FAQ

Retinitis Pigmentosa 11

Known as: RP11 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1996-2017
0102019962017

Related topics

Related topics

2 relations
Autosomal dominant inheritance

Broader (1)

Retinitis Pigmentosa

Related mentions per year

Related mentions per year

1937-2018
19401960198020002020
Retinitis Pigmentosa 11
Autosomal dominant inheritance
Retinitis Pigmentosa

Papers overview

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2015
2015
Three circulating long non-coding RNAs act as biomarkers for predicting NSCLC.
BACKGROUND/AIMS Circulating long non coding RNAs (lncRNAs) have emerged recently as major players in tumor biology and may be… (More)
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2015
2015
Circulation long non-coding RNAs act as biomarkers for predicting tumorigenesis and metastasis in hepatocellular carcinoma
BACKGROUND & AIMS Alpha Fetal Protein (AFP) was one of the traditional biomarker for diagnosis of Hepatocellular carcinoma (HCC… (More)
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2015
2015
Clinical significance of high expression of circulating serum lncRNA RP11-445H22.4 in breast cancer patients: a Chinese population-based study
Long noncoding RNAs (lncRNAs) have been gradually confirmed to be tumor-associated biological molecules and became interesting… (More)
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2014
2014
Aberrantly expressed long noncoding RNAs in human intervertebral disc degeneration: a microarray related study
INTRODUCTION In addition to the well-known short noncoding RNAs such as microRNAs (miRNAs), increasing evidence suggests that… (More)
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2009
2009
Study of gene-targeted mouse models of splicing factor gene Prpf31 implicated in human autosomal dominant retinitis pigmentosa (RP).
PURPOSE Pre-mRNA processing factor 31 (PRPF31) is a ubiquitous protein needed for the assembly of the pre-mRNA splicing machinery… (More)
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2006
2006
TPM3/PDGFRB fusion transcript and its reciprocal in chronic eosinophilic leukemia
Using metaphase fluorescence in situ hybridization (FISH) to narrow translocation breakpoints and polymerase chain reaction (PCR… (More)
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2004
2004
Elucidation of a cryptic interstitial 7q31.3 deletion in a patient with a language disorder and mild mental retardation by array-CGH.
We report on a 14-year-old boy who presented with bilateral cleft lip and palate, hearing loss, a language processing disorder… (More)
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2004
2004
Subtelomere specific microarray based comparative genomic hybridisation: a rapid detection system for cryptic rearrangements in idiopathic mental retardation.
N Harada, E Hatchwell, N Okamoto, M Tsukahara, K Kurosawa, H Kawame, T Kondoh, H Ohashi, R Tsukino, Y Kondoh, O Shimokawa, T Ida… (More)
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2003
2003
Expression of PRPF31 mRNA in patients with autosomal dominant retinitis pigmentosa: a molecular clue for incomplete penetrance?
PURPOSE To investigate whether the incomplete penetrance phenotype characteristic of adRP families linked to chromosome 19q13.4… (More)
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2002
2002
Double minute chromosomes in acute myeloid leukemia and myelodysplastic syndrome: identification of new amplification regions by fluorescence in situ hybridization and spectral karyotyping.
Double minute chromosomes (dmin) are small chromatin bodies consisting of genes amplified in an extrachromosomal location. dmins… (More)
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