Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Priscilla Cukier"'
Autor:
Marcos Tadashi Kakitani Toyoshima, Priscilla Cukier, Alexandre Barbosa Câmara de Souza, Juliana Pereira, Ana Oliveira Hoff, Marcia Nery
Publikováno v:
Einstein (São Paulo), Vol 20 (2022)
ABSTRACT Objective To analyze interstitial glucose behavior during glucocorticoid use in non-diabetic patients receiving chemotherapy for hematologic malignancies. Methods Prospective pilot study carried out to assess interstitial glucose levels in 1
Externí odkaz:
https://doaj.org/article/a933f1d0330841ffb8f3dfde69959145
Autor:
Priscilla Cukier
Publikováno v:
Biblioteca Digital de Teses e Dissertações da USPUniversidade de São PauloUSP.
O mecanismo de controle da secreção de GnRH inclui diversas vias neuronais. Estudos em modelos animais identificaram genes que codificam fatores de transcrição, tais como TTF-1 (thyroid transcription factor 1) e EAP1 (enhanced at puberty), que at
Autor:
Matheo Stumpf, Laís Lins, Priscilla Cukier, Márcia Nery, Maria Giannella, Maria Rossi da Silva
Publikováno v:
Revista Portuguesa de Endocrinologia, Diabetes e Metabolismo.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8b86da67425025843593d712ad561c7a
https://doi.org/10.26497/cc220052
https://doi.org/10.26497/cc220052
Autor:
Nathalia Lisboa Gomes, Maria Tereza Martins Ferrari, Andreia Watanabe, Mirian Yumie Nishi, Luiz F. Onuchic, Leila Cristina Pedroso de Paula, Rafael Loch Batista, Thatiane E da Silva, Berenice B. Mendonca, Priscilla Cukier, Elaine Maria Frade Costa, Sorahia Domenice, Eduardo Castro da Costa
Publikováno v:
Sexual Development. 16:46-54
Wilms’ tumor suppressor gene 1 (WT1) plays an essential role in urogenital and kidney development. Heterozygous germline pathogenic allelic variants of WT1 have been classically associated with Denys–Drash syndrome (DDS) and Frasier syndrome (FS)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84e9eddd84fe3c3041f24f750b1cc0ab
https://doi.org/10.1159/000517373
https://doi.org/10.1159/000517373
Autor:
Ana Claudia Latronico, Berenice B. Mendonca, Marina Cunha-Silva, Priscilla Cukier, Ivo J.P. Arnhold, Danielle S Bessa, Vinicius Nahime Brito, Delanie B. Macedo, Carolina Ramos
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
Background: Hypothalamic hamartoma (HH) represents the commonest cause of organic central precocious puberty (CPP). Follow-up of these patients in adulthood is scarce. Objective: To describe the anthropometric, metabolic, and reproductive parameters
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7b9ea75296ebc5872b224e61a1e73e6
Akademický článek
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Publikováno v:
Endocrine-related cancer. 24(12)
Immune checkpoint inhibitors have recently become a cornerstone for the treatment of different advanced cancers. These drugs, represented mainly by monoclonal antibodies anti-cytotoxic T-lymphocyte antigen 4 (CTLA-4), anti-programmed cell death prote
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bfc7be3668e6ced25a3834354a666f4f
https://pubmed.ncbi.nlm.nih.gov/29025857
https://pubmed.ncbi.nlm.nih.gov/29025857
Autor:
Andrew Dauber, Delanie B. Macedo, Ana Claudia S. Reis, Sonir Roberto Rauber Antonini, Guilherme Guaragna Filho, Leticia Ferreira Gontijo Silveira, Berenice B. Mendonca, Ana Paula Abreu, Daiane Beneduzzi, Ivo J.P. Arnhold, Zoran Gucev, Ayrton Custódio Moreira, Vinicius Nahime Brito, Carlos Eduardo Martinelli, Milena Gurgel Teles, Ursula B. Kaiser, Gil Guerra Júnior, Margaret de Castro, Luciana Ribeiro Montenegro, Joel N. Hirschhorn, Priscilla Cukier, Rona S. Carroll, Ana Claudia Latronico
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
Context: Loss-of-function mutations in makorin ring finger 3 (MKRN3), an imprinted gene located on the long arm of chromosome 15, have been recognized recently as a cause of familial central precocious puberty (CPP) in humans. MKRN3 has a potential i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cfcf7f420c32191733d52b251e4297a8
https://doi.org/10.1210/jc.2013-3126
https://doi.org/10.1210/jc.2013-3126
Autor:
Delanie B. Macedo, Ana Claudia Latronico, Priscilla Cukier, Berenice B. Mendonca, Vinicius Nahime Brito
Publikováno v:
Arquivos Brasileiros de Endocrinologia & Metabologia v.58 n.2 2014
Arquivos Brasileiros de Endocrinologia & Metabologia
Sociedade Brasileira de Endocrinologia e Metabologia (SBEM)
instacron:SBEM
Arquivos Brasileiros de Endocrinologia & Metabologia
Sociedade Brasileira de Endocrinologia e Metabologia (SBEM)
instacron:SBEM
The onset of puberty is first detected as an increase in the amplitude and frequency of pulses of gonadotropin-releasing hormone (GnRH) after a quiescent period during childhood. The reemergence of pulsatile GnRH secretion leads to increases in the s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0dc42a471927a3599179a833cb4b8c3a
https://doi.org/10.1590/0004-2730000002931
https://doi.org/10.1590/0004-2730000002931