Functional pri-miR-34b/c rs4938723 and KRAS 3′UTR rs61764370 SNPs: Novel phenotype modifiers in Li-Fraumeni Syndrome?-Reference-Cited by-同舟云学术

Functional pri-miR-34b/c rs4938723 and KRAS 3′UTR rs61764370 SNPs: Novel phenotype modifiers in Li-Fraumeni Syndrome?

Published:2024-03 Issue: Volume:898 Page:148069
ISSN:0378-1119
Container-title:Gene
language:en
Short-container-title:Gene

Author:

Vieira Igor Araujo,Pezzi Eduarda Heidrich,Bandeira Isabel Cristina,Reis Larissa Brussa,de Araújo Rocha Yasminne Marinho,Fernandes Bruna Vieira,Siebert Marina,Miyamoto Kendi Nishino,Siqueira Monique Banik,Achatz Maria I.,Galvão Henrique de Campos Reis,Garcia Felipe Antonio de Oliveira,Campacci Natalia,Carraro Dirce Maria,Formiga Maria Nirvana,Vianna Fernanda Sales Luiz,Palmero Edenir Inez,Macedo Gabriel S.,Ashton-Prolla Patricia

Publisher

Elsevier BV

Subject

Genetics,General Medicine

Reference79 articles.

1. The TP53 mutation, R337H, is associated with Li-Fraumeni and Li-Fraumeni-like syndromes in Brazilian families;Achatz;Cancer Lett.,2007

2. The inherited p53 mutation in the Brazilian population;Achatz;Cold Spring Harb. Perspect. Med.,2016

3. let-7 microRNA functions as a potential growth suppressor in human colon cancer cells;Akao;Biol. Pharm. Bull.,2006

4. The functions of animal microRNAs;Ambros;Nature,2004

5. 1000 Genomes Project Consortium, Auton A, Brooks LD et al (2015) A global reference for human genetic variation. Nature 526:68–74. https://doi.org/10.1038/nature15393.

Cited by 1 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. AI-guided identification of risk variants for adrenocortical tumours in TP53 p.R337H carrier children: a genetic association study;The Lancet Regional Health - Americas;2024-10