Disease on EC 3.1.2.12 - S-formylglutathione hydrolase

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DISEASE
TITLE OF PUBLICATION
LINK TO PUBMED
Acquired Immunodeficiency Syndrome
Splenomegaly in 2,505 patients at a large university medical center from 1913 to 1995. 1963 to 1995: 449 patients.
Adenocarcinoma of Lung
Activity-based proteomics: Identification of ABHD11 and ESD activities as potential biomarkers for human lung adenocarcinoma.
Agranulocytosis
A placebo-controlled trial of the immune modulator, lentinan, in HIV-positive patients: a phase I/II trial.
Alzheimer Disease
Synthesis of organophosphates with fluorine-containing leaving groups as serine esterase inhibitors with potential for Alzheimer disease therapeutics.
Amyloidosis
Activities of lysosomal enzymes and levels of serum amyloid A (SAA) in blood plasma of hamsters during casein induction of AA-amyloidosis.
Fibril amyloid enhancing factor (FAEF)-accelerated amyloidosis in the hamster is not dependent on serine esterase activity and mononuclear phagocytosis.
Anaphylaxis
A placebo-controlled trial of the immune modulator, lentinan, in HIV-positive patients: a phase I/II trial.
Characterization of two strains of selectively bred guinea-pigs. I. Skin transplantation experiments and screening for erythrocyte enzyme polymorphism.
Diisopropylfluorophosphate-evoked inhibition of anaphylactic histamine release from human skin: decrease of the inhibition by storing the skin specimens.
Aniridia
Toward clinical microcytogenetics: the aniridia and the retinoblastoma stories.
Bone Resorption
Inhibition of bone resorption in vitro by serine-esterase inhibitors.
Carcinogenesis
[Retinoblastoma and esterase D II. The oncogenesis of retinoblastoma and the phenotype of esterase D]
Carcinoma
Expression of acute and late-stage inflammatory antigens, c-fms, CSF-1, and human monocytic serine esterase 1, in tumor-associated macrophages of renal cell carcinomas.
The esterase D polymorphism in patients with diabetes or carcinoma of the bladder and a matched sample of non-donor controls.
Carcinoma, Hepatocellular
Differential inhibition of hepatic, pancreatic, and plasma fatty acid ethyl ester synthase by tri-o-tolylphosphate in rats.
Carcinoma, Renal Cell
Expression of acute and late-stage inflammatory antigens, c-fms, CSF-1, and human monocytic serine esterase 1, in tumor-associated macrophages of renal cell carcinomas.
Cholera
Interleukin 2 counteracts the inhibition of cytotoxic T lymphocytes by cholera toxin in vitro and in vivo.
Lack of target cell participation in cytotoxic T lymphocyte-mediated lysis.
Colonic Neoplasms
Colonic aberrant crypts in azoxymethane-treated F344 rats have decreased hexosaminidase activity.
Communicable Diseases
Splenomegaly in 2,505 patients at a large university medical center from 1913 to 1995. 1963 to 1995: 449 patients.
Diabetic Nephropathies
Renal oxidative stress and nitric oxide production in streptozotocin-induced diabetic nephropathy in rats: the possible modulatory effects of garlic (Allium sativum L.).
Digestive System Neoplasms
[Acid phosphatase activity and non-specific esterase D of alpha-naphthyl acetate in the lymphocytes of patients with digestive system neoplasms after surgical treatment]
Endometriosis
[Genetic aspects of endometriosis: features of the distribution of polymorphic gene frequencies]
Foot-and-Mouth Disease
Esterase D enhances type I interferon signal transduction to suppress foot-and-mouth disease virus replication.
Gardner Syndrome
Benign epithelial polyps of the stomach.
Glioblastoma
A human glioblastoma line with karyotypic nullisomy 13 containing several chromosome 13-specific sequences.
Granuloma
Fibroblast stimulation in schistosomiasis. V. Egg granuloma macrophages spontaneously secrete a fibroblast-stimulating factor.
