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Initially, the GeneCards database had two main features: delivery of integrated biomedical information for a gene in ‘card’ format, and a text-based search engine. Since 1998, the database has integrated more data resources and data types, such as protein expression and gene network information.
Database of different circuitry frameworks and neuroimaging datasets, including volumetric datasets, atlases, and connectomics research Human, mouse, bat, zebrafish, insect, other Multilevel: brain regions, connections, neurons, gene expression patterns Images and 3D data Healthy No [37] openfnirs: a meta-database specific to fNIRS data.
Down syndrome is a genetic syndrome marked by intellectual disability and distinct cranio-facial features and occurs in approximately 1 in 800 live births. [17] Experts believe the genetic cause for the syndrome is a lack of genes in the 21st chromosome. [17] However, the gene or genes responsible for the cognitive phenotype have yet to be ...
Human protein-coding gene pages: •Python code for maintaining the list •List of human protein-coding genes page 1 covers genes A1BG–EPGN •List of human protein-coding genes page 2 covers genes EPHA1–MTMR3 •List of human protein-coding genes page 3 covers genes MTMR4–SLC17A7
"All psychological traits show significant and substantial genetic influence." "No behavioural traits are 100% heritable." "Heritability is caused by many genes of small effect." "Phenotypic correlations between psychological traits show significant and substantial genetic mediation." "The heritability of intelligence increases throughout ...
The gene was first reported by two independent research groups Aaltonen et al. and Nagamine et al. in 1997 who were able to isolate and clone the gene from human chromosome 21q22.3. Their work was able to show that mutations in the AIRE gene are responsible for the pathogenesis of Autoimmune polyglandular syndrome type I. [ 5 ] [ 8 ] More ...
The GDB Human Genome Database was a community curated collection of human genomic data. It was a key database in the Human Genome Project [ 1 ] [ 2 ] and was in service from 1989 to 2008. History
In humans it is synthesised by the gene GLP1R, which is present on chromosome 6. [5] [6] It is a member of the glucagon receptor family of GPCRs. [7] GLP1R is composed of two domains, one extracellular (ECD) that binds the C-terminal helix of GLP-1, [8] and one transmembrane (TMD) domain [9] that binds the N-terminal region of GLP-1.