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Adelbert Roscher

Research Profile

Living Beings

Disorders

Adrenoleukodystrophy

Chemicals & Drugs

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Molecular Sequence Data

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Germany

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Sonja C Schriever; Adelbert A Roscher; Jerzy Adamski; Manuel J Deutsch; Regina Ensenauer
Cellular signaling of amino acids towards mTORC1 activation in impaired human leucine catabolism.
Simone Renner; Werner Römisch-Margl; Adelbert A Roscher; Karsten Suhre; Jerzy Adamski; Helmut Blum; Burkhard Göke; Stefan Krebs; Cornelia Prehn; Eckhard Wolf
Changing metabolic signatures of amino acids and lipids during the prediabetic period in a pig model with impaired incretin function and reduced β-cell mass.
Regina Ensenauer; Ralph Fingerhut; Barbara Fink; Andreas Kirschner; Bernhard Olgemöller; Philipp Pagel; Marc Becker; Torsten Dame; Wulf Röschinger; Sonja C Schriever; Nina C Sellerer; Adelbert A Roscher
In situ assay of fatty acid β-oxidation by metabolite profiling following permeabilization of cell membranes.

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All Publications

2013: Sonja C Schriever; Adelbert A Roscher; Jerzy Adamski; Manuel J Deutsch; Regina Ensenauer
Cellular signaling of amino acids towards mTORC1 activation in impaired human leucine catabolism.
The Journal of nutritional biochemistry 2013;24(5):824-31.
2012: Simone Renner; Werner Römisch-Margl; Adelbert A Roscher; Karsten Suhre; Jerzy Adamski; Helmut Blum; Burkhard Göke; Stefan Krebs; Cornelia Prehn; Eckhard Wolf
Changing metabolic signatures of amino acids and lipids during the prediabetic period in a pig model with impaired incretin function and reduced β-cell mass.
Diabetes 2012;61(8):2166-75.
2012: Regina Ensenauer; Ralph Fingerhut; Barbara Fink; Andreas Kirschner; Bernhard Olgemöller; Philipp Pagel; Marc Becker; Torsten Dame; Wulf Röschinger; Sonja C Schriever; Nina C Sellerer; Adelbert A Roscher
In situ assay of fatty acid β-oxidation by metabolite profiling following permeabilization of cell membranes.
Journal of lipid research 2012;53(5):1012-20.
2010: Soeren Gersting; Florian B Lagler; Anna Eichinger; Kristina F Kemter; Marta K Danecka; Dunja D Messing; Michael Staudigl; Katharina A Domdey; Clemens Zsifkovits; Ralph Fingerhut; Hartmut Glossmann; Adelbert A Roscher; Ania C Muntau
Pahenu1 is a mouse model for tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency and promotes analysis of the pharmacological chaperone mechanism in vivo.
Human molecular genetics 2010;19(10):2039-49.
2009: Esther M Maier; J Pongratz; Ania C Muntau; Bernhard Liebl; Uta Nennstiel-Ratzel; U Busch; Ralph Fingerhut; Bernhard Olgemöller; Adelbert A Roscher; Wulf Röschinger
Dissection of biochemical borderline phenotypes in carriers and genetic variants of medium-chain acyl-CoA dehyrogenase deficiency: implications for newborn screening [corrected].
Clinical genetics 2009;76(2):179-87.
2009: Ralph Fingerhut; Regina Ensenauer; Wulf Röschinger; Ralf Arnecke; Bernhard Olgemöller; Adelbert A Roscher
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 deficiency.
Analytical chemistry 2009;81(9):3571-5.
2008: Esther M Maier; Peter U Mayerhofer; Muriel Asheuer; Wolfgang Köhler; Martina Rothe; Ania C Muntau; Adelbert A Roscher; Andreas Holzinger; Patrick Aubourg; Johannes Berger
X-linked adrenoleukodystrophy phenotype is independent of ABCD2 genotype.
Biochemical and biophysical research communications 2008;377(1):176-80.
2008: Soeren Gersting; Kristina F Kemter; Michael Staudigl; Dunja D Messing; Marta K Danecka; Florian B Lagler; Christian P Sommerhoff; Adelbert A Roscher; Ania C Muntau
Loss of function in phenylketonuria is caused by impaired molecular motions and conformational instability.
American journal of human genetics 2008;83(1):5-17.
2007: Dominik Hartl; Philipp Latzin; Peter Hordijk; Veronica Marcos; Carsten Rudolph; Markus Woischnik; Susanne Krauss-Etschmann; Barbara Koller; Dietrich Reinhardt; Adelbert A Roscher; Dirk Roos; Matthias Griese
Cleavage of CXCR1 on neutrophils disables bacterial killing in cystic fibrosis lung disease.
Nature medicine 2007;13(12):1423-30.
