Published in Nat Genet on January 01, 1998
Progression of coronary artery calcification seems to be inevitable, but predictable - results of the Heinz Nixdorf Recall (HNR) study. Eur Heart J (2014) 2.23
The vitamin D receptor genotype predisposes to the development of calcific aortic valve stenosis. Heart (2001) 1.86
Redox control of renal function and hypertension. Antioxid Redox Signal (2008) 1.45
Pharmacogenetics of antidepressant response. J Psychiatry Neurosci (2011) 1.28
Association of NQO1 polymorphism with spontaneous breast cancer in two independent populations. Br J Cancer (2004) 1.11
The G-protein beta3 subunit 825 TT genotype is associated with epigastric pain syndrome-like dyspepsia. BMC Med Genet (2010) 1.04
Homozygous 825T allele of the GNB3 protein influences the susceptibility of Japanese to dyspepsia. Dig Dis Sci (2007) 1.04
G-Protein Beta3 Subunit C825T Polymorphism in Patients With Overlap Syndrome of Functional Dyspepsia and Irritable Bowel Syndrome. J Neurogastroenterol Motil (2012) 1.04
Common genetic variants in ARNTL and NPAS2 and at chromosome 12p13 are associated with objectively measured sleep traits in the elderly. Sleep (2013) 1.03
Association of α-adducin and G-protein β3 genetic polymorphisms with hypertension: a meta-analysis of Chinese populations. PLoS One (2011) 1.02
Expression profile of a gamma-deletion variant of the human telomerase reverse transcriptase gene. Neoplasia (2003) 1.01
Common variants of the beta and gamma subunits of the epithelial sodium channel and their relation to plasma renin and aldosterone levels in essential hypertension. BMC Med Genet (2005) 1.01
The genetics of normal platelet reactivity. Blood (2010) 0.98
Genetics of arterial hypertension and hypotension. Naunyn Schmiedebergs Arch Pharmacol (2007) 0.97
A new locus on chromosome 12p13.3 for pseudohypoaldosteronism type II, an autosomal dominant form of hypertension. Am J Hum Genet (2000) 0.97
Genetic variants in the alpha2C-adrenoceptor and G-protein contribute to ethnic differences in cardiovascular stress responses. Pharmacogenet Genomics (2008) 0.94
Race, common genetic variation, and therapeutic response disparities in heart failure. JACC Heart Fail (2014) 0.91
Pharmacogenetics of low dose clonidine in irritable bowel syndrome. Neurogastroenterol Motil (2009) 0.91
Mouse model implicates GNB3 duplication in a childhood obesity syndrome. Proc Natl Acad Sci U S A (2013) 0.90
Association of the C825T polymorphism in the GNB3 gene with obesity and metabolic phenotypes in a Taiwanese population. Genes Nutr (2012) 0.90
G-protein beta3 subunit gene splice variant and body fat distribution in Nunavut Inuit. Genome Res (1999) 0.90
Pharmacogenetics of antidepressant response: an update. Hum Genomics (2009) 0.89
Identification and characterization of G beta 3s2, a novel splice variant of the G-protein beta 3 subunit. Biochem J (2003) 0.88
The C825T polymorphism of the G-protein β3 subunit gene and its association with hypertension and stroke: an updated meta-analysis. PLoS One (2013) 0.87
Cognitive Functions across the GNB3 C825T Polymorphism in an Elderly Italian Population. Neurol Res Int (2013) 0.87
Are centenarians genetically predisposed to lower disease risk? Age (Dordr) (2011) 0.87
Genetic polymorphisms related to efficacy and overuse of triptans in chronic migraine. J Headache Pain (2010) 0.86
A new approach to SNP genotyping with fluorescently labeled mononucleotides. Nucleic Acids Res (2004) 0.85
Renal tubular transport and the genetic basis of hypertensive disease. Clin Exp Nephrol (2005) 0.85
Distribution of the GNB3 825C>T polymorphism among Brazilians: impact of population structure. Eur J Clin Pharmacol (2007) 0.84
Polymorphisms in the circadian expressed genes PER3 and ARNTL2 are associated with diurnal preference and GNβ3 with sleep measures. J Sleep Res (2014) 0.83
The genetic basis for altered blood vessel function in disease: large artery stiffening. Vasc Health Risk Manag (2005) 0.83
Biallelic Mutations in GNB3 Cause a Unique Form of Autosomal-Recessive Congenital Stationary Night Blindness. Am J Hum Genet (2016) 0.83
