Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Camila Simioni Vanzin"'
Autor:
Camila Simioni Vanzin, Caroline Paula Mescka, Bruna Donida, Desirèe Padilha Marchetti, Carlos Eduardo Jacques, Tatiane Hauschild, Jéssica Lamberty Faverzani, Marion Deon, Dinara Moura, Jenifer Saffi, Daniella de Moura Coelho, Moacir Wajner, Angela T.S. Wyse, Carmen Regla Vargas
Publikováno v:
Clinical and Biomedical Research, Vol 38, Iss 1 (2018)
Introduction: Homocysteine (Hcy) tissue accumulation occurs in a metabolic disease characterized biochemically by cystathionine β-synthase (CBS) deficiency and clinically by mental retardation, vascular problems, and skeletal abnormalities. Previous
Externí odkaz:
https://doaj.org/article/b36ae36dd098482790e2470350a1ab3d
Autor:
Desirèe Padilha Marchetti, Dinara Jaqueline Moura, Caroline Paula Mescka, Jéssica Lamberty Faverzani, Camila Simioni Vanzin, Moacir Wajner, Carlos Eduardo Diaz Jacques, Bruna Donida, Daniella de Moura Coelho, Tatiane Cristina Hauschild, Carmen Regla Vargas, Marion Deon, Jenifer Saffi, Angela T. S. Wyse
Publikováno v:
Clinical & Biomedical Research. 38:50-57
Introduction: Homocysteine (Hcy) tissue accumulation occurs in a metabolic disease characterized biochemically by cystathionine β-synthase (CBS) deficiency and clinically by mental retardation, vascular problems, and skeletal abnormalities. Previous
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9adb031f9988e372b465b2612940f765
https://doi.org/10.4322/2357-9730.76977
https://doi.org/10.4322/2357-9730.76977
Autor:
Janaína Kolling, Tatiane Grazieli Hammerschimidt, Bruna Donida, Adriana Simon Coitinho, Camila Simioni Vanzin, Caroline Paula Mescka, Angela T. S. Wyse, Emilene B. S. Scherer, Laura Vilarinho, Moacir Wajner, Graziela S. Ribas, Carmen Regla Vargas, Célia Nogueira
Publikováno v:
Cellular and Molecular Neurobiology. 35:899-911
Cystathionine-β-synthase (CBS) deficiency is the main cause of homocystinuria. Homocysteine (Hcy), methionine, and other metabolites of Hcy accumulate in the body of affected patients. Despite the fact that thromboembolism represents the major cause
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::969ad830a528916bcc9fa3946063c04a
https://doi.org/10.1007/s10571-015-0185-7
https://doi.org/10.1007/s10571-015-0185-7
Autor:
Carlos Alberto Yasin Wayhs, Carlos Severo Dutra-Filho, Gilian Guerreiro, Camila Simioni Vanzin, Vanusa Manfredini, Carolina Guerini de Souza, Moacir Wajner, Caroline Paula Mescka, Carmen Regla Vargas, Giovana Brondani Biancini
Publikováno v:
International Journal of Developmental Neuroscience. 31:21-24
Maple syrup urine disease (MSUD) is an inborn error of metabolism biochemically characterized by elevated levels of the branched chain amino acids (BCAA) leucine, isoleucine, valine and the corresponding branched-chain α-keto acids. This disorder is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ede93e08e3066fceb680ddf6eb601eb
https://doi.org/10.1016/j.ijdevneu.2012.10.109
https://doi.org/10.1016/j.ijdevneu.2012.10.109
Autor:
Carmen Regla Vargas, Camila Simioni Vanzin, Cristina Brinckmann Oliveira Netto, Roberto Giugliani, Graziela S. Ribas, Laura Bannach Jardim, Marion Deon, Alethea Gatto Barschak, Daiane Rodrigues, Giovana Brondani Biancini, Vanusa Manfredini
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1822:226-232
Fabry disease is an X-linked inborn error of glycosphingolipid catabolism due to deficient activity of α-galactosidase A that leads to accumulation of the enzyme substrates, mainly globotriaosylceramide (Gb3), in body fluids and lysosomes of many ce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8669dbf6f1a320682e8814f13e9e486
https://doi.org/10.1016/j.bbadis.2011.11.001
