Gotowe bibliografie tematyczne / Genomic imprinting

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  1. Artykuły w czasopismach
  2. Rozprawy doktorskie
  3. Książki
  4. Części książek
  5. Streszczenia konferencji
  6. Raporty organizacyjne

Gotowa bibliografia na temat „Genomic imprinting”

Autor: Grafiati
Data publikacji: 4 czerwca 2021
Data aktualizacji: 25 lipca 2025

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Artykuły w czasopismach na temat "Genomic imprinting"

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Bajrami, Emirjeta, and Mirko Spiroski. "Genomic Imprinting." Open Access Macedonian Journal of Medical Sciences 4, no. 1 (2016): 181–84. http://dx.doi.org/10.3889/oamjms.2016.028.

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BACKGROUND: Genomic imprinting is the inheritance out of Mendelian borders. Many of inherited diseases and human development violates Mendelian law of inheritance, this way of inheriting is studied by epigenetics.AIM: The aim of this review is to analyze current opinions and options regarding to this way of inheriting.RESULTS: Epigenetics shows that gene expression undergoes changes more complex than modifications in the DNA sequence; it includes the environmental influence on the gametes before conception. Humans inherit two alleles from mother and father, both are functional for the majority
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Monk, M. "Genomic imprinting." Genes & Development 2, no. 8 (1988): 921–25. http://dx.doi.org/10.1101/gad.2.8.921.

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Maher, E. R. "Genomic Imprinting." Journal of Medical Genetics 28, no. 9 (1991): 647. http://dx.doi.org/10.1136/jmg.28.9.647.

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Hall, J. G. "Genomic imprinting." Archives of Disease in Childhood 65, no. 10 Spec No (1990): 1013–15. http://dx.doi.org/10.1136/adc.65.10_spec_no.1013.

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Jones, Peter A. "Genomic Imprinting." American Journal of Human Genetics 63, no. 3 (1998): 927. http://dx.doi.org/10.1086/302003.

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Pedersen, C. "Genomic imprinting." Reproductive Toxicology 11, no. 2-3 (1997): 309–16. http://dx.doi.org/10.1016/s0890-6238(96)00213-4.

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da Rocha, Simao Teixeira, and Anne C. Ferguson-Smith. "Genomic imprinting." Current Biology 14, no. 16 (2004): R646—R649. http://dx.doi.org/10.1016/j.cub.2004.08.007.

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Hultén, M., A. Kerr, and WilliamH James. "Genomic imprinting." Lancet 338, no. 8760 (1991): 188–89. http://dx.doi.org/10.1016/0140-6736(91)90180-w.

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Lambertini, Luca. "Genomic imprinting." Current Opinion in Pediatrics 26, no. 2 (2014): 237–42. http://dx.doi.org/10.1097/mop.0000000000000072.

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Hodgson, Shirley. "Genomic Imprinting." Developmental Medicine & Child Neurology 33, no. 6 (2008): 552–56. http://dx.doi.org/10.1111/j.1469-8749.1991.tb14920.x.

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Rozprawy doktorskie na temat "Genomic imprinting"

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Santure, Anna Wensley, and n/a. "Quantitative genetic models for genomic imprinting." University of Otago. Department of Zoology, 2006. http://adt.otago.ac.nz./public/adt-NZDU20060811.134008.

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A gene is imprinted when its expression is dependent on the sex of the parent from which it was inherited. An increasing number of studies are suggesting that imprinted genes have a major influence on medically, agriculturally and evolutionarily important traits, such as disease severity and livestock production traits. While some genes have a large effect on the traits of an individual, quantitative characters such as height are influenced by many genes and by the environment, including maternal effects. The interaction between these genes and the environment produces variation in the charact
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Whitehead, Joanne. "Genomic Imprinting in Development and Evolution." Doctoral thesis, Uppsala universitet, Zoologisk utvecklingsbiologi, 2004. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-4491.

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Genetic information is encoded by the linear sequence of the DNA double helix, while epigenetic information is overlayed as the packaging of DNA and associated proteins into the chromatin structure. Variations in chromatin structure play a vital role in establishing and maintaining patterns of gene expression during differentiation and development of higher eukaryotes, and disruption of this epigenetic gene regulation can lead to cancer. Mammals display an epigenetic phenomenon known as genomic imprinting, which provides an ideal model system for the study of epigenetics. Genes subject to geno
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McCann, Jennifer. "Variability of genomic imprinting in human disease." Thesis, McGill University, 2004. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=84294.

