Zobrazeno 1 - 10
of 54
pro vyhledávání: '"Greice Andreotti De Molfetta"'
Autor:
Joel Del Bel Pádua, Carolline Fontes Alves Mariano, Alexandre Todorovic Fabro, Fermino Sanches Lizarte Neto, Rogério Lenotti Zuliani, Cláudia Tarcila Gomes Sares, José Sebastião dos Santos, Ajith Kumar Sankarankutty, Daniela Pretti da Cunha Tirapelli, Vanessa da Silva Silveira, Greice Andreotti de Molfetta, Wilson Araújo da Silva Júnior, Mariângela Ottoboni Brunaldi
Publikováno v:
Biomarker Insights, Vol 19 (2024)
Background: Immunohistochemical prognostic significance of the homologous recombination-related proteins RAD51, ATM, BRCA1, and BRCA2 is known in gastric adenocarcinoma, one of the deadliest cancers. Objective and design: This retrospective cohort st
Externí odkaz:
https://doaj.org/article/00cdf380685147fb9d7d7953a5654c4a
Autor:
Mariana Lima Mascarenhas Moreira, Iana Mizumukai de Araújo, Greice Andreotti de Molfetta, Wilson Araújo Silva Jr., Francisco José Albuquerque de Paula
Publikováno v:
Archives of Endocrinology and Metabolism, Vol 65, Iss 4, Pp 500-504 (2021)
SUMMARY The occurrence of fractures in young individuals is frequently overlooked by physicians, especially when associated with exercise or trauma. Nevertheless, multiple fractures should always be investigated since underlying conditions can predis
Externí odkaz:
https://doaj.org/article/1990b69343ce460ea11f1b39997694fc
Autor:
Aline Simoneti Fonseca, Anelisa Ramão, Matheus Carvalho Bürger, Jorge Estefano Santana de Souza, Dalila Lucíola Zanette, Greice Andreotti de Molfetta, Luiza Ferreira de Araújo, Rafaela de Barros e Lima Bueno, Graziela Moura Aguiar, Jessica Rodrigues Plaça, Cleidson de Pádua Alves, Anemari Ramos Dinarte dos Santos, Daniel Onofre Vidal, Gyl Eanes Barros Silva, Rodrigo Alexandre Panepucci, Fernanda Maris Peria, Omar Feres, José Joaquim Ribeiro da Rocha, Marco Antonio Zago, Wilson Araújo Silva
Publikováno v:
BMC Cancer, Vol 21, Iss 1, Pp 1-14 (2021)
Abstract Background Colorectal cancer (CRC) is one of the most common cancers worldwide; it is the fourth leading cause of death in the world and the third in Brazil. Mutations in the APC, DCC, KRAS and TP53 genes have been associated with the progre
Externí odkaz:
https://doaj.org/article/714a3d32697943ac85805bff473fd4b1
Autor:
Ana Vitoria Barban Margutti, Wilson Araújo Silva, Daniel Fantozzi Garcia, Greice Andreotti de Molfetta, Adriana Aparecida Marques, Tatiana Amorim, Vânia Mesquita Gadelha Prazeres, Raquel Tavares Boy da Silva, Irene Kazue Miura, João Seda Neto, Emerson de Santana Santos, Mara Lúcia Schmitz Ferreira Santos, Charles Marques Lourenço, Tássia Tonon, Fernanda Sperb-Ludwig, Carolina Fischinger Moura de Souza, Ida Vanessa Döederlein Schwartz, José Simon Camelo
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-11 (2020)
Abstract Background Maple syrup urine disease (MSUD) is an autosomal recessive inherited metabolic disease caused by deficient activity of the branched-chain α-keto acid dehydrogenase (BCKD) enzymatic complex. BCKD is a mitochondrial complex encoded
Externí odkaz:
https://doaj.org/article/2039cf41956a41fdbfad39b064da9a4f
Autor:
Léa Maria Zanini Maciel, Patrícia Künzle Ribeiro Magalhães, Ieda Regina Lopes Del Ciampo, Maria Luísa Barato de Sousa, Maria Inez Machado Fernandes, Regina Sawamura, Roberta Rodrigues Bittar, Greice Andreotti de Molfetta, Wilson Araújo da Silva Júnior
Publikováno v:
