Author

Gabriele Reinkensmeier

Observed name: G. Reinkensmeier

Institution: University of Oxford

Observed institutions: Monsanto (United States), National Institutes of Health, Peking University, University of Oxford, National Institute of Diabetes and Digestive and Kidney Diseases, State Key Laboratory of Natural and Biomimetic Drugs

OpenAlex ID: A5000447367

Infantile-onset symptomatic epilepsy syndrome caused by a homozygous loss-of-function mutation of GM3 synthase

2004 · Michael A Simpson, Harold Cross, et al. · Nature Genetics · 390

Prevention of Lysosomal Storage in Tay-Sachs Mice Treated with N -Butyldeoxynojirimycin

1997 · Frances M. Platt, Gabrielle R. Neises, et al. · Science · 340

Treatment with miglustat reverses the lipid-trafficking defect in Niemann–Pick disease type C

2004 · Robin H Lachmann, Danielle te Vruchte, et al. · Neurobiology of Disease · 150

Extensive Glycosphingolipid Depletion in the Liver and Lymphoid Organs of Mice Treated with N-Butyldeoxynojirimycin

1997 · Frances M. Platt, Gabriele Reinkensmeier, et al. · Journal of Biological Chemistry · 119

Combination of α-glucosidase inhibitor and ribavirin for the treatment of dengue virus infection in vitro and in vivo

2010 · Jinhong Chang, Wouter Schul, et al. · Antiviral Research · 100

Rational Design and Synthesis of Highly Potent Pharmacological Chaperones for Treatment of N370S Mutant Gaucher Disease

2009 · Guan-Nan Wang, Gabriele Reinkensmeier, et al. · Journal of Medicinal Chemistry · 65

High-Performance Liquid Chromatography Analysis of Ganglioside Carbohydrates at the Picomole Level after Ceramide Glycanase Digestion and Fluorescent Labeling with 2-Aminobenzamide

2001 · D.R. Wing, B. Garner, et al. · Analytical Biochemistry · 59

Selection of the biological activity of DNJ neoglycoconjugates through click length variation of the side chain

2011 · Nicolas Ardes-Guisot, Dominic S. Alonzi, et al. · Organic & Biomolecular Chemistry · 48

An Inducible Mouse Model of Late Onset Tay–Sachs Disease

2002 · Mylvaganam Jeyakumar, David Smith, et al. · Neurobiology of Disease · 30

Inhibition of glycogen breakdown by imino sugars in vitro and in vivo

2003 · Ulrika Andersson, Gabriele Reinkensmeier, et al. · Biochemical Pharmacology · 27

Human GM3 synthase deficiency: A novel form of hereditary childhood epilepsy

2005 · David A. Priestman, Neville Dca., et al. · UCL Discovery (University College London)

Human GM3 synthase deficiency: Autosomal recessive infantile onset symptomatic epilepsy syndrome.

2004 · David A. Priestman, Neville Dca., et al. · UCL Discovery (University College London)

Works count: 12

Citation count: 1,327

H-index: 10

I10-index: 10