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Allelic imbalance analysis of oral tongue squamous cell carcinoma by high-density single nucleotide polymorphism arrays using whole-genome amplified DNA.
- Published in:
- Human Genetics, 2005, v. 118, n. 3/4, p. 504, doi. 10.1007/s00439-005-0069-x
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- Article
Concurrent analysis of loss of heterozygosity (LOH) and copy number abnormality (CNA) for oral premalignancy progression using the Affymetrix 10K SNP mapping array.
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- Human Genetics, 2004, v. 115, n. 4, p. 327, doi. 10.1007/s00439-004-1163-1
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- Article
Cell adhesion molecules contribute to Alzheimer's disease: multiple pathway analyses of two genome-wide association studies.
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- Journal of Neurochemistry, 2012, v. 120, n. 1, p. 190, doi. 10.1111/j.1471-4159.2011.07547.x
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- Article
A genome-wide linkage scan of familial benign recurrent vertigo: linkage to 22q12 with evidence of heterogeneity.
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- Human Molecular Genetics, 2006, v. 15, n. 2, p. 251, doi. 10.1093/hmg/ddi441
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- Article
Joint mouse-human phenome-wide association to test gene function and disease risk.
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- Nature Communications, 2016, v. 7, n. 2, p. 10464, doi. 10.1038/ncomms10464
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- Article
Improving the efficiency of genomic loci capture usingoligonucleotide arrays for high throughput resequencing.
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- BMC Genomics, 2009, v. 10, p. 646, doi. 10.1186/1471-2164-10-646
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- Article
Cartilage-selective genes identified in genome-scale analysis of non-cartilage and cartilage gene expression.
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- BMC Genomics, 2007, v. 8, p. 165, doi. 10.1186/1471-2164-8-165
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- Article
A Quantitative High-Resolution Genetic Profile Rapidly Identifies Sequence Determinants of Hepatitis C Viral Fitness and Drug Sensitivity.
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- PLoS Pathogens, 2014, v. 10, n. 4, p. 1, doi. 10.1371/journal.ppat.1004064
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- Article
Convergent Genetic and Expression Datasets Highlight TREM2 in Parkinson's Disease Susceptibility.
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- Molecular Neurobiology, 2016, v. 53, n. 7, p. 4931, doi. 10.1007/s12035-015-9416-7
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- Article
CR1 rs3818361 Polymorphism Contributes to Alzheimer's Disease Susceptibility in Chinese Population.
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- Molecular Neurobiology, 2016, v. 53, n. 6, p. 4054, doi. 10.1007/s12035-015-9343-7
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- Article
Identifying the Association Between Alzheimer's Disease and Parkinson's Disease Using Genome-Wide Association Studies and Protein-Protein Interaction Network.
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- Molecular Neurobiology, 2015, v. 52, n. 3, p. 1629, doi. 10.1007/s12035-014-8946-8
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- Article
Analyzing 54,936 Samples Supports the Association Between CD2AP rs9349407 Polymorphism and Alzheimer's Disease Susceptibility.
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- Molecular Neurobiology, 2015, v. 52, n. 1, p. 1, doi. 10.1007/s12035-014-8834-2
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- Article
CD33 rs3865444 Polymorphism Contributes to Alzheimer's Disease Susceptibility in Chinese, European, and North American Populations.
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- Molecular Neurobiology, 2015, v. 52, n. 1, p. 414, doi. 10.1007/s12035-014-8880-9
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- Article
Integrating Genome-Wide Association Study and Brain Expression Data Highlights Cell Adhesion Molecules and Purine Metabolism in Alzheimer's Disease.
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- Molecular Neurobiology, 2015, v. 52, n. 1, p. 514, doi. 10.1007/s12035-014-8884-5
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- Article
An Updated Analysis with 85,939 Samples Confirms the Association Between CR1 rs6656401 Polymorphism and Alzheimer's Disease.
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- Molecular Neurobiology, 2015, v. 51, n. 3, p. 1017, doi. 10.1007/s12035-014-8761-2
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- Article
Melanomas acquire resistance to B-RAF(V600E) inhibition by RTK or N-RAS upregulation.
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- Nature, 2010, v. 468, n. 7326, p. 973, doi. 10.1038/nature09626
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- Article
Shotgun bisulphite sequencing of the Arabidopsis genome reveals DNA methylation patterning.
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- Nature, 2008, v. 452, n. 7184, p. 215, doi. 10.1038/nature06745
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- Article
U87MG Decoded: The Genomic Sequence of a Cytogenetically Aberrant Human Cancer Cell Line.
