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Neuropsychobiology|March 14, 2015
Integrating Different Aspects of Resting Brain Activity: A Review of Electroencephalographic Signatures in Resting State Networks Derived from Functional Magnetic Resonance ImagingKeiichiro Nishida, Nadja Razavi, Kay Jann, et al.
Psychopathology|September 20, 2002
Mood changes following acute tryptophan depletion in healthy adultsKlaus Schmeck, Shella Sadigorsky, Ekkehart Englert, et al.
Brain Topography|March 20, 2013
Quantification of network perfusion in ASL cerebral blood flow data with seed based and ICA approachesKay Jann, Ariane Orosz, Thomas Dierks, et al.
Brain Connectivity|May 12, 2012
Linking brain connectivity across different time scales with electroencephalogram, functional magnetic resonance imaging, and diffusion tensor imagingKay Jann, Andrea Federspiel, Stéphanie Giezendanner, et al.
The Journal of Biological Chemistry|August 30, 2013
Arylsulfatase K, a novel lysosomal sulfataseElena Marie Wiegmann, Eva Westendorf, Ina Kalus, et al.
Plos One|October 15, 2013
Shifted coupling of EEG driving frequencies and fMRI resting state networks in schizophrenia spectrum disordersNadja Razavi, Kay Jann, Thomas Koenig, et al.
Applied Microbiology and Biotechnology|January 12, 2019
Expression, characterization, and site-specific covalent immobilization of an L-amino acid oxidase from the fungus Hebeloma cylindrosporumSvenja Bloess, Tobias Beuel, Tobias Krüger, et al.
The Journal of Biological Chemistry|February 29, 2008
The non-catalytic N-terminal extension of formylglycine-generating enzyme is required for its biological activity and retention in the endoplasmic reticulumMalaiyalam Mariappan, Santosh Lakshmi Gande, Karthikeyan Radhakrishnan, et al.
European Journal of Human Genetics : EJHG|January 17, 2013
Rapid degradation of an active formylglycine generating enzyme variant leads to a late infantile severe form of multiple sulfatase deficiencyLars Schlotawa, Karthikeyan Radhakrishnan, Matthias Baumgartner, et al.
Biochimica Et Biophysica Acta|January 7, 2009
Molecular basis of multiple sulfatase deficiency, mucolipidosis II/III and Niemann-Pick C1 disease - Lysosomal storage disorders caused by defects of non-lysosomal proteinsThomas Dierks, Lars Schlotawa, Marc-André Frese, et al.
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