IGHD1-14 gene

Known as: DM2, IGHD1-14, immunoglobulin heavy diversity 1-14 (non-functional) 
 
National Institutes of Health

Papers overview

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Highly Cited
2011
Highly Cited
2011
Myotonic dystrophy is the most common muscular dystrophy in adults and the first recognized example of an RNA-mediated disease… (More)
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Highly Cited
2009
Highly Cited
2009
OBJECTIVES Patients with rheumatoid arthritis (RA) have an increased cardiovascular risk, but the magnitude of this risk is not… (More)
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Review
2007
Review
2007
There is a progressive deterioration in beta-cell function and mass in type 2 diabetics. It was found that islet function was… (More)
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Highly Cited
2006
Highly Cited
2006
AIM Exenatide, an incretin mimetic for the adjunct treatment of type 2 diabetes (DM2), reduced A1C and weight in 30-week placebo… (More)
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Highly Cited
2005
Highly Cited
2005
BACKGROUND We sought to compare metabolic syndrome (MetS) with the Framingham Risk Score (FRS) as predictors of coronary heart… (More)
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Highly Cited
2005
Highly Cited
2005
CONTEXT First-phase insulin secretion (within 10 min after a sudden rise in plasma glucose) is reduced in type 2 diabetes… (More)
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Highly Cited
2003
Highly Cited
2003
Two substrates of insulin-degrading enzyme (IDE), amyloid beta-protein (Abeta) and insulin, are critically important in the… (More)
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Highly Cited
2003
Highly Cited
2003
Two substrates of insulin-degrading enzyme (IDE), amyloid -protein (A ) and insulin, are critically important in the pathogenesis… (More)
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Highly Cited
2002
Highly Cited
2002
Myotonic dystrophy is a complex neuromuscular disorder associated with DNA expansion mutations in two different genes. In DM1 a… (More)
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Highly Cited
2001
Highly Cited
2001
The phenotypes in myotonic dystrophy types 1 and 2 (DM1 and DM2) are similar, suggesting a shared pathophysiologic mechanism. DM1… (More)
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