Zobrazeno 1 - 10
of 44
pro vyhledávání: '"Cristiane S. Rocha"'
Autor:
Amanda M. Canto, Alexandre B. Godoi, Alexandre H. B. Matos, Jaqueline C. Geraldis, Fabio Rogerio, Marina K. M. Alvim, Clarissa L. Yasuda, Enrico Ghizoni, Helder Tedeschi, Diogo F. T. Veiga, Barbara Henning, Welliton Souza, Cristiane S. Rocha, André S. Vieira, Elayne V. Dias, Benilton S. Carvalho, Rovilson Gilioli, Albert B. Arul, Renã A. S. Robinson, Fernando Cendes, Iscia Lopes‐Cendes
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 9, Iss 4, Pp 454-467 (2022)
Abstract Objectives We compared the proteomic signatures of the hippocampal lesion induced in three different animal models of mesial temporal lobe epilepsy with hippocampal sclerosis (MTLE+HS): the systemic pilocarpine model (PILO), the intracerebro
Externí odkaz:
https://doaj.org/article/f1b0e9ef2cfb478c82e204f073111d3e
Autor:
Rodrigo Secolin, Tânia K. de Araujo, Marina C. Gonsales, Cristiane S. Rocha, Michel Naslavsky, Luiz De Marco, Maria A. C. Bicalho, Vinicius L. Vazquez, Mayana Zatz, Wilson A. Silva, Iscia Lopes-Cendes
Publikováno v:
Human Genome Variation, Vol 8, Iss 1, Pp 1-9 (2021)
COVID-19: Variants related to susceptibility in a Brazilian population Genetic variants in the Brazilian population do not appear to explain the relatively high overall rates of COVID-19 cases compared to other countries, but could be relevant for ri
Externí odkaz:
https://doaj.org/article/837a8a8fd95843fc8e7711345c437392
Autor:
Rodrigo Secolin, Marina C. Gonsales, Cristiane S. Rocha, Michel Naslavsky, Luiz De Marco, Maria A. C. Bicalho, Vinicius L. Vazquez, Mayana Zatz, Wilson A. Silva, Iscia Lopes-Cendes
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
We recently reported a deviation of local ancestry on the chromosome (ch) 8p23.1, which led to positive selection signals in a Brazilian population sample. The deviation suggested that the genetic variability of candidate genes located on ch 8p23.1 m
Externí odkaz:
https://doaj.org/article/393e054902154532bb1fd24aca80a76f
Publikováno v:
Genetics and Molecular Biology, Vol 43, Iss 2 (2020)
Abstract For a better interpretation of variants, evidence-based databases, such as ClinVar, compile data on the presumed relationships between variants and phenotypes. In this study, we aimed to analyze the pattern of sequencing depth in variants fr
Externí odkaz:
https://doaj.org/article/add904e6946e40d9b5868988d071cb91
Autor:
Sâmia Cruz Tfaile Corbi, Alliny Souza Bastos, Rafael Nepomuceno, Thamiris Cirelli, Raquel Alves dos Santos, Catarina Satie Takahashi, Cristiane S. Rocha, Silvana Regina Perez Orrico, Claudia V. Maurer-Morelli, Raquel Mantuaneli Scarel-Caminaga
Publikováno v:
Journal of Diabetes Research, Vol 2017 (2017)
Despite increasing research in type 2 diabetes mellitus (T2D), there are few studies showing the impact of the poor glycemic control on biological processes occurring in T2D. In order to identify potential genes related to poorly/well-controlled pati
Externí odkaz:
https://doaj.org/article/196c20bd76ba40bf8a38aa0ba8fd4128
Autor:
Claudia V Maurer-Morelli, Jaira F de Vasconcellos, Estela M Bruxel, Cristiane S Rocha, Amanda M do Canto, Helder Tedeschi, Clarissa L Yasuda, Fernando Cendes, Iscia Lopes-Cendes
Publikováno v:
Exp Biol Med (Maywood)
Most patients with pharmacoresistant mesial temporal lobe epilepsy (MTLE) have hippocampal sclerosis on the postoperative histopathological examination. Although most patients with MTLE do not refer to a family history of the disease, familial forms
Autor:
de Campos Bm, Alvim Mkm, Cardoso TAMdO, Souza Tkas, Joao Rb, Fernando Cendes, Natalia S Brunetti, Waku T, Ludwig Gvn, Clarissa L. Yasuda, Boldrini VdO, Sousa JGDd, da Costa Ba, Mendes Mj, Baptista Sn, de Brito Mr, Alessandro S. Farias, Santos Lmb, Cristiane S. Rocha, Lucas Scardua Silva, Schmitt GdS, André Schwambach Vieira, Mateus Henrique Nogueira, ítalo Karmann Aventurato
Although post-acute cognitive dysfunction and neuroimaging abnormalities have been reported after hospital discharge in patients recovered from COVID-19, little is known about persistent, long-term alterations in patients who did not require hospital
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e4ab5bf7db6eb2cebcf16b205d6d5408
https://doi.org/10.21203/rs.3.rs-2339100/v1
https://doi.org/10.21203/rs.3.rs-2339100/v1
Autor:
Amanda M Canto, André Schwambach Vieira, Alexandre Hilário Berenguer de Matos, Benilton S. Carvalho, Rovilson Gilioli, Diogo F.T. Veiga, Vinicius D'Ávila Bitencourt Pascoal, Barbara Henning, Alexandre B Godoi, Cristiane S. Rocha, Iscia Lopes-Cendes, Fernando Cendes, Beatriz Bertelli Aoyama
Publikováno v:
Hippocampus. 31:122-139
Mesial temporal lobe epilepsy (MTLE) is a chronic neurological disorder characterized by the occurrence of seizures, and histopathological abnormalities in the mesial temporal lobe structures, mainly hippocampal sclerosis (HS). We used a multi-omics
Autor:
Bárbara Roque da Silva, Alliny de Souza Bastos, Catarina Satie Takahashi, Diego Girotto Bussaneli, Cláudia Vianna Maurer-Morelli, Silvana Regina Perez Orrico, Raquel M. Scarel-Caminaga, Silvana P. Barros, Sâmia Cruz Tfaile Corbi, Benilton S. Carvalho, Jaira F. de Vasconcellos, Cristiane S. Rocha, Raquel Alves dos Santos
Publikováno v:
Scientific Reports, Vol 10, Iss 1, Pp 1-14 (2020)
Scientific Reports
Scopus
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP
Scientific Reports
Scopus
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP
Made available in DSpace on 2020-12-12T02:06:26Z (GMT). No. of bitstreams: 0 Previous issue date: 2020-12-01 Type 2 diabetes mellitus (T2DM), dyslipidemia and periodontitis are frequently associated pathologies; however, there are no studies showing
Autor:
Simoni H Avansini, Francesca Puppo, Jason W Adams, Andre S Vieira, Ana C Coan, Fabio Rogerio, Fabio R Torres, Patricia A O R Araújo, Mariana Martin, Maria A Montenegro, Clarissa L Yasuda, Helder Tedeschi, Enrico Ghizoni, Andréa F E C França, Marina K M Alvim, Maria C Athié, Cristiane S Rocha, Vanessa S Almeida, Elayne V Dias, Lauriane Delay, Elsa Molina, Tony L Yaksh, Fernando Cendes, Iscia Lopes Cendes, Alysson R Muotri
Publikováno v:
Brain : a journal of neurology, vol 145, iss 6
Focal cortical dysplasia is a highly epileptogenic cortical malformation with few treatment options. Here, we generated human cortical organoids from patients with focal cortical dysplasia type II. Using this human model, we mimicked some focal corti