Works matching IS 14739542 AND DT 2016 AND VI 10
Results: 39
The status of Her2 amplification and Kras mutations in mucinous ovarian carcinoma.
- Published in:
- Human Genomics, 2016, v. 10, p. 1, doi. 10.1186/s40246-016-0096-9
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- Article
Head-and-neck squamous cell carcinoma risk in smokers: no association detected between phenotype and AHR, CYP1A1, CYP1A2, or CYP1B1 genotype.
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- Human Genomics, 2016, v. 10, p. 1, doi. 10.1186/s40246-016-0094-y
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- Article
Head-and-neck squamous cell carcinoma risk in smokers: no association detected between phenotype and AHR, CYP1A1, CYP1A2, or CYP1B1 genotype.
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- Human Genomics, 2016, v. 10, p. 1, doi. 10.1186/s40246-016-0094-y
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- Article
Targeted next generation sequencing identifies novel NOTCH3 gene mutations in CADASIL diagnostics patients.
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- Human Genomics, 2016, v. 10, p. 1, doi. 10.1186/s40246-016-0093-z
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- Article
An efficient method for protein function annotation based on multilayer protein networks.
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- Human Genomics, 2016, v. 10, p. 1, doi. 10.1186/s40246-016-0087-x
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- Article
A genomic case study of desmoplastic small round cell tumor: comprehensive analysis reveals insights into potential therapeutic targets and development of a monitoring tool for a rare and aggressive disease.
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- Human Genomics, 2016, v. 10, p. 1, doi. 10.1186/s40246-016-0092-0
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- Article
Navigating the dynamic landscape of long noncoding RNA and protein-coding gene annotations in GENCODE.
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- Human Genomics, 2016, v. 10, p. 1, doi. 10.1186/s40246-016-0090-2
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- Article
Novel genetic risk variants for pediatric celiac disease.
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- Human Genomics, 2016, v. 10, p. 1, doi. 10.1186/s40246-016-0091-1
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A first-line diagnostic assay for limb-girdle muscular dystrophy and other myopathies.
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- Human Genomics, 2016, v. 10, p. 1, doi. 10.1186/s40246-016-0089-8
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- Article
Transcriptome analysis reveals manifold mechanisms of cyst development in ADPKD.
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- Human Genomics, 2016, v. 10, p. 1, doi. 10.1186/s40246-016-0095-x
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- Article
Major influence of repetitive elements on disease-associated copy number variants (CNVs).
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- Human Genomics, 2016, v. 10, p. 1, doi. 10.1186/s40246-016-0088-9
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- Article
Variation of global DNA methylation levels with age and in autistic children.
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- Human Genomics, 2016, v. 10, p. 1, doi. 10.1186/s40246-016-0086-y
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- Article
MicroRNAs in acute kidney injury.
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- Human Genomics, 2016, v. 10, p. 1, doi. 10.1186/s40246-016-0085-z
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- Article
Transcriptome sequencing of gingival biopsies from chronic periodontitis patients reveals novel gene expression and splicing patterns.
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- Human Genomics, 2016, v. 10, p. 1, doi. 10.1186/s40246-016-0084-0
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- Article
Mutation analysis of the COL1A1 and COL1A2 genes in Vietnamese patients with osteogenesis imperfecta.
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- Human Genomics, 2016, v. 10, p. 1, doi. 10.1186/s40246-016-0083-1
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- Article
The up-regulation of Myb may help mediate EGCG inhibition effect on mouse lung adenocarcinoma.
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- Human Genomics, 2016, v. 10, p. 103, doi. 10.1186/s40246-016-0072-4
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- Article
Hypomethylation coordinates antagonistically with hypermethylation in cancer development: a case study of leukemia.
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- Human Genomics, 2016, v. 10, p. 83, doi. 10.1186/s40246-016-0071-5
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- Article
The clinical significance of snail protein expression in gastric cancer: a metaanalysis.
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- Human Genomics, 2016, v. 10, p. 71, doi. 10.1186/s40246-016-0070-6
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- Article
Identification of protein complexes from multi-relationship protein interaction networks.
