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Familial Partial Lipodystrophy, Type 3

Known as: FPLD3, Lipodystrophy, Familial Partial, Associated With PPARg Mutations, Lipodystrophy, Familial Partial, Type 3 
This type can be caused by mutation in the gene encoding PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR GAMMA.
National Institutes of Health

Papers overview

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Highly Cited
2014
Highly Cited
2014
Significance Genome sequencing of individuals in the population reveals new mutations in almost every protein coding gene… Expand
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Highly Cited
2009
Highly Cited
2009
Aims/hypothesisExercise training improves glucose homeostasis, but large inter-individual differences are reported, suggesting a… Expand
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Highly Cited
2008
Highly Cited
2008
OBJECTIVE—Recently, several genes have been shown to be associated with an increased risk of type 2 diabetes by genome-wide… Expand
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Highly Cited
2008
Highly Cited
2008
BackgroundConsidering that a portion of the heterogeneity amongst previous replication studies may be due to a variable… Expand
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Highly Cited
2007
Highly Cited
2007
BackgroundSusceptibility to type 2 diabetes may be conferred by genetic variants having modest effects on risk. Genome-wide fixed… Expand
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Review
2005
Review
2005
  • Michael Roden
  • International Journal of Obesity
  • 2005
  • Corpus ID: 24427594
INTRODUCTION:Obese and type 2 diabetic (T2DM) adolescents present with reduced insulin-stimulated glucose disposal and elevated… Expand
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Highly Cited
2005
Highly Cited
2005
Aims/hypothesisMorbid obesity (BMI>40 kg/m2) affecting 0.5–5% of the adult population worldwide is a major risk factor for type 2… Expand
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2005
2005
BackgroundFamilial partial lipodystrophy (Dunnigan) type 3 (FPLD3, Mendelian Inheritance in Man [MIM] 604367) results from… Expand
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Review
2005
Review
2005
The metabolic syndrome (MetS) is a common phenotype that is clinically defined by threshold values applied to measures of central… Expand
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2004
2004
Familial partial lipodystrophy (FPLD) results from coding sequence mutations either in LMNA, encoding nuclear lamin A/C, or in… Expand
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