47 research outputs found
ΠΠΈΠ°Π³Π½ΠΎΡΡΠΈΠΊΠ° Π·Π°Π±ΠΎΠ»Π΅Π²Π°Π½ΠΈΠΉ ΡΠ΅ΡΠ΄Π΅ΡΠ½ΠΎ-ΡΠΎΡΡΠ΄ΠΈΡΡΠΎΠΉ ΡΠΈΡΡΠ΅ΠΌΡ ΠΈ ΠΈΡΠ΅ΠΌΠΈΠΈ ΠΌΠΈΠΎΠΊΠ°ΡΠ΄Π° Ρ ΠΏΠΎΠΌΠΎΡΡΡ ΠΌΠ°Π³Π½ΠΈΡΠΎΡΠ΅Π·ΠΎΠ½Π°Π½ΡΠ½ΠΎΠΉ Π²ΠΈΠ·ΡΠ°Π»ΠΈΠ·Π°ΡΠΈΠΈ Ρ ΠΊΠΎΠ½ΡΡΠ°ΡΡΠ½ΡΠΌ ΡΡΠΈΠ»Π΅Π½ΠΈΠ΅ΠΌ
ΠΠΎΠΊΠ°Π·Π°Π½Π° Π²ΠΎΠ·ΠΌΠΎΠΆΠ½ΠΎΡΡΡ Π²ΡΡΠ²Π»Π΅Π½ΠΈΡ ΠΏΠ°ΡΠΎΠ»ΠΎΠ³ΠΈΡΠ΅ΡΠΊΠΈΡ
ΠΈΠ·ΠΌΠ΅Π½Π΅Π½ΠΈΠΉ Π² ΠΌΠΈΠΎΠΊΠ°ΡΠ΄Π΅ (ΠΈΠ½ΡΠ°ΡΠΊΡ, ΠΈΡΠ΅ΠΌΠΈΡ) ΠΈ ΡΠΎΡΡΠ΄ΠΈΡΡΠΎΠΉ ΡΠΈΡΡΠ΅ΠΌΠ΅ (ΡΡΠ΅Π½ΠΎΠ·) Ρ ΠΏΠΎΠΌΠΎΡΡΡ ΠΌΠ°Π³Π½ΠΈΡΠΎΡΠ΅Π·ΠΎΠ½Π°Π½ΡΠ½ΠΎΠΉ Π²ΠΈΠ·ΡΠ°Π»ΠΈΠ·Π°ΡΠΈΠΈ Ρ ΠΊΠΎΠ½ΡΡΠ°ΡΡΠ½ΡΠΌ ΡΡΠΈΠ»Π΅Π½ΠΈΠ΅ΠΌ.The possibility to reveal pathological changes in the myocardium (infarction, ischemia) and vascular system (stenosis) using magnetic resonance imaging with contrast enhancement is shown
On the sample size dependence of the critical current density in MgB superconductors
Sample size dependent critical current density has been observed in magnesium
diboride superconductors. At high fields, larger samples provide higher
critical current densities, while at low fields, larger samples give rise to
lower critical current densities. The explanation for this surprising result is
proposed in this study based on the electric field generated in the
superconductors. The dependence of the current density on the sample size has
been derived as a power law ( is the factor
characterizing curve ). This dependence provides one with
a new method to derive the factor and can also be used to determine the
dependence of the activation energy on the current density.Comment: Revtex, 4 pages, 5 figure
Brain Plasticity and Intellectual Ability Are Influenced by Shared Genes
Although the adult brain is considered to be fully developed and stable until senescence when its size steadily decreases, such stability seems at odds with continued human (intellectual) development throughout life. Moreover, although variation in human brain size is highly heritable, we do not know the extent to which genes contribute to individual differences in brain plasticity. In this longitudinal magnetic resonance imaging study in twins, we report considerable thinning of the frontal cortex and thickening of the medial temporal cortex with increasing age and find this change to be heritable and partly related to cognitive ability. Specifically, adults with higher intelligence show attenuated cortical thinning and more pronounced cortical thickening over time than do subjects with average or below average IQ. Genes influencing variability in both intelligence and brain plasticity partly drive these associations. Thus, not only does the brain continue to change well into adulthood, these changes are functionally relevant because they are related to intelligence. CopyrightΒ©2010 the authors
Is synthetic hexaploid wheat a useful germplasm source for increasing grain size and yield in bread wheat breeding?