2006: Sonja C Stadler; Roman Polanetz; Esther M Maier; Sylvia C Heidenreich; Birgit Niederer; Peter U Mayerhofer; Florian Lagler; Hans Georg Koch; René Santer; Janice M Fletcher; Enzo Ranieri; Anibh M Das; Ute Spiekerkötter; Karl O Schwab; Simone Pötzsch; Iris Marquardt; Julia B Hennermann; Ina Knerr; Saadet Mercimek-Mahmutoglu; Nicolai Kohlschmidt; Bernhard Liebl; Ralph Fingerhut; Bernhard Olgemöller; Ania C Muntau; Adelbert A Roscher; Wulf Röschinger
Newborn screening for 3-methylcrotonyl-CoA carboxylase deficiency: population heterogeneity of MCCA and MCCB mutations and impact on risk assessment.
Human mutation 2006;27(8):748-59.
2006: Esther M Maier; Stephanie Osterrieder; Catharina Whybra; Markus Ries; Andreas Gal; Michael Beck; Adelbert A Roscher; Ania C Muntau
Disease manifestations and X inactivation in heterozygous females with Fabry disease.
Acta paediatrica (Oslo, Norway : 1992). Supplement 2006;95(451):30-8.
2005: Yoshinori Kashiwayama; Kota Asahina; Hiroyuki Shibata; Masashi Morita; Ania C Muntau; Adelbert A Roscher; Ronald J A Wanders; Nobuyuki Shimozawa; Masao Sakaguchi; Hiroaki Kato; Tsuneo Imanaka
Role of Pex19p in the targeting of PMP70 to peroxisome.
Biochimica et biophysica acta 2005;1746(2):116-28.
2005: Sonja C Stadler; Roman Polanetz; Stephan Meier; Peter U Mayerhofer; Johannes M Herrmann; Katja Anslinger; Adelbert A Roscher; Wulf Röschinger; Andreas Holzinger
Mitochondrial targeting signals and mature peptides of 3-methylcrotonyl-CoA carboxylase.
Biochemical and biophysical research communications 2005;334(3):939-46.
2005: Peter Rittler; Beatrice Schiefer; Hans Demmelmair; Berthold Koletzko; Adelbert A Roscher; Rita Jacobs; Maximiliane Krick; Karl-Walter Jauch; Wolfgang H Hartl
Effect of amino acid infusion on human postoperative colon protein synthesis in situ.
JPEN. Journal of parenteral and enteral nutrition 2005;29(4):255-61.
2005: Uta Nennstiel-Ratzel; Stephan Arenz; Esther M Maier; Ina Knerr; Joachim Baumkötter; Wulf Röschinger; Bernhard Liebl; Hans-Beat Hadorn; Adelbert A Roscher; Rüdiger von Kries
Reduced incidence of severe metabolic crisis or death in children with medium chain acyl-CoA dehydrogenase deficiency homozygous for c.985A>G identified by neonatal screening.
Molecular genetics and metabolism 2005;85(2):157-9.
2005: Esther M Maier; Bernhard Liebl; Wulf Röschinger; Uta Nennstiel-Ratzel; Ralph Fingerhut; Bernhard Olgemöller; Ulrich Busch; Nils Krone; Rüdiger v Kries; Adelbert A Roscher
Population spectrum of ACADM genotypes correlated to biochemical phenotypes in newborn screening for medium-chain acyl-CoA dehydrogenase deficiency.
Human mutation 2005;25(5):443-52.
2005: Siegfried Kösel; Siegfried Burggraf; Ralph Fingerhut; Helmut G Dörr; Adelbert A Roscher; Bernhard Olgemöller
Rapid second-tier molecular genetic analysis for congenital adrenal hyperplasia attributable to steroid 21-hydroxylase deficiency.
Clinical chemistry 2005;51(2):298-304.
2004: Christian Baumgartner; C Böhm; Daniela Baumgartner; G Marini; K Weinberger; Bernhard Olgemöller; Bernhard Liebl; Adelbert A Roscher
Supervised machine learning techniques for the classification of metabolic disorders in newborns.
Bioinformatics (Oxford, England) 2004;20(17):2985-96.
2004: Chunming Ding; Esther Maier; Adelbert A Roscher; Andreas Braun; Charles R Cantor
Simultaneous quantitative and allele-specific expression analysis with real competitive PCR.
BMC genetics 2004;5():8.
2004: Ondine S von Ehrenstein; E M Maier; Stephan K Weiland; David Carr; T Hirsch; Thomas Nicolai; Adelbert A Roscher; Erika von Mutius
Alpha1 antitrypsin and the prevalence and severity of asthma.
Archives of disease in childhood 2004;89(3):230-1.
2004: Georg F Hoffmann; Rüdiger von Kries; Daniela Klose; Martin Lindner; Andreas Schulze; Ania C Muntau; Wulf Röschinger; Bernhard Liebl; Ertan Mayatepek; Adelbert A Roscher
Frequencies of inherited organic acidurias and disorders of mitochondrial fatty acid transport and oxidation in Germany.
