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15q22.3-q23

A chromosome band present on 15q
National Institutes of Health

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3 relations
15qChromosomesNEO1 wt Allele

Papers overview

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Highly Cited
2003
Highly Cited
2003
Evaluation of complex inheritance involving the most common Bardet-Biedl syndrome locus (BBS1).
Bardet-Biedl syndrome (BBS) is a genetic disorder with the primary features of obesity, pigmentary retinopathy, polydactyly… 
2003
2003
Cloning and identification of a novel ubiquitin-like protein, BMSC-UbP, from human bone marrow stromal cells.
2000
2000
Significant association between a silent polymorphism in the neuromedin B gene and body weight in German children and adolescents
Abstract Neuromedin B has been shown to exert an inhibiting effect on food consumption in rats. The corresponding gene NMB maps… 
Highly Cited
1998
Highly Cited
1998
New eukaryotic semaphorins with close homology to semaphorins of DNA viruses.
Semaphorins were initially described as a family of repulsive guidance molecules in embryonal development. Their basic structure… 
Highly Cited
1997
Highly Cited
1997
Linkage mapping in 29 Bardet-Biedl syndrome families confirms loci in chromosomal regions 11q13, 15q22.3-q23, and 16q21.
Bardet-Biedl syndrome (BBS) is a clinically and genetically heterogeneous autosomal recessive disorder characterized by retinitis… 
1997
1997
Molecular characterization of human neogenin, a DCC-related protein, and the mapping of its gene (NEO1) to chromosomal position 15q22.3-q23.
Neogenin was first identified in the chick embryo, and like a number of cell surface proteins of the immunoglobulin (Ig… 
1997
1997
Genetic analysis of autosomal recessive forms of retinitis pigmentosa
Retinitis pigmentosa (RP) is a heterogeneous group of genetic disorders characterised by a progressive pigmentary degeneration of… 
1995
1995
Localization of the gene encoding the putative human HLA class II associated protein (PHAPI) to chromosome 15q22.3-q23 by fluorescence in situ hybridization.
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