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ΠΠ΅ΡΠ°ΠΊΠ»ΠΈΡΡ β ΠΊΠ°ΡΠ±ΠΎΠ½Π°ΡΠ½ΡΠ΅ ΠΎΠ±ΡΠ°Π·ΠΎΠ²Π°Π½ΠΈΡ Π³Π°Π·ΠΎΠ²ΡΡ ΠΈΡΡΠΎΡΠ½ΠΈΠΊΠΎΠ² ΠΈ Π³ΡΡΠ·Π΅Π²ΡΡ Π²ΡΠ»ΠΊΠ°Π½ΠΎΠ² ΠΌΠΈΠΎΡΠ΅Π½Π°
ΠΠΎΡΡΠΎΠ»ΠΎΠ³ΠΈΡΠ΅ΡΠΊΠΈΠ΅ ΠΏΡΠΈΠ·Π½Π°ΠΊΠΈ, ΠΌΠΈΠ½Π΅ΡΠ°Π»ΠΎΠ³ΠΈΡ, Π³Π΅ΠΎΡ
ΠΈΠΌΠΈΡ ΠΈ ΡΠΎΡΡΠ°Π² Π³Π°Π·ΠΎΠ²ΠΎΠΉ ΡΡΠ°ΠΊΡΠΈΠΈ Π³Π΅ΡΠ°ΠΊΠ»ΠΈΡΠΎΠ² ΠΏΠΎΠ΄ΡΠ²Π΅ΡΠ΄ΠΈΠ»ΠΈ ΠΈΡ
Π³Π΅Π½Π΅ΡΠΈΡΠ΅ΡΠΊΡΡ ΠΎΠ±ΡΠ½ΠΎΡΡΡ Ρ ΡΠΎΠ²ΡΠ΅ΠΌΠ΅Π½Π½ΡΠΌΠΈ ΠΊΠ°ΡΠ±ΠΎΠ½Π°ΡΠ½ΡΠΌΠΈ ΠΎΠ±ΡΠ°Π·ΠΎΠ²Π°Π½ΠΈΡΠΌΠΈ ΠΌΠ΅ΡΠ°Π½ΠΎΠ²ΡΡ
ΠΈΡΡΠΎΡΠ½ΠΈΠΊΠΎΠ² ΠΈ Π³ΡΡΠ·Π΅Π²ΡΡ
Π²ΡΠ»ΠΊΠ°Π½ΠΎΠ² Π§Π΅ΡΠ½ΠΎΠ³ΠΎ ΠΌΠΎΡΡ. ΠΡΠΈΡΡΡΡΡΠ²ΠΈΠ΅ Π² Π³Π΅ΡΠ°ΠΊΠ»ΠΈΡΠ°Ρ
Π±ΠΈΡΡΠΌΠΎΠ², ΠΌΠ΅ΡΠ°Π½Π° ΠΈ ΡΡΠ°Π½Π° ΠΌΠΎΠΆΠ΅Ρ ΡΠ»ΡΠΆΠΈΡΡ ΠΈΠ½Π΄ΠΈΠΊΠ°ΡΠΎΡΠΎΠΌ Π½Π°Π»ΠΈΡΠΈΡ Π½Π΅ΡΡΠΈ ΠΈ Π³Π°Π·Π° Π½Π° ΠΠ΅ΡΠ°ΠΊΠ»Π΅ΠΉΡΠΊΠΎΠΌ ΠΏΠΎΠ»ΡΠΎΡΡΡΠΎΠ²Π΅ ΠΈ ΠΏΡΠΈΠ»Π΅Π³Π°ΡΡΠ΅ΠΌΡ ΠΊ Π½Π΅ΠΌΡ ΡΠ΅Π»ΡΡΠ΅.ΠΠΎΡΡΠΎΠ»ΠΎΠ³ΡΡΠ½Ρ ΠΎΠ·Π½Π°ΠΊΠΈ, ΠΌΡΠ½Π΅ΡΠ°Π»ΠΎΠ³ΡΡ, Π³Π΅ΠΎΡ
!ΠΌΡΡ i ΡΠΊΠ»Π°Π΄ Π³Π°Π·ΠΎΠ²ΠΎΡ ΡΡΠ°ΠΊΡΡΡ Π³Π΅ΡΠ°ΠΊΠ»ΠΈΡΡΠ² ΠΏΡΠ΄ΡΠ²Π΅ΡΠ΄ΠΈΠ»ΠΈ ΡΡ
Π³Π΅Π½Π΅ΡΠΈΡΠ½Ρ ΡΠΏΡΠ»ΡΠ½ΡΡΡΡ ΡΠ· ΡΡΡΠ°ΡΠ½ΠΈΠΌΠΈ ΠΊΠ°ΡΠ±ΠΎΠ½Π°ΡΠ½ΠΈΠΌΠΈ ΡΡΠ²ΠΎΡΠ΅Π½Π½ΡΠΌΠΈ ΠΌΠ΅ΡΠ°Π½ΠΎΠ²ΠΈΡ
Π΄ΠΆΠ΅ΡΠ΅Π» i Π³ΡΡΠ·ΡΠΎΠ²ΠΈΡ
Π²ΡΠ»ΠΊΠ°Π½ΡΠ² Π§ΠΎΡΠ½ΠΎΠ³ΠΎ ΠΌΠΎΡΡ. ΠΡΠΈΡΡΡΠ½ΡΡΡΡ Ρ Π³Π΅ΡΠ°ΠΊΠ»ΡΡΠ°Ρ
Π±ΡΡΡΠΌΡΠ², ΠΌΠ΅ΡΠ°Π½Ρ i Π΅ΡΠ°Π½Ρ ΠΌΠΎΠΆΠ΅ ΡΠ»ΡΠ³ΡΠ²Π°ΡΠΈ ΡΠΊ ΡΠ½Π΄ΠΈΠΊΠ°ΡΠΎΡ Π½Π°ΡΠ²Π½ΠΎΡΡΡ Π½Π°ΡΡΠΈ ΠΉ Π³Π°Π·Ρ Π½Π° ΠΠ΅ΡΠ°ΠΊΠ»Π΅ΠΉΡΡΠΊΠΎΠΌ niΠ²ocΡpoΠ²i i ΠΏΡΠΈΠ»Π΅Π³Π»ΠΎΠΌΡ Π΄ΠΎ Π½ΡΠΎΠ³ΠΎ ΡΠ΅Π»ΡΡΡ.Morphological attributes, mineralogy, geochemistry and structure of gas fraction Geraklit have confirmed their proximity to modern carbonate formations of methane sources and mud volcanoes in the Black sea. Presence of bitumen, methane and ethane in Geraklites serves as indicator of occurence of oil fields and gas on the Geraklejskij peninsula and adjoining to them a shelf
Contributing factors to advanced brain aging in depression and anxiety disorders
Depression and anxiety are common and often comorbid mental health disorders that represent risk factors for aging-related conditions. Brain aging has shown to be more advanced in patients with major depressive disorder (MDD). Here, we extend prior work by investigating multivariate brain aging in patients with MDD, anxiety disorders, or both, and examine which factors contribute to older-appearing brains. Adults aged 18-57 years from the Netherlands Study of Depression and Anxiety underwent structural MRI. A pretrained brain-age prediction model based on >2000 samples from the ENIGMA consortium was applied to obtain brain-predicted age differences (brain PAD, predicted brain age minus chronological age) in 65 controls and 220 patients with current