Pages that link to "Q5930325"
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The following pages link to Hugh Christian Watkins (Q5930325):
Displayed 50 items.
- Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations (Q21092458) (← links)
- Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution (Q21092459) (← links)
- Genome-wide mapping of susceptibility to coronary artery disease identifies a novel replicated locus on chromosome 17 (Q21145265) (← links)
- Relationship between CAD risk genotype in the chromosome 9p21 locus and gene expression. Identification of eight new ANRIL splice variants (Q21562338) (← links)
- Altered regulatory properties of human cardiac troponin I mutants that cause hypertrophic cardiomyopathy (Q22254076) (← links)
- Investigation of a truncated cardiac troponin T that causes familial hypertrophic cardiomyopathy: Ca(2+) regulatory properties of reconstituted thin filaments depend on the ratio of mutant to wild-type protein (Q22254242) (← links)
- Genetic studies of body mass index yield new insights for obesity biology (Q22305005) (← links)
- Personalized medicine: hope or hype? (Q24289193) (← links)
- Mutations in the gamma(2) subunit of AMP-activated protein kinase cause familial hypertrophic cardiomyopathy: evidence for the central role of energy compromise in disease pathogenesis (Q24291256) (← links)
- Novel associations of CPS1, MUT, NOX4, and DPEP1 with plasma homocysteine in a healthy population: a genome-wide evaluation of 13 974 participants in the Women's Genome Health Study (Q24293230) (← links)
- Cardiac myosin binding protein C: its role in physiology and disease (Q24294438) (← links)
- Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy (Q24304076) (← links)
- Dilated cardiomyopathy mutations in three thin filament regulatory proteins result in a common functional phenotype (Q24304085) (← links)
- Alterations in thin filament regulation induced by a human cardiac troponin T mutant that causes dilated cardiomyopathy are distinct from those induced by troponin T mutants that cause hypertrophic cardiomyopathy (Q24304998) (← links)
- Support for a trimeric collar of myosin binding protein C in cardiac and fast skeletal muscle, but not in slow skeletal muscle (Q24306769) (← links)
- Severe disease expression of cardiac troponin C and T mutations in patients with idiopathic dilated cardiomyopathy (Q24314590) (← links)
- Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere (Q24316399) (← links)
- Mutations in fast skeletal troponin I, troponin T, and beta-tropomyosin that cause distal arthrogryposis all increase contractile function (Q24338449) (← links)
- Genome-wide association analyses identify 18 new loci associated with serum urate concentrations (Q24620065) (← links)
- Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk (Q24630394) (← links)
- Blood pressure loci identified with a gene-centric array (Q24630508) (← links)
- Hundreds of variants clustered in genomic loci and biological pathways affect human height (Q24630979) (← links)
- Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes (Q24635872) (← links)
- Genetic Loci associated with C-reactive protein levels and risk of coronary heart disease (Q24649709) (← links)
- Localization of the binding site of the C-terminal domain of cardiac myosin-binding protein-C on the myosin rod (Q24671901) (← links)
- Familial Hypertrophic cardiomyopathy with Wolff-Parkinson-White syndrome maps to a locus on chromosome 7q3 (Q24679142) (← links)
- Analysis of protein-coding genetic variation in 60,706 humans (Q26831376) (← links)
- Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants (Q27008212) (← links)
- (Q28050006) (redirect page) (← links)
- Human stromelysin gene promoter activity is modulated by transcription factor ZBP-89 (Q28198820) (← links)
- Mutations in the genes for cardiac troponin T and alpha-tropomyosin in hypertrophic cardiomyopathy (Q28236892) (← links)
- Evidence from human myectomy samples that MYBPC3 mutations cause hypertrophic cardiomyopathy through haploinsufficiency (Q28250719) (← links)
- A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease (Q28267020) (← links)
- Mutations in the gene for cardiac myosin-binding protein C and late-onset familial hypertrophic cardiomyopathy (Q28268916) (← links)
- New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk (Q28270700) (← links)
- The molecular phenotype of human cardiac myosin associated with hypertrophic obstructive cardiomyopathy (Q28276519) (← links)
- Triglyceride-mediated pathways and coronary disease: collaborative analysis of 101 studies (Q28281855) (← links)
- A mutation in the alpha tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy NEM1 (Q28296701) (← links)
- A mutation in the alpha tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy (Q28299243) (← links)
- Sudden death due to troponin T mutations (Q28305351) (← links)
- Assignment of a locus for dominantly inherited venous malformations to chromosome 9p (Q28306091) (← links)
- A mutation in the mitochondrial fission gene Dnm1l leads to cardiomyopathy (Q28509163) (← links)
- Nprl3 is required for normal development of the cardiovascular system (Q28588831) (← links)
- Rare and low-frequency variants and their association with plasma levels of fibrinogen, FVII, FVIII, and vWF (Q28607764) (← links)
- Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility (Q28651068) (← links)
- Association between alcohol and cardiovascular disease: Mendelian randomisation analysis based on individual participant data (Q28655857) (← links)
- Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP Consortia (Q28656014) (← links)
- Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease (Q28661433) (← links)
- Functional significance of SRJ domain mutations in CITED2 (Q28716971) (← links)
- Homocysteine and coronary heart disease: meta-analysis of MTHFR case-control studies, avoiding publication bias (Q28731901) (← links)