Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Márcia Gonçalves"'
Autor:
Márcia R. Amorim, Thereza Quirico-Santos, Cláudia de Melo Moura, Márcia Gonçalves Ribeiro, Hazel N. Barboza, Marcelo Aguiar Costa-Lima, Joissy Aprigio
Publikováno v:
Journal of Molecular Neuroscience. 70:1410-1414
Down syndrome (DS) is the most common form of mental disability of genetic etiology. Nondisjunction of chromosome 21 is the leading cause of the syndrome. In general, free trisomy 21 cases originate from missegregation in maternal meiosis. Several re
Autor:
Allan E. Rubenstein, Mauro Geller, Carolina de Almeida Ito Brum, Márcia Gonçalves Ribeiro, Luiz Guilherme Darrigo, Karin Soares Gonçalves Cunha, Alessandra Santos, Allan Bernacchi, Sanyu Takirambudde, Lisa Oliveira, Spyros G.E. Mezitis
Publikováno v:
Heliyon, Vol 7, Iss 3, Pp e06518-(2021)
Heliyon
Heliyon
Background Neurofibromatosis type 1 (NF1) is an autosomal dominant genetic disorder with a prevalence of 1:3000 births and a wide variety of clinical manifestations. Cutaneous neurofibromas (cNF) are among the most common visible manifestations of NF
Autor:
João Hugo Abdalla Santos, Michele Silva de Jesus, Edson Delatorre, Felipe Gomes Naveca, Débora Duarte, Paola Cristina Resende, Cristiano Fernandes da Costa, André de Lima Corado, Luciana Márcia Gonçalves, Victor Costa de Souza, Tiago Gräf, Marineide Silva, Tirza Mattos, Valdinete Alves do Nascimento, Gemilson Soares Pontes, Gonzalo Bello, Maria Júlia Brandão, Daniel Barros, Ágatha Costa, Marilda M. Siqueira, Karina Pessoa, Vanderson de Souza Sampaio, Filipe Zimmer Dezordi, Gabriel Luz Wallau, Matilde Mejía, Ligia Fernandes Abdalla, George Silva, Fernanda Nascimento, Ighor Arantes
Publikováno v:
Nature medicine. 27(7)
The northern state of Amazonas is among the regions in Brazil most heavily affected by the COVID-19 epidemic and has experienced two exponentially growing waves, in early and late 2020. Through a genomic epidemiology study based on 250 severe acute r
Autor:
Belisia Vasconcelos de Barros, Thuane Silva da Cruz, Eduardo Vieira Neto, Lilian de Mattos Carvalho, Heber de Souza Maia Filho, Márcia Gonçalves Ribeiro, Claudia Braga Monteiro
Publikováno v:
Medical Science Monitor : International Medical Journal of Experimental and Clinical Research
BACKGROUND Phenylketonuria (PKU) is an inborn error of metabolism caused by mutations in the phenylalanine hydroxylase (PAH) gene. When untreated, PKU leads to a significant intellectual deficiency. Although early initiation of dietary therapy allows
Autor:
Ana Paula Muraro, Ana Paula de Matos, Márcia Gonçalves Ferreira, Lorena Barbosa Fonseca, Paulo Rogério Melo Rodrigues
Publikováno v:
Nutrition and health. 27(2)
Background: University students may be a vulnerable group to adopt unhealthy behaviors, including changes in eating behavior. Assessment of factors associated with the prevalence of disordered eating behaviors in this population may facilitate the ea
Autor:
Kátia Regina Netto dos Santos, Fernanda Sampaio Cavalcante, Ekaterini Goudouris, Eliane de Dios Abad, Alexandre S. Rosado, Jan Dirk van Elsas, Alexandre Marques Paes da Silva, Cristina Barroso Hofer, Simone Saintive, Evandro Prado, Márcia Gonçalves Ribeiro, Dennis de Carvalho Ferreira
Publikováno v:
Journal of microbiology, immunology, and infection = Wei mian yu gan ran za zhi, 53(5), 724-730
Journal of Microbiology, Immunology and Infection, Vol 53, Iss 5, Pp 724-730 (2020)
Journal of Microbiology, Immunology and Infection, Vol 53, Iss 5, Pp 724-730 (2020)
