16q22.1

A chromosome band present on 16q
National Institutes of Health

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Highly Cited
2012
Highly Cited
2012
Genome-wide association studies (GWAS) have identified more than a dozen loci associated with colorectal cancer (CRC) risk. Here… (More)
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Highly Cited
2009
Highly Cited
2009
Closely located at the tumor suppressor locus 16q22.1, CKLF-like MARVEL transmembrane domain-containing member 3 and 4 (CMTM3 and… (More)
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Highly Cited
2009
Highly Cited
2009
Spinocerebellar ataxia type 31 (SCA31) is an adult-onset autosomal-dominant neurodegenerative disorder showing progressive… (More)
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Highly Cited
2008
Highly Cited
2008
Genome-wide association (GWA) studies have identified multiple loci at which common variants modestly influence the risk of… (More)
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2007
2007
AbstractThe 16q22.1-linked autosomal dominant cerebellar ataxia (16q-ADCA; Online Mendelian Inheritance in Man [OMIN] #117210) is… (More)
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2005
2005
Autosomal dominant cerebellar ataxia (ADCA) is a group of heterogeneous neurodegenerative disorders. By positional cloning, we… (More)
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Review
2001
Review
2001
E-cadherin is a cell–cell adhesion protein fulfilling a prominent role in epithelial differentiation. Data from model systems… (More)
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Highly Cited
2001
Highly Cited
2001
Loss of heterozygosity (LOH) allows the expression of recessive mutation in tumor suppressor genes (TSG). Therefore, on the basis… (More)
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Highly Cited
1996
Highly Cited
1996
We report the cloning, sequence analysis, tissue distribution, and functional expression of the K-Cl cotransport protein, KCC1… (More)
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Highly Cited
1990
Highly Cited
1990
Loss of heterozygosity on chromosome 16 is a common genetic alteration in human hepatocellular carcinoma (HCC). To clarify the… (More)
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