Gotowa bibliografia na temat „Human genetics”
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Artykuły w czasopismach na temat "Human genetics"
Comai, L. "Human genetics: Human genetics discovering ourselves". Heredity 99, nr 5 (19.09.2007): 481–82. http://dx.doi.org/10.1038/sj.hdy.6801060.
Pełny tekst źródłaVázquez, José. "Human Genetics". American Biology Teacher 68, nr 2 (1.02.2006): 118–19. http://dx.doi.org/10.2307/4451943.
Pełny tekst źródłaHaas, John M. "Human Genetics". Ethics & Medics 21, nr 2 (1996): 1–3. http://dx.doi.org/10.5840/em19962123.
Pełny tekst źródłaConnors, Bernadette J. "Human Genetics". American Biology Teacher 77, nr 5 (1.05.2015): 393–94. http://dx.doi.org/10.1525/abt.2015.77.5.12c.
Pełny tekst źródłaAtramentova, L. A. "Bayesian statistics in human genetics". Faktori eksperimental'noi evolucii organizmiv 26 (1.09.2020): 316–19. http://dx.doi.org/10.7124/feeo.v26.1286.
Pełny tekst źródłaMotulsky, Arno G. "Societal problems in human and medical genetics". Genome 31, nr 2 (15.01.1989): 870–75. http://dx.doi.org/10.1139/g89-153.
Pełny tekst źródłaPassarge, Eberhard. "Origins of human genetics. A personal perspective". European Journal of Human Genetics 29, nr 7 (4.02.2021): 1038–44. http://dx.doi.org/10.1038/s41431-020-00785-7.
Pełny tekst źródłaKing, M. C. "HUMAN GENETICS: Mapping Human History". Science 298, nr 5602 (20.12.2002): 2342–43. http://dx.doi.org/10.1126/science.1080373.
Pełny tekst źródłaLupski, James R. "A Human in Human Genetics". Cell 177, nr 1 (marzec 2019): 9–15. http://dx.doi.org/10.1016/j.cell.2019.02.034.
Pełny tekst źródłaLorey, Fred. "Human Genetics Data Applied to Genetic Screening Programs". Practicing Anthropology 20, nr 2 (1.04.1998): 30–33. http://dx.doi.org/10.17730/praa.20.2.n84728r821185380.
Pełny tekst źródłaRozprawy doktorskie na temat "Human genetics"
Ingman, Max. "Mitochondria and Human Evolution". Doctoral thesis, Uppsala University, Department of Genetics and Pathology, 2003. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-3580.
Pełny tekst źródłaMitochondrial DNA (mtDNA) has been a potent tool in studies of the evolution of modern humans, human migrations and the dynamics of human populations over time. The popularity of this cytoplasmic genome has largely been due to its clonal inheritance (in Man) allowing the tracing of a direct genetic line. In addition, a comparatively high rate of nucleotide substitution facilitates phylogenetic resolution among relatively closely related individuals of the same species.
In this thesis, a statistically supported phylogeny based on complete mitochondrial genome sequences is presented which, for the first time, unambiguously places the root of modern human mitochondrial lineages in Africa in the last 200 thousand years. This conclusion provides strong support for the “recent African origin” hypothesis. Also, the complete genome data underline the problematic nature of traditional approaches to analyses of mitochondrial phylogenies.
The dispersal of anatomically modern humans from the African continent is examined through single nucleotide polymorphism (SNP) and sequence data. These data imply an expansion from Africa about 57 thousand years ago and a subsequent population dispersal into Asia. The dispersal coincides with a major population division that may be the result of multiple migratory routes to East Asia.
Also investigated is the question of a common origin for the indigenous peoples of Australia and New Guinea. Previous studies have been equivocal on this question with some presenting evidence for a common genetic origin and other proposing separate histories. Our data reveals an ancient genetic link between Australian Aborigines and the peoples of the New Guinea highlands.
Whitmore, Scott Anthony. "Positional cloning of genes associated with human disease /". Title page, contents and summary only, 1999. http://web4.library.adelaide.edu.au/theses/09PH/09phw616.pdf.
Pełny tekst źródłaCopies of author's previously published articles inserted. Amendments pasted onto back-end paper. Bibliography: leaves 255-286.
