Allelic variations in genes belonging to glutathione system increase proliferative retinopathy risk in type 1 diabetes individuals (2019)
- Authors:
- USP affiliated authors: CAVALEIRO, ANA MERCEDES DE SOUSA - FM ; GIANNELLA, MARIA LUCIA CARDILLO CORREA - FM
- Unidade: FM
- DOI: 10.1016/j.gene.2019.04.015
- Subjects: DIABETES MELLITUS INSULINO-DEPENDENTE; DOENÇAS RETINIANAS; ESTRESSE OXIDATIVO; ESTUDOS TRANSVERSAIS; OLIGOPEPTÍDEOS
- Agências de fomento:
- Language: Inglês
- Imprenta:
- Source:
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
PEREZ, Ricardo Vessoni et al. Allelic variations in genes belonging to glutathione system increase proliferative retinopathy risk in type 1 diabetes individuals. Gene, v. 703, p. 120-124, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.gene.2019.04.015. Acesso em: 28 dez. 2025. -
APA
Perez, R. V., Machado, C. G., Santos-bezerra, D. P., Admoni, S. N., Patente, T. A., Monteiro, M. B., et al. (2019). Allelic variations in genes belonging to glutathione system increase proliferative retinopathy risk in type 1 diabetes individuals. Gene, 703, 120-124. doi:10.1016/j.gene.2019.04.015 -
NLM
Perez RV, Machado CG, Santos-bezerra DP, Admoni SN, Patente TA, Monteiro MB, Cavaleiro AM de S, Queiroz MS, Nery M, Giannella MLCC. Allelic variations in genes belonging to glutathione system increase proliferative retinopathy risk in type 1 diabetes individuals [Internet]. Gene. 2019 ; 703 120-124.[citado 2025 dez. 28 ] Available from: https://doi.org/10.1016/j.gene.2019.04.015 -
Vancouver
Perez RV, Machado CG, Santos-bezerra DP, Admoni SN, Patente TA, Monteiro MB, Cavaleiro AM de S, Queiroz MS, Nery M, Giannella MLCC. Allelic variations in genes belonging to glutathione system increase proliferative retinopathy risk in type 1 diabetes individuals [Internet]. Gene. 2019 ; 703 120-124.[citado 2025 dez. 28 ] Available from: https://doi.org/10.1016/j.gene.2019.04.015 - Na DPH oxidase 4 and P22PHOX (CYBA) gene polymorphisms as risk factors dor arterial hypertension and overt nephrolopathy in type 1 diabetes
- Glutathione peroxidase 4 functional variant rs713041 modulates the risk for cardiovascular autonomic neuropathy in individuals with type 1 diabetes [Carta]
- Hyperinsulinism/hyperammonemia (HI/HA) syndrome due to a mutation in the glutamate dehydrogenase gene
- A novel mutation in the glycogen synthase 2 gene in a child with glycogen storage disease type 0
- Association of a variant in the regulatory region of NADPH oxidase 4 gene and metabolic syndrome in patients with chronic hepatitis C
- Influence of UCP3 gene polymorphisms on metabolic syndrome and cardiovascular risk in patients with in non-alcoholic fatty liver disease
- Hepatocyte growth factor-regulated tyrosine kinase substrate (HGS) and guanylate kinase 1 (GUK1) are differentially expressed in GH-secreting adenomas
- Rs4862705 in the melatonin receptor 1A gene is associated with renal function decline in type 1 diabetes individuals
- Association of single nucleotide polymorphisms in the gene encoding GLUT1 and diabetic nephropathy in Brazilian patients with type 1 diabetes mellitus
- Possible role of a radiation-induced p53 mutation in a Nelson’s syndrome patient with a fatal outcome
Informações sobre o DOI: 10.1016/j.gene.2019.04.015 (Fonte: oaDOI API)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas