U2AF1 and other splicing factor gene mutations in telomere biology disorders are associated with hematologic neoplasia and worse overall survival (2021)
- Authors:
- Autor USP: RODRIGUES, RODRIGO DO TOCANTINS CALADO DE SALOMA - FMRP
- Unidade: FMRP
- DOI: 10.1182/blood-2021-146946
- Subjects: MUTAÇÃO GENÉTICA; NEOPLASIAS; SANGUE; TELÔMERO; MEDULA ÓSSEA
- Language: Inglês
- Imprenta:
- Publisher place: Washington
- Date published: 2021
- Source:
- Conference titles: ASH Annual Meeting Abstracts
- Este periódico é de assinatura
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: bronze
-
ABNT
GROARKE, Emma M. et al. U2AF1 and other splicing factor gene mutations in telomere biology disorders are associated with hematologic neoplasia and worse overall survival. Blood. Washington: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. Disponível em: https://doi.org/10.1182/blood-2021-146946. Acesso em: 31 dez. 2025. , 2021 -
APA
Groarke, E. M., Gutierrez-Rodrigues, F., Ma, X., Patel, B. A., Spitofsky, N., Browne, P. V., et al. (2021). U2AF1 and other splicing factor gene mutations in telomere biology disorders are associated with hematologic neoplasia and worse overall survival. Blood. Washington: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. doi:10.1182/blood-2021-146946 -
NLM
Groarke EM, Gutierrez-Rodrigues F, Ma X, Patel BA, Spitofsky N, Browne PV, Chien KS, Wu CO, DiNardo CD, Colla S, Calado RT, Young NS. U2AF1 and other splicing factor gene mutations in telomere biology disorders are associated with hematologic neoplasia and worse overall survival [Internet]. Blood. 2021 ; 138 862-864.[citado 2025 dez. 31 ] Available from: https://doi.org/10.1182/blood-2021-146946 -
Vancouver
Groarke EM, Gutierrez-Rodrigues F, Ma X, Patel BA, Spitofsky N, Browne PV, Chien KS, Wu CO, DiNardo CD, Colla S, Calado RT, Young NS. U2AF1 and other splicing factor gene mutations in telomere biology disorders are associated with hematologic neoplasia and worse overall survival [Internet]. Blood. 2021 ; 138 862-864.[citado 2025 dez. 31 ] Available from: https://doi.org/10.1182/blood-2021-146946 - Variações da qPCR e seus usos
- Short telomeres result in chromosomal instability in hematopoietic cells and precede malignant evolution in human aplastic anemia
- Exome sequencing reveals a thrombopoietin ligand mutation in a Micronesian family with autosomal recessive aplastic anemia
- Telomerase variant A279T induces telomere dysfunction and inhibits non-canonical telomerase activity in esophageal carcinomas
- The future of aplastic anemia treatment in Brazil: lessons learned for global hematology
- Targeting complement to treat paroxysmal nocturnal hemoglobinuria (PNH)
- Telomere dynamics in mice and humans
- A mutation in the H/ACA box of telomerase RNA component gene (TERC) in a young patient with myelodysplastic syndrome
- Repeat course of rabbit antithymocyte globulin as salvage following initial therapy with rabbit antithymocyte globulin in acquired aplastic anemia
- Repeat course of rabbit antithymocyte globulin as salvage following initial therapy with rabbit antithymocyte globulin in acquired aplastic anemia. [Carta]
Informações sobre o DOI: 10.1182/blood-2021-146946 (Fonte: oaDOI API)
Download do texto completo
| Tipo | Nome | Link | |
|---|---|---|---|
 |
003237495.pdf |
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