Dubé, Marie-Pierre. "New approaches in human genetic analysis". Thesis, McGill University, 1999. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=36581.
Pełny tekst źródłaThe second part addresses linkage-disequilibrium based fine mapping in the French Canadian population. The performance of five linkage-disequilibrium based fine-mapping methods is evaluated using French Canadian chromosomes with one of three diseases found in this population: oculopharyngeal muscular dystrophy (OPMD), hidrotic ectodermal dysplasia (HED), and sensorimotor polyneuropathy with or without agenesis of the corpus callosum (ACCPN). The gene for OPMD was recently mapped and cloned, allowing us to evaluate the performance of the methods with the OPMD results, and to make predictions about the ACCPN and HED putative gene positions. In addition, a new approach to linkage-disequilibrium based fine mapping is presented using FrenchCanadian ascending genealogies. The method involves two steps. First, the likely founding couple of a mutation-bearing chromosome is identified using a computerised randomisation statistic. Then, using a delete-d jackknife resampling scheme, the distribution of gene mapping estimates is calculated from the count of ancestral recombinants and ancestral meioses joining the identified founding couple to the disease gene carriers. Gene mapping estimates are calculated from each marker individually, and confidence intervals of the estimates are derived from the jackknife distributions. The method, when applied to French Canadian families with OPMD, successfully confirmed the localisation of PABP2 responsible for OPMD and performed better than other linkage disequilibrium-based mapping models.
De, Bustos Cecilia. "Genetic and Epigenetic Variation in the Human Genome : Analysis of Phenotypically Normal Individuals and Patients Affected with Brain Tumors". Doctoral thesis, Uppsala : Acta Universitatis Upsaliensis : Univ.-bibl. [distributör], 2006. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-6629.
Pełny tekst źródłaHeilbronn, Leonie Kaye. "Gene/environment interactions in human obesity". Title page, table of contents and summary only, 2001. http://web4.library.adelaide.edu.au/theses/09PH/09phh466.pdf.
Pełny tekst źródłaBell, Christopher Graeme. "The genetics of human obesity". Thesis, Imperial College London, 2006. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.433662.
Pełny tekst źródłaJennings, Michael William. "Developmental genetics of human haemoglobin". Thesis, University of Oxford, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.236131.
Pełny tekst źródłaBell, Jordana Tzenova. "Epistasis in complex human traits". Thesis, University of Oxford, 2006. http://ora.ox.ac.uk/objects/uuid:547db446-c84c-4a6c-8b5c-ce960f7765c5.
Pełny tekst źródłaMelin, Malin. "Identification of Candidate Genes in Four Human Disorders". Doctoral thesis, Uppsala : Acta Universitatis Upsaliensis, 2006. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-7344.
Pełny tekst źródłaNelki, Daniel S. "The ownership of human genes and human tissue". Thesis, City University London, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.301178.
Pełny tekst źródłaKsiążki na temat "Human genetics"
Lewis, Ricki. Human genetics: Concepts and applications. Wyd. 7. Dubuque, IA: McGraw-Hill, 2007.
Znajdź pełny tekst źródłaNoël, Merino, red. Human genetics. Detroit: Greenhaven Press, 2010.
Znajdź pełny tekst źródłaJenkins, John B. Human genetics. Wyd. 2. New York: Harper & Row, 1990.
Znajdź pełny tekst źródłaVogel, Friedrich, i Arno G. Motulsky. Human Genetics. Berlin, Heidelberg: Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-662-02489-8.
Pełny tekst źródłaVogel, Friedrich, i Karl Sperling, red. Human Genetics. Berlin, Heidelberg: Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-642-71635-5.
Pełny tekst źródłaVogel, Friedrich, i Arno G. Motulsky. Human Genetics. Berlin, Heidelberg: Springer Berlin Heidelberg, 1997. http://dx.doi.org/10.1007/978-3-662-03356-2.
Pełny tekst źródłaJenkins, John B. Human genetics. Wyd. 2. New York: Harper & Row, 1990.
Znajdź pełny tekst źródłaMerino, Noël. Human genetics. Detroit: Greenhaven Press, 2010.
Znajdź pełny tekst źródłaMerino, Noël. Human genetics. Detroit, MI: Greenhaven Press, 2010.
