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Relevant bibliographies by topics / Proteins, Protein, Genes

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Dissertations / Theses
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Academic literature on the topic 'Proteins, Protein, Genes'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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Journal articles on the topic "Proteins, Protein, Genes"

1

Darwish, Kamel, Huiying Li, and Thomas Poulos. "Engineering proteins, subcloning and hyperexpressing oxidoreductase genes." "Protein Engineering, Design and Selection" 4, no. 6 (1991): 701–8. http://dx.doi.org/10.1093/protein/4.6.701.

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Darwish, K., H. Li, and T. L. Poulos. "Engineering proteins, subcloning and hyperexpressing xidoreductase genes." "Protein Engineering, Design and Selection" 4, no. 7 (1991): 850. http://dx.doi.org/10.1093/protein/4.7.850.

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Neff, Norma F. "Protein splicing: selfish genes invade cellular proteins." Current Opinion in Cell Biology 5, no. 6 (1993): 971–76. http://dx.doi.org/10.1016/0955-0674(93)90079-6.

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Yesilirmak, Filiz, and Zehra Sayers. "Heterelogous Expression of Plant Genes." International Journal of Plant Genomics 2009 (August 6, 2009): 1–16. http://dx.doi.org/10.1155/2009/296482.

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Heterologous expression allows the production of plant proteins in an organism which is simpler than the natural source. This technology is widely used for large-scale purification of plant proteins from microorganisms for biochemical and biophysical analyses. Additionally expression in well-defined model organisms provides insights into the functions of proteins in complex pathways. The present review gives an overview of recombinant plant protein production methods using bacteria, yeast, insect cells, and Xenopus laevis oocytes and discusses the advantages of each system for functional studi

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Gophna, Uri, and Yanay Ofran. "Lateral acquisition of genes is affected by the friendliness of their products." Proceedings of the National Academy of Sciences 108, no. 1 (2010): 343–48. http://dx.doi.org/10.1073/pnas.1009775108.

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A major factor in the evolution of microbial genomes is the lateral acquisition of genes that evolved under the functional constraints of other species. Integration of foreign genes into a genome that has different components and circuits poses an evolutionary challenge. Moreover, genes belonging to complex modules in the pretransfer species are unlikely to maintain their functionality when transferred alone to new species. Thus, it is widely accepted that lateral gene transfer favors proteins with only a few protein–protein interactions. The propensity of proteins to participate in protein–pr

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NG, SEE-KIONG, and SOON-HENG TAN. "DISCOVERING PROTEIN–PROTEIN INTERACTIONS." Journal of Bioinformatics and Computational Biology 01, no. 04 (2004): 711–41. http://dx.doi.org/10.1142/s0219720004000600.

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The ongoing genomics and proteomics efforts have helped identify many new genes and proteins in living organisms. However, simply knowing the existence of genes and proteins does not tell us much about the biological processes in which they participate. Many major biological processes are controlled by protein interaction networks. A comprehensive description of protein–protein interactions is therefore necessary to understand the genetic program of life. In this tutorial, we provide an overview of the various current high-throughput methods for discovering protein–protein interactions, coveri

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Medvedeva, Irina V., Pavel S. Demenkov, and Vladimir A. Ivanisenko. "SITEX 2.0: Projections of protein functional sites on eukaryotic genes. Extension with orthologous genes." Journal of Bioinformatics and Computational Biology 15, no. 02 (2017): 1650044. http://dx.doi.org/10.1142/s021972001650044x.

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Functional sites define the diversity of protein functions and are the central object of research of the structural and functional organization of proteins. The mechanisms underlying protein functional sites emergence and their variability during evolution are distinguished by duplication, shuffling, insertion and deletion of the exons in genes. The study of the correlation between a site structure and exon structure serves as the basis for the in-depth understanding of sites organization. In this regard, the development of programming resources that allow the realization of the mutual project

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Kuroda, Hirofumi, Naoki Takahashi, Hiroaki Shimada, Motoaki Seki, Kazuo Shinozaki, and Minami Matsui. "Classification and Expression Analysis of Arabidopsis F-Box-Containing Protein Genes." Plant and Cell Physiology 43, no. 10 (2002): 1073–85. http://dx.doi.org/10.1093/pcp/pcf151.