Hematologic Diseases
Splenomegaly in 2,505 patients at a large university medical center from 1913 to 1995. 1963 to 1995: 449 patients.
Hepatitis
Mechanism of killing by virus-induced cytotoxic T lymphocytes elicited in vivo.
Hepatolenticular Degeneration
A sialic acid-specific O-acetylesterase in human erythrocytes: possible identity with esterase D, the genetic marker of retinoblastomas and Wilson disease.
Assignment of the gene for Wilson disease to chromosome 13: linkage to the esterase D locus.
Carrier detection and early diagnosis of Wilson's disease by restriction fragment length polymorphism analysis.
Esterase D and retinoblastoma gene loci are tightly linked to Wilson's disease in Chinese pedigrees from Taiwan.
Evidence for linkage between Wilson disease and esterase D in three kindreds: detection of linkage for an autosomal recessive disorder by the family study method.
Human esterase D gene: complete cDNA sequence, genomic structure, and application in the genetic diagnosis of human retinoblastoma.
Linkage studies of the esterase D and retinoblastoma genes to canine copper toxicosis: a model for Wilson disease.
Mapping the Wilson disease locus to a cluster of linked polymorphic markers on chromosome 13.
Molecular cloning of the human esterase D gene, a genetic marker of retinoblastoma.
Hydatidiform Mole
[Polymorphic studies of the etiological mechanism of hydatidiform mole using phosphoglucomutase-1 and esterase D]
Hypertension
Potential of garlic and its active constituent, S-allyl cysteine, as antihypertensive and cardioprotective in presence of captopril.
Infections
Infection of the health-care worker by HIV and other blood-borne viruses: risks, protection, and education.
Inhibition of tryptase TL2 from human T4+ lymphocytes and inhibition of HIV-1 replication in H9 cells by recombinant aprotinin and bikunin homologues.
Paediatric nosocomial urinary tract infection at a regional hospital.
Influenza, Human
Selective induction of CD8+ cytotoxic T lymphocyte effector function by staphylococcus enterotoxin B.
The novel carboxylesterase 1 variant c.662A>G may decrease the bioactivation of oseltamivir in humans.
Leprosy
Genetic markers and leprosy in South African negroes: Part II. Erythrocyte enzyme polymorphisms.
Leukemia
Demonstration of the increase in serine esterase-positive T cells in hairy-cell leukemia patients undergoing alpha-interferon therapy.
IgE mediated triggering of rat basophil leukemia cells: lack of evidence for serine esterase activation.
Leukemia, Myeloid, Acute
Esterase D and gamma 1 actin level might predict results of induction therapy in patients with acute myeloid leukemia without and with maturation.
Lymphadenopathy
[In situ production and possible role of interleukins in clinical immunopathology]
Lymphocytosis
Lymphocyte activation and serine-esterase induction following recombinant interleukin-2 infusion for lymphomas and acute leukaemias.
Lymphoma
T-cell activation. I. Evidence for a functional linkage between class I MHC antigens and the Tc-Ti complex.
Migraine Disorders
Genetic markers: association study in migraine.
Nasopharyngeal Carcinoma
Impact of socioeconomic status on the diagnosis to treatment interval in Waldeyer's ring carcinoma.
Neoplasm Metastasis
Activity-based proteomics: Identification of ABHD11 and ESD activities as potential biomarkers for human lung adenocarcinoma.
Neoplasms
A null allele of esterase D is a marker for genetic events in retinoblastoma formation.
Antibody-dependent tumour cytolysis by human neutrophils: effect of synthetic serine esterase inhibitors and substrates.
Cationic lipid gene transfer of an IL-2 transgene leads to activation of natural killer cells in a SCID mouse human tumor xenograft.
Chromosome 13 instability and esterase D expression in an osteosarcoma cell line.
Compound A398, a novel podophyllotoxin analogue: cytotoxicity and induction of apoptosis in human leukemia cells.
