Výsledky vyhledávání - "M S, Brassesco"

RARE TUMORS

Autor: C. Kiyotani, T. Uno, H. Ogiwara, N. Morota, A. Nakazawa, Y. Tsutsumi, H. Masaki, T. Mori, J. A. S. Sanz, M. Guibelalde, A. Tavera, I. Herandez, J. Ibanez, M. Brell, A. Mas, H. L. Muller, U. Gebhardt, M. Warmuth-Metz, T. Pietsch, N. Sorensen, R.-D. Kortmann, S. Stapleton, I. Gonzalez, S. Steinbrueck, L. Rodriguez, G. Tuite, M. Krzyzankova, S. Mertsch, A. Jeibmann, U. Kordes, J. Wolff, W. Paulus, M. Hasselblatt, Y. Nonaka, S. Hara, S. Fukazawa, K. Shimizu, M. Ben-Arush, S. Postovsky, H. Toledano, M. Peretz-Nahum, J. Fujimura, S. Sakaguchi, A. Kondo, Y. Saito, K. Shimoji, Y. Ohara, A. Arakawa, M. Saito, T. Shimizu, M. Benesch, A. O. von Bueren, T. Dantonello, K. von Hoff, I. Leuschner, A. Claviez, U. Bierbach, G. Kropshofer, R. Korinthenberg, N. Graf, M. Suttorp, R. D. Kortmann, C. Friedrich, T. Klingebiel, E. Koscielniak, S. Rutkowski, M. Mesa, M. Sanchez, J. Mejia, G. Pena, R. Dussan, M. Cabeza, A. Storino, F. Dincer, T. Roffidal, M. Powell, S. Berrak, J. E. Wolff, F. Fouyssac, C. Delaunay, J.-M. Vignaud, E. Schmitt, O. Klein, L. Mansuy, P. Chastagner, O. Cruz, A. Guillen, G. Garcia, M. Alamar, S. Candela, I. Roussos, M. Garzon, M. Sunol, J. Muchart, M. Rebollo, J. Mora, B. Diez, A. Muggeri, N. Arakaki, F. Meli, G. Sevlever, V. Tsitouras, B. Pettorini, G. Fellows, J. Blair, M. Didi, C. Daousi, C. Steele, M. Javadpour, A. Sinha, M. Hishii, H. Ishii, M. Miyajima, H. Arai, R. Dvir, D. Sayar, D. Levin, L. Ben-Sirah, S. Constantini, R. Elhasid, E. Gertsch, N. Foreman, E. T. Valera, M. S. Brassesco, H. R. Machado, R. S. Oliveira, A. C. Santos, V. C. Terra, M. V. Barros, C. A. Scrideli, L. G. Tone, D. Merino, M. Pienkowska, A. Shlien, U. Tabori, R. Gilbertson, D. Malkin, I. Jeeva, B. Chang, V. Long, S. Picton, D. Burton, S. Clark, C. Kwok, B. Mokete, O. Rafiq, I. Simmons, M. M. K. Shing, C. K. Li, G. C. F. Chan, S. Y. Ha, H. L. Yuen, C. W. Luk, S. C. Ling, R. C. H. Li, J. H. Yoon, H. J. Park, H. J. Shin, B.-K. Park, J.-Y. Kim, H. L. Jung, Y. S. Ra, T. T. Ghim, S. Hartung, M. Garami, H. Traunecker, P. Thall, A. Mahajan, D. Sumerauer, P. Grillner, A. Orrego, M. Mosskin, B. Gustavsson, S. Holm, N. Peters, M. Rogers, S. Chowdry, W. Selman, A. Mitchell, B. Bangert, S. Ahuja, K. Laschinger, D. Gold, D. Stearns, K. Wright, K. Gupta, P. Klimo, D. Ellison, G. Keating, L. Eckel, C. Giannini, N. Wetjen, A. Patton, W. Zaky, G. McComb, J. Finlay, J. Grimm, K. Wong, G. Dhall, F. Gilles, D. Ormandy, R. Alston, E. Estlin, R. Gattamaneni, J. Birch, I. Kamaly-Asl, M. Hemenway, S. Rush, Y. A. Reginald, G. Nicolin, U. Bartel, J. R. Buncic, D. Aguilera, R. Flamini, C. Mazewski, M. Schniederjan, L. Hayes, W. Boydston, T. MacDonald, A. Fleming, N. Jabado, C. Saint-Martin, S. Albrecht, D. A. Ramsay, J. P. Farmer, A. Bendel, M. Hansen, S. Dugan, N. Mendelsohn

Publikováno v: Neuro-Oncology. 14:i148-i156

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a81d63bbcc3d5c1253fed5cb928aa1c5
https://doi.org/10.1093/neuonc/nos108

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PEDIATRICS LABORATORY RESEARCH

