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14q21-q22
A chromosome band present on 14q
National Institutes of Health
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2 relations
Chromosomes
chromosome 14q
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2009
2009
Localization of the gene encoding a novel isoform of lysyl hydroxylase
C. Szpirer
,
J. Szpirer
,
M. Rivière
,
P. Vanvooren
,
M. Valtavaara
,
R. Myllylä
Mammalian Genome
2009
Corpus ID: 9380716
Method of mapping: FISH and in situ hybridization Database depository information: GenBank J02921, M35368, M36682, M64303…
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2006
2006
A genome-wide scan maps a novel juvenile-onset primary open angle glaucoma locus to chromosome 5 q
C. Pang
,
B. Fan
,
+7 authors
R. Ritch
2006
Corpus ID: 45051917
Glaucoma is a leading cause of vision impairment and blindness in both developed and developing countries. Primary open angle…
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2005
2005
In vitro-induced resistance to the deoxycytidine analogues cytarabine (AraC) and 5-aza-2′-deoxycytidine (DAC) in a rat model for acute myeloid leukemia is mediated by mutations in the deoxycytidine…
A. Stegmann
,
M. Honders
,
A. Hagemeijer
,
B. Hoebee
,
R. Willemze
,
J. Landegent
Annals of Hematology
2005
Corpus ID: 9379344
The deoxycytidine kinase (dck) gene encodes the enzyme responsible for the metabolic activation of the antileukemic drugs…
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2001
2001
Hereditary spastic paraplegia linked to chromosome 14q11-q21: reduction of the SPG3 locus interval from 5.3 to 2.7 cM
S. Rainier
,
P. Hedera
,
+4 authors
J. Fink
Journal of medical genetics
2001
Corpus ID: 20138040
Editor—Recently, Reid et al 1 reported reduction of the chromosome 12q locus for autosomal dominant hereditary spastic paraplegia…
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2000
2000
A novel locus (DFNA23) for prelingual autosomal dominant nonsyndromic hearing loss maps to 14q21-q22 in a Swiss German kindred.
A. Salam
,
F. Häfner
,
T. E. Linder
,
T. Spillmann
,
A. Schinzel
,
S. Leal
American journal of human genetics
2000
Corpus ID: 42408940
DFNA23, a novel locus for autosomal dominant nonsyndromic hearing loss, was identified in a Swiss German kindred. DNA samples…
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1998
1998
cDNA cloning, genomic organization, and expression of the human RTN2 gene, a member of a gene family encoding reticulons.
A. Roebroek
,
B. Contreras
,
I. Pauli
,
W. V. D. Van de Ven
Genomics
1998
Corpus ID: 43006933
This paper describes the cDNA cloning, genomic organization, and expression of the human RTN2 gene on chromosome 19q13.3, which…
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1998
1998
Comparative genome mapping: mouse and rat homologies revealed by fluorescence in situ hybridization.
J. Scalzi
,
J. Hozier
Genomics
1998
Corpus ID: 25344126
Mouse and rat genome studies are vital to the use of rodents as models of biology and human genetic disease. In this study…
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1998
1998
The small subunits of human and mouse DNA polymerase epsilon are homologous to the second largest subunit of the yeast Saccharomyces cerevisiae DNA polymerase epsilon.
M. Jokela
,
M. Mäkiniemi
,
S. Lehtonen
,
C. Szpirer
,
U. Hellman
,
J. Syväoja
Nucleic acids research
1998
Corpus ID: 8728468
Human DNA polymerase epsilon is composed of a 261 kDa catalytic polypeptide and a 55 kDa small subunit of unknown function. cDNAs…
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1995
1995
Human GTP-cyclohydrolase I gene and sepiapterin reductase gene map to region 14q21-q22 and 2p14-p12, respectively, by in situ hybridization.
B. Thöny
,
C. Heizmann
,
M. Mattei
Genomics
1995
Corpus ID: 28029286
Highly Cited
1994
Highly Cited
1994
Chromosome locations of human EMX and OTX genes.
K. Kastury
,
T. Druck
,
+5 authors
E. Boncinelli
Genomics
1994
Corpus ID: 25022720
We have determined the chromosomal localization of four human homeobox-containing genes, EMX1, EMX2, OTX1, and OTX2, related to…
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