Familial Partial Lipodystrophy, Type 2

Known as: Syndrome, Dunnigan, Lipodystrophy, Familial Partial, Dunnigan Type, LIPOATROPHIC DIABETES 
This type can be caused by mutation in the gene encoding LAMIN TYPE A.

Topic mentions per year

Topic mentions per year

2004-2018
02420042018

Papers overview

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2017
2017
BACKGROUND Dipeptidyl peptidase-4 (DDP4) is an enzyme responsible for glucagon-like peptide-1 inactivation and plays an important… (More)
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2016
2016
We report the first described case of a heterozygous p.R545H (c.1634 G > A) missense mutation in the LMNA gene with clinical… (More)
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2015
2015
Nuclear lamins are involved in many cellular functions due to their ability to bind numerous partners including chromatin and… (More)
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2012
2012
UNLABELLED BACKGROUND Familial partial lipodystrophies (FPLD) are clinically heterogeneous disorders characterized by… (More)
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2009
2009
A number of metabolic conditions have been associated with Obstructive Sleep Apnea Syndrome (OSAS). Familial partial… (More)
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2009
2009
BACKGROUND Type 2 familial partial lipodystrophy (FPLD2) is characterised by loss of fat in the limbs and buttocks and results… (More)
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2009
2009
We investigated the role of LMNA in adipose tissue by developing a novel mouse model of lipodystrophy. Transgenic mice were… (More)
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2007
2007
CONTEXT Familial partial lipodystrophy (FPLD) results from coding sequence mutations either in LMNA, encoding nuclear lamin A/C… (More)
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2006
2006
CONTEXT To date, all cases of familial partial lipodystrophy type 2 (FPLD2; Mendelian Inheritance in Man 151660) result from… (More)
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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… (More)
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