Dissertations / Theses on the topic 'Saccharomyces cerevisiae Saccharomyces cerevisiae Proteins Signal Transduction'

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1

Powers, 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.

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2

Zeller, Corinne Eileen Dohlman Henrik G. "Regulation of signal transduction by G protein [beta] subunits in Saccharomyces cerevisiae." Chapel Hill, N.C. : University of North Carolina at Chapel Hill, 2007. http://dc.lib.unc.edu/u?/etd,1404.

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Thesis (Ph. D.)--University of North Carolina at Chapel Hill, 2007.<br>Title from electronic title page (viewed Apr. 25, 2008). "... in partial fulfillment of the requirements for the degree of Doctor of Philosophy in the Department of Biochemistry and Biophysics." Discipline: Biochemistry and Biophysics; Department/School: Medicine. On title page, [beta] appears as Greek character.
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3

Miller, Kristi E. "Negative Regulation of Polarity Establishment in Saccharomyces cerevisiae." The Ohio State University, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1555329407450767.

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4

Takahashi, Satoe. "Plasma Membrane Localization of Signaling Proteins in Yeast: a Dissertation." eScholarship@UMMS, 2008. https://escholarship.umassmed.edu/gsbs_diss/364.

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In response to external stimuli, many intracellular signaling proteins undergo dynamic changes in localization to the plasma membrane. Using the Saccharomyces cerevisiaemating pathway as a model, I investigated the molecular interactions that govern plasma membrane localization of signaling proteins, and how the plasma membrane compartmentalization of a signaling complex influences the overall signaling behavior of the pathway. Signaling proteins often consist of multiple interaction domains that collectively dictate their localization and function. Ste20 is a p21-activated kinase (PAK) that f
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5

Paulovich, Amanda G. "The regulation of S phase progression rate in yeast in response to DNA damage /." Thesis, Connect to this title online; UW restricted, 1996. http://hdl.handle.net/1773/10263.

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6

Robinson, Kevin Spencer. "The phosphatidylinositol signal transduction system in the yeast Saccharomyces cerevisiae." Thesis, University of Bath, 1992. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.316975.

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7

Van, Dyk Dewald 1975. "Genetic analysis of a signal transduction pathway : the regulation of invasive growth and starch degradation in Saccharomyces cerevisiae." Thesis, Stellenbosch : Stellenbosch University, 2004. http://hdl.handle.net/10019.1/49972.

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Dissertation (PhD)--University of Stellenbosch, 2004.<br>ENGLISH ABSTRACT: Cells of the yeast Saccharomyces cerevisiae are able to change their morphological appearance in response to a variety of extracellular and intracellular signals. The processes involved in morphogenesis are well characterised in this organism, but the exact mechanism by which information emanating from the environment is integrated into the regulation of the actin cytoskeleton and the yeast cell cycle, is still not clearly understood. Considerable progress has, however, been made. The processes are investigated o
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8

Roberts, Radclyffe L. (Radclyffe Lee) 1968. "Specificity determinants of a bifunctional signal transduction pathway in Saccharomyces cerevisiae." Thesis, Massachusetts Institute of Technology, 1997. http://hdl.handle.net/1721.1/43554.

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9

Kerwin, Christine. "Pho2 dependence in the phosphate signal transduction pathway of Saccharomyces cerevisiae and Candida glabrata." Click here for download, 2008. http://proquest.umi.com/pqdweb?did=1605126421&sid=1&Fmt=2&clientId=3260&RQT=309&VName=PQD.

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10

Nikolaou, Elissavet. "Phylogenetic diversity of fungal stress signaling pathways." Thesis, Available from the University of Aberdeen Library and Historic Collections Digital Resources, 2008. http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?application=DIGITOOL-3&owner=resourcediscovery&custom_att_2=simple_viewer&pid=24849.

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11

Kriel, Johan Hendrik. "Development of synthetic signal sequences for heterologous protein secretion from Saccharomyces cerevisiae." Thesis, Stellenbosch : Stellenbosch University, 2003. http://hdl.handle.net/10019.1/53364.

