Amanote Research
Register
Sign In
Discover open access scientific publications
Search, annotate, share and cite publications
Publications by Adelbert A Roscher
Genetic and Phenotypic Heterogeneity in Disorders of Peroxisome Biogenesis—A Complementation Study Involving Cell Lines From 19 Patients
Pediatric Research
Child Health
Pediatrics
Perinatology
Related publications
Temperature-Sensitive Mutation of PEX6 in Peroxisome Biogenesis Disorders in Complementation Group C (CG-C): Comparative Study of PEX6 and PEX1
Pediatric Research
Child Health
Pediatrics
Perinatology
Genetic Basis of Peroxisome-Assembly Mutants of Humans, Chinese Hamster Ovary Cells, and Yeast: Identification of a New Complementation Group of Peroxisome-Biogenesis Disorders Apparently Lacking Peroxisomal-Membrane Ghosts
American Journal of Human Genetics
Genetics
Temperature-Sensitive Phenotypes of Peroxisome-Assembly Processes Represent the Milder Forms of Human Peroxisome-Biogenesis Disorders
American Journal of Human Genetics
Genetics
PEX16: A Multifaceted Regulator of Peroxisome Biogenesis
Frontiers in Physiology
Physiology
Peroxisomal Biogenesis: Genetic Disorders Reveal the Mechanisms
Genetic and Phenotypic Characterization of Indolent T-Cell Lymphoproliferative Disorders of the Gastrointestinal Tract
Haematologica
Hematology
The NeuroDev Study: Phenotypic and Genetic Characterization of Neurodevelopmental Disorders in Kenya and South Africa
Neuron
Neuroscience
Genetic Disorders Involving Molecular-Chaperone Genes: A Perspective
Genetics in Medicine
Medicine
Genetics
Genotypic and Phenotypic Heterogeneity Among Mycobacterium Tuberculosis Isolates From Pulmonary Tuberculosis Patients
Journal of Clinical Microbiology
Microbiology
