Identification of a putative lysosomal cobalamin exporter altered in the cblF defect of vitamin B<sub>12</sub> metabolism.
- Published in:
- Nature Genetics, 2009, v. 41, n. 2, p. 234, doi. 10.1038/ng.294
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- Publication type:
- Article
Works matching AU Sagné, Corinne
Results: 6
1
2
Severe Serotonin Depletion after Conditional Deletion of the Vesicular Monoamine Transporter 2 Gene in Serotonin Neurons: Neural and Behavioral Consequences.
- Published in:
- Neuropsychopharmacology, 2011, v. 36, n. 12, p. 2538, doi. 10.1038/npp.2011.142
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- Publication type:
- Article
3
Differential regulation of tyrosine hydroxylase in the basal ganglia of mice lacking the dopamine transporter.
- Published in:
- European Journal of Neuroscience, 1999, v. 11, n. 10, p. 3499, doi. 10.1046/j.1460-9568.1999.00764.x
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- Publication type:
- Article
4
Molecular pathogenesis of sialic acid storage diseases: insight gained from four missense mutations and a putative polymorphism of human sialin.
- Published in:
- Biology of the Cell (Wiley-Blackwell), 2008, v. 100, n. 9, p. 551, doi. 10.1042/BC20070166
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- Publication type:
- Article
5
Lysosomal amino acid transporter LYAAT-1 in the rat central nervous system: An in situ hybridization and immunohistochemical study.
- Published in:
- Journal of Comparative Neurology, 2003, v. 462, n. 1, p. 71, doi. 10.1002/cne.10712
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- Publication type:
- Article
6
Functional characterization of wild-type and mutant human sialin.
- Published in:
- EMBO Journal, 2004, v. 23, n. 23, p. 4560, doi. 10.1038/sj.emboj.7600464
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- Publication type:
- Article