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[PDF] Top 20 Genetic variation of ITGB3 is associated with asthma in Chinese Han children.

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Genetic variation of ITGB3 is associated with asthma in Chinese Han children.

Genetic variation of ITGB3 is associated with asthma in Chinese Han children.

... Asthma is one of the most common chronic diseases in children, and it is characterised by bronchial hyperresponsiveness (BHR) and reversible airway ...Both genetic and ... See full document

7

The GG genotype of telomerase reverse transcriptase at genetic locus rs2736100 is associated with human atherosclerosis risk in the Han Chinese population.

The GG genotype of telomerase reverse transcriptase at genetic locus rs2736100 is associated with human atherosclerosis risk in the Han Chinese population.

... telomere is a region of repetitive nucleotide sequences at the end of each chromatid of most eukaryotic organisms that protects the end of the chromosome from deterioration or from ... See full document

5

Genetic variants in meiotic program initiation pathway genes are associated with spermatogenic impairment in a Han Chinese population.

Genetic variants in meiotic program initiation pathway genes are associated with spermatogenic impairment in a Han Chinese population.

... consistent with the phenotypes in STRA8 2/2 mice [8]. While in male mutant mice, the premeiotic DNA replication was conserved [8] and the germ cells could partly condense chromosomes, and initiate ... See full document

6

Filaggrin gene mutation c.3321delA is associated with various clinical features of atopic dermatitis in the Chinese Han population.

Filaggrin gene mutation c.3321delA is associated with various clinical features of atopic dermatitis in the Chinese Han population.

... analyses in the ...3). In the QTL analysis, we found that c.3321delA was associated with disease severity (P = ...compared with the patients with a wild-type genotype ...trend ... See full document

7

Genetic variants in MARCO are associated with the susceptibility to pulmonary tuberculosis in Chinese Han population.

Genetic variants in MARCO are associated with the susceptibility to pulmonary tuberculosis in Chinese Han population.

... consideration in addressing the significant genetic association is population stratification inherent to case control study, which however, could be minimized in the current research, as ... See full document

6

A common variant in the SIAH2 locus is associated with estrogen receptor-positive breast cancer in the Chinese Han population.

A common variant in the SIAH2 locus is associated with estrogen receptor-positive breast cancer in the Chinese Han population.

... study of women of Chinese descent, 21 SNPs from newly published GWAS of breast cancer were ...detected with $80% power, whereas 7 other SNPs (rs865686, rs1981867, rs10822013, rs9485372, ... See full document

5

Lymphotoxin alpha (LTA) polymorphism is associated with prognosis of non-Hodgkin's lymphoma in a Chinese population.

Lymphotoxin alpha (LTA) polymorphism is associated with prognosis of non-Hodgkin's lymphoma in a Chinese population.

... Despite of the strengths, our study also has ...effect of SNP on PFS and short-term outcome of NHL subtypes, but we did not analyze the overall ...role of inflammation and immune- related gene ... See full document

6

Genetic variants in MUC4 gene are associated with lung cancer risk in a Chinese population.

Genetic variants in MUC4 gene are associated with lung cancer risk in a Chinese population.

... gene is ~211 kb in size and is located on chromosome 3 in region q29 ...296 of MUC4 SNPs with minor allele frequency (MAF) > 5% from both dbSNP ...[Han Chinese]) ... See full document

11

Genetic Variation in the REL Gene Increases Risk of Behcet's Disease in a Chinese Han Population but That of PRKCQ Does Not.

Genetic Variation in the REL Gene Increases Risk of Behcet's Disease in a Chinese Han Population but That of PRKCQ Does Not.

... polymorphism in the REL gene has been previously reported as a risk factor for potential CD in Southern Italy populations, and the expression of the c-REL gene was higher in Marsh 0 potentials ... See full document

8

Polymorphisms of the DNA methyltransferase 1 associated with reduced risks of Helicobacter pylori infection and increased risks of gastric atrophy.

Polymorphisms of the DNA methyltransferase 1 associated with reduced risks of Helicobacter pylori infection and increased risks of gastric atrophy.

