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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… Expand
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2003
2003
Cloning and identification of a novel ubiquitin-like protein, BMSC-UbP, from human bone marrow stromal cells.
Ubiquitin is one of phylogenetically well-conserved proteins in all eukaryotes. Ubiquitin-dependent modification of protein… Expand
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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… Expand
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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… Expand
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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… Expand
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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… Expand
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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… Expand
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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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