Gotowe bibliografie tematyczne / Developmental neurophysiology Genetic aspects

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Gotowa bibliografia na temat „Developmental neurophysiology Genetic aspects”

Autor: Grafiati
Data publikacji: 4 czerwca 2021
Data aktualizacji: 28 stycznia 2023

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Artykuły w czasopismach na temat "Developmental neurophysiology Genetic aspects"

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Winter, R. M. "Genetic Aspects of Developmental Pathology." Journal of Medical Genetics 25, no. 2 (February 1, 1988): 141. http://dx.doi.org/10.1136/jmg.25.2.141.

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Scharloo, W. "Canalization: Genetic and Developmental Aspects." Annual Review of Ecology and Systematics 22, no. 1 (November 1991): 65–93. http://dx.doi.org/10.1146/annurev.es.22.110191.000433.

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Regehr, Sonya M. "The genetic aspects of developmental dyslexia." Canadian Journal of Behavioural Science / Revue canadienne des sciences du comportement 19, no. 3 (1987): 239–53. http://dx.doi.org/10.1037/h0079988.

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Postma, Alex V., Lukas R. C. Dekker, Alexandre T. Soufan, and Antoon F. M. Moorman. "Developmental and Genetic Aspects of Atrial Fibrillation." Trends in Cardiovascular Medicine 19, no. 4 (May 2009): 123–30. http://dx.doi.org/10.1016/j.tcm.2009.07.003.

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Paoli, Marco, and Giovanni C. Galizia. "Olfactory coding in honeybees." Cell and Tissue Research 383, no. 1 (January 2021): 35–58. http://dx.doi.org/10.1007/s00441-020-03385-5.

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Abstract With less than a million neurons, the western honeybee Apis mellifera is capable of complex olfactory behaviors and provides an ideal model for investigating the neurophysiology of the olfactory circuit and the basis of olfactory perception and learning. Here, we review the most fundamental aspects of honeybee’s olfaction: first, we discuss which odorants dominate its environment, and how bees use them to communicate and regulate colony homeostasis; then, we describe the neuroanatomy and the neurophysiology of the olfactory circuit; finally, we explore the cellular and molecular mecha
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Alkhzouz, Camelia, Simona Bucerzan, Maria Miclaus, Andreea-Manuela Mirea, and Diana Miclea. "46,XX DSD: Developmental, Clinical and Genetic Aspects." Diagnostics 11, no. 8 (July 30, 2021): 1379. http://dx.doi.org/10.3390/diagnostics11081379.

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Differences in sex development (DSD) in patients with 46,XX karyotype occur by foetal or postnatal exposure to an increased amount of androgens. These disorders are usually diagnosed at birth, in newborns with abnormal genitalia, or later, due to postnatal virilization, usually at puberty. Proper diagnosis and therapy are mostly based on the knowledge of normal development and molecular etiopathogenesis of the gonadal and adrenal structures. This review aims to describe the most relevant data that are correlated with the normal and abnormal development of adrenal and gonadal structures in dire
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Srivastava, Deepak. "Developmental and genetic aspects of congenital heart disease." Current Opinion in Cardiology 14, no. 3 (May 1999): 263. http://dx.doi.org/10.1097/00001573-199905000-00011.

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Levy, Avraham A., Anne Bagg Britt, Kenneth R. Luehrsen, Vicki L. Chandler, Christine Warren, and Virginia Walbot. "Developmental and genetic aspects ofMutator excision in maize." Developmental Genetics 10, no. 6 (1989): 520–31. http://dx.doi.org/10.1002/dvg.1020100611.

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Veenma, D. C. M., A. de Klein, and D. Tibboel. "Developmental and genetic aspects of congenital diaphragmatic hernia." Pediatric Pulmonology 47, no. 6 (March 29, 2012): 534–45. http://dx.doi.org/10.1002/ppul.22553.

