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16q24

A chromosome band present on 16q
National Institutes of Health

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4 relations
16qCBFA2T3 wt AlleleChromosomesIL17C wt Allele

Papers overview

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Highly Cited
2012
Highly Cited
2012
A genetic study of chronic venous insufficiency.
Highly Cited
2009
Highly Cited
2009
Twenty bone mineral density loci identified by large-scale meta-analysis of genome-wide association studies
Bone mineral density (BMD) is a heritable complex trait used in the clinical diagnosis of osteoporosis and the assessment of… 
Highly Cited
2009
Highly Cited
2009
Genome-wide association study identifies three loci associated with melanoma risk
We report a genome-wide association study of melanoma conducted by the GenoMEL consortium based on 317K tagging SNPs for 1,650… 
Highly Cited
2008
Highly Cited
2008
Deleterious mutations in the Zinc-Finger 469 gene cause brittle cornea syndrome.
Highly Cited
2004
Highly Cited
2004
DNA Hypomethylation and Ovarian Cancer Biology
Hypomethylation of some portions of the genome and hypermethylation of others are very frequent in human cancer. The… 
Highly Cited
2002
Highly Cited
2002
Frequent somatic mutations in PTEN and TP53 are mutually exclusive in the stroma of breast carcinomas
We have recently shown that loss of heterozygosity of specific markers, including those at 10q23, 17p13–p15 and 16q24, can occur… 
Highly Cited
1997
Highly Cited
1997
The Ig heavy chain gene is frequently involved in chromosomal translocations in multiple myeloma and plasma cell leukemia as detected by in situ hybridization.
Chromosome rearrangement of 14q32.33 has recurrently occurred with variable partner sites, including 11q13.3, 8q24.1, 18q21.3… 
Highly Cited
1996
Highly Cited
1996
H–cadherin, a novel cadherin with growth inhibitory functions and diminished expression in human breast cancer
A newly identified gene, H–cadherin, is reported. H–cadherin encodes a protein related to the cadherin superfamily of cell… 
Highly Cited
1994
Highly Cited
1994
17 beta-Hydroxysteroid dehydrogenase type 2: chromosomal assignment and progestin regulation of gene expression in human endometrium.
The cDNAs for two separate human 17 beta-hydroxysteroid dehydrogenases (17 beta-HSD) have been isolated and sequenced. The well… 
Highly Cited
1990
Highly Cited
1990
Human neutrophil cytochrome b light chain (p22-phox). Gene structure, chromosomal location, and mutations in cytochrome-negative autosomal recessive chronic granulomatous disease.
A membrane-bound cytochrome b, a heterodimer formed by a 91-kD glycoprotein (heavy chain) and a 22-kD polypeptide (light chain… 
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