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19q13

A chromosome band present on 19q
National Institutes of Health

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8 relations
19qACTN4 wt AlleleChromosomesKLK10 wt Allele

Papers overview

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Highly Cited
2006
Highly Cited
2006
1p/19q loss within oligodendroglioma is predictive for response to first line temozolomide but not to salvage treatment.
Highly Cited
2005
Highly Cited
2005
Allelic losses at 1p36 and 19q13 in gliomas: correlation with histologic classification, definition of a 150-kb minimal deleted region on 1p36, and evaluation of CAMTA1 as a candidate tumor…
PURPOSE Allelic loss at 1p is seen in 70% to 85% of oligodendrogliomas (typically in association with 19q allelic loss) and 20-30… 
Review
2004
Review
2004
Diseases associated with the extracellular calcium-sensing receptor.
Highly Cited
2002
Highly Cited
2002
The spectrum of pathology in central core disease
Highly Cited
2000
Highly Cited
2000
High-throughput tissue microarray analysis of cyclin E gene amplification and overexpression in urinary bladder cancer.
Highly Cited
1999
Highly Cited
1999
Detection of a cystic fibrosis modifier locus for meconium ileus on human chromosome 19q13
Detection of a cystic fibrosis modifier locus for meconium ileus on human chromosome 19q13 
Highly Cited
1999
Highly Cited
1999
Localization of a New Prostate-specific Antigen-related Serine Protease Gene, KLK4, Is Evidence for an Expanded Human Kallikrein Gene Family Cluster on Chromosome 19q13.3–13.4*
The human tissue kallikrein (KLK) family of serine proteases, which is important in post-translational processing events… 
Highly Cited
1999
Highly Cited
1999
Localization of familial benign hypercalcemia, Oklahoma variant (FBHOk), to chromosome 19q13.
Calcium homeostasis by the kidneys and parathyroids is mediated by the calcium-sensing receptor (CaSR), which is located on 3q21… 
Review
1997
Review
1997
Cytogenetic findings in 73 osteosarcoma specimens and a review of the literature.
Highly Cited
1995
Highly Cited
1995
Gene for progressive familial heart block type I maps to chromosome 19q13.
BACKGROUND Progressive familial heart block type I (PF-HBI) is a dominantly inherited cardiac bundle-branch conduction disorder… 
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