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Cancer Research, ISSN 0008-5472, 07/2017, Volume 77, Issue 13 Supplement, pp. 3360 - 3360
Journal Article
Oncotarget, ISSN 1949-2553, 2018, Volume 9, Issue 8, pp. 7844 - 7858
Glioblastoma presents as a heterogeneous disease with poor prognosis despite the use of multimodal therapy. Analysis of genomic DNA changes between initial... 
Tumor heterogeneity | Selection pressure | Neutral evolution | Glioblastoma | Mutation profiling
Journal Article
Neuro-Oncology, ISSN 1522-8517, 11/2017, Volume 19, Issue suppl_6, pp. vi190 - vi191
Malignant Rhabdoid Tumor (MRT) is a rare pediatric cancer predominant in the kidney and CNS that is resistant to current treatment regimes. MRT is genetically... 
Abstracts
Journal Article
Journal Article
Clinical Epigenetics, ISSN 1868-7075, 08/2018, Volume 10, Issue 1, pp. 114 - 13
Background: Beckwith-Wiedemann syndrome (BWS) is an imprinting disorder with a population frequency of approximately 1 in 10,000. The most common epigenetic... 
Beckwith-Wiedemann syndrome | DNA methyltransferase 1 | Methylation | One-carbon pathway | METHYLENETETRAHYDROFOLATE-REDUCTASE GENE | NEURAL-TUBE DEFECTS | CRYSTAL-STRUCTURE | HUMAN METHIONINE SYNTHASE | 5,10-METHYLENETETRAHYDROFOLATE REDUCTASE | COMMON MUTATION | VASCULAR-DISEASE | ONCOLOGY | PREIMPLANTATION DEVELOPMENT | CANCER-RISK | IN-VITRO FERTILIZATION | Genomic Imprinting | Humans | Male | Beckwith-Wiedemann Syndrome - metabolism | Mutation, Missense | Beckwith-Wiedemann Syndrome - genetics | DNA Methylation | DNA (Cytosine-5-)-Methyltransferase 1 - genetics | Metabolic Networks and Pathways | Methylenetetrahydrofolate Reductase (NADPH2) - genetics | Folic Acid - metabolism | Female | Polymorphism, Single Nucleotide | HeLa Cells | Potassium Channels, Voltage-Gated - genetics | Genetic disorders | Research | Genetic variation | DNA | Methyltransferase | Genomes | Methylenetetrahydrofolate reductase | Methionine adenosyltransferase | Folic acid | Enzymatic activity | Vitamin B | Imprinting | DNA methylation | Potassium channels (voltage-gated) | Genetic factors | Cystathionine b-synthase | Deoxyribonucleic acid--DNA | Crystal structure | 5-Methyltetrahydrofolate-homocysteine S-methyltransferase | DNMT1 protein | Methionine | KCNQ1OT1 protein | Genetic diversity | Dietary intake | Homocysteine S-methyltransferase | Infertility | Stem cells | Epigenetics | Mutation | Homocysteine
Journal Article
PLoS ONE, ISSN 1932-6203, 02/2009, Volume 4, Issue 2, p. e4482
Journal Article
Journal Article
Journal Article
Journal of Cancer Epidemiology, ISSN 1687-8558, 2014, Volume 2014, pp. 806076 - 4
We determined the extent and distribution of cancers in relatives of 379 children newly diagnosed with cancer. Family history was collected from 1,337... 
Prognosis | Research | Demographic aspects | Risk factors | Cancer | Cancer in children
Journal Article
Neuro-Oncology, ISSN 1522-8517, 11/2011, Volume 13, pp. 102 - 102
Journal Article
Journal of Medical Genetics, ISSN 0022-2593, 07/1999, Volume 36, Issue 7, pp. 524 - 531
In this study, we have examined CDKN1C expression in BWS patients with allele imbalance (AI) affecting the 11p15 region. Two of two informative patients with... 
CDKN1C | Allele imbalance | Beckwith-Wiedemann syndrome | WT1 GENE | GENETICS & HEREDITY | allele imbalance | IGF2 | GENE P57(KIP2) | MUTATIONS | DEPENDENT KINASE INHIBITOR | WILMS-TUMOR | DELETION | Signal transduction | Genotype & phenotype | Genes | Cell cycle | Mutation | Chromosomes | Patients
Journal Article
Journal Article