Дисертації з теми "Genomic screens"
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Wilson, Jennifer L. (Jennifer Lynn). "Network analyses for functional genomic screens in cancer." Thesis, Massachusetts Institute of Technology, 2016. http://hdl.handle.net/1721.1/104236.
Повний текст джерелаCataloged from PDF version of thesis.
Includes bibliographical references (pages 128-151).
Gene interference screens are a widely adopted and popular tool for uncovering gene function but imperfections in the technology limit the power of these investigations. There are many completed and on-going RNAi investigations across a multitude of biological systems because these experiments are scalable, cost-effective, and relatively easily adapted to multiple experimental environments. The most influential disadvantage is that many of the individual reagents are non-specific and interfere with genes other than the intended target. Efforts to improve limitations in RNAi have focused on statistical models and improving reagents, yet have not explored using biological context to select gene targets. This thesis uses network modeling and data integration to provide context for gene interference studies, and demonstrates the utility of this approach in two systems: Acute Lymphoblastic Leukemia (ALL) is a disease of undifferentiated B-cells that results from accumulation of genetic lesions, yet we have an incomplete understanding of all genes contributing to the disease and how they interact. To discover genetic mediators of this disease, we employ a genome-scale shRNA screen, and complement this data with differential mRNA expression and ChIP-seq data using network integration. The integrated model identifies processes not represented in any input set and predicts novel genes contributing to disease. We specifically validate the role of Wwpl as a tumor suppressor in ALL. Aberrant growth factor pathway activity drives cancer pathology and is the target of molecular cancer therapies. Specifically, the epidermal growth factor receptor (EFGR) pathway and its ligand, transforming growth factor alpha (TGF[alpha]) are clinically relevant to gastric cancer. We use an shRNA screen and Prize Collecting Steiner Forest (PCSF) algorithm to discover the pathway regulating TGF shedding. This pathway identifies common regulators of TGF[alpha] shedding and NF[chi]B regulation, yet targeting NF[chi]B and the EGFR pathway has thus far been unsuccessful in cancer therapies. Our network identifies IRAK1 as a viable path forward for modulating both TGF[alpha] and NF[chi]B in gastric cancer.
by Jennifer L. Wilson.
Ph. D.
Burrows, Anna. "Genome-Wide Loss-of-Function Genetic Screens Identify Novel Senescence Genes and Putative Tumor Suppressors." Thesis, Harvard University, 2012. http://dissertations.umi.com/gsas.harvard:10191.
Повний текст джерелаPickering, H. "Identification of Chlamydia trachomatis immune targets through immunological and population-genomic screens and elucidation of potential roles in bacterial pathogenesis." Thesis, London School of Hygiene and Tropical Medicine (University of London), 2017. http://researchonline.lshtm.ac.uk/3928322/.
Повний текст джерелаAllan, Kristina Jean. "Enhancing Oncolytic Virotherapy Using Functional Genomic Screening." Thesis, Université d'Ottawa / University of Ottawa, 2018. http://hdl.handle.net/10393/37910.
Повний текст джерелаLi, Shuzhao. "A genomic screen for Zic1 target genes in neural development." Thesis, Montana State University, 2006. http://etd.lib.montana.edu/etd/2006/li/LiS0806.pdf.
Повний текст джерелаPedro, Rodrigues Joana Cristina. "Yeast genome-wide telomere screens and insights into cancer." Thesis, University of Newcastle upon Tyne, 2017. http://hdl.handle.net/10443/3898.
Повний текст джерелаGiedraitis, Vilmantas. "Candidate gene analyses and genome-wide screens in multiple sclerosis /." Stockholm, 2002. http://diss.kib.ki.se/2002/91-7349-408-9/.
Повний текст джерелаSawcer, Stephen James. "A linkage genome screen in multiple sclerosis." Thesis, University of Cambridge, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.627121.
Повний текст джерелаJarvis, Morgan L. "Development of a novel screen protocol for the identification of genes causing replication associated genomic instability in Schizosaccharomyces pombe." Thesis, Kingston, Ont. : [s.n.], 2008. http://hdl.handle.net/1974/1227.
Повний текст джерелаDeligiannaki, Myrto. "Identification of novel septate junction components through genome-wide glial screens." Diss., Ludwig-Maximilians-Universität München, 2015. http://nbn-resolving.de/urn:nbn:de:bvb:19-183079.
Повний текст джерелаPedanou, Victoria E. "Identification of Novel Pathways that Promote Anoikis through Genome-wide Screens." eScholarship@UMMS, 2016. https://escholarship.umassmed.edu/gsbs_diss/889.
