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Chaudhry, M. Ahmad – Biochemistry and Molecular Biology Education, 2006
The expression of genes in cells of various tissue types varies considerably and is correlated with the function of a particular organ. The pattern of gene expression changes in diseased tissues, in response to therapy or infection and exposure to environmental mutagens, chemicals, ultraviolet light, and ionizing radiation. To better understand…
Descriptors: Radiation, Genetics, Human Body, Diseases
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Bonner, Janice M.; Holliday, William G. – Journal of Research in Science Teaching, 2006
A composite theory of college science student note-taking strategies was derived from a periodic series of five interviews with 23 students and with other variables, including original and final versions of notes analyzed during a semester-long genetics course. This evolving composite theory was later compared with Van Meter, Yokoi, and Pressley's…
Descriptors: College Science, Learning Strategies, Genetics, Notetaking
Papierno, Paul B.; Ceci, Stephen J.; Makel, Matthew C.; Williams, Wendy M. – Journal for the Education of the Gifted, 2005
Despite extensive research, questions underlying the nature and nurture of talent remain both numerous and diverse. In the current paper, we present an account that addresses 2 of the primary questions inspired by this debate: (a) the very existence of innate talents and (b) how exceptional abilities are developed. The development of exceptional…
Descriptors: Nature Nurture Controversy, Talent, Talent Development, Models
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Polderman, Tinca J. C.; Stins, John F.; Posthuma, Danielle; Gosso, M. Florencia; Verhulst, Frank C.; Boomsma, Dorret I. – Intelligence, 2006
This study examined the phenotypic and genotypic relationship between working memory speed (WMS) and working memory capacity (WMC) in 12-year-old twins and their siblings (N = 409). To asses WMS all children performed a reaction time task with three memory loads from which a basic mental speed measure and the derived slope were used. WMC was…
Descriptors: Short Term Memory, Children, Twins, Siblings
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Elks, Martin A. – Mental Retardation: A Journal of Practices, Policy and Perspectives, 2005
"The Kallikak Family" is a pre-eminent text in the history of mental retardation and psychology in which Goddard (1912) claimed he proved the heritability of feeble-mindedness and the necessity of institutionalization. The book contains 14 photographs, some of which have been retouched. These photographs were interpreted in this paper within the…
Descriptors: History, Mental Retardation, Psychology, Photography
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Pata, Kai; Sarapuu, Tago – International Journal of Science Education, 2006
This study investigated the possible activation of different types of model-based reasoning processes in two learning settings, and the influence of various terms of reasoning on the learners' problem representation development. Changes in 53 students' problem representations about genetic issue were analysed while they worked with different…
Descriptors: Logical Thinking, Genetics, Charts, Influences
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Valasek, Mark A.; Repa, Joyce J. – Advances in Physiology Education, 2005
In recent years, real-time polymerase chain reaction (PCR) has emerged as a robust and widely used methodology for biological investigation because it can detect and quantify very small amounts of specific nucleic acid sequences. As a research tool, a major application of this technology is the rapid and accurate assessment of changes in gene…
Descriptors: Research Methodology, Research Tools, Genetics, Molecular Biology
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Marcus, Jeffrey – Journal of College Science Teaching, 2005
It is not always easy for a teacher to relate to his or her students. To communicate with students, it is important for a teacher to relate the subject that he or she is trying to teach is something that the students know, or at least to something that the students care about. In this article, the author, a genetics teacher, relates how he used…
Descriptors: Cancer, Genetics, Entomology, Teaching Styles
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Kielinen, Marko; Rantala, Heikki; Timonen, Eija; Linna, Sirkka-Liisa; Moilanen, Irma – Autism: The International Journal of Research and Practice, 2004
A population-based survey was conducted among 152,732 Finnish children and adolescents aged under 16 years and living in northern Finland. Diagnoses and associated medical conditions were derived from the hospital and institutional records of this area. One hundred and eighty-seven children with DSM-IV autistic disorder were identified. Associated…
Descriptors: Foreign Countries, Down Syndrome, Hearing Impairments, Cerebral Palsy
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Whitfield, Keith E.; McClearn, Gerald – American Psychologist, 2005
Understanding the origins of racial health disparities is currently a central focus of health-oriented funding agencies and the health policy community. In particular, the role of genetics in the origin of racial health disparities is receiving growing attention and has been susceptible to considerable misinterpretation. In this article, the…
Descriptors: Race, Health Conditions, Genetics, Environment
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Bertella, L.; Girelli, L.; Grugni, G.; Marchi, S.; Molinari, E.; Semenza, C. – Journal of Intellectual Disability Research, 2005
This paper investigates mathematical skills in Prader-Willi Syndrome (PWS), a pathological condition because of congenital alterations of chromosome pair 15. The following questions were addressed: (1) Are mathematical skills in PWS relatively more impaired with respect to other cognitive functions (as has been repeatedly but anecdotally…
Descriptors: Measures (Individuals), Task Analysis, Cognitive Ability, Short Term Memory
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Wigg, Karen G.; Couto, Jillian M.; Feng, Yu; Crosbie, Jennifer; Anderson, Barbara; Cate-Carter, Tasha; Tannock, Rosemary; Lovett, Maureen W.; Humphries, Tom; Kennedy, James L.; Ickowicz, Abel; Pathare, Tejaswee; Roberts, Wendy; Malone, Molly; Schachar, Russell; Barr, Cathy L. – Scientific Studies of Reading, 2005
Recently a gene, termed EKN1, has been identified because of a chromosomal breakpoint that occurred in this gene. This chromosomal breakpoint was found in 4 family members that had specific reading disabilities (RDs), indicating that disruption of this gene may be contributing to the risk of developing RDs. This gene was further supported as…
Descriptors: Reading Difficulties, Hyperactivity, Genetics, Attention Deficit Disorders
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Lewis, Alison; Peat, Mary; Franklin, Sue – Journal of Biological Education, 2005
Protein synthesis is a complex process and students find it difficult to understand. This article describes an interactive discussion "game" used by first year biology students at the University of Sydney. The students, in small groups, use the game in which the processes of protein synthesis are actioned by the students during a…
Descriptors: Biology, Genetics, Scientific Concepts, Universities
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Bolte, Sven; Poustka, Fritz – Journal of Child Psychology and Psychiatry, 2006
Background: The objective of this study was to investigate the tendency for local processing style ("weak central coherence") and executive dysfunction in parents of subjects with an autism spectrum disorder (ASD) compared with parents of individuals with early onset schizophrenia (EOS) and mental retardation (MR). Method: Sixty-two…
Descriptors: Mental Retardation, Schizophrenia, Autism, Genetics
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Polleux, Franck; Lauder, Jean M. – Mental Retardation and Developmental Disabilities Research Reviews, 2004
Autism is a complex, behaviorally defined, developmental brain disorder with an estimated prevalence of 1 in 1,000. It is now clear that autism is not a disease, but a syndrome with a strong genetic component. The etiology of autism is poorly defined both at the cellular and the molecular levels. Based on the fact that seizure activity is…
Descriptors: Autism, Seizures, Inhibition, Etiology
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