A FRET-based analysis of SNPs without fluorescent probes. Nucleic Acids Res (2004) 0.82
Pharmacogenomics in depression and antidepressants. Dialogues Clin Neurosci (2005) 0.82
Clustering of distinct autoimmune diseases associated with functional abnormalities of T cell survival in children. Clin Exp Immunol (2000) 0.82
Association between 5-HT2A, TPH1 and GNB3 genotypes and response to typical neuroleptics: a serotonergic approach. BMC Psychiatry (2007) 0.81
Is gnb3 c825t polymorphism associated with elite status of polish athletes? Biol Sport (2014) 0.81
The Gβ3 splice variant associated with the C825T gene polymorphism is an unstable and functionally inactive protein. Cell Signal (2012) 0.81
The genetics of essential hypertension. Br J Clin Pharmacol (2001) 0.81
Further evidence supporting a role for gs signal transduction in severe malaria pathogenesis. PLoS One (2010) 0.81
G protein betagamma dimer expression in cardiomyocytes: developmental acquisition of Gbeta3. Biochem Biophys Res Commun (2008) 0.80
Novel quantitative trait locus is mapped to chromosome 12p11 for left ventricular mass in Dominican families: the Family Study of Stroke Risk and Carotid Atherosclerosis. BMC Med Genet (2009) 0.80
A follow-up study for left ventricular mass on chromosome 12p11 identifies potential candidate genes. BMC Med Genet (2011) 0.80
A genetic association study of single nucleotide polymorphisms in GNβ3 and COMT in elderly patients with irritable bowel syndrome. Med Sci Monit (2014) 0.80
Association study of the G-protein beta3 subunit C825T polymorphism with disease progression in patients with bladder cancer. World J Urol (2005) 0.80
Gβ2 and Gβ4 participate in the opioid and adrenergic receptor-mediated Ca2+ channel modulation in rat sympathetic neurons. J Physiol (2012) 0.80
Hypertension genes and retinal vascular calibre: the Cardiovascular Health Study. J Hum Hypertens (2009) 0.80
The association of genetic variations with sensitivity of blood pressure to dietary salt: A narrative literature review. ARYA Atheroscler (2014) 0.79
The C825T Polymorphism of the G-Protein β3 Gene as a Risk Factor for Depression: A Meta-Analysis. PLoS One (2015) 0.79
G-protein beta3 Subunit Gene 825C/T Polymorphism Is Not Associated with Olanzapine-Induced Weight Gain in Korean Schizophrenic Patients. Psychiatry Investig (2009) 0.79
Association between a functional polymorphism in the renin-angiotensin system and completed suicide. J Neural Transm (Vienna) (2006) 0.79
Interactions between the FTO and GNB3 genes contribute to varied clinical phenotypes in hypertension. PLoS One (2013) 0.79
Association of congenital cardiovascular malformations with 33 single nucleotide polymorphisms of selected cardiovascular disease-related genes. Birth Defects Res A Clin Mol Teratol (2010) 0.79
Interaction of gender and body mass index (BMI) reveals evidence of linkage for hypertension in the Framingham Heart Study. BMC Genet (2003) 0.79
Common genetic risk factors for psychiatric and simatic disorders. Dialogues Clin Neurosci (2003) 0.79
The GNB3 C825T polymorphism and depression among subjects with alcohol dependence. J Neural Transm (Vienna) (2006) 0.78
Association of genetic variants in GNβ3 with functional dyspepsia: a meta-analysis. Dig Dis Sci (2014) 0.78
No association of G-protein beta polypeptide 3 polymorphism with irritable bowel syndrome: evidence from a meta-analysis. World J Gastroenterol (2014) 0.78
Comparison of univariate and multivariate linkage analysis of traits related to hypertension. BMC Proc (2009) 0.78
G-protein beta 3 subunit polymorphisms and essential hypertension: a case-control association study in northern Han Chinese. J Geriatr Cardiol (2015) 0.78
The -308G/A of Tumor Necrosis Factor (TNF)-α and 825C/T of Guanidine Nucleotide Binding Protein 3 (GNB3) are associated with the onset of acute myocardial infarction and obesity in Taiwan. Int J Mol Sci (2012) 0.78
The I1-imidazoline agonist moxonidine decreases sympathetic tone under physical and mental stress. Br J Clin Pharmacol (2004) 0.77
