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14q21.3

A chromosome band present on 14q
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
Background & Aims Altered extrahepatic bile ducts, gut, and cardiovascular anomalies constitute the variable phenotype of biliary… Expand
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Highly Cited
2013
Highly Cited
2013
BACKGROUND Idiopathic pulmonary fibrosis (IPF) is a devastating disease that probably involves several genetic loci. Several rare… Expand
2012
2012
Sexual dysfunction is a major side effect of selective serotonin reuptake inhibitors (SSRIs) and serotonin-noradrenaline reuptake… Expand
2011
2011
Copy-number variants (CNVs) are a source of genetic variation that increasingly are associated with human disease. However, the… Expand
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2009
2009
The risk of osteoporotic fracture is a function of both applied muscle mass and bone tissue distribution. Leg lean mass (LLM) and… Expand
2009
2009
OBJECTIVES To determine the mechanism for the 46,XX/46,XY karyotype observed in a patient with an ovotesticular disorder of… Expand
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2008
2008
BackgroundLung cancer with EGFR mutation was shown to be a specific clinical entity. In order to better understand the biology… Expand
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2007
2007
A new human esophageal cancer cell line, HKESC-4, was established from a nude-mouse xenograft of a moderately differentiated… Expand
2006
2006
We have previously identified and characterized human KLHDC2/HCLP-1, a kelch repeat protein that interacts with and inhibits… Expand
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2002
2002
Factor B is a subunit of the mammalian ATP synthase complex, whose existence has been controversial. This paper describes the… Expand