Adelbert A. Roscher

Overview

Best Publications

• Genome-wide, large-scale production of mutant mice by ENU mutagenesis

  M. H. Hrabe de Angelis;H. Flaswinkel;H. Fuchs;B. Rathkolb

  802
  Citations

• Predicting phenotype in steroid 21-hydroxylase deficiency? Comprehensive genotyping in 155 unrelated, well defined patients from southern Germany.

  Nils Krone;Andreas Braun;Adelbert Anton Roscher;Dietrich Knorr

  457
  Citations

• Cleavage of CXCR1 on neutrophils disables bacterial killing in cystic fibrosis lung disease.

  Dominik Hartl;Dominik Hartl;Philipp Latzin;Peter Hordijk;Veronica Marcos

  385
  Citations

• Tetrahydrobiopterin as an Alternative Treatment for Mild Phenylketonuria

  Ania C Muntau;Wulf Röschinger;Matthias Habich;Hans Demmelmair

  356
  Citations

• Quantitative measurement of different ceramide species from crude cellular extracts by electrospray ionization tandem mass spectrometry (ESI-MS/MS)

  G. Liebisch;W. Drobnik;M. Reil;B. Trümbach

  291
  Citations

• Studies on the role of specific cell surface receptors in the removal of lipoprotein (a) in man.

  F Krempler;G M Kostner;A Roscher;F Haslauer

  280
  Citations

• CXCR2 mediates NADPH oxidase–independent neutrophil extracellular trap formation in cystic fibrosis airway inflammation

  Veronica Marcos;Zhe Zhou;Ali Önder Yildirim;Alexander Bohla

  271
  Citations

• Screening for Congenital Adrenal Hyperplasia: Adjustment of 17-Hydroxyprogesterone Cut-Off Values to Both Age and Birth Weight Markedly Improves the Predictive Value

  Bernhard Olgemöller;Adelbert A. Roscher;Bernhard Liebl;Ralph Fingerhut

  161
  Citations

• Disease manifestations and X inactivation in heterozygous females with Fabry disease.

  Esther M Maier;Stephanie Osterrieder;Catharina Whybra;Markus Ries

  161
  Citations

• Hepatic Carnitine Palmitoyltransferase I Deficiency: Acylcarnitine Profiles in Blood Spots Are Highly Specific

  Ralph Fingerhut;Wulf Röschinger;Ania C. Muntau;Torsten Dame

  150
  Citations

• Loss of Function in Phenylketonuria Is Caused by Impaired Molecular Motions and Conformational Instability

  Søren W. Gersting;Kristina F. Kemter;Michael Staudigl;Dunja D. Messing

  148
  Citations

• Cloning and characterization of the gene encoding the human peroxisomal assembly protein Pex3p

  Stefan Kammerer;Andreas Holzinger;Ulrich Welsch;Adelbert A Roscher

  145
  Citations

• The four murine peroxisomal ABC‐transporter genes differ in constitutive, inducible and developmental expression

  Johannes Berger;Sabrina Albet;Marc Bentejac;Angela Netik

  143
  Citations

• Digital image analysis approach for lipid droplet size quantitation of Oil Red O-stained cultured cells.

  Manuel J. Deutsch;Sonja C. Schriever;Adelbert A. Roscher;Regina Ensenauer

  142
  Citations

• Primary structure of human PMP69, a putative peroxisomal ABC-transporter.

  Andreas Holzinger;Stefan Kammerer;Adelbert A. Roscher

  139
  Citations

• Defective Peroxisome Membrane Synthesis Due To Mutations in Human PEX3 Causes Zellweger Syndrome, Complementation Group G

  Ania C. Muntau;Peter U. Mayerhofer;Barbara C. Paton;Stefan Kammerer

  132
  Citations

• cDNA cloning and mRNA expression of the human adrenoleukodystrophy related protein (ALDRP), a peroxisomal ABC transporter.

  Andreas Holzinger;Stefan Kammerer;Johannes Berger;Adelbert A. Roscher

  131
  Citations

• Molecular cloning and functional characterization of a mouse bradykinin B1 receptor gene.

  João B. Pesquero;Jorge L. Pesquero;Suzana M. Oliveira;Adelbert A. Roscher

  130
  Citations

• Age-related reference values for serum selenium concentrations in infants and children.

  Ania C. Muntau;Monika Streiter;Matthias Kappler;Wulf Röschinger

  129
  Citations

• Population spectrum of ACADM genotypes correlated to biochemical phenotypes in newborn screening for medium-chain acyl-CoA dehydrogenase deficiency.

  Esther M. Maier;Bernhard Liebl;Wulf Röschinger;Uta Nennstiel-Ratzel

  129
  Citations