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19q13.33

A chromosome band present on 19q.
National Institutes of Health

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7 relations
AKT1S1 wt AlleleCPT1C wt AlleleChromosomesMIR150 wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
Copy number variants associated with epilepsy from gene expression microarrays
2014
2014
Validation of association of genetic variants at 10q with prostate‐specific antigen (PSA) levels in men at high risk for prostate cancer
To validate six previously identified markers among men at increased risk of prostate cancer (African‐American men and those with… 
2014
2014
association studies cancer and the effect of control selection on genetic Genetic variation in protein specific antigen detected prostate
Review
2011
Review
2011
MIR125A (microRNA 125a)
Review on MIR125A (microRNA 125a), with data on DNA, on the protein encoded, and where the gene is implicated. 
2010
2010
DNA repair deficiency in a newly identified neurological disease.
Mutations in PNKP cause microcephaly, seizures and defects in DNA repair Shen et al. (2010) Nature Genetics 42(3… 
2010
2010
[c.359T>C mutation of the MYH14 gene in two autosomal dominant non-syndromic hearing impairment families with common ancestor].
OBJECTIVE To identify the gene mutation for two Chinese families with autosomal dominant non-syndromic hearing impairment(NSHI… 
2009
2009
Vaccinia-related kinase ( VRK ) signaling in cell and tumor biology
VRK (vaccinia-related kinase) is a group of three proteins in the human kinome. These proteins, mainly VRK1 and VRK2, have been… 
Highly Cited
2005
Highly Cited
2005
Molecular cytogenetic analysis of chromosomes 1 and 19 in glioma cell lines.
2004
2004
A novel PRPF31 splice-site mutation in a Chinese family with autosomal dominant retinitis pigmentosa.
PURPOSE The autosomal dominant form of retinitis pigmentosa (ADRP) can be caused by mutations in 13 genes and a further locus for… 
2004
2004
Refinement of the DFNA4 locus to a 1.44 Mb region in 19q13.33
Many forms of autosomal dominant non-syndromic hearing impairment are known. While the underlying gene defects and causative… 
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