Search Results - "Li, Jiaoxing"
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1
Unilateral Upper Cervical Posterior Spinal Cord Infarction Caused by Spontaneous Bilateral Vertebral Artery Dissection
Published in Neurology (13-09-2022)Get full text
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2
N6-Methyladenosine RNA modification in cerebrospinal fluid as a novel potential diagnostic biomarker for progressive multiple sclerosis
Published in Journal of translational medicine (22-07-2021)“…Abstract Background Progressive multiple sclerosis (PMS) is an uncommon and severe subtype of MS that worsens gradually and leads to irreversible disabilities…”
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3
Development and Validation of a Five-Gene Signature to Predict Relapse-Free Survival in Multiple Sclerosis
Published in Frontiers in neurology (03-12-2020)“…Multiple sclerosis (MS) is an inflammatory and demyelinating disease of the central nervous system with a variable natural history of relapse and remission…”
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4
Prevalence of RNF213 variants in symptomatic intracranial arterial stenosis/occlusion in China
Published in Molecular genetics and genomics : MGG (01-05-2020)“…The ring finger protein 213 gene ( RNF213 ) rs112735431 was significantly associated with intracranial artery stenosis/occlusion disease (ICASO) in Japan and…”
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5
AND score: a simple tool for predicting infection in acute ischemic stroke patients without a ventilator in the Chinese population
Published in Journal of international medical research (01-03-2020)“…Objective We aimed to develop a simple and user-friendly scoring system to predict all-cause hospital-acquired infections (HAIs) after acute ischemic stroke…”
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6
Mutation of rnf213a by TALEN causes abnormal angiogenesis and circulation defects in zebrafish
Published in Brain research (01-08-2016)“…Abstract Moyamoya disease (MMD) is characterized by a stenosis at the terminal of the internal carotid artery and an abnormal vascular network at the base of…”
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Bilateral cerebral infarction associated with severe arteriosclerosis in the A1 segment: a case report
Published in Journal of international medical research (01-03-2019)“…Large artery atherosclerosis and cardioembolism are the two major subtypes of ischemic stroke. We herein describe a 75-year-old man with acute complete…”
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8
Efficacy and Safety of Antiplatelet Agents for Adult Patients With Ischemic Moyamoya Disease
Published in Frontiers in neurology (15-01-2021)“…The use of antiplatelet agents in ischemic moyamoya disease (MMD) is controversial. This study aimed to investigate the effectiveness and safety of…”
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Interactions among Candidate Genes Selected by Meta-Analyses Resulting in Higher Risk of Ischemic Stroke in a Chinese Population
Published in PloS one (28-12-2015)“…Ischemic stroke (IS) is a multifactorial disorder caused by both genetic and environmental factors. The combined effects of multiple susceptibility genes might…”
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10
ABCB1 C3435T polymorphism and risk of adverse clinical events in clopidogrel treated patients: A meta-analysis
Published in Thrombosis research (01-06-2012)“…Abstract Introduction The ABCB1 C3435T polymorphism limits oral bioavailability of clopidogrel and may influence prognosis of patients treated with…”
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Association between 1425G/A SNP in PRKCH and ischemic stroke among Chinese and Japanese populations: A meta-analysis including 3686 cases and 4589 controls
Published in Neuroscience letters (06-01-2012)“…► All studies evaluating 1425G/A SNP in PRKCH and ischemic stroke were identified. ► We performed a comprehensive meta-analysis in Chinese and Japanese…”
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12
Development and Validation of a Nomogram to Predict the Individual Future Stroke Risk for Adult Patients With Moyamoya Disease: A Multicenter Retrospective Cohort Study in China
Published in Frontiers in neurology (13-05-2021)“…Background: Studies exploring the predictive performance of major risk factors associated with future stroke events are insufficient, and a useful tool to…”
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13
The -7351C/T polymorphism in the TPA gene and ischemic stroke risk: a meta-analysis
Published in PloS one (09-01-2013)“…A number of studies assessed the association of tissue plasminogen activator(TPA) gene polymorphisms with ischemic stroke, but the results were contradictory…”
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14
Decreased Pituitary Height and Stunted Linear Growth After Radiotherapy in Survivors of Childhood Nasopharyngeal Carcinoma Cases
Published in Frontiers in endocrinology (Lausanne) (19-11-2018)“…To examine the morphological changes of the pituitary glands and linear growth of childhood nasopharyngeal carcinoma (NPC) cases who accepted radiotherapy. A…”
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RNF213 loss-of-function promotes pathological angiogenesis in moyamoya disease via the Hippo pathway
Published in Brain (London, England : 1878) (02-11-2023)“…Abstract Moyamoya disease is an uncommon cerebrovascular disorder characterized by steno-occlusive changes in the circle of Willis and abnormal vascular…”
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16
Mapping cell diversity in human sporadic cerebral cavernous malformations
Published in Gene (05-10-2024)“…•We performed in-depth single-cell RNA sequencing and ATAC-seq in SCCM and control patients.•We identified six cell types in the SCCM and control vessels and…”
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Rnf-213 Knockout Induces Pericyte Reduction and Blood-Brain Barrier Impairment in Mouse
Published in Molecular neurobiology (01-11-2023)“…Moyamoya disease (MMD) is a rare cerebrovascular disorder characterized by progressive occlusion of the internal carotid artery and the formation of an…”
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Thymectomy is a beneficial therapy for patients with non-thymomatous ocular myasthenia gravis: a systematic review and meta-analysis
Published in Neurological sciences (01-10-2017)“…Ocular myasthenia gravis, an autoimmune disease, is characterized by extraocular muscle weakness. Myasthenia gravis is closely associated with the functional…”
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Bioinformatic Analysis of Coexpressed Differentially Expressed Genes and Potential Targets for Intracerebral and Subarachnoid Hemorrhage
Published in World neurosurgery (01-03-2022)“…Secondary brain injury following intracerebral hemorrhage (ICH) and subarachnoid hemorrhage (SAH) is life threatening, and effective therapeutic strategies are…”
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Mutations of RNF213 are responsible for sporadic cerebral cavernous malformation and lead to a mulberry-like cluster in zebrafish
Published in Journal of cerebral blood flow and metabolism (01-06-2021)“…Although familial forms of cerebral cavernous malformation are mainly attributed to three CCM genes (KRIT1, CCM2 and PDCD10), no mutation is identified in…”
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