نتائج البحث - "Denise Perone"

المصدر: 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

مصطلحات موضوعية: Male, 0301 basic medicine, medicine.medical_specialty, Endocrinology, Diabetes and Metabolism, medicine.medical_treatment, Gene Expression, heart failure, lcsh:Medicine, Heart failure, 030204 cardiovascular system & hematology, Ryanodine receptor 2, lcsh:Diseases of the endocrine glands. Clinical endocrinology, Sarcoplasmic Reticulum Calcium-Transporting ATPases, 03 medical and health sciences, chemistry.chemical_compound, 0302 clinical medicine, Internal medicine, medicine.artery, calcium channels, triiodothyronine, medicine, Animals, Thoracic aorta, RNA, Messenger, Thoracotomy, Rats, Wistar, Triiodothyronine, lcsh:RC648-665, business.industry, lcsh:R, Therapeutic use, Ryanodine Receptor Calcium Release Channel, Reverse triiodothyronine, Aortic Valve Stenosis, medicine.disease, Euthyroid Sick Syndromes, Thyroxine, Calcium channels, 030104 developmental biology, Endocrinology, chemistry, Aortic valve stenosis, therapeutic use, Models, Animal, business, Euthyroid sick syndrome

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4

Estrogen-Responsive Genes Overlap with Triiodothyronine-Responsive Genes in a Breast Carcinoma Cell Line

المؤلفون: Sílvia Helena Cestari, Denise Perone, Sandro José Conde, Dirce Maria Carraro, Célia Regina Nogueira, Maria Mitzi Brentani, Helena Brentani, Renata de Azevedo Melo Luvizotto, Maria Lucia Hirata Katayama, Nancy Bueno Figueiredo, Maria Teresa De Sibio

المساهمون: Universidade Estadual Paulista (Unesp), Universidade de São Paulo (USP), AC Camargo Hosp

المصدر: Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Celia Regina Nogueira
The Scientific World Journal
Web of Science
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP
The Scientific World Journal, Vol 2014 (2014)

مصطلحات موضوعية: Article Subject, Microarray, medicine.drug_class, lcsh:Medicine, Breast Neoplasms, Biology, Real-Time Polymerase Chain Reaction, lcsh:Technology, General Biochemistry, Genetics and Molecular Biology, Breast cancer, parasitic diseases, Gene expression, medicine, Humans, lcsh:Science, Gene, Oligonucleotide Array Sequence Analysis, General Environmental Science, Regulation of gene expression, lcsh:T, Reverse Transcriptase Polymerase Chain Reaction, lcsh:R, Carcinoma, EXPRESSÃO GÊNICA, Estrogens, General Medicine, medicine.disease, Molecular biology, Gene Expression Regulation, Neoplastic, Real-time polymerase chain reaction, Estrogen, MCF-7 Cells, Cancer research, Triiodothyronine, lcsh:Q, Female, Breast carcinoma, Research Article

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https://doi.org/10.1155/2014/969404

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5

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

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

المصدر: Pituitary. 17:30-37

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

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6

Analysis of the PAX8 gene in 32 children with thyroid dysgenesis and functional characterization of a promoter variant

المؤلفون: Geraldo Medeiros-Neto, Peter Kopp, Antônio J. Chagas, Denise Perone, Vera M. A. Dias, Maria de Fátima S. Viana, Célia Regina Nogueira

المصدر: Journal of pediatric endocrinologymetabolism : JPEM. 29(2)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9445db0e8a49ef1b05e6c30a5fde5c91
https://pubmed.ncbi.nlm.nih.gov/26495924

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7

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

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

المصدر: Endocrine Research. 31:397-405

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

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Molecular analysis of the Von Hippel-Lindau (VHL) gene in a family with non-syndromic pheochromocytoma: the importance of genetic testing

المؤلفون: Sueli A. Clara, Sandro José Conde, Juliana B. Cruz, Denise Perone, Peter Kopp, Célia Regina Nogueira, Leonardo Parr dos Santos Fernandes

المساهمون: Universidade Estadual Paulista (Unesp), Northwestern University (NU)

المصدر: Arquivos Brasileiros de Endocrinologia & Metabologia, Volume: 51, Issue: 9, Pages: 1463-1467, Published: DEC 2007
Arquivos Brasileiros de Endocrinologia & Metabologia v.51 n.9 2007
Arquivos Brasileiros de Endocrinologia & Metabologia
Sociedade Brasileira de Endocrinologia e Metabologia (SBEM)
instacron:SBEM
SciELO
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP

مصطلحات موضوعية: Oncology, Proband, Male, Von Hippel-Lindau disease, medicine.medical_specialty, Pathology, von Hippel-Lindau Disease, Genetic testing, endocrine system diseases, Adolescent, Doença de Von Hippel-Lindau, Endocrinology, Diabetes and Metabolism, Adrenal Gland Neoplasms, Mutation, Missense, Pheochromocytoma, Asymptomatic, Polymerase Chain Reaction, Germline mutation, Pre-Eclampsia, Pregnancy, Internal medicine, medicine, Humans, Von Hippel–Lindau disease, Child, Germ-Line Mutation, Mutação, medicine.diagnostic_test, Base Sequence, business.industry, General Medicine, Metanephrines, medicine.disease, Pedigree, Feocromocitoma, Von Hippel-Lindau Tumor Suppressor Protein, Mutation (genetic algorithm), Mutation, Female, medicine.symptom, business, Teste genético

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http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-27302007000900008&lng=en&tlng=en

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PAX8 and rTSH genes involvement in congenital hypothyrodism in patients with thyroid dysgenesis

المؤلفون: Denise Perone

المساهمون: Geraldo Antonio de Medeiros Neto, Célia Regina Nogueira, Tânia Aparecida Sartori Sanchez Bachega, Reinaldo Perrone Furlanetto, Meyer Knobel, Carlos Alberto Longui

المصدر: Biblioteca Digital de Teses e Dissertações da USP
Universidade de São Paulo (USP)
instacron:USP

مصطلحات موضوعية: Biology

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1c3efb858c3ca5fd30954f2ceb9bd9d

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[Genetic aspects in congenital hypothyrodism]

المؤلفون: Denise, Perone, Silvânia S, Teixeira, Sueli A, Clara, Daniela C dos, Santos, Célia R, Nogueira

المصدر: Arquivos brasileiros de endocrinologia e metabologia. 48(1)

مصطلحات موضوعية: Hypothyroidism, Congenital Hypothyroidism, Humans

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::d169752c3ee74d3175fa905efc5863b6
https://pubmed.ncbi.nlm.nih.gov/15611819

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