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17q11

A chromosome band present on 17q
National Institutes of Health

Papers overview

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Highly Cited
2008
Highly Cited
2008
Chromosomal rearrangements that create gene fusions are common features of human tumors. The prevailing view is that the… 
Highly Cited
2007
Highly Cited
2007
We analyzed the subchromosomal numerical aberrations of 44 surgically resected pancreatic adenocarcinomas by array‐based… 
Highly Cited
2004
Highly Cited
2004
A large body of research supports a multifactorial cause in multiple sclerosis (MS), with an underlying genetic susceptibility… 
Highly Cited
2004
Highly Cited
2004
We investigated the genetic aspects of the large sex bias in the prevalence of autism spectrum disorder by monitoring changes in… 
Highly Cited
2004
Highly Cited
2004
Two known recurrent constitutional translocations, t(11;22) and t(17;22), as well as a non-recurrent t(4;22), display derivative… 
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Highly Cited
2001
Highly Cited
2001
A novel human gene, SARM, encodes the orthologue of a Drosophila protein (CG7915) and contains a unique combination of the… 
Highly Cited
1999
Highly Cited
1999
To search for recurrent and specific genomic alterations in human hepatocellular carcinoma (HCC), we examined 18 cell lines by… 
Review
1999
Review
1999
  • M. Rothenberg
  • American journal of respiratory cell and…
  • 1999
  • Corpus ID: 18245564
Eosinophil accumulation in the peripheral blood and tissues is a hallmark feature of several important medical diseases… 
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Highly Cited
1997
Highly Cited
1997
The group of autosomal recessive (AR) muscular dystrophies includes, among others, two main clinical entities, the limb-girdle… 
Highly Cited
1995
Highly Cited
1995
Clonal chromosome aberrations were detected in 8 short‐term cultured malignant peripheral nerve sheath tumors (MPNST). Seven had…