Search results for "Forensic"

showing 10 items of 1701 documents

Immunohistochemistry of primary central nervous system malignant rhabdoid tumors: report of five cases and review of the literature

1996

Malignant rhabdoid tumors (MRT) are characterized by a typical light microscopic morphology with uniformly round tumor cells, vacuolated cytoplasm with occasional round, hyaline intracytoplasmic, periodic acid-Schiff-positive inclusions, vesicular nuclei with prominent nucleoli and positive immunoreactivity for vimentin. The histogenesis of MRT is controversial. Five cases of primary central nervous system (CNS) rhabdoid tumors in children are presented. Immunohistochemical, light and electron microscopic features are compared with primary CNS malignant rhabdoid tumors reported in the literature. Expression of various neurofilaments in our cases of primary CNS rhabdoid tumors was prominent …

Central Nervous SystemMalePathologymedicine.medical_specialtyNeurofilamentCentral nervous systemVimentinHistogenesisBiologyPathology and Forensic MedicineCentral nervous system disease03 medical and health sciencesCellular and Molecular Neuroscience0302 clinical medicinemedicineHumansRhabdoid TumorHyalineBrain NeoplasmsRhabdoid tumorsInfantmedicine.diseaseImmunohistochemistry3. Good healthMicroscopy Electronmedicine.anatomical_structureChild Preschool030220 oncology & carcinogenesisbiology.proteinImmunohistochemistryFemaleNeurology (clinical)030217 neurology & neurosurgeryActa Neuropathologica
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GAL4-responsive UAS- tau as a tool for studying the anatomy and development of the Drosophila central nervous system

1997

To improve the quality of cytoplasmic labelling of GAL4-expressing cells in Drosophila enhancer-trap and transgenic strains, a new GAL4-responsive reporter UAS-tau, which features a bovine tau cDNA under control of a yeast upstream activation sequence (UAS), was tested. Tau, a microtubule-associated protein, is distributed actively and evenly into all cellular processes. Monoclonal anti-bovine Tau antibody reveals the axonal structure of the labelled cells with detail similar to that of Golgi impregnation. We demonstrate that the UAS-tau system is especially useful for studying processes of differentiation and reorganisation of identified neurones during postembryonic development.

Central Nervous SystemSaccharomyces cerevisiae ProteinsHistologyTransgenetau ProteinsBiologyProteomicsPathology and Forensic MedicineAnimals Genetically ModifiedFungal ProteinsUpstream activating sequenceGenes ReporterComplementary DNAmental disordersAnimalsEnhancer trapGenetic TestingTranscription factorNeuronsRegulation of gene expressionMetamorphosis BiologicalAntibodies MonoclonalGene Expression Regulation DevelopmentalCell BiologyAnatomyDNA-Binding ProteinsEnhancer Elements GeneticCytoplasmCattleDrosophilaTranscription FactorsCell and Tissue Research
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Exacerbated experimental autoimmune encephalomyelitis in mast-cell-deficient KitW-sh/W-sh mice

2011

Mast cell (MC)-deficient c-Kit mutant Kit(W/W-v) mice are protected against experimental autoimmune encephalomyelitis (EAE), an animal model of multiple sclerosis, suggesting a detrimental role for MCs in this disease. To further investigate the role of MCs in EAE, we took advantage of a recently characterized model of MC deficiency, Kit(W-sh/W-sh). Surprisingly, we observed that myelin oligodendrocyte glycoprotein (MOG)(35-55)-induced chronic EAE was exacerbated in Kit(W-sh/W-sh) compared with Kit(+/+) mice. Kit(W-sh/W-sh) mice showed more inflammatory foci in the central nervous system (CNS) and increased T-cell response against myelin. To understand whether the discrepant results obtaine…