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Thesis (MSc)--Stellenbosch University, 2003.<br>ENGLISH ABSTRACT: Protein secretion and intracellular transport are highly regulated processes and involve the interplay of a multitude of proteins. A unique collection of thermosensitive secretory mutants allowed scientists to demonstrate that the secretory pathway of the yeast Saccharomyces cerevisiae is very similar to that of the higher eukaryotes. All proteins commence their journey in the endoplasmic reticulum, where they undergo amino-linked core glycosyl modification. After passage through the Golgi apparatus, where the remodelling
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12

Tsujimoto, Yoshiyuki. "Regulation of DOG2 Gene Expression and Signal Transduction in Environmental Stress Response of saccharomyces cerevisiae." Kyoto University, 1998. http://hdl.handle.net/2433/157117.

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本文データは平成22年度国立国会図書館の学位論文(博士)のデジタル化実施により作成された画像ファイルを基にpdf変換したものである<br>Kyoto University (京都大学)<br>0048<br>新制・課程博士<br>博士(農学)<br>甲第7406号<br>農博第990号<br>新制||農||762(附属図書館)<br>学位論文||H10||N3152(農学部図書室)<br>UT51-98-G335<br>京都大学大学院農学研究科食品工学専攻<br>(主査)教授 木村 光, 教授 天知 輝夫, 教授 江﨑 信芳<br>学位規則第4条第1項該当
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13

Ketela, Troy W. "Functional characterization of the Saccharomyces cerevisiae SKN7 and MID2 genes, and their roles in osmotic stress and cell wall integrity signaling." Thesis, McGill University, 1999. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=36620.

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The yeast SKN7 gene encodes a transcription factor that is involved in a variety of processes in cell physiology including cell wall synthesis, cell cycle progression, and oxidative stress resistance. Using a transcriptional reporter-based system, it has been demonstrated that Skn7p is regulated by the two-component osmosensor Sln1p in a manner that requires the phosphorelay molecule Ypd1p, but not the response regulator Ssk1p. Consistent with its regulation by an osmosensor, Skn7p is involved in negative regulation of the osmoresponsive HOG MAP kinase cascade. Cells lacking SKN7 and the prote
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14

Andréasson, Claes. "Ligand-activated proteolysis in nutrient signaling /." Stockholm, 2004. http://diss.kib.ki.se/2004/91-7140-075-3/.

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15

Bonizec, Mélanie. "Nouvelles fonctions de la protéine Cdc48 : une ATPase, chez la levure Saccharomyces cerevisiae." Paris 7, 2012. http://www.theses.fr/2012PA077123.

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L'ubiquitylation est une modification post-traductionnelle impliquée dans de nombreux processus cellulaires qui nécessite une régulation fine. La protéine Cdc48, qui appartient à la famille des ATPases AÂA (ATPase associated with various activities), participe à cette régulation. En effet, il s'agit d'une chaperonne dépendante de l'ubiquitine, essentielle à la viabilité cellulaire, qui est capable de réguler le devenir de protéines ubiquitylées, directement ou indirectement via des cofacteurs. Cdc48 est impliquée dans la régulation de nombreuses fonctions biologiques et contribue à l'homéostas
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16

Rivoyre, Matthieu de. "Expression et purification de protéines membranaires mammifères impliquées dans des pathologies." Nice, 2006. http://www.theses.fr/2006NICE4062.

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À l’interface entre la cellule et le milieu extérieur, les protéines membranaires ont un rôle indispensable au fonctionnement cellulaire. Elles jouent un grand nombre de fonctions et peuvent être impliquées dans des pathologies graves. La connaissance de ces protéines membranaire peut permettre de mieux comprendre de nombreux phénomènes biologiques et pathologiques et leur localisation, accessible, en fait de bonne cibles thérapeutique. La connaissance de la structure des protéines apporte une quantité d’information très importante sur leur fonctionnement. À ce jour si plusieurs dizaines de mi
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17

Strickfaden, Shelly Catherine. "Regulation of Cell Polarization and Map Kinase Signaling in the Saccharomyces Cerevisiae Pheromone Response Pathway: a Dissertation." eScholarship@UMMS, 2007. https://escholarship.umassmed.edu/gsbs_diss/321.

