20 research outputs found
Papillomas And Carcinomas Of The Choroid Plexus: Histological And Immunohistochemical Studies And Comparison With Normal Fetal Choroid Plexus
Background: Choroid plexus tumors are rare. Results on immunohistochemical features are scanty and controversial even regarding normal plexus. Method: Thirteen cases of choroid plexus tumors and five samples of normal fetal choroid plexus were submitted to immunohistochemical study using a panel of epithelial, neuronal and stromal markers. Results/Conclusions: Relevant histological findings were presence of clear cells in 3/5 papillomas (PP) and 7/8 carcinomas (CA) and all 5 fetal plexuses; rhabdoid cells, desmoplasia and vascular proliferation were found respectively in 3, 4 and 5 cases out of 6 poorly differentiated CA and were absent in PP and well differentiated CA. Pancytokeratin AE1/AE3 was strongly positive in all 13 cases, even in the undifferentiated component of poorly differentiated CA, where reactivity was focal in 3 and diffuse in 3 cases. Low molecular weight cytokeratin (35βH11) was not expressed in any of the 8 CA, but was present in all 5 PP. In 4 of 6 poorly differentiated CA there was reactivity for smooth muscle actin (1A4) in 10 to 30% of the cells. This was true also for one case lacking rhabdoid cells. Laminin was undetectable in all 6 cases of poorly differentiated CA but was present in 4 PP and 2 well differentiated CA. All 5 fetal plexuses expressed GFAP.623 A600607Pianetti, G., Fonseca, L.F., Tumores do plexo coróideo (1998) Arq Neuropsiquiatr, 56, pp. 223-231Pencalet, P., Sainte-Rose, C., Lellouch-Tubiana, A., Papillomas and carcinomas of the choroid plexus in children (1998) J Neurosurg, 88, pp. 521-528Lynch, J.C., Moraes, G.P., Duarte, F., Xantogranuloma do plexo coróide (1988) Arq Neuropsiquiatr, 46, pp. 191-194Aguiar, M.F.M., Cavalcanti, M., Barbosa, H., Vilela, S.L., Mendonça, J.L., Horta, E., Síndrome de Aicardi e papiloma do plexo coróide: Uma associação rara (1996) Arq Neuropsiquiatr, 54, pp. 313-317Filho, P.G., Fonseca, L.F., Suva, M.C., Choroid plexus papilloma and Aicardi syndrome: Case report (2002) Arq Neuropsiquiatr, 60, pp. 1008-1010Matsushima, T., Choroid plexus papillomas and human choroid plexus, a light and electron microscopic study (1983) J Neurosurg, 59, pp. 1054-1062Marrazzoni, D.R., Barbosa-Coutinho, L.M., Plexos coróides: Estudo histopatológico em diferentes faixas etärias (1986) Arq Neuropsiquiatr, 44, pp. 341-350Kasper, M., Goertchen, R., Stosiek, P., Perry, G., Karsten, U., Coexistence of cytokeratin, vimentin and neurofilament protein in human choroid plexus: An immunohistochemical study of intermediate filaments in neuroepithelial tissues (1986) Virchows Arch A, 410, pp. 173-177Miettinen, M., Clark, R., Virtanen, I., Intermediate filament proteins in choroid plexus and ependyma and their tumors (1986) Am J Pathol, 123, pp. 231-240Doglioni, C., Dell'Orto, P., Coggi, G., Iuzzolino, P., Bontempini, L., Viale, G., Choroid plexus tumors: An imunocytochemical study with particular reference to the coexpression of intermediate filament proteins (1987) Am J Pathol, 127, pp. 519-529Felix, I., Phudhichareonrat, S., Halliday, W.C., Becker, L.E., Choroid plexus tumors in children: Immunohistochemical and scanning-electron-microscopic features (1987) Pediat Neurosci, 13, pp. 263-269Gabrion, J., Peraldi, S., Faivre-Bauman, A., Characterization of ependymal cells in hypothalamic and choroidal primary cultures (1988) Neuroscience, 24, pp. 993-1007Kouno, M., Kumanishi, T., Washiyama, K., Sekiguchi, K., Saito, T., Tanaka, R., An immunohistochemical study of cytokeratin and glial fibrillary acidic protein in choroid plexus papilloma (1988) Acta Neuropathol (Berl), 75, pp. 317-320Cruz-Sanchez, F.F., Rossi, M.L., Hughes, J.T., Coakham, H.B., Figols, J., Eynaud, P.M., Choroid plexus papillomas: An immunohistological study of 16 cases (1989) Histopathology, 15, pp. 61-69Sarnat, H.B., Regional differentiation of the human fetal ependyma: Immunocytochemical markers (1992) J Neuropathol Exp Neurol, 51, pp. 58-75Rubinstein, L.J., Brucher, J.M., Focal ependymal differentiation in choroid plexus papillomas: An immunoperoxidase study (1981) Acta Neuropathol (Berl), 53, pp. 29-33Taratuto, A.L., Molina, H., Monges, J., Choroid plexus tumors in infancy and childhood: Focal ependymal differentiation. 