Fetal cardiac troponin isoforms rescue the increased Ca2+ sensitivity produced by a novel double deletion in cardiac troponin T linked to restrictive cardiomyopathy: a clinical, genetic, and functional approach (Q35063399)

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English	Fetal cardiac troponin isoforms rescue the increased Ca2+ sensitivity produced by a novel double deletion in cardiac troponin T linked to restrictive cardiomyopathy: a clinical, genetic, and functional approach	scientific article

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29 January 2020

Fetal cardiac troponin isoforms rescue the increased Ca2+ sensitivity produced by a novel double deletion in cardiac troponin T linked to restrictive cardiomyopathy: a clinical, genetic, and functional approach (English)

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29 January 2020

restrictive cardiomyopathy

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José Renato Pinto

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29 January 2020

Nicolas Tremblay

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29 January 2020

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Mario Talajic

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29 January 2020

Michelle S Parvatiyar

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Michelle S Parvatiyar

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29 January 2020

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Shi Wei Yang

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29 January 2020

Marc-Phillip Hitz

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29 January 2020

Michelle A Jones

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29 January 2020

Jingsheng Liang

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29 January 2020

Victor Kokta

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29 January 2020

Michelle Jaeggi

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29 January 2020

Gregor Andelfinger

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29 January 2020

James D Potter

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29 January 2020

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18 April 2011

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29 January 2020

Journal of Biological Chemistry

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29 January 2020

286

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29 January 2020

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29 January 2020

20901-20912

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29 January 2020

Neonatal gene transfer of Serca2a delays onset of hypertrophic remodeling and improves function in familial hypertrophic cardiomyopathy

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8 July 2018

Cardiac troponin mutations and restrictive cardiomyopathy

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8 July 2018

Correcting diastolic dysfunction by Ca2+ desensitizing troponin in a transgenic mouse model of restrictive cardiomyopathy

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8 July 2018

Malignant and benign mutations in familial cardiomyopathies: insights into mutations linked to complex cardiovascular phenotypes.

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8 July 2018

Ca2+ cycling and new therapeutic approaches for heart failure

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8 July 2018

Clinical and functional characterization of TNNT2 mutations identified in patients with dilated cardiomyopathy

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8 July 2018

Mutations in Troponin that cause HCM, DCM AND RCM: what can we learn about thin filament function?

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8 July 2018

Functional effects of a restrictive-cardiomyopathy-linked cardiac troponin I mutation (R145W) in transgenic mice

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8 July 2018

A functional and structural study of troponin C mutations related to hypertrophic cardiomyopathy.

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8 July 2018

Myofilament Ca2+ sensitization causes susceptibility to cardiac arrhythmia in mice.

1 reference

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8 July 2018

Cardiac troponin T mutation in familial cardiomyopathy with variable remodeling and restrictive physiology

1 reference

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8 July 2018

The role of cardiac troponin T quantity and function in cardiac development and dilated cardiomyopathy.

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8 July 2018

Structural basis for tropomyosin overlap in thin (actin) filaments and the generation of a molecular swivel by troponin-T

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8 July 2018

Myofilament degradation and dysfunction of human cardiomyocytes in Fabry disease.

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8 July 2018

Idiopathic restrictive cardiomyopathy in children is caused by mutations in cardiac sarcomere protein genes

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8 July 2018

Allele and species dependent contractile defects by restrictive and hypertrophic cardiomyopathy-linked troponin I mutants

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8 July 2018

Calcium and cardiomyopathies.

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8 July 2018

Troponin and cardiomyopathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3121488

8 July 2018

Pediatric restrictive cardiomyopathy associated with a mutation in beta-myosin heavy chain.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3121488

8 July 2018

Sarcomeric proteins and inherited cardiomyopathies.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3121488

8 July 2018

A troponin T mutation that causes infantile restrictive cardiomyopathy increases Ca2+ sensitivity of force development and impairs the inhibitory properties of troponin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3121488

8 July 2018

Genetic basis of hypertrophic cardiomyopathy: from bench to the clinics

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3121488

8 July 2018

Thin filament disinhibition by restrictive cardiomyopathy mutant R193H troponin I induces Ca2+-independent mechanical tone and acute myocyte remodeling

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3121488

8 July 2018

Infantile restrictive cardiomyopathy resulting from a mutation in the cardiac troponin T gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3121488

8 July 2018

Pediatric brain natriuretic peptide and N-terminal pro-brain natriuretic peptide reference intervals

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8 July 2018

Expression of slow skeletal troponin I in adult mouse heart helps to maintain the left ventricular systolic function during respiratory hypercapnia

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3121488

8 July 2018

Mutations in human cardiac troponin I that are associated with restrictive cardiomyopathy affect basal ATPase activity and the calcium sensitivity of force development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3121488

