A mutation in the CCAAT box of the TERC promoter region causes telomere disease (2011)
- Authors:
- Autor USP: RODRIGUES, RODRIGO DO TOCANTINS CALADO DE SALOMA - FMRP
- Unidade: FMRP
- Subjects: CROMOSSOMOS; MUTAÇÃO GENÉTICA
- Language: Inglês
- Imprenta:
- Source:
- Título: Abstracts
- Conference titles: Meeting of the Telomeres & Telomerase
-
ABNT
AALBERS, Anna M. et al. A mutation in the CCAAT box of the TERC promoter region causes telomere disease. 2011, Anais.. New York: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, 2011. . Acesso em: 15 mar. 2026. -
APA
Aalbers, A. M., Kajigaya, S., Heuvel, M. M. van den, Velden, V. van der, Zwaan, M., Pieters, R., et al. (2011). A mutation in the CCAAT box of the TERC promoter region causes telomere disease. In Abstracts. New York: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. -
NLM
Aalbers AM, Kajigaya S, Heuvel MM van den, Velden V van der, Zwaan M, Pieters R, Calado RT, Young NS. A mutation in the CCAAT box of the TERC promoter region causes telomere disease. Abstracts. 2011 ;[citado 2026 mar. 15 ] -
Vancouver
Aalbers AM, Kajigaya S, Heuvel MM van den, Velden V van der, Zwaan M, Pieters R, Calado RT, Young NS. A mutation in the CCAAT box of the TERC promoter region causes telomere disease. Abstracts. 2011 ;[citado 2026 mar. 15 ] - 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
- Exome sequencing reveals a thrombopoietin ligand mutation in a Micronesian family with autosomal recessive 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]
- Telomeres in disease
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