Повний текст джерелаPedanou, Victoria E. "Identification of Novel Pathways that Promote Anoikis through Genome-wide Screens." eScholarship@UMMS, 2010. http://escholarship.umassmed.edu/gsbs_diss/889.
Повний текст джерелаLi, Hubo. "Genome-Wide RNAi Screens for Novel Regulators of Acute Myeloid Leukemia." Thesis, Harvard University, 2015. http://nrs.harvard.edu/urn-3:HUL.InstRepos:14226105.
Повний текст джерелаBowen, Emma. "A genomic screen for the identification of novel components of the S-phase checkpoint." Thesis, University of Sheffield, 2015. http://etheses.whiterose.ac.uk/8190/.
Повний текст джерелаSerra, Ryan W. "Investigating Cancer Molecular Genetics using Genome-wide RNA Interference Screens: A Dissertation." eScholarship@UMMS, 2013. https://escholarship.umassmed.edu/gsbs_diss/676.
Повний текст джерелаSerra, Ryan W. "Investigating Cancer Molecular Genetics using Genome-wide RNA Interference Screens: A Dissertation." eScholarship@UMMS, 2006. http://escholarship.umassmed.edu/gsbs_diss/676.
Повний текст джерелаAmberkar, Sandeep [Verfasser], and Roland [Akademischer Betreuer] Eils. "Integrative bioinformatics analyses of genome-wide RNAi screens / Sandeep Amberkar ; Betreuer: Roland Eils." Heidelberg : Universitätsbibliothek Heidelberg, 2014. http://d-nb.info/1180032608/34.
Повний текст джерелаXiong, Zikai. "Genome-wide recessive screens for DNA mismatch repair genes in mouse ES cells." Thesis, University of Cambridge, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.612055.
Повний текст джерелаNg, Cheuk-Him (Andy). "Genome-Wide Screen Identifies Novel Genes Involved in Mitochondrial Quality Control." Thesis, Université d'Ottawa / University of Ottawa, 2015. http://hdl.handle.net/10393/33204.
Повний текст джерелаNewbury, Dianne F. "A genome wide screen for loci involved in specific language impairment." Thesis, University of Oxford, 2002. http://ora.ox.ac.uk/objects/uuid:2b30517a-cecd-49f3-8a5d-556cef6d6723.
Повний текст джерелаKiritsy, Michael C. "Functional Genomics of Mammalian Innate Immunity." eScholarship@UMMS, 2020. https://escholarship.umassmed.edu/gsbs_diss/1102.
Повний текст джерелаMeisner, Sarah. "The genetics of susceptibility to leprosy." Thesis, University of Oxford, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.298995.
Повний текст джерелаDuPree, Michael G. "A candidate gene study and a full genome screen for male homosexuality." Connect to this title online, 2002. http://etda.libraries.psu.edu/theses/approved/WorldWideIndex/ETD-209/index.html.
Повний текст джерелаTran, Grant. "Modeling drug efficacy in the tumour microenvironment with Saccharomyces cerevisiae genome-wide screens in hypoxic conditions." Thesis, University of British Columbia, 2017. http://hdl.handle.net/2429/60210.
Повний текст джерелаPharmaceutical Sciences, Faculty of
Graduate
Deligiannaki, Myrto Verfasser], and Ulrike [Akademischer Betreuer] [Gaul. "Identification of novel septate junction components through genome-wide glial screens / Myrto Deligiannaki. Betreuer: Ulrike Gaul." München : Universitätsbibliothek der Ludwig-Maximilians-Universität, 2015. http://d-nb.info/1072376601/34.
Повний текст джерелаPrüßing, Katja [Verfasser]. "Genome-wide screen for modifiers of Abeta42-induced neurodegeneration in Drosophila / Katja Prüßing." Aachen : Hochschulbibliothek der Rheinisch-Westfälischen Technischen Hochschule Aachen, 2012. http://d-nb.info/1026309840/34.
Повний текст джерелаFernandes, Caroline. "Genome-wide screen for novel regulators of Parkinson's disease genes in «Drosophila melanogaster»." Thesis, McGill University, 2011. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=103725.
