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Szyf, Moshe; Bick, Johanna – Child Development, 2013
Although epidemiological data provide evidence that early life experience plays a critical role in human development, the mechanism of how this works remains in question. Recent data from human and animal literature suggest that epigenetic changes, such as DNA methylation, are involved not only in cellular differentiation but also in the…
Descriptors: Genetics, Early Experience, Individual Development, Cytology
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Braverman, Nancy E.; D'Agostino, Maria Daniela; MacLean, Gillian E. – Developmental Disabilities Research Reviews, 2013
The peroxisome biogenesis disorders (PBD) are a heterogeneous group of autosomal recessive disorders in which peroxisome assembly is impaired, leading to multiple peroxisome enzyme deficiencies, complex developmental sequelae and progressive disabilities. Mammalian peroxisome assembly involves the protein products of 16 "PEX" genes;…
Descriptors: Genetic Disorders, Congenital Impairments, Biochemistry, Symptoms (Individual Disorders)
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Kanungo, Shibani; Soares, Neelkamal; He, Miao; Steiner, Robert D. – Developmental Disabilities Research Reviews, 2013
Cholesterol has numerous quintessential functions in normal cell physiology, as well as in embryonic and postnatal development. It is a major component of cell membranes and myelin, and is a precursor of steroid hormones and bile acids. The development of the blood brain barrier likely around 12-18 weeks of human gestation makes the developing…
Descriptors: Genetic Disorders, Metabolism, Neurological Impairments, Symptoms (Individual Disorders)
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Kerkhoff, Annemarie; de Bree, Elise; de Klerk, Maartje; Wijnen, Frank – Journal of Child Language, 2013
This study tests the hypothesis that developmental dyslexia is (partly) caused by a deficit in implicit sequential learning, by investigating whether infants at familial risk of dyslexia can track non-adjacent dependencies in an artificial language. An implicit learning deficit would hinder detection of such dependencies, which mark grammatical…
Descriptors: Genetics, Dyslexia, Child Language, Language Acquisition
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Lebowitz, Matthew S.; Ahn, Woo-Kyoung; Nolen-Hoeksema, Susan – Journal of Consulting and Clinical Psychology, 2013
Objective: Previous research has shown that biological (e.g., genetic, biochemical) accounts of depression--currently in ascendancy--are linked to the general public's pessimism about the syndrome's prognosis. This research examined for the first time whether people with depressive symptoms would associate biological accounts of depression with…
Descriptors: Biology, Depression (Psychology), Adults, Beliefs
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Little, Katie; Riby, Deborah M.; Janes, Emily; Clark, Fiona; Fleck, Ruth; Rodgers, Jacqui – Research in Developmental Disabilities: A Multidisciplinary Journal, 2013
The developmental disorder of Williams syndrome (WS) is associated with an overfriendly personality type, including an increased tendency to approach strangers. This atypical social approach behaviour (SAB) has been linked to two potential theories: the amygdala hypothesis and the frontal lobe hypothesis. The current study aimed to investigate…
Descriptors: Inhibition, Personality Traits, Brain Hemisphere Functions, Children
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Haworth, Claire M. A.; Davis, Oliver S. P.; Hanscombe, Ken B.; Kovas, Yulia; Dale, Philip S.; Plomin, Robert – Learning and Individual Differences, 2013
Previous studies have shown that environmental influences on school science performance increase in importance from primary to secondary school. Here we assess for the first time the relationship between the science-learning environment and science performance using a genetically sensitive approach to investigate the aetiology of this link. 3000…
Descriptors: Foreign Countries, Educational Environment, Science Education, Twins
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Marschik, Peter B.; Kaufmann, Walter E.; Sigafoos, Jeff; Wolin, Thomas; Zhang, Dajie; Bartl-Pokorny, Katrin D.; Pini, Giorgio; Zappella, Michele; Tager-Flusberg, Helen; Einspieler, Christa; Johnston, Michael V. – Research in Developmental Disabilities: A Multidisciplinary Journal, 2013
We delineated the achievement of early speech-language milestones in 15 young children with Rett syndrome ("MECP2" positive) in the first two years of life using retrospective video analysis. By contrast to the commonly accepted concept that these children are normal in the pre-regression period, we found markedly atypical development of…
Descriptors: Pathology, Video Technology, Language Acquisition, Genetic Disorders
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Ashworth, Anna; Hill, Catherine M.; Karmiloff-Smith, Annette; Dimitriou, Dagmara – Research in Developmental Disabilities: A Multidisciplinary Journal, 2013
Based on previous findings of frequent sleep problems in children with Down syndrome (DS) and Williams syndrome (WS), the present study aimed to expand our knowledge by using parent report and actigraphy to define sleep problems more precisely in these groups. Twenty-two school-aged children with DS, 24 with WS and 52 typically developing (TD)…
Descriptors: Sleep, Genetic Disorders, Down Syndrome, Symptoms (Individual Disorders)
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Chen, Mu-Hong; Su, Tung-Ping; Chen, Ying-Sheue; Hsu, Ju-Wei; Huang, Kai-Lin; Chang, Wen-Han; Chen, Tzeng-Ji; Bai, Ya-Mei – Research in Autism Spectrum Disorders, 2013
Previous clinical and genetic studies have suggested autism spectrum disorders (ASDs) is associated with immunological abnormalities involving cytokines, immunoglobulins, inflammation, and cellular immunity, but epidemiological reports are still limited. Patients with ASDs were identified in the National Health Insurance Database from 1996 to…
Descriptors: Health Insurance, Autism, Etiology, Control Groups
Gulsoy, Gunhan – ProQuest LLC, 2013
New experimental methods has resulted in increasing amount of genetic interaction data to be generated every day. Biological networks are used to store genetic interaction data gathered. Increasing amount of data available requires fast large scale analysis methods. Therefore, we address the problem of querying large biological network datasets.…
Descriptors: Biological Sciences, Biomedicine, Databases, Genetics
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Eggleson, Kathleen – American Biology Teacher, 2013
The controversy and uncertainty surrounding use of nanosilver in consumer products can be used to stimulate a question-based discussion that integrates ethical and social implications with biology.
Descriptors: Science and Society, Genetics, Ethics, Biology
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Priess-Groben, Heather A.; Hyde, Janet Shibley – Journal of Abnormal Child Psychology, 2013
Depression surges in adolescence, especially among girls. Most evidence indicates that the short allele of a polymorphism in the promoter region of the serotonin transporter gene (5-HTTLPR) interacts with stress to influence the onset of depression. This effect appears to be less robust in adolescents, particularly among boys, and may be moderated…
Descriptors: Females, Adolescents, Depression (Psychology), Interaction
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Kohlman, Michael J. – Alberta Journal of Educational Research, 2012
This article examines the history of the American Eugenics movement's penetration into the formal and popular educational milieu during the first half of the 20th Century, and includes a review of some recent scholarly research on eugenic themes in education and popular culture. Apologists have dismissed the American Eugenics movement as a…
Descriptors: Scholarship, Social Sciences, Popular Culture, Historiography
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Duan, Xiaoju – High Ability Studies, 2012
A promising future has been drawn by Ziegler and Phillipson through illustrating how gifted education works as a system to be beneficial to everyone. Gifted education is individually designed and fostered. The whole system requires continuous adaptation and adjustment of both the individual and environment including schools, teachers, parents, and…
Descriptors: Gifted, Genetics, Futures (of Society), Instructional Design
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