Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Cong-Xia Lu"'
Autor:
Wen-Qing Huang, Hui-Ming Ye, Liang-Liang Cai, Qi-Lin Ma, Cong-Xia Lu, Sui-Jun Tong, Chi-Meng Tzeng, Qing Lin
Publikováno v:
Frontiers in Genetics, Vol 10 (2019)
Background: Leukoaraiosis (LA) is shown as white matter hyperintensities on T2-weighted magnetic resonance imaging brain scans. Together with candidate gene association studies (CGAS), multiple genome-wide association studies (GWAS) have reported lar
Externí odkaz:
https://doaj.org/article/85d1b9c995bf4264a1da1ef61de19836
Autor:
Wen-Qing Huang, Cong-Xia Lu, Ya Zhang, Ke-Hui Yi, Liang-Liang Cai, Ming-Li Li, Han Wang, Qing Lin, Chi-Meng Tzeng
Publikováno v:
Frontiers in Aging Neuroscience, Vol 8 (2016)
Background: Cerebral cavernous malformations (CCMs) are common vascular malformations that predominantly arise in the central nervous system and are mainly characterized by enlarged vascular cavities without intervening brain parenchyma. Familial CCM
Externí odkaz:
https://doaj.org/article/5b8ba850a065412fb81661eaaa6d845e
Autor:
Enque Biniam Tesfaye, Liang-Liang Cai, Chi-Meng Tzeng, Hui-Ling Wang, Hsin-Chih Lai, Qing Lin, Ye Zhao, Fanrong Meng, Cong-Xia Lu
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 19, Iss, Pp 398-410 (2020)
Epilepsy affects around 70 million people worldwide, with a 65% rate of unknown etiology. This rate is known as epilepsy of unknown etiology (EUE). Dysregulation of microRNAs (miRNAs) is recognized to contribute to mental disorders, including epileps
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3055a5e2284e0d0c19ea378623cf543b
https://doi.org/10.1016/j.omtm.2020.10.005
https://doi.org/10.1016/j.omtm.2020.10.005
Publikováno v:
Clinical Genetics. 92:143-149
Several genome-wide association studies (GWASs) in Caucasian populations have identified 12 loci that are significantly associated with migraine. More evidence suggests that serotonin receptors are also involved in migraine pathophysiology. In the pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::099eff73cc79507fea05842a447dbb9f
https://doi.org/10.1111/cge.12962
https://doi.org/10.1111/cge.12962
Autor:
Cong-Xia Lu, Qi-Lin Ma, Yi-Hong Zhan, Ning Wang, Cen Yue, Xiao-Rong Zhang, Qi-Cong Luo, Nai-An Xiao
Publikováno v:
Biochemistry (Moscow). 81:591-599
Cadherin is an epidermal growth factor and laminin-G seven-pass G-type receptor 1 (CELSR1) is a key component of the noncanonical Wnt/planar cell polarity (PCP) pathway that critically regulates endothelial cell proliferation and angiogenesis. In thi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0d161db9c3475d2f53d4de913bd4068
https://doi.org/10.1134/s0006297916060055
https://doi.org/10.1134/s0006297916060055
Publikováno v:
Journal of neurology. 264(1)
Migraine is a common and disabling nervous system disease with a significant genetic predisposition. The sex hormones play an important role in the pathogenesis of migraine. However, the conclusions of the previous genetic relation studies are confli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21ca7f39d57e84d9b942ccd08de054cc
https://pubmed.ncbi.nlm.nih.gov/27778160
https://pubmed.ncbi.nlm.nih.gov/27778160
Autor:
Qi-Lin Ma, Bin Cai, Sui-Jun Tong, Wei Wei, Yi-Hong Zhan, Ling Fang, Yi Lin, Ning Wang, Cong-Xia Lu
Recently, CELSR1 was identified by genome-wide association studies (GWAS) as a susceptibility gene for ischaemic stroke (IS) in Japanese individuals.The goal was to examine whether CELSR1 variants are associated with IS in the Chinese Han population.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a407bb6e661812aaccade3e34180f89a
Autor:
Sui-Jun Tong, Qilin Ma, Liang-Liang Cai, Chi-Meng Tzeng, Ke-Hui Yi, Wen-Qing Huang, Hui-Nuan Lin, Jin-Hu Ye, Long Gu, Cong-Xia Lu, Qing Lin
Publikováno v:
Medicine. 96:e7682
Leukoaraiosis (LA) refers to white matter hyperintensities or white matter lesions (WMLs) on magnetic resonance imaging (MRI) scans of the brain; this disease is associated with an increased risk of stroke, dementia, and cognitive decline. The aims o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b527b9c0d3ee2a4236681afc43925983
https://doi.org/10.1097/md.0000000000007682
https://doi.org/10.1097/md.0000000000007682
Publikováno v:
European journal of medical genetics. 57(9)
Wilson's disease (WD) is a rare autosomal recessive genetic disorder of copper metabolism resulting in brain damage, liver failure, and neurological impairment and psychiatric disturbances, as a result of excessive copper accumulation in the brain, l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::308e8c613a9d74c745a06367bcaec175
https://pubmed.ncbi.nlm.nih.gov/24878384
https://pubmed.ncbi.nlm.nih.gov/24878384
Publikováno v:
Headache. 53(10)
Recent genome-wide association studies (GWAS) have identified 3 loci in or near PRDM16 (1p36.32, rs2651899), LRP1 (12q13.3, rs11172113) and TRPM8 (2q37.1, rs10166942) in the population-based Women's Genome Health Study (WGHS) of migraine, and 2 loci
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7bfee55884232bb6f9887bb2f73e216
https://pubmed.ncbi.nlm.nih.gov/24021092
https://pubmed.ncbi.nlm.nih.gov/24021092