Ablation of the GNB3 gene in mice does not affect body weight, metabolism or blood pressure, but causes bradycardia. Cell Signal (2014) 0.77
Gene polymorphisms associated with functional dyspepsia. World J Gastroenterol (2015) 0.77
Association of insulin sensitivity and glucose tolerance with the c.825C>T variant of the G protein beta-3 subunit gene. J Diabetes Complications (2008) 0.77
Alterations in Fibronectin Type III Domain Containing 1 Protein Gene Are Associated with Hypertension. PLoS One (2016) 0.77
C825T G-protein beta3 subunit gene polymorphism, tilt test results and point score in syncopal patients. Clin Auton Res (2008) 0.77
Combination of the C1429T polymorphism in the G-protein beta-3 subunit gene and the A1330V polymorphism in the low-density lipoprotein receptor-related protein 5 gene is a risk factor for hypercholesterolaemia. Clin Exp Med (2007) 0.76
Pharmacogenomics and migraine: possible implications. J Headache Pain (2008) 0.76
G protein β3 subunit polymorphism and long-term prognosis of functional dyspepsia. Gut Liver (2014) 0.76
The role of G protein gene GNB3 C825T polymorphism in HIV-1 acquisition, progression and immune activation. Retrovirology (2012) 0.76
Pharmacogenetic Associations of Antipsychotic Drug-Related Weight Gain: A Systematic Review and Meta-analysis. Schizophr Bull (2016) 0.76
Interaction of G-protein beta3 subunit and nitric oxide synthase gene polymorphisms on carotid artery intima-media thickness in young adults: the Bogalusa Heart Study. Am J Hypertens (2008) 0.76
The C825T Polymorphism of the G-Protein β3 Gene as a Risk Factor for Functional Dyspepsia: A Meta-Analysis. Gastroenterol Res Pract (2015) 0.76
Polymorphisms in the GNB3 and ADD1 genes and blood pressure in a Chinese population. Hum Genet (2010) 0.76
Differences in genotype frequencies of salt-sensitive genes between fishing and nonfishing communities in Japan. Int J Gen Med (2016) 0.75
Association between polymorphisms in genes related to common adult diseases and fetal growth. Clin Med Pediatr (2009) 0.75
GNB3 C825T Polymorphism and Myocardial Recovery in Peripartum Cardiomyopathy: Results of the Multicenter Investigations of Pregnancy-Associated Cardiomyopathy Study. Circ Heart Fail (2016) 0.75
Hypertension-associated C825T polymorphism impairs the function of Gβ3 to target GRK2 ubiquitination. Cell Discov (2016) 0.75
Estimation of the relationship between the polymorphisms of selected genes: ACE, AGTR1, TGFβ1 and GNB3 with the occurrence of primary vesicoureteral reflux. Int Urol Nephrol (2016) 0.75
Association between GNB3 c.825C > T polymorphism and the risk of overweight and obesity: A meta-analysis. Meta Gene (2016) 0.75
Does the GNB3 C825T Polymorphism Influence Swimming Performance in Competitive Swimmers? J Hum Kinet (2015) 0.75
Metabolic and haemodynamic effects of oral glucose loading in young healthy men carrying the 825T-allele of the G protein beta3 subunit. Cardiovasc Diabetol (2003) 0.75
β-blocker therapy and heart rate control during exercise testing in the general population: role of a common G-protein β-3 subunit variant. Pharmacogenomics (2010) 0.75
G proteins propel surprise. Nat Genet (1998) 0.75
Influence of G-protein β-Polypeptide 3 C825T Polymorphism on Antihypertensive Response to Telmisartan and Amlodipine in Chinese Patients. Chin Med J (Engl) (2016) 0.75
Cardiovascular diseases-related GNB3 C825T polymorphism has a significant sex-specific effect on serum soluble E-selectin levels. J Inflamm (Lond) (2016) 0.75
The D153del mutation in GNB3 gene causes tissue specific signalling patterns and an abnormal renal morphology in Rge chickens. PLoS One (2011) 0.75
Prediction of the Risk for Essential Hypertension among Carriers of C825T Genetic Polymorphism of G Protein β3 (GNB3) Gene. Biomark Insights (2016) 0.75
A longitudinal study of the association between the GNB3 C825T polymorphism and metabolic disturbance in bipolar II patients treated with valproate. Pharmacogenomics J (2016) 0.75
Renoprotective effect of the angiotensin-receptor antagonist irbesartan in patients with nephropathy due to type 2 diabetes. N Engl J Med (2001) 17.24
