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7q21.3

A chromosome band present on 7q
National Institutes of Health

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7 relations
Chromosome 7qChromosomesDBF4 wt AlleleDLX5 wt Allele

Papers overview

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2009
2009
Comparative expression analysis reveals differences in the regulation of intestinal paraoxonase family members.
2008
2008
Identification of SMURF1 as a possible target for 7q21.3‐22.1 amplification detected in a pancreatic cancer cell line by in‐house array‐based comparative genomic hybridization
Pancreatic cancer (PC) cell lines provide a useful starting point for the discovery and functional analysis of genes driving the… 
2006
2006
Homozygous SLC25A13 mutation in a Taiwanese patient with adult-onset citrullinemia complicated with steatosis and hepatocellular carcinoma.
Review
2002
Review
2002
Mitochondrial aspartate glutamate carrier (citrin) deficiency as the cause of adult-onset type II citrullinemia (CTLN2) and idiopathic neonatal hepatitis (NICCD)
AbstractBy using homozygosity mapping and positional cloning, we have shown that adult-onset type II citrullinemia (CTLN2) is… 
Highly Cited
1998
Highly Cited
1998
Genetic variation in paraoxonase-1 and paraoxonase-2 is associated with variation in plasma lipoproteins in Alberta Hutterites.
Highly Cited
1997
Highly Cited
1997
Molecular cytogenetic delineation of deletions and translocations involving chromosome band 7q22 in myeloid leukemias.
Loss of chromosome 7 (-7) or deletion of its long arm (7q-) are recurring chromosome abnormalities in myeloid disorders… 
1997
1997
The phenotypic effects of chromosome rearrangement involving bands 7q21.3 and 22q13.3.
We report a family in which the proband has a direct insertion of band 7q21.3 into chromosome 22 at 22q13.3, karyotype 46,XX,dir… 
Highly Cited
1996
Highly Cited
1996
Cloning and Characterization of PDK4 on 7q21.3 Encoding a Fourth Pyruvate Dehydrogenase Kinase Isoenzyme in Human*
Different isoenzymes of pyruvate dehydrogenase kinase (PDK) inhibit the mitochondrial pyruvate dehydrogenase complex by… 
1996
1996
Split hand/split foot malformation, deafness, and mental retardation with a complex cytogenetic rearrangement involving 7q21.3.
Split hand/split foot malformation (SHSF) has been described in several patients associated with cytogenetically visible… 
Highly Cited
1994
Highly Cited
1994
Type I procollagen COOH-terminal proteinase enhancer protein: identification, primary structure, and chromosomal localization of the cognate human gene (PCOLCE).
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