European journal of pediatrics 2004;163(2):76-80.
2003: Bernhard Olgemöller; Adelbert A Roscher; Bernhard Liebl; Ralph Fingerhut
Screening for congenital adrenal hyperplasia: adjustment of 17-hydroxyprogesterone cut-off values to both age and birth weight markedly improves the predictive value.
The Journal of clinical endocrinology and metabolism 2003;88(12):5790-4.
2003: Wulf Röschinger; Bernhard Olgemöller; Ralph Fingerhut; Bernhard Liebl; Adelbert A Roscher
Advances in analytical mass spectrometry to improve screening for inherited metabolic diseases.
European journal of pediatrics 2003;162 Suppl 1():S67-76.
2003: Bernhard Liebl; Uta Nennstiel-Ratzel; Adelbert A Roscher; Rüdiger von Kries
Data required for the evaluation of newborn screening programmes.
European journal of pediatrics 2003;162 Suppl 1():S57-61.
2003: Joachim F Kuebler; Elisabeth Schremmer-Danninger; Kanti D Bhoola; Adelbert A Roscher; Konrad Messmer; Tomas F Hoffmann
Kinin-B1 receptors in ischaemia-induced pancreatitis: functional importance and cellular localisation.
Biological chemistry 2003;384(9):1311-9.
2003: Pablo Landgraf; Peter U Mayerhofer; Roman Polanetz; Adelbert A Roscher; Andreas Holzinger
Targeting of the human adrenoleukodystrophy protein to the peroxisomal membrane by an internal region containing a highly conserved motif.
European journal of cell biology 2003;82(8):401-10.
2003: Ania C Muntau; Adelbert A Roscher; Wolf-H Kunau; Gabriele Dodt
The interaction between human PEX3 and PEX19 characterized by fluorescence resonance energy transfer (FRET) analysis.
European journal of cell biology 2003;82(7):333-42.
2003: René Santer; Ralph Fingerhut; Uta Lässker; Patrick J Wightman; David R FitzPatrick; Bernhard Olgemöller; Adelbert A Roscher
Tandem mass spectrometric determination of malonylcarnitine: diagnosis and neonatal screening of malonyl-CoA decarboxylase deficiency.
Clinical chemistry 2003;49(4):660-2.
2003: Ania C Muntau; Adelbert A Roscher; Wolf-H Kunau; Gabriele Dodt
Interaction of PEX3 and PEX19 visualized by fluorescence resonance energy transfer (FRET).
Advances in experimental medicine and biology 2003;544():221-4.
2003: Andreas Holzinger; Peter U Mayerhofer; Esther M Maier; Adelbert A Roscher; Johannes Berger
Evidence against the adrenoleukodystrophy-related gene acting as a modifier of X-adrenoleukodystrophy.
Advances in experimental medicine and biology 2003;544():95-6.
2002: Ania C Muntau; Wulf Röschinger; Matthias Habich; Hans Demmelmair; Björn Hoffmann; Christian P Sommerhoff; Adelbert A Roscher
Tetrahydrobiopterin as an alternative treatment for mild phenylketonuria.
The New England journal of medicine 2002;347(26):2122-32.
2002: Esther M Maier; Stefan Kammerer; Ania C Muntau; Maria Wichers; Andreas Braun; Adelbert A Roscher
Symptoms in carriers of adrenoleukodystrophy relate to skewed X inactivation.
Annals of neurology 2002;52(5):683-8.
2002: P Meyer; A Braun; Adelbert A Roscher
Analysis of the two common alpha-1-antitrypsin deficiency alleles PiMS and PiMZ as modifiers of Pseudomonas aeruginosa susceptibility in cystic fibrosis.
Clinical genetics 2002;62(4):325-7.
2002: Ondine S von Ehrenstein; Erika von Mutius; E Maier; T Hirsch; David Carr; W Schaal; Adelbert A Roscher; Bernhard Olgemöller; Thomas Nicolai; Stephan K Weiland
Lung function of school children with low levels of alpha1-antitrypsin and tobacco smoke exposure.
The European respiratory journal : official journal of the European Society for Clinical Respiratory Physiology 2002;19(6):1099-106.
2002: Nils Krone; Andreas Braun; Stefanie Weinert; Michael Peter; Adelbert A Roscher; Carl-Joachim Partsch; Wolfgang G Sippell
Multiplex minisequencing of the 21-hydroxylase gene as a rapid strategy to confirm congenital adrenal hyperplasia.
Clinical chemistry 2002;48(6 Pt 1):818-25.
2002: Peter U Mayerhofer; Tanja Kattenfeld; Adelbert A Roscher; Ania C Muntau
Two splice variants of human PEX19 exhibit distinct functions in peroxisomal assembly.
