Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Marcelo Razera Baruffi"'
Autor:
Marcelo Razera Baruffi, Edgard Edward Engel, Jeremy Andrew Squire, Luis Gonzaga Tone, Silvia Regina Rogatto
Publikováno v:
Genetics and Molecular Biology, Vol 26, Iss 2, Pp 107-113 (2003)
We applied a combination of comparative genomic hybridization (CGH) and fluorescence in situ hybridization (FISH), to characterize the genetic aberrations in three osteosarcomas (OS) and one Ewing's sarcoma. CGH identified recurrent chromosomal losse
Externí odkaz:
https://doaj.org/article/79194d7f97fa45059d5d8b4ae38a082a
Autor:
Marcelo Razera Baruffi, J. Barbieri-Neto, João Monteiro Pina-Neto, C.E. Suerzut, Cacilda Casartelli
Publikováno v:
Genetics and Molecular Biology, Vol 25, Iss 3, Pp 265-270 (2002)
Cytogenetic analyses were performed on a bone giant cell reparative granuloma (GCRG) and on three bone giant cell tumors (GCT). The present GCRG case is the second to be described cytogenetically. A modal chromosome number of 46 was observed in all s
Externí odkaz:
https://doaj.org/article/4dd82b701cff45518397a11924b5be46
Autor:
Marcelo Razera Baruffi, Deise Helena de Souza, Rosana Aparecida Bicudo da Silva, Ester Silveira Ramos, Danilo Moretti-Ferreira
Publikováno v:
Case Reports in Genetics, Vol 2012 (2012)
Balanced X-autosome translocations are rare, and female carriers are a clinically heterogeneous group of patients, with phenotypically normal women, history of recurrent miscarriage, gonadal dysfunction, X-linked disorders or congenital abnormalities
Externí odkaz:
https://doaj.org/article/d1df6b0d2918418a848d5b588e431aed
Autor:
Plínio Cerqueira dos Santos Cardoso, Marcelo de Oliveira Bahia, Marcelo Razera Baruffi, Juliana Simão Nina de Azevedo, André Salim Khayat, Marilia de Arruda Cardoso Smith, Paulo Pimentel de Assumpção, Rommel Rodríguez Burbano, Luiz Gonzaga Tone
Publikováno v:
Revista Brasileira de Cancerologia, Vol 51, Iss 1 (2005)
Os rabdomiossarcomas (RMS) são considerados tumores clinicamente agressivos com origem a partir de células mesenquimais imaturas e que se caracterizam pela presença de células com diferenciação pouco definida. O emprego das técnicas citogenét
Externí odkaz:
https://doaj.org/article/a45f52a22f6149588527a164fe9f4b58
Autor:
Marcelo Razera Baruffi, Deise Helena Souza, Rosana Aparecida Bicudo Silva, Ester Silveira Ramos, Danilo Moretti-Ferreira
Publikováno v:
São Paulo Medical Journal, Vol 131, Iss 6, Pp 427-431
CONTEXT: Robertsonian translocations (RT) are among the most common balanced structural rearrangements in humans and comprise complete chromatin fusion of the long arm of two acrocentric chromosomes. Nevertheless, non-Robertsonian translocation invol
Externí odkaz:
https://doaj.org/article/6e4c7cc52936450682c5edef1236c0bc
Autor:
Ricardo Defavery, Silvia Regina Rogatto, Elvis Terci Valera, Marcelo Razera Baruffi, Carlos Alberto Scrideli, Luiz Gonzaga Tone
Publikováno v:
Leukemia Research. 27:371-374
This report describes the case of an 8-month-old infant with a diagnosis of juvenile myelomonocytic leukemia (JMML) and type 1 neurofibromatosis that presented progression to B lineage acute lymphoid leukemia (ALL). The same rearrangement of gene T-c
Publikováno v:
Cancer Genetics and Cytogenetics. 129:177-180
An aneurysmal bone cyst was submitted to cytogenetic analysis. The modal chromosome number was 46. The composite karyotype was 40 approximately 48,XY,-Y[4],-6[3],del(7)(q32)[3],-9[3],+12[2],+13[2], inv(16)(p13.1q24)[4],-17[3],-19[4],-20[3][cp13]. The
Autor:
Ester Silveira Ramos, Carlos Alberto Scrideli, Luiz Gonzaga Tone, Jana Karaskova, Jeremy A. Squire, Marcelo Razera Baruffi, Benjamin Heck
Publikováno v:
Leukemia Research. 29:1465-1467
Patients with 1q duplication have demonstrated a wide range of multiple congenital abnormalities. Alterations involving this chromosomal region have being described in hematopoietic malignancies and a series of candidate genes that may be associated
Autor:
Rosana Aparecida Bicudo da Silva, Ester Silveira Ramos, Danilo Moretti-Ferreira, Deise Helena de Souza, Marcelo Razera Baruffi
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
SciELO
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP
São Paulo Medical Journal, Vol 131, Iss 6, Pp 427-431
Universidade de São Paulo (USP)
instacron:USP
SciELO
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP
São Paulo Medical Journal, Vol 131, Iss 6, Pp 427-431
Made available in DSpace on 2014-09-30T18:18:31Z (GMT). No. of bitstreams: 0 Previous issue date: 2013Bitstream added on 2014-10-01T14:03:26Z : No. of bitstreams: 1 S1516-31802013000600427.pdf: 891821 bytes, checksum: b9c0c42585e6052852c3070567cd8869
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1edf75de50dbdebada8c57dfe422288
Autor:
Juliana Simão Nina de Azevedo, Luiz Gonzaga Tone, Marcelo de Oliveira Bahia, Marcelo Razera Baruffi, Plínio Cerqueira dos Santos Cardoso, André Salim Khayat, Paulo Pimentel de Assumpção, Marília de Arruda Cardoso Smith, Rommel Rodríguez Burbano
Publikováno v:
Revista Brasileira de Cancerologia, Vol 51, Iss 1 (2005)
Revista Brasileira de Cancerologia; Vol. 51 No. 1 (2005): Jan./Feb./Mar.; 59-65
Revista Brasileira de Cancerologia; Vol. 51 Núm. 1 (2005): ene./feb./mar.; 59-65
Revista Brasileira de Cancerologia; v. 51 n. 1 (2005): jan./fev./mar.; 59-65
Revista Brasileira de Cancerologia
Instituto Nacional de Câncer José Alencar Gomes da Silva (INCA)
instacron:INCA
Revista Brasileira de Cancerologia; Vol. 51 No. 1 (2005): Jan./Feb./Mar.; 59-65
Revista Brasileira de Cancerologia; Vol. 51 Núm. 1 (2005): ene./feb./mar.; 59-65
Revista Brasileira de Cancerologia; v. 51 n. 1 (2005): jan./fev./mar.; 59-65
Revista Brasileira de Cancerologia
Instituto Nacional de Câncer José Alencar Gomes da Silva (INCA)
instacron:INCA
Os rabdomiossarcomas (RMS) são considerados tumores clinicamente agressivos com origem a partir de células mesenquimais imaturas e que se caracterizam pela presença de células com diferenciação pouco definida. O emprego das técnicas citogenét