Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Fernanda S. G. Kehdy"'
Autor:
Daniela P. Mendes-de-Almeida, Fernanda S. G. Kehdy, Remy Martins-Gonçalves, Joanna Bokel, Eduarda Grinsztejn, Patrícia Mouta Nunes de Oliveira, Maria de Lourdes de Sousa Maia, Brenda Hoagland, Sandra Wagner Cardoso, Beatriz Grinsztejn, Marilda M. Siqueira, Pedro Kurtz, Patricia T. Bozza, Cristiana C. Garcia
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 10 (2023)
The emergence of the rare syndrome called vaccine-induced immune thrombocytopenia and thrombosis (VITT) after adenoviral vector vaccines, including ChAdOx1 nCov-19, raises concern about one's predisposing risk factors. Here we report the case of a 56
Externí odkaz:
https://doaj.org/article/ba389ae50dfb4ddc9339e1bb0fea71c9
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
Externí odkaz:
https://doaj.org/article/d1e1cacf622145bbb91567a86c3b9ef9
Autor:
Kelly Nunes, Vitor R. C. Aguiar, Márcio Silva, Alexandre C. Sena, Danielli C. M. de Oliveira, Carla L. Dinardo, Fernanda S. G. Kehdy, Eduardo Tarazona-Santos, Vanderson G. Rocha, Anna Barbara F. Carneiro-Proietti, Paula Loureiro, Miriam V. Flor-Park, Claudia Maximo, Shannon Kelly, Brian Custer, Bruce S. Weir, Ester C. Sabino, Luís Cristóvão Porto, Diogo Meyer
Publikováno v:
Frontiers in Immunology, Vol 11 (2020)
A match of HLA loci between patients and donors is critical for successful hematopoietic stem cell transplantation. However, the extreme polymorphism of HLA loci – an outcome of millions of years of natural selection – reduces the chances that tw
Externí odkaz:
https://doaj.org/article/7135c23b854d4ea48891ccb520ebe641
Publikováno v:
Molecules, Vol 13, Iss 8, Pp 1759-1772 (2008)
Fanconi anaemia (FA) is a rare genetic chromosomal instability syndrome caused by impairment of DNA repair and reactive oxygen species (ROS) imbalance. This disease is also related to bone marrow failure and cancer. Treatment of these complications w
Externí odkaz:
https://doaj.org/article/6f27a88ef62f4dcab00fdbed78789497
Autor:
Meddly L. Santolalla, Fernanda S G Kehdy, Thiago P. Leal, Michel S Naslavsky, Meredith Yeager, Moara Machado, Eduardo Tarazona-Santos, Shane A. Norris, Hanaisa P Sant'Anna, Francisco Pereira Lobo, Victor Borda, Lucas Michelin, Alexandre C. Pereira, Sam M. Mbulaiteye, Robert H. Gilman, Guilherme L. Yamamoto, Edward D. Yeboah, Marcelo R. Luizon, Matthew E. B. Hansen, Sérgio Viana Peixoto, Camila Zolini, Nathalia M. Araujo, Julie Dutil, Timothy D O Connor, Isabela Alvim, Mateus H. Gouveia, Maria Rita Passos-Bueno, Ricardo Lyra, Marilia O. Scliar, Michèle Ramsay, Gilderlanio S. Araújo, Yeda Aparecida de Oliveira Duarte, Heinner Guio, Mayana Zatz, Maria Fernanda Lima-Costa, Wagner C. S. Magalhães, Sarah A. Tishkoff, Ananyo Choudhury, Bernardo L. Horta, Maíra R. Rodrigues, James E. Mensah, Mauricio Lima Barreto, Ann W. Hsing
Publikováno v:
Int J Obes (Lond)
Background/objectives: Admixed populations are a resource to study the global genetic architecture of complex phenotypes, which is critical, considering that non-European populations are severely underrepresented in genomic studies. Here, we study th
Publikováno v:
Frontiers in Genetics
Frontiers in Genetics, Vol 12 (2021)
Frontiers in Genetics, Vol 12 (2021)
Autor:
Meddly Santollala, Victor Borda, Carolina Silva-Carvalho, Rennan G. Moreira, Isabela Alvim, Lucas Michelin, Luis Jaramillo-Valverde, Murilo Pita-Oliveira, Fernanda S G Kehdy, Mariana Scudeler, Ricardo A. Verdugo, Timothy D. O’Connor, Andres Vasquez-Dominguez, Giordano B. Soares-Souza, Fernanda Rodrigues-Soares, Heinner Guio, Eduardo Tarazona-Santos, Vinicius Furlan, Cesar Neira, Sabrina Torres-Loureiro, Marla M. Aquino, Thiago P. Leal, Renato Santana Aguiar, Camila Zolini
