Found: 15
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Identification and characterization of a complete carnitine biosynthesis pathway in Candida albicans.
- Published in:
- FASEB Journal, 2009, v. 23, n. 8, p. 2349, doi. 10.1096/fj.08-127985
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- Publication type:
- Article
The Role of Virulence Proteins in Protection Conferred by Bordetella pertussis Outer Membrane Vesicle Vaccines.
- Published in:
- Vaccines, 2020, v. 8, n. 3, p. 429, doi. 10.3390/vaccines8030429
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- Publication type:
- Article
Prediction of phenotypic severity in mucopolysaccharidosis type IIIA.
- Published in:
- 2017
- By:
- Publication type:
- journal article
An algorithm to predict phenotypic severity in mucopolysaccharidosis type I in the first month of life.
- Published in:
- Orphanet Journal of Rare Diseases, 2013, v. 8, n. 1, p. 1, doi. 10.1186/1750-1172-8-99
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- Publication type:
- Article
An algorithm to predict phenotypic severity in mucopolysaccharidosis type I in the first month of life.
- Published in:
- 2013
- By:
- Publication type:
- journal article
Submitochondrial localization of 6- N-trimethyllysine dioxygenase − implications for carnitine biosynthesis.
- Published in:
- FEBS Journal, 2007, v. 274, n. 22, p. 5845, doi. 10.1111/j.1742-4658.2007.06108.x
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- Publication type:
- Article
Slc22a5 haploinsufficiency does not aggravate the phenotype of the long‐chain acyl‐CoA dehydrogenase KO mouse.
- Published in:
- Journal of Inherited Metabolic Disease, 2020, v. 43, n. 3, p. 486, doi. 10.1002/jimd.12204
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- Publication type:
- Article
Newborn screening for mucopolysaccharidoses: a pilot study of measurement of glycosaminoglycans by tandem mass spectrometry.
- Published in:
- Journal of Inherited Metabolic Disease, 2017, v. 40, n. 1, p. 151, doi. 10.1007/s10545-016-9981-6
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- Publication type:
- Article
Genistein increases glycosaminoglycan levels in mucopolysaccharidosis type I cell models.
- Published in:
- Journal of Inherited Metabolic Disease, 2014, v. 37, n. 5, p. 813, doi. 10.1007/s10545-014-9703-x
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- Publication type:
- Article
Plasma and urinary levels of dermatan sulfate and heparan sulfate derived disaccharides after long-term enzyme replacement therapy (ERT) in MPS I: correlation with the timing of ERT and with total urinary excretion of glycosaminoglycans.
- Published in:
- Journal of Inherited Metabolic Disease, 2013, v. 36, n. 2, p. 247, doi. 10.1007/s10545-012-9538-2
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- Publication type:
- Article
Functional analysis of TMLH variants and definition of domains required for catalytic activity and mitochondrial targeting.
- Published in:
- Journal of Cellular Physiology, 2005, v. 204, n. 3, p. 839, doi. 10.1002/jcp.20332
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- Publication type:
- Article
In vitro alternative for reactogenicity assessment of outer membrane vesicle based vaccines.
- Published in:
- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-39908-7
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- Publication type:
- Article
Abnormal sodium and water homeostasis in mice with defective heparan sulfate polymerization.
- Published in:
- PLoS ONE, 2019, v. 14, n. 7, p. 1, doi. 10.1371/journal.pone.0220333
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- Publication type:
- Article
In vitro alternative for reactogenicity assessment of outer membrane vesicle based vaccines.
- Published in:
- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-39908-7
- By:
- Publication type:
- Article
A Multiplex Assay for the Diagnosis of Mucopolysaccharidoses and Mucolipidoses.
- Published in:
- PLoS ONE, 2015, v. 10, n. 9, p. 1, doi. 10.1371/journal.pone.0138622
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- Publication type:
- Article