Biochemical and biophysical research communications 2002;291(5):1180-6.
2002: Ania C Muntau; Monika Streiter; Matthias Kappler; Wulf Röschinger; Irene Schmid; Albert Rehnert; Peter Schramel; Adelbert A Roscher
Age-related reference values for serum selenium concentrations in infants and children.
Clinical chemistry 2002;48(3):555-60.
2002: Bernhard Liebl; Uta Nennstiel-Ratzel; Rüdiger von Kries; Ralph Fingerhut; Bernhard Olgemöller; Andreas Zapf; Adelbert A Roscher
Expanded newborn screening in Bavaria: tracking to achieve requested repeat testing.
Preventive medicine 2002;34(2):132-7.
2002: Bernhard Liebl; Uta Nennstiel-Ratzel; Rüdiger von Kries; Ralph Fingerhut; Bernhard Olgemöller; Andreas Zapf; Adelbert A Roscher
Very high compliance in an expanded MS-MS-based newborn screening program despite written parental consent.
Preventive medicine 2002;34(2):127-31.
2002: Andreas Holzinger; Esther M Maier; Cornelius Bück; Peter U Mayerhofer; Matthias Kappler; James C Haworth; Stanley P Moroz; Hans-Beat Hadorn; J Evan Sadler; Adelbert A Roscher
Mutations in the proenteropeptidase gene are the molecular cause of congenital enteropeptidase deficiency.
American journal of human genetics 2002;70(1):20-5.
2001: Skadi Beblo; H Reinhardt; Ania C Muntau; W Mueller-Felber; Adelbert A Roscher; Berthold Koletzko
Fish oil supplementation improves visual evoked potentials in children with phenylketonuria.
Neurology 2001;57(8):1488-91.
2001: Nils Krone; I Wachter; M Stefanidou; Adelbert A Roscher; H P Schwarz
Mothers with congenital adrenal hyperplasia and their children: outcome of pregnancy, birth and childhood.
Clinical endocrinology 2001;55(4):523-9.
2001: Ralph Fingerhut; Wulf Röschinger; Ania C Muntau; T Dame; J Kreischer; Ralf Arnecke; andrea superti-furga; H Troxler; Bernhard Liebl; Bernhard Olgemöller; Adelbert A Roscher
Hepatic carnitine palmitoyltransferase I deficiency: acylcarnitine profiles in blood spots are highly specific.
Clinical chemistry 2001;47(10):1763-8.
2001: Andreas Holzinger; Wulf Röschinger; Florian Lagler; Peter U Mayerhofer; P Lichtner; T Kattenfeld; LP Thuy; William L Nyhan; Hans Georg Koch; Ania C Muntau; Adelbert A Roscher
Cloning of the human MCCA and MCCB genes and mutations therein reveal the molecular cause of 3-methylcrotonyl-CoA: carboxylase deficiency.
Human molecular genetics 2001;10(12):1299-306.
2001: B Rolinski; F A M Baumeister; Adelbert A Roscher
Determination of amino acid tissue concentrations by microdialysis: method evaluation and relation to plasma values.
Amino acids 2001;21(2):129-38.
2000: Ania C Muntau; Peter U Mayerhofer; B C Paton; Stefan Kammerer; Adelbert A Roscher
Defective peroxisome membrane synthesis due to mutations in human PEX3 causes Zellweger syndrome, complementation group G.
American journal of human genetics 2000;67(4):967-75.
2000: Wulf Röschinger; Ania C Muntau; Marinus Duran; L Dorland; Lodewijk IJlst; Ronald J A Wanders; Adelbert A Roscher
Carnitine-acylcarnitine translocase deficiency: metabolic consequences of an impaired mitochondrial carnitine cycle.
Clinica chimica acta; international journal of clinical chemistry 2000;298(1-2):55-68.
2000: C Randak; W Roschinger; B Rolinski; Hans-Beat Hadorn; D A Applegarth; Adelbert A Roscher
Three siblings with nonketotic hyperglycinaemia, mildly elevated plasma homocysteine concentrations and moderate methylmalonic aciduria.
Journal of inherited metabolic disease 2000;23(5):520-2.
2000: B Rolinski; Ralf Arnecke; T Dame; J Kreischer; Bernhard Olgemöller; Eckhard Wolf; Rudi Balling; Martin Hrabé De Angelis; Adelbert A Roscher
The biochemical metabolite screen in the Munich ENU Mouse Mutagenesis Project: determination of amino acids and acylcarnitines by tandem mass spectrometry.
Mammalian genome : official journal of the International Mammalian Genome Society 2000;11(7):547-51.
2000: Ania C Muntau; Wulf Röschinger; Andreas Merkenschlager; M S van der Knaap; C Jakobs; Marinus Duran; G F Hoffmann; Adelbert A Roscher
Combined D-2- and L-2-hydroxyglutaric aciduria with neonatal onset encephalopathy: a third biochemical variant of 2-hydroxyglutaric aciduria?