Publikováno v:
Genetics and Molecular Biology, Vol 44, Iss 1 suppl 1 (2021)
Genetics and Molecular Biology
Genetics and Molecular Biology, Volume: 44, Issue: 1 Supplement 1, Article number: e20200484, Published: 25 AUG 2021
Genetics and Molecular Biology
Genetics and Molecular Biology, Volume: 44, Issue: 1 Supplement 1, Article number: e20200484, Published: 25 AUG 2021
The current search for host-susceptibility variants for COVID-19 contrasts with the fact that the study of the genetic architecture of Severe Acute Respiratory Syndrome (SARS) has been neglected. For human/SARS-CoV-2 interactome genes ACE2, TMPRSS2 a
Autor:
André Luiz Leturiondo, Fabíola da Costa Rodrigues, Jamile Leão Rêgo, Antonio G. Pacheco, Fernanda S G Kehdy, Nédio Mabunda, Ilesh V. Jani, Graca Salomé, Ohanna Cavalcanti de Lima Bezerra, Ann W. Hsing, Eduardo Tarazona-Santos, Diogo Meyer, Léa Cristina Castellucci, Caroline de Sales-Marques, Edward D. Yeboah, Rafaela Mota Andrade, Lucia Elena Alvarado-Arnez, Carolina Talhari, Lais F. Pereira, Amina de Sousa, Sam M. Mbulaiteve, Milton Ozório Moraes, Mateus H. Gouveia, Ariani Batista Noronha, Roberta Olmo Pinheiro, Elizeu Fagundes de Carvalho, Cynthia de Oliveira Ferreira, Fernanda Saloum de Neves Manta, Thyago Leal Calvo, Ana Carla Pereira Latini, Kelly Nunes
Publikováno v:
SSRN Electronic Journal.
Background: Pyruvate kinase (PK) gene (PKLR) is a key player in glycolysis controlling the integrity of erythrocytes. Due to Plasmodium selection, mutations for PK deficiency, leading to hemolytic anemia, are associated with resistance to malaria in
Autor:
Vinicius Furlan, Sarah A. Tishkoff, Raquel Liboredo, Rennan Garcias Moreira, Stephen J. Chanock, Roxana Zamudio, Camila Zolini, Michael Dean, Maria Cátira Bortolini, Maria Fernanda Lima-Costa, Isabela Alvim, Wagner C. S. Magalhães, Mateus H. Gouveia, Heinner Guio, Fernanda Rodrigues-Soares, Meddly L. Santolalla, Marla M. Aquino, Gilderlanio S. Araújo, Victor Borda, Andrew W. Bergen, Lucas Michelin, Fernanda S G Kehdy, Giordano B. Soares-Souza, Robert H. Gilman, Bernardo L. Horta, Sam M. Mbulaiteye, Maíra R. Rodrigues, Meredith Yeager, Nathalia M. Araujo, Thiago P. Leal, Moara Machado, Mauricio Lima Barreto, Marilia O. Scliar, Hanaisa P. Sant Anna, Eduardo Tarazona-Santos, Jorge Rocha, Alexandre C. Pereira
Publikováno v:
Mol Biol Evol
The Transatlantic Slave Trade transported more than 9 million Africans to the Americas between the early 16th and the mid-19th centuries. We performed genome-wide analysis of 6,267 individuals from 22 populations and observed an enrichment in West-Af
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc280cc6d2b4f2d5838ce6edbcab599f
https://doi.org/10.1101/652701
https://doi.org/10.1101/652701
Autor:
Fernanda S G Kehdy, Rosemeire L. Fiaccone, Gisel Lorena Fattore, Eduardo Tarazona-Santos, Caroline Alves Feitosa, Alvaro A. Cruz, Letícia Marques dos Santos, Mauricio Lima Barreto, Neuza Maria Alcantara-Neves, Laura C. Rodrigues, Camila Alexandrina Figueiredo, Thiago Magalhães da Silva, Gustavo Nunes de Oliveira Costa, Darci Neves dos Santos
Publikováno v:
Pediatric Pulmonology.
Background Genetic variants underlying African ancestry have been suggested be implicated in the ethnic-racial inequalities reported for asthma and allergies. Objectives To investigate the association between individual African ancestry and asthma sy