RFC-180G>A Polymorphism in Case-Mother/Control-Mother Dyads Is Associated with Risk of Nephroblastoma and Neuroblastoma-Reference-Cited by-同舟云学术

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RFC-180G>A Polymorphism in Case-Mother/Control-Mother Dyads Is Associated with Risk of Nephroblastoma and Neuroblastoma

Published:2015-02 Issue:2 Volume:19 Page:75-81
ISSN:1945-0265
Container-title:Genetic Testing and Molecular Biomarkers
language:en
Short-container-title:Genetic Testing and Molecular Biomarkers

Author:

Montalvão-de-Azevedo Rafaela¹,Vasconcelos Gisele M.¹,Vargas Fernando R.²,Thuler Luiz Claudio³,Pombo-de-Oliveira Maria S.¹,de Camargo Beatriz¹,

Affiliation:

1. Pediatric Hematology-Oncology Research Program, Instituto Nacional de Câncer, Rio de Janeiro, Brazil.

2. Genetic Program, Research Center, Instituto Nacional de Câncer, Rio de Janeiro, Brazil.

3. Research Center, Clinical Research Program, Instituto Nacional de Câncer, Rio de Janeiro, Brazil.

Publisher

Mary Ann Liebert Inc

Subject

Genetics(clinical),General Medicine

Link

http://www.liebertpub.com/doi/pdf/10.1089/gtmb.2014.0177

Reference29 articles.

1. Prevention of Neural-Tube Defects with Folic Acid in China

2. Folate deficiency causes uracil misincorporation into human DNA and chromosome breakage: Implications for cancer and neuronal damage

3. Association between theMTHFRA1298C polymorphism and increased risk of acute myeloid leukemia in Brazilian children

4. MTR polymorphic variant A2756G and retinoblastoma risk in Brazilian children

Cited by 7 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Influence of maternal folate depletion on Art3 DNA methylation in the murine adult brain; potential consequences for brain and neurocognitive health;Mutagenesis;2024-02-28

2. Decisive evidence corroborates a null relationship between MTHFR C677T and chronic kidney disease;Medicine;2020-07-17

3. In silico analysis of the structural and functional implications of SLC19A1 R27H polymorphism;Journal of Genetics;2019-08-23

4. Maternal Haplotypes in DHFR Promoter and MTHFR Gene in Tuning Childhood Acute Lymphoblastic Leukemia Onset-Latency: Genetic/Epigenetic Mother/Child Dyad Study (GEMCDS);Genes;2019-08-22

5. Base Excision Repair Gene Polymorphisms and Wilms Tumor Susceptibility;EBioMedicine;2018-07

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