-
1
-
-
53249134368
-
Beyond silencing - engineering applications of RNA interference and antisense technology for altering cellular phenotype
-
Hebert CG, Valdes JJ, Bentley WE. Beyond silencing - engineering applications of RNA interference and antisense technology for altering cellular phenotype. Curr Opin Biotechnol 2008; 19:500-505.
-
(2008)
Curr Opin Biotechnol
, vol.19
, pp. 500-505
-
-
Hebert, C.G.1
Valdes, J.J.2
Bentley, W.E.3
-
2
-
-
59149106521
-
Downregulation of α-galactosidase A upregulates CD77:functional impact for Fabry nephropathy
-
Thomaidis T, Relle M, Golbas M et al. Downregulation of α-galactosidase A upregulates CD77:functional impact for Fabry nephropathy. Kidney Int 2009; 75:399-407.
-
(2009)
Kidney Int
, vol.75
, pp. 399-407
-
-
Thomaidis, T.1
Relle, M.2
Golbas, M.3
-
3
-
-
33947718746
-
Narrative review: Fabry disease
-
Clarke JT. Narrative review: Fabry disease. Ann Intern Med 2007; 146:425-433.
-
(2007)
Ann Intern Med
, vol.146
, pp. 425-433
-
-
Clarke, J.T.1
-
4
-
-
55849108852
-
Characterization of Fabry disease in 352 pediatric patients in the Fabry registry
-
Hopkin RJ, Bissler J, Banikazemi M et al. Characterization of Fabry disease in 352 pediatric patients in the Fabry registry . Pediatr Res 2008; 64:550-555.
-
(2008)
Pediatr Res
, vol.64
, pp. 550-555
-
-
Hopkin, R.J.1
Bissler, J.2
Banikazemi, M.3
-
5
-
-
0025343134
-
Biochemical and clinical analysis of accumulated glycolipids in symptomatic heterozygotes of angiokeratoma corporis diffusum (Fabry's disease) in comparison with hemizygotes
-
Hozumi I, Nishizawa M, Ariga T et al. Biochemical and clinical analysis of accumulated glycolipids in symptomatic heterozygotes of angiokeratoma corporis diffusum (Fabry's disease) in comparison with hemizygotes. J Lipid Res 1990; 31:335-340.
-
(1990)
J Lipid Res
, vol.31
, pp. 335-340
-
-
Hozumi, I.1
Nishizawa, M.2
Ariga, T.3
-
6
-
-
33846447796
-
The Dutch Fabry cohort: Diversity of clinical manifestations and Gb3 levels
-
Vedder AC, Linthorst GE, van Breemen MJ et al. The Dutch Fabry cohort: diversity of clinical manifestations and Gb3 levels. J Inherit Metab Dis 2007; 30:68-78.
-
(2007)
J Inherit Metab Dis
, vol.30
, pp. 68-78
-
-
Vedder, A.C.1
Linthorst, G.E.2
van Breemen, M.J.3
-
7
-
-
25444446897
-
The relationship of vascular glycolipid storage to clinical manifestations of Fabry disease: A cross-sectional study of a large cohort of clinically affected heterozygous women
-
Gupta S, Ries M, Kotsopoulos S et al. The relationship of vascular glycolipid storage to clinical manifestations of Fabry disease: a cross-sectional study of a large cohort of clinically affected heterozygous women. Medicine (Baltimore) 2005; 84:261-268.
-
(2005)
Medicine (Baltimore)
, vol.84
, pp. 261-268
-
-
Gupta, S.1
Ries, M.2
Kotsopoulos, S.3
-
8
-
-
42949119819
-
Elevated globotriaosylsphingosine is a hallmark of Fabry disease
-
Aerts JM, Groener JE, Kuiper S et al. Elevated globotriaosylsphingosine is a hallmark of Fabry disease. Proc Natl Acad Sci USA 2008; 105:2812-2817.
-
(2008)
Proc Natl Acad Sci USA
, vol.105
, pp. 2812-2817
-
-
Aerts, J.M.1
Groener, J.E.2
Kuiper, S.3
-
9
-
-
12644284502
-
Alpha-galactosidase A deficient mice: A model of Fabry disease
-
Ohshima T, Murray GJ, Swaim WD et al. Alpha-galactosidase A deficient mice: a model of Fabry disease. Proc Natl Acad Sci USA 1997; 94:2540-2544.
-
(1997)
Proc Natl Acad Sci USA
, vol.94
, pp. 2540-2544
-
-
Ohshima, T.1
Murray, G.J.2
Swaim, W.D.3
-
10
-
-
13044281563
-
Aging accentuates and bone marrow transplantation ameliorates metabolic defects in Fabry disease mice
-
Ohshima T, Schiffmann R, Murray GJ et al. Aging accentuates and bone marrow transplantation ameliorates metabolic defects in Fabry disease mice. Proc Natl Acad Sci USA 1999; 96:6423-6427.
