Megalobrama amblycephala cardiac troponin T variants: molecular cloning, expression and response to nitrite.

No abstract is available for this paper.

• Publication year

  2013

• Venue

  Gene

• Publication date

  2013-09-25

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1016/j.gene.2013.05.089PMID 23816406
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Prolonged intravenous infusion of sodium nitrite delivers nitric oxide (NO) in humans.

  2013cited by this paper
• Sequence analysis and expression differentiation of chemokine receptor CXCR4b among three populations of Megalobrama amblycephala.

  2013cited by this paper
• The N-terminal extension of cardiac troponin T stabilizes the blocked state of cardiac thin filament.

  2012cited by this paper
• [Variation and clinical significance of serum CTnT and CK-MB in patients with acute organophosphorus pesticid poisoning].

  2011cited by this paper
• Myofibrillogenesis in the developing zebrafish heart: A functional study of tnnt2.

  2009cited by this paper
• Cloning of TNNT2,a Key Gene during Heart Function and Its Expression in Rat

  2008cited by this paper
• Molecular and immunohistochemical analyses of cardiac troponin T during cardiac development in the Mexican axolotl, Ambystoma mexicanum

  2007cited by this paper
• Role of myofibril-inducing RNA in cardiac TnT expression in developing Mexican axolotl.

  2007cited by this paper
• Cytoprotective effects of nitrite during in vivo ischemia-reperfusion of the heart and liver.

  2005cited by this paper
• Familial Hypertrophic Cardiomyopathy Mutations from Different Functional Regions of Troponin T Result in Different Effects on the pH and Ca2+ Sensitivity of Cardiac Muscle Contraction*

  2004cited by this paper
• Molecular structure and developmental expression of three muscle‐type troponin T genes in zebrafish

  2003influential reference
• Cardiac troponin T mutation R141W found in dilated cardiomyopathy stabilizes the troponin T-tropomyosin interaction and causes a Ca2+ desensitization.

  2003cited by this paper
• Autopsy findings in siblings with hypertrophic cardiomyopathy caused by Arg92Trp mutation in the cardiac troponin T gene showing dilated cardiomyopathy‐like features

  2003cited by this paper
• A novel mutation Lys273Glu in the cardiac troponin T gene shows high degree of penetrance and transition from hypertrophic to dilated cardiomyopathy.

  2002cited by this paper
• Cardiac troponin T is essential in sarcomere assembly and cardiac contractility

  2002cited by this paper
• Ca2+-desensitizing effect of a deletion mutation ΔK210 in cardiac troponin T that causes familial dilated cardiomyopathy

  2002cited by this paper
• Comparative studies on the expression patterns of three troponin T genes during mouse development

  2001cited by this paper
• Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy.

  2001cited by this paper
• Novel Cardiac Troponin T Mutation as a Cause of Familial Dilated Cardiomyopathy

  2001cited by this paper
• Genes encoding troponin I and troponin T are organized as three paralogous pairs in the mouse genome

  2000cited by this paper
• Alternative splicing, muscle calcium sensitivity, and the modulation of dragonfly flight performance.

  1999cited by this paper
• Structure and Evolution of the Alternatively Spliced Fast Troponin T Isoform Gene*

  1999cited by this paper
• Functional consequences of a carboxyl terminal missense mutation Arg278Cys in human cardiac troponin T.

  1999cited by this paper
• National Academy of Clinical Biochemistry Standards of Laboratory Practice: recommendations for the use of cardiac markers in coronary artery diseases.

  1999cited by this paper
• Troponin T: genetics, properties and function

  1998influential reference
• Genomic organisation, alternative splicing and polymorphisms of the human cardiac troponin T gene.

  1998cited by this paper
• Primary structure and developmental acidic to basic transition of 13 alternatively spliced mouse fast skeletal muscle troponin T isoforms.

  1997cited by this paper
• Expression of cDNAs encoding mouse cardiac troponin T isoforms: characterization of a large sample of independent clones.

  1996influential reference
• Molecular diversity of myofibrillar proteins: gene regulation and functional significance.

  1996cited by this paper
• Molecular basis of human cardiac troponin T isoforms expressed in the developing, adult, and failing heart.

  1995cited by this paper
• Molecular cloning of human cardiac troponin T isoforms: expression in developing and failing heart.

  1995cited by this paper
• Structure and regulation of the mouse cardiac troponin I gene.

  1994cited by this paper
• Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere.

  1994cited by this paper
• Variation in morphology and biochemical genetic markers among populations of blunt snout bream (Megalobrama amblycephala)

  1993cited by this paper
• Molecular cloning and developmental expression of human cardiac troponin T

  1993cited by this paper
• Drosophila melanogaster troponin-T mutations engender three distinct syndromes of myofibrillar abnormalities.

  1990cited by this paper
• Structure-function relationships in cardiac troponin T.

  1989cited by this paper
• Complete nucleotide sequence of the fast skeletal troponin T gene. Alternatively spliced exons exhibit unusual interspecies divergence.

  1986cited by this paper
• A single cardiac troponin T gene generates embryonic and adult isoforms via developmentally regulated alternate splicing.

  1985influential reference

• Genome-Wide Population Structure and Selection Signatures of Yunling Goat Based on RAD-seq

  2022cites this paper
• Isolation and characterization of three skeletal troponin genes and association with growth-related traits in Exopalaemon carinicauda

  2018cites this paper