Impact of the endothelial nitric oxide synthase gene G894T polymorphism on renal endothelial function in patients with type 2 diabetes.

Martin Ritt; Christian Ott; Christian Delles; Markus Schneider; Roland E Schmieder

doi:10.1097/FPC.0b013e32830500b1

Impact of the endothelial nitric oxide synthase gene G894T polymorphism on renal endothelial function in patients with type 2 diabetes.

Martin Ritt
, Christian Ott
, Christian Delles
, Markus Schneider
, Roland E Schmieder

Department of Internal Medicine IV, Division of Nephrology and Hypertensiology

Research output: Contribution to journal › Original Article › peer-review

16 Citations (Web of Science)

Original language	English
Pages (from-to)	699-707
Journal	PHARMACOGENETICS AND GENOMICS
Volume	18
Issue number	8
DOIs	https://doi.org/10.1097/FPC.0b013e32830500b1
Publication status	Published - 2008

Keywords

ENOS GLU298ASP POLYMORPHISM
VITAMIN-C
DEPENDENT VASODILATION
VASCULAR-DISEASE
COMMON VARIANT
HEART-DISEASE
RISK-FACTOR
L-ARGININE
HYPERTENSION
NEPHROPATHY

Access to Document

10.1097/FPC.0b013e32830500b1

Cite this

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title = "Impact of the endothelial nitric oxide synthase gene G894T polymorphism on renal endothelial function in patients with type 2 diabetes.",

keywords = "ENOS GLU298ASP POLYMORPHISM, VITAMIN-C, DEPENDENT VASODILATION, VASCULAR-DISEASE, COMMON VARIANT, HEART-DISEASE, RISK-FACTOR, L-ARGININE, HYPERTENSION, NEPHROPATHY",

author = "Martin Ritt and Christian Ott and Christian Delles and Markus Schneider and Schmieder, \{Roland E\}",

year = "2008",

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volume = "18",

pages = "699--707",

journal = "PHARMACOGENETICS AND GENOMICS",

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publisher = "Lippincott Williams \& Wilkins ",

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T1 - Impact of the endothelial nitric oxide synthase gene G894T polymorphism on renal endothelial function in patients with type 2 diabetes.

AU - Ritt, Martin

AU - Ott, Christian

AU - Delles, Christian

AU - Schneider, Markus

AU - Schmieder, Roland E

PY - 2008

Y1 - 2008

KW - ENOS GLU298ASP POLYMORPHISM

KW - VITAMIN-C

KW - DEPENDENT VASODILATION

KW - VASCULAR-DISEASE

KW - COMMON VARIANT

KW - HEART-DISEASE

KW - RISK-FACTOR

KW - L-ARGININE

KW - HYPERTENSION

KW - NEPHROPATHY

U2 - 10.1097/FPC.0b013e32830500b1

DO - 10.1097/FPC.0b013e32830500b1

M3 - Original Article

C2 - 18622262

SN - 1744-6872

VL - 18

SP - 699

EP - 707

JO - PHARMACOGENETICS AND GENOMICS

JF - PHARMACOGENETICS AND GENOMICS

IS - 8

ER -