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Diffusion Lung Capacity of Patients with Arterial Hypertension.
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- Collegium Antropologicum, 2009, v. 33, p. 165
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- Article
Prevalence and Risk Factors of the Rheumatoid Arthritis in Herzegovina Region in 2003-2005.
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- Collegium Antropologicum, 2009, v. 33, p. 73
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- Publication type:
- Article
Implication of the Immune System in Alzheimer's Disease: Evidence from Genome-Wide Pathway Analysis.
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- Journal of Alzheimer's Disease, 2010, v. 20, n. 4, p. 1107, doi. 10.3233/JAD-2010-100018
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- Article
Systematic Analysis of Candidate Genes for Alzheimer's Disease in a French, Genome-Wide Association Study.
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- Journal of Alzheimer's Disease, 2010, v. 20, n. 4, p. 1181, doi. 10.3233/JAD-2010-100126
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- Publication type:
- Article
Genetic Variants of FOXP2 and KIAA0319/TTRAP/THEM2 Locus Are Associated with Altered Brain Activation in Distinct Language-Related Regions.
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- Journal of Neuroscience, 2012, v. 32, n. 3, p. 817, doi. 10.1523/JNEUROSCI.5996-10.2012
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- Article
High-resolution autosomal radiation hybrid maps of the pig genome and their contribution to the genome sequence assembly.
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- BMC Genomics, 2012, v. 13, n. 1, p. 585, doi. 10.1186/1471-2164-13-585
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- Publication type:
- Article
Development and implementation of a highlymultiplexed SNP array for genetic mapping in maritime pine and comparative mapping with loblolly pine.
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- BMC Genomics, 2011, v. 12, n. 1, p. 368, doi. 10.1186/1471-2164-12-368
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- Article
A new locus ( SPG46) maps to 9p21.2-q21.12 in a Tunisian family with a complicated autosomal recessive hereditary spastic paraplegia with mental impairment and thin corpus callosum.
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- Neurogenetics, 2010, v. 11, n. 4, p. 441, doi. 10.1007/s10048-010-0249-2
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- Article
Refinement of the SPG15 candidate interval and phenotypic heterogeneity in three large Arab families.
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- Neurogenetics, 2007, v. 8, n. 4, p. 307, doi. 10.1007/s10048-007-0097-x
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- Article
Deciphering the 8q24.21 association for glioma.
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- Human Molecular Genetics, 2013, v. 22, n. 11, p. 2293, doi. 10.1093/hmg/ddt063
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- Publication type:
- Article
Genome-wide association study identifies loci on 12q24 and 13q32 associated with Tetralogy of Fallot.
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- Human Molecular Genetics, 2013, v. 22, n. 7, p. 1473, doi. 10.1093/hmg/dds552
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- Article
A genome-wide association study identifies a novel susceptibility locus for renal cell carcinoma on 12p11.23.
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- Human Molecular Genetics, 2012, v. 21, n. 2, p. 456, doi. 10.1093/hmg/ddr479
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- Publication type:
- Article
Chromosome 7p11.2 (EGFR) variation influences glioma risk.
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- Human Molecular Genetics, 2011, v. 20, n. 14, p. 2897, doi. 10.1093/hmg/ddr192
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- Publication type:
- Article
Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population.
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- Human Molecular Genetics, 2011, v. 20, n. 3, p. 615
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- Article
TCF12 is mutated in anaplastic oligodendroglioma.
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- Nature Communications, 2015, v. 6, n. 6, p. 7207, doi. 10.1038/ncomms8207
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- Article
Incidence of Breast Cancer and Its Subtypes in Relation to Individual and Multiple Low-Penetrance Genetic Susceptibility Loci.
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- JAMA: Journal of the American Medical Association, 2010, v. 304, n. 4, p. 426, doi. 10.1001/jama.2010.1042
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- Article
AP1S2 is mutated in X-linked Dandy-Walker malformation with intellectual disability, basal ganglia disease and seizures (Pettigrew syndrome).