Znajdź pełny tekst źródłaHonig, George R. Human hemoglobin genetics. Berlin: Springer-Verlag, 1985.
Znajdź pełny tekst źródłaCzęści książek na temat "Human genetics"
Vogel, Friedrich, i Arno G. Motulsky. "Population Genetics: Consanguinity, Genetic Drift". W Human Genetics, 549–82. Berlin, Heidelberg: Springer Berlin Heidelberg, 1997. http://dx.doi.org/10.1007/978-3-662-03356-2_14.
Pełny tekst źródłaKowles, Richard. "Human Genetics". W Solving Problems in Genetics, 389–445. New York, NY: Springer New York, 2001. http://dx.doi.org/10.1007/978-1-4613-0205-6_11.
Pełny tekst źródłaLancaster, H. O. "Human Genetics". W Quantitative Methods in Biological and Medical Sciences, 45–57. New York, NY: Springer New York, 1994. http://dx.doi.org/10.1007/978-1-4612-2658-1_5.
Pełny tekst źródłaVogel, Friedrich, i Arno G. Motulsky. "Human Chromosomes". W Human Genetics, 20–110. Berlin, Heidelberg: Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-662-02489-8_3.
Pełny tekst źródłaVogel, Friedrich, i Arno G. Motulsky. "Human Evolution". W Human Genetics, 512–42. Berlin, Heidelberg: Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-662-02489-8_8.
Pełny tekst źródłaVogel, Friedrich, i Arno G. Motulsky. "Human Evolution". W Human Genetics, 583–621. Berlin, Heidelberg: Springer Berlin Heidelberg, 1997. http://dx.doi.org/10.1007/978-3-662-03356-2_15.
Pełny tekst źródłaVogel, Friedrich, i Arno G. Motulsky. "Population Genetics". W Human Genetics, 433–511. Berlin, Heidelberg: Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-662-02489-8_7.
Pełny tekst źródłaCraig, A., F. Michiels, G. Zehetner, B. Sproat, M. Burmeister, M. Bućan, A. Poustka, T. Pohl, A. M. Frischauf i H. Lehrach. "Molecular Techniques in Mammalian Genetics: A New Era in Genetic Analysis". W Human Genetics, 126–32. Berlin, Heidelberg: Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-642-71635-5_11.
Pełny tekst źródłaEastwood, Martin. "Genetics". W Principles of Human Nutrition, 37–66. Boston, MA: Springer US, 1997. http://dx.doi.org/10.1007/978-1-4899-3025-5_2.
Pełny tekst źródłaDye, Frank J. "Genetics". W Human Life Before Birth, 33–47. Second edition. | Boca Raton : Taylor & Francis, 2019.: CRC Press, 2019. http://dx.doi.org/10.1201/9781351130288-5.
Pełny tekst źródłaStreszczenia konferencji na temat "Human genetics"
YAMAGUCHI, TETSUTARO, RYOSUKE KIMURA, AKIRA KAWAGUCHI, YOKO TOMOYASU i KOUTARO MAKI. "Craniofacial Morphology in Human Genetics". W Proceedings of the 2nd International Symposium. WORLD SCIENTIFIC, 2013. http://dx.doi.org/10.1142/9789814518413_0005.
Pełny tekst źródłaGuan, Hannah. "The genetics of human aging". W BCB '21: 12th ACM International Conference on Bioinformatics, Computational Biology and Health Informatics. New York, NY, USA: ACM, 2021. http://dx.doi.org/10.1145/3459930.3469508.
Pełny tekst źródłaDronamraju, Krishna R. "The History & Development of Human Genetics". W Progress in Different Countries. WORLD SCIENTIFIC, 1992. http://dx.doi.org/10.1142/9789814537919.
Pełny tekst źródłaCleaver, James E. "Genetics of human sensitivity to ultraviolet radiation". W Ultraviolet Radiation Hazards. SPIE, 1994. http://dx.doi.org/10.1117/12.180813.
Pełny tekst źródłaMitrofanova, Antonina, i Bud Mishra. "Population genetics of human copy number variations". W the 2008 ACM symposium. New York, New York, USA: ACM Press, 2008. http://dx.doi.org/10.1145/1363686.1363990.
