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8q21

A chromosome band present on 8q
National Institutes of Health

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8 relations
CYP11B1 wt AlleleChromosomesFABP4 wt AlleleHEY1 wt Allele

Papers overview

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2015
2015
AB013. Long-range modulation of PAG1 expression by 8q21 allergy risk variants
The gene(s) whose expression is regulated by allergy risk variants is unknown for many loci identified through genome-wide… 
2012
2012
Kombination der FISH- und TMA-Technik zur Aufklärung der molekularen Architektur des 8q21 Amplikons beim Mammakarzinom
Amplifikationen auf Chromosom 8q21 wurden bei ca. 3-58,3 % der Mammakarzinome beschrieben. Studien, die diesen Bereich kartiert… 
2012
2012
A study of chromosome 8q24 and 8q21 association with prostate cancer in Chinese population
Objective to explore the correlation between chro-mosome 8q24:rs6983561(C)、rs13252298(T)、rs12543663(T)and8q21 rs1512268(T) and… 
2012
2012
Prävalenz und klinische Signifikanz von TPD52-Gen-Amplifikationen im humanen Prostatakarzinom
Das Prostatakarzinom ist das am haufigsten diagnostizierte Malignom bei Mannern in den Industrienationen. Die molekularen… 
2012
2012
4 MRE 11 A Gene Mutations Responsible for the Rare Ataxia Telangiectasia-Like Disorder
Ataxia telangiectasia like disorder (ATLD) is a rare variant of ataxia telangiectasia (A-T) that share a number of clinical… 
2009
2009
Award Number: W81XWH-08-1-0660 TITLE: TPD52: A Novel Vaccine Target for Prostate Cancer
Expression studies have consistently identified tumor protein D52 (TPD52) overexpression in tumor cells. Murine TPD52 (mD52… 
2001
2001
Fluorescence in Situ Hybridization Evaluation of c-erbB2 Gene Amplification and Chromosomal Anomalies in Bladder Cancer 1
Oncogene amplification and chromosomal anomalies are found in many solid tumors and are often associated with aggressiveness of… 
1998
1998
A molecular marker for the bovine ciliary neurotrophic factor receptor gene (CNTFR) maps to 8q21.
1997
1997
Genetic MappingUsingMicrocell-Mediat ed Chromosome Transfer Suggests a LocusforNijmegen Breakage Syndrome atChromosome 8q21-24
Summary Nijmegen breakage syndrome (NBS)isanautosomal recessive disorder characterized bymicrocephaly, short stature… 
1983
1983
Del (8) (q212q2200) de novo in a boy without Langer-Giedion syndrome.
A two year-old boy with congenital malformations, psychomotor retardation and absence of phenotypical features of the Langer…