Повний текст джерелаIntroduction : L'altération de la fonction mitochondriale entraîne la dégénérescence de certains neurones chez les personnes atteintes de maladies neurodégénératives dont la maladie de Parkinson. Les cellules saines sont dotées d'un système de contrôle leur permettant de faire face et de réparer les dysfonctionnements des mitochondries et ainsi de préserver leur intégrité. Des études récentes ont révélé l'implication de deux gènes à l'origine de syndromes parkinsoniens autosomiques récessifs, Pink1 et Parkin, dans une voie de signalisation commune contrôlant le maintien de la fonction mitochondriale. Pink1 et Parkin interviennent ensemble dans l'isolation et la dégradation des mitochondries défectueuses. Cependant, à l'heure actuelle, les mécanismes moléculaires contrôlant ce processus restent à élucider. Méthodes : Le but de notre étude a été d'identifier de nouveaux régulateurs de la voie de signalisation Pink1/Parkin par crible génétique dans un modèle drosophile de la maladie de Parkinson. Pour cela, nous avons criblé une collection de lignées de drosophiles déficientes sur les chromosomes deux et trois pour leur capacité à modifier (augmenter ou diminuer) le phénotype de posture de l'aile caractéristique de la mutation de Pink1/Parkin. Résultats: Nous avons identifié plusieurs régions cytologiques qui interagissent fortement avec Parkin et/ou Pink1. Quatre de ces régions ont été disséquées de façon à révéler cinq gènes. Parmi eux, opa1 et drp1 avaient déjà été impliques dans la voie de signalisation Pink1/Parkin. Les trois autres gènes p60, β4galNacTA et debra représentent de nouveaux régulateurs de la fonction de Pink1 et Parkin. Conclusion/implications : D'une part, l'identification non biaisée de gènes déjà connus comme interagissant avec Pink1/Parkin démontre la validité de cette approche. D'autre part, la découverte de nouveaux gènes candidats de la voie Pink1/Parkin pour le maintien de l'intégrité mitochondriale permettra de mieux comprendre les mécanismes moléculaires contrôlant ce processus et aidera à l'élaboration de traitements.
Mendez, Jamie Elizabeth. "Investigation of Hsf1 Interacting Partners via a Genome-wide Yeast Two-hybrid Screen." Scholar Commons, 2013. http://scholarcommons.usf.edu/etd/4543.
Повний текст джерелаMcKnight, N. C. "A genome-wide screen for starvation-induced autophagy : identifies new modulators of autophagy." Thesis, University College London (University of London), 2011. http://discovery.ucl.ac.uk/1302281/.
Повний текст джерелаDrake, Peter. "The first genome-wide screen for animal peroxins using RNAi in Drosophila melanogaster." Thesis, University of Sheffield, 2013. http://etheses.whiterose.ac.uk/3777/.
Повний текст джерелаPowers, Ralph Wilson. "Genome-wide screens reveal that reduced TOR signaling extends chronological and replicative life span in S. cerevisiae /." Thesis, Connect to this title online; UW restricted, 2006. http://hdl.handle.net/1773/5044.
Повний текст джерелаGore, Tanvi. "Analyse génétique du trafic intracellulaire du morphogène Hedgehog chez la Drosophile." Thesis, Nice, 2015. http://www.theses.fr/2015NICE4110.
Повний текст джерелаHedgehog (Hh) is a conserved secreted morphogen involved in an array of developmental processes. Using Drosophila as a model, during my thesis we aimed to ask how the secretion, extraction and transport of Hh protein are regulated at the site of its production. To understand the positive regulators of Hh secretion and transport we designed and performed a genome-wide RNAi screen in Drosophila to identify new regulators of Hh transport and identified the small GTPase Rab8 as a novel component required for Hh trafficking. According to our proposed model, there are two pools of secreted Hh. The apical pool is needed for long range target gene activation, and basolateral pool for short range target gene activation. It is not clear how Hh is sorted apico-basally in the producing cells. Interfering with Rab8 function in the Hh producing cells extends Hh short range targets. Conversely, it reduces the long range Hh targets, suggesting that interfering with Rab8 function in the Hh producing cells impairs Hh trafficking, thus hampering the fine tuning between the two secreted pools of Hh. Moreover, using live assays to track the dynamics of endogenous Hh internalization, we observed that loss of Rab8 in Hh producing cells does not affect its primary secretion, but causes defects in Hh endocytosis, subsequently affecting its gradient activity. We hypothesize a model where Hh is targeted for primary secretion to the apical side of the wing disc, which then is internalized, and this internalized Hh is then directed for recycling which is essential for its long range activity
Scheich, Christoph. "High-throughput evaluation of protein folding conditions and expression constructs for structural genomics." Phd thesis, [S.l. : s.n.], 2004. http://pub.ub.uni-potsdam.de/2004/0055/scheich.pdf.
Повний текст джерелаIvatt, R. M. "A whole genome RNAi screen to identify novel promoters of PINK1/Parkin-mediated mitophagy." Thesis, University of Sheffield, 2013. http://etheses.whiterose.ac.uk/4899/.
Повний текст джерелаYamanoi, Kouji. "Suppression of ABHD2, identified through a functional genomics screen, causes anoikis resistance, chemoresistance and poor prognosis in ovarian cancer." Kyoto University, 2017. http://hdl.handle.net/2433/227585.
