Search results for "Histochemistry"

showing 10 items of 1604 documents

CHK1-targeted therapy to deplete DNA replication-stressed, p53-deficient, hyperdiploid colorectal cancer stem cells.

2017

ObjectiveCancer stem cells (CSCs) are responsible for tumour formation and spreading, and their targeting is required for tumour eradication. There are limited therapeutic options for advanced colorectal cancer (CRC), particularly for tumours carrying RAS-activating mutations. The aim of this study was to identify novel CSC-targeting strategies.DesignTo discover potential therapeutics to be clinically investigated as single agent, we performed a screening with a panel of FDA-approved or investigational drugs on primary CRC cells enriched for CSCs (CRC-SCs) isolated from 27 patients. Candidate predictive biomarkers of efficacy were identified by integrating genomic, reverse-phase protein mic…

0301 basic medicinep53DNA ReplicationCELL CYCLE CONTROLDNA damageColorectal cancerColonmedicine.medical_treatmentAntineoplastic AgentsBiologyBioinformaticsmedicine.disease_causeDNA DAMAGETargeted therapy03 medical and health sciencesCancer stem cellCell Line TumormedicineHumansCHEK11506DRUG DEVELOPMENTOligonucleotide Array Sequence AnalysisMutationCOLORECTAL CANCERSettore MED/06 - ONCOLOGIA MEDICAGastroenterologyCHEMOTHERAPYmedicine.diseaseImmunohistochemistryPrexasertib030104 developmental biologyPyrazinesCheckpoint Kinase 1MutationCancer researchNeoplastic Stem CellsPyrazolesStem cellTumor Suppressor Protein p53Colorectal NeoplasmsGut
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Ataluren for the Treatment of Usher Syndrome 2A Caused by Nonsense Mutations

2019

The identification of genetic defects that underlie inherited retinal diseases (IRDs) paves the way for the development of therapeutic strategies. Nonsense mutations caused approximately 12% of all IRD cases, resulting in a premature termination codon (PTC). Therefore, an approach that targets nonsense mutations could be a promising pharmacogenetic strategy for the treatment of IRDs. Small molecules (translational read-through inducing drugs

0301 basic medicinepatient-derived fibroblastsUsher syndromechemistry.chemical_compound0302 clinical medicineMedicineTRIDSpectroscopyCells CulturedExtracellular Matrix ProteinsOxadiazolesGeneral MedicinePhenotypeImmunohistochemistryComputer Science ApplicationsRetinitis pigmentosaCodon Nonsenseocular therapyUsher syndromeUsher SyndromesNonsense mutationModels BiologicalCatalysisArticleInorganic Chemistry03 medical and health sciencesStructure-Activity RelationshipAtalurenCiliogenesisparasitic diseasesRetinitis pigmentosaHumansGenetic Predisposition to DiseasePhysical and Theoretical ChemistryMolecular BiologyGenetranslational read-throughbusiness.industryOrganic ChemistryHEK 293 cellsFibroblastsmedicine.diseaseAtaluren030104 developmental biologyHEK293 CellschemistryProtein BiosynthesisMutationCancer researchbusiness030217 neurology & neurosurgeryInternational Journal of Molecular Sciences
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Improved Models of Human Endometrial Organoids Based on Hydrogels from Decellularized Endometrium

2021

Organoids are three-dimensional (3D) multicellular tissue models that mimic their corresponding in vivo tissue. Successful efforts have derived organoids from primary tissues such as intestine, liver, and pancreas. For human uterine endometrium, the recent generation of 3D structures from primary endometrial cells is inspiring new studies of this important tissue using precise preclinical models. To improve on these 3D models, we decellularized pig endometrium containing tissue-specific extracellular matrix and generated a hydrogel (EndoECM). Next, we derived three lines of human endometrial organoids and cultured them in optimal and suboptimal culture expansion media with or without EndoEC…

0301 basic medicineproliferationMedicine (miscellaneous)EndometriumArticleExtracellular matrix03 medical and health sciences0302 clinical medicineIn vivomedicineOrganoidendometriumorganoids030219 obstetrics & reproductive medicineDecellularizationChemistryECM hydrogelRCell biology030104 developmental biologymedicine.anatomical_structureSelf-healing hydrogelsImmunohistochemistryMedicinedecellularizationPancreasJournal of Personalized Medicine
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Cytology, Histology and Histochemistry

1986

0303 health sciences03 medical and health sciencesPathologymedicine.medical_specialtyCytology030302 biochemistry & molecular biologymedicineImmunohistochemistryAnimal Science and ZoologyHistologyBiology030304 developmental biologyBolletino di zoologia
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Evaluating the suitability of nicotinic acetylcholine receptor antibodies for standard immunodetection procedures

2007

Nicotinic acetylcholine receptors play important roles in numerous cognitive processes as well as in several debilitating central nervous system (CNS) disorders. In order to fully elucidate the diverse roles of nicotinic acetylcholine receptors in CNS function and dysfunction, a detailed knowledge of their cellular and subcellular localizations is essential. To date, methods to precisely localize nicotinic acetylcholine receptors in the CNS have predominantly relied on the use of anti-receptor subunit antibodies. Although data obtained by immunohistology and immunoblotting are generally in accordance with ligand binding studies, some discrepancies remain, in particular with electrophysiolog…