BACKGROUND: Methicillin-resistant Staphylococcus aureus (MRSA) colonization in Atopic Dermatitis (AD) patients can contribute to worsening their clinical condition.OBJECTIVE: A cohort study was carried out to determine the incidence of MRSA acquisiti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4532940ee8029587ccc0e4a6f993c50
https://research.rug.nl/en/publications/336d7d38-b390-4d3c-8950-9018fa79547d
https://research.rug.nl/en/publications/336d7d38-b390-4d3c-8950-9018fa79547d
Autor:
Edmilson Moutinho dos Santos, Taissa Pereira dos Santos, Marcelo Quintela Gomes, Danilo Simonini Teixeira, Maycon Sebastião Alberto Santos Neves, Vanessa de Oliveira Santos, Filipe Vieira Santos de Abreu, Christophe Paupy, Andréa Marques Vieira da Silva, Camilla Bayma Fernandes, Márcia Gonçalves de Castro, Luzia Maria de Oliveira-Pinto, Sara Moutailler, Myrna C. Bonaldo, José Henrique Rezende Linhares, Sheila Maria Barbosa de Lima, Ana Paula Dinis Ano Bom, Lena Yousfi, Emily Hime Miranda, Adriana de Souza Azevedo, Alessandro Pecego Martins Romano, Ricardo Lourenço-de-Oliveira, Ieda Pereira Ribeiro, Monique da Rocha Queiroz Lima, Alexandre Dos Santos, Anielly Ferreira-de-Brito, Monique de Albuquerque Motta
Publikováno v:
Viruses
Viruses, MDPI, 2020, 12 (4), ⟨10.3390/v12040364⟩
Viruses, Vol 12, Iss 4, p 364 (2020)
Volume 12
Issue 4
Viruses, 2020, 12 (4), ⟨10.3390/v12040364⟩
Viruses, MDPI, 2020, 12 (4), ⟨10.3390/v12040364⟩
Viruses, Vol 12, Iss 4, p 364 (2020)
Volume 12
Issue 4
Viruses, 2020, 12 (4), ⟨10.3390/v12040364⟩
In the last decade, Flaviviruses such as yellow fever (YFV) and Zika (ZIKV) have expanded their transmission areas. These viruses originated in Africa, where they exhibit both sylvatic and interhuman transmission cycles. In Brazil, the risk of YFV ur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19c76287339f02d9e2198e2fd19599f9
https://hal.umontpellier.fr/hal-03002400
https://hal.umontpellier.fr/hal-03002400
Autor:
Márcia Mattos Gonçalves Pimentel, Jussara Mendonça dos Santos, Rafael Mina Piergiorge, Raquel Tavares Boy da Silva, Enrique Medina-Acosta, Carla Rosenberg, Veluma Calassara, Suely Rodrigues dos Santos, Márcia Gonçalves Ribeiro, Filipe Brum Machado, Ana Cristina Victorino Krepischi, Cíntia Barros Santos-Rebouças, Andressa Pereira Gonçalves, Evelyn Quintanilha Vianna
Publikováno v:
Molecular neurobiology. 57(9)
Intellectual disability (ID) affects 30% more males than females. This sex bias can be attributed to the enrichment of genes on the X chromosome playing essential roles in the central nervous system and their hemizygous state on males. Moreover, as a
Autor:
Ricardo Lourenço-de-Oliveira, Anielly Ferreira-de-Brito, Erich Loza Telleria, Myrna C. Bonaldo, Lidiane Menezes Souza Raphael, Rosilainy Surubi Fernandes, Maria Ignez Lima Bersot, Márcia Gonçalves de Castro
Publikováno v:
Scientific Reports, Vol 9, Iss 1, Pp 1-7 (2019)
Scientific Reports
Scientific Reports
Zika virus (ZIKV) has spread in the Americas since 2015 and the potential establishment of a sylvatic transmission cycle in the continent has been hypothesized. We evaluated vector competence of five sylvatic Neotropical mosquito species to two ZIKV
Autor:
Isaura Ribeiro, Dulce Quelhas, Lúcia Lacerda, Nicole Mineiro, Francisco Ferraz Laranjeira, Márcia Gonçalves Ribeiro, Lilian de Mattos Carvalho, Alexandre L. Seabra, Eduardo Vieira Neto
Publikováno v:
Molecular Genetics & Genomic Medicine
Background Phenylketonuria (PKU) is an autosomal recessive disease resulting from mutations in the PAH gene. Most of the patients are compound heterozygotes, and genotype is a major factor in determining the phenotypic variability of PKU. More than 1