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6p22.1

A chromosome band present on 6p
National Institutes of Health

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Chromosome 6 Short ArmChromosomesGMNN wt AlleleHIST1H3B wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Genome-wide association study of wheezing phenotypes in the Avon longitudinal study of parents and children
Asthma is a polygenic heterogeneous condition with phenotypic variation through the life course. Using 5 wheezing phenotypes from… 
2015
2015
Single Nucleotide Polymorphisms (5p15.33, 6p22.1 and 15q25.1), Smoking and Lung Cancer Survival
Background: Genome-wide studies of single nucleotide polymorphisms (SNPs) reported associations between chromosomal regions (5p15… 
2014
2014
DNA methylation analysis of the evolution of Wilms tumour from its precursor nephrogenic rests
Recurrent loss of imprinting at 11p15, paucity of recurrent genetic mutations and associated nephrogenic rests (NR; precursor… 
2010
2010
Candidate variants at 6p21.33 and 6p22.1 and risk of non-small cell lung cancer in a Chinese population.
Chromosome 6p21.33, containing BAT3 and MSH5 genes, together with chromosome 6p22.1 were recently identified as susceptible… 
2010
2010
Original Article Candidate variants at 6p21.33 and 6p22.1 and risk of non-small cell lung cancer in a Chinese population
Chromosome 6p21.33, containing BAT3 and MSH5 genes, together with chromosome 6p22.1 were recently identified as susceptible… 
2001
2001
[Preliminary study of the gene structure of human glycosylphosphatidylinositol specific phospholipase D].
To explore the cDNA and its genomic gene structure of human glycosylphosphatidylinositol specific phospholipase D (GPI-PLD), the… 
1999
1999
Monosomy 6 in human cultured fibroblast-like cells permanently stimulated by fibroblast growth factor 1: evidence for selection
The appearance of cells with monosomy 6 (mono6 cells) in cultures of human fibroblast-like cells during long-term stimulation… 
1997
1997
Physical mapping of two histone gene clusters on human chromosome 6p22.1-22.2.
Histones are basic proteins which are responsible for the assembly and maintenance of the nucleosomal structure within the… 
Review
1997
Review
1997
The mouse HFE gene
Idiopathic hemochromatosis is believed to represent the most frequent hereditary condition in Caucasian populations (for review… 
1997
1997
Complex duplications at 6p22.1, 6p11.2, 5q13, 5p15.1 and 5p13 revealed by fluorescent in situ hybridisation.
A complex pattern of fluorescent in situ hybridisation (FISH) has been detected using PAC clones from the short arm of chromosome… 
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