Glossmann, Hartmut

Mutations in the Δ7-sterol reductase gene in patients with the Smith–Lemli–Opitz syndrome

Fitzky, B. U., Witsch-Baumgartner, M., Erdel, M., Lee, J. N., Paik, Y.-K., Glossmann, H., Utermann, G., & Moebius, F. F. (1998) · Proceedings of the National Academy of Sciences

Metabolism and Genetic DisordersCholesterol and Lipid Metabolism

Cited by 384

Mutations in the gene encoding 3β- hydroxysteroid-Δ8,Δ7- isomerase cause X-linked dominant Conradi-Hünermann syndrome

Braverman, N., Lin, P., Moebius, F. F., Obie, C., Moser, A., Glossmann, H., Wilcox, W. R., Rimoin, D. L., Smith, M., Kratz, L., et al. (1999) · Nature Genetics

Metabolism and Genetic DisordersCholesterol and Lipid Metabolism

Cited by 285

Metformin and Aging: A Review

Glossmann, H. H., & Lutz, O. M. D. (2019) · Gerontology

Metabolism, Diabetes, and CancerGenetics, Aging, and Longevity in Model Organisms

Cited by 149

Pharmacological Analysis of Sterol Δ8-Δ7 Isomerase Proteins with [3H]Ifenprodil

Moebius, F. F., Reiter, R. J., Bermoser, K., Glossmann, H., Cho, S. Y., & Paik, Y.-K. (1998) · Molecular Pharmacology

Pharmacological Receptor Mechanisms and EffectsCholesterol and Lipid Metabolism

Cited by 81

Purification and amino-terminal sequencing of the high affinity phenylalkylamine Ca2+ antagonist binding protein from guinea pig liver endoplasmic reticulum.

Moebius, F. F., Hanner, M., Knaus, H. G., Weber, F., Striessnig, J., & Glossmann, H. (1994) · Journal of Biological Chemistry

Ion channel regulation and functionIon Channels and Receptors

Cited by 39

Histidine77, Glutamic Acid81, Glutamic Acid123, Threonine126, Asparagine194, and Tryptophan197 of the Human Emopamil Binding Protein Are Required for in Vivo Sterol Δ8−Δ7 Isomerization

Moebius, F. F., Soellner, K. E. M., Fiechtner, B., Huck, C. W., Bonn, G., & Glossmann, H. (1999) · Biochemistry

Cholesterol and Lipid MetabolismLipid Membrane Structure and Behavior

Cited by 36