Results 131 to 140 of about 92,663 (299)

Missense Variant rs28362680 in BTNL2 Reduces Risk of Coronary Heart Disease

open access: yesPharmacogenomics and Personalized Medicine, 2022
Jian Zhuo,1 Yingchun Wu,2 Wei Li,1 Zerong Li,1 Yipeng Ding,3 Tianbo Jin4,5 1Department of Emergency Service, People’s Hospital of Wanning, Wanning, Hainan, 571500, People’s Republic of China; 2Department of Intensive Care Unit, Hainan General Hospital ...
Zhuo J, Wu Y, Li W, Li Z, Ding Y, Jin T
doaj  

Trends in educational assortative marriage in China from 1970 to 2000 [PDF]

open access: yes
This research examines trends in educational assortative marriage in China among first marriages from 1970 to 2000 using data from the 2000 China Population Census and the 2001 Chinese Demographic Reproductive Health Survey. The results reveal decreasing
Hongyun Han
core  

Innate Immune Reprogramming Mediated by Endogenous Retroelement Dysregulation Drives Multiple Sclerosis Progression

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
Epigenetic reprogramming in hematopoietic stem and progenitor cells (HSPCs) and downstream myeloid cells, mediated by H3.3 downregulation and endogenous retroelement (ERE) overexpression, contributes to the progression of multiple sclerosis (MS). ABSTRACT Background Skewed myelopoiesis in the bone marrow has been identified as a key driver of multiple ...
Li‐Mei Xiao   +6 more
wiley   +1 more source

Location‐Specific Hematoma Volume Predicts Early Neurological Deterioration in Supratentorial ICH

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Early neurological deterioration (END) adversely affects outcomes in patients with intracerebral hemorrhage (ICH). This study aimed to determine the location‐specific hematoma volumes for END in supratentorial ICH patients. Methods We retrospectively analyzed supratentorial ICH patients presenting from two prospective cohorts.
Zuoqiao Li   +10 more
wiley   +1 more source

Polymorphisms of the _ENPP1_ gene are not associated with type 2 diabetes or obesity in the Chinese Han population

open access: yes, 2008
*Objective:* Type 2 Diabetes mellitus is a metabolic disorder characterized by chronic hyperglycemia and with a major feature of insulin resistance. Genetic association studies have suggested that _ENPP1_ might play a potential role in susceptibility to ...
Daizhan Zhou   +11 more
core  

Genetic structure adds power to detect schizophrenia susceptibility at SLIT3 in the Chinese Han population

open access: yes, 2004
The Chinese Han population, the largest population in the world, has traditionally been geographically divided into two parts, the Southern Han and Northern Han. In practice, however, these commonly used ethnic labels are both insufficient and inaccurate
Yu, L   +14 more
core   +1 more source

CSF Monoamine Metabolites and Cognitive Trajectory in Early Parkinson's Disease

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background Imaging and postmortem studies indicate that abnormalities in monoaminergic neurotransmission contribute to cognitive impairment in Parkinson's disease (PD). However, it remains uncertain if cerebrospinal fluid (CSF) monoamine metabolites can serve as biomarkers of cognitive decline in early PD.
Jing‐Yu Shao   +7 more
wiley   +1 more source

Clinical Outcomes of SEEG‐Guided Radiofrequency Thermocoagulation in Children With Focal Drug‐Resistant Epilepsy: A Multicenter Real‐World Study

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Stereoelectroencephalography‐guided radiofrequency thermocoagulation (SEEG‐RFTC) has emerged as a safe and effective minimally invasive treatment for children with drug‐resistant focal epilepsy. Although evidence from real‐world studies remains limited, numerous pediatric cases have demonstrated promising outcomes. This retrospective
Weitao Chen   +7 more
wiley   +1 more source

Association of Genetic Variants in Senataxin and Alzheimer’s Disease in a Chinese Han Population in Taiwan

open access: yes, 2014
[[abstract]]Development of Alzheimer's disease (AD) is characterized by progressive neuronal death and a decline in learning and memory. Mutations in human senataxin (SETX), an ortholog yeast protein of Sen1, have been identified to cause the syndrome of
Che-Piao She(Che-Piao Shen)、Wei-Yong Lin(Wei-Yong Lin)、Ting-Fang Li(Ting-Fang Lin)、Wen-Fu Wang(Wen-Fu Wang)、Chon-Haw Tsa(Chon-Haw Tsai)、Ban-Dar Hsu(Ban-Dar Hsu)、黃志揚(CHIH-YANG HUANG)*、Hsin-Ping Li(Hsin-Ping Liu)、蔡輔仁(Tsai, Fuu-Jen)*
core   +1 more source

RNA Sequencing Resolves Cryptic Pathogenic Variants in Mitochondrial Disease

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Mitochondrial diseases are the most common inherited metabolic disorders, characterized by pronounced clinical and genetic heterogeneity that complicates molecular diagnosis. Although DNA‐based sequencing approaches have become standard in genetic testing, up to half of patients remain without a definitive diagnosis.
Zhimei Liu   +21 more
wiley   +1 more source

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