Výsledky vyhledávání - "R. R. Capela de Matos"

Somatic homozygous loss of SH2B3, and a non-Robertsonian translocation t(15;21)(q25.3;q22.1) with NTRK3 rearrangement, in an adolescent with progenitor B-cell acute lymphoblastic leukemia with the iAMP21

Autor: R R, Capela de Matos, Mak, Othman, G M, Ferreira, Kca, Monteso, M T, de Souza, M, Rouxinol, J B, Melo, I M, Carreira, E, Abdelhay, T, Liehr, R C, Ribeiro, Mlm, Silva

Publikováno v: Cancer Genetics. :16-22

Intrachromosomal amplification of chromosome 21 (iAMP21) occurs in ∼2% of B-cell acute lymphoblastic leukemia (ALL) and is considered to confer a poor prognosis. The relapse risk is associated with therapy intensity, suggesting that other somatic m

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a4da803d7306aa1ce8d8fcf9f08788a
https://doi.org/10.1016/j.cancergen.2021.12.003

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Childhood B-cell progenitor acute lymphoblastic leukemia presenting a three-way t(11;12;21)(q14;p13;q22) with a RUNX1 gene signal on chromosome 11

Autor: Thomas Liehr, R. R. Capela de Matos, Raul C. Ribeiro, Samarth Bhatt, Maria Luiza Macedo Silva, W. Pulcheri, M. T. de Souza, Daniela Ribeiro Ney-Garcia, Eliana Abdelhay, G. Pimenta

Publikováno v: International Journal of Hematology. 95:112-114

The ETV6/RUNX1 (TEL/AML1) gene fusion is the most common gene rearrangement in childhood B-cell progenitor acute lymphoblastic leukemia (BCP-ALL) that occurs in 19–27% of cases [1]. This gene fusion is caused by the t(12;21)(p13;q22) mutation, whic

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::8fbd9d478931db415a3b9fe392e7441a
https://doi.org/10.1007/s12185-011-0981-x

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