Повний текст джерелаYang, Dingyi. "Identifying novel immune modulating factors in a genome-wide Staphylococcus aureus screen in human neutrophils." Thesis, University of Sheffield, 2017. http://etheses.whiterose.ac.uk/19447/.
Повний текст джерелаSharma, Sumana. "Genome-scale identification of cellular pathways required for cell surface recognition." Thesis, University of Cambridge, 2018. https://www.repository.cam.ac.uk/handle/1810/271825.
Повний текст джерелаTran, Anh Thuy. "Genome-wide RNA-interference screen for human host factors vital to influenza A virus-induced cell death and viral replication." Journal of Virology, 2013. http://hdl.handle.net/1993/18323.
Повний текст джерелаLee, Liam Changwoo. "Functional identification of molecular oncotargets associated with the resistance to ALK inhibition in neuroblastoma via genome-wide CRISPR-Cas9 screens." Thesis, University of Cambridge, 2017. https://www.repository.cam.ac.uk/handle/1810/267921.
Повний текст джерелаNorton, Matthew. "Genome-wide RNAi Screen Identifies Romo1 as a Novel Regulator of Mitochondrial Fusion and Cristae Integrity." Thesis, Université d'Ottawa / University of Ottawa, 2013. http://hdl.handle.net/10393/23701.
Повний текст джерелаRose, Elaine. "Identifying Mechanisms of Resistance to Oncolytic Virotherapy in Acute Leukemia Through a Genome-wide CRISPR Screen." Thesis, Université d'Ottawa / University of Ottawa, 2018. http://hdl.handle.net/10393/38112.
Повний текст джерелаPfannenstiel, Brandon T., Xixi Zhao, Jennifer Wortman, Philipp Wiemann, Kurt Throckmorton, Joseph E. Spraker, Alexandra A. Soukup, et al. "Revitalization of a Forward Genetic Screen Identifies Three New Regulators of Fungal Secondary Metabolism in the Genus Aspergillus." AMER SOC MICROBIOLOGY, 2017. http://hdl.handle.net/10150/626452.
Повний текст джерелаZahoor, Muhammad kashif. "Genome wide analysis for novel regulators of growth and lipid metabolism in drosophila melanogaster." Phd thesis, Université Paris Sud - Paris XI, 2011. http://tel.archives-ouvertes.fr/tel-00664844.
Повний текст джерелаAdamson, Brittany Susan. "A Genome-Wide Study of Homologous Recombination in Mammalian Cells Identifies RBMX, a Novel Component of the DNA Damage Response." Thesis, Harvard University, 2012. http://dissertations.umi.com/gsas.harvard:10723.
Повний текст джерелаAmai, Takamitsu. "Development of genome editing technology of mitochondrial DNA in Saccharomyces cerevisiae." Doctoral thesis, Kyoto University, 2021. http://hdl.handle.net/2433/263707.
Повний текст джерелаVoß, Felizia Katharina [Verfasser]. "Molecular identification of the volume-regulated anion channel VRAC by a genome-wide siRNA screen / Felizia Katharina Voß." Berlin : Freie Universität Berlin, 2015. http://d-nb.info/1068809906/34.
Повний текст джерелаBuchholz, Frank, Mikołaj Słabicki, Mirko Theis, Dragomir B. Krastev, Sergey Samsonov, Emeline Mundwiller, Magno Junqueira, et al. "A Genome-Scale DNA Repair RNAi Screen Identifies SPG48 as a Novel Gene Associated with Hereditary Spastic Paraplegia." Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2015. http://nbn-resolving.de/urn:nbn:de:bsz:14-qucosa-180795.
Повний текст джерелаRambani, Komal. "A genome wide screen in C. elegans identifies cell non-autonomous regulators of oncogenic Ras mediated over-proliferation." The Ohio State University, 2016. http://rave.ohiolink.edu/etdc/view?acc_num=osu1461288131.
Повний текст джерелаBuchholz, Frank, Mikołaj Słabicki, Mirko Theis, Dragomir B. Krastev, Sergey Samsonov, Emeline Mundwiller, Magno Junqueira, et al. "A Genome-Scale DNA Repair RNAi Screen Identifies SPG48 as a Novel Gene Associated with Hereditary Spastic Paraplegia." Public Library of Science, 2010. https://tud.qucosa.de/id/qucosa%3A28927.
Повний текст джерелаBoquete, Vilarino Lorena. "Development of shRNA screens to identify effectors of three complex traits : neighbour suppression of tumour growth and proliferation and protection from lipotoxicity in β-cells". Thesis, University of Exeter, 2016. http://hdl.handle.net/10871/27635.
Повний текст джерела