Zobrazeno 1 - 10
of 44
pro vyhledávání: '"Fernanda Timm"'
Publikováno v:
Pesquisa Agropecuária Tropical, Vol 54, p e79612 (2024)
The conventional vegetable farming model aggravates the climate crisis, whereas the no-tillage system provides a sustainable alternative. This study aimed to identify winter cover crops for single cropping and intercropping by evaluating the biomass
Externí odkaz:
https://doaj.org/article/f7a78301edaa47978f256cc23e7fef5c
Autor:
Paulo José Lorenzoni, Elaine Cardoso, Ana C. S. Crippa, Charles Marques Lourenço, Fernanda Timm Seabra Souza, Roberto Giugliani, Maria Luiza Saraiva-Pereira, Salmo Raskin, Isac Bruck, Cláudia S. K. Kay, Rosana H. Scola, Lineu C.Werneck, Hélio A. G. Teive
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 72, Iss 3, Pp 214-218 (2014)
The aim of the study was to analyze a series of Brazilian patients with Niemann-Pick disease type C (NP-C). Method Correlations between clinical findings, laboratory data, molecular findings and treatment response are presented. Result The sample con
Externí odkaz:
https://doaj.org/article/a02badeda6ba48cc82dfe4d8ace2fc43
Autor:
Fernanda Timm Seabra Souza, Alexandre Silva de Mello, Kristiane Michelin, Janice Carneiro Coelho
Publikováno v:
Genetics and Molecular Biology, Vol 27, Iss 3, Pp 454-459 (2004)
The effect of four antibiotics (amikacin, clindamycin, cephalothin and vancomycin) was investigated considering that bacterial infection in fibroblasts cultures is a very frequent event. The investigation included the effect of the antibiotics on fib
Externí odkaz:
https://doaj.org/article/9633d1141aa84b828c317d07a5ee833b
Autor:
Marcella Borges, Luissa Araujo, Bruno Lima, Laura Vagnini, Alberto Salles, Guerino Magalhaes, Joao Cristofolo, Joao Freitas, Pedro Aranas, Jacqueline Fonseca, Fernanda Timm, Charles Lourenco
Publikováno v:
Residência Pediátrica.
Lysosomal acid lipase deficiency (LAL-D) is a lysosomal storage disorder involved in cholesterol ester metabolism. It is a poorly understood genetic cause of cirrhosis, dyslipidemia and premature atherosclerotic disease in children and adults. As the
Autor:
Bruno Previdelli Coghi, Beatriz Bettiol Nicoletti, Bruna Sandy Pastre, Bruna Isepão Barboza da-Silva, Zumira Aparecida Carneiro, Jacqueline Fonseca, Laura Vagnini, Regina Albuquerque, Marcela Almeida, Debora de Cassia Tomaz, Fernanda Veiga Goes, Tainá Regina Damaceno Silveira, Ana Paula Andrade Hamad, Fernanda Timm, Charles Marques Lourenco
Publikováno v:
Rev Ped SOPERJ. 22
Autor:
Maria Luiza Saraiva-Pereira, Roberto Giugliani, Fernanda Timm Seabra Souza, Felipe C Nepomuceno, Rafaella Mergener, Hugo Bock, Ana Carolina Silva Rodrigues Farias, Márcia Polese-Bonatto, Mirela Severo Gil, Rejane Gus, Maria Cristina Cotta Matte
Publikováno v:
Molecular Neurobiology. 56:6426-6435
Niemann-Pick type C (NP-C) is a rare autosomal recessive disorder characterized by storage of unesterified glycolipids and cholesterol in lysosome and/or late endosome due to mutations in either NPC1 or NPC2 gene. This study aims to identify the spec
Autor:
Seabra Souza, Fernanda Timm, Souza Sostruznik, Luana, Casagrande Scolari, Roberta, Maciel de Castro, Karen Joana, Giugliani, Roberto, Coelho, Janice Carneiro
Publikováno v:
In Clinical Biochemistry 2007 40(8):521-525
Autor:
Verônica Bidinotto Brito, Roberto Giugliani, Fernanda Poletto, Rudimar Luiz Frozza, Bruna Donida, Luiza Steffens Reinhardt, Bárbara Tauffner, Fernanda Timm, Marco Raabe, Andryele Zaffari Machado, Andressa Bernardi, Rejane Gus Kessler, Carmen Regla Vargas, Dinara Jaqueline Moura, Marcelo Alexandre de Farias, Tatiane Grazieli Hammerschmidt, Rodrigo Villares Portugal
Publikováno v:
Journal of inherited metabolic diseaseREFERENCES. 43(3)
β-Cyclodextrin (β-CD) is being considered a promising therapy for Niemann-Pick C (NPC) disease because of its ability to mobilise the entrapped cholesterol from lysosomes, however, a major limitation is its inability to cross the blood-brain barrie
Autor:
Maira Graeff Burin, Márcia Polese Bonatto, Rejane Gus Kessler, Fernanda Timm Seabra Souza, Carmen Regla Vargas, Graziela de Oliveira Schmitt Ribas, Kristiane Michelin-Tirelli, Maria Luiza Saraiva-Pereira, Tatiane Grazieli Hammerschmidt, Franciele Barbosa Trapp, Roberto Giugliani
Publikováno v:
International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience. 66
Background Niemann-Pick type C (NP-C), one of 50 inherited lysosomal storage disorders, is caused by NPC protein impairment that leads to unesterified cholesterol accumulation in late endosomal/lysosomal compartments. The clinical manifestations of N
Autor:
Pardo Echeverría, Liz Carolina, Arrieta Violet, Leopoldo Antonio, Seabra Souza, Fernanda Timm
Publikováno v:
Ciencia en Desarrollo, Volume: 7, Issue: 2, Pages: 31-41, Published: DEC 2016
Resumen Se realizó diagnóstico bioquímico en cultivos de fibroblastos, provenientes de biopsias de piel de 73 pacientes candidatos clínicamente de padecer la enfermedad neurodegenerativa de herencia autosómica recesiva de Niemann Pick C, remitid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______618::92bf191bc83f99c5b90ac84924431d14
http://www.scielo.org.co/scielo.php?script=sci_arttext&pid=S0121-74882016000200003&lng=en&tlng=en
http://www.scielo.org.co/scielo.php?script=sci_arttext&pid=S0121-74882016000200003&lng=en&tlng=en