Zobrazeno 1 - 10
of 62
pro vyhledávání: '"Kiyoko Abe Sandes"'
Autor:
Cleyton Soares dos Santos, Renata Giannecchini Bongiovanni Kishi, Daniel Lima Gomes da Costa, Danniel Sann Dias da Silva, Tânia Regina Franco Narciso, Lucimar Retto da Silva de Avó, Carla Maria Ramos Germano, Kiyoko Abe Sandes, Angelina Xavier Acosta, Débora Gusmão Melo
Publikováno v:
Revista Brasileira de Medicina de Família e Comunidade, Vol 15, Iss 42 (2020)
Problema: Embora individualmente raras, somadas, as doenças genéticas têm prevalência global estimada de 31,5 a 73,0 por 1.000 indivíduos. Além disto, doenças genéticas e defeitos congênitos representam a segunda causa de mortalidade infanti
Externí odkaz:
https://doaj.org/article/6c338704fefc4e3db7461674bcf1e2aa
Autor:
Ingrid Petroni Ewald, Silvia Liliana Cossio, Edenir Inez Palmero, Manuela Pinheiro, Ivana Lucia de Oliveira Nascimento, Taisa Manuela Bonfim Machado, Kiyoko Abe Sandes, Betânia Toralles, Bernardo Garicochea, Patricia Izetti, Maria Luiza Saraiva Pereira, Hugo Bock, Fernando Regla Vargas, Miguel Ângelo Martins Moreira, Ana Peixoto, Manuel R. Teixeira, Patricia Ashton-Prolla
Publikováno v:
Genetics and Molecular Biology, Vol 39, Iss 2, Pp 223-231 (2016)
Abstract Approximately 5-10% of breast cancers are caused by germline mutations in high penetrance predisposition genes. Among these, BRCA1 and BRCA2, which are associated with the Hereditary Breast and Ovarian Cancer (HBOC) syndrome, are the most fr
Externí odkaz:
https://doaj.org/article/1d77d237f8334302a3adb2fb5bfe5798
Autor:
Polyanna Oliveira, Paula Correa, Angelina Acosta, Juliana Freitas, Taísa Machado-Lopes, Thais Bomfim-Palma, Ândrea Ribeiro-dos-Santos, Sidney Santos, Roberto Nascimento, Ivana Nascimento, Kiyoko Abe-Sandes
Publikováno v:
Global Medical Genetics, Vol 10, Iss 04, Pp 376-381 (2023)
Introduction Cancer is a multifactorial disease dependent on the influence of genetic and environmental factors. About 10% of cancers are associated with germline mutations, which predispose to a higher risk of developing cancer. Currently, the use o
Externí odkaz:
https://doaj.org/article/07e37ab30a0f4284b513e8a1b03b0848
Autor:
Gabriela E. S. Felix, Rodrigo Santa Cruz Guindalini, Yonglan Zheng, Tom Walsh, Elisabeth Sveen, Taisa Manuela Machado Lopes, Juliana Côrtes, Jing Zhang, Polyanna Carôzo, Irlânia Santos, Thaís Ferreira Bonfim, Bernardo Garicochea, Maria Betânia Pereira Toralles, Roberto Meyer, Eduardo Martins Netto, Kiyoko Abe-Sandes, Mary-Claire King, Ivana Lucia de Oliveira Nascimento, Olufunmilayo I. Olopade
Publikováno v:
Breast Cancer Research and Treatment. 193:485-494
Purpose There is a paucity of data on the spectrum and prevalence of pathogenic variants among women of African ancestry in the Northeast region of Brazil. Methods We performed BROCA panel sequencing to identify inherited loss-of-function variants in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6763ad6e4df118bddee2f616dd3cb21a
https://doi.org/10.1007/s10549-022-06560-0
https://doi.org/10.1007/s10549-022-06560-0
Autor:
Selma Alves Valente do Amaral Lopes, Isabel Cristina Brito Guimarães, Sofia Fontes Oliva Costa, Angelina Xavier Acosta, Kiyoko Abe-Sandes, Carlos Maurício Cardeal Mendes