Neuropediatrics 2000;31(3):137-40.
2000: Christian Johannes Gloeckner; Peter U Mayerhofer; Pablo Landgraf; Ania C Muntau; Andreas Holzinger; Josef-Karl Gerber; Stefan Kammerer; Jerzy Adamski; Adelbert A Roscher
Human adrenoleukodystrophy protein and related peroxisomal ABC transporters interact with the peroxisomal assembly protein PEX19p.
Biochemical and biophysical research communications 2000;271(1):144-50.
2000: Bernhard Liebl; Ralph Fingerhut; Wulf Röschinger; Ania C Muntau; Ina Knerr; Bernhard Olgemöller; Andreas Zapf; Adelbert A Roscher
[Model project for updating neonatal screening in Bavaria: concept and initial results].
Gesundheitswesen (Bundesverband der Ärzte des Öffentlichen Gesundheitsdienstes (Germany)) 2000;62(4):189-95.
2000: Ania C Muntau; Peter U Mayerhofer; S Albet; T E Schmid; Maurice Bugaut; Adelbert A Roscher; Stefan Kammerer
Genomic organization, expression analysis, and chromosomal localization of the mouse PEX3 gene encoding a peroxisomal assembly protein.
Biological chemistry 2000;381(4):337-42.
2000: Wulf Röschinger; Ania C Muntau; Günther Rudolph; Adelbert A Roscher; Stefan Kammerer
Carrier assessment in families with lowe oculocerebrorenal syndrome: novel mutations in the OCRL1 gene and correlation of direct DNA diagnosis with ocular examination.
Molecular genetics and metabolism 2000;69(3):213-22.
2000: Nils Krone; A Braun; Adelbert A Roscher; D Knorr; H P Schwarz
Predicting phenotype in steroid 21-hydroxylase deficiency? Comprehensive genotyping in 155 unrelated, well defined patients from southern Germany.
The Journal of clinical endocrinology and metabolism 2000;85(3):1059-65.
2000: Ania C Muntau; Andreas Holzinger; Peter U Mayerhofer; Jutta Gärtner; Adelbert A Roscher; Stefan Kammerer
The human PEX3 gene encoding a peroxisomal assembly protein: genomic organization, positional mapping, and mutation analysis in candidate phenotypes.
Biochemical and biophysical research communications 2000;268(3):704-10.
1999: Johannes Berger; S Albet; Marc Bentejac; Angela Netik; Andreas Holzinger; Adelbert A Roscher; Maurice Bugaut; Sonja Forss-Petter
The four murine peroxisomal ABC-transporter genes differ in constitutive, inducible and developmental expression.
European journal of biochemistry / FEBS 1999;265(2):719-27.
1999: Elisabeth Schremmer-Danninger; A Hermann; Edwin Fink; Hans Fritz; Adelbert A Roscher
Identification and occurrence of mRNAs for components of the kallikrein-kinin system in human skin and in skin diseases.
Immunopharmacology 1999;43(2-3):287-91.
1999: Andreas Holzinger; Peter U Mayerhofer; Johannes Berger; P Lichtner; Stefan Kammerer; Adelbert A Roscher
Full length cDNA cloning, promoter sequence, and genomic organization of the human adrenoleukodystrophy related (ALDR) gene functionally redundant to the gene responsible for X-linked adrenoleukodystrophy.
Biochemical and biophysical research communications 1999;258(2):436-42.
1999: Esther M Maier; Adelbert A Roscher; Stefan Kammerer; K Mehnert; E Conzelmann; Andreas Holzinger
Prenatal diagnosis of X-linked adrenoleukodystrophy combining biochemical, immunocytochemical and DNA analyses.
Prenatal diagnosis 1999;19(4):364-8.
1999: Uwe Wintergerst; B Rolinski; B Sölder; Johannes R Bogner; Eckhard Wolf; H Jäger; Adelbert A Roscher; Bernd H Belohradsky
Lack of absorption of didanosine after rectal administration in human immunodeficiency virus-infected patients.
Antimicrobial agents and chemotherapy 1999;43(3):699-701.
1999: Nils Krone; A Braun; Adelbert A Roscher; H P Schwarz
A novel frameshift mutation (141delT) in exon 1 of the 21-hydroxylase gene (CYP21) in a patient with the salt wasting form of congenital adrenal hyperplasia. Mutation in brief no. 255. Online.
Human mutation 1999;14(1):90-1.
1998: Nils Krone; Adelbert A Roscher; H P Schwarz; A Braun
Comprehensive analytical strategy for mutation screening in 21-hydroxylase deficiency.
Clinical chemistry 1998;44(10):2075-82.
1998: Andreas Holzinger; Ania C Muntau; Peter U Mayerhofer; Stefan Kammerer; S Albet; Maurice Bugaut; Adelbert A Roscher
The mouse gene encoding the peroxisomal membrane protein 1-like protein (PXMP1-L): cDNA cloning, genomic organization and comparative expression studies.
