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10q21

A chromosome band present on 10q
National Institutes of Health

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4 relations
10qCCDC6 wt AlleleChromosomesTET1 wt Allele

Papers overview

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Highly Cited
2008
Highly Cited
2008
Positive association of genetic variants in the upstream region of NKX2-3 with Crohn’s disease in Japanese patients
Background and aims: A number of genome-wide association studies have been performed as a robust means of identifying… 
2006
2006
Influence of lysosomal acid lipase polymorphisms on chromosome 10 on the risk of Alzheimer's disease and cholesterol metabolism
2004
2004
Genome scan for QTLs underlying bone size variation at 10 refined skeletal sites: genetic heterogeneity and the significance of phenotype refinement.
To identify quantitative trait loci (QTLs) underlying variation in bone size, we conducted a whole-genome linkage scan in 53… 
2002
2002
Human Surfactant Protein – A Gene Locus for Genetic Studies in the Finnish Population
Lung surfactant lowers the surface tension but surfactant proteins also have other functions. Surfactant protein A (SP-A) has a… 
2001
2001
Genetic abnormalities specifically associated with varying metastatic potential of prostate cancer cell lines as detected by comparative genomic hybridization.
2000
2000
Abnormal levels of human mitochondrial transcription factor A in skeletal muscle in mitochondrial encephalomyopathies
Abstract Human mitochondrial transcription factor A (h-mtTFA or Tfam), a 25-kDa protein encoded by a nuclear gene located on… 
1998
1998
Characterization and chromosomal mapping of the human gene for SFT, a stimulator of Fe transport.
Hemochromatosis is the most common genetic disorder known in man and results in progressive tissue deposition of iron leading to… 
1997
1997
De novo der(X)t(X;10)(q26;q21) with features of distal trisomy 10q: case report of paternal origin identified by late replication with BrdU and the human androgen receptor assay (HAR).
We describe an 11 year old girl with a de novo unbalanced t(X;10) that resulted in a deletion of Xq26-->Xqter and a trisomy of… 
1992
1992
Karyotype at relapse following allogeneic bone marrow transplantation for chronic myelogenous leukemia.
1977
1977
[Two new cases of trisomy 10q21 to 10qter in two sisters due to paternal translocation t(9;10) (q34;q24)].
Two sisters with multiple congenital malformations were shown to be trisomic for 10q24 to 10qter as a consequence of… 
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