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If head morphology and brain size are also integrated, eco-morphological adaptations might indirectly affect brain size evolution [ 12, 15].
Given the strong and general association of ecology and head shape in teleost fishes [ 32- 36], our results indicate that eco-morphological adaptation and cognitive adaptation can interact through phenotypic integration of head morphology and brain size.
Those hypothesis are further supported by neuroimaging research, which provides an accurate way to measure the relationship between behaviors or symptoms and underlying brain morphology and brain functioning.
Therefore, further studies on brain morphology and brain metabolism are essential to elucidate the (neuro physiological basis of fatigue.
Notably, gross brain morphology and brain mass (Fig 1E) and body mass (Supporting Information Fig S1) were normal in Hdac6 −/− mice.
Our assessment of covariation between head morphology and brain size, feeding mode, and body size involved testing for correlated evolution between two sets of several variables.
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We have evaluated the efficacy of enriched environment on the dendritic morphology and brain-derived neurotrophic factor (BDNF) expression in the hippocampus of ventral subicular lesioned rats.
These findings link PAK/LIMK1-dependent regulatiof of actin polymerization to the control of spine morphology and higher brain function.
Unique to songbirds is the complex syringeal morphology and underlying brain circuitry for vocal learning, the ability to imitate a tutor's song transmitted across successive generations [ 4, 5].
Our multivariate phylogenetic comparative study found support for integration of the head morphology of Lake Tanganyika cichlids, and that evolutionary associations exist among head morphology, feeding mode, and brain size.
Our study supports the hypothesis that brain surface morphology, gyral patterns, and brain volumes underlie lesser genetic control than supposed [ 3, 5].
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