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21q22.2

A chromosome band present on 21q
National Institutes of Health

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5 relations
21qCBR3 wt AlleleChromosomesETS2 wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2003
2003
Down syndrome: a study of chromosomal mosaicism.
2001
2001
Molecular mechanisms of human single-minded 2 (SIM2) gene expression: identification of a promoter site in the SIM2 genomic sequence.
2001
2001
Association of deletions and translocation of the reduced folate carrier gene with profound loss of gene expression in methotrexate-resistant K562 human erythroleukemia cells.
2000
2000
Assignment1 of SYNJ1 to human chromosome 21q22.2 and Synj12 to the murine homologous region on chromosome 16C3–4 by in situ hybridization
Synaptojanin 1 is a polyphosphoinositide phosphatase highly enriched in nerve terminals (McPherson et al., 1996). The NH2… 
1998
1998
Mapping of a novel human carbonyl reductase, CBR3, and ribosomal pseudogenes to human chromosome 21q22.2.
To find the genes contributing to Down syndrome, we constructed a 4-Mb sequence-ready map spanning chromosome 21q22.2 with… 
Review
1997
Review
1997
Functional screening and complex traits: human 21q22.2 sequences affecting learning in mice.
Libraries of the mammalian genome have generally been propagated in single cells and have been used for gene discovery through in… 
1997
1997
Altered expression of Erg and Ets-2 transcription factors is associated with genetic changes at 21q22.2-22.3 in immortal and cervical carcinoma cell lines
Human Papillomavirus (HPV) type 16 is the most frequently detected HPV in cervical cancer. Although epidemiologic and… 
1997
1997
Localisation of a human homologue of the Drosophila mnb and rat Dyrk genes to chromosome 21q22.2
Abstract Exon trapping was used to identify portions of human chromosome 21-encoded genes. More than 600 potential exons on the… 
1997
1997
The murine Dyrk protein maps to chromosome 16, localizes to the nucleus, and can form multimers.
We mapped the murine copy of the Dyrk gene and examined its subcellular localization and self-interaction. We found that: (1… 
1976
1976
[Partial trisomy 21 (21q21 - 21q22.2)].
An abnormal chromosome 21 is reported in a child with a phenotype strongly reminiscent of trisomy 21 syndrome. It is shown to… 
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