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15q22.3-q23
A chromosome band present on 15q
National Institutes of Health
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Related topics
Related topics
3 relations
15q
Chromosomes
NEO1 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).
K. Mykytyn
,
D. Nishimura
,
+18 authors
V. Sheffield
American Journal of Human Genetics
2003
Corpus ID: 10941594
Bardet-Biedl syndrome (BBS) is a genetic disorder with the primary features of obesity, pigmentary retinopathy, polydactyly…
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2003
2003
Cloning and identification of a novel ubiquitin-like protein, BMSC-UbP, from human bone marrow stromal cells.
Shuxun Liu
,
Yizhi Yu
,
+6 authors
Xuetao Cao
Immunology Letters
2003
Corpus ID: 23128613
2000
2000
Significant association between a silent polymorphism in the neuromedin B gene and body weight in German children and adolescents
F. Oeffner
,
D. Bornholdt
,
+8 authors
K. Grzeschik
Acta Diabetologica
2000
Corpus ID: 29703298
Abstract Neuromedin B has been shown to exert an inhibiting effect on food consumption in rats. The corresponding gene NMB maps…
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Highly Cited
1998
Highly Cited
1998
New eukaryotic semaphorins with close homology to semaphorins of DNA viruses.
C. Lange
,
T. Liehr
,
M. Goen
,
E. Gebhart
,
B. Fleckenstein
,
A. Ensser
Genomics
1998
Corpus ID: 27465094
Semaphorins were initially described as a family of repulsive guidance molecules in embryonal development. Their basic structure…
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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.
E. Bruford
,
R. Riise
,
+12 authors
A. Wright
Genomics
1997
Corpus ID: 27342384
Bardet-Biedl syndrome (BBS) is a clinically and genetically heterogeneous autosomal recessive disorder characterized by retinitis…
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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.
J. Vielmetter
,
X. Chen
,
+4 authors
W. Dreyer
Genomics
1997
Corpus ID: 20495675
Neogenin was first identified in the chick embryo, and like a number of cell surface proteins of the immunoglobulin (Ig…
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1997
1997
Genetic analysis of autosomal recessive forms of retinitis pigmentosa
E. Bruford
1997
Corpus ID: 79978962
Retinitis pigmentosa (RP) is a heterogeneous group of genetic disorders characterised by a progressive pigmentary degeneration of…
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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.
T. Fink
,
M. Vaesen
,
H. Kratzin
,
P. Lichter
,
M. Zimmer
Genomics
1995
Corpus ID: 36361532
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