Constitutional translocation breakpoint mapping by genome-wide paired-end sequencing identifies HACE1 as a putative Wilms tumour susceptibility gene-Reference-Cited by-同舟云学术

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Constitutional translocation breakpoint mapping by genome-wide paired-end sequencing identifies HACE1 as a putative Wilms tumour susceptibility gene

Published:2009-11-30 Issue:5 Volume:47 Page:342-347
ISSN:0022-2593
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Slade I.,Stephens P.,Douglas J.,Barker K.,Stebbings L.,Abbaszadeh F.,Pritchard-Jones K.,Cole R.,Pizer B.,Stiller C.,Vujanic G.,Scott R. H.,Stratton M. R.,Rahman N.,

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Cited by 44 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. The HACE1 E3 ligase mediates RAC1‐dependent control of mTOR signaling complexes;EMBO reports;2023-10-17

2. Chromosome 6;Cancer Genes;2023-07-09

3. In silico assessment of DNA damage response gene variants associated with head and neck cancer;Journal of Biomolecular Structure and Dynamics;2022-01-17

4. HACE1-mediated NRF2 activation causes enhanced malignant phenotypes and decreased radiosensitivity of glioma cells;Signal Transduction and Targeted Therapy;2021-11-24

5. Wilms tumour surveillance in at-risk children: Literature review and recommendations from the SIOP-Europe Host Genome Working Group and SIOP Renal Tumour Study Group;European Journal of Cancer;2021-08

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