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BMC Biochemistry|January 12, 2013
Hepatoma-derived growth factor and nucleolin exist in the same ribonucleoprotein complexStephanie Bremer, Katharina Klein, Angela Sedlmaier, et al.
Biological Chemistry|November 15, 2008
Mannose 6-phosphate receptor-dependent endocytosis of lysosomal enzymes is increased in sulfatide-storing kidney cellsDiana Klein, Afshin Yaghootfam, Ullrich Matzner, et al.
Irish Journal of Psychological Medicine|February 19, 2026
Opportunities and challenges of joint crisis plans in mental healthcare: a qualitative interview study with mental health professionalsAstrid Gieselmann, Anna Werning, Sarah Potthoff, et al.
American Journal of Medical Genetics. Part A|December 28, 2002
Biochemical characterization of two (C300F, P425T) arylsulfatase a missense mutationsAna Marcão, Heidi Simonis, Frank Schestag, et al.
Human Mutation|January 1, 1995
Molecular basis of late infantile metachromatic leukodystrophy in the Habbanite JewsJ Zlotogora, G Bach, C Bösenberg, et al.
Developmental Neuroscience|January 1, 1991
Molecular genetics of metachromatic leukodystrophyV Gieselmann, A Polten, J Kreysing, et al.
American Journal of Human Genetics|December 1, 1991
Two new arylsulfatase A (ARSA) mutations in a juvenile metachromatic leukodystrophy (MLD) patientA L Fluharty, C B Fluharty, W Bohne, et al.
Brain Research|November 27, 1999
Decline in brainstem auditory-evoked potentials coincides with loss of spiral ganglion cells in arylsulfatase A-deficient miceR D'Hooge, R Coenen, V Gieselmann, et al.
BMC Cancer|October 22, 2011
Overexpression of hepatoma-derived growth factor in melanocytes does not lead to oncogenic transformationAngela Sedlmaier, Nicolas Wernert, Rainer Gallitzendörfer, et al.
Human Molecular Genetics|November 20, 2020
Decreased turnover of the CNS myelin protein Opalin in a mouse model of hereditary spastic paraplegia 35Robert Hardt, Silvia Jordans, Dominic Winter, et al.
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