Results 251 to 260 of about 2,765,821 (261)

Mutation in saposin D domain of sphingolipid activator protein gene causes urinary system defects and cerebellar Purkinje cell degeneration with accumulation of hydroxy fatty acid-containing ceramide in mouse.

Human Molecular Genetics, 2004
J. Matsuda, M. Kido, K. Tadano-Aritomi, I. Ishizuka, K. Tominaga, K. Toida, E. Takeda, Kunihiko Suzuki, Y. Kuroda   +8 more
semanticscholar   +1 more source

Sphingolipid activator protein D (sap-D) stimulates the lysosomal degradation of ceramide in vivo.

Biochemical and Biophysical Research Communications - BBRC, 1994
A. Klein, M. Henseler, C. Klein, Kunihiko Suzuki, K. Harzer, Konrad Sandhoff   +5 more
semanticscholar   +1 more source

Synthesis of the sphingolipid activator protein, saposin C, using an azido-protected O-acyl isopeptide as an aggregation-disrupting element

, 2011
H. Hojo, Hidekazu Katayama, C. Tano, Y. Nakahara, Azusa Yoneshige, J. Matsuda, Youhei Sohma, Y. Kiso, Y. Nakahara   +8 more
semanticscholar   +1 more source

A mutation in the saposin A domain of the sphingolipid activator protein (prosaposin) gene results in a late-onset, chronic form of globoid cell leukodystrophy in the mouse.

Human Molecular Genetics, 2001
J. Matsuda, M. Vanier, Y. Saito, J. Tohyama, K. Suzuki   +4 more
semanticscholar   +1 more source

Sphingolipid activator proteins.

Essays in biochemistry, 1997
openaire   +1 more source

Sphingolipid Activator Protein (SAP, Saposin)

2008
openaire   +1 more source

MICE WITH TOTAL ABSENCE OF SPHINGOLIPID ACTIVATOR PROTEINS (SAP KNOCKOUT)

Journal of Neuropathology and Experimental Neurology, 1997
Y. Oya, H. Nakayasu, N. Fujita, K. Suzuki   +3 more
openaire   +1 more source

[Sphingolipid activator protein deficiency].

Tanpakushitsu kakusan koso. Protein, nucleic acid, enzyme, 1990
openaire   +1 more source

[Sphingolipid activator protein deficiency].

Ryoikibetsu shokogun shirizu, 2001
openaire   +1 more source

Sphingolipid Activator Proteins

Konrad Sandhoff
exaly