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7q21-q22

A chromosome band present on 7q
National Institutes of Health

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6 relations
AKAP9 wt AlleleCDK6 wt AlleleChromosome 7qChromosomes

Papers overview

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Highly Cited
2007
Highly Cited
2007
Identification of PFTAIRE protein kinase 1, a novel cell division cycle‐2 related gene, in the motile phenotype of hepatocellular carcinoma cells
Metastasis is a major cause of cancer morbidity and mortality in individuals with hepatocellular carcinoma (HCC), yet little is… 
2006
2006
Characterization of the 7q21-q22 amplicon in pancreatic cancer
1999
1999
Human-mouse comparative mapping of the genomic region containing CDK6: localization of an evolutionary breakpoint
The striking success of the ongoing Human Genome Project has resulted in the formulation of accelerated plans for completing the… 
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… 
1996
1996
Assignment of pig immunoglobulin kappa gene IGKC, to Chromosome 3ql2-ql4 by fluorescence in situ hybridization (FISH)
Method of mapping: Fluorescence in situ hybridization (FISH) [3,4]; probe tagged with biotin and labeled with FITC; blood… 
1995
1995
Chromosomal localization of two KOX zinc finger genes on chromosome bands 7q21-q22.
Human cDNAs encoding Krüppel-type zinc finger domains, designated KOX 1-32, have been cloned from human T lymphocyte cell line… 
1994
1994
Evidence for locus heterogeneity in human autosomal dominant split hand/split foot malformation.
Review
1994
Review
1994
A contiguous gene deletion syndrome at 7q21‐q22 and implications for a relationship between isolated ectrodactyly and syndromic ectrodactyly
Ectrodactyly is a genetically heterogeneous human limb developmental malformation with an autosomal locus at 7q21 designated… 
1994
1994
Familial split hand/split foot long bone deficiency does not segregate with markers linked to the SHFD1 locus in 7q21.3-q22.1.
Ectrodactyly (split hand/split foot, SHSF) is characterized by the absence of middle rays of the hand or the foot. Cytogenetic… 
1994
1994
Localization of the gene encoding the alpha 2/delta subunit (CACNL2A) of the human skeletal muscle voltage-dependent Ca2+ channel to chromosome 7q21-q22 by somatic cell hybrid analysis.
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