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Ed., , London: ArnoldSreenan, J.J., Prayson, R.A., Gliosarcoma: A study of 13 tumors, including p53 and CD34 immunohistochemistrty (1997) Arch Pathol Lab Med, 121, pp. 129-133Gessi, M., Giangaspero, F., Pietsch, T., Atypical teratoid/rhabdoid tumors and choroid plexus tumors: When genetics "surprise" pathology (2003) Brain Pathol, 13, pp. 409-414Lopes, M.B., Rosemberg, S., Almeida, P.C., Pestana, C.B., Glial fibrillary acidic protein and cytokeratin in choroid plexus tumors: An immunohistochemical study (1989) Pathol Res Pract, 185, pp. 339-341Jay, V., Ho, M., Chan, F., Malkin, D., p53 expression in choroid plexus neoplasms: An immunohistochemical study (1996) Arch Pathol Lab Med, 120, pp. 1061-1065Carlotti Jr., C.G., Salhia, B., Weitzman, S., Evaluation of proliferative index and cell cycle protein expression in choroid plexus tumors in children (2002) Acta Neuropathol, 103, pp. 1-10Ohgaki, H., Eibl, R.H., Schwab, M., Mutations of the p53 tumor suppressor gene in neoplasms of the human nervous system (1993) Mol Carcinog, 8, pp. 74-8
Search for single top quarks in the tau+jets channel using 4.8 fb of collision data
We present the first direct search for single top quark production using tau
leptons. The search is based on 4.8 fb of integrated luminosity
collected in collisions at =1.96 TeV with the D0 detector
at the Fermilab Tevatron Collider. We select events with a final state
including an isolated tau lepton, missing transverse energy, two or three jets,
one or two of them tagged. We use a multivariate technique to discriminate
signal from background. The number of events observed in data in this final
state is consistent with the signal plus background expectation. We set in the
tau+jets channel an upper limit on the single top quark cross section of
\TauLimObs pb at the 95% C.L. This measurement allows a gain of 4% in expected
sensitivity for the observation of single top production when combining it with
electron+jets and muon+jets channels already published by the D0 collaboration
with 2.3 fb of data. We measure a combined cross section of
\SuperCombineXSall pb, which is the most precise measurement to date.Comment: 12 pages, 5 figure
Measurement of Z/gamma*+jet+X angular distributions in ppbar collisions at sqrt{s}=1.96 TeV
We present the first measurements at a hadron collider of differential cross
sections for Z+jet+X production in delta phi(Z, jet), |delta y(Z, jet)| and
|y_boost(Z, jet)|. Vector boson production in association with jets is an
excellent probe of QCD and constitutes the main background to many small cross
section processes, such as associated Higgs production. These measurements are
crucial tests of the predictions of perturbative QCD and current event
generators, which have varied success in describing the data. Using these
measurements as inputs in tuning event generators will increase the
experimental sensitivity to rare signals.Comment: Published in Physics Letters B 682 (2010), pp. 370-380. 15 pages, 6
figure
Search for the associated production of a b quark and a neutral supersymmetric Higgs boson which decays to tau pairs
We report results from a search for production of a neutral Higgs boson in
association with a quark. We search for Higgs decays to pairs with
one subsequently decaying to a muon and the other to hadrons. The data
correspond to 2.7fb of \ppbar collisions recorded by the D0 detector
at TeV. The data are found to be consistent with background
predictions. The result allows us to exclude a significant region of parameter
space of the minimal supersymmetric model.Comment: Submitted to Phys. Rev. Letter
Search for charged Higgs bosons in top quark decays
We present a search for charged Higgs bosons in top quark decays. We analyze
the \eplus, \muplus, , , , \etau and \mutau final states from
top quark pair production events, using data from about 1 of
integrated luminosity recorded by the \dzero experiment at the Fermilab
Tevatron Collider. We consider different scenarios of possible charged Higgs
boson decays, one where the charged Higgs boson decays purely hadronically into