FEBS letters 1998;433(1-2):179-83.
1998: Bernhard Liebl; Adelbert A Roscher
[Neonatal screening for congenital metabolic disorders in Bavaria--assessment of current status and planned reorganization].
Gesundheitswesen (Bundesverband der Ärzte des Öffentlichen Gesundheitsdienstes (Germany)) 1998;60 Suppl 1():S20-3.
1998: Stefan Kammerer; Andreas Holzinger; U Welsch; Adelbert A Roscher
Cloning and characterization of the gene encoding the human peroxisomal assembly protein Pex3p.
FEBS letters 1998;429(1):53-60.
1998: Andreas Holzinger; E Maier; S Stöckler-Ipsiroglu; A Braun; Adelbert A Roscher
Characterization of a novel mutation in exon 10 of the adrenoleukodystrophy gene.
Clinical genetics 1998;53(6):482-7.
1998: Andreas Holzinger; Adelbert A Roscher; Pablo Landgraf; P Lichtner; Stefan Kammerer
Genomic organization and chromosomal localization of the human peroxisomal membrane protein-1-like protein (PXMP1-L) gene encoding a peroxisomal ABC transporter.
FEBS letters 1998;426(2):238-42.
1998: Elisabeth Schremmer-Danninger; A Offner; Matthias Siebeck; Adelbert A Roscher
B1 bradykinin receptors and carboxypeptidase M are both upregulated in the aorta of pigs after LPS infusion.
Biochemical and biophysical research communications 1998;243(1):246-52.
1998: Jutta Gärtner; A Braun; Andreas Holzinger; Peter Roerig; Hans-Gerd Lenard; Adelbert A Roscher
Clinical and genetic aspects of X-linked adrenoleukodystrophy.
Neuropediatrics 1998;29(1):3-13.
1998: Elisabeth Schremmer-Danninger; E Toepfer-Petersen; Hans Fritz; Adelbert A Roscher
Bradykinin-induced tyrosine phosphorylation of proteins in cultured human keratinocytes.
Biological research 1998;31(3):189-98.
1997: Andreas Holzinger; Stefan Kammerer; Johannes Berger; Adelbert A Roscher
cDNA cloning and mRNA expression of the human adrenoleukodystrophy related protein (ALDRP), a peroxisomal ABC transporter.
Biochemical and biophysical research communications 1997;239(1):261-4.
1997: Stefan Kammerer; N Arnold; W Gutensohn; H W Mewes; Wolf-H Kunau; Gerald Hoefler; Adelbert A Roscher; A Braun
Genomic organization and molecular characterization of a gene encoding HsPXF, a human peroxisomal farnesylated protein.
Genomics 1997;45(1):200-10.
1997: A Feussner; B Rolinski; N Weiss; T Deufel; Günther Wolfram; Adelbert A Roscher
Determination of total homocysteine in human plasma by isocratic high-performance liquid chromatography.
European journal of clinical chemistry and clinical biochemistry : journal of the Forum of European Clinical Chemistry Societies 1997;35(9):687-91.
1997: Andreas Holzinger; Stefan Kammerer; Adelbert A Roscher
Primary structure of human PMP69, a putative peroxisomal ABC-transporter.
Biochemical and biophysical research communications 1997;237(1):152-7.
1997: B Flath; B Rolinski; Adelbert A Roscher
Simple high-performance liquid chromatographic method for the detection of phenylpropionylglycine in urine as a diagnostic tool in inherited medium-chain acyl-coenzyme A dehydrogenase deficiency.
Journal of chromatography. B, Biomedical sciences and applications 1997;694(1):227-32.
1997: Uwe Wintergerst; B Rolinski; Johannes R Bogner; Gundula Notheis; Frank-Detlef Goebel; Adelbert A Roscher; Bernd H Belohradsky
Pharmacokinetics of zidovudine after rectal administration in human immunodeficiency virus-infected patients.
Antimicrobial agents and chemotherapy 1997;41(5):1143-5.
1996: C Randak; Peter Neth; Ennes A Auerswald; Irmgard Assfalg-Machleidt; Adelbert A Roscher; Hans-Beat Hadorn; Werner Machleidt
A recombinant polypeptide model of the second predicted nucleotide binding fold of the cystic fibrosis transmembrane conductance regulator is a GTP-binding protein.
FEBS letters 1996;398(1):97-100.
1996: A Braun; P Meyer; H Cleve; Adelbert A Roscher
Rapid and simple diagnosis of the two common alpha 1-proteinase inhibitor deficiency alleles Pi*Z and Pi*S by DNA analysis.
European journal of clinical chemistry and clinical biochemistry : journal of the Forum of European Clinical Chemistry Societies 1996;34(9):761-4.
