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The Biochemical Journal|May 15, 2002
The family of hepatoma-derived growth factor proteins: characterization of a new member HRP-4 and classification of its subfamiliesFrank Dietz, Sebastian Franken, Kenya Yoshida, et al.
Human Mutation|January 1, 1994
Molecular genetics of metachromatic leukodystrophyV Gieselmann, J Zlotogora, A Harris, et al.
Biochimica Et Biophysica Acta|August 27, 2009
Compensatory expression of human N-acetylglucosaminyl-1-phosphotransferase subunits in mucolipidosis type III gammaSandra Pohl, Stephan Tiede, Monica Castrichini, et al.
American Journal of Medical Genetics. Part A|August 25, 2004
Novel mutations associated with metachromatic leukodystrophy: phenotype and expression studies in nine Czech and Slovak patientsLinda Berná, Volkmar Gieselmann, Helena Poupetová, et al.
The FEBS Journal|February 22, 2005
Missense mutations as a cause of metachromatic leukodystrophy. Degradation of arylsulfatase A in the endoplasmic reticulumPeter Poeppel, Matthias Habetha, Ana Marcão, et al.
The Journal of Biological Chemistry|January 28, 1999
Interaction of arylsulfatase A with UDP-N-acetylglucosamine:Lysosomal enzyme-N-acetylglucosamine-1-phosphotransferaseA Schierau, F Dietz, H Lange, et al.
Biochemical and Biophysical Research Communications|June 29, 2000
Enzymatic properties, tissue-specific expression, and lysosomal location of two highly homologous rat SULT1C2 sulfotransferasesL Xiangrong, C Jöhnk, D Hartmann, et al.
Frontiers in Psychiatry|November 7, 2022
Opportunities and risks of self-binding directives: A qualitative study involving stakeholders and researchers in GermanySarah Potthoff, Marleen Finke, Matthé Scholten, et al.
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