Exome sequencing reveals a thrombopoietin ligand mutation in a Micronesian family with autosomal recessive aplastic anemia (2013)
- Authors:
- Autor USP: RODRIGUES, RODRIGO DO TOCANTINS CALADO DE SALOMA - FMRP
- Unidade: FMRP
- DOI: 10.1182/blood-2012-12-473538
- Subjects: ANEMIA (QUIMIOTERAPIA); MUTAÇÃO GENÉTICA; HIBRIDIZAÇÃO
- Language: Inglês
- Imprenta:
- Publisher place: Washington
- Date published: 2013
- Source:
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
-
ABNT
DASOUKI, Majed J. et al. Exome sequencing reveals a thrombopoietin ligand mutation in a Micronesian family with autosomal recessive aplastic anemia. Blood, v. 122, n. 20, p. 3440-3449, 2013Tradução . . Disponível em: https://doi.org/10.1182/blood-2012-12-473538. Acesso em: 15 fev. 2026. -
APA
Dasouki, M. J., Rafi, S. K., Olm-Shipman, A. J., Wilson, N. R., Abhyankar, S., Ganter, B., et al. (2013). Exome sequencing reveals a thrombopoietin ligand mutation in a Micronesian family with autosomal recessive aplastic anemia. Blood, 122( 20), 3440-3449. doi:10.1182/blood-2012-12-473538 -
NLM
Dasouki MJ, Rafi SK, Olm-Shipman AJ, Wilson NR, Abhyankar S, Ganter B, Furness LM, Fang J, Calado RT, Saadi I. Exome sequencing reveals a thrombopoietin ligand mutation in a Micronesian family with autosomal recessive aplastic anemia [Internet]. Blood. 2013 ; 122( 20): 3440-3449.[citado 2026 fev. 15 ] Available from: https://doi.org/10.1182/blood-2012-12-473538 -
Vancouver
Dasouki MJ, Rafi SK, Olm-Shipman AJ, Wilson NR, Abhyankar S, Ganter B, Furness LM, Fang J, Calado RT, Saadi I. Exome sequencing reveals a thrombopoietin ligand mutation in a Micronesian family with autosomal recessive aplastic anemia [Internet]. Blood. 2013 ; 122( 20): 3440-3449.[citado 2026 fev. 15 ] Available from: https://doi.org/10.1182/blood-2012-12-473538 - Defective telomere elongation and hematopoiesis from telomerase-mutant aplastic anemia iPSCs
- Cell senescence and malignant transformation in the inherited bone marrow failure syndromes: overlapping pathophysiology with therapeutic implications
- Short telomeres result in chromosomal instability in hematopoietic cells and precede malignant evolution in human aplastic anemia
- Telomere shortening in hepatocyte proliferation and predisposition to alcohol-induced steatosis
- Telomerase enzyme deficiency promotes metabolic dysfunction in murine hepatocytes upon dietary stress
- Telomere dynamics in iPS cells derived from human patients with telomerase mutations
- Predictors of early mortality after rabbit antithymocyte globulin as first-line treatment in severe aplastic anemia
- Células reprogramadas. [Depoimento a Hérika Dias e Luis Ribeiro]
- A mutation in the CCAAT box of the TERC promoter region causes telomere disease
- Telomeres in disease
Informações sobre o DOI: 10.1182/blood-2012-12-473538 (Fonte: oaDOI API)
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