Central Nervous SystemT-LymphocytesEncephalomyelitisexperimental autoimmune encephalomyelitismast cellsInbred C57BLSeverity of Illness IndeximmunologyMiceMyelinPeptide Fragmentimmune system diseasesMast CellEncephalomyelitisMyelin SheathbiologyExperimental autoimmune encephalomyelitisMast cellProto-Oncogene Proteins c-kitPhenotypemedicine.anatomical_structuremastcell-deficient miceBone Marrow Cellgenetics/immunology/pathology/prevention /&/ controlc-kit mutationsc-kit mutations; experimental autoimmune encephalomyelitis; granulocytes; mast cellsEncephalomyelitis Autoimmune ExperimentalCentral nervous systemBone Marrow CellsPathology and Forensic MedicineMyelin oligodendrocyte glycoproteinExperimentalAnimals Antibody Formation Bone Marrow Cells; pathology Central Nervous System; pathology Encephalomyelitis; Autoimmune; Experimental; genetics/immunology/pathology/prevention /&/ control Glycoproteins; immunology Granulocytes; pathology Immunization Mast Cells; pathology Mice Mice; Inbred C57BL Mutation Myelin Sheath; immunology Myelin-Oligodendrocyte Glycoprotein Peptide Fragments; immunology Phenotype Proto-Oncogene Proteins c-kit; deficiency/genetics/metabolism Severity of Illness Index T-Lymphocytes; pathologyAntigendeficiency/genetics/metabolismmedicineAnimalsMolecular BiologyGlycoproteinsAnimalMultiple sclerosismast-cell-deficient Kit W-sh/W-sh mice.Experimental autoimmune encephalomyelitis; mast-cell-deficient Kit W-sh/W-sh mice.GranulocytegranulocytesCell Biologymedicine.diseaseEncephalomyelitiExperimental autoimmune encephalomyelitiPeptide FragmentsMice Inbred C57BLT-LymphocyteAntibody FormationMutationImmunologybiology.proteinexperimental autoimmune encephalomyelitis; mastcell-deficient mice; mast cellspathologyImmunizationMyelin-Oligodendrocyte GlycoproteinGlycoproteinAutoimmuneLaboratory Investigation
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Degeneration of the Cerebellum in Huntington's Disease (HD): Possible Relevance for the Clinical Picture and Potential Gateway to Pathological Mechan…

2012

Huntington's disease (HD) is a polyglutamine disease and characterized neuropathologically by degeneration of the striatum and select layers of the neo- and allocortex. In the present study, we performed a systematic investigation of the cerebellum in eight clinically diagnosed and genetically confirmed HD patients. The cerebellum of all HD patients showed a considerable atrophy, as well as a consistent loss of Purkinje cells and nerve cells of the fastigial, globose, emboliform and dentate nuclei. This pathology was obvious already in HD brains assigned Vonsattel grade 2 striatal atrophy and did not correlate with the extent and distribution of striatal atrophy. Therefore, our findings sug…

CerebellumPathologymedicine.medical_specialtyAtaxiaGeneral NeuroscienceNeurodegenerationmedicine.diseasePathology and Forensic MedicinePathogenesisDysarthriamedicine.anatomical_structureAtrophynervous systemHuntington's diseasemedicineCorticobasal degenerationNeurology (clinical)medicine.symptomPsychologyNeuroscienceBrain Pathology
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A fatal iatrogenic right vertebral injury after transoral odontoidectomy and posterior cervical stabilization for a type II odontoid fracture.

2014

Abstract The authors present a singular case of an iatrogenic right vertebral artery injury, involving a 67 year-old man, who reported a type II odontoid fracture (Anderson and D'Alonzo Classification) and posterior atlantoaxial dislocation following a road traffic accident. A small injury involving the right vertebral artery occurred as a consequence of transoral odontoidectomy and posterior cervical stabilization. It was caused by bone spicules of spinal origin and their presence was confirmed by the histological section of the right vertebral artery at the level of C1–C2. The case confirms how iatrogenic vertebral artery injuries during cervical spine surgery may be potentially lethal, e…

Cervical spine surgeryMalemedicine.medical_specialtyVertebral arteryIatrogenic DiseaseJoint DislocationsArterial Occlusive DiseasesOdontoid fracturePathology and Forensic MedicineFatal OutcomeSettore MED/43 - Medicina Legalemedicine.arteryOdontoid ProcessingleseRight vertebral arteryMedicineHumansSingular caseVertebral ArteryOdontoid fractureAgedbusiness.industryAtlantoaxial dislocationTransoral odontoidectomyAccidents TrafficOsteonecrosisVertebral injuryThrombosisGeneral MedicineDecompression SurgicalSurgeryRoad traffic accidentAtlanto-Axial JointVertebral artery injuryCerebrovascular CirculationHypoxia-Ischemia BrainCervical VertebraeSpinal FracturesRadiologybusinessLawJournal of forensic and legal medicine
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Vascular Patterns in Dermoscopy

2012

Under the right conditions, dermoscopy allows us to observe the vascular features of many different types of skin lesions. The visualization and identification of vessels with a characteristic morphology can be the key to diagnosis, especially in hypopigmented lesions in which the typical pigmented structures are not visible. Some of the more characteristic associations are the presence of crown vessels in sebaceous hyperplasia, arborizing telangiectasias in basal cell carcinoma, comma-shaped vessels in intra- dermal and compound nevi, dotted vessels in Spitz nevi and melanoma, and hairpin vessels in seborrheic keratoses. The recognition of distinctive vascular features can be of great help…

Characteristic morphologymedicine.medical_specialtyPathologyHistologyintegumentary systemSeborrheic keratosesbusiness.industryMelanomaSebaceous hyperplasiaDermatologymedicine.diseaseDermatologyPathology and Forensic MedicinemedicineBasal cell carcinomaSkin lesionbusinessActas Dermo-Sifiliográficas (English Edition)
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Zum polymorphismus der alkalischen phosphatase (EC3.1.3.1.)

