Neutral Sphingomyelinase 1 Deficiency in the Mouse Causes No Lipid Storage Disease

Por Zumbansen, Markus, Stoffel, Wilhelm
Publicado em 2002

Functional breakdown of the lipid bilayer of the myelin membrane in central and peripheral nervous system by disrupted galactocerebroside synthesis

Por Bosio, Andreas, Binczek, Erika, Stoffel, Wilhelm
Publicado em 1996

Interactions of a photosensitive analog of cholesterol with hydroxymethylglutaryl-CoA reductase (NADPH) and acyl-CoA:cholesterol acyltransferase

Por Heller, Renu A., Klotzbücher, Rainer, Stoffel, Wilhelm
Publicado em 1979

Cloning and characterization of the mammalian brain-specific, Mg(2+)-dependent neutral sphingomyelinase

Por Hofmann, Kay, Tomiuk, Stefan, Wolff, Gabriela, Stoffel, Wilhelm
Publicado em 2000

(13)C Nuclear Magnetic Resonance Spectroscopic Evidence for Hydrophobic Lipid-Protein Interactions in Human High Density Lipoproteins

Por Stoffel, Wilhelm, Zierenberg, Ottfried, Tunggal, Budi, Schreiber, Ekkehard
Publicado em 1974

Cloned mammalian neutral sphingomyelinase: Functions in sphingolipid signaling?

Por Tomiuk, Stefan, Hofmann, Kay, Nix, Michael, Zumbansen, Markus, Stoffel, Wilhelm
Publicado em 1998

Neutral sphingomyelinase 2 (smpd3) in the control of postnatal growth and development

Por Stoffel, Wilhelm, Jenke, Britta, Blöck, Barbara, Zumbansen, Markus, Koebke, Jürgen
Publicado em 2005

Assembly of Myelin by Association of Proteolipid Protein with Cholesterol- and Galactosylceramide-Rich Membrane Domains

Por Simons, Mikael, Krämer, Eva-Maria, Thiele, Christoph, Stoffel, Wilhelm, Trotter, Jacqueline
Publicado em 2000

SMPD3 deficiency perturbs neuronal proteostasis and causes progressive cognitive impairment

Por Stoffel, Wilhelm, Jenke, Britta, Schmidt-Soltau, Inga, Binczek, Erika, Brodesser, Susanne, Hammels, Ina
Publicado no Cell Death Dis (2018)

Altered Phenotype of the Vestibular Organ in GLAST-1 Null Mice

Por Schraven, Sebastian P., Franz, Christoph, Rüttiger, Lukas, Löwenheim, Hubert, Lysakowski, Anna, Stoffel, Wilhelm, Knipper, Marlies
Publicado em 2012

Neutral Sphingomyelinase (SMPD3) Deficiency Causes a Novel Form of Chondrodysplasia and Dwarfism That Is Rescued by Col2A1-Driven smpd3 Transgene Expression

Por Stoffel, Wilhelm, Jenke, Britta, Holz, Barbara, Binczek, Erika, Günter, Robert Heinz, Knifka, Jutta, Koebke, Jürgen, Niehoff, Anja
Publicado em 2007

Obesity resistance and deregulation of lipogenesis in Δ6-fatty acid desaturase (FADS2) deficiency

Por Stoffel, Wilhelm, Hammels, Ina, Jenke, Britta, Binczek, Erika, Schmidt-Soltau, Inga, Brodesser, Susanne, Odenthal, Margarete, Thevis, Mario
Publicado no EMBO Rep (2014)

Neutral sphingomyelinase (SMPD3) deficiency disrupts the Golgi secretory pathway and causes growth inhibition

Por Stoffel, Wilhelm, Hammels, Ina, Jenke, Bitta, Binczek, Erika, Schmidt-Soltau, Inga, Brodesser, Susanne, Schauss, Astrid, Etich, Julia, Heilig, Juliane, Zaucke, Frank
Publicado no Cell Death Dis (2016)

Δ6-Desaturase (FADS2) deficiency unveils the role of ω3- and ω6-polyunsaturated fatty acids

Por Stoffel, Wilhelm, Holz, Barbara, Jenke, Britta, Binczek, Erika, Günter, Robert Heinz, Kiss, Christine, Karakesisoglou, Iakowos, Thevis, Mario, Weber, Artur-Aron, Arnhold, Stephan, Addicks, Klaus
Publicado em 2008