TNNT1 gene

Known as: ANM, MGC104241, STNT 
 

Topic mentions per year

Topic mentions per year

1992-2016
0246819922016

Papers overview

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2016
2016
INTRODUCTION Nemaline myopathy is a rare disorder characterized by skeletal muscle weakness of varying severity and onset, with… (More)
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2016
2016
Troponin T (TnT) is the tropomyosin (Tm)-binding and thin filament-anchoring subunit of troponin and plays a central role in… (More)
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2015
2015
INTRODUCTION Nemaline myopathy (NM) is a congenital neuromuscular disorder often characterized by hypotonia, facial weakness… (More)
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2014
2014
Slow skeletal muscle troponin T (TNNT1) pre-messenger RNA alternative splicing (AS) provides transcript diversity and increases… (More)
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2014
2014
Chromosome 1p36 deletion syndrome is one of the most common terminal deletions observed in humans and is related to congenital… (More)
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2013
2013
In recent years, epigenetic markers emerged as a new tool to understand the influence of lifestyle factors on obesity phenotypes… (More)
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2012
2012
AIM This study aims to assess whether epigenetic changes may account for high-density lipoprotein cholesterol (HDL-C) level… (More)
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2008
2008
Myostatin (GDF-8) is a key protein responsible for skeletal muscle growth and development, thus mutations in themstn gene can… (More)
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Highly Cited
2000
Highly Cited
2000
The nemaline myopathies are characterized by weakness and eosinophilic, rodlike (nemaline) inclusions in muscle fibers. Amish… (More)
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2000
2000
The nonpathogenic human virus adeno-associated virus type 2 (AAV) has evolved the potentially unique strategy to establish… (More)
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