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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

Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
Bedeutung und Charakterisierung der 6q-Deletion beim Prostatakarzinom
Ein primares Ziel in der Prostatakarzinomforschung ist die Identifizierung neuer prognostischer molekularer Marker, welche dazu… 
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
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… 
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… 
2000
2000
Achromatopsia on chromosome 8q21 is caused by mutations in the CNGB3 gene encoding the beta-subunit of the cone photoreceptor cGMP gated channel
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…