Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Raysa Samanta Moraes Laranjeira"'
Autor:
Juliana Vieira de Barros Arcoverde, Carla Fernandes dos Santos, Maria Cecília Magalhães Luckwu, Raysa Samanta Moraes Laranjeira, Aldianne Milene dos Santos Barbosa, Thays Maria Costa de Lucena, Jaqueline de Azevêdo Silva, Neide Santos
Publikováno v:
Genetics and Molecular Biology, Vol 47, Iss 4 (2024)
Abstract Down syndrome (DS), affecting 1 in 700 live births, is the most prevalent chromosomal disorder among newborns. Recognizable by classical clinical features, patients with DS are susceptible to various immunological misbalances. Inflammasome i
Externí odkaz:
https://doaj.org/article/1cf3810f7ce54fb9893195bd9e428e97
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:
Raysa Samanta Moraes Laranjeira, Luana Oliveira dos Santos, Maria Eduarda de Albuquerque Borborema, Rarysa Ferraz de Almeida e Silva, Adriana Valéria Sales Bispo, Andréa de Rezende Duarte, Jacqueline Araújo, Jaqueline de Azevêdo Silva, Neide Santos
Publikováno v:
Scandinavian Journal of Immunology. 97
Autor:
Luana Oliveira dos Santos, J de Azevêdo Silva, A. de R. Duarte, M. E. B. de A. Borborema, J. Araujo, Raysa Samanta Moraes Laranjeira, Neide Santos, Cibele G. Sotero-Caio
Publikováno v:
Journal of Endocrinological Investigation. 43:505-513
Turner syndrome (TS) patients display considerable immune misregulation, and it is hypothesized that Vitamin D (VTD) activity may fluctuate according to Vitamin D receptor (VDR) polymorphisms and/or expression profile. To uncover a possible relations
Autor:
Sergio Crovella, Jaqueline de Azevêdo Silva, Maria do Socorro Cavalcanti, Andréa de Rezende Duarte, Marcos André Cavalcanti Bezerra, Taciana Furtado de Mendonça Belmont, Raysa Samanta Moraes Laranjeira, Rafaella do Nascimento Pinto, Luana Oliveira dos Santos, Paula Sandrin-Garcia, Jacqueline Araújo, Juliana Vieira de Barros, Adriana Valéria Sales Bispo, Neide Santos
Publikováno v:
Genetics and Molecular Biology, Issue: ahead, Published: 29 NOV 2018
Genetics and Molecular Biology
Genetics and Molecular Biology, Vol 41, Iss 4, Pp 727-734 (2018)
Genetics and Molecular Biology, Volume: 41, Issue: 4, Pages: 727-734, Published: 29 NOV 2018
Genetics and Molecular Biology v.41 n.4 2018
Sociedade Brasileira de Genética (SBG)
instacron:SBG
Genetics and Molecular Biology
Genetics and Molecular Biology, Vol 41, Iss 4, Pp 727-734 (2018)
Genetics and Molecular Biology, Volume: 41, Issue: 4, Pages: 727-734, Published: 29 NOV 2018
Genetics and Molecular Biology v.41 n.4 2018
Sociedade Brasileira de Genética (SBG)
instacron:SBG
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 (rs231775)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75397ce93017ea28f1d05821392ab4c5
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572018005021104&lng=en&tlng=en
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572018005021104&lng=en&tlng=en