Phenotypes and malignancy risk of different FUS mutations in genetic amyotrophic lateral sclerosis
出版年份 2019 全文链接
标题
Phenotypes and malignancy risk of different
FUS
mutations in genetic amyotrophic lateral sclerosis
作者
关键词
-
出版物
Annals of Clinical and Translational Neurology
Volume 6, Issue 12, Pages 2384-2394
出版商
Wiley
发表日期
2019-11-04
DOI
10.1002/acn3.50930
参考文献
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注意:仅列出部分参考文献,下载原文获取全部文献信息。- Comprehensive analysis of the mutation spectrum in 301 German ALS families
- (2018) Kathrin Müller et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- Impaired DNA damage response signaling by FUS-NLS mutations leads to neurodegeneration and FUS aggregate formation
- (2018) Marcel Naumann et al. Nature Communications
- Epidemiology of amyotrophic lateral sclerosis in Southern Germany
- (2017) Angela Rosenbohm et al. JOURNAL OF NEUROLOGY
- Amyotrophic Lateral Sclerosis
- (2017) Robert H. Brown et al. NEW ENGLAND JOURNAL OF MEDICINE
- A novel mutation of the C-terminal amino acid of FUS (Y526C) strengthens FUS gene as the most frequent genetic factor in aggressive juvenile ALS
- (2017) Philippe Corcia et al. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
- Mechanisms of FUS mutations in familial amyotrophic lateral sclerosis
- (2016) Yulei Shang et al. BRAIN RESEARCH
- Genotype-phenotype relationships in familial amyotrophic lateral sclerosis withFUS/TLSmutations in Japan
- (2016) Tetsuya Akiyama et al. MUSCLE & NERVE
- FUS Mislocalization and Vulnerability to DNA Damage in ALS Patients Derived hiPSCs and Aging Motoneurons
- (2016) Julia Higelin et al. Frontiers in Cellular Neuroscience
- Ataxia-telangiectasia — A historical review and a proposal for a new designation: ATM syndrome
- (2015) Hélio A.G. Teive et al. JOURNAL OF THE NEUROLOGICAL SCIENCES
- De novo FUS mutations are the most frequent genetic cause in early-onset German ALS patients
- (2015) Annemarie Hübers et al. NEUROBIOLOGY OF AGING
- ALS-associated mutation FUS-R521C causes DNA damage and RNA splicing defects
- (2014) Haiyan Qiu et al. JOURNAL OF CLINICAL INVESTIGATION
- TARDBPandFUSMutations Associated with Amyotrophic Lateral Sclerosis: Summary and Update
- (2013) Serena Lattante et al. HUMAN MUTATION
- Interaction of FUS and HDAC1 regulates DNA damage response and repair in neurons
- (2013) Wen-Yuan Wang et al. NATURE NEUROSCIENCE
- State of play in amyotrophic lateral sclerosis genetics
- (2013) Alan E Renton et al. NATURE NEUROSCIENCE
- Amyotrophic lateral sclerosis and cancer: A register-based study in Sweden
- (2013) Fang Fang et al. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
- Truncating mutations inFUS/TLSgive rise to a more aggressive ALS-phenotype than missense mutations: a clinico-genetic study in Germany
- (2012) S. Waibel et al. EUROPEAN JOURNAL OF NEUROLOGY
- Cancer incidence in patients with polyglutamine diseases: a population-based study in Sweden
- (2012) Jianguang Ji et al. LANCET ONCOLOGY
- Lymphoid tumours and breast cancer in ataxia telangiectasia; substantial protective effect of residual ATM kinase activity against childhood tumours
- (2011) A Reiman et al. BRITISH JOURNAL OF CANCER
- P525L FUS mutation is consistently associated with a severe form of juvenile Amyotrophic Lateral Sclerosis
- (2011) Amelia Conte et al. NEUROMUSCULAR DISORDERS
- German cancer statistics 2004
- (2010) Jörg Haberland et al. BMC CANCER
- Parkinson’s disease and cancer risk: a systematic review and meta-analysis
- (2010) Archna Bajaj et al. CANCER CAUSES & CONTROL
- Mutant FUS proteins that cause amyotrophic lateral sclerosis incorporate into stress granules
- (2010) Daryl A. Bosco et al. HUMAN MOLECULAR GENETICS
- TDP-43 and FUS/TLS: emerging roles in RNA processing and neurodegeneration
- (2010) C. Lagier-Tourenne et al. HUMAN MOLECULAR GENETICS
- Prognostic factors in ALS: A critical review
- (2009) Adriano Chiò et al. Amyotrophic Lateral Sclerosis
- The occurrence of mutations inFUSin a Belgian cohort of patients with familial ALS
- (2009) P. Van Damme et al. EUROPEAN JOURNAL OF NEUROLOGY
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