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Abstract F-box proteins regulate diverse cellular processes, including cell cycle transition, transcriptional regulation and signal transduction, by playing roles in Skp1p-cullin-F-box protein (SCF) complexes or non-SCF complexes. F-box proteins are encoded by a large gene family. Our database search revealed that at least 568 F-box protein genes are present in the Arabidopsisthaliana (Arabidopsis) genome. Domain search analysis using SMART and Pfam-A databases revealed that 67 of the F-box proteins contained Kelch repeats and 29 contained leucine-rich repeats (LRRs). Interestingly only two F-

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Biernat, Jacek, and Hubert Köster. "Expression of synthetic genes coding for completely new, nutritionally rich, artificial proteins." "Protein Engineering, Design and Selection" 1, no. 4 (1987): 353–58. http://dx.doi.org/10.1093/protein/1.4.353.

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Chakraborty, Sandip, and David Alvarez-Ponce. "Positive Selection and Centrality in the Yeast and Fly Protein-Protein Interaction Networks." BioMed Research International 2016 (2016): 1–12. http://dx.doi.org/10.1155/2016/4658506.

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Proteins within a molecular network are expected to be subject to different selective pressures depending on their relative hierarchical positions. However, it is not obvious what genes within a network should be more likely to evolve under positive selection. On one hand, only mutations at genes with a relatively high degree of control over adaptive phenotypes (such as those encoding highly connected proteins) are expected to be “seen” by natural selection. On the other hand, a high degree of pleiotropy at these genes is expected to hinder adaptation. Previous analyses of the human protein-pr

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Dissertations / Theses on the topic "Proteins, Protein, Genes"

1

Lin, Da. "Regulation of MICA and MICB expression." Thesis, University of Oxford, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.509978.

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Baisden, Joseph M. "AFAP-110 is a cSrc activator." Morgantown, W. Va. : [West Virginia University Libraries], 2003. http://etd.wvu.edu/templates/showETD.cfm?recnum=2766.

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Thesis (Ph. D.)--West Virginia University, 2003.<br>Title from document title page. Document formatted into pages; contains v, 149 p. : ill. (some col.). Vita. Includes abstract. Includes bibliographical references.

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Dobson, Richard James Butler. "Global analysis of SNPs, proteins and protein-protein interactions : approaches for the prioritisation of candidate disease genes." Thesis, Queen Mary, University of London, 2009. http://qmro.qmul.ac.uk/xmlui/handle/123456789/463.

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Understanding the etiology of complex disease remains a challenge in biology. In recent years there has been an explosion in biological data, this study investigates machine learning and network analysis methods as tools to aid candidate disease gene prioritisation, specifically relating to hypertension and cardiovascular disease. This thesis comprises four sets of analyses: Firstly, non synonymous single nucleotide polymorphisms (nsSNPs) were analysed in terms of sequence and structure based properties using a classifier to provide a model for predicting deleterious nsSNPs. The degree of sequ

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Östensson, Frida. "Grain protein content and its assocoation with the NAC-protein genes HvNAM1 and HvNAM2 in Nordic barley." Thesis, Linköpings universitet, Biologi, 2016. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-129390.

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Hunger is a problem faced by many people all over the world, and as the population grows, so does the need for food such as cereals. Because of this, the need for food with higher protein and nutrient content will be increasingly important. NAM-B1, a NAC-protein gene in wheat, has been shown to control the grain protein content and nutrient values, as well as senescence. In barley, two orthologous genes have been found, HvNAM1 and HvNAM2. This study focuses on Nordic barley accessions and how haplotypes of HvNAM1 and HvNAM2 correlate to the grain protein content (GPC) and nutrient content. No

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Protopopova, Marina. "Modulation of activity of the tumour suppressor p53 by small molecules and damaged DNA /." Stockholm, 2004. http://diss.kib.ki.se/2004/91-7349-926-9/.

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Williams, Corey L. "Analysis of cystic kidney disease-related genes in Caenorhabditis elegans." Thesis, Birmingham, Ala. : University of Alabama at Birmingham, 2009. https://www.mhsl.uab.edu/dt/2009p/williams.pdf.

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James, Leonard Philip. "Myc and Mad target genes /." Thesis, Connect to this title online; UW restricted, 2000. http://hdl.handle.net/1773/5093.

