Skip to search formSkip to main contentSkip to account menu

18q21.3

A chromosome band present on 18q
National Institutes of Health

Related topics

Related topics

7 relations
BCL2 wt AlleleChromosomesDCC wt AlleleKDSR wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2005
2005
Identification of an HLA-A1 restricted CTL epitope from Mcl-1
The lymphochip: a specialized cDNA microarray for the genomicscale analysis of gene expression in normal and malignant… 
2001
2001
Allelic loss of chromosome 2p21-16.3 is associated with reduced survival in sporadic colorectal cancer.
BACKGROUND Since allelic loss of genes involved in the development of colorectal cancer could serve as prognostic markers, we… 
2001
2001
De novo deletion of chromosome 18q in a baby with harlequin ichthyosis.
Harlequin ichthyosis, (MIM 242500), is a rare, autosomal recessive skin disorder due to an inborn error of epidermal… 
1999
1999
Structural analysis of human SCC antigen 2 promoter.
1999
1999
Erythropoietic protoporphyria: identification of novel mutations in the ferrochelatase gene and comparison of biochemical markers versus molecular analysis as diagnostic strategies.
BACKGROUND Erythropoietic protoporphyria (EPP) results from an inherited deficiency of the last enzyme of the heme biosynthetic… 
1997
1997
Human Gene Mapping Report: Proteinase inhibitor 8 Map position 18q21.3
Functional T-cell antigen receptors are diverse structures in obligate association with CD3 proteins and the zeta chain protein… 
1997
1997
Expression, purification, and characterization of recombinant mammalian ferrochelatase.
1995
1995
Translocations and amplification of the BCL2 gene are detected in interphase nuclei of non-Hodgkin's lymphoma by in situ hybridization with yeast artificial chromosome clones.
Translocation of the BCL2 gene in B-cell malignancies carrying t(14;18) and amplification of the BCL2 gene in a cell line (HBL-2… 
1995
1995
The 18q- syndrome: analysis of chromosomes by bivariate flow karyotyping and the PCR reveals a successive set of deletion breakpoints within 18q21.2-q22.2.
The 18q- syndrome is one of several terminal deletion disorders that occur in humans. Previous G-banding studies suggest that the… 
1987
1987
c‐yes and bc1‐2 genes located on 18q21.3 in a follicular lymphoma cell line carrying a t(14;18) chromosomal translocation
The c‐yes‐1 and bc1‐2 genes have been independently mapped at the same position of the chromosome band, 18q21.3, which is a… 
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)