Cloning defined regions of the human genome by microdissection of banded chromosomes and enzymatic amplification. Nature (1989) 7.14
American College of Cardiology Clinical Expert Consensus Document on Standards for Acquisition, Measurement and Reporting of Intravascular Ultrasound Studies (IVUS). A report of the American College of Cardiology Task Force on Clinical Expert Consensus Documents. J Am Coll Cardiol (2001) 6.12
Use of transesophageal echocardiography to guide cardioversion in patients with atrial fibrillation. N Engl J Med (2001) 5.67
Effect of the angiotensin-converting-enzyme inhibitor benazepril on the progression of chronic renal insufficiency. The Angiotensin-Converting-Enzyme Inhibition in Progressive Renal Insufficiency Study Group. N Engl J Med (1996) 5.46
Increased plasma viscosity during an air pollution episode: a link to mortality? Lancet (1997) 5.45
The Heidelberg classification of renal cell tumours. J Pathol (1997) 5.36
Respiratory effects are associated with the number of ultrafine particles. Am J Respir Crit Care Med (1997) 5.35
Tobacco and cancer: recent epidemiological evidence. J Natl Cancer Inst (2004) 4.83
Residential exposure to traffic is associated with coronary atherosclerosis. Circulation (2007) 4.68
Identification of brain-specific and imprinted small nucleolar RNA genes exhibiting an unusual genomic organization. Proc Natl Acad Sci U S A (2000) 4.54
Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene. Nat Genet (1996) 4.36
Particulate air pollution is associated with an acute phase response in men; results from the MONICA-Augsburg Study. Eur Heart J (2001) 4.21
KORA--a research platform for population based health research. Gesundheitswesen (2005) 3.95
Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15. Nat Genet (1995) 3.79
Multicenter case-control study of exposure to environmental tobacco smoke and lung cancer in Europe. J Natl Cancer Inst (1998) 3.74
Safety of transesophageal echocardiography. A multicenter survey of 10,419 examinations. Circulation (1991) 3.70
Prognostic implications of monosomy 3 in uveal melanoma. Lancet (1996) 3.26
A gene for the mouse pink-eyed dilution locus and for human type II oculocutaneous albinism. Nature (1993) 3.24
The nephrotic syndrome. N Engl J Med (1998) 3.22
Botulinum C2 toxin ADP-ribosylates actin. Nature (1986) 3.16
Job strain in relation to body mass index: pooled analysis of 160 000 adults from 13 cohort studies. J Intern Med (2011) 3.14
The IC-SNURF-SNRPN transcript serves as a host for multiple small nucleolar RNA species and as an antisense RNA for UBE3A. Hum Mol Genet (2001) 3.07
Protein kinase C phosphorylates the inhibitory guanine-nucleotide-binding regulatory component and apparently suppresses its function in hormonal inhibition of adenylate cyclase. Eur J Biochem (1985) 3.04
Imprinting in Prader-Willi and Angelman syndromes. Trends Genet (1998) 2.85
Air pollution and daily mortality in Erfurt, east Germany, 1980-1989. Environ Health Perspect (1993) 2.84
Ultraviolet B and blood pressure. Lancet (1998) 2.83
Epigenetic changes may contribute to the formation and spontaneous regression of retinoblastoma. Hum Genet (1989) 2.80
New signs characteristic of myocardial bridging demonstrated by intracoronary ultrasound and Doppler. Eur Heart J (1999) 2.67
Effects of air pollution on blood pressure: a population-based approach. Am J Public Health (2001) 2.64
Early clinical experience with the 6 French Angio-Seal device: immediate closure of femoral puncture sites after diagnostic and interventional coronary procedures. Catheter Cardiovasc Interv (2001) 2.62
Traffic-related air pollution and respiratory health during the first 2 yrs of life. Eur Respir J (2002) 2.50
Nonsurgical retrieval of embolized coronary stents. Catheter Cardiovasc Interv (2000) 2.48
A new phospholipase-C-calcium signalling pathway mediated by cyclic AMP and a Rap GTPase. Nat Cell Biol (2001) 2.45
Polarization-sensitive optical coherence tomography of dental structures. Caries Res (2000) 2.43
Age of entry to day nursery and allergy in later childhood. Lancet (1999) 2.42