Esterase D assay in Brazilian retinoblastoma families.
Esterase D: evaluation of a potential derived gene marker for hereditary retinoblastoma.
Gene for hereditary retinoblastoma assigned to human chromosome 13 by linkage to esterase D.
Immunotherapy with anti-CD3 monoclonal antibodies and recombinant interleukin 2: stimulation of molecular programs of cytotoxic killer cells and induction of tumor regression.
Impact of socioeconomic status on the diagnosis to treatment interval in Waldeyer's ring carcinoma.
Mechanism of killing by virus-induced cytotoxic T lymphocytes elicited in vivo.
Patient with 13 chromosome deletion: evidence that the retinoblastoma gene is a recessive cancer gene.
Somatic inactivation of genes on chromosome 13 is a common event in retinoblastoma.
[Acid phosphatase activity and non-specific esterase D of alpha-naphthyl acetate in the lymphocytes of patients with digestive system neoplasms after surgical treatment]
Obesity
An exploratory investigation of genetic linkage with body composition and fatness phenotypes: the Québec Family Study.
Osteosarcoma
Chromosome 13 instability and esterase D expression in an osteosarcoma cell line.
Pneumonia
Intensive care of patients with the acquired immunodeficiency syndrome. Outcome and changing patterns of utilization.
Psoriasis
Esterase D phenotypes in psoriasis vulgaris, atopic diseases and healthy controls.
Respiratory Insufficiency
Intensive care of patients with the acquired immunodeficiency syndrome. Outcome and changing patterns of utilization.
Retinoblastoma
A "new" allele of esterase D in a retinoblastoma family.
A case report of a patient with retinoblastoma and chromosome 13q deletion: assignment of a new gene (gene for LCP1) on human chromosome 13.
A chromosomal breakpoint that separates the esterase D and retinoblastoma predisposition loci in a patient with del(13)(q14q31).
A genetic study of retinoblastoma.
A null allele of esterase D is a marker for genetic events in retinoblastoma formation.
A sialic acid-specific O-acetylesterase in human erythrocytes: possible identity with esterase D, the genetic marker of retinoblastomas and Wilson disease.
Accuracy of detection of the retinoblastoma gene by esterase D linkage.
Activity of red cell esterase D in 50 cases of retinoblastoma patients and their family members.
Assignment of retinoblastoma susceptibility gene to mouse chromosome 14.
Association of autism, retinoblastoma, and reduced esterase D activity.
Chromosome 13 instability and esterase D expression in an osteosarcoma cell line.
Cloning of the esterase D gene: a polymorphic gene probe closely linked to the retinoblastoma locus on chromosome 13.
Closely linked loci on the long arm of chromosome 13 flank a specific 2;13 translocation breakpoint in childhood rhabdomyosarcoma.
Colonic aberrant crypts in azoxymethane-treated F344 rats have decreased hexosaminidase activity.
Crystal structure of human esterase D: a potential genetic marker of retinoblastoma.
De novo complex autosomal translocation involving chromosomes 8, 13 and 15 in a girl with a sporadic retinoblastoma.
Deletion of chromosome region 13q14 is transmissible and does not always predispose to retinoblastoma.
Deletions of the esterase D locus from a survey of 200 retinoblastoma patients.
Esterase D analysis in familial retinoma and retinoblastoma.
Esterase D and hereditary retinoblastoma.
Esterase D and retinoblastoma gene loci are tightly linked to Wilson's disease in Chinese pedigrees from Taiwan.
Esterase D assay in Brazilian retinoblastoma families.
Esterase D studies in human retinoblastoma.
Esterase D: evaluation of a potential derived gene marker for hereditary retinoblastoma.
Familial retinoblastoma (mother and son) with 13q14 deletion.
Gene for hereditary retinoblastoma assigned to human chromosome 13 by linkage to esterase D.
Geographic variations in Wilson's disease.
Human esterase D gene: complete cDNA sequence, genomic structure, and application in the genetic diagnosis of human retinoblastoma.