Publikováno v:
Progress in Pediatric Cardiology. 68:101612
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b81ee1f4ce594c6ddf90ba7d29caa18d
https://doi.org/10.1016/j.ppedcard.2022.101612
https://doi.org/10.1016/j.ppedcard.2022.101612
Autor:
Karin Alvarez, Walter Hernán Pavicic, Taisa Manuela Bonfim Machado-Lopes, Tamara Alejandra Piñero, Maria Betânia Pereira Toralles, Francisco López-Köstner, Kiyoko Abe Sandes, Benedito Mauro Rossi, Carlos A. Vaccaro, Marion Rolain, Juliana Côrtes Freitas, Joanna Goes Castro Meira, Alexandra Martins, Thais Bomfim, Ivana Nascimento, Dirce Maria Carraro, Mev Dominguez-Valentin, Omar Soukarieh, Pål Møller, Giovana Tardin Torrezan, Samuel Aguiar Junior
Publikováno v:
Familial Cancer. 19:323-336
Germline pathogenic variants in the DNA mismatch repair genes (MMR): MLH1, MSH2, MSH6, and PMS2, are causative of Lynch syndrome (LS). However, many of the variants mapping outside the invariant splice site positions (IVS ± 1, IVS ± 2) are classifi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a52a4b06a14942471efd67b378c5c619
https://doi.org/10.1007/s10689-020-00182-5
https://doi.org/10.1007/s10689-020-00182-5
Autor:
Gabriela ES Felix, Rodrigo Santa Cruz Guindalini, Yonglan Zheng, Tom Walsh, Elisabeth Sveen, Taisa Manuela Machado Lopes, Juliana Côrtes, Jing Zhang, Polyanna Carôzo, Irlânia Santos, Thaís Ferreira Bonfim, Bernardo Garicochea, Betânia Pereira Toralles, Roberto Meyer, Eduardo Martins Netto, Kiyoko Abe-Sandes, Mary-Claire King, Ivana Lucia de Oliveira Nascimento, Olufunmilayo I. Olopade
Purpose: There is a paucity of data on the spectrum and prevalence of pathogenic variants among women of African ancestry in the Northeast region of Brazil. Methods: We performed BROCA panel sequencing to identify inherited loss-of-function variants
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e8292f71545cf1d22464688b7f33af55
https://doi.org/10.21203/rs.3.rs-1065243/v1
https://doi.org/10.21203/rs.3.rs-1065243/v1
Autor:
Maria Nirvana Formiga, Joseph A. Pinto, Caroline U. Sa, Celia Aparecida Marques Pimenta, Julio Sanchez del Monte, Carlos A. Vaccaro, Mabel Bohorquez, Patricia Esperon, Florencia Spirandelli, Patricia Ashton-Prolla, Carmelo Caballero, Gutiérrez Angulo Melva, Maria del Carmen Castro-Mujica, Edite P. Oliveira, Norma Teresa Rossi, Sergio Chialina, Ivana Nascimento, Claudia Barletta-Carrillo, Larissa Souza Mario Bueno, Geth, Yesilda Balavarca, Jorge Padron, Edenir Inêz Palmero, Francisco López-Köstner, Sabrina Daniela da Silva, Nora Manoukian Forones, Juan Carlos Bazo-Alvarez, Florencia Neffa, Alcides Recalde Cañete, Mariela Torres Loarte, Pål Møller, Constantino Dominguez-Barrera, Mev Dominguez-Valentin, Pablo Kalfayan, John-Paul Plazzer, Jose Buleje, Kiyoko Abe-Sandes, Florencia C. Cardoso, Dirce Maria Carraro, Eivind Hovig, Patrik Wernhoff, Rodrigo Santa Cruz Guindalini, María Laura Gonzalez, Paola Montenegro Beltran, Marina Antelo, Angela R. Solano, Henrique de Campos Reis Galvão, Sonia Tereza dos Santos Nogueira, Samuel Aguiar Junior, Carlos Sarroca, Alberto Ignacio Herrando, Leonardo S. Lino-Silva, Carlos Mario Muñetón Peña, Tamara Alejandra Piñero, Erika Maria Monteiro Santos, Benedito Mauro Rossi, Mariano Golubicki, Yasser Sullcahuaman, Enrique Spirandelli, Geiner Jimenez, Karin Alvarez, Giovana Tardin Torrezan, Daniel Cisterna, Yenni Rodriguez, Richard Quispe, Ricardo Fujita, Claudia Martin, Della Valle Adriana, Renata Gondim Meira Velame de Azevedo, Lina Nuñez