Serum cystatin C concentration as a marker of renal dysfunction in the elderly. Am J Kidney Dis (2001) 2.42
Molecular diagnosis of the Prader-Willi and Angelman syndromes by detection of parent-of-origin specific DNA methylation in 15q11-13. Hum Genet (1992) 2.41
Hantavirus infection presenting as acute renal failure. Lancet (1990) 2.40
Morphology of coronary atherosclerotic lesions in patients with end-stage renal failure. Nephrol Dial Transplant (2000) 2.38
Tei-index in patients with mild-to-moderate congestive heart failure. Eur Heart J (2000) 2.37
Molecular dissection of the Prader-Willi/Angelman syndrome region (15q11-13) by YAC cloning and FISH analysis. Hum Mol Genet (1992) 2.35
De novo deletions of SNRPN exon 1 in early human and mouse embryos result in a paternal to maternal imprint switch. Nat Genet (2000) 2.30
Physiology and pathophysiology of the adipose tissue renin-angiotensin system. Hypertension (2000) 2.30
Cloning of the putative tumour suppressor gene for hereditary multiple exostoses (EXT1). Nat Genet (1995) 2.29
A nucleotide substitution in the promoter of human angiotensinogen is associated with essential hypertension and affects basal transcription in vitro. J Clin Invest (1997) 2.23
Mutations in a new gene, encoding a zinc-finger protein, cause tricho-rhino-phalangeal syndrome type I. Nat Genet (2000) 2.23
Prevalence and clinical significance of accidental findings in electron-beam tomographic scans for coronary artery calcification. Eur Heart J (2001) 2.15
Contemporary percutaneous treatment of unprotected left main coronary stenoses: initial results from a multicenter registry analysis 1994-1996. Circulation (1997) 2.15
Increases in heart rate during an air pollution episode. Am J Epidemiol (1999) 2.13
Informatics and medicine--from molecules to populations. Methods Inf Med (2008) 2.13
Diagnosis of heart tumours by transoesophageal echocardiography: a multicentre study in 154 patients. European Cooperative Study Group. Eur Heart J (1993) 2.10
Analysis of interinstitutional observer agreement in interpretation of dobutamine stress echocardiograms. J Am Coll Cardiol (1996) 2.09
[The radial artery as an approach to diagnostic coronary angiography]. Z Kardiol (1997) 2.07
Comparison of intravascular ultrasound and angiography in the assessment of myocardial bridging. Circulation (1994) 2.06
The rising tide of endstage renal failure from diabetic nephropathy type II--an epidemiological analysis. Nephrol Dial Transplant (1995) 2.06
The ancestral gene for transcribed, low-copy repeats in the Prader-Willi/Angelman region encodes a large protein implicated in protein trafficking, which is deficient in mice with neuromuscular and spermiogenic abnormalities. Hum Mol Genet (1999) 2.02
A genome-wide search for linkage to asthma. German Asthma Genetics Group. Genomics (1999) 2.00
A gene for hereditary multiple exostoses maps to chromosome 19p. Hum Mol Genet (1994) 2.00
[Intima-media thickness is a suitable surrogate marker for systemic atherosclerosis - pro]. Dtsch Med Wochenschr (2009) 1.99
Identification and regulation of 1,25-dihydroxyvitamin D3 receptor activity and biosynthesis of 1,25-dihydroxyvitamin D3. Studies in cultured bovine aortic endothelial cells and human dermal capillaries. J Clin Invest (1989) 1.98
A prognostic computer model to individually predict post-procedural complications in interventional cardiology: the INTERVENT Project. Eur Heart J (1999) 1.98
Maternal methylation imprints on human chromosome 15 are established during or after fertilization. Nat Genet (2001) 1.97
Characterization of the 7S RNA and its gene from halobacteria. Nucleic Acids Res (1985) 1.97
Stepwise intravascular ultrasound (IVUS) guidance of high-pressure coronary stenting does not result in an improved acute or long-term outcome: a randomized comparison to "final-look" IVUS assessment. Catheter Cardiovasc Interv (1999) 1.93
Imprinting-mutation mechanisms in Prader-Willi syndrome. Am J Hum Genet (1999) 1.93
A single-tube PCR test for the diagnosis of Angelman and Prader-Willi syndrome based on allelic methylation differences at the SNRPN locus. Eur J Hum Genet (1997) 1.90