Autor: M. S. Brassesco, E. T. Valera, J. A. Pezuk, A. G. Morales, J. C. Oliveira, K. Umezawa, E. M. Rego, G. C. Carlotti, C. A. Scrideli, L. G. Tone, J.-i. Adachi, T. Suzuki, T. Yanagisawa, K. Fukuoka, K. Mishima, K. Wakiya, M. Matsutani, R. Nishikawa, A. Fernandez-L, M. Squatrito, P. Northcott, E. C. Holland, M. D. Taylor, Z. Nahle, A. M. Kenney, D. M. Ashley, A. Muscat, L. Gordon, L. Rigby, D. Birks, N. Foreman, E. Algar, L. K. Donovan, N. Potter, T. Warr, G. Pilkington, A. Erdreich-Epstein, H. Zhou, X. Ren, T. B. Davidson, M. Schur, L. Ji, R. Sposto, S. Asgharzadeh, L. Hiddingh, V. Caretti, E. Hulleman, G.-J. L. Kaspers, W. P. Vandertop, D. P. Noske, T. Wurdinger, T. Lagerweij, P. W. Koken, G. G. Kaspers, E. E. Bar, K. Schreck, C. G. Eberhart, D. A. Largaespada, J. D. Larson, F. J. Rodriquez, A. M. Demer, A. L. Sarver, A. Dubuc, R. B. Jenkins, A. J. Dupuy, N. G. Copeland, N. A. Jenkins, M. A. Taylor, M. Monje, M. E. Freret, P. A. Beachy, M. H. Jansen, P. W. Vandertop, K. Dorris, M. Sobo, E. Panditharatna, C. Liu, M.-O. Kim, L. Miles, S. Goldman, S. Gardner, C. Stevenson, T. Maugans, M. Fouladi, R. Drissi, D. W. Fults, M. Mumert, C. A. Pedone, X. Wu, P. A. Northcott, A. M. Saratsis, S. Magge, B. Rood, A. Hill, J. Nazarian, D. G. van Vuurden, M. Bugiani, P. Wesseling, G. J. Kaspers, V. Gopalakrishnan, C. Das, M. Gireud, P. Taylor, A. Singh, D. Lee, K. Aldape, G. Fuller, J. Fangusaro, V. Rajaram, C. Eberhart

Publikováno v: Neuro-Oncology. 13:iii102-iii106

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::761bd56d684fb9f0b433a153dfd52ca9
https://doi.org/10.1093/neuonc/nor157

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Case report. Familial balanced translocation leading to an offspring with phenotypic manifestations of 9p syndrome

Autor: M. S. Brassesco, M. L. C. Moreira, J M Pina-Neto, L. S. Abreu

Publikováno v: Genetics and molecular research : GMR. 13(2)

We report two similarly affected cousins (children of monozygotic twin sisters) with phenotypic features consistent with 9p deletion syndrome, including dysmorphic craniofacial features (trigonocephaly, midface hypoplasia, upward-slanting palpebral f

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad6f4109e3cf8889301743851268a9df
https://pubmed.ncbi.nlm.nih.gov/25036174

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PLK1 expression and BI 2536 effects in childhood acute lymphoblastic leukemia

Autor: J C, Oliveira, J A, Pezuk, M S, Brassesco, A G, Morales, R G P, Queiroz, C A, Scrideli, L G, Tone

Publikováno v: Pediatric bloodcancer. 61(7)

Polo-like kinase 1 (PLK1) is a conserved kinase that mediates various mitotic events. Compelling data have repeatedly demonstrated its upregulation in different neoplasia, being frequently associated with poor prognosis. However, in childhood acute l

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::5b7829579785087f8716a7edc0f8f314
https://pubmed.ncbi.nlm.nih.gov/24519995

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Osteosarcoma arising from osteochondroma of the tibia: case report and cytogenetic findings

Autor: E E, Engel, M H, Nogueira-Barbosa, M S, Brassesco, G E B, Silva, E T, Valera, F M, Peria, T C, Motta, L G, Tone

Publikováno v: Genetics and molecular research : GMR. 11(1)

Osteochondroma is a cartilage capped benign tumor developing mainly at the juxta-epiphyseal region of long bones. The rate of malignant transformation, mainly into chondrosarcoma, is estimated to be less than 1-3%. Transformation into osteosarcoma is

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::ed97059910a0782ab6648fb264f60c8e
https://pubmed.ncbi.nlm.nih.gov/22427037

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Tetraploidization in Wilms tumor in an infant

Autor: E T, Valera, M S, Brassesco, C A, Scrideli, L G, Tone

Publikováno v: Genetics and molecular research : GMR. 9(3)

Genetic instability is frequent in human cancer. Unscheduled tetraploidization can trigger cell transformation and tumorigenesis. We made a cytogenetic analysis by Giemsa-trypsin banding of a stage I, biphasic Wilms tumor diagnosed in a 10-month-old

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::be6dfedb1b5545d958fff54527fd4ef2
https://pubmed.ncbi.nlm.nih.gov/20715000

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Cytogenetic findings in an epithelioid sarcoma with angiomatoid features. A case report

Autor: M S, Brassesco, E T, Valera, A M, Castro-Gamero, D A, Moreno, T P, Silveira, B M, Mori, E E, Engel, C A, Scrideli, L G, Tone

Publikováno v: Genetics and molecular research : GMR. 8(4)

Epithelioid sarcoma is a rare, aggressive soft tissue tumor of unknown histogenesis showing predominantly epithelioid cytomorphology. We conducted a conventional and molecular cytogenetic study of a 27-year-old male with epithelioid sarcoma with angi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::a43a5c82c10fa14b9bc5a1461a518a0f
https://pubmed.ncbi.nlm.nih.gov/19866439

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Comparative cytogenetic studies of Curimatidae (Pisces, Characiformes) from the middle Paraná River (Argentina)

Autor: M S, Brassesco, M C, Pastori, H A, Roncati, A S, Fenocchio

Publikováno v: Genetics and molecular research : GMR. 3(2)

Almost all species of the Curimatidae family have a stable karyotype, with a diploid number of 54 metacentric (M) and submetacentric (SM) chromosomes, and one sole nucleolus organizer pair. This family has considerable specific diversity in Argentine

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::78d488d9aae1c9b4d5897ce4ac474331
https://pubmed.ncbi.nlm.nih.gov/15266401

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