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MORSE, ANDREW C., JOHN L. BEARD, and BYRON C. JONES. "A Genetic Developmental Model of Iron Deficiency: Biological Aspects." Proceedings of the Society for Experimental Biology and Medicine 220, no. 3 (March 1999): 147–52. http://dx.doi.org/10.1046/j.1525-1373.1999.d01-22.x.

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Rozprawy doktorskie na temat "Developmental neurophysiology Genetic aspects"

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Tosch, Paul. "Investigations of ephrin ligands during development." Title page, abstract and table of contents only, 2002. http://web4.library.adelaide.edu.au/theses/09PH/09pht713.pdf.

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"May 2002." Addendum inside back cover. Bibliography: p. 139-157. Aims to isolate ephrin ligands from Drosophila melanogaster and analyse their involvement in Drosophila deveopment. Also investigates the potential of ephrin B-1 as a causative gene in the human condition Aicardi's syndrome.
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Gauthier, Julie. "Genetic investigation of pervasive developmental disorders in the Quebec population." Thesis, McGill University, 2005. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=100369.

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Pervasive developmental disorders are a group of neurodevelopmental-neuropsychiatric disorders that are characterized by variable and severe pervasive impairments in several areas of child development, notably social interaction, communication and imagination. They all share clinical features but differ in the severity and age of onset of the impairments. Except for Rett Syndrome (RTT), the etiology of these disorders is unknown, but there is strong evidence that genetic factors contribute to their pathogenesis. While no major genes have been linked to theses disorders linkages, association an
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Law, Kit-fong Stephanie, and 羅潔芳. "The molecular consequences of Indian hedgehog mutations in distal digit patterning." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2004. http://hub.hku.hk/bib/B31353253.

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Morgan, Vera Anne. "Intellectual disability co-occurring with schizophrenia and other psychiatric illness : epidemiology, risk factors and outcome." University of Western Australia. School of Psychiatry and Clinical Neurosciences, 2008. http://theses.library.uwa.edu.au/adt-WU2008.0209.

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(Truncated abstract) The aims of this thesis are: (i) To estimate the prevalence of psychiatric illness among persons with intellectual disability and, conversely, the prevalence of intellectual disability among persons with a psychiatric illness; (ii) To describe the disability and service utilisation profile of persons with conjoint disorder; (iii) To examine, in particular, intellectual disability co-occurring with schizophrenia; and (iv) To explore the role of hereditary and environmental (specifically obstetric) risk factors in the aetiology of (i) intellectual disability and (ii) intelle
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Moers, Virginie. "Contribution à l'étude de la fonction des facteurs BTBD6 et DMRT5 au cours du développement embryonnaire." Doctoral thesis, Universite Libre de Bruxelles, 2008. http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/210408.

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Au cours de ce travail de thèse, nous avons abordé l’étude des gènes BTBD6 et Dmrt5 au cours du développement embryonnaire en utilisant les avantages complémentaires de plusieurs organismes modèles.<p>\<br>Doctorat en Sciences<br>info:eu-repo/semantics/nonPublished
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Tosch, Paul. "Investigations of ephrin ligands during development / by Paul Tosch." Thesis, 2002. http://hdl.handle.net/2440/21884.

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"May 2002."<br>Addendum inside back cover.<br>Bibliography: p. 139-157.<br>174 p. : ill. (some col.), col. plates ; 30 cm.<br>Aims to isolate ephrin ligands from Drosophila melanogaster and analyse their involvement in Drosophila deveopment. Also investigates the potential of ephrin B-1 as a causative gene in the human condition Aicardi's syndrome.<br>Thesis (Ph.D.)--University of Adelaide, Dept. of Molecular Biosciences, 2003
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Qi, Hongjian. "Computational genomics and genetics of developmental disorders." Thesis, 2018. https://doi.org/10.7916/D8N02QDR.