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Genomic imprinting is the differential expression of genetic material depending on the parent from which it is transmitted. It is involved in the pathogenesis of many diseases, especially those involved in development, growth abnormalities and cancer. We examined the extent of and the variability of genomic imprinting amongst individuals in three human diseases, Wilms' tumour, Type 1 diabetes and Silver-Russell syndrome.<br>Wilms' tumour (WT) is a renal embryonal cancer associated with overexpression of the insulin-like growth factor 2 (IGF2). IGF2 is directed to the lysosomes for degra
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Sun, Bowen. "Genomic imprinting in mouse pluripotent stem cells." Thesis, University of Cambridge, 2011. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.609478.

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Zhou, Jiyuan. "Single-marker and haplotype analyses for detecting parent-of-origin effects using family and pedigree data." Click to view the E-thesis via HKUTO, 2009. http://sunzi.lib.hku.hk/hkuto/record/B4308543X.

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Lucifero, Diana. "Developmental regulation of genomic imprinting by DNA methylation." Thesis, McGill University, 2004. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=85573.

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Maintaining appropriate patterns of gene expression in the gametes and during early embryogenesis is essential for normal development. DNA methylation is an epigenetic means of regulating gene expression and is an important molecular mark regulating the sex-specific expression of genes subject to genomic imprinting. Imprinted genes are expressed from only one of two inherited chromosomes and are differentially marked during gametogenesis to allow for their parental allele specific expression. These genes affect embryo growth, placental function, behavior after birth and are implicated i
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Rancourt, Rebecca Catherine. "Functional genomic analysis of an imprinting control region." Thesis, University of Cambridge, 2010. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.608514.

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Adams, Sally. "Genomic imprinting in the endosperm of Arabidopsis thaliana." Thesis, University of Bath, 2002. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.760803.

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Coan, Philip Michael. "Placental development and genomic imprinting in the mouse." Thesis, University of Cambridge, 2006. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.613928.

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Hore, Timothy Alexander, and timothy hore@anu edu au. "THE EVOLUTION OF GENOMIC IMPRINTING AND X CHROMOSOME INACTIVATION IN MAMMALS." The Australian National University. Research School of Biological Sciences, 2008. http://thesis.anu.edu.au./public/adt-ANU20081216.152553.

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Genomic imprinting is responsible for monoallelic gene expression that depends on the sex of the parent from which the alleles (one active, one silent) were inherited. X-chromosome inactivation is also a form of monoallelic gene expression. One of the two X chromosomes is transcriptionally silenced in the somatic cells of females, effectively equalising gene dosage with males who have only one X chromosome that is not complemented by a gene poor Y chromosome. X chromosome inactivation is random in eutherian mammals, but imprinted in marsupials, and in the extraembryonic membranes of some place
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Książki na temat "Genomic imprinting"

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Ward, Andrew, ed. Genomic Imprinting. Humana Press, 2002. http://dx.doi.org/10.1385/1592592112.

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Engel, Nora, ed. Genomic Imprinting. Humana Press, 2012. http://dx.doi.org/10.1007/978-1-62703-011-3.

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Ohlsson, Rolf, ed. Genomic Imprinting. Springer Berlin Heidelberg, 1999. http://dx.doi.org/10.1007/978-3-540-69111-2.

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Wilkins, Jon F., ed. Genomic Imprinting. Springer New York, 2008. http://dx.doi.org/10.1007/978-0-387-77576-0.

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Wolf, Reik, and Surani Azim, eds. Genomic imprinting. IRL Press at Oxford University Press, 1997.

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F, Wilkins Jon, ed. Genomic imprinting. Springer Science+Business Media, 2008.

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R, Ohlsson, Hall Kerstin, and Ritzén Martin 1937-, eds. Genomic imprinting: Causes and consequences. Cambridge University Press, 1995.

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R, Ohlsson, ed. Genomic imprinting: An interdisciplinary approach. Springer, 1999.

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Eric, Engel. Genomic imprinting and uniparental disomy in medicine: Clinical and molecular aspects. Wiley, 2002.

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Flint, Jonathan. How genes influence behavior. Oxford University Press, 2010.

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Części książek na temat "Genomic imprinting"

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Paro, Renato, Ueli Grossniklaus, Raffaella Santoro, and Anton Wutz. "Genomic Imprinting." In Introduction to Epigenetics. Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-68670-3_5.

