Search Results - "Braeutigam, C"
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The RNA-binding protein Rbfox2: an essential regulator of EMT-driven alternative splicing and a mediator of cellular invasion
Published in Oncogene (27-02-2014)“…The epithelial–mesenchymal transition (EMT), a prerequisite for cancer progression and metastasis formation, is regulated not only at the transcriptional but…”
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STAT6 and STAT1 are essential antagonistic regulators of cell survival in classical Hodgkin lymphoma cell line
Published in Leukemia (01-10-2009)“…Classical Hodgkin lymphoma (cHL) is a malignant lymphoid disorder characterized by aberrant activation of signaling pathways. Constitutive activation of…”
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Exploring behavioral adjustments of proportion congruency manipulations in an Eriksen flanker task with visual and auditory distractor modalities
Published in Memory & cognition (01-01-2024)“…The present study investigated global behavioral adaptation effects to conflict arising from different distractor modalities. Three experiments were conducted…”
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Proactive reward in conflict tasks: Does it only enhance general performance or also modulate conflict effects?
Published in Attention, perception & psychophysics (01-08-2024)“…In the present study, we investigated the influence of performance-contingent reward prospects on task performance across three visual conflict tasks with…”
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Aromatic L-amino acid decarboxylase deficiency with hyperdopaminuria. Clinical and laboratory findings in response to different therapies
Published in Neuropediatrics (01-08-2002)“…Aromatic L-amino acid decarboxylase (AADC - E.C. 4.1.1.28) converts L-dopa to dopamine and 5-hydroxytryptophan to serotonin. Inherited deficiency of this…”
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Clinical and laboratory findings in twins with neonatal epileptic encephalopathy mimicking aromatic L-amino acid decarboxylase deficiency
Published in Neuropediatrics (01-06-2002)“…Aromatic L-amino acid decarboxylase (AADC) is a vitamin B 6 requiring enzyme involved in the biosynthesis of the neurotransmitters dopamine (DA) and serotonin…”
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A review of biochemical and molecular genetic aspects of tyrosine hydroxylase deficiency including a novel mutation (291delC)
Published in Journal of inherited metabolic disease (01-06-1999)“…An overview is given of the current knowledge on the human tyrosine hydroxylase gene and on the biochemical aspects of diagnosing defects in this gene…”
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