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Smith, Marissa B. "Using gain of function genetics to explore the role of non-histone chromosomal protein D1 in Drosophila melanogaster." Morgantown, W. Va. : [West Virginia University Libraries], 2007. https://eidr.wvu.edu/etd/documentdata.eTD?documentid=5533.

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Thesis (M.S.)--West Virginia University, 2007.<br>Title from document title page. Document formatted into pages; contains vii, 124 p. : ill. (some col.). Includes abstract. Includes bibliographical references (p. 116-124).

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Bryant, Helen Elizabeth. "Analysis of cellular and viral proteins that interact with the IE63 protein of herpes simplex virus type 1." Thesis, University of Glasgow, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.312135.

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Khorram, Khorshid Hamid Reza. "Analysis of the genes encoding the spp24 protein in human and mouse and identification of interacting proteins." Thesis, University of Leicester, 2003. http://hdl.handle.net/2381/30347.

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Secreted phosphoprotein 24 (spp24) is a member of the cystatin superfamily.;This study identifies a rare single-amino acid polymorphism (p.S38F) of human spp24 and its importance has been assessed by comparing the sequence of human spp24 with that of eight other species. The gene encoding spp24 in mouse (Spp2), like its human ortholog, comprises eight exons with an apparently TATA-les promoter. The exon-intron structure is identical in mouse and human and the size and location of intron 1 is conserved between many species. Using several strategies, the gene encoding spp24 in mouse has been map

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Books on the topic "Proteins, Protein, Genes"

1

Tropp, Burton E. Molecular biology: Genes to proteins. 3rd ed. Jones and Bartlett, 2008.

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Blum-Moonesinghe, Janaki Kumari. Expression of calcium-binding proteins in chemically transformed rat fibroblasts. Hartung-Gorre Verlag, 1993.

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Berchtold, Martin W. Structure and expression of genes for parvalbumin and other EF-hand type CA²⁺--binding proteins. Hartung-Gorre, 1990.

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Berchtold, Martin W. Structure and expression of genes for parvalbumin and other EF-hand type CA2 - binding proteins. Hartung-Gorre, 1990.

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International Workshop on the CCN Family of Genes (5th 2008 Toronto, Canada). CCN proteins in health and disease: An overview of the Fifth International Workshop on the CCN Family of Genes. Edited by Perbal Annick, Takigawa Masaharu, and Perbal Bernard V. Springer, 2010.

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Näthke, Inke S. APC proteins. Springer Science+Business Media, 2009.

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European, Symposium on Calcium Binding Proteins in Normal and Transformed Cells (1st 1989 Brussels Belgium). Calcium binding proteins in normal and transformed cells. Plenum Press, 1990.

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Loftus, Brendan. Analysis of the prion protein (PrP) and PrP genes from Ovis aries and Oryctalagus cuniculus. University College Dublin, 1996.

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Stefánsson, Stefán Einar. Characterization of a repressor element and purification of its cognate DNA-binding protein for the transcription of the genes for the antifreeze proteins in wolffish (Anarhichas lupus). National Library of Canada = Bibliothèque nationale du Canada, 1997.

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Ludlow, John W. Tumor suppressors: Involvement in human diseases, viral protein interactions, and growth regulation. R.G. Landes, 1994.

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Book chapters on the topic "Proteins, Protein, Genes"

1

Larkins, Brian A. "Modification of Proteins Encoded by Seed Storage Protein Genes." In Tailoring Genes for Crop Improvement. Springer US, 1987. http://dx.doi.org/10.1007/978-1-4684-5329-4_14.

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Lerosey, Isabelle, Véronique Pizon, Armand Tavitian, and Jean de Gunzburg. "Phosphorylation of rap Proteins by the cAMP-Dependent Protein Kinase." In The Superfamily of ras-Related Genes. Springer US, 1991. http://dx.doi.org/10.1007/978-1-4684-6018-6_4.

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Graham, Brett H. "Mitochondrial Protein Translation-Related Disease: Mitochondrial Ribosomal Proteins and Translation Factors." In Mitochondrial Disorders Caused by Nuclear Genes. Springer New York, 2012. http://dx.doi.org/10.1007/978-1-4614-3722-2_17.