Publikováno v:
Repositorio Académico USMP
Universidad San Martín de Porres-USMP
USMP-Institucional
Universidad de San Martín de Porres
instacron:USMP
International Journal of Cancer
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
Universidad San Martín de Porres-USMP
USMP-Institucional
Universidad de San Martín de Porres
instacron:USMP
International Journal of Cancer
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
Colorectal cancer (CRC) is one of the most common cancers in Latin America and the Caribbean, with the highest rates reported for Uruguay, Brazil and Argentina. We provide a global snapshot of the CRC patterns, how screening is performed, and compare
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::877aeca091c95233becfe121cbeb957b
https://doi.org/10.1002/ijc.31920
https://doi.org/10.1002/ijc.31920
Autor:
Patrik Wernhoff, Sergio Chialina, María Luisa Guevara Gil, María Laura Gonzalez, Luis José Palacios Fuenmayor, Constantino Dominguez-Barrera, Ana Protzel, Leonardo S. Lino-Silva, Michael Vallejo, Francisco López-Köstner, Karin Alvarez, Celia Aparecida Marques Pimenta, Julio Sanchez del Monte, Nadia Cambados Héritas, Carlos Mario Muñetón Peña, Jorge Andres Rugeles Mindiola, Elizabeth Lemos Silveira-Lucas, Eivind Hovig, Luisina Inés Bruno, Carlos Reyes-Silva, Alicia Cock-Rada, Florencia Neffa, Thais F Bonfim Palma, Richard Quispe, Alcides Recalde, Gabriela Jaramillo-Koupermann, Fabiana Alejandra Ferro, Norma Teresa Rossi, Mev Dominguez-Valentin, Florencia Spirandelli, Edenir Inêz Palmero, John-Paul Plazzer, Tirzah Braz Petta-Lajus, Sandra Patricia Bello Uyaban, Adriana Della Valle, Pål Møller, Ivana Nascimento, Marina Antelo, Jose Buleje, Kiyoko Abe-Sandes, Alejandra Mampel, Ana Rafaela de Souza Timoteo, Enrique Spirandelli, Julyann Pérez-Mayoral, Mariano Golubicki, Yasser Sullcahuaman, Alfonso Suárez, Mariela Torres, Henrique de Campos Reis Galvão, Carlos Sarroca, Magdalena Echeverry, Carlos Afanador Ayala, Claudia Martin, Guiliana Chávez, Jesús Arturo Hernández-Sandoval, Angélica Hernandez Guerrero, Geiner Jimenez, Yeni Rodriguez, Cladelis Rubio, Tamara Alejandra Piñero, Marcia Cruz-Correa, Pablo Kalfayan, Benedito Mauro Rossi, Florencia Petracchi, María de la Luz Ayala-Madrigal, Yesilda Balavarca, Juan Carlos Bazo-Alvarez, Carlos A. Vaccaro, Mabel Bohorquez, Milagros Dueñas, Nora Manoukian Forones, Claudio Benavides Yañez
Publikováno v:
European journal of cancer (Oxford, England : 1990). 119
We aimed to assess the current genetics practice to manage patients with Lynch syndrome (LS) across Latin America. A Latin American LS survey was sent out to 52 centres/registries, comprising a total of 12 countries from the region. Overall, 33 centr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e288aad80099e1069fea7e6d4d5a63c6
https://pubmed.ncbi.nlm.nih.gov/31442815
https://pubmed.ncbi.nlm.nih.gov/31442815