Publications

The mg$Δ$lpn mouse model for Marfan syndrome recapitulates the ocular phenotypes of the disease
Rodrigo Barbosa de Souza, Isabela Gerdes Gyuricza, Luara Lucena Cassiano, Luis Ernesto Farinha-Arcieri, Ana Maria Alvim Liberatore, Sheila Schuindt do Carmo, Waldir Caldeira, Marcio V. Cruz, Alberto F. Ribeiro, Roberto Carlos Tedesco, Dieter P. Reinhardt, Ricardo Smith, Ivan Hong Jun Koh, Lygia V. Pereira
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Proteomic and transcriptomic profiling reveal different aspects of aging in the kidney
textlessptextgreaterLittle is known about the molecular changes that take place in the kidney during the aging process. In order to …
Yuka Takemon, Joel M Chick, Isabela Gerdes Gyuricza, Daniel A Skelly, Olivier Devuyst, Steven P Gygi, Gary A Churchill, Ron Korstanje
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Is HSPG2 a modifier gene for Marfan syndrome?
Marfan syndrome (MFS) is a connective tissue disease caused by variants in the FBN1 gene. Nevertheless, other genes influence the …
Isabela Gerdes Gyuricza, Rodrigo Barbosa de Souza, Luis Ernesto Farinha-Arcieri, Gustavo Ribeiro Fernandes, Lygia Veiga Pereira
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Induced Pluripotent Stem Cell for the Study and Treatment of Sickle Cell Anemia
Sickle cell anemia (SCA) is a monogenic disease of high mortality, affecting millions of people worldwide. There is no broad, …
Luiza Cunha Junqueira Reis, Virgínia Picanço-Castro, Bárbara Cristina Martins Fernandes Paes, Olívia Ambrozini Pereira, Isabela Gerdes Gyuricza, Fabiano Tófoli De Araújo, Mariana Morato-Marques, Lílian Figueiredo Moreira, Everton De Brito Oliveira Costa, Tálita Pollyanna Moreira Dos Santos, Dimas Tadeu Covas, Lygia Da Veiga Pereira Carramaschi, Elisa Maria De Sousa Russo
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