Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Tatiana S. Pelaes"'
Autor:
Maria Beatriz Monteiro, Tatiana S. Pelaes, Daniele P. Santos-Bezerra, Karina Thieme, Antonio M. Lerario, Sueli M. Oba-Shinjo, Ubiratan F. Machado, Marisa Passarelli, Suely K. N. Marie, Maria Lúcia Corrêa-Giannella
Publikováno v:
Frontiers in Endocrinology, Vol 11 (2020)
Introduction: Using a discovery/validation approach we investigated associations between a panel of genes selected from a transcriptomic study and the estimated glomerular filtration rate (eGFR) decline across time in a cohort of type 1 diabetes (T1D
Externí odkaz:
https://doaj.org/article/5a4e3390fcd54a8196ea42af99e1dff6
Autor:
Daniele P. Santos-Bezerra, Aritania S. Santos, Gabriel C. Guimarães, Sharon N. Admoni, Ricardo V. Perez, Cleide G. Machado, Tatiana S. Pelaes, Marisa Passarelli, Ubiratan F. Machado, Marcia S. Queiroz, Maria Elizabeth R. da Silva, Maria Lucia Correa-Giannella
Publikováno v:
Frontiers in Endocrinology, Vol 10 (2019)
Objective: To compare the serum micro-RNAs (miRNAs) profile of individuals with type 1 diabetes without microvascular complications vs. those with multiple severe microvascular complications, in order to identify epigenetically modulated pathways in
Externí odkaz:
https://doaj.org/article/8bf04c94bc564131b053d915eb8dbc84
Genetic variants in DNMT1 and the risk of cardiac autonomic neuropathy in women with type 1 diabetes
Autor:
Maria Candida Ribeiro Parisi, Tatiana S. Pelaes, Cleide Guimarães Machado, Daniele Pereira Santos-Bezerra, Maria Beatriz Monteiro, Elizabeth João Pavin, Ubiratan Fabres Machado, Marisa Passarelli, Márcia Silva Queiroz, Ricardo Vesoni Perez, Rosana Cristina Tieko Mori, Maria Lúcia Corrêa-Giannella, Sharon Nina Admoni
Publikováno v:
Journal of Diabetes Investigation, Vol 10, Iss 4, Pp 985-989 (2019)
Journal of Diabetes Investigation
Journal of Diabetes Investigation
Aims/Introduction Epigenetics participate in the pathogenesis of metabolic memory, a situation in which hyperglycemia exerts prolonged deleterious effects even after its normalization. We tested the hypothesis that genetic variants in an epigenetic g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1943a76cc16f062b1e0ea6c12a0e10e0
https://doaj.org/article/a12e2c6a042d43d98e39dfcebac8cc10
https://doaj.org/article/a12e2c6a042d43d98e39dfcebac8cc10
Autor:
Tatiana S. Pelaes, Maria Lúcia Corrêa-Giannella, Vishal S. Vaidya, Daniele Pereira Santos-Bezerra, Maria Beatriz Monteiro
Publikováno v:
Clin Chem
To the Editor: Diabetic kidney disease (DKD)1 is the leading cause of end-stage renal disease worldwide (1). Microalbuminuria is the earliest indicator of DKD in diabetes mellitus (DM). Microalbuminuria is clinically sensitive but not specific to thi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f9198347f62ca99aa9a3f23d368184ce
https://pubmed.ncbi.nlm.nih.gov/31427290
https://pubmed.ncbi.nlm.nih.gov/31427290
Autor:
Ricardo Vessoni Perez, Cleide Guimarães Machado, Maria Lúcia Corrêa-Giannella, Tatiana S. Pelaes, Rosana Cristina Tieko Mori, Ubiratan Fabres Machado, Sharon Nina Admoni, Maria Beatriz Monteiro, Márcia Silva Queiroz, Daniele Pereira Santos-Bezerra
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 AND AIM 11β-Hydroxysteroid dehydrogenase 1 has been implicated in insulin resistance (IR) in the setting of metabolic disorders, and single nucleotide polymorphisms (SNPs) in its encoding gene (HSD11B1) have been associated with type 2 di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e04a10ba09836ea3f2653dc3c6a5bed
https://pubmed.ncbi.nlm.nih.gov/32453474
https://pubmed.ncbi.nlm.nih.gov/32453474
Autor:
Márcia Silva Queiroz, Silvia M. Titan, Marcia Nery, Aécio Lopes de Araújo Lira, Tatiana S. Pelaes, Carolina C. R. Betônico, Maria Lúcia Corrêa-Giannella
Publikováno v:
Clinical Therapeutics. 41:2008-2020.e3
Purpose Glycemic control in patients with chronic kidney disease (CKD) is particularly hard to achieve because of a slower insulin degradation by the kidney. It might modify the long-acting insulin analogue pharmacokinetics, increasing its time–act
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6078792fce290dfab15df25d5d92566
https://doi.org/10.1016/j.clinthera.2019.07.011
https://doi.org/10.1016/j.clinthera.2019.07.011
Autor:
Regina Matsunaga Martin, Sorahia Domenice, Rodrigo Rocha Codarin, P.H.M. Bianchi, Luciane Carneiro de Carvalho, Tatiana S. Pelaes, Berenice B. Mendonca, Marlene Inácio, Elaine Maria Frade Costa, Gabriela Romanenghi Fanti Carvalho Araujo Gouveia, Rossana Pulcineli Vieira Francisco, Paulo C. Serafini, Edmund Chada Baracat, Maria Beatriz Sator de Faria
Publikováno v:
The Journal of clinical endocrinology and metabolism. 101(2)
Congenital adrenal hyperplasia (CAH) due to 17α-hydroxylase deficiency in 46,XX patients is characterized by primary amenorrhea, absent or incomplete sexual maturation, infertility, low serum levels of estradiol, and elevated progesterone (P). There
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17d45bda6c59fea803f3ab9409b96120
https://pubmed.ncbi.nlm.nih.gov/26647153
https://pubmed.ncbi.nlm.nih.gov/26647153