8 July 2018

Structure of the core domain of human cardiac troponin in the Ca(2+)-saturated form

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3121488

8 July 2018

Idiopathic restrictive cardiomyopathy is part of the clinical expression of cardiac troponin I mutations

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3121488

8 July 2018

Cardiac troponin T isoforms affect the Ca2+ sensitivity and inhibition of force development. Insights into the role of troponin T isoforms in the heart

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3121488

8 July 2018

Cardiac troponin T is essential in sarcomere assembly and cardiac contractility

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3121488

8 July 2018

Disease-causing mutations in cardiac troponin T: identification of a critical tropomyosin-binding region

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3121488

8 July 2018

Clinical utility of Doppler echocardiography and tissue Doppler imaging in the estimation of left ventricular filling pressures: A comparative simultaneous Doppler-catheterization study

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3121488

8 July 2018

Regulation of contraction in striated muscle

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8 July 2018

Troponin I: inhibitor or facilitator

2 references

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8 July 2018

https://api.crossref.org/works/10.1074%2FJBC.M111.234336

21 January 2018

Cardiac troponin I gene knockout: a mouse model of myocardial troponin I deficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3121488

8 July 2018

Troponin I gene expression during human cardiac development and in end-stage heart failure

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3121488

8 July 2018

Molecular basis of human cardiac troponin T isoforms expressed in the developing, adult, and failing heart.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3121488

8 July 2018

Effects of acidosis on ventricular muscle from adult and neonatal rats

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3121488

8 July 2018

Troponin T isoform expression in humans. A comparison among normal and failing adult heart, fetal heart, and adult and fetal skeletal muscle

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3121488

8 July 2018

Outcomes of children with restrictive cardiomyopathy listed for heart transplant: a multi-institutional study.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3121488

27 September 2018

Targeted disruption of the cardiac troponin T gene causes sarcomere disassembly and defects in heartbeat within the early mouse embryo.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3121488

27 September 2018

Deletion in TNNI3 gene is associated with restrictive cardiomyopathy.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3121488

27 September 2018

Expanding the range of free calcium regulation in biological solutions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3121488

27 September 2018

Drastic Ca2+ sensitization of myofilament associated with a small structural change in troponin I in inherited restrictive cardiomyopathy.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3121488

27 September 2018

F110I and R278C troponin T mutations that cause familial hypertrophic cardiomyopathy affect muscle contraction in transgenic mice and reconstituted human cardiac fibers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3121488

27 September 2018

Protection against endotoxemia-induced contractile dysfunction in mice with cardiac-specific expression of slow skeletal troponin I.

1 reference

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27 September 2018

Impact of cardiac growth on Doppler tissue imaging velocities: a study in healthy children.

1 reference

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27 September 2018

Sarcomere thin filament regulatory isoforms. Evidence of a dominant effect of slow skeletal troponin I on cardiac contraction.

1 reference

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27 September 2018

Outcome of idiopathic restrictive cardiomyopathy in children.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3121488

27 September 2018

Clinical profile and outcome of idiopathic restrictive cardiomyopathy

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3121488

27 September 2018

Molecular cloning of human cardiac troponin T isoforms: expression in developing and failing heart.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3121488

27 September 2018

A de novo mutation of the beta cardiac myosin heavy chain gene in an infantile restrictive cardiomyopathy

1 reference

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Outcomes of children with cardiomyopathy listed for transplant: a multi-institutional study

1 reference

https://pubmed.ncbi.nlm.nih.gov/21502316

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Altered regulation of cardiac muscle contraction by troponin T mutations that cause familial hypertrophic cardiomyopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/21502316

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical spectrum of restrictive cardiomyopathy in children

1 reference

https://pubmed.ncbi.nlm.nih.gov/21502316

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hypertrophic cardiomyopathy: histopathological features of sudden death in cardiac troponin T disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/21502316

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A direct regulatory role for troponin T and a dual role for troponin C in the Ca2+ regulation of muscle contraction

1 reference

https://pubmed.ncbi.nlm.nih.gov/21502316

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Increased Ca2+ affinity of cardiac thin filaments reconstituted with cardiomyopathy-related mutant cardiac troponin I

1 reference

https://pubmed.ncbi.nlm.nih.gov/21502316

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A point mutation (R192H) in the C-terminus of human cardiac troponin I causes diastolic dysfunction in transgenic mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/21502316

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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10.1074/JBC.M111.234336

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21502316%20AND%20SRC:MED&resulttype=core&format=json

29 January 2020

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Europe PubMed Central

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29 January 2020

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21502316%20AND%20SRC:MED&resulttype=core&format=json

29 January 2020

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