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Wasylyk, B. "Promoter Elements of Eukaryotic Protein-Coding Genes." In Chromosomal Proteins and Gene Expression. Springer US, 1985. http://dx.doi.org/10.1007/978-1-4684-7615-6_7.

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GÜnther, E. "Heat Shock Protein Genes and the Major Histocompatibility Complex." In Heat Shock Proteins and Immune Response. Springer Berlin Heidelberg, 1991. http://dx.doi.org/10.1007/978-3-642-75875-1_3.

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Loopstra, C. A., E. G. No, H. Wang, and J. Puryear. "Xylem-Specific Expression of Arabinogalactan-Protein-Like Genes." In Cell and Developmental Biology of Arabinogalactan-Proteins. Springer US, 2000. http://dx.doi.org/10.1007/978-1-4615-4207-0_16.

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Meyers, Marian B. "A 22 kDa Calcium-Binding Protein, Sorcin, is Encoded by Amplified Genes in Multidrug-Resistant Cells." In Novel Calcium-Binding Proteins. Springer Berlin Heidelberg, 1991. http://dx.doi.org/10.1007/978-3-642-76150-8_22.

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Hood, L., S. Kent, L. Smith, et al. "The Development of a Facility to Analyze and Synthesize Genes and Proteins." In Methods in Protein Sequence Analysis · 1986. Humana Press, 1987. http://dx.doi.org/10.1007/978-1-59259-480-1_2.

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Ciliberto, G. "Transcriptional Regulation of Acute Phase Response Genes with Emphasis on the Human C-reactive Protein Gene." In Acute Phase Proteins in the Acute Phase Response. Springer London, 1989. http://dx.doi.org/10.1007/978-1-4471-1739-1_3.

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Gupta, Radhey S. "Microbial Phylogeny and Evolution Based on Protein Sequences (The Change from Targeted Genes to Proteins)." In Mass Spectrometry for Microbial Proteomics. John Wiley & Sons, Ltd, 2010. http://dx.doi.org/10.1002/9780470665497.ch2.

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Conference papers on the topic "Proteins, Protein, Genes"

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Rajput, B., D. Alaimo, A. M. Asselbergs, and E. Reich. "CONSTRUCTION AND EXPRESSION OF HYBRID PLASMINOGEN ACTIVATOR GENES." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644412.

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Hybrid plasminogen activator (PA) genes containing fragments of cDNA encoding the non-catalytic part of tissue-PA and the .catalytic domain of urokinase and vice versa were constructed and expressed in Chinese Hamster ovary (CHO) cells. The hybrid nature of the products in stably transformed cells was analyzed at the level of DNA and RNA using probes derived from different regions of the urokinase and tissue-PA cDNAs and at the protein level by means of polyclonal antibodies raised against tissue-PA and urokinase. The hybrid genes made hybrid RNAs and proteins of the expected sizes. The protei

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Kim, Moon K., Byeongsoo Lim, and Wing Kam Liu. "Multiscale Elastic Network Model for Macromolecular Machines." In ASME 2010 First Global Congress on NanoEngineering for Medicine and Biology. ASMEDC, 2010. http://dx.doi.org/10.1115/nemb2010-13090.

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In the early year of this century the human genome sequencing project was successfully completed so that we can understand all the human genes and their corresponding protein sequences. Now our interests have naturally moved from genetics to proteomics in which we challenge to elucidate the relationship between functions and structures of proteins. In particular, understanding large conformational changes occurring at molecular machinery systems or protein assemblies have received great attentions. However, it has been rarely studied both experimentally and theoretically because of limitation

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Furis, B. C., M. J. Jorgensem, M. J. Rabiet, et al. "RECOGNITION SITE DIRECTING GAMMA-CARBOXYLATION RESIDES ON THE PROPEPTIDES OF FACTOR IX AND PROTRROMBIN." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643992.

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Factor IX and prothrombin vitamin K-dependent proteins that participate in blood coagulation undergo post-translationalmodification in which glutamic acid residues in the amino terminus of the protein are converted to gamma-carboxyglutamic acid residues. This modification confers divalent metal ion binding ability upon the proteins.As a consequence of binding divalent metal ions these proteins undergoconformational changes necessary for biological function.The vitamin K-dependent proteins are synthesized with an NH2-terminal extension. The region distal to the NH2-terminus of the mature protei

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Pannekok, H., A. J. Van Zonneveid, C. J. M. de vries, M. E. MacDonald, H. Veerman, and F. Blasi. "FUNCTIONAL PROPERTIES OF DELETION-MUTANTS OF TISSUE-TYPE PLASMINOGEN ACTIVATOR." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643724.

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Over the past twenty-five years, genetic methods have generated a wealth of information on the regulation and the structure-function relationship of bacterial genes.These methods are based on the introduction of random mutations in a gene to alter its function. Subsequently, genetic techniques cure applied to localize the mutation, while the nature of the impairedfunction could be determined using biochemical methods. Classic examples of this approach is now considered to be the elucidation of the structure and function of genes, constituting the Escherichia coli lactose (lac) and tryptophan (

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de Vries, C. J. M., N. K. Veerman, and H. Pannekoek. "ARTIFICIAL EXON SHUFFLING: CONSTRUCTION OF HYBRID cDNAS CONTAINING DOMAINS OF TISSUE-TYPE PLASMINOGEN ACTIVATOR (T-PA) AND UROKINASE (u-PA)." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643940.

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The intriguing finding that functions of t-PA coincide with structural domains and that these domains occur in related proteins, has been the basis to construct hybrid proteins by artificial exon shuffling to prove the conservation of functions in the shuffled domains. The heavy chain (Hch) of t-PA mediates both binding to fibrin and stimulation of plasminogen activator activity via its Finger- and Kringle-2 domain, whereas the light chain (Lch) contains the serine protease moiety of the protein. The Hch of u-PA is very homologous to the Lch of t-PA, but exhibits a higher plasminogen activator

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Butler-Zimrin, A. E., J. S. Bennett, M. Poncz, et al. "ISOLATION AND CHARACTERIZATION OF cDNA CLONES FOR THE PLATELET MEMBRANE GLYCOPROTEINS IIb and IIIa." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643961.

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The platelet membrane GPIIb/GPIIIa complex on activated platelets contains receptors for fibrinogen, von Willebrand factor, and fibronectin. GPIIb and GPIlia also appear to be members of a family of membrane receptors involved in cell-cell and cell-matrix interactions. To study the structure of GPIIb and GPIIIa, we have constructed an expression library in the vector lambda gtll using mRNA from the HEL cell line and screened it with polyclonal antibody against each platelet protein. HEL cells constitutively express proteins similar to platelet GPIIb and GPIIIa. A 3.2kb GPIIb cDNA clone was ide

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Giannelli, B. F. "MOLECULAR GENETICS OF HAEMOPHILIA." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643981.

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Haemophilia B, an X-linked recessive disease with an incidence of 1/30,000 newborn males, is due to defects in the gene for coagulation factor IX, which is on the long am of the X chromosome at band Xq27.1. This gene consists of approximately 34 Kb and contains 8 exons which specify a mRtfc of 2803 residues coding for a protein of 415 aa preceded by a prepro signal peptide of 46 aa. Coripanson of the functional domains of the factor IX protein with the exon structure of the gene supports the exon/protein domain hypothesis of gene evolution. The factor IX gene seems to be formed by a number of

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O'hara, Patrick J., Frank A. Grant, A. Betty, J. Haldmen, and Mark J. Murray. "Structure of the Human Factor VII Gene." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643786.

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Factor VII is a member of a family of vitamin K-dependent, gamma-carboxylated plasma protein which includes factor IX, factor X, protein C, protein S and prothrombin. Activated factor VII (factor Vila) is a plasma serine protease which participates in a cascade of reactions leading to the coagulation of blood. Two overlapping genomic clones containing sequences encoding human factor VII were isolated and characterized. The complete sequence of the gene was determined and found to span 12.8 kilobases. The mRNA for factor VII as demonstrated by cDNA cloning is polyadenylated at multiple sites bu

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Pannekoek, H., M. Linders, J. Keijer, H. Veerman, H. Van Heerikhuizen, and D. J. Loskutoff. "THE STRUCTURE OF THE HUMAN ENDOTHELIAL PLASMINOGEN ACTIVATOR INHIBITOR (PAI-1) GENE: NON-RANDOM POSITIONING OF INTRONS." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644767.