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- European Journal of Human Genetics, 2014, v. 22, n. 3, p. 363, doi. 10.1038/ejhg.2013.135
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- Article
Association Analysis Indicates That a Variant GATA-Binding Site in the PIK3CB Promoter Is a Cis-Acting Expression Quantitative Trait Locus for This Gene and Attenuates Insulin Resistance in Obese Children.
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- Diabetes, 2008, v. 57, n. 2, p. 494, doi. 10.2337/db07-1273
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- Article
Serial translocation by means of circular intermediates underlies colour sidedness in cattle.
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- Nature, 2012, v. 482, n. 7383, p. 81, doi. 10.1038/nature10757
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- Article
Novel Breast Cancer Susceptibility Locus at 9q31.2: Results of a Genome-Wide Association Study.
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- JNCI: Journal of the National Cancer Institute, 2011, v. 103, n. 5, p. 425, doi. 10.1093/jnci/djq563
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- Article
Antiviral agent Cidofovir decreases Epstein-Barr virus (EBV) oncoproteins and enhances the radiosensitivity in EBV-related malignancies.
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- Oncogene, 2003, v. 22, n. 15, p. 2260, doi. 10.1038/sj.onc.1206402
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- Publication type:
- Article
Combining gene mapping and phenotype assessment for fast mutation finding in non-consanguineous autosomal recessive retinitis pigmentosa families.
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- European Journal of Human Genetics, 2011, v. 19, n. 12, p. 1256, doi. 10.1038/ejhg.2011.133
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- Publication type:
- Article
Bivariate association analysis in selected samples: application to a GWAS of two bone mineral density phenotypes in males with high or low BMD.
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- European Journal of Human Genetics, 2011, v. 19, n. 6, p. 710, doi. 10.1038/ejhg.2011.22
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- Publication type:
- Article
Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease.
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- Nature Genetics, 2013, v. 45, n. 12, p. 1452, doi. 10.1038/ng.2802
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- Article
Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16.
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- Nature Genetics, 2013, v. 45, n. 7, p. 822, doi. 10.1038/ng.2637
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- Article
Multiple apical plasma membrane constituents are associated with susceptibility to meconium ileus in individuals with cystic fibrosis.
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- Nature Genetics, 2012, v. 44, n. 5, p. 562, doi. 10.1038/ng.2221
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- Article
Genome-wide association study of renal cell carcinoma identifies two susceptibility loci on 2p21 and 11q13.3.
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- Nature Genetics, 2011, v. 43, n. 1, p. 60, doi. 10.1038/ng.723
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- Article
Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease.
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- Nature Genetics, 2009, v. 41, n. 10, p. 1094, doi. 10.1038/ng.439
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- Publication type:
- Article
Genome-wide association study identifies five susceptibility loci for glioma.
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- Nature Genetics, 2009, v. 41, n. 8, p. 899, doi. 10.1038/ng.407
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- Article
Common variants at 30 loci contribute to polygenic dyslipidemia.
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- Nature Genetics, 2009, v. 41, n. 1, p. 56, doi. 10.1038/ng.291
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- Article
A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15.
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- Nature Genetics, 2007, v. 39, n. 10, p. 1197, doi. 10.1038/ng2108
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- Article
A New Family of Transcripts of the Myelin Basic Protein Gene: Expression in Brain and in Immune System.
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- Journal of Neurochemistry, 1993, v. 60, n. 4, p. 1574, doi. 10.1111/j.1471-4159.1993.tb03325.x
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- Article
A Novel Transcript Overlapping the Myelin Basic Protein Gene.
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- Journal of Neurochemistry, 1992, v. 59, n. 6, p. 2318, doi. 10.1111/j.1471-4159.1992.tb10126.x
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- Publication type:
- Article
Isolation of a Novel cDNA Corresponding to a Transcript Expressed in the Choroid Plexus and Leptomeninges.
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- Journal of Neurochemistry, 1991, v. 56, n. 6, p. 2133, doi. 10.1111/j.1471-4159.1991.tb03476.x
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- Article
Comprehensive Linkage and Association Analyses Identify Haplotype, Near to the TNFSF15 Gene, Significantly Associated with Spondyloarthritis.