1976

1. Plazenta-Extrakte weisen in der horizontalen Starkegel-Elektrophorese einen Polymorphismus der alkalischen Phosphatase auf, der nach ROBSON und HARRIS vom Genotyp des Feten bestimmt wird. In 73 untersuchten Plazentaproben wurden 5 der 6 haufigen Phanotypen beobachtet, deren Frequenz sehr gute Ubereinstimmung mit den Werten der englischen Autoren aufwies. Die Typisierung war allerdings wegen undeutlicher Darstellung der Muster sehr schwierig. 2.In 66 Seren von Muttern wurde zum Geburtstermin zwar auch ein Polymorphismus der hitzestabilen alkalischen Phosphatase beobachtet, der jedoch nur 4 Typen umfaste und keine sichere Zuordnung zu den Plazentamustern gestattete. 3. Die 66 untersuchten …

ChemistryAlkalische phosphataseAnatomyMolecular biologyPathology and Forensic MedicineZeitschrift f�r Rechtsmedizin
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Nachweis der Faktoren Gm (1,2,4,5,21) und In V(1) in menschlichen Sekreten: Speichel, Schwei�, Nasensekret und Sperma

1977

Im Sperma sind bei genugend Substrat Gm- und InV-Faktoren nachweisbar. An Uberlagerungen durch Nasen- oder Scheidensekret mus gedacht werden. Dagegen wirkt sich Schweis als Verunreinigung nicht storend aus. Im Speichel konnen keine Gm-, wohl aber InV-Merkmale festgestellt werden. Die Gummierung der Briefmarken reagiert unspezifisch mit InV-Antiseren und kommt daher als Fehlerquelle in Betracht. Der Beweiswert von Gm- und InV-Befunden bei Spurenuntersuchungen ergibt sich aus den Phanotyp-Frequenzen, die im Serum von 400 nichtverwandten Personen festgestellt wurden.

ChemistryAnatomyMolecular biologyAntibody formationPathology and Forensic MedicineBlood group antigensZeitschrift f�r Rechtsmedizin
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Aktivit�tsbestimmungen der sauren phosphatase in verschiedenen biologischen medien unter verwendung von o-Carboxyphenylphosphat

1971

Unter den fur die Bestimmung der menschlichen sauren Spermaphosphatase festgestellten Bedingungen wurden die Spaltungsraten verschiedener Substanzen menschlicher, tierischer und pflanzlicher Herkunft bestimmt. Im Humansperma wurden etwa 104–106 U, im bovinen etwa 102–104 und im Blumenkohlpressaft 103–104 U festgestellt. In den ubrigen Substanzen ist zwar eine geringe Hydrolyserate, die auch durch saure Phosphataseaktivitat bedingt sein kann, nicht auszuschliesen, jedoch ist dieses Ferment nicht mit Sicherheit nachweisbar. Die Untersuchungsergebnisse zeigen, das die saure Phosphatase des menschlichen Ejaculates o-Carboxyphenylphosphat sehr schnell hydrolysiert, aber auch im Blumenkohlpressaf…

ChemistryAnatomyMolecular biologyPathology and Forensic MedicineZeitschrift f�r Rechtsmedizin
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Vergleichende elektronenmikroskopische Untersuchungen am Dr�senepithel und am sog. lobul�ren Carcinom der Mamma

1969

In vergleichenden elektronenmikroskopischen Untersuchungen am Drusenacinus einer normalen weiblichen Mamma und eines lobularen Carcinoms werden verschiedene Zelltypen beschrieben: A-Zellen sind ribosomenreich und uberwiegend basal lokalisiert. B-Zellen enthalten weniger Ribosomen, sind luminal lokalisiert und haben prismatische Form. Myoepithelzellen sind durch ihre Topik, Funktion und durch den Gehalt an Myofilamenten charakterisiert.

ChemistryCell BiologyGeneral MedicineMolecular BiologyMolecular biologyPathology and Forensic MedicineVirchows Archiv Abteilung A Pathologische Anatomie
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