DLK1 Is a Novel Link Between Reproduction and Metabolism (2019)
- Authors:
- USP affiliated authors: MONTENEGRO, LUCIANA RIBEIRO - FM ; MACIEL, GUSTAVO ARANTES ROSA - FM ; BARACAT, EDMUND CHADA - FM ; JORGE, ALEXANDER AUGUSTO DE LIMA - FM ; MENDONÇA, BERENICE BILHARINHO DE - FM ; XAVIER, ANA CLAUDIA LATRÔNICO - FM
- Unidade: FM
- DOI: 10.1210/jc.2018-02010
- Subjects: PUBERDADE PRECOCE; MUTAÇÃO GENÉTICA; PROTEÍNAS DA MEMBRANA; DIFERENCIAÇÃO CELULAR; TECIDO ADIPOSO; GANHO DE PESO; HIPERLIPIDEMIA
- Agências de fomento:
- Language: Inglês
- Imprenta:
- Publisher place: Washington
- Date published: 2019
- Source:
- Título: Journal of clinical endocrinology & metabolism
- ISSN: 0021-972X
- Volume/Número/Paginação/Ano: v. 104, n. 6, p. 2112-2120, 2019
- Status:
- Artigo possui acesso gratuito no site do editor (Bronze Open Access)
- Versão do Documento:
- Versão publicada (Published version)
- Acessar versão aberta:
-
ABNT
GAMES, Larissa G et al. DLK1 Is a Novel Link Between Reproduction and Metabolism. Journal of clinical endocrinology & metabolism, v. 104, n. 6, p. 2112-2120, 2019Tradução . . Disponível em: https://doi.org/10.1210/jc.2018-02010. Acesso em: 14 abr. 2026. -
APA
Games, L. G., Cunha-silva, M., Crespo, R. P., Ramos, C. O., Montenegro, L. R., Maciel, G. A. R., et al. (2019). DLK1 Is a Novel Link Between Reproduction and Metabolism. Journal of clinical endocrinology & metabolism, 104( 6), 2112-2120. doi:10.1210/jc.2018-02010 -
NLM
Games LG, Cunha-silva M, Crespo RP, Ramos CO, Montenegro LR, Maciel GAR, Baracat EC, Jorge AA de L, Mendonça BB de, Xavier ACL. DLK1 Is a Novel Link Between Reproduction and Metabolism [Internet]. Journal of clinical endocrinology & metabolism. 2019 ; 104( 6): 2112-2120.[citado 2026 abr. 14 ] Available from: https://doi.org/10.1210/jc.2018-02010 -
Vancouver
Games LG, Cunha-silva M, Crespo RP, Ramos CO, Montenegro LR, Maciel GAR, Baracat EC, Jorge AA de L, Mendonça BB de, Xavier ACL. DLK1 Is a Novel Link Between Reproduction and Metabolism [Internet]. Journal of clinical endocrinology & metabolism. 2019 ; 104( 6): 2112-2120.[citado 2026 abr. 14 ] Available from: https://doi.org/10.1210/jc.2018-02010 - Clinical and Genetic Characterization of Familial Central Precocious Puberty
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- Two rare loss-of-function variants in the STAG3 gene leading to primary ovarian insufficiency
- High Frequency of MKRN3 Mutations in Male Central Precocious Puberty Previously Classified as Idiopathic
- Loss-of-function mutations in a gene cause central precocius puberty
- Paternally inherited DLK1 deletion as novel cause of familial central precocious puberty
- Central Precocious Puberty Caused by a Heterozygous Deletion in the MKRN3 Promoter Region
- Novel mutations (P.G6R and P.R511W) in IGF1R gene in children born small for gestational age (SGA) without catch-up growth
- Contribution of Clinical and Genetic Approaches for Diagnosing 209 Index Cases With 46,XY Differences of Sex Development
- Novel OTX2 loss of function variant associated with congenital hypopituitarism without eye abnormalities
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