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Computational genomics is at the intersection of computational applied physics, math, statistics, computer science and biology. With the advances in sequencing technology, large amounts of comprehensive genomic data are generated every year. However, the nature of genomic data is messy, complex and unstructured; it becomes extremely challenging to explore, analyze and understand the data based on traditional methods. The needs to develop new quantitative methods to analyze large-scale genomics datasets are urgent. By collecting, processing and organizing clean genomics datasets and using these
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"Studies of candidate genes for susceptibility to developmental dyslexia." 2012. http://library.cuhk.edu.hk/record=b5934633.

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讀寫障礙是最普遍的一種學習障礙（80%)，影響全球大約一成的學童。讀寫障礙患者於閱讀及書寫能力方面出現困難，而這並非因為患者本身的智力、學習動機或學習機會引致。對於引至讀寫障礙的理仍未清楚，但在西方人士的遺傳研究方面已發現多個與讀寫障礙相聯的基因位點及基因。本研究針對其中4個基因位點（DYX1 ’ DYX2 ’ DYX3 ’ DKX8)及其覆蓋的11基因測試了 131讀寫障礙的中國人家庭與讀寫障礙的關聯性。是項研究從國際人類基因組單體型圖(HapMap)中選擇標籤單核苷酸多型性(Tag-SNPs)及選擇以往報告與讀寫障礙有關的單核苷酸多型性進行測試。並在DYXZa基因（rs3743205 ’ padjusted =0.0072' OR = 0.08 ( 95% CI: 0.01 - 0.64 ))私MRPL19 (風險單体型rs2422229-rs7570229,風險單体型T-G, Padjusted=0.0020, OR = 2.345 (95% CI: 1.402 - 3.923))發現與讀寫障礙有正關聯性。單核苷酸多態性亦與閱讀的幾個特徵相關：DYX1C1 ( rs3743205 )與快速命名（Digit Rapid Naming ) ’語音記憶（Non-word repetition)，字型結構的左右逆轉（Left-Right Reversal )相關；KIAA0319 (
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Queitsch, Christine. "Thermotolerance, buffering of genetic variation and developmental stability : different aspects of chaperone function in the plant Arabidopsis thaliana /." 2001. http://gateway.proquest.com/openurl?url_ver=Z39.88-2004&res_dat=xri:pqdiss&rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&rft_dat=xri:pqdiss:3029529.

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"Pathogenesis of retinoic acid-induced developmental ocular defects studied using mouse models." Thesis, 2009. http://library.cuhk.edu.hk/record=b6074726.

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As exogenously administered RA suppressed the expression of the RA synthesizing enzymes, further investigation on whether this would lead to deficiency in endogenous RA concentrations was conducted. Results showed that exogenously administered RA significantly reduced the endogenous RA level in the head region with C57 embryos showing a greater reduction than ICR embryos.<br>In addition, detailed morphological and histological studies were conducted to determine if RA treatment caused early embryonic changes with strain difference. When compared with ICR embryos, C57 embryos exhibited more pro
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Książki na temat "Developmental neurophysiology Genetic aspects"

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Annapia, Verri, ed. Life span development in genetic disorders: Behavioral and neurological aspects. New York: Nova Science Publishers, 2008.

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Smith, Moyra. Mental retardation and developmental delay: Genetic and epigenetic factors. New York, N.Y: Oxford University Press, 2006.

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Marco, Cappa, ed. Endocrine involvement in developmental syndromes. Basel: Karger, 2009.

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1952-, Butler Merlin Gene, and Meaney F. John, eds. Genetics of developmental disabilities. Boca Raton: Taylor & Francis, 2005.

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1939-, Colombo Jorge A., ed. Poverty and brain development during childhood: An approach from cognitive psychology and neuroscience. Washington, DC: American Psychological Association, 2009.

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Aging of the genome: The dual role of the DNA in life and death. Oxford ; New York: Oxford University Press, 2007.