https://doi.org/10.1016/j.bbadis.2011.11.001
Autor:
Angela T. S. Wyse, Angela Sitta, Camila Simioni Vanzin, Moacir Wajner, Ida Vanessa Doederlein Schwartz, Izabela Netto Pereira, Solange Cristina Garcia, Carmen Regla Vargas, Francieli J Rockenbach, Giovana Brondani Biancini, Carlos Alberto Yasin Wayhs
Publikováno v:
Molecular Genetics and Metabolism. 104:112-117
Homocystinuria is an inherited disorder biochemically characterized by high urinary excretion of homocystine and increased levels of homocysteine (Hcy) and methionine in biological fluids. Affected patients usually have a variety of clinical and path
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae9417a4f298746ca08ffee86dc148bb
https://doi.org/10.1016/j.ymgme.2011.06.013
https://doi.org/10.1016/j.ymgme.2011.06.013
Autor:
Luciana Giugliani, Vanusa Manfredini, Camila Simioni Vanzin, Giovana Brondani Biancini, Angela Sitta, Denise Bohrer, Moacir Wajner, Ida Vanessa Doederlein Schwartz, A. B. de Oliveira, Solange Cristina Garcia, C. R. Vargas, Carlos Alberto Yasin Wayhs, Graziela de Oliveira Schmitt Ribas
Publikováno v:
Cellular and Molecular Neurobiology. 31:429-436
It is well established that the involvement of reactive species in the pathophysiology of several neurological diseases, including phenylketonuria (PKU), a metabolic genetic disorder biochemically characterized by elevated levels of phenylalanine (Ph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7ed492a40b9af437a6dab8a6ef42a10
https://doi.org/10.1007/s10571-010-9636-3
https://doi.org/10.1007/s10571-010-9636-3
Autor:
Helena Maria Tannhauser Barros, Angela Sitta, Giovana Brondani Biancini, Marion Deon, Graziela S. Ribas, Maurício Schüler Nin, Carlos Alberto Yasin Wayhs, Vanusa Manfredini, Carmen Regla Vargas, Camila Simioni Vanzin
Publikováno v:
Mutation Research/Genetic Toxicology and Environmental Mutagenesis. 703:187-190
Diabetes mellitus (DM) is a chronic hyperglycemic state. DM may be associated with moderate cognitive deficits and neurophysiologic/structural changes in the brain (diabetic encephalopathy). Psychiatric manifestations seem to accompany this encephalo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bdbf3fc0f63e5836255a52b7132fcc2a
https://doi.org/10.1016/j.mrgentox.2010.08.017
https://doi.org/10.1016/j.mrgentox.2010.08.017
Autor:
Moacir Wajner, Carmen Regla Vargas, Camila Simioni Vanzin, Vanusa Manfredini, Carlos Alberto Yasin Wayhs, Rosana B. Vieira, Giovana Brondani Biancini, Graziela S. Ribas, Maria Gilda De Marco
Publikováno v:
Mutation Research/Genetic Toxicology and Environmental Mutagenesis. 702:123-128
Propionic acidemia (PAemia) and methylmalonic acidemia (MMAemia) are inborn errors of propionate metabolism characterized by the accumulation of, respectively, propionic and l-methylmalonic acids (and their metabolites) in the blood and tissues of af
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::448bf62354b959879d797373826c25a1
https://doi.org/10.1016/j.mrgentox.2010.07.008
https://doi.org/10.1016/j.mrgentox.2010.07.008
Autor:
Giovana Brondani Biancini, Maria do Carmo Ruaro Peralba, Carmen Regla Vargas, Anna Maria Ribeiro Dal Vesco, Franciele Cipriani, Moacir Wajner, Vanusa Manfredini, Camila Simioni Vanzin, Roberta Treméa, Marion Deon, Lidiana Biasi
Publikováno v:
Cell Biochemistry and Function. 28:360-366
Type 2 diabetes (T2D) is associated with increased oxidative stress as indicated by elevated levels of lipid peroxidation and protein oxidation products. Since reactive oxygen species (ROS) can cause damage to biological macromolecules including DNA,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ceabccd0ea2da4c4b29bb69666fd114a
https://doi.org/10.1002/cbf.1654
https://doi.org/10.1002/cbf.1654