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AbstractA typical cell contains two sets of chromosomes: one that was inherited from the mother, the other from the father. Usually, autosomal alleles are expressed at similar levels from the maternally and paternally inherited chromosomes. This chapter is dedicated to an exception of this rule: the expression of genes that are regulated by genomic imprinting depends on the parental origin of the allele, leading to the non-equivalence of maternal and paternal genomes. Genomic imprinting is a paradigm of epigenetic gene regulation as genetically identical alleles can exist in two expression sta
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Manji, Husseini K., Jorge Quiroz, R. Andrew Chambers, et al. "Genomic Imprinting." In Encyclopedia of Psychopharmacology. Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-540-68706-1_4273.

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Feinberg, Andrew P. "Genomic Imprinting." In Encyclopedia of Cancer. Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-642-27841-9_2390-2.

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Magenis, R. Ellen. "Genomic imprinting." In The AGT Cytogenetics Laboratory Manual. John Wiley & Sons, Inc., 2017. http://dx.doi.org/10.1002/9781119061199.ch10.

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Choufani, Sanaa, and Rosanna Weksberg. "Genomic Imprinting." In The Functional Nucleus. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-38882-3_19.

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Khan, Scheherazade, and Angela Hilliker. "Genomic Imprinting." In Molecular Life Sciences. Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4614-6436-5_759-1.

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Carlberg, Carsten, and Ferdinand Molnár. "Genomic Imprinting." In Mechanisms of Gene Regulation. Springer Netherlands, 2016. http://dx.doi.org/10.1007/978-94-017-7741-4_9.

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Brahmachari, Vani, and Shruti Jain. "Genomic Imprinting." In Encyclopedia of Systems Biology. Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4419-9863-7_848.

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Feinberg, Andrew P. "Genomic Imprinting." In Encyclopedia of Cancer. Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-46875-3_2390.

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Feinberg, Andrew P. "Genomic Imprinting." In Encyclopedia of Cancer. Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-16483-5_2390.

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Streszczenia konferencji na temat "Genomic imprinting"

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Guo, Chenkai, and Yaoxuan Wu. "Genomic imprinting in haemopoietic stem cells and leukemia." In 4TH INTERNATIONAL CONFERENCE ON FRONTIERS OF BIOLOGICAL SCIENCES AND ENGINEERING (FBSE 2021). AIP Publishing, 2022. http://dx.doi.org/10.1063/5.0095078.

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Anisimova, Inga V. "The etiology of intellectual development disorders." In Proceedings of III Research-to-Practice Conference with International Participation “The Value of Everyone. The Life of a Person with Mental Disorder: Support, Life Arrangements, Social Integration”. Terevinf, 2023. http://dx.doi.org/10.61157/978-5-4212-0676-7-2023-73-76.

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the causes of intellectual developmental disorders of various etiologies are described: the impact of external factors, hypoxic-ischemic brain lesions, the influence of genetic factors: chromosomal pathologies, monogenic diseases, genomic imprinting diseases
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Gonzalez-Pons, Maria, Mercedes Y. Lacourt, Sharon Fonseca-Williams, et al. "Abstract 5362: Analysis of loss of IGF2 genomic imprinting and colorectal cancer risk in Puertorrican Hispanics." In Proceedings: AACR 104th Annual Meeting 2013; Apr 6-10, 2013; Washington, DC. American Association for Cancer Research, 2013. http://dx.doi.org/10.1158/1538-7445.am2013-5362.

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Wang, Xu. "Allele-specific transcriptome and methylome analysis revealscis-regulation of DNA methylation and lack of genomic imprinting inNasonia." In 2016 International Congress of Entomology. Entomological Society of America, 2016. http://dx.doi.org/10.1603/ice.2016.105137.

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Kenny, D., R. D. Sleator, C. P. Murphy, R. D. Evans, and D. P. Berry. "370. Detecting the presence of genomic imprinting for carcass traits in cattle using imputed high-density genotypes." In World Congress on Genetics Applied to Livestock Production. Wageningen Academic Publishers, 2022. http://dx.doi.org/10.3920/978-90-8686-940-4_370.

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Raporty organizacyjne na temat "Genomic imprinting"

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Ohad, Nir, and Robert Fischer. Regulation of plant development by polycomb group proteins. United States Department of Agriculture, 2008. http://dx.doi.org/10.32747/2008.7695858.bard.

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Our genetic and molecular studies have indicated that FIE a WD-repeat Polycomb group (PcG) protein takes part in multi-component protein complexes. We have shown that FIE PcG protein represses inappropriate programs of development during the reproductive and vegetative phases of the Arabidopsis life cycle. Moreover, we have shown that FIE represses the expression of key regulatory genes that promote flowering (AG and LFY), embryogenesis (LEC1), and shoot formation (KNAT1). These results suggest that the FIE PcG protein participates in the formation of distinct PcG complexes that repress inappr
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