B. E. Reuber

Cloning and Functional Expression of a Mammalian Gene for a Peroxisomal Sarcosine Oxidase*

S. Mihalik, G. Dodt, Bernadette E. Reuber, 1997, The Journal of Biological Chemistry.

Genotyping of human platelet antigen‐1 by gene amplification and labelling in one system and automated fluorescence correlation spectroscopy

A. Weber, Bernadette E. Reuber, S. Weber, 2002, British journal of haematology.

Disruption of a PEX1-PEX6 interaction is the most common cause of the neurologic disorders Zellweger syndrome, neonatal adrenoleukodystrophy, and infantile Refsum disease.

B. Geisbrecht, S. Gould, B. E. Reuber, 1998, Proceedings of the National Academy of Sciences of the United States of America.

Expression of PEX11β Mediates Peroxisome Proliferation in the Absence of Extracellular Stimuli*

C. Obie, D. Valle, G. Jiménez-Sánchez, 1998, The Journal of Biological Chemistry.

Mutations in PEX1 are the most common cause of peroxisome biogenesis disorders

H. Moser, D. Valle, S. Gould, 1997, Nature Genetics.