MDD and/or anxiety. Brain-PAD estimates were associated with clinical, somatic, lifestyle, and biological factors. After correcting for antidepressant use, brain PAD was significantly higher in MDD (+2.78 years, Cohen's d=0.25, 95% CI -0.10-0.60) and anxiety patients (+2.91 years, Cohen's d=0.27, 95% CI -0.08-0.61), compared with controls. There were no significant associations with lifestyle or biological stress systems. A multivariable model indicated unique contributions of higher severity of somatic depression symptoms (b=4.21 years per unit increase on average sum score) and antidepressant use (-2.53 years) to brain PAD. Advanced brain aging in patients with MDD and anxiety was most strongly associated with somatic depressive symptomatology. We also present clinically relevant evidence for a potential neuroprotective antidepressant effect on the brain-PAD metric that requires follow-up in future research.Education and Child Studie
Genetic contributions to human brain morphology and intelligence
Variation in gray matter (GM) and white matter (WM) volume of the adult human brain is primarily genetically determined. Moreover, total brain volume is positively correlated with general intelligence, and both share a common genetic origin. However, although genetic effects on morphology of specific GM areas in the brain have been studied, the heritability of focal WM is unknown. Similarly, it is unresolved whether there is a common genetic origin of focal GM and WM structures with intelligence. We explored the genetic influence on focal GM and WM densities in magnetic resonance brain images of 54 monozygotic and 58 dizygotic twin pairs and 34 of their siblings. For genetic analyses, we used structural equation modeling and voxel-based morphometry. To explore the common genetic origin of focal GM and WM areas with intelligence, we obtained cross-trait/cross-twin correlations in which the focal GM and WM densities of each twin are correlated with the psychometric intelligence quotient of his/her cotwin. Genes influenced individual differences in left and right superior occipitofrontal fascicle (heritability up to 0.79 and 0.77), corpus callosum (0.82, 0.80), optic radiation (0.69, 0.79), corticospinal tract (0.78, 0.79), medial frontal cortex (0.78, 0.83), superior frontal cortex (0.76, 0.80), superior temporal cortex (0.80, 0.77), left occipital cortex (0.85), left postcentral cortex (0.83), left posterior cingulate cortex (0.83), right parahippocampal cortex (0.69), and amygdala (0.80, 0.55). Intelligence shared a common genetic origin with superior occipitofrontal, callosal, and left optical radiation WM and frontal, occipital, and parahippocampal GM (phenotypic correlations up to 0.35). These findings point to a neural network that shares a common genetic origin with human intelligence