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- PLoS Genetics, 2010, v. 6, n. 1, p. 1, doi. 10.1371/journal.pgen.1000832
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- Article
A new histone deacetylase inhibitor remodels the tumor microenvironment by deletion of polymorphonuclear myeloid-derived suppressor cells and sensitizes prostate cancer to immunotherapy.
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- BMC Medicine, 2023, v. 21, n. 1, p. 1, doi. 10.1186/s12916-023-03094-0
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- Article
A forward-backward fragment assembling algorithm for the identification of genomic amplification and deletion breakpoints using high-density single nucleotide polymorphism (SNP) array.
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- BMC Bioinformatics, 2007, v. 8, p. 145, doi. 10.1186/1471-2105-8-145
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- Article
Measles Contributes to Rheumatoid Arthritis: Evidence from Pathway and Network Analyses of Genome-Wide Association Studies.
- Published in:
- PLoS ONE, 2013, v. 8, n. 10, p. 1, doi. 10.1371/journal.pone.0075951
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- Article
Prediction of Antimicrobial Peptides Based on Sequence Alignment and Feature Selection Methods.
- Published in:
- PLoS ONE, 2011, v. 6, n. 4, p. 1, doi. 10.1371/journal.pone.0018476
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- Article
Phenotype Sequencing: Identifying the Genes That Cause a Phenotype Directly from Pooled Sequencing of Independent Mutants.
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- PLoS ONE, 2011, v. 6, n. 2, p. 1, doi. 10.1371/journal.pone.0016517
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- Article
SATB1 Chromatin Loops Regulate Megakaryocyte/Erythroid Progenitor Expansion by Facilitating HSP70 and GATA1 Induction.
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- Stem Cells, 2023, v. 41, n. 6, p. 560, doi. 10.1093/stmcls/sxad025
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- Article
The CLU Gene rs11136000 Variant is Significantly Associated with Alzheimer's Disease in Caucasian and Asian Populations.
- Published in:
- NeuroMolecular Medicine, 2014, v. 16, n. 1, p. 52, doi. 10.1007/s12017-013-8250-1
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- Article
PICALM Gene rs3851179 Polymorphism Contributes to Alzheimer's Disease in an Asian Population.
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- NeuroMolecular Medicine, 2013, v. 15, n. 2, p. 384, doi. 10.1007/s12017-013-8225-2
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- Article
MicroRNA Profiling and Head and Neck Cancer.
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- Comparative & Functional Genomics, 2009, p. 1, doi. 10.1155/2009/837514
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- Article
Identification of allele-specific alternative mRNA processing via transcriptome sequencing.
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- Nucleic Acids Research, 2012, v. 40, n. 13, p. e104, doi. 10.1093/nar/gks280
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- Article
Molecular diagnosis of putative Stargardt disease probands by exome sequencing.
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- BMC Medical Genetics, 2012, v. 13, n. 1, p. 67, doi. 10.1186/1471-2350-13-67
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- Article
Representational oligonucleotide microarray analysis (ROMA) and comparison of binning and change-point methods of analysis: application to detection of del22q11.2 (DiGeorge) Syndrome.
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- Human Mutation, 2008, v. 29, n. 1, p. 176, doi. 10.1002/humu.20593
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- Article
Deletion mapping in Xp21 for patients with complex glycerol kinase deficiency using SNP mapping arrays.
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- Human Mutation, 2007, v. 28, n. 3, p. 235, doi. 10.1002/humu.20424
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- Article
Correction: U87MG Decoded: The Genomic Sequence of a Cytogenetically Aberrant Human Cancer Cell Line.
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- 2018
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- Correction Notice
Dusp6 is a genetic modifier of growth through enhanced ERK activity.
- Published in:
- Human Molecular Genetics, 2019, v. 28, n. 2, p. 279, doi. 10.1093/hmg/ddy349
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- Article
Pathway analysis of genome-wide association study and transcriptome data highlights new biological pathways in colorectal cancer.
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- Molecular Genetics & Genomics, 2015, v. 290, n. 2, p. 603, doi. 10.1007/s00438-014-0945-y
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- Article
Ribosomal Proteins RPS11 and RPS20, Two Stress-Response Markers of Glioblastoma Stem Cells, Are Novel Predictors of Poor Prognosis in Glioblastoma Patients.
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- PLoS ONE, 2015, v. 10, n. 10, p. 1, doi. 10.1371/journal.pone.0141334
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- Article
The γ-Carbonic Anhydrase Subcomplex of Mitochondrial Complex I Is Essential for Development and Important for Photomorphogenesis of Arabidopsis.
- Published in:
- Plant Physiology, 2012, v. 160, n. 3, p. 1373, doi. 10.1104/pp.112.204339
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- Article