Decreased nitric oxide bioavailability in a mouse model of Fabry disease.
about
The balance of powers: Redox regulation of fibrogenic pathways in kidney injuryRole of Tyrosine Isomers in Acute and Chronic Diseases Leading to Oxidative Stress - A ReviewCardiomyopathy and response to enzyme replacement therapy in a male mouse model for Fabry diseaseAngiotensin II type 1A receptors in vascular smooth muscle cells do not influence aortic remodeling in hypertension.Prevalence of chronic kidney disease in fabry disease patients: Multicenter cross sectional study in Argentina.The development and use of small molecule inhibitors of glycosphingolipid metabolism for lysosomal storage diseases.Establishing 3-nitrotyrosine as a biomarker for the vasculopathy of Fabry disease.Multi-system disorders of glycosphingolipid and ganglioside metabolismGlobotriaosylsphingosine accumulation and not alpha-galactosidase-A deficiency causes endothelial dysfunction in Fabry disease.Quantitative analysis of amino Acid oxidation markers by tandem mass spectrometrySerum high concentrations of homocysteine and low levels of folic acid and vitamin B12 are significantly correlated with the categories of coronary artery diseasesHomocysteine and erythrocyte sedimentation rate correlate with cerebrovascular disease in fabry disease.Progressive podocyte injury and globotriaosylceramide (GL-3) accumulation in young patients with Fabry diseaseEndothelial nitric oxide synthase uncoupling and microvascular dysfunction in the mesentery of mice deficient in α-galactosidase A.An association of metabolic syndrome constellation with cellular membrane caveolaeFabry Disease: Recognition, Diagnosis, and Treatment of Neurological Features.Tetrahydrobiopterin deficiency in the pathogenesis of Fabry disease.The urea decomposition product cyanate promotes endothelial dysfunction.Glycosphingolipid Mediated Caveolin-1 Oligomerization.Fabry disease: characterisation of the plasma proteome pre- and post-enzyme replacement therapy.Globotriaosylceramide leads to K(Ca)3.1 channel dysfunction: a new insight into endothelial dysfunction in Fabry disease.Blocking hyperactive androgen receptor signaling ameliorates cardiac and renal hypertrophy in Fabry mice.Fabry disease
P2860
Q26786137-E37DD9DF-DD96-4F00-BF51-D751696907FCQ28072656-3EE75F5B-DEC8-4D88-B98C-B8C98CF0DC8AQ28730130-14C72C0E-1703-4EB6-B399-0F93154EBA87Q30428077-C5D0BEB0-FB1B-400E-8F6B-C5F3F4BEDBC8Q33726258-B5C2C655-3251-445C-B47F-13755B669267Q33825097-0A5683D0-056E-4C0B-AA6C-210F05F3EE76Q33831482-7C699C42-815A-4123-8B5E-1A6421EB8C48Q33902037-75E6B56C-29B2-4D48-AA4F-81793AE465FEQ34257466-5534255A-1F8A-4F4A-945C-E6D0F1443C6CQ35173711-AAADC22A-2FDC-4787-9FD4-C9F421258FBCQ36256320-53907BCB-6FB5-4FCF-80E3-4A6EF70B5861Q36590911-4A0E1526-1E62-48AB-86D2-BC003DB7321BQ36808226-152022E4-E0BE-483D-8D11-66783E503F87Q37575656-7AB2D1DD-3CE4-489A-9F64-FB8CF293B54FQ37589401-15B6D8B3-A411-49B2-8B38-BB66DD11CF28Q38844401-7A8D4388-C904-4EFD-A961-ED795140EBFAQ40351353-2DDD458C-A3AE-4611-A01C-290B694D1845Q42025075-38EB80FD-1BF4-4174-821F-8EB3CE7B757EQ42148671-56DC2992-ABC4-490D-A19F-69370A5017B4Q47123134-1A051EC1-17B0-4090-8CCF-50EC3BAF9052Q53453652-A3452164-1ED4-4416-BA73-E44BB2EDEAD5Q53608980-43621148-A573-4675-99EA-CD9D633CB5B0Q56905945-052ACF17-E1BA-4E30-8187-80F688D4B438
P2860
Decreased nitric oxide bioavailability in a mouse model of Fabry disease.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 23 July 2009
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Decreased nitric oxide bioavailability in a mouse model of Fabry disease.
@en
Decreased nitric oxide bioavailability in a mouse model of Fabry disease.
@nl
type
label
Decreased nitric oxide bioavailability in a mouse model of Fabry disease.
@en
Decreased nitric oxide bioavailability in a mouse model of Fabry disease.
@nl
prefLabel
Decreased nitric oxide bioavailability in a mouse model of Fabry disease.
@en
Decreased nitric oxide bioavailability in a mouse model of Fabry disease.
@nl
P2093
P2860
P356
P1476
Decreased nitric oxide bioavailability in a mouse model of Fabry disease.
@en
P2093
Jaeman Byun
James A Shayman
James L Park
Jessica Kollmeyer
Liming Shu
Subramaniam Pennathur
P2860
P304
P356
10.1681/ASN.2008111190
P577
2009-07-23T00:00:00Z