Zobrazeno 1 - 10
of 80
pro vyhledávání: '"Luiz F Onuchic"'
Autor:
Precil D Neves, Ramaiane A Bridi, Janaína A Ramalho, Lectícia B Jorge, Elieser H Watanabe, Andreia Watanabe, Luis Yu, Viktoria Woronik, Rafaela B Pinheiro, Leonardo A Testagrossa, Lívia B Cavalcante, Denise M Malheiros, Cristiane B Dias, Luiz F Onuchic
Publikováno v:
PLoS Neglected Tropical Diseases, Vol 14, Iss 10, p e0008582 (2020)
BackgroundSchistosoma mansoni schistosomiasis (SM) remains a public health problem in Brazil. Renal involvement is classically manifested as a glomerulopathy, most often membranoproliferative glomerulonephritis or focal and segmental glomeruloscleros
Externí odkaz:
https://doaj.org/article/b3da16565a04432f9badbda9d9798932
Autor:
Luciana S. Feltran, Andreia Watanabe, Mara S. Guaragna, Ivan C. Machado, Fernanda M.S. Casimiro, Precil D.M.M. Neves, Lilian M. Palma, Patrícia Varela, Maria H. Vaisbich, Suely K.N. Marie, Inalda Facincani, João B. Pesquero, Vera M.S. Belangero, Matthew G. Sampson, Paulo C. Koch Nogueira, Luiz F. Onuchic
Publikováno v:
Kidney International Reports, Vol 5, Iss 3, Pp 358-362 (2020)
Externí odkaz:
https://doaj.org/article/199ec3e071334eb9a0072e65f0d5627f
Autor:
Renata Meca, Bruno E. Balbo, Milene Subtil Ormanji, Jonathan M. Fonseca, Leandro R. Iannuzzi, Eliene Santana Costa, Luiz F. Onuchic, Ita Pfeferman Heilberg
Publikováno v:
Cellular Physiology and Biochemistry, Vol 52, Iss 5, Pp 1061-1074 (2019)
Externí odkaz:
https://doaj.org/article/a4f63db4b10d46a99af8871a28206d6b
Autor:
Nathalia Lisboa Gomes, Maria Tereza Martins Ferrari, Andreia Watanabe, Mirian Yumie Nishi, Luiz F. Onuchic, Leila Cristina Pedroso de Paula, Rafael Loch Batista, Thatiane E da Silva, Berenice B. Mendonca, Priscilla Cukier, Elaine Maria Frade Costa, Sorahia Domenice, Eduardo Castro da Costa
Publikováno v:
Sexual Development. 16:46-54
Wilms’ tumor suppressor gene 1 (WT1) plays an essential role in urogenital and kidney development. Heterozygous germline pathogenic allelic variants of WT1 have been classically associated with Denys–Drash syndrome (DDS) and Frasier syndrome (FS)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84e9eddd84fe3c3041f24f750b1cc0ab
https://doi.org/10.1159/000517373
https://doi.org/10.1159/000517373
Autor:
Precil D. Neves, Renato A. Caires, Manoel P. Guimarães, Elerson C. Costalonga, Livia B. Cavalcante, Verônica T. Costa e Silva, Francisco Z. Mattedi, Leonardo F. Santana, Antônio A. Teixeira-Júnior, Orlando V. Gomes, Gyl E. Silva, Emmanuel A. Burdmann, Luiz F. Onuchic
Publikováno v:
Kidney International. 101:637-639
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::57675172469fed0a3d3d59b68884435f
https://doi.org/10.1016/j.kint.2021.12.016
https://doi.org/10.1016/j.kint.2021.12.016
Autor:
Henrique Proença, José Osmar Medina Pestana, Luiz F. Onuchic, Andreia Watanabe, Elieser H. Watanabe, Valkercyo A. Feitosa, Precil Diego Miranda de Menezes Neves, Vega F S Azevedo, Fernanda Trani Ferreira
Publikováno v:
Kidney International Reports
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d3f8730253cc37867d6673ded37caf5
https://doi.org/10.1016/j.ekir.2020.10.021
https://doi.org/10.1016/j.ekir.2020.10.021
Autor:
