Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Tatiane Cristina Hauschild"'
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
Autor:
Tatiane Cristina Hauschild, Eduard A. Struys, Carmen Regla Vargas, Vanusa Manfredini, Carlos Eduardo Diaz Jacques, Ângela Sitta, Moacir Wajner, Daiane Rodrigues, Abdellatif Bakkali, Cornelis Jakobs, Daniella de Moura Coelho
Publikováno v:
Rodrigues, D G B, de Moura Coelho, D, Sitta, Â, Jacques, C E D, Hauschild, T, Manfredini, V, Bakkali, A, Struys, E A, Jakobs, C, Wajner, M & Vargas, C R 2017, ' Experimental evidence of oxidative stress in patients with L-2-hydroxyglutaric aciduria and that L-carnitine attenuates in vitro DNA damage caused by D-2-hydroxyglutaric and L-2-hydroxyglutaric acids ', Toxicology in Vitro, vol. 42, pp. 47-53 . https://doi.org/10.1016/j.tiv.2017.04.006
Toxicology in Vitro, 42, 47-53. Elsevier Limited
Toxicology in Vitro, 42, 47-53. Elsevier Limited
D-2-hydroxyglutaric (D-2-HGA) and L-2-hydroxyglutaric (L-2-HGA) acidurias are rare neurometabolic disorders biochemically characterized by increased levels of D-2-hydroxyglutaric acid (D-2-HG) and L-2-hydroxyglutaric acid (L-2-HG) respectively, in bi
Autor:
Vanusa Manfredini, Luiza Steffens, Tatiane Cristina Hauschild, Daniella de Moura Coelho, Dinara Jaqueline Moura, Caroline Paula Mescka, Carmen Regla Vargas, Gilian Guerreiro
Publikováno v:
Toxicology in vitro : an international journal published in association with BIBRA. 57
Maple syrup urine disease (MSUD) is an inherited deficiency of the branched-chain α-keto dehydrogenase complex, characterized by accumulation of the branched-chain amino acids (BCAAs) and their respective branched chain α-keto-acids (BCKAs), as wel
Autor:
Desirèe Padilha Marchetti, Patricia Koehler-Santos, Bruna Donida, Adriana Simon Coitinho, Carmen Regla Vargas, Laura Bannach Jardim, Daniella de Moura Coelho, Tatiane Cristina Hauschild, Marion Deon, Carlos Eduardo Diaz Jacques
Publikováno v:
Journal of cellular biochemistry. 119(1)
X-linked adrenoleukodystrophy (X-ALD) is an inherited disease characterized by progressive inflammatory demyelization in the brain, adrenal insufficiency, and an abnormal accumulation of very long chain fatty acids (VLCFA) in tissue and body fluids.