1996: Said Abdalla; Jasminka Godovac-Zimmermann; A Braun; Adelbert A Roscher; Werner Müller-Esterl; Ursula Quitterer
Structure of the bradykinin B2 receptors' amino terminus.
Biochemistry 1996;35(23):7514-9.
1996: Elisabeth Schremmer-Danninger; A Offner; Matthias Siebeck; P Heinz-Erian; Peter Gais; Adelbert A Roscher
Autoradiographic visualization of B1 bradykinin receptors in porcine vascular tissues in the presence or absence of inflammation.
Immunopharmacology 1996;33(1-3):95-100.
1996: A Braun; Stefan Kammerer; E Maier; E Böhme; Adelbert A Roscher
Polymorphisms in the gene for the human B2-bradykinin receptor. New tools in assessing a genetic risk for bradykinin-associated diseases.
Immunopharmacology 1996;33(1-3):32-5.
1996: A Braun; E Maier; Stefan Kammerer; B Müller; Adelbert A Roscher
A novel sequence polymorphism in the promoter region of the human B2-bradykinin receptor gene.
Human genetics 1996;97(5):688-9.
1996: A Braun; Stefan Kammerer; H Ambach; Adelbert A Roscher
Characterization of a partial pseudogene homologous to the adrenoleukodystrophy gene and application to mutation detection.
Human mutation 1996;7(2):105-8.
1996: A M Kasel; A Faussner; A Pfeifer; U Müller; K Werdan; Adelbert A Roscher
B2 bradykinin receptors in cultured neonatal rat cardiomyocytes mediate a negative chronotropic and negative inotropic response.
Diabetes 1996;45 Suppl 1():S44-50.
1995: Johannes Berger; Hanno Bernheimer; Ingrid Faé; A Braun; Adelbert A Roscher; Brunhilde Molzer; G Fischer
Association of X-linked adrenoleukodystrophy with HLA DRB1 alleles.
Biochemical and biophysical research communications 1995;216(2):447-51.
1995: Uwe Wintergerst; B Rolinski; M Vocks-Hauck; V Wahn; K M Debatin; Gundula Notheis; I Grosch-Wörner; Frank-Detlef Goebel; Adelbert A Roscher; Bernd H Belohradsky
Pharmacokinetics of orally administered zidovudine in HIV-infected children and adults.
Infection 1995;23(6):344-8.
1995: Elisabeth Schremmer-Danninger; P Heinz-Erian; E Töpfer-Petersen; Adelbert A Roscher
Autoradiographic localization and characterization of bradykinin receptors in human skin.
European journal of pharmacology 1995;283(1-3):207-16.
1995: A Braun; Stefan Kammerer; E Böhme; B Müller; Adelbert A Roscher
Identification of polymorphic sites of the human bradykinin B2 receptor gene.
Biochemical and biophysical research communications 1995;211(1):234-40.
1995: Stefan Kammerer; A Braun; Norbert Arnold; Adelbert A Roscher
The human bradykinin B2 receptor gene: full length cDNA, genomic organization and identification of the regulatory region.
Biochemical and biophysical research communications 1995;211(1):226-33.
1995: C Randak; Adelbert A Roscher; Hans-Beat Hadorn; Irmgard Assfalg-Machleidt; Ennes A Auerswald; Werner Machleidt
Expression and functional properties of the second predicted nucleotide binding fold of the cystic fibrosis transmembrane conductance regulator fused to glutathione-S-transferase.
FEBS letters 1995;363(1-2):189-94.
1995: A Braun; H Ambach; Stefan Kammerer; B Rolinski; S Stöckler; W Rabl; Jutta Gärtner; S Zierz; Adelbert A Roscher
Mutations in the gene for X-linked adrenoleukodystrophy in patients with different clinical phenotypes.
American journal of human genetics 1995;56(4):854-61.
1995: A Braun; H Ambach; R Bichlmaier; Stefan Kammerer; Adelbert A Roscher
Population study of a sequence polymorphism in intron 2 of the human beta-globin gene.
Human genetics 1995;95(3):352.
1994: A Deufel; T Deufel; Astrid Golla; H Achatz; R Bertele-Harms; Adelbert A Roscher; Thomas Meitinger
Three novel mutations (I506S, S466X, 1651A-->T) in exon 10 of the cystic fibrosis transmembrane conductance regulator (CFTR) detected in patients of southern German descent.
Human mutation 1994;3(1):64-6.
1993: T Deufel; H Rabe; T Wieser; Thomas Meitinger; J Rosenecker; R Bertele-Harms; K Harms; Hans-Beat Hadorn; Adelbert A Roscher
Mutation analysis in the diagnosis of cystic fibrosis.
European journal of pediatrics 1993;152(11):909-11.
1993: S Huber; D Költgen; Adelbert A Roscher; P Heinz-Erian
A linear 16 pS Cl- channel in the apical membrane of Caco-2 cells.