Andressa G. Amaral, Camille C.C. da Silva, Julian D.C. Serna, Kinulpe Honorato-Sampaio, Jéssica A. Freitas, Amaro N. Duarte-Neto, Antonio C. Bloise, Laura Cassina, Marcos Y. Yoshinaga, Adriano B. Chaves-Filho, Feng Qian, Sayuri Miyamoto, Alessandra Boletta, Silvana Bordin, Alicia J. Kowaltowski, Luiz F. Onuchic
Publikováno v:
Biochimica et biophysica acta. Molecular basis of disease. 1868(6)
Cardiovascular manifestations account for marked morbi-mortality in autosomal dominant polycystic kidney disease (ADPKD). Pkd1- and Pkd2-deficient mice develop cardiac dysfunction, however the underlying mechanisms remain largely unclear. It is unkno
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4773c3a8296d1a8129f8e06f6cbafa2c
https://pubmed.ncbi.nlm.nih.gov/35218894
https://pubmed.ncbi.nlm.nih.gov/35218894
Autor:
Luiz F. Onuchic, Guilherme Jinson de Oliveira Ahn, Neide Missae Murai, Eny Maria Goloni Bertollo, David Campos Wanderley, Vinicius Augusto Ferreira Baptista, Osvaldo Merege Vieira-Neto, Márcio Dantas, Elieser Hitoshi Watanabe, Joaquim Nelito da Silveira-Neto, Precil Diego Miranda de Menezes Neves, Miguel Moyses-Neto, Sergio R. De Antonio, Andreia Watanabe, Maria Alice Sperto Ferreira Baptista, Stanley de Almeida Araújo, Roberto Silva Costa
Publikováno v:
Diagnostic Pathology
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Diagnostic Pathology, Vol 16, Iss 1, Pp 1-6 (2021)
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Diagnostic Pathology, Vol 16, Iss 1, Pp 1-6 (2021)
Background Lipoprotein glomerulopathy (LPG) is a rare autosomal dominant disease caused by mutations in APOE, the gene which encodes apolipoprotein E. LPG mainly affects Asian individuals, however occasional cases have also been described in American
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79f484a5ac214cf0959f732f9d9477e0
https://doi.org/10.1186/s13000-021-01119-x
https://doi.org/10.1186/s13000-021-01119-x
Autor:
Juan J Muñoz, Ana C Anauate, Andressa G Amaral, Frederico M Ferreira, Elieser H Watanabe, Renata Meca, Milene S Ormanji, Mirian A Boim, Luiz F Onuchic, Ita Pfeferman Heilberg
Autosomal Dominant Polycystic Kidney Disease (ADPKD) is the most common inherited renal disorder, characterized by renal cyst development leading to end-stage renal disease. Although the appropriate choice of suitable reference is critical for quanti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::10ffd426ee4ce6a484fd3a515ba95737
https://doi.org/10.21203/rs.3.rs-551245/v1
https://doi.org/10.21203/rs.3.rs-551245/v1
Autor:
Ita Pfeferman Heilberg, Milene S Ormanji, Mirian A. Boim, Renata Meca, Elieser H. Watanabe, Ana Carolina Anauate, Juan José Augusto Moyano Muñoz, Luiz F. Onuchic, Frederico Moraes Ferreira, Andressa Godoy Amaral
Publikováno v:
Scientific Reports
Scientific Reports, Vol 11, Iss 1, Pp 1-14 (2021)
Scientific Reports, Vol 11, Iss 1, Pp 1-14 (2021)
Autosomal Dominant Polycystic Kidney Disease (ADPKD) is the most common inherited renal disorder, characterized by renal cyst development leading to end-stage renal disease. Although the appropriate choice of suitable reference is critical for quanti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0175fdc2a47385e6be2e8fdb37abf4bd
https://pubmed.ncbi.nlm.nih.gov/34611276
https://pubmed.ncbi.nlm.nih.gov/34611276