Six novel rare non-synonymous mutations for migraine without aura identified by exome sequencing
出版年份 2015 全文链接
标题
Six novel rare non-synonymous mutations for migraine without aura identified by exome sequencing
作者
关键词
-
出版物
JOURNAL OF NEUROGENETICS
Volume 29, Issue 4, Pages 188-194
出版商
Informa UK Limited
发表日期
2016-01-27
DOI
10.3109/01677063.2015.1122787
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。- The association between candidate migraine susceptibility loci and severe migraine phenotype in a clinical sample
- (2015) Ann-Louise Esserlind et al. CEPHALALGIA
- Migraine pathophysiology: lessons from mouse models and human genetics
- (2015) Michel D Ferrari et al. LANCET NEUROLOGY
- Replication of Migraine GWAS Susceptibility Loci in Chinese Han Population
- (2014) Xiaoping Fan et al. HEADACHE
- Migraine genetics: current findings and future lines of research
- (2014) A. M. Persico et al. NEUROGENETICS
- Investigation of the male pattern baldness major genetic susceptibility loci AR/EDA2R and 20p11 in female pattern hair loss
- (2012) S. Redler et al. BRITISH JOURNAL OF DERMATOLOGY
- Association analysis of TNFRSF1B polymorphism with susceptibility for migraine in the Chinese Han population
- (2012) Wanli Dong et al. JOURNAL OF CLINICAL NEUROSCIENCE
- Confirmation that Xq27 and Xq28 are susceptibility loci for migraine in independent pedigrees and a case-control cohort
- (2012) B. H. Maher et al. NEUROGENETICS
- Rho-kinase: important new therapeutic target in cardiovascular diseases
- (2011) Kimio Satoh et al. AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY
- Brainstem changes in 5-HT1A receptor availability during migraine attack
- (2010) G Demarquay et al. CEPHALALGIA
- A Novel Locus for Familial Migraine on Xp22
- (2010) Thomas Wieser et al. HEADACHE
- Crosstalk of EDA-A2/XEDAR in the p53 Signaling Pathway
- (2010) C. Tanikawa et al. MOLECULAR CANCER RESEARCH
- Evidence of shared genetic risk factors for migraine and rolandic epilepsy
- (2009) Tara Clarke et al. EPILEPSIA
- Targeted capture and massively parallel sequencing of 12 human exomes
- (2009) Sarah B. Ng et al. NATURE
- Exome sequencing identifies the cause of a mendelian disorder
- (2009) Sarah B Ng et al. NATURE GENETICS
- XEDAR as a putative colorectal tumor suppressor that mediates p53-regulated anoikis pathway
- (2009) C Tanikawa et al. ONCOGENE
- Genetic diagnosis by whole exome capture and massively parallel DNA sequencing
- (2009) Murim Choi et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Migraine: Sex-influenced trait model?
- (2008) Xiao-Ping Wang et al. MEDICAL HYPOTHESES
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