14q21-q22

A chromosome band present on 14q
National Institutes of Health

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Chromosomeschromosome 14q

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2006
2006
A genome-wide scan maps a novel juvenile-onset primary open angle glaucoma locus to chromosome 5 q
Glaucoma is a leading cause of vision impairment and blindness in both developed and developing countries. Primary open angle… Expand
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2001
2001
Hereditary spastic paraplegia linked to chromosome 14q11-q21: reduction of the SPG3 locus interval from 5.3 to 2.7 cM.
Editor—Recently, Reid et al 1 reported reduction of the chromosome 12q locus for autosomal dominant hereditary spastic paraplegia… Expand
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2000
2000
A novel locus (DFNA23) for prelingual autosomal dominant nonsyndromic hearing loss maps to 14q21-q22 in a Swiss German kindred.
DFNA23, a novel locus for autosomal dominant nonsyndromic hearing loss, was identified in a Swiss German kindred. DNA samples… Expand
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1998
1998
Comparative genome mapping: mouse and rat homologies revealed by fluorescence in situ hybridization.
Mouse and rat genome studies are vital to the use of rodents as models of biology and human genetic disease. In this study… Expand
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1998
1998
cDNA cloning, genomic organization, and expression of the human RTN2 gene, a member of a gene family encoding reticulons.
This paper describes the cDNA cloning, genomic organization, and expression of the human RTN2 gene on chromosome 19q13.3, which… Expand
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1998
1998
The small subunits of human and mouse DNA polymerase epsilon are homologous to the second largest subunit of the yeast Saccharomyces cerevisiae DNA polymerase epsilon.
Human DNA polymerase epsilon is composed of a 261 kDa catalytic polypeptide and a 55 kDa small subunit of unknown function. cDNAs… Expand
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1997
1997
Localization of the gene encoding a novel isoform of lysyl hydroxylase
Method of mapping: FISH and in situ hybridization Database depository information: GenBank J02921, M35368, M36682, M64303… Expand
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1995
1995
Human GTP-cyclohydrolase I gene and sepiapterin reductase gene map to region 14q21-q22 and 2p14-p12, respectively, by in situ hybridization.
The two cDNA clones pHGCH1 and pHSR1, harboring partial coding sequences for GTPCH and SR, respectively, were tritium-labeled by… Expand
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1995
1995
In vitro-induced resistance to the deoxycytidine analogues cytarabine (AraC) and 5-aza-2′-deoxycytidine (DAC) in a rat model for acute myeloid leukemia is mediated by mutations in the deoxycytidine…
The deoxycytidine kinase (dck) gene encodes the enzyme responsible for the metabolic activation of the antileukemic drugs… Expand
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1994
1994
Chromosome locations of human EMX and OTX genes.
We have determined the chromosomal localization of four human homeobox-containing genes, EMX1, EMX2, OTX1, and OTX2, related to… Expand
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