Biocytin and biotin uptake into NB2a neuroblastoma and C6 astrocytoma cells

Author:

Baur Barbara,Suormala Terttu,Baumgartner E.Regula

Publisher

Elsevier BV

Subject

Developmental Biology,Neurology (clinical),Molecular Biology,General Neuroscience

Reference24 articles.

1. Multiple carboxylase deficiency: Inherited and acquired disorders of biotin metabolism;Baumgartner;Intern. J. Vit. Nutr. Res.,1997

2. Biotinidase deficiency: Factors responsible for the increased biotin requirement;Baumgartner;J. Inher. Metab. Dis.,1985

3. E.R. Baumgartner, T. Suormala, H. Wick, A. Probst, U. Blauenstein, C. Bachmann, M. Vest, Biotinidase deficiency: a cause of subacute necrotizing encephalomyelopathy (Leigh syndrome). Report of a case with lethal outcome, Pediatr. Res. (1989) 260–266.

4. Biotin and biocytin uptake into cultured primary calf brain microvessel endothelial cells of the blood–brain barrier;Baur;Brain Res.,2000

5. C. Bernouilli, Entwicklung einer sensitiven Methode zur Biotinbestimmung in Plasma und Liquor: Ermittlung von Referenzwerten in der Pädiatrie, Erstellen des Biotinstatus bei Biotinidasemangel-Patienten und Bestimmen der Proteinbindung in Plasma. Inauguraldissertation, Philosophisch-Naturwissenschaftliche Fakultät der Universität Basel, 1999.

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