Adelbert A Roscher


Ontology type: schema:Person     


Person Info

NAME

Adelbert A

SURNAME

Roscher

Publications in SciGraph latest 50 shown

  • 2017-05 Abstracts of the 52nd Workshop for Pediatric Research in MOLECULAR AND CELLULAR PEDIATRICS
  • 2016-12 The leukemogenic fusion gene MLL-AF9 alters microRNA expression pattern and inhibits monoblastic differentiation via miR-511 repression in JOURNAL OF EXPERIMENTAL & CLINICAL CANCER RESEARCH
  • 2015-02 Neue Zielerkrankungen im Neugeborenenscreening in MONATSSCHRIFT KINDERHEILKUNDE
  • 2014-12 RNAi-mediated silencing of MLL-AF9 reveals leukemia-associated downstream targets and processes in MOLECULAR CANCER
  • 2011-07 Retraction: CXCR2 mediates NADPH oxidase–independent neutrophil extracellular trap formation in cystic fibrosis airway inflammation in NATURE MEDICINE
  • 2010-09 CXCR2 mediates NADPH oxidase–independent neutrophil extracellular trap formation in cystic fibrosis airway inflammation in NATURE MEDICINE
  • 2007-12 Cleavage of CXCR1 on neutrophils disables bacterial killing in cystic fibrosis lung disease in NATURE MEDICINE
  • 2007 Peroxisomale Krankheiten in PÄDIATRIE
  • 2004-12 Simultaneous quantitative and allele-specific expression analysis with real competitive PCR in BMC GENETICS
  • 2004-02 Frequencies of inherited organic acidurias and disorders of mitochondrial fatty acid transport and oxidation in Germany in EUROPEAN JOURNAL OF PEDIATRICS
  • 2004 Stoffwechselerkrankungen in PÄDIATRISCHE NOTFALL- UND INTENSIVMEDIZIN
  • 2003-12 Data required for the evaluation of newborn screening programmes in EUROPEAN JOURNAL OF PEDIATRICS
  • 2003-12 Early diagnosis of inherited metabolic diseases: towards improving outcome in EUROPEAN JOURNAL OF PEDIATRICS
  • 2003-12 Advances in analytical mass spectrometry to improve screening for inherited metabolic diseases in EUROPEAN JOURNAL OF PEDIATRICS
  • 2003 Evidence against the Adrenoleukodystrophy-related Gene acting as a Modifier of X-adrenoleukodystrophy in PEROXISOMAL DISORDERS AND REGULATION OF GENES
  • 2003 Interaction of PEX3 and PEX19 Visualized by Fluorescence Resonance Energy Transfer (FRET) in PEROXISOMAL DISORDERS AND REGULATION OF GENES
  • 2001-12 Ethisch-rechtliche Aspekte des Neugeborenenscreenings in MONATSSCHRIFT KINDERHEILKUNDE
  • 2001-12 Erweiterung des Neugeborenenscreenings durch Tandemmassenspektrometrie in MONATSSCHRIFT KINDERHEILKUNDE
  • 2001-09 Determination of amino acid tissue concentrations by microdialysis: method evaluation and relation to plasma values in AMINO ACIDS
  • 2001 Diagnostik der cystischen Fibrose in CYSTISCHE FIBROSE
  • 2001 Tandem-Massenspektrometrie in SCREENING AUF ANGEBORENE ENDOKRINE UND METABOLE STÖRUNGEN
  • 2001 Stoffwechselkrankheiten in PÄDIATRIE
  • 2000-07 Three siblings with nonketotic hyperglycinaemia, mildly elevated plasma homocysteine concentrations and moderate methylmalonic aciduria in JOURNAL OF INHERITED METABOLIC DISEASE
  • 2000-07 The biochemical metabolite screen in the Munich ENU Mouse Mutagenesis Project: determination of amino acids and acylcarnitines by tandem mass spectrometry in MAMMALIAN GENOME
  • 1996-06 Successful treatment of heart failure with enoximone in a patient with cytochrome c oxidase deficiency in EUROPEAN JOURNAL OF PEDIATRICS
  • 1996-05 A novel sequence polymorphism in the promoter region of the human B2-bradykinin receptor gene in HUMAN GENETICS
  • 1995-03 Population study of a sequence polymorphism in intron 2 of the human β-globin gene in HUMAN GENETICS
  • 1995-02 Influence of different states of hydration on injured tissue (bowel anastomosis) in a rat model in PEDIATRIC SURGERY INTERNATIONAL
  • 1993-11 Mutation analysis in the diagnosis of cystic fibrosis in EUROPEAN JOURNAL OF PEDIATRICS
  • 1993-08 A linear 16 pS Cl− channel in the apical membrane of Caco-2 cells in PFLÜGERS ARCHIV - EUROPEAN JOURNAL OF PHYSIOLOGY
  • 1993-03 Protein Binding of Zidovudine in the Sera of Healthy Controls and Patients Infected with Human Immunodeficiency Virus in CLINICAL DRUG INVESTIGATION
  • 1992-12 Hartnup syndrome, progressive encephalopathy and allo-albuminaemia in EUROPEAN JOURNAL OF PEDIATRICS
  • 1992 Anti-Idiotypic Antibodies Against the Kinin Receptor in RECENT PROGRESS ON KININS
  • 1991-12 157 COMPARISON OF VIP-STIMULATED CHILORIDE SECRETION AND PROTEIN PHOSPHORYLATION IN ISOLATED RAT COLONIC CRYPTS AND CACO-2 CELLS in PEDIATRIC RESEARCH
  • 1989-09 ISOLATION OF APICAL MEMBRANES FROM HORMONE-SENSITIVE RAT COLONIC CRYPT CELLS in PEDIATRIC RESEARCH
  • 1989-07 Genetic and Phenotypic Heterogeneity in Disorders of Peroxisome Biogenesis—A Complementation Study Involving Cell Lines from 19 Patients in PEDIATRIC RESEARCH
  • 1989 Fluorescence Studies on Membranes from Human Skin Fibroblasts Deficient in Plasmalogens in FLUORESCENT BIOMOLECULES
  • 1987-09 Ornithine transcarbamylase variant in a male patient in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1987-03 The effect ofd-(+)-glucosamine on levels of freeN-acetylneuraminic acid and UDP-N-acetylhexosamines in infantile sialic acid storage disease (ISSD) fibroblasts in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1986-08 Infantile Sialic Acid Storage Disease: The Fate of Biosynthetically Labeled N-Acetyl-(3H)-Neuraminic Acid in Cultured Human Fibroblasts in PEDIATRIC RESEARCH
  • 1985-09 The Cerebrohepatorenal (Zellweger) Syndrome: An Improved Method for the Biochemical Diagnosis and its Potential Value for Prenatal Detection in PEDIATRIC RESEARCH
  • 1985-03 Plasma lipids and lipoproteins of a patient with cholesteryl ester storage disease in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1980-08 Elevated CSF cyclic AMP concentrations in patients with inflammatory diseases of cerebral and extracerebral origin in EUROPEAN JOURNAL OF PEDIATRICS
  • 1980-03 ENHANCED ADENOSINE 3': 5' - MONOPHOSPHATE RESPONSE TO BETAADRENERGIC STIMULATION IN CYSTIC FIBROSIS FIBROBLASTS AFTER REMOVAL OF CONDITIONED MEDIUM in PEDIATRIC RESEARCH
  • 1979-10 Reduced plating efficiency of Turner's syndrome fibroblasts. Evidence for a peripheral resistance to growth factors? in PEDIATRIC RESEARCH
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