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1p22-p21

A chromosome band present on 1p
National Institutes of Health

Papers overview

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2014
2014
GPR88, coding for a G protein-coupled orphan receptor that is highly represented in the striatum, is a strong functional… Expand
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2010
2010
The discovery of the genetic factors implicated in the predisposition to complex diseases may greatly profit from genetic studies… Expand
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2008
2008
ABSTRACT Type 2 diabetes mellitus (T2DM) is a common complex phenotype that by the year 2010 is predicted to affect 221 million… Expand
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2008
2008
BackgroundThe General Transcription Apparatus (GTA) comprises more than one hundred proteins, including RNA Polymerases, GTFs… Expand
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2002
2002
Primary intraosseous vascular anomaly, previously called intraosseous hemangioma, is a very rare malformation that is usually… Expand
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2001
2001
Paralemmin is a protein implicated in plasma membrane dynamics. Here we describe the identification of two new paralemmin-related… Expand
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1996
1996
Pigmented villonodular synovitis (PVNS) is a relatively uncommon benign lesion that is characterized by diffuse synovial… Expand
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1996
1996
Abstract Stargardt disease (STGD) is one of the most frequent causes of macular degeneration in childhood. Linkage analysis in… Expand
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