MAPT mutations, tauopathy, and mechanisms of neurodegeneration | Laboratory Investigation
Comprehensive Survey of SNPs in the Affymetrix Exon Array Using the 1000 Genomes Dataset | PLOS ONE
Frequency of three Hex A mutant alleles among Jewish and non-Jewish carriers identified in a Tay-Sachs screening program. - Abstract - Europe PMC
Tau and MAPT genetics in tauopathies and synucleinopathies - ScienceDirect
PTX3 genetic variations affect the risk of Pseudomonas aeruginosa airway colonization in cystic fibrosis patients | Genes & Immunity
Finding Protein-Coding Genes through Human Polymorphisms | PLOS ONE
Two Genetic Determinants Acquired Late in Mus Evolution Regulate the Inclusion of Exon 5, which Alters Mouse APOBEC3 Translation Efficiency | PLOS Pathogens
PDF) Comprehensive Survey of SNPs in the Affymetrix Exon Array Using the 1000 Genomes Dataset
Frontiers | Functional Genetic Variant of Long Pentraxin 3 Gene Is Associated With Clinical Aspects of Oral Cancer in Male Patients
Genome‐wide analysis of European sea bass provides insights into the evolution and functions of single‐exon genes - Tine - 2021 - Ecology and Evolution - Wiley Online Library
IJMS | Free Full-Text | Non-Rodent Genetic Animal Models for Studying Tauopathy: Review of Drosophila, Zebrafish, and C. elegans Models
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
Table of Contents page: Journal of Biological Chemistry
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
Coding SNPs included in exon arrays for the study of psychiatric disorders | Molecular Psychiatry
