[PDF] Top 20 A Non-Synonymous Single Nucleotide Polymorphism in the HJURP Gene Associated with Susceptibility to Hepatocellular Carcinoma among Chinese.
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A Non-Synonymous Single Nucleotide Polymorphism in the HJURP Gene Associated with Susceptibility to Hepatocellular Carcinoma among Chinese.
... limitations in the present study. First, the patients with HCC were recruited from hospitals, while the controls were selected from community ...Therefore, the inherent selection ... See full document
15
Is a non-synonymous SNP in the HvAACT1 coding region associated with
... variation in the HvAACT1 gene sequence among barley genotypes (Furukawa et ...2015), with one single nucleotide polymorphism (SNP) oc- curring per 29 bp of this ... See full document
11
CHRNA5 polymorphism and susceptibility to lung cancer in a Chinese population
... Polymorphisms in the nicotinic acetylcholine receptor subunit CHRNA5 gene have been associated with lung cancer positive susceptibility in European and American ... See full document
6
A 3' UTR SNP in COL18A1 is associated with susceptibility to HBV related hepatocellular carcinoma in Chinese: three independent case-control studies.
... Hepatocellular carcinoma (HCC) is one of the most common malignancy and ranks fifth in men and eighth in women among causes of cancer mortality ...throughout the world ... See full document
6
The 10 bp duplication insertion/deletion in the promoter region within paired box 7 gene is associated with growth traits in cattle
... knowledge, the promoter sequence is an impor- tant part of a gene regulatory region, which can regulate the expression of target genes by interacting with trans-acting factors (Mottagui-Tabar ... See full document
8
Uncovering the rare variants of DLC1 isoform 1 and their functional effects in a Chinese sporadic congenital heart disease cohort.
... is the most common birth defect affecting the structure and function of fetal ...studies, the genetic mechanism of sporadic CHD remains obscure. Deleted in liver cancer 1 (DLC1) gene, ... See full document
9
Single nucleotide polymorphisms of the angiotensin-converting enzyme (ACE) gene are associated with essential hypertension and increased ACE enzyme levels in Mexican individuals.
... and the study complies with the Declaration of Helsinki and was approved by the Ethics Committee of the Instituto Nacional de Cardiologı´a ‘‘Ignacio Cha´a´vez’’ ...referred to ... See full document
7
Genotype at the P554L variant of the hexose-6 phosphate dehydrogenase gene is associated with carotid intima-medial thickness.
... of the ER luminal store of NADPH, sensitizes cells to oxidative stress and thus promotes apoptosis, which is a key process in the vessel wall in the initiation and progression of ... See full document
7
Rev. Bras. Reumatol. vol.53 número4 en v53n4a05
... rs7700944 polymorphism with covari- ate sex (adjusted for age) was done (Table ...3). In females, no signii cant association was found between the groups regard- ing TIM-4 rs7700944 ... See full document
5
Farmacogenética da esquizofrenia
... of the most potent neurotrophic factors for these neurons, GDNF is widely expressed throughout the brain, and exerts neuroprotective effects in several central and peripheral neuronal ...Changes ... See full document
147
The BCL2 -938C>A Promoter Polymorphism Is Associated with Risk for and Time to Aseptic Loosening of Total Hip Arthroplasty.
... necessary to understand the pathophysiology and identify mechanisms triggering aseptic ...is the induction of a non-infectious inflammatory cas- cade caused by wear debris of the ... See full document
10
The association between gene polymorphism of TCF7L2 and type 2 diabetes in Chinese Han population: a meta-analysis.
... is associated with type 2 diabetes mellitus (T2DM) in multiple ethnic groups, especially its single nucleotide polymorphisms of rs7903146C/T, rs12255372G/T and ...However, the ... See full document
13
Polymorphisms in the Toll-Like Receptor and the IL-23/IL-17 Pathways Were Associated with Susceptibility to Inflammatory Bowel Disease in a Danish Cohort.
... found. In the light of the obtained P-values and the number of statistical tests performed we cannot exclude, that some of our positive findings may be due to ...If the results ... See full document
14
Single nucleotide polymorphisms of Toll-like receptor 4 decrease the risk of development of hepatocellular carcinoma.
... role in neoplastic transformation [26]. In our study, the TLR4 SNPs may potentially exert regulator effects and therefore might decrease the risk for hepatocellular ...Due to ... See full document
7
Single nucleotide polymorphisms of microRNA processing machinery genes and outcome of hepatocellular carcinoma.
... Hepatocellular carcinoma (HCC) is the fifth most common cancer and is responsible for more than half a million deaths each year, which makes it the third leading cause of cancer deaths ... See full document
4
Polymorphisms in the interleukin 18 receptor 1 gene and tuberculosis susceptibility among Chinese.
... sites in the promoter region is a well-defined epigenetic phenomenon generally associated with active gene expression [29], for DNA methylation may have both direct effects, by ... See full document
8
Association of T174M polymorphism of angiotensinogen gene with essential hypertension: A meta-analysis
... for the discrepancies among these studies. The first possi- ble cause may be genetic differences in the population sam- ples and phenotypic differences in the hypertensive ... See full document
7
COL9A1 gene polymorphism is associated with Kashin-Beck disease in a northwest Chinese Han population.
... al’s susceptibility to KBD ...result in a secondary chronic osteoarthropathy [25]. The electron microscopic analysis have confirmed the chondrocyte necrosis and revealed a reduction ... See full document
11
Arq. NeuroPsiquiatr. vol.72 número6
... of the central nervous system (CNS) that affects mainly young ...seems to be a polygenic and multifactorial disease, and genetic susceptibility has been associated mainly with ... See full document
1
Association study of genetic variants at single nucleotide polymorphism rs109231409 of mannose-binding lectins 1 gene with mastitis susceptibility in Vrindavani crossbred cattle
... on the MBL1 gene was genotyped using polymerase chain reaction-restriction fragment length poly- morphisms ...for the PCR reaction for amplifying the introns 1 of MBL1 gene was ... See full document
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