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Cornish, Kim. Attention, genes, and developmental disorders. Oxford: Oxford University Press, 2010.

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S, Tuan Rocky, and Lo Cecilia W, eds. Developmental biology protocols. Totowa, N.J: Humana Press, 2000.

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Dodge, Kenneth A. Gene-environment interactions in developmental psychopathology. New York: Guilford Press, 2011.

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Kazemie, Mirabotalib. The designs of biological forms, development, and initiation of cancer. Bloomington, IN: Authorhouse, 2009.

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Części książek na temat "Developmental neurophysiology Genetic aspects"

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Davson, Hugh. "Neurophysiology of Perception: Developmental Aspects of Visual Field Characteristics." In Physiology of the Eye, 603–27. London: Macmillan Education UK, 1990. http://dx.doi.org/10.1007/978-1-349-09997-9_22.

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Goudie, R. B., A. S. Jack, and B. M. Goudie. "Genetic and Developmental Aspects of Pathological Pigmentation Patterns." In Current Topics in Pathology, 103–39. Berlin, Heidelberg: Springer Berlin Heidelberg, 1985. http://dx.doi.org/10.1007/978-3-642-69574-2_3.

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Ivanov, I. "Some Ethical Aspects of Genetic Aproaches to Human Health Care: A Developmental Geneticist’s Point of View." In Ethical Issues of Molecular Genetics in Psychiatry, 57–60. Berlin, Heidelberg: Springer Berlin Heidelberg, 1991. http://dx.doi.org/10.1007/978-3-642-76429-5_5.

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Eyre, J. A. "Developmental aspects of corticospinal projections." In Handbook of Clinical Neurophysiology, 27–57. Elsevier, 2004. http://dx.doi.org/10.1016/s1567-4231(04)04003-1.

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Dahl, Niklas. "Chapter 6 Genetic aspects of diagnosis." In Handbook of Clinical Neurophysiology, 99–112. Elsevier, 2003. http://dx.doi.org/10.1016/s1567-4231(09)70116-9.

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Baloh, MD, FAAN, Robert W., Vicente Honrubia, MD, DMSc, and Kevin A. Kerber, MD. "Developmental and Genetic Disorders." In Baloh and Honrubia's Clinical Neurophysiology of the Vestibular System, Fourth Edition, 383–401. Oxford University Press, 2011. http://dx.doi.org/10.1093/med/9780195387834.003.0018.

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Barbara, Whitman Y. "Neuropsychiatric Aspects of Genetic Disorders." In Genetics of Developmental Disabilities, 743–98. CRC Press, 2019. http://dx.doi.org/10.1201/9780429264078-20.

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"Neuropsychiatric Aspects of Genetic Disorders." In Genetics of Developmental Disabilities, 769–92. CRC Press, 2005. http://dx.doi.org/10.1201/b14171-24.

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Kotagal, Suresh. "Pediatric Sleep Assessment." In Clinical Neurophysiology, edited by Devon I. Rubin, 895–904. 5th ed. Oxford University PressNew York, 2021. http://dx.doi.org/10.1093/med/9780190067854.003.0051.

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Abstract There is considerable overlap in the categories of sleep-wake disorders of adults and children. The indications for various sleep diagnostic tests, the recording scenarios, scoring of various sleep-related events in children, and reference values, however, differ from those of adults. Many childhood sleep disorders are treatable, hence their early recognition and diagnosis is important. Certain aspects of the pediatric sleep history and examination are also unique due to developmental influences that change with age. This chapter provides an overview of these aspects. The optimum assessment requires integration of patient and parental concerns, questionnaire surveys, a sleep-focused examination and data from the various diagnostic modalities.
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Gleissberg, Stefan. "Comparative developmental and molecular genetic aspects of leaf dissection." In Systematics Association Special Volumes, 404–17. CRC Press, 2002. http://dx.doi.org/10.1201/9781420024982.ch21.

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