Zobrazeno 1 - 10
of 97
pro vyhledávání: '"Marcos André Cavalcanti, Bezerra"'
Autor:
Ronaldo Celerino da Silva, Suelen Cristina de Lima, Wendell Palôma Maria Dos Santos Reis, Jurandy Júnior Ferraz de Magalhães, Ronaldo Nascimento de Oliveira, Brijesh Rathi, Alain Kohl, Marcos André Cavalcanti Bezerra, Lindomar Pena
Publikováno v:
PLoS ONE, Vol 19, Iss 11, p e0314215 (2024)
[This corrects the article DOI: 10.1371/journal.pone.0287551.].
Externí odkaz:
https://doaj.org/article/807207a2310148b997a95fa0a47448f8
Autor:
Ronaldo Celerino da Silva, Suelen Cristina de Lima, Wendell Palôma Maria Dos Santos Reis, Jurandy Júnior Ferraz de Magalhães, Ronaldo Nascimento de Oliveira Magalhães, Brijesh Rathi, Alain Kohl, Marcos André Cavalcanti Bezerra, Lindomar Pena
Publikováno v:
PLoS ONE, Vol 18, Iss 10, p e0287551 (2023)
The coronavirus disease 2019 (COVID-19) pandemic has resulted in global shortages in supplies for diagnostic tests, especially in the developing world. Risk factors for COVID-19 severity include pre-existing comorbidities, older age and male sex, but
Externí odkaz:
https://doaj.org/article/04c24465fbc44aa89f693df4c9c85edd
Autor:
Okeke Chinedu, Wouitchékpo Vincent Tonassé, Dulcinéia Martins Albuquerque, Igor de Farias Domingos, Aderson da Silva Araújo, Marcos André Cavalcanti Bezerra, Maria de Fátima Sonati, Magnun Nueldo Nunes dos Santos
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 43, Iss 2, Pp 165-170 (2021)
Introduction: Mutations affecting genes involved in oxidative and signaling pathways may be associated with kidney disease in sickle cell anemia. We determined the allele and genotype frequencies of some polymorphisms in the promoter regions of the H
Externí odkaz:
https://doaj.org/article/874eebcef95940afb6c1fe7c4b2627a6
Autor:
Ó. do Kleyton Palmeira, Ana Karla da Silva Freire, Débora Nascimento de Nóbrega, Roberta dos Santos Souza, Isabela Cristina Cordeiro Farias, Taciana Furtado de Mendonça Belmont, Andreia Soares da Silva, Gabriela da Silva Arcanjo, Aderson da Silva Araujo, Ana Cláudia Mendonça dos Anjos, Antônio Roberto Lucena de Araujo, Marcos André Cavalcanti Bezerra, Patricia Muniz Mendes Freire de Moura, Maria do Socorro Mendonça Cavalcanti, Luydson Richardson Silva Vasconcelos
Publikováno v:
Molecular Biology Reports. 50:3341-3353
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::621f7b2fa94439bfe9a4d5c22f870666
https://doi.org/10.1007/s11033-023-08262-2
https://doi.org/10.1007/s11033-023-08262-2
Autor:
Luana Oliveira dos Santos, Adriana Valéria Sales Bispo, Juliana Vieira de Barros, Raysa Samanta Moraes Laranjeira, Rafaella do Nascimento Pinto, Jaqueline de Azevêdo Silva, Andréa de Rezende Duarte, Jacqueline Araújo, Paula Sandrin-Garcia, Sergio Crovella, Marcos André Cavalcanti Bezerra, Taciana Furtado de Mendonça Belmont, Maria do Socorro Cavalcanti, Neide Santos
Publikováno v:
Genetics and Molecular Biology, Vol 41, Iss 4, Pp 727-734 (2018)
Abstract Turner syndrome (TS) is characterized by a set of clinical conditions, including autoimmune/inflammatory diseases and infectious conditions, that can compromise a patient’s quality of life. Here we assessed polymorphisms in CTLA-4 +49A/G (
Externí odkaz:
https://doaj.org/article/b2e74d74f8134dda8a2786d07b465466
Autor:
Fernanda Silva Medeiros, Taciana Furtado de Mendonça, Katiuscia Araújo de Miranda Lopes, Laís Medeiros da Câmara França, Andreia Soares da Silva, Luydson Richardson Silva Vasconcelos, Maria do Carmo Valgueiro Costa de Oliveira, Ana Cláudia Mendonça dos Anjos, Betânia Lucena Domingues Hatzlhofer, Marcos André Cavalcanti Bezerra, Aderson da Silva Araújo, Patrícia Moura, Maria do Socorro de Mendonça Cavalcanti
Publikováno v:
Genetics and Molecular Biology, Vol 40, Iss 3, Pp 600-603 (2017)
