(Q33559617)

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Cardiac signaling genes exhibit unexpected sequence diversity in sporadic cardiomyopathy, revealing HSPB7 polymorphisms associated with disease

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scholarly article

1 reference

Europe PubMed Central

28 July 2017

Cardiac signaling genes exhibit unexpected sequence diversity in sporadic cardiomyopathy, revealing HSPB7 polymorphisms associated with disease (English)

1 reference

Europe PubMed Central

28 July 2017

1 reference

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inferred from title

Scot J Matkovich

object named as

Scot J Matkovich

1

0 references

object named as

Todd E Druley

5

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Muredach P. Reilly

object named as

Muredach P Reilly

8

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7

object named as

Robi D Mitra

1 reference

Europe PubMed Central

28 July 2017

author name string

Derek J Van Booven

2

1 reference

Europe PubMed Central

28 July 2017

Anna Hindes

3

1 reference

Europe PubMed Central

28 July 2017

Min Young Kang

4

1 reference

Europe PubMed Central

28 July 2017

Francesco L M Vallania

6

1 reference

Europe PubMed Central

28 July 2017

Thomas P Cappola

9

1 reference

Europe PubMed Central

28 July 2017

Gerald W Dorn

10

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Europe PubMed Central

28 July 2017

language of work or name

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publication date

14 December 2009

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Europe PubMed Central

28 July 2017

Journal of Clinical Investigation

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Europe PubMed Central

28 July 2017

120

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Europe PubMed Central

28 July 2017

1

1 reference

Europe PubMed Central

28 July 2017

280-289

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Europe PubMed Central

28 July 2017

Clinical and genetic modifiers of long-term survival in heart failure

1 reference

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Quantification of rare allelic variants from pooled genomic DNA

1 reference

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Next-generation sequencing: from basic research to diagnostics

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The UCSC Genome Browser Database: update 2009

1 reference

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Genetic mapping in human disease

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Accurate whole human genome sequencing using reversible terminator chemistry

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Autoimmune diseases: insights from genome-wide association studies

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Human mutation in the anti-apoptotic heat shock protein 20 abrogates its cardioprotective effects

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The cardiac sarcoplasmic/endoplasmic reticulum calcium ATPase: a potent target for cardiovascular diseases

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A GRK5 polymorphism that inhibits beta-adrenergic receptor signaling is protective in heart failure

1 reference

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Translating insights from the cancer genome into clinical practice

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Adrenergic gene polymorphisms and cardiovascular risk in the NHLBI-sponsored Women's Ischemia Syndrome Evaluation

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Beta-1 and beta-2 adrenoceptor polymorphisms: functional importance, impact on cardiovascular diseases and drug responses

1 reference

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Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

1 reference

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A common allele on chromosome 9 associated with coronary heart disease

1 reference

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21 June 2018

Transcriptional genomics associates FOX transcription factors with human heart failure

1 reference

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Alpha1-adrenergic receptors prevent a maladaptive cardiac response to pressure overload

1 reference

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21 June 2018

A mutation in the human phospholamban gene, deleting arginine 14, results in lethal, hereditary cardiomyopathy.

1 reference

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Admixture mapping for hypertension loci with genome-scan markers

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Pathways of chaperone-mediated protein folding in the cytosol

1 reference

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Advanced sequencing technologies: methods and goals

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A simple correction for multiple testing for single-nucleotide polymorphisms in linkage disequilibrium with each other

1 reference

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The natural history, epidemiology, and prognosis of heart failure in African Americans

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The inherited basis of diabetes mellitus: implications for the genetic analysis of complex traits

1 reference

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21 June 2018

Efficiency of single-nucleotide polymorphism haplotype estimation from pooled DNA.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2798680

21 June 2018

Human phospholamban null results in lethal dilated cardiomyopathy revealing a critical difference between mouse and human

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2798680

21 June 2018

Dilated cardiomyopathy and heart failure caused by a mutation in phospholamban

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2798680

21 June 2018

Human non-synonymous SNPs: server and survey

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2798680

21 June 2018

Accounting for human polymorphisms predicted to affect protein function

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2798680

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Positive and negative selection on the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2798680

21 June 2018

Phospholamban and cardiac contractile function

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2798680

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Identification and characterization of cvHsp. A novel human small stress protein selectively expressed in cardiovascular and insulin-sensitive tissues

1 reference

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The Ile164 beta2-adrenergic receptor polymorphism adversely affects the outcome of congestive heart failure

1 reference

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Genetics of essential hypertension

1 reference

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A multiple testing correction method for genetic association studies using correlated single nucleotide polymorphisms

1 reference

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Association of alpha1A adrenergic receptor gene variants on chromosome 8p21 with human stage 2 hypertension.

1 reference

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Alpha- and beta-adrenergic receptor polymorphisms in hypertensive and normotensive offspring.

1 reference

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Race, quality of care, and outcomes of elderly patients hospitalized with heart failure.

1 reference

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Low sequence variation in the gene encoding the human beta-myosin heavy chain.

1 reference

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Simple method to analyze SNP-based association studies using DNA pools

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Beta2-adrenergic receptor genotype and survival among patients receiving beta-blocker therapy after an acute coronary syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/20038796

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phospholamban R14 deletion results in late-onset, mild, hereditary dilated cardiomyopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/20038796

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular genetics of atrial fibrillation

1 reference

https://pubmed.ncbi.nlm.nih.gov/20038796

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polymorphisms of beta-adrenergic receptors in heart failure

1 reference

https://pubmed.ncbi.nlm.nih.gov/20038796

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1172/JCI39085

1 reference

Europe PubMed Central

28 July 2017

1 reference

Europe PubMed Central

28 July 2017

1 reference

Europe PubMed Central

28 July 2017

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