Zobrazeno 1 - 10
of 31
pro vyhledávání: '"F. Richeti"'
Autor:
Mirna Duarte Barros, Carla Sant`Anna Correa, F. Richeti, Carlos Alberto Longui, Ieda Millas, Rodrigo Nishihara Jorge
Publikováno v:
International Journal of Morphology v.39 n.4 2021
SciELO Chile
CONICYT Chile
instacron:CONICYT
SciELO Chile
CONICYT Chile
instacron:CONICYT
SUMMARY: Estrogen receptors (ER) have been identified in human nasal mucosa, but its physiologic and pathologic impacts are not totally established. ER have been demonstrated in nasal mucosa by several authors, mainly by immunohistochemical method in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34419dbdbc7297edc3b7ee938b150817
https://doi.org/10.4067/s0717-95022021000401147
https://doi.org/10.4067/s0717-95022021000401147
Autor:
J. Q. de Souza Leão, Tatiane Sousa e Silva, D.P.P. S. Cunha, Carlos Alberto Longui, A.C. M. Amarante, F. Richeti
Publikováno v:
Hormone and Metabolic Research. 45:495-500
Androgen action is exerted through the androgen receptor. The normal 46,XY genital virilization depends on androgen receptor gene expression, which is tissue specific, and requires normal androgen receptor mRNA levels in androgen sensitive tissues. H
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e13905990b48c7952d6f7297a61234df
https://doi.org/10.1055/s-0033-1333717
https://doi.org/10.1055/s-0033-1333717
Autor:
R F Mendonça, Cristiane Kochi, M N Rocha, Carlos Alberto Longui, R M Guazzelli, C Sant'Anna Corrêa, F. Richeti, R Lazzarini, Murilo Rezende Melo
Publikováno v:
Genetics and Molecular Research. 12:1834-1840
Normal testosterone levels are frequently observed in women with androgenetic alopecia (AGA), suggesting the involvement of androgen sensitivity in this condition. Androgen sensitivity is related to androgen receptor (AR) messenger RNA (mRNA) product
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3ef57689a10524933a2099734bda9391
https://doi.org/10.4238/2013.february.28.19
https://doi.org/10.4238/2013.february.28.19
Autor:
Cristiane Kochi, C. S. A. Corrêa, Carlos Alberto Longui, F. Richeti, C. D. C. Faria, M N Rocha, Murilo Rezende Melo
Publikováno v:
Hormone and Metabolic Research. 42:677-681
Turner syndrome (TS) is the complete or partial loss of the second sex chromosome, occurring in 1:5 000 girls. Early recognition allows appropriate therapy for short stature and puberty. Neonatal diagnosis of TS permits detection of associated malfor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0d3d32f31eacc9cbe4777799cf26833
https://doi.org/10.1055/s-0030-1253351
https://doi.org/10.1055/s-0030-1253351
Autor:
M N Rocha, L.A. Silva e Lima, Cristiane Kochi, S.C. Corrêa, Carlos Alberto Longui, Maísa Lamounier Magalhães, F. Richeti
Publikováno v:
Genetics and molecular research : GMR. 13(4)
Turner syndrome (TS) is characterized by the presence of one full X chromosome and total or partial deletion of the second sex chromosome. Diagnosis of TS is often delayed, resulting in inappropriate treatment. Early diagnosis of TS using a neonatal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f3219cc8a4f60fae5962c2e6239da6b
https://pubmed.ncbi.nlm.nih.gov/25366798
https://pubmed.ncbi.nlm.nih.gov/25366798
Autor:
Carlos Alberto Longui, M N Rocha, E G Chamlian, Cláudia Dutra Costantin Faria, W L Pereira, L A Rivetti, Murilo Rezende Melo, R. B. Castro, T S Silva, F. Richeti
Publikováno v:
Genetics and molecular research : GMR. 11(4)
Insulin resistance is an underlying cause of metabolic changes associated with cardiovascular diseases. Glucocorticoids are known determinant factors of insulin resistance. We quantified glucocorticoid receptor alpha (GRα) mRNA and 11 beta-hydroxyst
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd524cadeb1de4a8f60ba09a320614ca
https://pubmed.ncbi.nlm.nih.gov/23212335
https://pubmed.ncbi.nlm.nih.gov/23212335
Autor:
M N Rocha, C.C. Umbelino, Niro Kasahara, F. Richeti, Vital Paulino Costa, Anderson Tavares, Maurício Della Paolera, José Paulo Cabral de Vasconcellos, M B Melo
Publikováno v:
Journal of glaucoma. 19(3)
Purpose To determine the spectrum of CYP1B1 gene mutations in Brazilian patients with primary congenital glaucoma, and to correlate the presence of alterations in the CYP1B1 gene sequence with clinical aspects of the disease. Materials and methods Th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::640bb1b8624918a7013b2bbf9a5d0276
https://pubmed.ncbi.nlm.nih.gov/19528825
https://pubmed.ncbi.nlm.nih.gov/19528825
Autor:
Geraldo Vicente de Almeida, Carmo Mandia, Cristiano Caixeta-Umbelino, M B Melo, Niro Kasahara, Vital Paulino Costa, José Paulo Cabral de Vasconcellos, F. Richeti, Carlos Alberto Longui, Maurício Della Paolera, Ralph Cohen, M N Rocha
Publikováno v:
Ophthalmic genetics. 30(1)
Purpose: To verify the frequencies of T34T, E50K, M98K, 691_692insAG, and R545Q variants in the optineurin (OPTN) gene in Brazilian subjects with primary open-angle glaucoma (POAG) and controls. Patients and Methods: Ninety-nine patients with POAG an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3de4bcedb17fdf38b29ff93d989f7777
https://pubmed.ncbi.nlm.nih.gov/19172505
https://pubmed.ncbi.nlm.nih.gov/19172505
Akademický článek
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Autor:
Osmar Monte, Luis Eduardo Calliari, Cristiane Kochi, Carlos Alberto Longui, N M A Evangelista, C C Figueiredo, F. Richeti, M N Rocha
Publikováno v:
Scopus-Elsevier
Turner syndrome (TS) is one of the most common chromosomal abnormalities among girls. Complete monosomy of X chromosome is responsible for almost 50% of all cases of TS, and mosaicism and X anomaly are detected in the other half. It has already been
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a769758176a625ba11d8a5ff6aaeaac3
http://www.scopus.com/inward/record.url?eid=2-s2.0-40749107046&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-40749107046&partnerID=MN8TOARS