a charm and a strange quark, another where it decays into a lepton and a
neutrino and a third one where both decays appear. We extract limits on
the branching ratio for all these models. We use two methods,
one where the production cross section is fixed, and one where the
cross section is fitted simultaneously with . Based on the
extracted limits, we exclude regions in the charged Higgs boson mass and parameter space for different scenarios of the minimal supersymmetric
standard model.Comment: 10 pages, 8 figures, submitted to PL
Pervasive gaps in Amazonian ecological research
Biodiversity loss is one of the main challenges of our time,1,2 and attempts to address it require a clear un derstanding of how ecological communities respond to environmental change across time and space.3,4
While the increasing availability of global databases on ecological communities has advanced our knowledge
of biodiversity sensitivity to environmental changes,5–7 vast areas of the tropics remain understudied.8–11 In
the American tropics, Amazonia stands out as the world’s most diverse rainforest and the primary source of
Neotropical biodiversity,12 but it remains among the least known forests in America and is often underrepre sented in biodiversity databases.13–15 To worsen this situation, human-induced modifications16,17 may elim inate pieces of the Amazon’s biodiversity puzzle before we can use them to understand how ecological com munities are responding. To increase generalization and applicability of biodiversity knowledge,18,19 it is thus
crucial to reduce biases in ecological research, particularly in regions projected to face the most pronounced
environmental changes. We integrate ecological community metadata of 7,694 sampling sites for multiple or ganism groups in a machine learning model framework to map the research probability across the Brazilian
Amazonia, while identifying the region’s vulnerability to environmental change. 15%–18% of the most ne glected areas in ecological research are expected to experience severe climate or land use changes by
2050. This means that unless we take immediate action, we will not be able to establish their current status,
much less monitor how it is changing and what is being lostinfo:eu-repo/semantics/publishedVersio
Pervasive gaps in Amazonian ecological research
Biodiversity loss is one of the main challenges of our time,1,2 and attempts to address it require a clear understanding of how ecological communities respond to environmental change across time and space.3,4 While the increasing availability of global databases on ecological communities has advanced our knowledge of biodiversity sensitivity to environmental changes,5,6,7 vast areas of the tropics remain understudied.8,9,10,11 In the American tropics, Amazonia stands out as the world's most diverse rainforest and the primary source of Neotropical biodiversity,12 but it remains among the least known forests in America and is often underrepresented in biodiversity databases.13,14,15 To worsen this situation, human-induced modifications16,17 may eliminate pieces of the Amazon's biodiversity puzzle before we can use them to understand how ecological communities are responding. To increase generalization and applicability of biodiversity knowledge,18,19 it is thus crucial to reduce biases in ecological research, particularly in regions projected to face the most pronounced environmental changes. We integrate ecological community metadata of 7,694 sampling sites for multiple organism groups in a machine learning model framework to map the research probability across the Brazilian Amazonia, while identifying the region's vulnerability to environmental change. 15%–18% of the most neglected areas in ecological research are expected to experience severe climate or land use changes by 2050. This means that unless we take immediate action, we will not be able to establish their current status, much less monitor how it is changing and what is being lost
Search for squark production in events with jets, hadronically decaying tau leptons and missing transverse energy at root s=1.96 TeV
Contains fulltext :
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