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- PLoS Genetics, 2009, v. 5, n. 6, p. 1, doi. 10.1371/journal.pgen.1000528
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- Publication type:
- Article
Novel Crohn Disease Locus Identified by Genome-Wide Association Maps to a Gene Desert on 5p13.1 and Modulates Expression of PTGER4.
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- PLoS Genetics, 2007, v. 3, n. 4, p. e58, doi. 10.1371/journal.pgen.0030058
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- Article
Global Genetic Architecture of an Erythroid Quantitative Trait Locus, HMIP-2.
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- Annals of Human Genetics, 2014, v. 78, n. 6, p. 434, doi. 10.1111/ahg.12077
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- Article
Quantitative Variation in Plasma Angiotensin-I Converting Enzyme Activity Shows Allelic Heterogeneity in the ABO Blood Group Locus.
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- Annals of Human Genetics, 2013, v. 77, n. 6, p. 465, doi. 10.1111/ahg.12034
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- Article
Genome wide association study for plasma levels of natural anticoagulant inhibitors and protein C anticoagulant pathway: the MARTHA project.
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- British Journal of Haematology, 2012, v. 157, n. 2, p. 230, doi. 10.1111/j.1365-2141.2011.09025.x
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- Publication type:
- Article
Common and Rare Variant Analysis in Early-Onset Bipolar Disorder Vulnerability.
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- PLoS ONE, 2014, v. 9, n. 8, p. 1, doi. 10.1371/journal.pone.0104326
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- Article
CpG Methylation Changes within the <i>IL2RA</i> Promoter in Type 1 Diabetes of Childhood Onset.
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- PLoS ONE, 2013, v. 8, n. 7, p. 1, doi. 10.1371/journal.pone.0068093
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- Article
Caution in Interpreting Results from Imputation Analysis When Linkage Disequilibrium Extends over a Large Distance: A Case Study on Venous Thrombosis.
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- PLoS ONE, 2012, v. 7, n. 6, p. 1, doi. 10.1371/journal.pone.0038538
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- Article
Association of the CpG Methylation Pattern of the Proximal Insulin Gene Promoter with Type 1 Diabetes.
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- PLoS ONE, 2012, v. 7, n. 5, p. 1, doi. 10.1371/journal.pone.0036278
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- Article
Genetics of Venous Thrombosis: Insights from a New Genome Wide Association Study.
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- PLoS ONE, 2011, v. 6, n. 9, p. 1, doi. 10.1371/journal.pone.0025581
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- Article
Genome-Wide Population-Based Association Study of Extremely Overweight Young Adults - The GOYA Study.
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- PLoS ONE, 2011, v. 6, n. 9, p. 1, doi. 10.1371/journal.pone.0024303
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- Article
Regulatory T cells and dendritic cells in transplantation tolerance: molecular markers and mechanisms.
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- Immunological Reviews, 2003, v. 196, n. 1, p. 109, doi. 10.1046/j.1600-065X.2003.00078.x
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- Article
The role of CD4+ T-cell subsets in determining transplantation rejection or tolerance.
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- Immunological Reviews, 2001, v. 182, n. 1, p. 164, doi. 10.1034/j.1600-065x.2001.1820113.x
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- Article
Complete exon sequencing of all known Usher syndrome genes greatly improves molecular diagnosis.
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- Orphanet Journal of Rare Diseases, 2011, v. 6, n. 1, p. 21, doi. 10.1186/1750-1172-6-21
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- Publication type:
- Article
A novel locus (CORD12) for autosomal dominant cone-rod dystrophy on chromosome 2q24.2-2q33.1.
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- BMC Medical Genetics, 2011, v. 12, n. 1, p. 54, doi. 10.1186/1471-2350-12-54
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- Article
Erratum to: Childhood acute leukemia, maternal beverage intake during pregnancy, and metabolic polymorphisms.
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- 2014
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- Publication type:
- Erratum