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The Journal of Clinical Endocrinology and Metabolism|December 13, 2003
Screening for congenital adrenal hyperplasia: adjustment of 17-hydroxyprogesterone cut-off values to both age and birth weight markedly improves the predictive valueBernhard Olgemöller, Adelbert A Roscher, Bernhard Liebl, et al.
Molecular Cancer|February 13, 2014
RNAi-mediated silencing of MLL-AF9 reveals leukemia-associated downstream targets and processesKatrin K Fleischmann, Philipp Pagel, Irene Schmid, et al.
Biochemical and Biophysical Research Communications|March 9, 2002
Two splice variants of human PEX19 exhibit distinct functions in peroxisomal assemblyPeter U Mayerhofer, Tanja Kattenfeld, Adelbert A Roscher, et al.
Analytical Biochemistry|October 15, 2013
Digital image analysis approach for lipid droplet size quantitation of Oil Red O-stained cultured cellsManuel J Deutsch, Sonja C Schriever, Adelbert A Roscher, et al.
European Journal of Pediatrics|November 18, 2003
Advances in analytical mass spectrometry to improve screening for inherited metabolic diseasesWulf Röschinger, Bernhard Olgemöller, Ralph Fingerhut, et al.
European Journal of Cell Biology|August 20, 2003
The interaction between human PEX3 and PEX19 characterized by fluorescence resonance energy transfer (FRET) analysisAnia C Muntau, Adelbert A Roscher, Wolf-H Kunau, et al.
European Journal of Cell Biology|October 10, 2003
Targeting of the human adrenoleukodystrophy protein to the peroxisomal membrane by an internal region containing a highly conserved motifPablo Landgraf, Peter U Mayerhofer, Roman Polanetz, et al.
BMC Genetics|May 7, 2004
Simultaneous quantitative and allele-specific expression analysis with real competitive PCRChunming Ding, Esther Maier, Adelbert A Roscher, et al.
The Journal of Nutritional Biochemistry|August 18, 2012
Cellular signaling of amino acids towards mTORC1 activation in impaired human leucine catabolismSonja C Schriever, Manuel J Deutsch, Jerzy Adamski, et al.
Analytical Chemistry|March 28, 2009
Stability of acylcarnitines and free carnitine in dried blood samples: implications for retrospective diagnosis of inborn errors of metabolism and neonatal screening for carnitine transporter deficiencyRalph Fingerhut, Regina Ensenauer, Wulf Röschinger, et al.
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