Pełny tekst źródłaMoore, Jason H., Nate Barney i Bill C. White. "Towards human-human-computer interaction for biologically-inspired problem-solving in human genetics". W the 9th annual conference. New York, New York, USA: ACM Press, 2007. http://dx.doi.org/10.1145/1276958.1277052.
Pełny tekst źródłaGillespie, Marc. "Capturing, Curating, and Sharing Viral Disease in Reactome". W Genomics and Human Genetics: The New York Symposium. Reactome, 2024. http://dx.doi.org/10.3180/poster/20240126gillespie.
Pełny tekst źródła"Redesign of starch biosynthetic pathway in rice by CRISPR/Cas9-mediated genome editing toward human diets". W Plant Genetics, Genomics, Bioinformatics, and Biotechnology. Institute of Cytology and Genetics, Siberian Branch of the Russian Academy of Sciences, 2019. http://dx.doi.org/10.18699/plantgen2019-074.
Pełny tekst źródła"The study of the cross-interaction of antibodies with antigens of different types of human papillomaviruses (HPV)". W Plant Genetics, Genomics, Bioinformatics, and Biotechnology. Novosibirsk ICG SB RAS 2021, 2021. http://dx.doi.org/10.18699/plantgen2021-193.
Pełny tekst źródłaŠpernjak, Andreja, i Andrej Šorgo. "PRE-SERVICE AND IN-SERVICE TEACHERS´ VIEWS OF HUMAN GENETICS AND HUMAN BRAIN". W 13th International Technology, Education and Development Conference. IATED, 2019. http://dx.doi.org/10.21125/inted.2019.2209.
Pełny tekst źródłaRaporty organizacyjne na temat "Human genetics"
Loyd, Peter. An Evaluation of Genetics 308X/508X Biotechnology in Agriculture, Food, and Human Health. Ames (Iowa): Iowa State University, styczeń 1997. http://dx.doi.org/10.31274/cc-20240624-170.
Pełny tekst źródłaCollins, D. L., L. Segebrecht i R. N. Schimke. Human genetics education for middle and secondary science teachers. Third annual report, April 1, 1994--March 30, 1995. Office of Scientific and Technical Information (OSTI), grudzień 1994. http://dx.doi.org/10.2172/34255.
Pełny tekst źródłaCahaner, Avigdor, Susan J. Lamont, E. Dan Heller i Jossi Hillel. Molecular Genetic Dissection of Complex Immunocompetence Traits in Broilers. United States Department of Agriculture, sierpień 2003. http://dx.doi.org/10.32747/2003.7586461.bard.
Pełny tekst źródłaSeger, Yvette R. Genetic Requirements for the Transformation of Human Cells. Fort Belvoir, VA: Defense Technical Information Center, lipiec 2002. http://dx.doi.org/10.21236/ada410207.
Pełny tekst źródłaSeger, Yvette. Genetic Requirements for the Transformation of Human Cells. Fort Belvoir, VA: Defense Technical Information Center, lipiec 2004. http://dx.doi.org/10.21236/ada429117.
Pełny tekst źródłaSeger, Yvette M. Genetic Requirements for the Transformation of Human Cells. Fort Belvoir, VA: Defense Technical Information Center, lipiec 2003. http://dx.doi.org/10.21236/ada418793.
Pełny tekst źródłaKarlan, Beth Y. Genetic Definition and Phenotypic Determinants of Human Ovarian Carcinomas. Fort Belvoir, VA: Defense Technical Information Center, październik 2000. http://dx.doi.org/10.21236/ada394004.
Pełny tekst źródłaHait, William. Genetic Susceptibility to Cancer Chemotherapy in Human Breast Cancer. Fort Belvoir, VA: Defense Technical Information Center, lipiec 2000. http://dx.doi.org/10.21236/ada396563.
Pełny tekst źródłaHait, William N. Genetic Susceptibility to Cancer Chemotherapy in Human Breast Cancer. Fort Belvoir, VA: Defense Technical Information Center, lipiec 2001. http://dx.doi.org/10.21236/ada398401.
Pełny tekst źródłaDR. Howard B. Lieberman. Human Genetic Marker for Resistance to Radiation and Chemicals. Office of Scientific and Technical Information (OSTI), maj 2001. http://dx.doi.org/10.2172/789807.
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