Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Ana Cláudia Mendonça dos Anjos"'
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:
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:
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:
Taciana Furtado de Mendonça Belmont, Kleyton Palmeira do Ó, Andreia Soares da Silva, Kamila de Melo Vilar, Fernanda Silva Medeiros, Luydson Richardson Silva Vasconcelos, Ana Claudia Mendonça Dos Anjos, Betânia Lucena Domingues Hatzlhofer, Maíra Galdino da Rocha Pitta, Marcos André Cavalcanti Bezerra, Aderson da Silva Araújo, Moacyr Jesus Barreto de Melo Rego, Patrícia Moura, Maria do Socorro Mendonça Cavalcanti
Publikováno v:
PLoS ONE, Vol 11, Iss 9, p e0162297 (2016)
INTRODUCTION:Patients with sickle cell anemia (SCA) may present chronic hemolytic anemia, vaso-occlusion and respiratory tract infection (RTI) episodes. Galectin-3 (GAL-3) is a multifunctional protein involved in inflammation, apoptosis, adhesion and
Externí odkaz:
https://doaj.org/article/b76fc6fdf9364d74b98985bbdfab4927
Autor:
Clarisse Lopes de Castro Lobo, Rodolfo Delfini Cançado, Ana Claudia Celestino Bezerra Leite, Ana Claudia Mendonça dos Anjos, Ana Cristina Silva Pinto, Andre Palma da Cunha Matta, Célia Maria Silva, Gisele Sampaio Silva, João Ricardo Friedrisch, Josefina Aparecida Pellegrini Braga, Marcos Christiano Lange, Maria Stella Figueiredo, Marília Álvares Rugani, Orlando Veloso, Patrícia Gomes Moura, Paulo Ivo Cortez, Robert Adams, Sandra Fátima Menosi Gualandro, Shirley Lopes de Castilho, Ursula Thomé, Viviane Flumignan Zetola
Publikováno v:
Revista Brasileira de Hematologia e Hemoterapia, Vol 33, Iss 1, Pp 43-48 (2011)
BACKGROUND: Sickle cell disease is the most common monogenic hereditary disease in Brazil. Although strokes are one of the main causes of morbidity and mortality in these patients, the use of transcranial Doppler to identify children at risk is not u
Externí odkaz:
https://doaj.org/article/419146d56716416796ca8cf81fec6e0a