| 1 |
24872419 | Mesotrypsin and caspase-14 participate in prosaposin processing: potential relevance to epidermal permeability barrier formation. | 2014 Jul 18 |
1 |
| 2 |
20175216 | A mutation in the saposin C domain of the sphingolipid activator protein (Prosaposin) gene causes neurodegenerative disease in mice. | 2010 Aug 1 |
3 |
| 3 |
19907127 | Regional expression of prosaposin in the wild-type and saposin D-deficient mouse brain detected by an anti-mouse prosaposin-specific antibody. | 2009 |
1 |
| 4 |
15743835 | The exon 8-containing prosaposin gene splice variant is dispensable for mouse development, lysosomal function, and secretion. | 2005 Mar |
1 |
| 5 |
15345707 | 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. | 2004 Nov 1 |
1 |
| 6 |
10196186 | Sphingolipid activator proteins are required for epidermal permeability barrier formation. | 1999 Apr 16 |
2 |
| 7 |
9582364 | Role of Sp proteins and RORalpha in transcription regulation of murine prosaposin. | 1998 May 22 |
1 |