Pflügers Archiv : European journal of physiology 1993;424(3-4):364-6.
1992: K Schmidtke; W Endres; Adelbert A Roscher; H Ibel; N Herschkowitz; C Bachmann; E Plöchl; Hans-Beat Hadorn
Hartnup syndrome, progressive encephalopathy and allo-albuminaemia. A clinico-pathological case study.
European journal of pediatrics 1992;151(12):899-903.
1992: Adelbert A Roscher; B Rolinski
Peroxisomal disorders in man.
Cell biochemistry and function 1992;10(3):201-7.
1992: M Haasemann; J Buschko; A Faussner; Adelbert A Roscher; J Hoebeke; R Burch; Werner Müller-Esterl
Anti-idiotypic antibodies against the kinin receptor.
Journal of cardiovascular pharmacology 1992;20 Suppl 9():S47-54.
1992: M Haasemann; J Buschko; A Faussner; Adelbert A Roscher; J Hoebeke; R Burch; W Muller-Esterl
Anti-idiotypic antibodies against the kinin receptor.
Agents and actions. Supplements 1992;38 ( Pt 1)():497-512.
1991: M Haasemann; J Buschko; A Faussner; Adelbert A Roscher; J Hoebeke; R M Burch; Werner Müller-Esterl
Anti-idiotypic antibodies bearing the internal image of a bradykinin epitope. Production, characterization, and interaction with the kinin receptor.
Journal of immunology (Baltimore, Md. : 1950) 1991;147(11):3882-92.
1991: A Faussner; P Heinz-Erian; C Klier; Adelbert A Roscher
Solubilization and characterization of B2 bradykinin receptors from cultured human fibroblasts.
The Journal of biological chemistry 1991;266(15):9442-6.
1990: R Dengler; A Faussner; Werner Müller-Esterl; Adelbert A Roscher
[Hyp3]-bradykinin and [Hyp3]-Lys-bradykinin interact with B2-bradykinin receptors and stimulate inositol phosphate production in cultured human fibroblasts.
FEBS letters 1990;262(1):111-4.
1990: Adelbert A Roscher; C Klier; R Dengler; A Faussner; Werner Müller-Esterl
Regulation of bradykinin action at the receptor level.
Journal of cardiovascular pharmacology 1990;15 Suppl 6():S39-43.
1989: Adelbert A Roscher; S Hoefler; Gerald Hoefler; Eduard Paschke; F Paltauf; Ann B Moser; H Moser
Genetic and phenotypic heterogeneity in disorders of peroxisome biogenesis--a complementation study involving cell lines from 19 patients.
Pediatric research 1989;26(1):67-72.
1989: K Kremser; Adelbert A Roscher
Plasmalogen biosynthesis in the diagnosis of peroxisomal disorders.
Journal of clinical chemistry and clinical biochemistry. Zeitschrift für klinische Chemie und klinische Biochemie 1989;27(5):315-7.
1987: S Stöckler; U Kastner; B Pokits; W Müller; Adelbert A Roscher
[Blood propionic acid with hyperammonemic coma].
Klinische Pädiatrie 1987;199(5):348-50.
1987: S Stöckler; F Grossschädl; C Bachmann; Adelbert A Roscher
Ornithine transcarbamylase variant in a male patient.
Journal of inherited metabolic disease 1987;10(3):272.
1987: Eduard Paschke; Gerald Hoefler; Adelbert A Roscher
The effect of D-(+)-glucosamine on levels of free N-acetylneuraminic acid and UDP-N-acetylhexosamines in infantile sialic acid storage disease (ISSD) fibroblasts.
Journal of inherited metabolic disease 1987;10(1):48-51.
1986: Brunhilde Molzer; M Korschinsky; Hanno Bernheimer; R Schmid; C Wolf; Adelbert A Roscher
Very long chain fatty acids in genetic peroxisomal disease fibroblasts: differences between the cerebro-hepato-renal (Zellweger) syndrome and adrenoleukodystrophy variants.
Clinica chimica acta; international journal of clinical chemistry 1986;161(1):81-90.
1986: Eduard Paschke; Gerald Hoefler; Adelbert A Roscher
Infantile sialic acid storage disease: the fate of biosynthetically labeled N-acetyl-(3H)-neuraminic acid in cultured human fibroblasts.
Pediatric research 1986;20(8):773-7.
1986: Eduard Paschke; G Trinkl; W Erwa; M Pavelka; I Mutz; Adelbert A Roscher
Infantile type of sialic acid storage disease with sialuria.
Clinical genetics 1986;29(5):417-24.
1985: Adelbert A Roscher; Brunhilde Molzer; Hanno Bernheimer; S Stöckler; I Mutz; F Paltauf
The cerebrohepatorenal (Zellweger) syndrome: an improved method for the biochemical diagnosis and its potential value for prenatal detection.
Pediatric research 1985;19(9):930-3.