PDF) Comprehensive Survey of SNPs in the Affymetrix Exon Array Using the 1000 Genomes Dataset
Comprehensive Survey of SNPs in the Affymetrix Exon Array Using the 1000 Genomes Dataset | PLOS ONE
Haplotype Diversity and Linkage Disequilibrium at Human G6PD: Recent Origin of Alleles That Confer Malarial Resistance | Science
Reading TE leaves: New approaches to the identification of transposable element insertions
Integrative genomics and transcriptomics analysis of human embryonic and induced pluripotent stem cells | BioData Mining | Full Text
PDF) Comprehensive Survey of SNPs in the Affymetrix Exon Array Using the 1000 Genomes Dataset
Biomedicines | Free Full-Text | Tau mRNA Metabolism in Neurodegenerative Diseases: A Tangle Journey
Long pentraxin 3 in pulmonary infection and acute lung injury | American Journal of Physiology-Lung Cellular and Molecular Physiology
Invited review: Frontotemporal dementia caused by microtubule‐associated protein tau gene (MAPT) mutations: a chameleon for neuropathology and neuroimaging - Ghetti - 2015 - Neuropathology and Applied Neurobiology - Wiley Online Library
Functions, structure, and read-through alternative splicing of feline APOBEC3 genes | Genome Biology | Full Text
Protective effects of long pentraxin PTX3 on lung injury in a severe acute respiratory syndrome model in mice | Laboratory Investigation
Cardiovascular Disease in Duchenne Muscular Dystrophy: Overview and Insight Into Novel Therapeutic Targets | JACC: Basic to Translational Science
IJMS | Free Full-Text | Non-Rodent Genetic Animal Models for Studying Tauopathy: Review of Drosophila, Zebrafish, and C. elegans Models
Integrative genomics and transcriptomics analysis of human embryonic and induced pluripotent stem cells | BioData Mining | Full Text
PDF) Comprehensive Survey of SNPs in the Affymetrix Exon Array Using the 1000 Genomes Dataset
Coding SNPs included in exon arrays for the study of psychiatric disorders | Molecular Psychiatry
Frontiers | Functional Genetic Variant of Long Pentraxin 3 Gene Is Associated With Clinical Aspects of Oral Cancer in Male Patients
Frequency of three Hex A mutant alleles among Jewish and non-Jewish carriers identified in a Tay-Sachs screening program. - Abstract - Europe PMC
