Výsledky vyhledávání - "Splendore, Alessandra"

Estudo molecular do gene TCOF1 em pacientes portadores da síndrome de Treacher Collins

A síndrome de Treacher Collins (STC) é um distúrbio do desenvolvimento craniofacial de herança autossômica dominante causada por mutações no gene TCOF1, localizado no cromossomo 5 (5q32). Utilizando as técnicas de SSCP e seqüenciamento, esta

Externí odkaz: http://www.teses.usp.br/teses/disponiveis/41/41131/tde-22092004-222503/

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Akademický článek

T-cell lymphoblastic leukemia in early childhood presents NOTCH1 mutations and MLL rearrangements

Autor: Mansur, Marcela Braga, Emerenciano, Mariana, Splendore, Alessandra, Brewer, Lilian, Hassan, Rocio, Pombo-de-Oliveira, Maria S.

Publikováno v: In Leukemia Research 2010 34(4):483-486

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Akademický článek

GATA1 mutations in acute leukemia in children with Down syndrome

Autor: Magalhães, Isis Quezado, Splendore, Alessandra, Emerenciano, Mariana, Figueiredo, Alexandre, Ferrari, Íris, Pombo-de-Oliveira, Maria S.

Publikováno v: In Cancer Genetics and Cytogenetics 2006 166(2):112-116

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Akademický článek

Impact of complex NOTCH1 mutations on survival in paediatric T-cell leukaemia

Autor: Mansur Marcela, Hassan Rocio, Barbosa Thayana C, Splendore Alessandra, Jotta Patricia Y, Yunes José, Wiemels Joseph L, Pombo-de-Oliveira Maria S

Publikováno v: BMC Cancer, Vol 12, Iss 1, p 9 (2012)

Abstract Background Molecular alterations occur frequently in T-ALL and the potential impact of those abnormalities on outcome is still controversial. The current study aimed to test whether NOTCH1 mutations and additional molecular abnormalities wou

Externí odkaz: https://doaj.org/article/65d36b1065a946c3960573ca985b4441

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Akademický článek

Parental origin of mutations in sporadic cases of Treacher Collins syndrome.

Autor: Splendore, Alessandra¹, Jabs, Ethylin Wang², Têmis Maria Félix³, Passos-Bueno, Maria Rita¹ passos@ib.usp.br

Publikováno v: European Journal of Human Genetics. Sep2003, Vol. 11 Issue 9, p718. 5p.

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Influência da metileno-tetrahidrofolato redutase na patogênese das leucemias agudas infantis

Autor: Zanrosso, Crisiane Wais, Emerenciano, Mariana, Figueiredo, Alexandre, Reis, Marcelo, Cordeiro, Synara Nô Seara, Splendore, Alessandra, Pombo-de-Oliveira, Maria S

Publikováno v: Revista Brasileira de Cancerologia; Vol. 51 No. 4 (2005): Oct./Nov./Dec.; 289-295
Revista Brasileira de Cancerologia; Vol. 51 Núm. 4 (2005): oct./nov./dic.; 289-295
Revista Brasileira de Cancerologia; v. 51 n. 4 (2005): out./nov./dez.; 289-295
Revista Brasileira de Cancerologia
Instituto Nacional de Câncer José Alencar Gomes da Silva (INCA)
instacron:INCA

ILeukemia is a result of an adverse gene-environment interaction, with a susceptibility related to polymorphisms. Since the methylenetetrahydrofolate reductase (MTHFR) plays a key role in folate metabolism, changes in its activity (resulting from pol

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3056::198b8fccfcb70671b5434dbd925166e0
https://rbc.inca.gov.br/index.php/revista/article/view/1920

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