Abstract Sickle cell anemia (SCA) presents heterogenous clinical manifestations that cannot be explained solely by alterations to hemoglobin (Hb); other components such as endothelial adhesion, thrombosis and inflammation may be involved. The mannose
Externí odkaz:
https://doaj.org/article/8d6b488b9ac8486bbb5511d9e9285af2
Autor:
Antonio R. Lucena-Araujo, Diego A Pereira-Martins, Rafael F. O. França, Igor de Farias Domingos, Pedro L Franca-Neto, Juan L Coelho-Silva, Aderson S Araujo, Isabel Weinhäuser, Marcos André Cavalcanti Bezerra
Publikováno v:
Annals of Hematology. 101:281-287
One of the physiologic mechanisms responsible to maintain asymmetric phospholipid distribution (in particular phosphatidylserine, PS) in human erythrocyte membranes is orchestrated by the balance between enzymes responsible for active transport of PS
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6ddde6cc215a94a5e7e72d7984ef59ea
https://doi.org/10.1007/s00277-021-04696-5
https://doi.org/10.1007/s00277-021-04696-5
Autor:
Kleyton Palmeira do Ó, Ana Karla da Silva Freire, Debora Nascimento de Nóbrega, Roberta dos Santos Souza, Isabela Cristina Cordeiro Farias, Taciana Furtado de Mendonça Belmont, Andreia Soares da Silva, Gabriela da Silva Arcanjo, Aderson da Silva Araujo, Ana Cláudia Mendonça dos Anjos, Antônio Roberto Lucena de Araujo, Marcos André Cavalcanti Bezerra, Patricia Muniz Mendes Freire de Moura, Maria do Socorro Mendonça Cavalcanti, Luydson Richardson Silva Vasconcelos
Background Sickle cell anemia (SCA) is a genetic disease with great clinical heterogeneity and few viable strategies for treatment; hydroxyurea (HU) is the only widely used drug. Thus, the study of single nucleotide polymorphisms (SNPs) and the gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ce094b4cc8874fb6ff26cb91e5bff4bb
https://doi.org/10.21203/rs.3.rs-2285360/v1
https://doi.org/10.21203/rs.3.rs-2285360/v1
Autor:
Manuela F. Hazin, Thais Helena Chaves Batista, Gabriela da Silva Arcanjo, Aderson S Araujo, Betânia Lucena Domingues Hatzlhofer, Antonio R. Lucena-Araujo, Diego Arruda Falcão, Jéssica Vitória Gadelha de Freitas Batista, Pablo Ramon Gualberto Cardoso, Maira Galdino da Rocha Pitta, Marcos André Cavalcanti Bezerra, Diego A Pereira-Martins, Igor de Farias Domingos, Fernando Ferreira Costa, Ana Claudia Mendonça dos Anjos, Isabel Weinhäuser
Publikováno v:
Annals of Hematology. 100:1921-1927
The clinical and phenotypic heterogeneity of patients with sickle cell anemia (SCA) is influenced by environmental and genetic factors. Several genetic modifiers, such as the KLOTHO (KL) gene, have been associated with SCA clinical outcomes. The KL g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::40f3803ddc7dc752fca5574ce5027dd6
https://doi.org/10.1007/s00277-021-04532-w
https://doi.org/10.1007/s00277-021-04532-w
Autor:
Magnun N. N. Santos, Okeke Chinedu, Igor de Farias Domingos, Aderson S Araujo, Maria de Fátima Sonati, Marcos André Cavalcanti Bezerra, Wouitchékpo Vincent Tonassé, Dulcineia M. Albuquerque
Publikováno v:
Hematology, Transfusion and Cell Therapy, Volume: 43, Issue: 2, Pages: 165-170, Published: 07 JUL 2021
Hematology, Transfusion and Cell Therapy, Vol 43, Iss 2, Pp 165-170 (2021)
Hematology, Transfusion and Cell Therapy
Hematology, Transfusion and Cell Therapy, Vol 43, Iss 2, Pp 165-170 (2021)
Hematology, Transfusion and Cell Therapy
Introduction Mutations affecting genes involved in oxidative and signaling pathways may be associated with kidney disease in sickle cell anemia. We determined the allele and genotype frequencies of some polymorphisms in the promoter regions of the He
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e617ffa144cc27fe6880e900e7b49f72
https://doi.org/10.1016/j.htct.2020.01.009
https://doi.org/10.1016/j.htct.2020.01.009