Structural analysis of human NHLRC2, mutations of which are associated with FINCA disease-Reference-Cited by-同舟云学术

Structural analysis of human NHLRC2, mutations of which are associated with FINCA disease

Published:2018-08-23 Issue:8 Volume:13 Page:e0202391
ISSN:1932-6203
Container-title:PLOS ONE
language:en
Short-container-title:PLoS ONE

Author:

Biterova Ekaterina,Ignatyev Alexander,Uusimaa Johanna,Hinttala Reetta,Ruddock Lloyd W.^ORCID

Funder

Academy of Finland

Biocenter Oulu

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference53 articles.

1. ROS-induced cleavage of NHLRC2 by caspase-8 leads to apoptotic cell death in the HCT116 human colon cancer cell line;K Nishi;Cell Death Dis,2017

2. NHLRC2 variants identified in patients with fibrosis, neurodegeneration, and cerebral angiomatosis (FINCA): characterisation of a novel cerebropulmonary disease;J Uusimaa;Acta Neuropathol,2018

3. A novel repeat domain that is often associated with RING finger and B-box motifs;FJ Slack;Trends Biochem Sci,1998

4. TRIM-NHL proteins in development and disease;C Tocchini;Semin Cell Dev Biol,2015

5. Discovery of Novel Biomarkers for Alzheimer’s Disease from Blood;J Long;Dis Markers,2016

Cited by 18 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. Case Report: Clinical manifestations and treatment of two Chinese patients with FINCA syndrome carrying a novel variant of NHLRC2;Frontiers in Pediatrics;2024-09-12

2. FINCA disease mouse model exhibits altered behaviour and immune response;2024-06-14

3. Broadening the phenotypic and molecular spectrum of FINCA syndrome: Biallelic NHLRC2 variants in 15 novel individuals;European Journal of Human Genetics;2023-05-15

4. Novel patients with NHLRC2 variants expand the phenotypic spectrum of FINCA disease;Frontiers in Neuroscience;2023-04-27

5. FINCA syndrome beyond pulmonary affection: biallelic NHLRC2 variants in eight families with intellectual disability and epilepsy;2022-11-11