FOXG1 Syndrome (FS) is a devastating neurodevelopmental disorder that is caused by a heterozygous loss-of-function (LOF) mutation of the FOXG1 gene, which encodes a transcriptional regulator important for telencephalic brain development.People with FS have marked developmental delays, impaired ambulation, movement disorders, seizures, and behavior
As high-throughput genomic tools, such as the DNA microarray platform, g5210t-p90 have lead to the development of novel genotyping procedures, such as Diversity Arrays Technology (DArT) and Single Nucleotide Polymorphisms (SNPs), it is likely that, in the future, high density linkage maps will be constructed from both dominant and co-dominant marke
Abstract Delirium is a multifactorial medical condition of waxing and waning impairment across various domains of mental functioning over time.Importantly, delirium is also one of the greatest risk factors for prolonged hospitalization, morbidity, and mortality.Studying this important condition is challenging due to the difficulty in both objective
Plant root systems are essential for sustainable agriculture, conveying resource-efficient genotypes and species with benefits to soil ecosystem functions.Targeted selection of species/genotypes depends on available root system information.Currently there is no standardized approach for comprehensive root system characterization, suggesting the nee