-
(1999)
Proc Natl Acad Sci USA
, vol.96
, pp. 6423-6427
-
-
Ohshima, T.1
Schiffmann, R.2
Murray, G.J.3
-
11
-
-
0037306593
-
Fabry disease in mice is associated with age-dependent susceptibility to vascular thrombosis
-
Eitzman DT, Bodary PF, Shen Y et al. Fabry disease in mice is associated with age-dependent susceptibility to vascular thrombosis. J Am Soc Nephrol 2003; 14:298-302.
-
(2003)
J Am Soc Nephrol
, vol.14
, pp. 298-302
-
-
Eitzman, D.T.1
Bodary, P.F.2
Shen, Y.3
-
12
-
-
33645830674
-
-
S hen Y, Bodary PF, Vargas FB et al. Alpha-galactosidase A deficiency leads to increased tissue fibrin deposition and thrombosis in mice homozygous for the factor V Leiden mutation. Stroke 2006; 37:1106-1108.
-
S hen Y, Bodary PF, Vargas FB et al. Alpha-galactosidase A deficiency leads to increased tissue fibrin deposition and thrombosis in mice homozygous for the factor V Leiden mutation. Stroke 2006; 37:1106-1108.
-
-
-
-
13
-
-
13444283308
-
Alpha-galactosidase A deficiency accelerates atherosclerosis in mice with apolipoprotein E deficiency
-
Bodary PF, Shen Y, Vargas FB et al. Alpha-galactosidase A deficiency accelerates atherosclerosis in mice with apolipoprotein E deficiency. Circulation 2005; 111:629-632.
-
(2005)
Circulation
, vol.111
, pp. 629-632
-
-
Bodary, P.F.1
Shen, Y.2
Vargas, F.B.3
-
14
-
-
50649111889
-
Vascular dysfunction in the α-galactosidase A-knockout mouse is an endothelial cell-, plasma membrane-based defect
-
Park JL, Whitesall SE, D'Alecy LG et al. Vascular dysfunction in the α-galactosidase A-knockout mouse is an endothelial cell-, plasma membrane-based defect. Clin Exp Pharmacol Physiol 2008; 35:1156-1163.
-
(2008)
Clin Exp Pharmacol Physiol
, vol.35
, pp. 1156-1163
-
-
Park, J.L.1
Whitesall, S.E.2
D'Alecy, L.G.3
-
15
-
-
34547118621
-
Caveolin-associated accumulation of globotriaosylceramide in the vascular endothelium of alpha-galactosidase A null mice
-
Shu L, Shayman JA. Caveolin-associated accumulation of globotriaosylceramide in the vascular endothelium of alpha-galactosidase A null mice. J Biol Chem 2007; 282:20960-20967.
-
(2007)
J Biol Chem
, vol.282
, pp. 20960-20967
-
-
Shu, L.1
Shayman, J.A.2
-
16
-
-
57449093386
-
Glycosphingolipids Gb3 and iGb3: In vivo roles in hemolytic-uremic syndrome and iNKT cell function] (article in German)
-
publication, 31 August, doi:10.1007/s00292-008-1040-0
-
Porubsky S, Luckow B, Bonrouhi M et al. [Glycosphingolipids Gb3 and iGb3: in vivo roles in hemolytic-uremic syndrome and iNKT cell function] (article in German). Pathologe advance online publication, 31 August 2008, doi:10.1007/s00292-008-1040-0.
-
(2008)
Pathologe advance online
-
-
Porubsky, S.1
Luckow, B.2
Bonrouhi, M.3
-
17
-
-
51449114507
-
Lipid composition of microdomains is altered in a cell model of Gaucher disease
-
Hein LK, Duplock S, Hopwood JJ et al. Lipid composition of microdomains is altered in a cell model of Gaucher disease. J Lipid Res 2008; 49:1725-1734.
-
(2008)
J Lipid Res
, vol.49
, pp. 1725-1734
-
-
Hein, L.K.1
Duplock, S.2
Hopwood, J.J.3
-
19
-
-
0020549842
-
A glycolipid antigen associated with Burkitt lymphoma defined by a monoclonal antibody
-
Nudelman E, Kannagi R, Hakomori S et al. A glycolipid antigen associated with Burkitt lymphoma defined by a monoclonal antibody. Science 1983; 220:509-511.
-
(1983)
Science
, vol.220
, pp. 509-511
-
-
Nudelman, E.1
Kannagi, R.2
Hakomori, S.3
-
20
-
-
0027366926
-
Apoptosis induced in Burkitt's lymphoma cells via Gb3/CD77, a glycolipid antigen
-
Mangeney M, Lingwood CA, Taga S et al. Apoptosis induced in Burkitt's lymphoma cells via Gb3/CD77, a glycolipid antigen. Cancer Res 1993; 53:5314-5319.
-
(1993)
Cancer Res
, vol.53
, pp. 5314-5319
-
-
Mangeney, M.1
Lingwood, C.A.2
Taga, S.3
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