0303 health sciencesCentral nervous systemContext (language use)BiologyBiochemistry3. Good healthBlot03 medical and health sciencesCellular and Molecular NeuroscienceNicotinic acetylcholine receptor0302 clinical medicinemedicine.anatomical_structureNicotinic agonistmedicineImmunohistochemistryReceptorNeuroscience030217 neurology & neurosurgery030304 developmental biologyAcetylcholine receptorJournal of Neurochemistry
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Data on in vivo PGC-1alpha overexpression model via local transfection in aged mouse muscle

2018

The data presented in this article are related to the research paper entitled “Intensified mitophagy in skeletal muscle with aging is downregulated by PGC-1alpha overexpression in vivo” (Yeo et al., 2019). The data explained the surgical procedure of in vivo local transfection by electroporation method in aged mouse tibialis anterior muscle, and plasmid DNA preparation and verification protocol. The data also showed the transfection efficiency levels of GFP or GFP-tagged PGC-1alpha through immunohistochemistry method for frozen muscle cross-sections.

0303 health sciencesMultidisciplinaryChemistryElectroporationfungiSkeletal muscleTransfectionlcsh:Computer applications to medicine. Medical informaticsGreen fluorescent proteinCell biology03 medical and health sciences0302 clinical medicinemedicine.anatomical_structureTibialis anterior muscleIn vivoBiochemistry Genetics and Molecular BiologyMitophagymedicinelcsh:R858-859.7Immunohistochemistrylcsh:Science (General)030217 neurology & neurosurgerylcsh:Q1-390030304 developmental biologyData in Brief
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Immunohistopathology in Diagnostic Neuropathology

1983

Within the field of surgical pathology, immunohistochemistry is now frequently applied to the morphological diagnosis of lymphomas (11), certain carcinomas and other selected types of tumor (12). In neuropathology, the study of neuro-oncological and non-neoplastic diseases may also receive diagnostic support from performing immunohistological techniques, which encompass immunofluorescent and immunoperoxidase methods. The following report represents a survey of our experience in this recently developed field of diagnostic neuropathology.

0303 health sciencesPathologymedicine.medical_specialtyGlial fibrillary acidic proteinbiologyImmunoperoxidaseNeuropathologymedicine.disease3. Good healthSurgical pathology03 medical and health sciences0302 clinical medicinePituitary adenoma030220 oncology & carcinogenesisbiology.proteinmedicineImmunohistochemistry030304 developmental biology
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Third International Congress of Histochemistry and Cytochemistry

1968

The tissue distribution of enzymatic activities in intestinal metaplasia stomachs exhibiting chronic gastritis was compared histochemically with that of the small intestine in man.

0303 health sciencesPathologymedicine.medical_specialtybiology030302 biochemistry & molecular biologyAcridine orangeAcid phosphataseChronic gastritisIntestinal metaplasiamedicine.diseaseSmall intestine03 medical and health scienceschemistry.chemical_compoundmedicine.anatomical_structurechemistryInternational congressmedicineCytochemistrybiology.proteinImmunohistochemistry030304 developmental biology
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Clinicopathological Significance of Syndecan-1 in Cholangiocarcinoma: A Study Based on Immunohistochemistry and Public Sequencing Data

2021

Background: Syndecan-1 (CD138

<i>SDC1</i>Pathologymedicine.medical_specialtyanimal structuresArticleSyndecan 1SDC103 medical and health sciences0302 clinical medicinemedicineLymph nodeIntrahepatic Cholangiocarcinoma030304 developmental biology0303 health sciencesbusiness.industryGallbladderRCancersyndecan-1General Medicinemedicine.diseasecarbohydrates (lipids)medicine.anatomical_structure030220 oncology & carcinogenesisBiliary Intraepithelial NeoplasiaMedicineImmunohistochemistrybiomarkerPancreasbusinesscholangiocarcinomaJournal of Clinical Medicine
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60KDa chaperonin (HSP60) is over-expressed during colorectal carcinogenesis

2003

The aim of the present study was to evaluate the expression of the heat shock protein 60 (HSP60), a mitochondrial matrix-associated protein belonging to the chaperonin family, in colorectal adenomas and cancers, comparing them to normal colonic tissues and hyperplastic polyps. We performed both immunohistochemistry and Western blot analysis for HSP60. Immunohistochemistry resulted positive in all tubular adenomas and infiltrating adenocarcinomas. By contrast, normal tissues and hyperplastic polyps were negative. Quantitative analysis showed that tubular adenomas with different levels of dysplasia did not present statistical differences concerning HSP60 positivity. In addition, carcinomas al…

AdenomaDysplasiaPathologymedicine.medical_specialtyanimal structuresHistologyBlotting WesternBiophysicsColonic PolypsAdenocarcinomaBiologymedicine.disease_causeChaperoninImmunoenzyme TechniquesWestern blotHeat shock proteinmedicineHumanslcsh:QH301-705.5Dysplasia; Heat shock proteins; Pre-neoplastic lesions; Cell Biology; Anatomy; Animal Science and Zoology; Developmental BiologyHyperplasiaHeat shock proteinmedicine.diagnostic_testChaperonin 60Cell Biologymedicine.diseasedigestive system diseaseslcsh:Biology (General)Hyperplastic PolypDysplasiaImmunohistochemistryAnimal Science and ZoologyHSP60AnatomyColorectal NeoplasmsCarcinogenesisPrecancerous ConditionsPre-neoplastic lesionDevelopmental Biology
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