Molecular and gene network analysis of thyroid transcription factor 1(TFF1) and enhanced at puberty (EAP1) gene in patients with GnRH-dependent pubertal disorders (2013)
- Authors:
- USP affiliated authors: MENDONÇA, BERENICE BILHARINHO DE - FM ; XAVIER, ANA CLAUDIA LATRÔNICO - FM
- Unidade: FM
- Subjects: PUBERDADE (ANORMALIDADES); GONADOTROFINAS; EXPRESSÃO GÊNICA; HIPOGONADISMO
- Language: Inglês
- Imprenta:
- Source:
- Título: Hormone Research in Paediatrics
- ISSN: 1663-2818
- Volume/Número/Paginação/Ano: v. 80, n. 2, p. 257-266, 2013
-
ABNT
CUKIER, Priscilla et al. Molecular and gene network analysis of thyroid transcription factor 1(TFF1) and enhanced at puberty (EAP1) gene in patients with GnRH-dependent pubertal disorders. Hormone Research in Paediatrics, v. 80, n. 2, p. 257-266, 2013Tradução . . Disponível em: http://www.karger.com/Article/FullText/354643. Acesso em: 25 jan. 2026. -
APA
Cukier, P., Wright, H., Rulfs, T., Silveira, L. F. G., Teles, M. G., Mendonça, B. B. de, et al. (2013). Molecular and gene network analysis of thyroid transcription factor 1(TFF1) and enhanced at puberty (EAP1) gene in patients with GnRH-dependent pubertal disorders. Hormone Research in Paediatrics, 80( 2), 257-266. Recuperado de http://www.karger.com/Article/FullText/354643 -
NLM
Cukier P, Wright H, Rulfs T, Silveira LFG, Teles MG, Mendonça BB de, Arnhold IJP, Heger S, Xavier ACL, Ojeba SR, Brito VN. Molecular and gene network analysis of thyroid transcription factor 1(TFF1) and enhanced at puberty (EAP1) gene in patients with GnRH-dependent pubertal disorders [Internet]. Hormone Research in Paediatrics. 2013 ; 80( 2): 257-266.[citado 2026 jan. 25 ] Available from: http://www.karger.com/Article/FullText/354643 -
Vancouver
Cukier P, Wright H, Rulfs T, Silveira LFG, Teles MG, Mendonça BB de, Arnhold IJP, Heger S, Xavier ACL, Ojeba SR, Brito VN. Molecular and gene network analysis of thyroid transcription factor 1(TFF1) and enhanced at puberty (EAP1) gene in patients with GnRH-dependent pubertal disorders [Internet]. Hormone Research in Paediatrics. 2013 ; 80( 2): 257-266.[citado 2026 jan. 25 ] Available from: http://www.karger.com/Article/FullText/354643 - Methylome profiling of healthy and central precocious puberty girls
- Mutational analysis of the necdin gene in patients with congenital isolated hypogonadotropic hypogonadism
- New mutation at GNAS1 in a man with progressive osseous heteroplasia-like heterotopic ossification and pseudo-pseudohypoparathyroidism
- Avanços na etiologia, no diagnóstico e no tratamento da puberdade precoce central
- Mutação na subunidade alfa da proteína G em paciente com heteroplasia óssea hereditária e estigmas da osteodistrofia de Albright
- Mutação ativadora do gene KISSI em um menino com puberdade precoce dependente de gonadotrofinas idiopática
- Phenotype–Genotype Correlations in Patients with Inactivating Gonadotropin Hormone Receptor Mutations
- Analysis of LH determination 2 hours after depot leuprolide acetate in monitoring gonadotropin-dependent precocious puberty treatment
- Novel mutation in the gonadotropin-releasing hormone receptor (GNRHR) gene in a patient with normosmic isolated hypogonadotropic hypogonadism
- Anthropometric, metabolic and reproductive outcome of patients with central precocious puberty due to hypothalamic hamartoma in adult life
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas