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Relevant bibliographies by topics / Human Mutagenesis

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Academic literature on the topic 'Human Mutagenesis'

Author: Grafiati

Published: 4 June 2021

Last updated: 3 February 2022

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Journal articles on the topic "Human Mutagenesis"

1

Rosenkranz, Herbert S., Ying Ping Zhang, Orest T. Macina, Donald R. Mattison, and Gilles Klopman. "Human developmental toxicity and mutagenesis." Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis 422, no. 2 (1998): 347–50. http://dx.doi.org/10.1016/s0027-5107(98)00170-5.

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Everson, Richard B., Karen L. Milne, Dorothy Warburton, Howard D. McClamrock, and Philip D. Buchanan. "Mutagenesis assays of human amniotic fluid." Environmental Mutagenesis 7, no. 2 (1985): 171–84. http://dx.doi.org/10.1002/em.2860070206.

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Bielli, Pamela, Gian Carlo Bellenchi, and Lilia Calabrese. "Site-directed Mutagenesis of Human Ceruloplasmin." Journal of Biological Chemistry 276, no. 4 (2000): 2678–85. http://dx.doi.org/10.1074/jbc.m007176200.

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Olins, Peter O., S. Christopher Bauer, Sarah Braford-Goldberg, et al. "Saturation Mutagenesis of Human Interleukin-3." Journal of Biological Chemistry 270, no. 40 (1995): 23754–60. http://dx.doi.org/10.1074/jbc.270.40.23754.

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Inouye, Satoshi, Yili Guo, Nicholas Ling, and Shunichi Shimasaki. "Site-specific mutagenesis of human follistatin." Biochemical and Biophysical Research Communications 179, no. 1 (1991): 352–58. http://dx.doi.org/10.1016/0006-291x(91)91377-o.

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Shedlovsky, A., J. D. McDonald, D. Symula, and W. F. Dove. "Mouse models of human phenylketonuria." Genetics 134, no. 4 (1993): 1205–10. http://dx.doi.org/10.1093/genetics/134.4.1205.

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Abstract Phenylketonuria (PKU) results from a deficiency in phenylalanine hydroxylase, the enzyme catalyzing the conversion of phenylalanine (PHE) to tyrosine. Although this inborn error of metabolism was among the first in humans to be understood biochemically and genetically, little is known of the mechanism(s) involved in the pathology of PKU. We have combined mouse germline mutagenesis with screens for hyperphenylalaninemia to isolate three mutants deficient in phenylalanine hydroxylase (PAH) activity and cross-reactive protein. Two of these have reduced PAH mRNA and display characteristic

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Kaluka, Daniel, Dipanwita Batabyal, Bing-Yu Chiang, Thomas L. Poulos, and Syun-Ru Yeh. "Spectroscopic and Mutagenesis Studies of Human PGRMC1." Biochemistry 54, no. 8 (2015): 1638–47. http://dx.doi.org/10.1021/bi501177e.

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Marcelino, Luisa A., and William G. Thilly. "Mitochondrial mutagenesis in human cells and tissues." Mutation Research/DNA Repair 434, no. 3 (1999): 177–203. http://dx.doi.org/10.1016/s0921-8777(99)00028-2.

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Gang, Spencer S., Michelle L. Castelletto, Astra S. Bryant, et al. "Targeted mutagenesis in a human-parasitic nematode." PLOS Pathogens 13, no. 10 (2017): e1006675. http://dx.doi.org/10.1371/journal.ppat.1006675.

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Barbone, Francis P., Steven A. Middleton, Dana L. Johnson, et al. "Mutagenesis Studies of the Human Erythropoietin Receptor." Journal of Biological Chemistry 272, no. 8 (1997): 4985–92. http://dx.doi.org/10.1074/jbc.272.8.4985.

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Dissertations / Theses on the topic "Human Mutagenesis"

1

Warburton, Johnny. "Selection and mutagenesis in cultured African violet plantlets." Thesis, University of Edinburgh, 1986. http://hdl.handle.net/1842/11945.

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Gan, Shu Uin. "Retroviral insertional mutagenesis of human myeloid HL-60 cells." Thesis, King's College London (University of London), 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.244680.

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Kozlenkov, Alexey. "Structural/functional studies on human alkaline phosphatases /." Umeå : Univ, 2003. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-136.

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Leontiou, Chrysoula. "Mechanisms of drug resistance to acridine derivatives mediated by human DNA topoisomerase IIÎ²." Thesis, University of Newcastle Upon Tyne, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.273685.

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Gebhard, Daniel [Verfasser]. "Solar-induced mitochondrial mutagenesis and dysfunction in human skin / Daniel Gebhard." Konstanz : Bibliothek der Universität Konstanz, 2014. http://d-nb.info/1081016450/34.

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Ellis, James. "Structural analysis of the human angiotensin type 1 receptor through mutagenesis." Thesis, University of Leeds, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.418731.

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Clapham, Peter C. "The radiobiology of human colorectal cell lines : an investigation into transformation and radiosensitivity." Thesis, University of Bristol, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.265322.

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Nie, Mei. "The transcriptional regulation of the human IL-8 and MCP-1 genes in cultured primary mesangial cells." Thesis, University of Nottingham, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.368257.

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Wang, Jen-Yeu. "Human PC4 Prevents Mutagenesis and Killing by Oxidative DNA Damage: a Dissertation." eScholarship@UMMS, 2012. http://escholarship.umassmed.edu/gsbs_diss/287.

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Chapter II Abstract Human positive cofactor 4 (PC4) is a transcriptional coactivator with a highly conserved single-strand DNA (ssDNA) binding domain of unknown function. We identified PC4 as a suppressor of the oxidative mutator phenotype of the Escherichia coli fpg mutY mutant and demonstrate that this suppression requires its ssDNA binding activity. Saccharomyces cerevisiae mutants lacking their PC4 ortholog Sub1 are sensitive to hydrogen peroxide and exhibit spontaneous and peroxide-induced hypermutability. PC4 expression suppresses the peroxide sensitivity of the yeast sub1Δ mutant, sugge

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Wang, Jen-Yeu. "Human PC4 Prevents Mutagenesis and Killing by Oxidative DNA Damage: a Dissertation." eScholarship@UMMS, 2004. https://escholarship.umassmed.edu/gsbs_diss/287.

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Chapter II Abstract Human positive cofactor 4 (PC4) is a transcriptional coactivator with a highly conserved single-strand DNA (ssDNA) binding domain of unknown function. We identified PC4 as a suppressor of the oxidative mutator phenotype of the Escherichia coli fpg mutY mutant and demonstrate that this suppression requires its ssDNA binding activity. Saccharomyces cerevisiae mutants lacking their PC4 ortholog Sub1 are sensitive to hydrogen peroxide and exhibit spontaneous and peroxide-induced hypermutability. PC4 expression suppresses the peroxide sensitivity of the yeast sub1Δ mutant, sugge

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Books on the topic "Human Mutagenesis"

1

International Conference on Environmental Mutagens in Human Populations (2nd 1995 Prague, Czech Republic). Second International Conference on Environmental Mutagens in Human Populations: August 20-25, 1995, Prague, Czech Republic / sponsored by Prague Institute of Advanced Studies, Regional Institute of Hygiene of Central Bohemia, University of Texas Medical Branch ; co-editors, William W. Au, Radim J. Sram ; assistant editor, Sherif Abdel-Rahman. U.S. Dept. of Health and Human Services, Public Health Service, National Institutes of Health, National Institute of Environmental Health Sciences, 1996.

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International Conference on Environmental Mutagenesis in Human Population at Risk (1st 1992 Cairo, Egypt). First International Conference on Environmental Mutagenesis in Human Population at Risk: Cairo, Egypt, January 19-24, 1992. Ain Shams University, Faculty of Medicine, 1992.

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3

Siderovski, David Peter. Human immunodeficiency virus type-1 trans-activator of transcription (HIV-1 Tat): Random mutagenesis and interaction with PKR. National Library of Canada = Bibliothèque nationale du Canada, 1997.

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4

Stepanova, Tatʹi͡ana. Demony bez angelov: [roman]. Ėksmo, 2012.

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5

Brusick, David. Principles of genetic toxicology. 2nd ed. Plenum Press, 1987.

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6

Environmental mutagenesis in human populations at risk. National Institutes of Health, National Institute of Environmental Health Sciences, 1993.

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(Editor), David H. Phillips, and Stanley Venitt (Editor), eds. Environmental Mutagenesis (A Volume in the Human Molecular Genetics Series) (Human Molecular Genetics). Academic Press, 1995.

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(Editor), David H. Phillips, and Stanley Venitt (Editor), eds. Environmental Mutagenesis (A Volume in the Human Molecular Genetics Series) (Human Molecular Genetics). Academic Press, 1995.

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9

Cooper, Stephen. Human Gene Evolution (Human Molecular Genetics). Academic Press, 1999.

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Cooper, Stephen. Human Gene Evolution (Human Molecular Genetics). Academic Press, 1999.

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Book chapters on the topic "Human Mutagenesis"

1

Chiba, Kunitoshi, and Dirk Hockemeyer. "Genome Editing in Human Pluripotent Stem Cells Using Site-Specific Nucleases." In Chromosomal Mutagenesis. Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4939-1862-1_15.

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Adachi, Noritaka, Aya Kurosawa, and Hideki Koyama. "Highly Proficient Gene Targeting by Homologous Recombination in the Human Pre-B Cell Line Nalm-6." In Chromosomal Mutagenesis. Humana Press, 2008. http://dx.doi.org/10.1007/978-1-59745-232-8_2.

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Revelle, Roger. "Toxins in the Human Food System." In Basic and Applied Mutagenesis. Springer US, 1985. http://dx.doi.org/10.1007/978-1-4684-4976-1_3.

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Abel, Ernest L. "Identifying Human Behavioral Teratogens." In Behavioral Teratogenesis and Behavioral Mutagenesis. Springer US, 1989. http://dx.doi.org/10.1007/978-1-4613-0735-8_6.

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Stich, H. F., W. Stich, and M. P. Rosin. "The Micronucleus Test on Exfoliated Human Cells." In Basic and Applied Mutagenesis. Springer US, 1985. http://dx.doi.org/10.1007/978-1-4684-4976-1_22.

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Hazra, P. "6. Mutagenesis for human nutrition." In Mutagenesis: exploring novel genes and pathways. Wageningen Academic Publishers, 2014. http://dx.doi.org/10.3920/978-90-8686-787-5_6.

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Huber, R., and M. Bauchinger. "Development and Perspectives of the Human Lymphocyte Micronucleus Assay." In Advances in Mutagenesis Research. Springer Berlin Heidelberg, 1990. http://dx.doi.org/10.1007/978-3-642-74955-1_4.

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Deaven, Larry L. "General Human Health Risks Associated with the Use of Chemicals." In Basic and Applied Mutagenesis. Springer US, 1985. http://dx.doi.org/10.1007/978-1-4684-4976-1_4.

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Natarajan, A. T., and A. D. Tates. "Current Techniques for Human Population Monitoring for Genetic Effects." In Mechanisms of Environmental Mutagenesis-Carcinogenesis. Springer US, 1990. http://dx.doi.org/10.1007/978-1-4615-3808-0_18.

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Crespan, Emmanuele, Alessandra Amoroso, and Giovanni Maga. "DNA Polymerases and Mutagenesis in Human Cancers." In Subcellular Biochemistry. Springer Netherlands, 2009. http://dx.doi.org/10.1007/978-90-481-3471-7_9.

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Conference papers on the topic "Human Mutagenesis"

1

Ashok Kumar, A., Margaret Insley, Jay Gambee, Sharon J. Busby, and Kathleen L. Berkner. "SITE SPECIFIC MUTAGENESIS WITHIN THE GLA-DOMAIN OF HUMAN FACTOR IX." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644079.

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Factor IX, a plasma protein, plays a critical role in blood coagulation. The biological activity of factor IX as well as several other plasma proteins depends on the presence of gamma-carboxy glutamic acid (Gla) residues in their amino terminal region. In vitro mutagenesis has been used to selectively replace Gla residues of factor IX with aspartic acid (Asp) residues in order to establish the contribution of individual as well as paired Gla residues to the normal functioning of the protein. These substitutions were made at positions 7, 15, 20 and 26 in human factor IX. In addition, residue nu

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2

Banday, A. Rouf, Ariunaa Bayanjargal, Krizia-Ivana Udquim, Olusegun O. Onabajo, and Ludmila Prokunina-Olsson. "Abstract 1292: Germline genetic, molecular and environmental factors modulate APOBEC mutagenesis in human tumors." In Proceedings: AACR Annual Meeting 2017; April 1-5, 2017; Washington, DC. American Association for Cancer Research, 2017. http://dx.doi.org/10.1158/1538-7445.am2017-1292.

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Datta, Shalini, Jean-Charles Nault, Andrea Franconi, et al. "Abstract 919: Adeno-associated virus 2 (AAV2) induces recurrent insertional mutagenesis in human hepatocellular carcinomas." In Proceedings: AACR 106th Annual Meeting 2015; April 18-22, 2015; Philadelphia, PA. American Association for Cancer Research, 2015. http://dx.doi.org/10.1158/1538-7445.am2015-919.

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4

Lord, S. T. "DIRECTED MUTAGENESIS OF HUMAN FIBRINOGEN: Aα CHAIN SUBSTITUTIONS THAT ALTER THROMBIN CLEAVAGE AND ANTIBODY RECOGNITION". У XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1642887.

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The initial event in fibrin clot formation is the thrombin catalized cleavage of the Aa chain of fibrinogen between Argl6 and Glyl7, releasing fibrinopeptide A. Previous data indicate that most of the information required for thrombin recognition and cleavage of the Aa chain lies within the amino terminal 51 residue CNBr fragment. In order to use protein engineering techniques to study the interaction of thrombin with the Aa chain, we have constructed a plasmid expression vector which encodes a tripartite protein consisting of amino acids 1-50 of the Aa chain of human fibrinogen followed by 60

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Arruda, Paulo, and Lucas Adjafre. "Use of Site-directed mutagenesis in the understanding of the catalytic domain activity of the human SDH enzyme." In XXIII Congresso de Iniciação Científica da Unicamp. Galoá, 2015. http://dx.doi.org/10.19146/pibic-2015-38296.

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Holmes, W. E., H. R. Lijnen та D. Collen. "CHARACTERIZATION OFα2-ANTIPLASMIN.REACTIVE SITE VARIANTS PRODUCED BY SITE-DIRECTED MUTAGENESIS". У XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644766.

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α2-Antiplasmin (α2AP) is the primary physiological plasmin inhibitor in human plasma. The inhibition is rapid (second order rate constants (k1) are expressed as M−1 s−1 ) (k1 = 2 × 107) and occurs as the consequence of an irreversible 1:1 stoichiometric complex formation; the exact nature of and the forces involved in complex formation are not fully understood. In fact, what makes α2AP an inhibitor, rather than simply a substrate remains unresolved. Recently, we deduced the primary structure of α2 AP from the sequence of its cDNA. 95%of this sequence was confirmed by amino acid (aa) sequence a

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Wha Lin, Shu, J. Ware, H. Roberts, N. McGraw, W. McAllister, and D. Stafford. "EXPRESSION OF HUMAN FACTOR IX IN MAMMALIAN CELLS." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643567.

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Human factor IX has been expressed in mammalian cells. A cloned factor IX cDNA missing the first 15 nucleotides of the 5’ end was modified by in vitro mutagenesis to restore the missing codons and add the translation consensus sequence, CCACC, proposed by Kozak to be optimal for translational initiation. Additionally, Bgl II and BamHI sites were added immediately upstream of the CCACC sequence for ease of portability of the fragment. This modified cDNA was inserted into a bovine papillomavirus (BPV) vector under the control of a mouse met alio thionein promoter. The constructed plasmid pBPV-IX

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Hasselbacher, Carol A., Elena Rusinova, Evan Waxman, et al. "Probing the structure of human tissue factor by site-directed mutagenesis of tryptophan residues and in-vivo incorporation of tryptophan analogs." In OE/LASE '94, edited by Joseph R. Lakowicz. SPIE, 1994. http://dx.doi.org/10.1117/12.182739.

