Leucemia mielóide aguda t(8;21): freqüência em pacientes brasileiros Acute myeloid leukemia with t(8;21): frequency among Brazilians

Autor: Maria de Lourdes L. F. Chauffaille, Daniela Borri, Sergio L. R. Martins

Publikováno v: Revista Brasileira de Hematologia e Hemoterapia, Vol 26, Iss 2, Pp 99-103 (2004)

A leucemia mielóide aguda (LMA) com diferenciação e t(8;21) ou LMA M2 com t(8;21), pela classificação FAB, tem sido descrita entre 6% e 12% dos casos nas grandes séries. Em nosso meio há poucas descrições com números expressivos de casos. O

Externí odkaz: https://doaj.org/article/d2995a29238b48a5bc8fc62cc3121946

Validation of interphase fluorescence in situ hybridization (iFISH) for multiple myeloma using CD138 positive cells

Autor: Cristina Alonso Ratis, Elvira Deolinda Rodrigues Pereira Velloso, Daniela Borri, Sarah Lee Vaughan Vulcani de Freitas, Roberta Sitnik, RK Kishimoto

Publikováno v: Revista Brasileira de Hematologia e Hemoterapia, Volume: 38, Issue: 2, Pages: 113-120, Published: JUN 2016
Revista Brasileira de Hematologia e Hemoterapia, Vol 38, Iss 2, Pp 113-120 (2016)
Revista Brasileira de Hematologia e Hemoterapia v.38 n.2 2016
Revista brasileira de hematologia e hemoterapia
Associação Brasileira de Hematologia e Hemoterapia e Terapia Celular (ABHHTC)
instacron:ABHHTC
Revista Brasileira de Hematologia e Hemoterapia

BACKGROUND: Multiple myeloma is a plasma cell neoplasm with acquired genetic abnormalities of clinical and prognostic importance. Multiple myeloma differs from other hematologic malignancies due to a high fraction of low proliferating malignant plasm

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c907f2f330d32784992d5d6952c4460

Identification of genes located at breakpoints of uncharacterized chromosomal translocations by the use of chromosomal microdissection and next generation DNA sequencing

Autor: Patrícia Severino, Daniela Borri, Paulo Vidal Campregher, Fernando Ferreira Costa, Natália Torres, Elvira Rp Velloso, Nelson Hamerschlak

Publikováno v: BMC Proceedings

Background Cancer results from accumulation of pathogenic genetic changes in a somatic cell. Chromosomal translocations (CT) are among the most common molecular changes associated with the development of cancer. The mechanism by which CT causes cance

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e64fed6422d43e6d90581c2c377052d
https://doi.org/10.1186/1753-6561-7-s2-p55

Chronic lymphocytic leukaemia/Small lymphocytic lymphoma (CLL/SLL) associated with translocation t(1;6)(p35;p25) as part of complex karyotype

Autor: Ratis C Alonso, Nelson Hamerschlak, Perin G Fleury, DC Pasqualin, Amps Bezerra, Daniela Borri, Pereira Velloso Ed Rodrigues, NS Bacal, Paa Silveira

Publikováno v: Atlas of Genetics and Cytogenetics in Oncology and Haematology.

Case report of a translocation : Chronic lymphocytic leukaemia/Small lymphocytic lymphoma (CLL/SLL) associated with translocation t(1;6)(p35;p25) as part of complex karyotype.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::8eecee84963945648b467602156bda8d
https://doi.org/10.4267/2042/45028

Acute Promyelocytic Leukemia with T(15;17): Frequency of Additional Clonal Chromosome Abnormalities and FLT3

Autor: Daniela Borri, Fernando L. Alberto, Eloisa de Sá Moreira, Rodrigo Proto Siqueira, Maria de Lourdes Lopes Ferrari Chauffaille

Publikováno v: Blood. 112:4857-4857

Acute promyelocytic leukemia (APL) is a distinct subtype of acute myeloid leukemia (AML) characterized by t(15;17)(q22;q21), a balanced reciprocal translocation involving PML and RARA genes. Studies conducted in animal models with PML/RARA suggest th

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::077b7bfe14072255ac5cdad3d341b856
https://doi.org/10.1182/blood.v112.11.4857.4857