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The endothelium plays a crucial role in the regulation of the fibrinolytic process, since it synthesizes and secretes tissue-type plasminogen activator (t-PA) as well as the fast-acting plasminogen activator inhibitor (PAI-1). Molecular cloning of full-length PAI-1 cDNA, employing a human endothelial cDNA expression library, and a subsequent determination of the complete nucleotide sequence, allowed a prediction of the amino-acid sequence of the PAI-1 glycoprotein. It was observed that the amino-acid sequence is significantly homologous to those of members of the serine protease inhibitor ("Se

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Kute, Stephanie M., and David A. Vorp. "Regional Association of Biological and Hemodynamic Parameters in Distal End-to-Side Vascular Anastomoses Perfused Ex Vivo." In ASME 2002 International Mechanical Engineering Congress and Exposition. ASMEDC, 2002. http://dx.doi.org/10.1115/imece2002-32513.

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Vascular bypass graft failure is a significant clinical problem and is frequently due to the formation of intimal hyperplasia (IH) [1–3]. IH is characterized by the accumulation of smooth muscle cells (SMC) and extracellular matrix in the intima of the vessel, which occurs when the normal balance between vascular cell proliferation and apoptosis (regulated cell death) is altered [4]. The disturbed flow present at the anastomosis has been implicated in the formation of IH and the link between hemodynamics and graft failure is via a complex cascade of events whereby biomechanical forces cause bi

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Reports on the topic "Proteins, Protein, Genes"

1

Arnett, Clint, Justin Lange, Ashley Boyd, Martin Page, and Donald Cropek. Expression and secretion of active Moringa oleifera coagulant protein in Bacillus subtilis. Engineer Research and Development Center (U.S.), 2021. http://dx.doi.org/10.21079/11681/41546.

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Cationic polypeptide proteins found in the seeds of the tropical plant Moringa oleifera have coagulation efficiencies similar to aluminum and ferric sulfates without their recalcitrant nature. Although these proteins possess great potential to augment or replace traditional coagulants in water treatment, harvesting active protein from seeds is laborious and not cost-effective. Here, we describe an alternative method to express and secrete active M. oleifera coagulant protein (MO) in Bacillus subtilis. A plasmid library containing the MO gene and 173 different types of secretory signal peptides

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Albala, J. S. Challenges in biotechnology at LLNL: from genes to proteins. Office of Scientific and Technical Information (OSTI), 1999. http://dx.doi.org/10.2172/14370.

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Atasoy, Ulus, J. W. Davis, and Tim Hoffman. RNA Binding Proteins Posttranscriptionally Regulate Genes Involved In Oncogenesis. Defense Technical Information Center, 2010. http://dx.doi.org/10.21236/ada540837.

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Somerville, Ronald L. Novel Approaches to the Characterization of Specific Protein-Protein Interactions Important in Gene Expression. Defense Technical Information Center, 1994. http://dx.doi.org/10.21236/ada300480.

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Somerville, Ronald L. Novel Approaches to the Characterization of Specific Protein-Protein Interactions Important in Gene Expression. Defense Technical Information Center, 1995. http://dx.doi.org/10.21236/ada300572.

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Foy, Brent D. Simulating the Interactions of Genes, Proteins, and Metabolities in Cell-Like Entities. Defense Technical Information Center, 2005. http://dx.doi.org/10.21236/ada438522.

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Prakash, L. Repair of uv damaged DNA: Genes and proteins of yeast and human. Office of Scientific and Technical Information (OSTI), 1992. http://dx.doi.org/10.2172/5400958.

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Rauscher, Frank J. Characterization of Two Proteins Which Interact With the BRCA1 Gene. Defense Technical Information Center, 1999. http://dx.doi.org/10.21236/ada381176.

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Rauscher, Frank J. Characterization of Two Proteins which Interact with the BRCA1 Gene. Defense Technical Information Center, 1997. http://dx.doi.org/10.21236/ada330246.

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Sanders, Michel. Regulation of the Multidrug Resistance-Associated Protein Gene by Estrogen. Defense Technical Information Center, 1999. http://dx.doi.org/10.21236/ada381694.

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