Using structural MRI to identify bipolar disorders - 13 site machine learning study in 3020 individuals from the ENIGMA Bipolar Disorders Working Group.
Bipolar disorders (BDs) are among the leading causes of morbidity and disability. Objective biological markers, such as those based on brain imaging, could aid in clinical management of BD. Machine learning (ML) brings neuroimaging analyses to individual subject level and may potentially allow for their diagnostic use. However, fair and optimal application of ML requires large, multi-site datasets. We applied ML (support vector machines) to MRI data (regional cortical thickness, surface area, subcortical volumes) from 853 BD and 2167 control participants from 13 cohorts in the ENIGMA consortium. We attempted to differentiate BD from control participants, investigated different data handling strategies and studied the neuroimaging/clinical features most important for classification. Individual site accuracies ranged from 45.23% to 81.07%. Aggregate subject-level analyses yielded the highest accuracy (65.23%, 95% CIβ=β63.47-67.00, ROC-AUCβ=β71.49%, 95% CIβ=β69.39-73.59), followed by leave-one-site-out cross-validation (accuracy = 58.67%, 95% CIβ=β56.70-60.63). Meta-analysis of individual site accuracies did not provide above chance results. There was substantial agreement between the regions that contributed to identification of BD participants in the best performing site and in the aggregate dataset (Cohen's Kappaβ=β0.83, 95% CIβ=β0.829-0.831). Treatment with anticonvulsants and age were associated with greater odds of correct classification. Although short of the 80% clinically relevant accuracyΒ threshold, the results are promising and provide a fair and realistic estimate of classification performance, which can be achieved in a large, ecologically valid, multi-site sample of BD participants based on regional neurostructural measures. Furthermore, the significant classification in different samples was based on plausible and similar neuroanatomical features. Future multi-site studies should move towards sharing of raw/voxelwise neuroimaging data
Do we measure gray matter activation with functional diffusion tensor imaging?
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