The Susceptibility Pathogenesis of Moyamoya Disease

scientific article published on 30 January 2017

The Susceptibility Pathogenesis of Moyamoya Disease is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1016/J.WNEU.2017.01.083
P698PubMed publication ID28153617

P2093author name stringJie Luo
Qianxue Chen
Juntao Hu
P2860cites workTemporal profile of the vascular anatomy evaluated by 9.4-T magnetic resonance angiography and histopathological analysis in mice lacking RNF213: a susceptibility gene for moyamoya diseaseQ87123847
The moyamoya disease susceptibility variant RNF213 R4810K (rs112735431) induces genomic instability by mitotic abnormalityQ87340542
Identification of RNF213 as a susceptibility gene for moyamoya disease and its possible role in vascular developmentQ24317590
A genome-wide association study identifies RNF213 as the first Moyamoya disease gene.Q34147943
Mapping of a familial moyamoya disease gene to chromosome 3p24.2-p26.Q34388898
The role of VEGF and KDR polymorphisms in moyamoya disease and collateral revascularizationQ34450594
Molecular analysis of RNF213 gene for moyamoya disease in the Chinese Han populationQ34461040
Prevalence and clinicoepidemiological features of moyamoya disease in Japan: findings from a nationwide epidemiological surveyQ34720010
The promise of minocycline in neurology.Q35958974
Moyamoya disease: current concepts and future perspectivesQ37305024
Outer-diameter narrowing of the internal carotid and middle cerebral arteries in moyamoya disease detected on 3D constructive interference in steady-state MR image: is arterial constrictive remodeling a major pathogenesis?Q40060007
Matrix metalloproteinase-9 pretreatment level predicts intracranial hemorrhagic complications after thrombolysis in human stroke.Q40607050
Lessons learned from moyamoya disease: outcome of direct/indirect revascularization surgery for 150 affected hemispheresQ44112798
Ablation of Rnf213 retards progression of diabetes in the Akita mouseQ45164699
Downregulation of Securin by the variant RNF213 R4810K (rs112735431, G>A) reduces angiogenic activity of induced pluripotent stem cell-derived vascular endothelial cells from moyamoya patients.Q48014638
Early appearance of activated matrix metalloproteinase-9 and blood-brain barrier disruption in mice after focal cerebral ischemia and reperfusionQ48087981
Temporary neurologic deterioration due to cerebral hyperperfusion after superficial temporal artery-middle cerebral artery anastomosis in patients with adult-onset moyamoya diseaseQ48263056
Epidemiological and clinical features of Moyamoya disease in Nanjing, ChinaQ48381792
Ultrastructural studies of cerebral arteries and collateral vessels in moyamoya diseaseQ48651322
Histopathology of the brain vascular network in moyamoya diseaseQ48810229
Cerebrovascular "moyamoya" disease. Disease showing abnormal net-like vessels in base of brainQ49052312
Plasma matrix metalloproteinases, cytokines and angiogenic factors in moyamoya disease.Q52597321
Predictors and clinical features of postoperative hyperperfusion after surgical revascularization for moyamoya disease: a serial single photon emission CT/positron emission tomography study.Q53148379
Significance of focal cerebral hyperperfusion as a cause of transient neurologic deterioration after extracranial-intracranial bypass for moyamoya disease: comparative study with non-moyamoya patients using N-isopropyl-p-[(123)I]iodoamphetamine singQ53250907
Incidence and risk factors for symptomatic cerebral hyperperfusion after superficial temporal artery-middle cerebral artery anastomosis in patients with moyamoya disease.Q53413414
Transient hyperperfusion after superficial temporal artery/middle cerebral artery bypass surgery as a possible cause of postoperative transient neurological deterioration.Q53540015
Linkage of Familial Moyamoya Disease (Spontaneous Occlusion of the Circle of Willis) to Chromosome 17q25Q57269479
Homozygous c.14576G>A variant of RNF213 predicts early-onset and severe form of moyamoya disease.Q59697640
Worldwide Distribution of Moyamoya DiseaseQ67466822
Cerebral haemorrhage in Moyamoya disease at autopsyQ70891849
Angiogenic factors in moyamoya diseaseQ71905100
Moyamoya diseaseQ73090978
Remodeling of carotid artery is associated with increased expression of matrix metalloproteinases in mouse blood flow cessation modelQ73265468
Linkage analysis of moyamoya disease on chromosome 6Q73658136
Remodeling with neointima formation in the mouse carotid artery after cessation of blood flowQ73832982
Histological features of middle cerebral arteries from patients treated for Moyamoya diseaseQ79632750
A novel susceptibility locus for moyamoya disease on chromosome 8q23Q80553325
Increased expression of hepatocyte growth factor in cerebrospinal fluid and intracranial artery in moyamoya diseaseQ80968092
Increased expression of serum Matrix Metalloproteinase-9 in patients with moyamoya diseaseQ83193829
Increased thyroid function and elevated thyroid autoantibodies in pediatric patients with moyamoya disease: a case-control studyQ83474001
Guidelines for diagnosis and treatment of moyamoya disease (spontaneous occlusion of the circle of Willis)Q84745917
Association of thyroid autoantibodies with moyamoya-type cerebrovascular disease: a prospective studyQ84933149
P304page(s)731-741
P577publication date2017-01-30
P1433published inWorld NeurosurgeryQ26853866
P1476titleThe Susceptibility Pathogenesis of Moyamoya Disease
P478volume101

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cites work (P2860)
Q91716470Clinical efficacy of extracranial-intracranial bypass for the treatment of adult patients with moyamoya disease: A protocol of systematic review of randomized controlled trials
Q57170001MinION rapid sequencing: Review of potential applications in neurosurgery
Q55340113Moyamoya disease in a Moroccan baby: a case report.
Q88413676Noninvasive Assessment of Hemodynamic Stress Distribution after Indirect Revascularization for Pediatric Moyamoya Vasculopathy
Q58608274Proximal internal carotid artery stenosis associates with diffuse wall thickening in petrous arterial segment of moyamoya disease patients: a three-dimensional magnetic resonance vessel wall imaging study
Q98466910RNF213 gene polymorphism rs9916351 and rs8074015 significantly associated with moyamoya disease in Chinese population

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