Human gene mapping, genetic linkage, and clinical applications.
Human retinoblastoma susceptibility gene: cloning, identification, and sequence.
Interstitial deletion of chromosome 13 involving the region 13q14.
Linkage of genes for human esterase D and hereditary retinoblastoma.
Linkage studies of the esterase D and retinoblastoma genes to canine copper toxicosis: a model for Wilson disease.
Location of the retinoblastoma susceptibility gene(s) and the human esterase D locus.
Low incidence of deletion of the esterase D locus in retinoblastoma patients.
Molecular cloning of the human esterase D gene, a genetic marker of retinoblastoma.
Molecular definition in a somatic cell hybrid of a specific 2:13 translocation breakpoint in childhood rhabdomyosarcoma.
Old syndromes and new cytogenetics.
Patient with 13 chromosome deletion: evidence that the retinoblastoma gene is a recessive cancer gene.
Purification, biochemical characterization, and biological function of human esterase D.
Re-evaluation of the sublocalization of esterase D and its relation to the retinoblastoma locus by in situ hybridization.
Regional assignment of genes for human esterase D and retinoblastoma to chromosome band 13q14.
Retinoblastoma and esterase D.
Retinoblastoma, deletion 13q14, and esterase D: application of gene dosage effect to prenatal diagnosis.
Retinoblastoma-del(13q14): report of two patients, one with a trisomic sib due to maternal insertion. Gene-dosage effect for esterase D.
Separation of retinoblastoma and esterase D loci in a patient with sporadic retinoblastoma and del(13)(q14.1q22.3).
Somatic inactivation of genes on chromosome 13 is a common event in retinoblastoma.
The need to screen all retinoblastoma patients for esterase D activity: detection of submicroscopic chromosome deletions.
Toward clinical microcytogenetics: the aniridia and the retinoblastoma stories.
[Clinical features and red cell esterase D in retinoblastoma over a 23-year period]
[Lausanne study of retinoblastoma, 1986-90: deletion of esterase D locus in a collective of 128 patients]
[Retinoblastoma and esterase D II. The oncogenesis of retinoblastoma and the phenotype of esterase D]
[Retinoblastoma and esterase D. I. The esterase D activity of RBC of retinoblastoma patients]
Rhabdomyosarcoma
Closely linked loci on the long arm of chromosome 13 flank a specific 2;13 translocation breakpoint in childhood rhabdomyosarcoma.
s-formylglutathione hydrolase deficiency
Deletions of the esterase D locus from a survey of 200 retinoblastoma patients.
Sarcoma
Chromosome 13 instability and esterase D expression in an osteosarcoma cell line.
Sexually Transmitted Diseases
Soft tissue infections among injection drug users--San Francisco, California, 1996-2000.
Splenic Diseases
Splenomegaly in 2,505 patients at a large university medical center from 1913 to 1995. 1963 to 1995: 449 patients.
Thrombosis
The red blood cell esterase D polymorphism in Europe and Asia.
Tongue Neoplasms
Impact of socioeconomic status on the diagnosis to treatment interval in Waldeyer's ring carcinoma.
Tonsillar Neoplasms
Impact of socioeconomic status on the diagnosis to treatment interval in Waldeyer's ring carcinoma.
Trisomy 13 Syndrome
Determination of esterase D (EsD) genotype in cases with trisomy 13.
Expression of esterase D and other gene markers in trisomy 13.
Overexpression of esterase D in kidney from trisomy 13 fetuses.
[Gene-dosage effect of esterase D enzyme on erythrocytes in a patient with Patau's syndrome]
Tuberculosis
In situ characterization of mycobacterial growth inhibition by lytic enzymes expressed in vectorized E. coli.
Urinary Tract Infections
Paediatric nosocomial urinary tract infection at a regional hospital.
Uveitis
Proteomic surveillance of retinal autoantigens in endogenous uveitis: implication of esterase D and brain-type creatine kinase as novel autoantigens.