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Functional gene set analyses were performed to create reference libraries of gene families and functional gene ontology categories that have importance for brain function and developmental neurobiology.
This points toward potential health risks for humans, including cardiovascular disease, pulmonary diseases, impairment of brain function and developmental toxicity (Buzea et al. 2007; Wick et al. 2010).
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We can now measure brain structure and function on the same brains, and thus relate structural connections to brain function and behavior, 38 analyze developmental pathways of structural connections, 39 and relate structural connections to functional segregation, 40 among many other possibilities that were unavailable two decades ago.
The hormonal influence on brain function and behavior is caused by developmental organizational effects and later on through modification and activation-related effects during maturation and adulthood [4], [7], [8], [11], [12], [13].
Furthermore, it is clear that the achievement of the ultimate goal - the elucidation of a genetic network underpinning language processes - will have an impact on our understanding not only of language impairment and acquisition, but also of human development, brain function and the neuropathology of associated developmental disorders.
Indeed, since most lncRNAs are expressed in the brain (Mercer et al., 2008) and many are primate-specific (Derrien et al., 2012), it may be that much of the lncRNA-mediated genetic information in humans (and in mammals generally) is devoted to brain function, and therefore not easily detectable in developmental, as opposed to cognitive, screens.
During the past five decades, enormous progress has been made towards understanding the local energy demands of living brain and the relationships between brain function and fluxes in metabolic pathways that satisfy developmental, energetic, neuroprotective, and biosynthetic requirements of working brain cells.
Some chemicals, known as endocrine disruptors, interfere with the natural hormones in our bodies that regulate reproduction, brain function and immune response, and may be linked to increased risk for developmental and reproductive problems in both humans and wildlife.
The characteristic surface morphology of the mammalian brain is closely correlated with brain function and dysfunction.
Another potential application of our finding comes from the pleiotropic role of IGF1 in many developmental and physiological or pathological processes related to aging, longevity, energy metabolism, brain functions, and cancer.
Ideally, these tests would explore the entire brain functions (and confirm whole brain death) including supra-tentorial cortex (neocortical brain death) and brain stem (brain stem death).
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