Refinements in stress echocardiographic techniques improve inter-institutional agreement in interpretation of dobutamine stress echocardiograms. Eur Heart J (2002) 1.87
Sporadic imprinting defects in Prader-Willi syndrome and Angelman syndrome: implications for imprint-switch models, genetic counseling, and prenatal diagnosis. Am J Hum Genet (1998) 1.87
Relationship between HbA1c levels and risk of cardiovascular adverse outcomes and all-cause mortality in overweight and obese cardiovascular high-risk women and men with type 2 diabetes. Diabetologia (2012) 1.85
Gender-specific association of adiponectin as a predictor of progression of chronic kidney disease: the Mild to Moderate Kidney Disease Study. Kidney Int (2007) 1.83
Randomized comparison of rescue angioplasty with conservative management of patients with early failure of thrombolysis for acute anterior myocardial infarction. Circulation (1994) 1.82
Short-term effects of particulate air pollution on respiratory morbidity in asthmatic children. Eur Respir J (1997) 1.80
Genotypic and phenotypic spectrum in tricho-rhino-phalangeal syndrome types I and III. Am J Hum Genet (2000) 1.80
Imprinting mutations suggested by abnormal DNA methylation patterns in familial Angelman and Prader-Willi syndromes. Am J Hum Genet (1994) 1.79
Totally endoscopic coronary artery bypass grafting on cardiopulmonary bypass with robotically enhanced telemanipulation: report of forty-five cases. J Thorac Cardiovasc Surg (2002) 1.78
Insulin resistance and hyperinsulinemia are already present in patients with incipient renal disease. Kidney Int (1998) 1.77
Worldwide ethnic distribution of the G protein beta3 subunit 825T allele and its association with obesity in Caucasian, Chinese, and Black African individuals. J Am Soc Nephrol (1999) 1.76
Minimal definition of the imprinting center and fixation of chromosome 15q11-q13 epigenotype by imprinting mutations. Proc Natl Acad Sci U S A (1996) 1.76
Air pollution and acute respiratory illness in five German communities. Environ Res (1991) 1.74
A previously unrecognised phenotype characterised by obesity, muscular hypotonia, and ability to speak in patients with Angelman syndrome caused by an imprinting defect. Eur J Hum Genet (1999) 1.74
Baseline recruitment and analyses of nonresponse of the Heinz Nixdorf Recall Study: identifiability of phone numbers as the major determinant of response. Eur J Epidemiol (2005) 1.73
Safety of ultrasound-guided percutaneous renal biopsy-retrospective analysis of 1090 consecutive cases. Nephrol Dial Transplant (1998) 1.71
Failure of familial Alzheimer's disease to segregate with the A4-amyloid gene in several European families. Nature (1987) 1.68
Bariatric surgery: a systematic review and network meta-analysis of randomized trials. Obes Rev (2011) 1.68
Effects on oral soft tissue produced by a diode laser in vitro. Lasers Surg Med (1999) 1.64
A common DNA polymorphism of the low-density lipoprotein (LDL) receptor gene and its use in diagnosis. Lancet (1985) 1.64
Modulation of vascular function by perivascular adipose tissue: the role of endothelium and hydrogen peroxide. Br J Pharmacol (2007) 1.63
A study of DNA polymorphisms around the human apolipoprotein AI gene in hyperlipidaemic and normal individuals. Clin Genet (1985) 1.62
A prognostic computer model to predict individual outcome in interventional cardiology. The INTERVENT Project. Eur Heart J (1997) 1.61
Disturbed calcium metabolism in subjects with elevated diastolic blood pressure. Clin Investig (1992) 1.61
Effect of 1,25 (OH)2 vitamin D3 on glomerulosclerosis in subtotally nephrectomized rats. Kidney Int (1998) 1.61
Characterization of deletions at the retinoblastoma locus in patients with bilateral retinoblastoma. Am J Med Genet (1991) 1.59
Evidence for impaired hepatic vitamin K1 metabolism in patients treated with N-methyl-thiotetrazole cephalosporins. Thromb Haemost (1984) 1.59
Molecular basis of human salt sensitivity: the role of the 11beta-hydroxysteroid dehydrogenase type 2. J Clin Endocrinol Metab (1999) 1.59
Impact of restenosis 10 years after coronary angioplasty. Eur Heart J (1998) 1.59