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Reshat, Reshat, Catherine Priestley, and Nigel J. Gooderham. "Abstract 6: A triple-helix forming oligonucleotide targeting a genomic locus is capable of sequence specific mutagenesis in human lymphoblastoid TK6 cells." In Proceedings: AACR 101st Annual Meeting 2010‐‐ Apr 17‐21, 2010; Washington, DC. American Association for Cancer Research, 2010. http://dx.doi.org/10.1158/1538-7445.am10-6.

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Nelles, L., H. R. Linjnen, E. Demarsin, D. Collen, and W. E. Holmes. "CHARACTERIZATION OF SINGLE CHAIN UROKINASE-TYPE PLASMINOGEN ACTIVATOR MUTANTS PRODUCED BY SITE-SPECIFIC MUTAGENESIS OF LYS." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1642909.

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A cDNA encoding full length single chain urokinase-type plasminogen activator (scu-PA) was cloned and sequenced. The recombinant scu-PA (rscu-PA) cDNA as well as the cDNA of two mutants constructed by deoxyoligonucleotide directed mutagenesis of Lys158 in rscu-PA to Gly158 (rscu-PA-Gly158 ) or to Glu158 (rscu-PA-Glu158 ) were inserted into SV40 early promoter/enhancer based expression vectors, which were used to transfect Chinese Hamster Ovary (CHO) cells. The expression products were purified from serum-free conditioned media by immunoadsorption on an insolubilized monoclonal antibody raised

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Reports on the topic "Human Mutagenesis"

1

Sun, LuZhe. Effect of Estrogen on Mutagenesis in Human Mammary Epithelial Cells. Defense Technical Information Center, 2005. http://dx.doi.org/10.21236/ada443767.

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Thilly, W. G. Comparative mutagenesis of human cells in vivo and in vitro. Office of Scientific and Technical Information (OSTI), 1992. http://dx.doi.org/10.2172/10152396.

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Thilly, W. G. Comparative mutagenesis of human cells in vivo and in vitro. Office of Scientific and Technical Information (OSTI), 1990. http://dx.doi.org/10.2172/7279262.

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Thilly, W. G. Comparative mutagenesis of human cells in vivo and in vitro. Office of Scientific and Technical Information (OSTI), 1993. http://dx.doi.org/10.2172/6878550.

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Thilly, W. G. Comparative mutagenesis of human cells in vivo and in vitro. Office of Scientific and Technical Information (OSTI), 1992. http://dx.doi.org/10.2172/5115937.

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Thilly, W. G. (Comparative) mutagenesis of human cells in vivo and in vitro. Office of Scientific and Technical Information (OSTI), 1989. http://dx.doi.org/10.2172/7235709.

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Thilly, W. G. [Comparative] mutagenesis of human cells in vivo and in vitro. Progress report, 1989. Office of Scientific and Technical Information (OSTI), 1989. http://dx.doi.org/10.2172/10158113.

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Thilly, W. G. Comparative mutagenesis of human cells in vivo and in vitro. Progress report, 1990. Office of Scientific and Technical Information (OSTI), 1990. http://dx.doi.org/10.2172/10158116.

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Thilly, W. G. Comparative mutagenesis of human cells in vivo and in vitro. Progress report, November 1, 1992--April 30, 1993. Office of Scientific and Technical Information (OSTI), 1993. http://dx.doi.org/10.2172/10142521.

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Thilly, W. G., K. Khrapko, X. C. Li, A. Tomita, and P. Herrero. Comparative mutagenesis of human cells in vitro and in vivo. Final progress report, 1 November 1995--31 October 1996. Office of Scientific and Technical Information (OSTI), 1998. http://dx.doi.org/10.2172/666235.

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