Search results for "blas"

showing 10 items of 2217 documents

Biological Description of 109 Cases of Blastic Plasmacytoid Dendritic Cell Neoplasm (BPDCN) from the French Network of BPDCN

2015

Abstract Blastic plasmacytoid dendritic cell neoplasm is a clonal disease derived from precursors of plasmacytoid dendritic cells (pDC). It is a rare neoplasm involving the skin which may or may not be associated from the outset with a leukemic component. The disease invariably progresses to aggressive leukemic dissemination, leading to a differential diagnosis with acute leukemia. In 2004, we set up a French network to recruit biological data at diagnosis. Diagnosis was according to recommendations (Swerdlow et al, 2008), with, in addition, a mandatory panel of pDC markers (Garnache-Ottou et al, 2009) detected by flow cytometry or by immunohistochemistry on infiltrated blood, bone marrow o…

0303 health sciencesPathologymedicine.medical_specialty[ SDV ] Life Sciences [q-bio][SDV]Life Sciences [q-bio]ImmunologyCell BiologyHematologyBlastic plasmacytoid dendritic cell neoplasmBiologyBiochemistry3. Good health[SDV] Life Sciences [q-bio]03 medical and health sciences0302 clinical medicineMyeloid cellsmedicineSkin lesion030304 developmental biology030215 immunology
researchProduct

2015

The clarification of complete cell lineages, which are produced by specific stem cells, is fundamental for understanding mechanisms, controlling the generation of cell diversity and patterning in an emerging tissue. In the developing Central Nervous System (CNS) of Drosophila, neural stem cells (neuroblasts) exhibit two periods of proliferation: During embryogenesis they produce primary lineages, which form the larval CNS. After a phase of mitotic quiescence, a subpopulation of them resumes proliferation in the larva to give rise to secondary lineages that build up the CNS of the adult fly. Within the ventral nerve cord (VNC) detailed descriptions exist for both primary and secondary lineag…

0303 health sciencesfungiEmbryogenesisAnatomyBiologyNeuromereEmbryonic stem cellGeneral Biochemistry Genetics and Molecular BiologyNeural stem cellCell biology03 medical and health sciences0302 clinical medicineNeuroblastVentral nerve cordStem cellGeneral Agricultural and Biological SciencesGanglion mother cell030217 neurology & neurosurgery030304 developmental biologyBiology Open
researchProduct

Cribra orbitalia as a potential indicator of childhood stress: Evidence from paleopathology, stable C, N, and O isotopes, and trace element concentra…

2016

Cribra orbitalia (CO), or porotic hyperostosis (PH) of the orbital roof, is one of the most common pathological conditions found in archaeological subadult skeletal remains. Reaching frequencies higher than 50% in many prehistoric samples, CO has been generally attributed to a variety of factors including malnutrition (e.g., megaloblastic anemia) and parasitism. In this study, we tested the relationship between CO, trace element concentrations, and stable isotope values (δ13C, δ15N, δ18O) in subadult skeletons from a 17th to 18th century cemetery in the historic town of Jēkabpils, Latvia. A total of 28 subadults were examined, seven of which (25%) showed evidence of CO. Bioarchaeological ev…

060101 anthropology060102 archaeologyδ13CStable isotope ratioTrace elementMineralogy06 humanities and the artsBiologymedicine.diseaseBiochemistryIsotopes of nitrogenInorganic ChemistryAnimal sciencemedicineMolecular Medicine0601 history and archaeologyMegaloblastic anemiaPaleopathologyTrophic levelPorotic hyperostosisJournal of Trace Elements in Medicine and Biology
researchProduct

Tres tablas más que añadir al catálogo de Vicente Macip. (Albaida, h. 1468- Valencia, 1551)

2013

1551) Samper EmbizUNESCO::CIENCIAS DE LAS ARTES Y LAS LETRAS:CIENCIAS DE LAS ARTES Y LAS LETRAS [UNESCO]h. 1468- ValenciaVicente 29 360211-5808 9678 Archivo de arte valenciano 367242 2013 94 4718364 Tres tablas más que añadir al catálogo de Vicente Macip. (Albaida
researchProduct

Integrated CGH/WES Analyses Advance Understanding of Aggressive Neuroblastoma Evolution: A Case Study

