Non-synonymous single-nucleotide polymorphisms associated with blood pressure and hypertension

Pharmacological characterization of the inhibition by moxonidine and agmatine on the cardioaccelerator sympathetic outflow in pithed rats

(2009) Luis E. Cobos-Puc et al.   EUROPEAN JOURNAL OF PHARMACOLOGY

Genome-wide scan identifies CDH13 as a novel susceptibility locus contributing to blood pressure determination in two European populations

(2009) Elin Org et al.   HUMAN MOLECULAR GENETICS

Hemodynamic and Cardiac Effects of Chronic Eprosartan and Moxonidine Therapy in Stroke-Prone Spontaneously Hypertensive Rats

(2009) Suhayla Mukaddam-Daher et al.   HYPERTENSION

Replication of the Wellcome Trust genome-wide association study on essential hypertension in a Korean population

(2009) Kyung-Won Hong et al.   HYPERTENSION RESEARCH

Association Study of the Decreased Serum BDNF Concentrations in Amnestic Mild Cognitive Impairment and the Val66Met Polymorphism in Chinese Han

(2009) Hui Yu et al.   JOURNAL OF CLINICAL PSYCHIATRY

A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits

(2009) Yoon Shin Cho et al.   NATURE GENETICS

Genome-wide association study identifies eight loci associated with blood pressure

(2009) Christopher Newton-Cheh et al.   NATURE GENETICS

Genome-wide association study of blood pressure and hypertension

(2009) Daniel Levy et al.   NATURE GENETICS

Validating, augmenting and refining genome-wide association signals

(2009) John P. A. Ioannidis et al.   NATURE REVIEWS GENETICS

BDNF Val66Met polymorphism is associated with unstable angina

(2008) Hong Jiang et al.   CLINICA CHIMICA ACTA

Replication of the Wellcome Trust genome-wide association study of essential hypertension: the Family Blood Pressure Program

(2008) Georg B Ehret et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

BDNFgene: functional Val66Met polymorphism in mood disorders and schizophrenia

(2008) Janusz K Rybakowski   PHARMACOGENOMICS

Whole-genome association study identifies STK39 as a hypertension susceptibility gene

(2008) Y. Wang et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Crystallographic and biochemical studies revealing the structural basis for antizyme inhibitor function

(2008) Shira Albeck et al.   PROTEIN SCIENCE