190 related articles for article (PubMed ID: 24872419)
1. Mesotrypsin and caspase-14 participate in prosaposin processing: potential relevance to epidermal permeability barrier formation.
Yamamoto-Tanaka M; Motoyama A; Miyai M; Matsunaga Y; Matsuda J; Tsuboi R; Hibino T
J Biol Chem; 2014 Jul; 289(29):20026-38. PubMed ID: 24872419
[TBL] [Abstract][Full Text] [Related]
2. Combined saposin C and D deficiencies in mice lead to a neuronopathic phenotype, glucosylceramide and alpha-hydroxy ceramide accumulation, and altered prosaposin trafficking.
Sun Y; Witte DP; Zamzow M; Ran H; Quinn B; Matsuda J; Grabowski GA
Hum Mol Genet; 2007 Apr; 16(8):957-71. PubMed ID: 17353235
[TBL] [Abstract][Full Text] [Related]
3. Regional expression of prosaposin in the wild-type and saposin D-deficient mouse brain detected by an anti-mouse prosaposin-specific antibody.
Yoneshige A; Suzuki K; Kojima N; Matsuda J
Proc Jpn Acad Ser B Phys Biol Sci; 2009; 85(9):422-34. PubMed ID: 19907127
[TBL] [Abstract][Full Text] [Related]
4. Lysosomal proteolysis of prosaposin, the precursor of saposins (sphingolipid activator proteins): its mechanism and inhibition by ganglioside.
Hiraiwa M; Martin BM; Kishimoto Y; Conner GE; Tsuji S; O'Brien JS
Arch Biochem Biophys; 1997 May; 341(1):17-24. PubMed ID: 9143348
[TBL] [Abstract][Full Text] [Related]
5. Saposin B is the dominant saposin that facilitates lipid binding to human CD1d molecules.
Yuan W; Qi X; Tsang P; Kang SJ; Illarionov PA; Besra GS; Gumperz J; Cresswell P
Proc Natl Acad Sci U S A; 2007 Mar; 104(13):5551-6. PubMed ID: 17372201
[TBL] [Abstract][Full Text] [Related]
6. 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.
Matsuda J; Kido M; Tadano-Aritomi K; Ishizuka I; Tominaga K; Toida K; Takeda E; Suzuki K; Kuroda Y
Hum Mol Genet; 2004 Nov; 13(21):2709-23. PubMed ID: 15345707
[TBL] [Abstract][Full Text] [Related]
7. Role of saposin C and D in auditory and vestibular function.
Lustig LR; Alemi S; Sun Y; Grabowski G; Akil O
Laryngoscope; 2016 Feb; 126(2):452-9. PubMed ID: 26198053
[TBL] [Abstract][Full Text] [Related]
8. Keratinocyte-specific mesotrypsin contributes to the desquamation process via kallikrein activation and LEKTI degradation.
Miyai M; Matsumoto Y; Yamanishi H; Yamamoto-Tanaka M; Tsuboi R; Hibino T
J Invest Dermatol; 2014 Jun; 134(6):1665-1674. PubMed ID: 24390132
[TBL] [Abstract][Full Text] [Related]
9. A mutation in the saposin C domain of the sphingolipid activator protein (Prosaposin) gene causes neurodegenerative disease in mice.
Yoneshige A; Suzuki K; Suzuki K; Matsuda J
J Neurosci Res; 2010 Aug; 88(10):2118-34. PubMed ID: 20175216
[TBL] [Abstract][Full Text] [Related]
10. Isolation, characterization, and proteolysis of human prosaposin, the precursor of saposins (sphingolipid activator proteins).
Hiraiwa M; O'Brien JS; Kishimoto Y; Galdzicka M; Fluharty AL; Ginns EI; Martin BM
Arch Biochem Biophys; 1993 Jul; 304(1):110-6. PubMed ID: 8323276
[TBL] [Abstract][Full Text] [Related]
11. Ex vivo localization of the mouse saposin C activation region for acid beta-glucosidase.
Qi X; Kondoh K; Yin H; Wang M; Ponce E; Sun Y; Grabowski GA
Mol Genet Metab; 2002 Jul; 76(3):189-200. PubMed ID: 12126932
[TBL] [Abstract][Full Text] [Related]
12. Proteolytic processing patterns of prosaposin in insect and mammalian cells.
Leonova T; Qi X; Bencosme A; Ponce E; Sun Y; Grabowski GA
J Biol Chem; 1996 Jul; 271(29):17312-20. PubMed ID: 8663398
[TBL] [Abstract][Full Text] [Related]
13. Modulation of human saposin B sphingolipid-binding specificity by alternative splicing. A study with saposin B-derived synthetic peptides.
Lamontagne S; Potier M
J Biol Chem; 1994 Aug; 269(32):20528-32. PubMed ID: 8051151
[TBL] [Abstract][Full Text] [Related]
14. Identification of a novel sequence involved in lysosomal sorting of the sphingolipid activator protein prosaposin.
Zhao Q; Morales CR
J Biol Chem; 2000 Aug; 275(32):24829-39. PubMed ID: 10818106
[TBL] [Abstract][Full Text] [Related]
15. Identification of prosaposin as a neurotrophic factor.
O'Brien JS; Carson GS; Seo HC; Hiraiwa M; Kishimoto Y
Proc Natl Acad Sci U S A; 1994 Sep; 91(20):9593-6. PubMed ID: 7937812
[TBL] [Abstract][Full Text] [Related]
16. Seminolipid and its precursor/degradative product, galactosylalkylacylglycerol, in the testis of saposin A- and prosaposin-deficient mice.
Tadano-Aritomi K; Matsuda J; Fujimoto H; Suzuki K; Ishizuka I
J Lipid Res; 2003 Sep; 44(9):1737-43. PubMed ID: 12810822
[TBL] [Abstract][Full Text] [Related]
17. A saposin deficiency model in Drosophila: Lysosomal storage, progressive neurodegeneration and sensory physiological decline.
Hindle SJ; Hebbar S; Schwudke D; Elliott CJH; Sweeney ST
Neurobiol Dis; 2017 Feb; 98():77-87. PubMed ID: 27913291
[TBL] [Abstract][Full Text] [Related]
18. Saposin C promotes survival and prevents apoptosis via PI3K/Akt-dependent pathway in prostate cancer cells.
Lee TJ; Sartor O; Luftig RB; Koochekpour S
Mol Cancer; 2004 Nov; 3():31. PubMed ID: 15548330
[TBL] [Abstract][Full Text] [Related]
19. Structural analysis of the mouse prosaposin (SGP-1) gene reveals the presence of an exon that is alternatively spliced in transcribed mRNAs.
Zhao Q; Hay N; Morales CR
Mol Reprod Dev; 1997 Sep; 48(1):1-8. PubMed ID: 9266755
[TBL] [Abstract][Full Text] [Related]
20. Prosaposin deficiency and saposin B deficiency (activator-deficient metachromatic leukodystrophy): report on two patients detected by analysis of urinary sphingolipids and carrying novel PSAP gene mutations.
Kuchar L; Ledvinová J; Hrebícek M; Mysková H; Dvoráková L; Berná L; Chrastina P; Asfaw B; Elleder M; Petermöller M; Mayrhofer H; Staudt M; Krägeloh-Mann I; Paton BC; Harzer K
Am J Med Genet A; 2009 Feb; 149A(4):613-21. PubMed ID: 19267410
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