Cadernos de Saúde Pública, Vol 36, Iss 10 (2020)
The Hospital of the Ribeirão Preto Medical School, University of São Paulo is one of the three screening centers in São Paulo State, Brazil, and has included a test for cystic fibrosis (CF) since February 6, 2010, by a court order. We evaluated th
Externí odkaz:
https://doaj.org/article/e770eb5539fd4dfb94ddb8193b599a1e
Autor:
Simone da Costa e Silva Carvalho, Carlos Henrique Paiva Grangeiro, Clarissa Gondim Picanço-Albuquerque, Thaís Oliveira dos Anjos, Greice Andreotti De Molfetta, Wilson Araujo Silva, Victor Evangelista de Faria Ferraz
Publikováno v:
BMC Research Notes, Vol 11, Iss 1, Pp 1-7 (2018)
Abstract Objective Hereditary hearing loss (HL) is the most common sensorineural disorder in humans. Besides mutations in GJB2 and GJB6 genes, pathogenic variants in the SLC26A4 gene have been reported as a cause of hereditary HL due to its role in t
Externí odkaz:
https://doaj.org/article/5d30c5e00d8441329e94246976220085
Autor:
Bruna Rodrigues Muys, Júlio Cesar Cetrulo Lorenzi, Dalila Luciola Zanette, Rafaela de Barros Lima e Bueno, Luíza Ferreira de Araújo, Anemari Ramos Dinarte-Santos, Cleidson Pádua Alves, Anelisa Ramão, Greice Andreotti de Molfetta, Daniel Onofre Vidal, Wilson Araújo Silva
Publikováno v:
PLoS ONE, Vol 11, Iss 3, p e0151560 (2016)
LINC00629 and MIR503HG are long intergenic non-coding RNAs (lincRNAs) mapped on chromosome X (Xq26), a region enriched for genes associated with human reproduction. Genes highly expressed in normal reproductive tissues and cancers (CT genes) are well
Externí odkaz:
https://doaj.org/article/69b9cc2606f54e88aefe7b9d1b22c12b
Autor:
João M. de Pina-Neto, Victor Evangelista F. Ferraz, Greice Andreotti de Molfetta, Jess Buxton, Sarah Richards, Sue Malcolm
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 55, Iss 2, Pp 199-208 (1997)
The Prader-Willi syndrome (PWS) and the Angelman syndrome (AS) are human neurogenetic disorders involving the imprinting mechanism, at the 15q11-13 chromosome region. The predominant genetic defects in PW are 15q 11-13 deletions of paternal origin an
Externí odkaz:
https://doaj.org/article/c263e5933130443c813308f5fba70f53
Autor:
Wilson A. Silva, Markus Hafner, Daniel Onofre Vidal, Ashish Lal, Anelisa Ramão, Greice Andreotti de Molfetta, Xiao Ling Li, Xiantao Wang, Dimitrios G. Anastasakis, Aishe A. Sarshad, Luíza Ferreira de Araújo, Jessica Rodrigues Plaça, Josane F. Sousa, Bruna Rodrigues Muys
Supplementary Figure 3. Protein blot from AGO proteins from nuclear and cytoplasmic portions of A2780.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::04e8dcfc2bb5d0a02174e3b8f1844f2a
https://doi.org/10.1158/0008-5472.22420899.v1
https://doi.org/10.1158/0008-5472.22420899.v1
Autor:
Wilson A. Silva, Markus Hafner, Daniel Onofre Vidal, Ashish Lal, Anelisa Ramão, Greice Andreotti de Molfetta, Xiao Ling Li, Xiantao Wang, Dimitrios G. Anastasakis, Aishe A. Sarshad, Luíza Ferreira de Araújo, Jessica Rodrigues Plaça, Josane F. Sousa, Bruna Rodrigues Muys
Dysregulation of miRNA expression is associated with multiple diseases, including cancers, in which small RNAs can have either oncogenic or tumor suppressive functions. Here we investigated the potential tumor suppressive function of miR-450a, one of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ccb27b600b22ad4e04f08d09d2a0805c
https://doi.org/10.1158/0008-5472.c.6510780
https://doi.org/10.1158/0008-5472.c.6510780