2021

Neuroblastoma (NB) is the most common extra-cranial malignancy in preschool children. To portray the genetic landscape of an overly aggressive NB leading to a rapid clinical progression of the disease, tumor DNA collected pre- and post-treatment has been analyzed. Array comparative genomic hybridization (aCGH), whole-exome sequencing (WES), and pharmacogenetics approaches, respectively, have identified relevant copy number alterations (CNAs), single nucleotide variants (SNVs), and polymorphisms (SNPs) that were then combined into an integrated analysis. Spontaneously formed 3D tumoroids obtained from the recurrent mass have also been characterized. The results prove the power of combining C…

3D tumoroids; Array CGH; Clonal evolution; Neuroblastoma; Pharmacogenetics; Recurrent tumor; Single nucleotide variants; Whole exome sequencing; Child Preschool; Disease Progression; Drug Resistance Neoplasm; Fatal Outcome; Humans; Immunophenotyping; Neuroblastoma; Polymorphism Single Nucleotide; Comparative Genomic Hybridization; Whole Exome SequencingQH301-705.5Drug Resistanceclonal evolutionCase Report3D tumoroidsSingle-nucleotide polymorphismDiseaseComputational biologyBiologyMalignancyPolymorphism Single NucleotideSomatic evolution in cancerImmunophenotypingwhole exome sequencingNeuroblastomaFatal OutcomeNeuroblastomaExome SequencingmedicineHumansarray CGHrecurrent tumorPolymorphismBiology (General)ChildPreschoolExome sequencingTumorsComparative Genomic HybridizationSingle NucleotideGeneral Medicinemedicine.diseaseSingle nucleotide variantsDrug Resistance NeoplasmPharmacogeneticsChild PreschoolDisease ProgressionFarmacogenèticaNeoplasmPharmacogeneticsComparative genomic hybridization
researchProduct

Retinoic-Acid-Induced Downregulation of the 67 KDa Laminin Receptor Correlates with Reduced Biological Aggressiveness of Human Neuroblastoma Cells

2012

Neuroblastoma is a common tumor of the childhood arising from embryonal sympathetic neural cell precursors. Despite of the improved therapeutic strategies, the survival rate of high-risk neuroblastoma patients is poor. Although complete clinical remissions can be achieved, relapse is relatively frequent, indicating a role for the persistence of the minimal residual disease (for review, Maris, 2010). Treatments with derivatives of retinoic acid (RA), the biologically active form of vitamin A, produce significant improvements on the therapy of high-risk neuroblastoma patients, when used together with intensive multimodal therapies (Reynolds et al., 2003, for review). Despite some controversy …

67 kDa Laminin Receptorchemistry.chemical_compoundDifferential displayDownregulation and upregulationChemistryApoptosisNeuroblastomaRetinoic acidmedicinemedicine.diseaseReceptorMolecular biologyMinimal residual disease
researchProduct

A subset of flavaglines inhibits KRAS nanoclustering and activation.

2020

The RAS oncogenes are frequently mutated in human cancers and among the three isoforms (KRAS, HRAS and NRAS), KRAS is the most frequently mutated oncogene. Here, we demonstrate that a subset of flavaglines, a class of natural anti-tumour drugs and chemical ligands of prohibitins, inhibit RAS GTP loading and oncogene activation in cells at nanomolar concentrations. Treatment with rocaglamide, the first discovered flavagline, inhibited the nanoclustering of KRAS, but not HRAS and NRAS, at specific phospholipid-enriched plasma membrane domains. We further demonstrate that plasma membrane-associated prohibitins directly interact with KRAS, phosphatidylserine and phosphatidic acid, and these int…

:Bioengineering [Engineering]Neuroblastoma RAS viral oncogene homologGene isoformLung NeoplasmsGTP'[SDV]Life Sciences [q-bio]AucunBiology: Biochemistry biophysics & molecular biology [F05] [Life sciences]medicine.disease_causeProto-Oncogene Proteins p21(ras)03 medical and health scienceschemistry.chemical_compound0302 clinical medicineRocaglamideCarcinoma Non-Small-Cell LungmedicineKRASHumansdrug therapy;geneticsgeneticsHRASProhibitin: Biochimie biophysique & biologie moléculaire [F05] [Sciences du vivant]neoplasmsComputingMilieux_MISCELLANEOUS030304 developmental biology0303 health sciencesOncogeneLipid nanoclusterOncogenesCell Biologydigestive system diseases3. Good healthrespiratory tract diseasesPhospholipidchemistry030220 oncology & carcinogenesisMutationCancer researchKRASFlavaglineRocaglamideProhibitinSignal Transduction
researchProduct

