Disease phenotypes trang 1 tải miễn phí từ TAILIEUCHUNG

"Disease phenotypes" trang 1 - tải miễn phí từ Tailieuchung

The study on clinical phenotypes of pulmonary hypertension due to left heart disease at pre-operation time in patients with isolated mitral valve replacement or double valve replacement

The study on clinical phenotypes of pulmonary hypertension due to left heart disease at pre-operation time in patients with isolated mitral valve replacement or double valve replacement

6 81 0

Integrating gene set analysis and nonlinear predictive modeling of disease phenotypes using a Bayesian multitask formulation

Integrating gene set analysis and nonlinear predictive modeling of disease phenotypes using a Bayesian multitask formulation

13 41 1

Clinical phenotypes and heath-related quality of life of COPD patients in a rural setting in Malaysia – a cross-sectional study

Clinical phenotypes and heath-related quality of life of COPD patients in a rural setting in Malaysia – a cross-sectional study

9 27 1

Integration of metabolomics, genomics, and immune phenotypes reveals the causal roles of metabolites in disease

Integration of metabolomics, genomics, and immune phenotypes reveals the causal roles of metabolites in disease

22 42 1

Family-based association analysis: A fast and efficient method of multivariate association analysis with multiple variants

Family-based association analysis: A fast and efficient method of multivariate association analysis with multiple variants

14 26 1

Genetic determinants of growth hormone and GH-related phenotypes

Genetic determinants of growth hormone and GH-related phenotypes

9 14 1

Báo cáo y học: "‘CFTR-opathies’: disease phenotypes associated with cystic fibrosis transmembrane regulator gene mutations"

5 47 0

Báo cáo y học: "Interstitial lung disease in children – genetic background and associated phenotypes"

16 28 0

Selective mode of action of plumbagin through BRCA1 deficient breast cancer stem cells

Selective mode of action of plumbagin through BRCA1 deficient breast cancer stem cells

16 42 1

Identifying novel associations in GWAS by hierarchical Bayesian latent variable detection of differentially misclassified phenotypes

Identifying novel associations in GWAS by hierarchical Bayesian latent variable detection of differentially misclassified phenotypes

25 50 1

IntLIM: Integration using linear models of metabolomics and gene expression data

IntLIM: Integration using linear models of metabolomics and gene expression data

12 38 1

Cluster analysis-based clinical phenotypes of idiopathic interstitial pneumonia: Associations with acute exacerbation and overall survival

Cluster analysis-based clinical phenotypes of idiopathic interstitial pneumonia: Associations with acute exacerbation and overall survival

9 22 1

Functional genomics analysis identifies T and NK cell activation as a driver of epigenetic clock progression

Functional genomics analysis identifies T and NK cell activation as a driver of epigenetic clock progression

21 9 1

Evolutionary conservation and divergence of the human brain transcriptome

Evolutionary conservation and divergence of the human brain transcriptome

33 20 1

Dietary and lifestyle indices for hyperinsulinemia with the risk of obesity phenotypes: A prospective cohort study among Iranian adult population

Dietary and lifestyle indices for hyperinsulinemia with the risk of obesity phenotypes: A prospective cohort study among Iranian adult population

11 13 1

A random set scoring model for prioritization of disease candidate genes using protein complexes and data-mining of GeneRIF, OMIM and PubMed records

A random set scoring model for prioritization of disease candidate genes using protein complexes and data-mining of GeneRIF, OMIM and PubMed records

13 53 1

CoNVaQ: A web tool for copy number variation-based association studies

CoNVaQ: A web tool for copy number variation-based association studies

9 33 1

High type II error and interpretation inconsistencies when attempting to refute transgenerational epigenetic inheritance

High type II error and interpretation inconsistencies when attempting to refute transgenerational epigenetic inheritance

4 39 1

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