Hypermethylation of genomic 3.3-kb repeats is frequent event in HPV-positive cervical cancer. - Wikidata - wikimedia - TriplyDB

Hypermethylation of genomic 3.3-kb repeats is frequent event in HPV-positive cervical cancer.

Hypermethylation of genomic 3.3-kb repeats is frequent event in HPV-positive cervical cancer.

http://www.wikidata.org/entity/Q33453988

about

DNA hypomethylation in cancer cells.DNA polymorphism and epigenetic marks modulate the affinity of a scaffold/matrix attachment region to the nuclear matrix.Diagnostic approach for FSHD revisited: SMCHD1 mutations cause FSHD2 and act as modifiers of disease severity in FSHD1 Cancer-related genes in the transcription signature of facioscapulohumeral dystrophy myoblasts and myotubes.Epigenetic reprogramming of host genes in viral and microbial pathogenesis Hypomethylation of repeated DNA sequences in cancer.Dux4 controls migration of mesenchymal stem cells through the Cxcr4-Sdf1 axis.RASSF2 hypermethylation is present and related to shorter survival in squamous cervical cancer.

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P2860

Hypermethylation of genomic 3.3-kb repeats is frequent event in HPV-positive cervical cancer.

http://www.wikidata.org/entity/Q33453988

description

2009 nî lūn-bûn

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2009 թուականի Մայիսին հրատարակուած գիտական յօդուած

@hyw

2009 թվականի մայիսին հրատարակված գիտական հոդված

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2009年の論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年论文

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name

Hypermethylation of genomic 3. ...... HPV-positive cervical cancer.

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Hypermethylation of genomic 3. ...... HPV-positive cervical cancer.

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type

label

Hypermethylation of genomic 3. ...... HPV-positive cervical cancer.

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Hypermethylation of genomic 3. ...... HPV-positive cervical cancer.

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prefLabel

Hypermethylation of genomic 3. ...... HPV-positive cervical cancer.

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Hypermethylation of genomic 3. ...... HPV-positive cervical cancer.

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BMC Medical Genomics

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Hypermethylation of genomic 3. ...... HPV-positive cervical cancer.

@en

P2093

Alexey N Katargin

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Fjodor L Kisseljov

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Larissa S Pavlova

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Natalia P Kisseljova

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P2860

DUX4, a candidate gene of facioscapulohumeral muscular dystrophy, encodes a transcriptional activator of PITX1

Characterization of a double homeodomain protein (DUX1) encoded by a cDNA homologous to 3.3 kb dispersed repeated elements

The DUX4 gene at the FSHD1A locus encodes a pro-apoptotic protein

Overexpression of a splice variant of DNA methyltransferase 3b, DNMT3b4, associated with DNA hypomethylation on pericentromeric satellite regions during human hepatocarcinogenesis.

The retinoblastoma gene product interacts with maintenance human DNA (cytosine-5) methyltransferase and modulates its activity

Nucleotide sequence of the partially deleted D4Z4 locus in a patient with FSHD identifies a putative gene within each 3.3 kb element

Loss of acetylation at Lys16 and trimethylation at Lys20 of histone H4 is a common hallmark of human cancer

A genetic screen identifies PITX1 as a suppressor of RAS activity and tumorigenicity

Evolutionary conservation of a coding function for D4Z4, the tandem DNA repeat mutated in facioscapulohumeral muscular dystrophy

Hypomethylation of D4Z4 in 4q-linked and non-4q-linked facioscapulohumeral muscular dystrophy

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scholarly article

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10.1186/1755-8794-2-30

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2

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1027782932

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19473516

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2695481

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