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PDF) Comprehensive Survey of SNPs in the Affymetrix Exon Array Using the 1000 Genomes Dataset
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
Gen RPGR - Asociación Mácula Retina
Integrative genomics and transcriptomics analysis of human embryonic and induced pluripotent stem cells | BioData Mining | Full Text
Two Genetic Determinants Acquired Late in Mus Evolution Regulate the Inclusion of Exon 5, which Alters Mouse APOBEC3 Translation Efficiency | PLOS Pathogens
Coding SNPs included in exon arrays for the study of psychiatric disorders | Molecular Psychiatry
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
Biomedicines | Free Full-Text | Tau mRNA Metabolism in Neurodegenerative Diseases: A Tangle Journey
PDF) Comprehensive Survey of SNPs in the Affymetrix Exon Array Using the 1000 Genomes Dataset
Reading TE leaves: New approaches to the identification of transposable element insertions
Tau and MAPT genetics in tauopathies and synucleinopathies - ScienceDirect
Retrotransposons Revisited: The Restraint and Rehabilitation of Parasites: Cell
Frequency of three Hex A mutant alleles among Jewish and non-Jewish carriers identified in a Tay-Sachs screening program. - Abstract - Europe PMC
Evolution of the Primate APOBEC3A Cytidine Deaminase Gene and Identification of Related Coding Regions | PLOS ONE
PDF) Comprehensive Survey of SNPs in the Affymetrix Exon Array Using the 1000 Genomes Dataset
Cells | Free Full-Text | The Role of Immune Checkpoint Receptors in Regulating Immune Reactivity in Lupus
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
Long pentraxin 3 in pulmonary infection and acute lung injury | American Journal of Physiology-Lung Cellular and Molecular Physiology
PDF) Case Report: Whole-Exome Sequencing With MLPA Revealed Variants in Two Genes in a Patient With Combined Manifestations of Spinal Muscular Atrophy and Duchenne Muscular Dystrophy