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LMNB2 gene

Known as: LAMIN B2, LMNB2 
National Institutes of Health

Papers overview

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2015
2015
We studied a consanguineous Palestinian Arab family segregating an autosomal recessive progressive myoclonus epilepsy (PME) with… 
2014
2014
The Barraquer–Simons syndrome or acquired parital lipodystrophy is a rare form of partial lipodystrophy characterized by gradual… 
Highly Cited
2011
Highly Cited
2011
Nuclear lamins are usually classified as A-type (lamins A and C) or B-type (lamins B1 and B2). A-type lamins have been implicated… 
Review
2009
Review
2009
  • E. Neilan
  • American Journal of Medical Genetics. Part A
  • 2009
  • Corpus ID: 29770319
In this issue of the Journal, McPherson et al. [2009] describe a unique constellation of clinical findings—including premature… 
Highly Cited
2006
Highly Cited
2006
The etiology of acquired partial lipodystrophy (APL, also called "Barraquer-Simons syndrome") is unknown. Genomic DNA mutations… 
2006
2006
The lamins are components of nuclear lamina and they have a profound influence on nuclear structure and functions. They are… 
Highly Cited
2004
Highly Cited
2004
ABSTRACT The cis-acting elements necessary for the activity of DNA replication origins in metazoan cells are still poorly… 
2001
2001
AbstractFamilial partial lipodystrophy (FPLD) has been shown to be due to mutations in the LMNA gene encoding nuclear lamins A… 
1998
1998
The recently developed procedure of topoisomerase II‐mediated DNA loop excision has been used to analyze the topological…