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4q21.2
A chromosome band present on 4q
National Institutes of Health
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Related topics
Related topics
3 relations
CXCL11 wt Allele
Chromosomes
GNRHR wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Concurrence of chromosome 3 and 4 aberrations in human uveal melanoma
É. Sipos
,
K. Hegyi
,
+8 authors
G. Halmos
Oncology Report
2017
Corpus ID: 35303070
Uveal melanoma (UM) is the most common primary intraocular malignancy with a very poor prognosis. The most frequent chromosome…
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2012
2012
Association of Common Variants in TNFRSF13B, TNFSF13, and ANXA3 with Serum Levels of Non-Albumin Protein and Immunoglobulin Isotypes in Japanese
Wael M. Osman
,
Y. Okada
,
Y. Kamatani
,
M. Kubo
,
K. Matsuda
,
Yusuke Nakamura
PLoS ONE
2012
Corpus ID: 15929997
We performed a genome-wide association study (GWAS) on levels of serum total protein (TP), albumin (ALB), and non-albumin protein…
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2005
2005
Frequent microsatellite alterations of chromosome locus 4q13.1 in oral squamous cell carcinomas.
Shu-Chun Lin
,
M. Chang
,
+4 authors
Kuo-Wei Chang
Journal of Oral Pathology & Medicine
2005
Corpus ID: 27125362
BACKGROUND Studies have revealed that losses of chromosome 4q24-25 regions are frequent in cancers including head and neck…
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2004
2004
Comparative mapping of the gene coding for Inhibin-α (INHA) to Chromosome 2 in sheep and cattle
R. Brunner
,
T. Goldammer
,
S. Hiendleder
,
C. Jäger
,
M. Schwerin
Mammalian Genome
2004
Corpus ID: 13547604
age with a NIKON epifluorescence microscope. FLcen was calculated according to [4], Previously identified homologs: Human and…
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2003
2003
Class II neocentromeres: a putative common neocentromere site in band 4q21.2
P. Warburton
,
J. Barwell
,
M. Splitt
,
D. Maxwell
,
S. Bint
,
C. Ogilvie
European Journal of Human Genetics
2003
Corpus ID: 25121022
Neocentromeres are rare functional centromeres formed within noncentromeric chromosomal regions. We report the finding of a…
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Review
2002
Review
2002
[Normosmic idiopathic hypogonadotropic hypogonadism with GnRH receptor mutation(review)].
T. Tamaya
Nihon rinsho. Japanese journal of clinical…
2002
Corpus ID: 21847764
Mutations in gonadotropin releasing hormone receptor(GnRHR) gene(chromosome location, 4q21.2) cause autosomal recessive…
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2001
2001
High-resolution mapping of the human 4q21 and the mouse 5E3 SCYB chemokine cluster by fiber-fluorescence in situ hybridization
M. Erdel
,
M. Theurl
,
M. Meyer
,
H. Duba
,
G. Utermann
,
G. Werner-Felmayer
Immunogenetics
2001
Corpus ID: 53492
Abstract. The CXC chemokine or small inducible cytokine B (SCYB) subfamily includes the T-cell chemoattractants MIG (CXCL9, SCYB9…
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2000
2000
Cloning, genomic sequence, and chromosome mapping of Scyb11, the murine homologue of SCYB11 (alias βR1/H174/SCYB9B/I-TAC/IP-9/CXCL11)
M. Meyer
,
M. Erdel
,
H. Duba
,
E. Werner
,
G. Werner-Felmayer
Cytogenetic and Genome Research
2000
Corpus ID: 32192833
A T-cell attracting CXC chemokine phylogenetically related to MIG and SCYB10 was recently characterized and termed SCYB11 (alias…
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1995
1995
Assignment of the human homolog of mouse Dlx3 to Chromosome 17q21.3-q22 by analysis of somatic cell hybrids and fluorescence in situ hybridization
S. Scherer
,
H. Heng
,
G. Robinson
,
K. Mahon
,
J. Evans
,
L. Tsui
Mammalian Genome
1995
Corpus ID: 3088522
Species: Human Locus name: Gonadotropin-releasing hormone receptor Locus symbol: GNRHR Map position: Chromosome 4q21.2 Methods of…
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1995
1995
Mapping of the gonadotropin-releasing hormone (GnRH) receptor gene to human Chromosome 4q21.2 by fluorescence in situ hybridization
Peter C. K. Leung
,
J. Squire
,
Chung-Kang Peng
,
N. Fan
,
Michael R. Hayden
,
Jan I. Olofsson
Mammalian Genome
1995
Corpus ID: 22885474
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