Thyroxine increases Serca2 and Ryr2 gene expression in heart failure rats with euthyroid sick syndrome

Autor: Fábio V. G. Campanha, Denise Perone, Dijon H. S. de Campos, Renata de A. M. Luvizotto, Maria T. De Síbio, Miriane de Oliveira, Regiane M. C. Olimpio, Fernanda C. F. Moretto, Carlos R. Padovani, Gláucia M. F. S. Mazeto, Antonio C. Cicogna, Célia R. Nogueira

Publikováno v: Archives of Endocrinology and Metabolism, Vol 60, Iss 6, Pp 582-586 (2016)

ABSTRACT Objective The current study was aimed at analyzing sarcoplasmic reticulum Ca2+ ATPase (Serca2) and ryanodine receptor type 2 (Ryr2) gene expression in rats subjected to surgery that induced HF and were subsequently treated with T4 using phys

Externí odkaz: https://doaj.org/article/82f57e02a05c4408b034c5b8045ca997

Thyroxine increases Serca2 and Ryr2 gene expression in heart failure rats with euthyroid sick syndrome

Autor: Regiane Marques Castro Olimpio, Gláucia Maria Ferreira da Silva Mazeto, Maria Teresa De Sibio, Antonio Carlos Cicogna, Miriane de Oliveira, Renata de Azevedo Melo Luvizotto, Dijon Henrique Salomé de Campos, Denise Perone, Célia Regina Nogueira, Carlos Roberto Padovani, Fábio V. G. Campanha, Fernanda Cristina Fontes Moretto

Publikováno v: Archives of Endocrinology and Metabolism, Vol 60, Iss 6, Pp 582-586 (2016)
Scopus
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP
Archives of Endocrinology and Metabolism v.60 n.6 2016
Arquivos de Endocrinologia e Metabolismo
Sociedade Brasileira de Endocrinologia e Metabologia (SBEM)
instacron:SBEM
Archives of Endocrinology and Metabolism, Volume: 60, Issue: 6, Pages: 582-586, Published: 10 OCT 2016

Made available in DSpace on 2018-12-11T17:08:19Z (GMT). No. of bitstreams: 0 Previous issue date: 2016-01-01. Added 1 bitstream(s) on 2019-10-09T18:30:42Z : No. of bitstreams: 1 S2359-39972016000600582.pdf: 208346 bytes, checksum: d4024e8a967f9479c53

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c2f80a6c91a454e1744b2e2e3e2abc5
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S2359-39972016000600582&lng=en&tlng=en

Frequency of multiple endocrine neoplasia type 1 in a group of patients with pituitary adenoma: genetic study and familial screening

Autor: Vânia dos Santos Nunes, G. L. Souza, Denise Perone, Célia Regina Nogueira, Sandro José Conde

Publikováno v: Pituitary. 17:30-37

The purpose of this study it was to evaluate the frequency of Multiple Endocrine Neoplasia type 1 (MEN1) in patients with pituitary adenoma and to perform genetic analysis and familial screening of those individuals afflicted with MEN1. 144 patients

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f8626eb52eb620969886bb45fa2f1e1d
https://doi.org/10.1007/s11102-013-0462-8

Low Triiodothyronine (T3) or Reverse Triiodothyronine (rT3) Syndrome Modifies Gene Expression in Rats With Congestive Heart Failure

Autor: R. C. M. Bauab, Célia Regina Nogueira, Antonio Carlos Cicogna, Ana Valeria B. Castro, Denise Perone

Publikováno v: Endocrine Research. 31:397-405

Heart failure (HF) is frequently associated with euthyroid "sick" syndrome (low T3 and elevated rT3). We investigated if altered thyroid hormone in HF could affect expression of the TH receptor (TRalpha1), and alpha and beta myosin heavy chains (alph

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd58cea17e441158faab3fb7377532b0
https://doi.org/10.1080/07435800500467942

'Avaliação do envolvimento dos genes PAX8 e rTSH no hipotireoidismo congênito em pacientes com disgenesia tireoidiana'

Autor: Denise Perone

Publikováno v: Biblioteca Digital de Teses e Dissertações da USPUniversidade de São PauloUSP.

Estudamos 32 crianças com HC devido à agenesia ou ectopia tireoideana para mutações no PAX8 e 30 crianças com hipoplasia da tireóide para mutações no rTSH. Todos os exons de ambos os genes foram amplificados a partir do DNA genômico, seguido

Externí odkaz: http://www.teses.usp.br/teses/disponiveis/5/5135/tde-05082005-125433/