[PDF] Top 20 The NPC1L1 Polymorphism 1679C>G Is Associated with Gallstone Disease in Chinese Patients.
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The NPC1L1 Polymorphism 1679C>G Is Associated with Gallstone Disease in Chinese Patients.
... heart disease at baseline compared with homozygous carriers of the common alleles, owing to alterations in cholesterol absorption ...that the G allele contrib- utes to increased ... See full document
9
A promoter polymorphism (rs17222919, -1316T/G) of ALOX5AP gene is associated with decreased risk of ischemic stroke in two independent Chinese populations.
... evaluate the ALOX5AP promoter SNP rs17222919 in rela- tion to IS risk and then to validate any promising associations in a second independent popula- ...tion. In the initial ... See full document
11
Gallbladder gallstone disease is associated with newly diagnosed coronary artery atherosclerotic disease: a cross-sectional study.
... and gallstone disease share several common risk factors such as higher total cholesterol and lower HDL cholesterol ...related with CAD even after matching for age, gender and MetS. The ... See full document
7
Adiponectin gene polymorphism rs2241766 T/G is associated with response to pioglitazone treatment in type 2 diabetic patients from southern China.
... outpatients with T2DM. All patients were derived from the Chinese Han population treated at the Department of Endocrinology of the Third Affiliated Hospital of Wenzhou Medical ... See full document
9
A functional polymorphism in the promoter region of microRNA-146a is associated with the risk of Alzheimer disease and the rate of cognitive decline in patients.
... method with Lymphoprep TM (Axis-Shield PoCAS, Oslo, Norway). In brief, blood samples were mixed with equal volume of ...NaCl. The diluted blood was then slowly added to tubes containing a ... See full document
8
Clinics vol.68 número11
... into the potent vasoconstrictor angiotensin II (ang II), inactivating the vasodilator peptide ...of the RAS pathway plays an important role in the develop- ment and perpetuation of AF ... See full document
5
COL9A1 gene polymorphism is associated with Kashin-Beck disease in a northwest Chinese Han population.
... result in a secondary chronic osteoarthropathy [25]. The electron microscopic analysis have confirmed the chondrocyte necrosis and revealed a reduction in the collagen fibril diameter, ... See full document
11
A Common Polymorphism of the Human Cardiac Sodium Channel Alpha Subunit (SCN5A) Gene Is Associated with Sudden Cardiac Death in Chronic Ischemic Heart Disease.
... of the rs11720524 polymorphism remains to be ...our in silico analysis revealed that the presence of the protective G allele creates a DNA binding site for the POU domain ... See full document
10
Lymphotoxin alpha (LTA) polymorphism is associated with prognosis of non-Hodgkin's lymphoma in a Chinese population.
... rs1800683 G .A was associated with progression free survival of DLBCL ...patients. The carriers of LTA rs1800683 AA genotype had poorer prognosis. This is the first study ... See full document
6
The co-existence of the IL-18+183 A/G and MMP-9 -1562 C/T polymorphisms is associated with clinical events in coronary artery disease patients.
... on the NanoDrop, ND-1000 (Saveen Werner, Sweden). The 3 9UTR +183A/G polymorphism (rs5744292) was genotyped with a Custom Design Assay manufactured by Applied Biosystems’ The ... See full document
6
Lin Gao1 , Hong Li1 , Kai Li1 , Zhu Shen1 , Ling Liu1 , Chunying Li1 , Zhengdong Zhang2 and Yufeng Liu1
... vulgaris is defined by a series of linked cellular changes in the skin: hyperplasia of epidermal keratinocytes, vascular hyperplasia and ectasia, and infiltration of T lymphocytes, neutrophils and ... See full document
5
The association between gene polymorphism of TCF7L2 and type 2 diabetes in Chinese Han population: a meta-analysis.
... assess the quality of the studies employed in this work. The NOS contains eight ...It is categorized into three dimensions including selection, comparability, and exposure for ... See full document
13
The polymorphism of the serotonin-2A receptor T102C is associated with age
... T102C polymorphism of gene 5-HT2A may be associated with mean life span because diseases and behaviors related to this polymorphism, such as schizophrenia, suicide, aggression, and addiction, ... See full document
6
O componente genético da determinação dos lipídeos séricos.
... A variação dos níveis lipídicos é uma carac- terística de etiologia multifatorial, pois é deter- minada por uma ampla gama de fatores, tanto ambientais quanto genéticos. Variações em um grande número de genes envolvidos ... See full document
8
The ACTN3 R577X Polymorphism Is Associated with Cardiometabolic Fitness in Healthy Young Adults.
... solubilized in SDS-lysis buffer and electrophoresed in a 10 well, 4–20% SDS-polyacrylamide gradient gel, followed by electroblotting onto PVDF ...washed with 0.05% Tween-PBS (PBST) and blocked ... See full document
13
Polimorfismos dos genes apolipoproteínas E e A5 e relação com parâmetros bioquímicos e hemostáticos em dislipidêmicos
... Atherosclerosis is a complex process due to multiple genetic and environmental interactions that modify not only lipid metabolism but also the coagulation system and inflammatory ...Dyslipidemia is ... See full document
176
A polymorphism in the HLA-DPB1 gene is associated with susceptibility to multiple sclerosis.
... LD with polymorphisms not genotyped in the discovery dataset we downloaded phased data for individuals from the HapMap CEU population (Utah residents with ancestry from northern and ... See full document
7
The Pro12Ala polymorphism in the peroxisome proliferator-activated receptor gamma-2 gene (PPARγ2) is associated with increased risk of coronary artery disease: a meta-analysis.
... examined the extent of the association between the PPARc2 pro12ala polymorphism and CAD risk by calculating odd ratio (OR) with 95% confidence interval ...(CI). The result of ... See full document
14
Multi-analytic approach elucidates significant role of hormonal and hepatocanalicular transporter genetic variants in gallstone disease in North Indian population.
... regarding the ADRB3 confirms that it is localized in the smooth muscles of the vasculature and the muscularis propria of the gallbladder [30] where it is thought to ... See full document
9
XmnI polymorphism is associated with fetal hemoglobin levels in hypoplastic syndromes
... change the level of HbF in adults, such as age, sex, polymorphisms, β-globin locus control region (LCR) and HbF ...Among the poly- morphic genetic markers of the β-globin gene cluster, ... See full document
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