Epigenetic and copy number variation analysis in retinoblastoma by MS-MLPA. - Wikidata - wikimedia - TriplyDB

Epigenetic and copy number variation analysis in retinoblastoma by MS-MLPA.

Epigenetic and copy number variation analysis in retinoblastoma by MS-MLPA.

http://www.wikidata.org/entity/Q46043772

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Orchestrating epigenetic roles targeting ocular tumors Epigenetics and Common Ophthalmic Diseases Diagnostic utility of MS-MLPA in DNA methylation profiling of adenocarcinomas and neuroendocrine carcinomas of the colon-rectum.Gestational hypoxia and epigenetic programming of brain development disorders.Molecular subtypes in stage II-III colon cancer defined by genomic instability: early recurrence-risk associated with a high copy-number variation and loss of RUNX3 and CDKN2A.Retinoic Acid Signaling Regulates Differential Expression of the Tandemly-Duplicated Long Wavelength-Sensitive Cone Opsin Genes in Zebrafish Increased incidence and disparity of diagnosis of retinoblastoma patients in Guatemala A Tox21 Approach to Altered Epigenetic Landscapes: Assessing Epigenetic Toxicity Pathways Leading to Altered Gene Expression and Oncogenic Transformation In Vitro Time-course gene profiling and networks in demethylated retinoblastoma cell line.Epigenetics in ocular diseases.Multiplexed methylation profiles of tumor suppressor genes and clinical outcome in oligodendroglial tumors.Epigenetic-dependent regulation of drug transport and metabolism: an update.More epigenetic hits than meets the eye: microRNAs and genes associated with the tumorigenesis of retinoblastoma.Epigenetic regulation of hypoxia inducible factor in diseases and therapeutics.The genomic landscape of retinoblastoma: a review.Screening for large rearrangements of the RB1 gene in Iranian patients with retinoblastoma using multiplex ligation-dependent probe amplification.Global patterns of large copy number variations in the human genome reveal complexity in chromosome organization.DNA methylation at the 9p21 glaucoma susceptibility locus is associated with normal-tension glaucoma.

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Epigenetic and copy number variation analysis in retinoblastoma by MS-MLPA.

http://www.wikidata.org/entity/Q46043772

description

2012 nî lūn-bûn

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2012年の論文

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2012年学术文章

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2012年学术文章

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2012年学术文章

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2012年学术文章

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2012年学术文章

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2012年學術文章

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2012年學術文章

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name

Epigenetic and copy number variation analysis in retinoblastoma by MS-MLPA.

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Epigenetic and copy number variation analysis in retinoblastoma by MS-MLPA.

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type

label

Epigenetic and copy number variation analysis in retinoblastoma by MS-MLPA.

@en

Epigenetic and copy number variation analysis in retinoblastoma by MS-MLPA.

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prefLabel

Epigenetic and copy number variation analysis in retinoblastoma by MS-MLPA.

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Epigenetic and copy number variation analysis in retinoblastoma by MS-MLPA.

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Pathology Oncology Research

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Epigenetic and copy number variation analysis in retinoblastoma by MS-MLPA.

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Alessandra Renieri

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Alfonso D'Ambrosio

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Annabella Marozza

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Francesca Ariani

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Gabriella Livide

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Maria Antonietta Mencarelli

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Maria Carmela Epistolato

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Mariangela Amenduni

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Paolo Toti

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Sonia De Francesco

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P2860

Chfr defines a mitotic stress checkpoint that delays entry into metaphase

Association of hereditary nonpolyposis colorectal cancer-related tumors displaying low microsatellite instability with MSH6 germline mutations.

Sensitive and efficient detection of RB1 gene mutations enhances care for families with retinoblastoma

Mutation and cancer: statistical study of retinoblastoma

GATA-4 and GATA-5 transcription factor genes and potential downstream antitumor target genes are epigenetically silenced in colorectal and gastric cancer

Methylation-specific MLPA (MS-MLPA): simultaneous detection of CpG methylation and copy number changes of up to 40 sequences

Familial endometrial cancer in female carriers of MSH6 germline mutations

Aberrant promoter methylation and silencing of the RASSF1A gene in pediatric tumors and cell lines

TSLC1 is a tumor-suppressor gene in human non-small-cell lung cancer

The H-cadherin (CDH13) gene is inactivated in human lung cancer

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