Výsledky vyhledávání - "Jéssica Barletto de Sousa Barros"

Akademický článek

No association of GSTP1 rs1695 polymorphism with amyotrophic lateral sclerosis: A case-control study in the Brazilian population.

Autor: Jéssica Barletto de Sousa Barros, Kamilla de Faria Santos, Rômulo Morais Azevedo, Rayana Pereira Dantas de Oliveira, Ana Carolina Dourado Leobas, Dhiogo da Cruz Pereira Bento, Rodrigo da Silva Santos, Angela Adamski da Silva Reis

Publikováno v: PLoS ONE, Vol 16, Iss 2, p e0247024 (2021)

Amyotrophic Lateral Sclerosis (ALS) is a rare neurodegenerative disease that affects motor neurons and promotes progressive muscle atrophy. It has a multifactorial etiology, where environmental conditions playing a remarkable role through the increas

Externí odkaz: https://doaj.org/article/a55f488fd634418d8792d552c0e8d30e

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Akademický článek

Acute Zika Virus Infection in an Endemic Area Shows Modest Proinflammatory Systemic Immunoactivation and Cytokine-Symptom Associations

Autor: Jéssica Barletto de Sousa Barros, Paulo Alex Neves da Silva, Rosemary de Carvalho Rocha Koga, Patrícia Gonzalez-Dias, José Rodrigues Carmo Filho, Patrícia Resende Alo Nagib, Verônica Coelho, Helder I. Nakaya, Simone Gonçalves Fonseca, Irmtraut Araci Hoffmann Pfrimer

Publikováno v: Frontiers in Immunology, Vol 9 (2018)

An early immune response to Zika virus (ZIKV) infection may determine its clinical manifestation and outcome, including neurological effects. However, low-grade and transient viremia limits the prompt diagnosis of acute ZIKV infection. We have invest

Externí odkaz: https://doaj.org/article/1dc96a30e4404206a8f85949bc812917

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Influence of GSTP1 rs1695 polymorphism on survival in male patients’ amyotrophic lateral sclerosis: a genetic association study in Brazilian population

Autor: Dhiogo da Cruz Pereira Bento, Leandro do Prado Assunção, Angela Adamski da Silva Reis, Jéssica Barletto de Sousa Barros, Rodrigo da Silva Santos, Kamilla de Faria Santos

Publikováno v: Molecular Biology Reports. 49:1655-1659

Glutathione S-transferase Pi (GSTP1) enzyme has a major antioxidant effect on the central nervous system (CNS), where it acts against oxidative damage, an established risk factor for amyotrophic lateral sclerosis (ALS). Hence, the purpose of this stu

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::154fd00f7b9d6eec6c5a42717227617f
https://doi.org/10.1007/s11033-021-06724-z

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O gene CFTR e sua associação com o desenvolvimento da Fibrose Cística

Autor: Nayane Soares de Lima, Kamilla de Faria Santos, Caroline Christine Pincela da Costa, Jéssica Barletto de Sousa Barros, Rayana Pereira Dantas de Oliveira

Publikováno v: Genética na Escola. 16:150-157

A Fibrose Cística (FC), também conhecida por mucoviscidose, é uma doença genética de herança autossômica recessiva causada por mutações no gene CFTR (do inglês Cystic Fibrosis Transmembrane Conductance Regulator). Esse gene codifica uma pro

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::fe18dd34177c1364603e3f5c832fbb94
https://doi.org/10.55838/1980-3540.ge.2021.363

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Gene DMD e a distrofia muscular de Duchenne

Autor: Caroline Christine Pincela da Costa, Rayana Pereira Dantas de Oliveira, Jéssica Barletto de Sousa Barros, Kamilla de Faria Santos, Nayane Soares de Lima

Publikováno v: Genética na Escola. 15:218-225

O gene DMD localiza-se no cromossomo X e codifica a distrofina, uma proteína do citoesqueleto responsável pela manutenção da integridade e da função contrátil das fibras musculares. Alterações moleculares no gene DMD interferem na produção

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::eb7e90624e88e52d3a4ef548bf580dc9
https://doi.org/10.55838/1980-3540.ge.2020.345

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O gene C4 e a susceptibilidade a esquizofrenia

Autor: Jéssica Barletto de Sousa Barros, Sarah Luana Ferreira dos Santos, Angela Adamski da Silva Reis, Rodrigo da Silva Santos

Publikováno v: Genética na Escola. 15:88-95

Sabe-se que a esquizofrenia possui origem multifatorial na qual fatores ambientais e genéticos influenciam diretamente o seu desenvolvimento. Nesse contexto, estudos recentes demonstram que existe uma forte associação entre o gene C4 e a susceptib

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::66b30e469a1218a0c306fa372e83674f
https://doi.org/10.55838/1980-3540.ge.2020.334

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No association of GSTP1 rs1695 polymorphism with amyotrophic lateral sclerosis: A case-control study in the Brazilian population

Autor: Rayana Pereira Dantas de Oliveira, Jéssica Barletto de Sousa Barros, Rômulo Morais Azevedo, Dhiogo da Cruz Pereira Bento, Ana Carolina Dourado Leobas, Kamilla de Faria Santos, Angela Adamski da Silva Reis, Rodrigo da Silva Santos

Publikováno v: PLoS ONE, Vol 16, Iss 2, p e0247024 (2021)
PLoS ONE

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51fd03dc724df6c0f9f919411fc271ac
https://doaj.org/article/a55f488fd634418d8792d552c0e8d30e

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Genotyping of the rs1695 polymorphism of the GSTP1 gene by PCR-RFLP v1

Glutathione S-transferases (GSTs) are enzymes that act in the cellular detoxification of harmful compounds. Due to the role of the GSTP1 isoenzyme in the brain, the presence of the single nucleotide polymorphism (SNP) rs1695 in the GSTP1 gene may pla

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::4fb8771b26eddf1231c80b1227168eed
https://doi.org/10.17504/protocols.io.bqgqmtvw

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