Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Cinthia Castro Do Nascimento"'
Publikováno v:
Frontiers in Molecular Biosciences, Vol 8 (2021)
Background: Lysosomal storage diseases (LSDs) are caused by a mutation in a specific gene. Enzymatic dysfunction results in a progressive storage of substrates that gradually affects lysosomal, cellular and tissue physiology. Their pathophysiological
Externí odkaz:
https://doaj.org/article/694f3ffcda534b1486cb45e58cfb6706
Autor:
Mariana Simões Garcia, Deborah Navit de Carvalho Cavalcante, Marcella da Silva Araújo Santiago, Paloma Da Cunha de Medeiros, Cinthia Castro do Nascimento, Gustavo Fernandes Camargo Fonseca, Luciana Le Sueur-Maluf, Juliana Elaine Perobelli
Publikováno v:
Ecotoxicology and Environmental Safety, Vol 209, Iss , Pp 111766- (2021)
The management of agrochemicals in Brazilian agriculture impacts global environmental sustainability and food security, since this country is one of the major agro-food exporters in the world. Acephate, carbendazim, and dithiocarbamates (DTCs) such a
Externí odkaz:
https://doaj.org/article/c6bb04c4b5b0413a99f6a41c5064ba49
Publikováno v:
PLoS ONE, Vol 14, Iss 12, p e0220429 (2019)
Mucopolysaccharidosis Type I (MPS I) is a rare genetic lysosomal storage disease caused by a mutation of IDUA gene. IDUA codes for α-L-iduronidase (IDUA), a lysosomal hydrolase that degrades glycosaminoglycans (GAGs): heparan sulphate and dermatan s
Externí odkaz:
https://doaj.org/article/ae07fd1185a546e688c7043217e3dce0
Autor:
Matheus Trovão De Queiroz, Cinthia Castro do Nascimento, Vanessa Gonçalves Pereira, Vânia D'Almeida
Publikováno v:
Frontiers in Endocrinology, Vol 7 (2016)
Non-coding RNAs (ncRNA) are a functional class of RNA involved in the regulation of several cellular processes which may modulate disease onset, progression and prognosis. Lysosomal storage diseases (LSD) are a group of rare disorders caused by mutat
Externí odkaz:
https://doaj.org/article/c25428f64a394b91b204df2e5227122b
Publikováno v:
Molecular Biology Reports. 48:363-370
Mucopolysaccharidosis type I (MPS I) is a lysosomal storage disease caused by a mutation in the IDUA gene, which codes α-L-iduronidase (IDUA), a lysosomal hydrolase that degrades two glycosaminoglycans (GAGs): heparan sulfate (HS) and dermatan sulfa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e812b0ec90c5b71781bc779b3cb2f8b
https://doi.org/10.1007/s11033-020-06055-5
https://doi.org/10.1007/s11033-020-06055-5
Publikováno v:
Journal of Molecular Histology. 51:137-145
Mucopolysaccharidosis type I (MPS I) is a genetic disease caused by a deficiency of the lysosomal hydrolase α-L-iduronidase (IDUA). IDUA degrades two types of glycosaminoglycans (GAGs): heparan and dermatan sulfates, important components of extracel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5893b2789a4ed30273fa5b03696704d3
https://doi.org/10.1007/s10735-020-09864-x
https://doi.org/10.1007/s10735-020-09864-x
Autor:
Vanessa Gonçalves Pereira, Nicole Yolanda Ferreira, Vanessa Cavalcante da Silva, Flavia de Oliveira, Vânia D'Almeida, Cinthia Castro do Nascimento, Carla Cristina Medalha
Publikováno v:
Acta histochemica. 123(2)
Mucopolysaccharidosis type I (MPS I) is a lysosomal storage disorder characterized by alpha-L-iduronidase (IDUA) deficiency, an enzyme responsible for glycosaminoglycan degradation. Musculoskeletal impairment is an important component of the morbidit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::204d53dd771ae01ef67ec302691e7fb9
https://pubmed.ncbi.nlm.nih.gov/33434858
https://pubmed.ncbi.nlm.nih.gov/33434858
Autor:
Guilherme Baldo, Marcelo A. Lima, Alexey V. Pshezhetsky, Vânia D'Almeida, Gustavo Monteiro Viana, Renan P. Cavalheiro, Helena B. Nader, Esteban Alberto Gonzalez, Marcela Maciel Palacio Alvarez, Cinthia Castro do Nascimento
Publikováno v:
International Journal of Molecular Sciences
International Journal of Molecular Sciences, Vol 21, Iss 4, p 1459 (2020)
Volume 21
Issue 4
International Journal of Molecular Sciences, Vol 21, Iss 4, p 1459 (2020)
Volume 21
Issue 4
Mucopolysaccharidosis type I (MPS I) is caused by genetic deficiency of &alpha
l-iduronidase and impairment of lysosomal catabolism of heparan sulfate and dermatan sulfate. In the brain, these substrates accumulate in the lysosomes of neurons an
l-iduronidase and impairment of lysosomal catabolism of heparan sulfate and dermatan sulfate. In the brain, these substrates accumulate in the lysosomes of neurons an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54c638b78a31b0b342db804032ce53d7
https://pubmed.ncbi.nlm.nih.gov/32093427
https://pubmed.ncbi.nlm.nih.gov/32093427
Autor:
Cinthia Castro do Nascimento, Paloma da Cunha de Medeiros, Deborah Navit de Carvalho Cavalcante, Juliana Elaine Perobelli, Luciana Le Sueur-Maluf, Gustavo Fonseca, Marcella da Silva Araujo Santiago, Mariana Simões Garcia
Publikováno v:
Ecotoxicology and Environmental Safety, Vol 209, Iss, Pp 111766-(2021)
The management of agrochemicals in Brazilian agriculture impacts global environmental sustainability and food security, since this country is one of the major agro-food exporters in the world. Acephate, carbendazim, and dithiocarbamates (DTCs) such a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f607cc007e3b4cc3efa5e7ac5aa25ae
https://doi.org/10.1016/j.ecoenv.2020.111766
https://doi.org/10.1016/j.ecoenv.2020.111766
Publikováno v:
Reproduction, Fertility and Development. 32:304
Mucopolysaccharidosis type I (MPS I) is a lysosomal storage disease caused by a deficiency of the lysosomal hydrolase, α-L-iduronidase (IDUA). IDUA degrades heparan and dermatan sulfates, two types of glycosaminoglycan (GAG), important signalling an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4acc1e4025e3ff2f2e88449ea1566369
https://doi.org/10.1071/rd19144
https://doi.org/10.1071/rd19144