Sobre la vegetación de la alianza Homalothecio-Polypodion serrati en las montañas valencianas

1983

Se han estudiado las comunidades de la alianza Homalothecio-Polypodion serrati en las montañas de la región valenciana y alrededores, encontrándose que las mismas pueden atribuirse a cuatro asociaciones: Anomodonio-Polypodietum serrati, Saxifragetum cossonianae, Saxifragetum latepetiolatae y Homalothecio-Asplenietum fontani. Se presentan sendas tablas fitosociológicas de cada una de las tres últimas, de las cuales se comentan, asimismo, sus principales notas características. The communities included in the alliance Homalothecio-Polypodio serrati are studied in Valencia region and neighbouring areas. 4 associations can be assigned to them: Anomodonio-Polypodietum serrati, Saxifragetum cosson…

:CIENCIAS DE LA VIDA::Biología vegetal (Botánica) [UNESCO]Homalothecio-Polypodion serratiValenciaHomalothecio-Polypodion serrati ; Valencia ; Tablas fitosociológicasUNESCO::CIENCIAS DE LA VIDA::Biología vegetal (Botánica)Tablas fitosociológicas
researchProduct

Análisis digital del infiltrado inmune en neuroblastoma. Impacto pronóstico.

2018

El neuroblastoma es el tumor sólido extracraneal más común en la niñez con un índice de supervivencia a los cinco años del 40% en pacientes de riesgo elevado a pesar de terapias intensivas. Recientemente, aunque la inmunoterapia, incluida la terapia de células T con receptor de antígeno quimérico, representa un tratamiento revolucionario para las neoplasias hematológicas, sigue habiendo grandes desafíos para aplicar esta estrategia terapéutica con los tumores sólidos, incluido el neuroblastoma, como resultado de la naturaleza inmunosupresiva del microambiente tumoral. Se ha descrito que las células cancerosas desarrollan múltiples mecanismos para escapar del reconocimiento inmune o para mod…

:CIENCIAS MÉDICAS ::Patología::Neuropatología [UNESCO]digital:CIENCIAS MÉDICAS ::Patología::Inmunopatología [UNESCO]:CIENCIAS MÉDICAS ::Ciencias clínicas::Oncología [UNESCO]UNESCO::CIENCIAS MÉDICAS ::Patología::Neuropatologíasistema inmuneneuroblastomaUNESCO::CIENCIAS MÉDICAS ::Ciencias clínicas::OncologíapediátricoUNESCO::CIENCIAS MÉDICAS ::Ciencias clínicas::Pediatríacáncer:CIENCIAS MÉDICAS ::Ciencias clínicas::Pediatría [UNESCO]UNESCO::CIENCIAS MÉDICAS ::Patología::Inmunopatologíapatología
researchProduct

Estudios sobre los problemas ternarios de probabilidad condicional de nivel N0

2014

Esta tesis aborda el problema de la enseñanza y aprendizaje de la probabilidad condicional, desde la resolución de problemas. Concretamente nos interesamos por una familia particular de problemas, que denominamos problemas ternarios de probabilidad condicional de nivel N0 y que se caracterizan por no presentar ninguna probabilidad condicional como dato conocido en el enunciado. Los objetivos concretos de la tesis son tres: primero, profundizar en el estudio de la estructura matemática de los problemas ternarios de nivel N0; segundo, observar la actuación de un grupo de nueve estudiantes cursando la asignatura Matemáticas Opción B de 4º de ESO resolviendo problemas de nivel N0; y tercero, di…

:MATEMÁTICAS [UNESCO]Tablas de contingencia 2x2Probabilidad condicionalResolución de problemasDidáctica de la Matemática:PEDAGOGÍA [UNESCO]UNESCO::PEDAGOGÍAUNESCO::MATEMÁTICASProcesos de enseñanza
researchProduct