... Over-expression of DNMT1 mRNA and protein is detected in gastric cancer suggesting that DNMT1 may contribute to tumorgenesis ...not associated with gastric cancer, consistent ... See full document

6

Obesity-related genomic loci are associated with type 2 diabetes in a Han Chinese population.

Obesity-related genomic loci are associated with type 2 diabetes in a Han Chinese population.

... resistance is a major risk factor leading to type 2 diabetes ...that genetic loci related to obesity could contribute to the risk for type 2 diabetes ...A of SNP rs9939609 in the FTO gene was ... See full document

9

The NPC1L1 Polymorphism 1679C>G Is Associated with Gallstone Disease in Chinese Patients.

The NPC1L1 Polymorphism 1679C>G Is Associated with Gallstone Disease in Chinese Patients.

... role in intestinal and hepatic cholesterol metabolism in ...humans. Genetic variation in NPC1L1 has been widely studied in recent ...polymorphisms in Chinese ... See full document

9

Association of germline variation in CCNE1 and CDK2 with breast cancer risk, progression and survival among Chinese Han women.

Association of germline variation in CCNE1 and CDK2 with breast cancer risk, progression and survival among Chinese Han women.

... analysis is a good way to determine whether one SNP is the causal ...effects of at-risk SNPs in CCNE1 on its mRNA and protein expression, and on cellular growth, centrosome amplification, DNA ... See full document

11

Genetic polymorphism of NOS3 with susceptibility to deep vein thrombosis after orthopedic surgery: a case-control study in Chinese Han population.

Genetic polymorphism of NOS3 with susceptibility to deep vein thrombosis after orthopedic surgery: a case-control study in Chinese Han population.

... thrombosis is one of the common complications of orthopedic ...that genetic factors played a considerable role in the pathogenesis of deep vein ...oxide in endothelial ... See full document

5

The common variant rs11646213 is associated with preeclampsia in Han Chinese women.

The common variant rs11646213 is associated with preeclampsia in Han Chinese women.

... First, genetic factors that influence the pathogenesis of preeclampsia differ by ethnic group, and the association between CDH13 and preeclampsia need to be confirmed in a larger sample size composed ... See full document

4

COL9A1 gene polymorphism is associated with Kashin-Beck disease in a northwest Chinese Han population.

COL9A1 gene polymorphism is associated with Kashin-Beck disease in a northwest Chinese Han population.

... KBD in our population, even though the heterozygosity of rs3765462 in gene COL9A3 showed a weak association with an evaluated KBD ...example, genetic study in a Finnish ... See full document

11

Pooled Sequencing of Candidate Genes Implicates Rare Variants in the Development of Asthma Following Severe RSV Bronchiolitis in Infancy.

Pooled Sequencing of Candidate Genes Implicates Rare Variants in the Development of Asthma Following Severe RSV Bronchiolitis in Infancy.

... It is important to note two limitations of using the ESP as controls in our ...characteristics of the ESP samples they cannot strictly be considered “population controls” as some individuals ... See full document

15

FAMILY HISTORY IS ASSOCIATED WITH THE PRESENCE OF DYSLIPIDEMIA IN PRE‑SCHOOL CHILDREN

FAMILY HISTORY IS ASSOCIATED WITH THE PRESENCE OF DYSLIPIDEMIA IN PRE‑SCHOOL CHILDREN

... criteria of the study - identifi- cation data that revealed the children’s location, if they had a full-term birth, appropriate weight, and a date of birth com- patible with the ages between 4 and 7 ... See full document

8

Genetic variation in the interleukin-28B gene is associated with spontaneous clearance and progression of hepatitis C virus in Moroccan patients.

Genetic variation in the interleukin-28B gene is associated with spontaneous clearance and progression of hepatitis C virus in Moroccan patients.

... influence of IL28B polymorphisms on the severity and progression of liver disease remains unclear with controversial results ...studies in ethnically diverse populations. In our study, ... See full document

6

Family history is associated with the presence of dyslipidemia in pre‑school children

Family history is associated with the presence of dyslipidemia in pre‑school children

... study with 257 children aged 4 to 7 years old from Viçosa, Minas Gerais, Southeast ...history of dyslipidemia in parents were carried ...presence of dyslipidemia in ... See full document

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