.
Hereditary leucodystrophy in the mouse: the new mutant twitcher.
Progressive accumulation of toxic metabolite in a genetic leukodystrophy.
The Twitcher mouse: an enzymatically authentic model of human globoid cell leukodystrophy (Krabbe disease).
Twenty five years of the "psychosine hypothesis": a personal perspective of its history and present status.
Transplantation of umbilical-cord blood in babies with infantile Krabbe's disease.
False positive and false negative FDG-PET scans in various thoracic diseases.
Early lesions of Kaposi's sarcoma in homosexual men. An ultrastructural comparison with other vascular proliferations in skin.
Clinicopathologic re-evaluation of 100 malignant fibrous histiocytomas: prognostic relevance of subclassification.
Malignant fibrous histiocytoma: a retrospective study of 167 cases.
Chest Pain, Shortness, labored breathing
A multivariate analysis of the prognosis after surgical treatment of malignant soft-tissue tumors.
Prosthetic knee replacement after resection of a malignant tumor of the distal part of the femur. Medium to long-term results.
Curcumin mediated apoptosis in AK-5 tumor cells involves the production of reactive oxygen intermediates.
Isolated limb perfusion with tumor necrosis factor and melphalan for limb salvage in 186 patients with locally advanced soft tissue extremity sarcomas. The cumulative multicenter European experience.
Sclerosing hemangioma (histiocytoma, xanthoma) of the lung.
Brief report: inhibition of renal phosphate transport by a tumor product in a patient with oncogenic osteomalacia.
A mutation in the canine BHD gene is associated with hereditary multifocal renal cystadenocarcinoma and nodular dermatofibrosis in the German Shepherd dog.
Chest Pain, Shortness labored breathing
The management of soft-tissue sarcomas of the extremities.
Incidence patterns of soft tissue sarcomas, regardless of primary site, in the surveillance, epidemiology and end results program, 1978-2001: An analysis of 26,758 cases.
Pleomorphic malignant fibrous histiocytoma: fact or fiction? A critical reappraisal based on 159 tumors diagnosed as pleomorphic sarcoma.
Receptors for B cell stimulatory factor 2. Quantitation, specificity, distribution, and regulation of their expression.
Direct evidence that hepatocyte growth factor is a hepatotrophic factor for liver regeneration and has a potent antihepatitis effect in vivo.
The hedgehog pathway regulates remodelling responses to biliary obstruction in rats.
Role of Kupffer cells in the pathogenesis of liver disease.
Regression of cholangiocyte proliferation after cessation of ANIT feeding is coupled with increased apoptosis.
Atp8b1 deficiency in mice reduces resistance of the canalicular membrane to hydrophobic bile salts and impairs bile salt transport.
Hepatocyte-specific ablation of Foxa2 alters bile acid homeostasis and results in endoplasmic reticulum stress.
Bile acid-activated nuclear receptor FXR suppresses apolipoprotein A-I transcription via a negative FXR response element.
Targeted inactivation of sister of P-glycoprotein gene (spgp) in mice results in nonprogressive but persistent intrahepatic cholestasis.
The rat canalicular conjugate export pump (Mrp2) is down-regulated in intrahepatic and obstructive cholestasis.
The endothelin antagonist bosentan inhibits the canalicular bile salt export pump: a potential mechanism for hepatic adverse reactions.
Hepatocanalicular bile salt export pump deficiency in patients with progressive familial intrahepatic cholestasis.
Mutations in the MDR3 gene cause progressive familial intrahepatic cholestasis.
Genome screening by searching for shared segments: mapping a gene for benign recurrent intrahepatic cholestasis.
A gene encoding a liver-specific ABC transporter is mutated in progressive familial intrahepatic cholestasis.
Apoptosis and necrosis in the liver: a tale of two deaths?
The nuclear receptor PXR is a lithocholic acid sensor that protects against liver toxicity.
Phase-shifts of 24-h rhythms of hormonal release and body temperature following early evening administration of the melatonin agonist agomelatine in healthy older men.
Melatonin phase shifts human circadian rhythms in a placebo-controlled simulated night-work study.
Disruption of circadian coordination and malignant growth.
Cross-talks between circadian timing system and cell division cycle determine cancer biology and therapeutics.
Chronic jet lag produces cognitive deficits.
Advancing human circadian rhythms with afternoon melatonin and morning intermittent bright light.
Jet lag: trends and coping strategies.
Melatonin for the prevention and treatment of jet lag.
How to trick mother nature into letting you fly around or stay up all night.
Differential resynchronisation of circadian clock gene expression within the suprachiasmatic nuclei of mice subjected to experimental jet lag.
Preflight adjustment to eastward travel: 3 days of advancing sleep with and without morning bright light.
Adrenal glucocorticoids have a key role in circadian resynchronization in a mouse model of jet lag.
Measurement of internal body time by blood metabolomics.
Visualizing jet lag in the mouse suprachiasmatic nucleus and peripheral circadian timing system.
Chronic 'jet lag' produces temporal lobe atrophy and spatial cognitive deficits.
Effects of chronic jet lag on tumor progression in mice.
Circadian rhythm sleep disorders: part I, basic principles, shift work and jet lag disorders. An American Academy of Sleep Medicine review.
Dysregulation of inflammatory responses by chronic circadian disruption.
Chronic jet-lag increases mortality in aged mice.
Large Hand, Prolactin Increased
Social jetlag: misalignment of biological and social time.
When top-down meets bottom-up: auditory training enhances verbal memory in schizophrenia.
Developmental disruptions and behavioral impairments in rats following in utero RNAi of Dyx1c1.
Blindness and auditory impairment caused by loss of the sodium bicarbonate cotransporter NBC3.
Involuntary attention and distractibility as evaluated with event-related brain potentials.
Deficient brainstem encoding of pitch in children with Autism Spectrum Disorders.
Congenital amusia: a group study of adults afflicted with a music-specific disorder.
Abnormal monitoring of inner speech: a physiological basis for auditory hallucinations.
Brainstem timing: implications for cortical processing and literacy.
Early experience impairs perceptual discrimination.
Auditory verbal hallucinations predominantly activate the right inferior frontal area.
The neural code of auditory phantom perception.
Mismatch negativity: different water in the same river.