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- Human Genomics, 2016, v. 10, p. 61, doi. 10.1186/s40246-016-0069-z
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- Article
A comparative study of k-spectrum-based error correction methods for next-generation sequencing data analysis.
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- Human Genomics, 2016, v. 10, p. 49, doi. 10.1186/s40246-016-0068-0
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- Article
Association of six CpG-SNPs in the inflammation-related genes with coronary heart disease.
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- Human Genomics, 2016, v. 10, p. 41, doi. 10.1186/s40246-016-0067-1
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Exome sequencing discloses KALRN homozygous variant as likely cause of intellectual disability and short stature in a consanguineous pedigree.
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- Human Genomics, 2016, v. 10, p. 1, doi. 10.1186/s40246-016-0082-2
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Letter to the editor for "Update of the human and mouse Fanconi anemia genes".
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- Human Genomics, 2016, v. 10, p. 1, doi. 10.1186/s40246-016-0081-3
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Experience of a multidisciplinary task force with exome sequencing for Mendelian disorders.
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- Human Genomics, 2016, v. 10, p. 1, doi. 10.1186/s40246-016-0080-4
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- Article
AMD and the alternative complement pathway: genetics and functional implications.
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- Human Genomics, 2016, v. 10, p. 1, doi. 10.1186/s40246-016-0079-x
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Proposed nomenclature for microhaplotypes.
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- Human Genomics, 2016, v. 10, p. 1, doi. 10.1186/s40246-016-0078-y
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- Article
Genetic risk factors for restenosis after percutaneous coronary intervention in Kazakh population.
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- Human Genomics, 2016, v. 10, p. 1, doi. 10.1186/s40246-016-0077-z
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- Article
Systematic analysis of the molecular mechanism underlying atherosclerosis using a text mining approach.
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- Human Genomics, 2016, v. 10, p. 1, doi. 10.1186/s40246-016-0075-1
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Human genome meeting 2016.
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- Human Genomics, 2016, v. 10, p. 1, doi. 10.1186/s40246-016-0063-5
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- Article
Exploring the interaction among EPHX1, GSTP1, SERPINE2, and TGFB1 contributing to the quantitative traits of chronic obstructive pulmonary disease in Chinese Han population.
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- Human Genomics, 2016, v. 10, p. 1, doi. 10.1186/s40246-016-0076-0
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Multiplex SNaPshot--a new simple and efficient CYP2D6 and ADRB1 genotyping method.
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- Human Genomics, 2016, v. 10, p. 1, doi. 10.1186/s40246-016-0073-3
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Organization, evolution and functions of the human and mouse Ly6/uPAR family genes.
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- Human Genomics, 2016, v. 10, p. 1, doi. 10.1186/s40246-016-0074-2
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Three-hour analysis of non-invasive foetal sex determination: application of Plexor chemistry.
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- Human Genomics, 2016, v. 10, p. 1, doi. 10.1186/s40246-016-0066-2
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The impact of common polymorphisms in CETP and ABCA1 genes with the risk of coronary artery disease in Saudi Arabians.
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- Human Genomics, 2016, v. 10, p. 1, doi. 10.1186/s40246-016-0065-3
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- Article
A review of the new HGNC gene family resource.
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- Human Genomics, 2016, v. 10, p. 1, doi. 10.1186/s40246-016-0062-6
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The clinical trial landscape in oncology and connectivity of somatic mutational profiles to targeted therapies.
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- Human Genomics, 2016, v. 10, p. 1, doi. 10.1186/s40246-016-0061-7
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Genetic studies of Polish migraine patients: screening for causative mutations in four migraine-associated genes.
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- Human Genomics, 2016, v. 10, p. 1, doi. 10.1186/s40246-015-0057-8
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Intragraft transcriptional profiling of renal transplant patients with tubular dysfunction reveals mechanisms underlying graft injury and recovery.
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- Human Genomics, 2016, v. 10, p. 1, doi. 10.1186/s40246-015-0059-6
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- Article
Whole exome sequencing identifies novel candidate genes that modify chronic obstructive pulmonary disease susceptibility.
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- Human Genomics, 2016, v. 10, p. 1, doi. 10.1186/s40246-015-0058-7
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