Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Marcela Cavalcante de Andrade Silva"'
Autor:
Jesus Paula Carvalho, Edmund Chada Baracat, Maria Del Pilar Esteves Diz, Heloisa de Andrade Carvalho, Filomena Marino de Carvalho, Marcela Cavalcante de Andrade Silva, Altamiro Ribeiro Dias Jr.
Publikováno v:
Rare Tumors, Vol 4, Iss 1, Pp e4-e4 (2012)
Fanconi Anemia (FA) is an autosomal recessive disease characterized by chromosome instability, cellular hypersensitivity to DNA cross-linking agents, and increased predisposition to malignancies. We describe here a 28 year-old female with FA and vagi
Externí odkaz:
https://doaj.org/article/5b9df50458e3420b90bd0727031c1706
Autor:
Michael W, Drazer, Claire C, Homan, Kai, Yu, Marcela, Cavalcante de Andrade Silva, Kelsey E, McNeely, Matthew J, Pozsgai, Maria G, Acevedo-Mendez, Jeremy P, Segal, Peng, Wang, Jinghua, Feng, Sarah L, King-Smith, Erika, Kim, Sophia, Korotev, David M, Lawrence, Andreas W, Schreiber, Christopher N, Hahn, Hamish S, Scott, Raman, Sood, Elvira D R P, Velloso, Anna L, Brown, Paul P, Liu, Lucy A, Godley
Publikováno v:
Blood Advances. 6:4357-4359
Autor:
Lia DeRoin, Marcela Cavalcante de Andrade Silva, Kristin Petras, Kelly Arndt, Nathaniel Phillips, Pankhuri Wanjari, Hari Prasanna Subramanian, David Montes, James McElherne, Megan Theissen, Renee Briese, Soma Das, Lucy A. Godley, Jeremy Segal, Daniela del Gaudio, Carrie Fitzpatrick, Jane E. Churpek
Publikováno v:
Human mutation. 43(7)
To avoid acquired variants found in the blood, cultured skin fibroblasts are a recommended DNA source for germline genetic testing in patients with hematologic disorders, but data are lacking regarding practicality and limitations. We conducted a ret
Autor:
Emery H. Bresnick, Elvira Deolinda Rodrigues Pereira Velloso, Lucy A. Godley, Marcela Cavalcante de Andrade Silva, Koichi R. Katsumura, Charu Mehta
Publikováno v:
Leukemia. 35:264-268
Autor:
Christopher N. Hahn, Raman Sood, Sophia C. Korotev, Erika Kim, David M. Lawrence, Elvira Deolinda Rodrigues Pereira Velloso, Lucy A. Godley, Nisc Comparative Sequencing Program, Peng Wang, Paul P. Liu, Andreas W. Schreiber, Matthew J. Pozsgai, Kelsey E. McNeely, Claire C. Homan, Marcela Cavalcante de Andrade Silva, Anna L. Brown, Kai Yu, Jeremy P. Segal, Sarah L King-Smith, Jinghua Feng, Michael W. Drazer, Hamish S. Scott, Maria G. Acevedo
Currently, there are at least a dozen recognized hereditary hematopoietic malignancies (HHMs), some of which phenocopy others. Among these, three HHMs driven by germline mutations in ANKRD26, ETV6, or RUNX1 share a phenotype of thrombocytopenia, qual
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::580d2a5488fc8813180c959ea5b48040
https://doi.org/10.1101/2021.11.17.468983
https://doi.org/10.1101/2021.11.17.468983
Autor:
Marcela, Cavalcante de Andrade Silva, Koichi R, Katsumura, Charu, Mehta, Elvira D R P, Velloso, Emery H, Bresnick, Lucy A, Godley
Publikováno v:
Leukemia. 35(1)
Autor:
Luciana Nardinelli, Evelin Aline Zanardo, Nair Hideki Muto, Ana Cristina Victorino Krepischi, Marcela Cavalcante de Andrade Silva, Vanderson Rocha, Silvia S. Costa, Elvira Deolinda Rodrigues Pereira Velloso, AM Leal, Leslie Domenici Kulikowski
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
Familial platelet disorder with propensity to acute myeloid leukemia (FPD/AML) associated with RUNX1 mutations is an autosomal dominant disorder included in the group of the myeloid neoplasms with germ line predisposition. We describe two brothers wh
Autor:
Soma Das, Pankhuri Wanjari, Hari Prasanna Subramanian, Lia DeRoin, Carrie Fitzpatrick, Daniela del Gaudio, Jeremy P. Segal, Jane E. Churpek, Marcela Cavalcante de Andrade Silva, Kelly Arndt, Lucy A. Godley, Nathaniel Phillips, David Montes, Kristin Petras
Publikováno v:
Blood. 136:35-36
Introduction Peripheral blood is the standard tissue source for germline genetic testing in most scenarios. In patients with hematologic malignancies, however, peripheral blood frequently contains tumor- or clonal hematopoiesis-related acquired genet
Publikováno v:
Cancer genetics.
With improvements in DNA sequencing technologies and the consequent reduction in costs, next generation sequencing is being utilized increasingly in panel-based testing to perform molecular profiling of tumors. Such tumor-based panels are often refer
Autor:
Marcela Cavalcante de Andrade Silva, Carolina Bárbara Belli, Silvia Maria Meira Magalhães, M. Rosenhain, Pedro Negri Aranguren, Yesica Soledad Bestach, Jacqueline Gonzalez, María Soledad Undurraga, Irene Larripa, Ronald Feitosa Pinheiro, Graciela Alfonso, Roberta Sandra da Silva Tanizawa, Ximena Valladares, Elvira Deolinda Rodrigues Pereira Velloso, Nora Watman, Hernán García Rivello
Publikováno v:
American Journal of Hematology. 90:851-858
Fil: Belli, Carolina Barbara. Consejo Nacional de Investigaciones Cientificas y Tecnicas. Instituto de Medicina Experimental. Academia Nacional de Medicina de Buenos Aires. Instituto de Medicina Experimental; Argentina