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Exposure to external stimuli promotes a variety of cellular responses including changes in morphology, gene expression and cell division status. These responses are promoted by signaling pathways composed of modules that are conserved from lower to higher eukaryotes. In Saccharomyces cerevisiae response to the external stimuli provided by mating pheromone is governed by the pheromone response pathway. This pathway is composed of a G protein coupled receptor/heterotrimeric G protein (Gαβγ) module and a MAP kinase cascade. Activation of this pathway allows the heterotrimeric G protein βγ dimer (
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18

Müller, Dirk [Verfasser]. "Model-Assisted Analysis of Cyclic AMP Signal Transduction in Saccharomyces cerevisiae – cAMP as Dynamic Coordinator of Energy Metabolism and Cell Cycle Progression / Dirk Müller." Aachen : Shaker, 2006. http://d-nb.info/1170528538/34.

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19

Fabre, Anne-Lise. "Synthèse et modification des glycanes glycosylphosphatidylinositol chez Saccharomyces cerevislae et d'autres levures." Angers, 2007. http://www.theses.fr/2007ANGE0053.

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Les glycosylphosphatidylinositols (GPIs) sont des modifications glycolipidiques permettant d'ancrer certaines protéines eucaryotes secrétées à la surface cellulaire. Les ancres GPI partagent la même sructure centrale très conservée protéine-PEthN-6Manα1-2Man&amp;l-6Manαl-4GlcNH2&amp;l-6inositol-PO4-lipide, synthétisée en plus de 12 étapes enzymatiques. Au moins une protéine a déja été identifiée pour chacune de ces étapes, à l'exception de l'addition du second mannose. Une stratégie bioinformatique m'a permis d'identifier une protéine non caractérisée, Gpi 18p, responsable de l'ajout de Man2.
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20

Jiang, Ying. "Transfer of the Ribosome-Nascent Chain Complex to the Translocon in Cotranslational Translocation: A Thesis." eScholarship@UMMS, 2007. https://escholarship.umassmed.edu/gsbs_diss/332.

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Cotranslational translocation is initiated by targeting of a ribosome-bound nascent polypeptide chain (RNC) to the endoplasmic reticulum (ER) membrane. The targeting reaction is coordinated by the signal recognition particle (SRP) through its interaction with the RNC and the membrane-bound SRP receptor (SR). A vacant translocon is a prerequisite for the subsequent nascent chain release from SRP-SR-RNC complex. It has been proposed that the protease-accessible cytosolic domains of the Sec61p complex play an important role in posttargeting steps by providing the binding site for the ribosome or
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21

Schmitt, Kerstin. "Ribosomal Asc1p/RACK1 in the phosphorylation signaling network of Saccharomyces cerevisiae." Doctoral thesis, 2016. http://hdl.handle.net/11858/00-1735-0000-002B-7D37-0.

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22

Rachfall, Nicole. "Translational control by the ribosomal protein Asc1p/Cpc2p in Saccharomyces cerevisiae." Thesis, 2010. http://hdl.handle.net/11858/00-1735-0000-0006-AE00-4.

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23

Schwartz, Monica A. "Signaling specificity in Saccharomyces cerevisiae mating and filamentous growth MAPK pathways /." 2005. http://wwwlib.umi.com/cr/ucsf/fullcit?p3199376.

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24

Opitz, Nadine. "Analysis of the Asc1p/RACK1 microenvironment in Saccharomyces cerevisiae using proximity-dependent Biotin Identification (BioID) and high-resolution mass spectrometry." Doctoral thesis, 2016. http://hdl.handle.net/11858/00-1735-0000-0023-3F29-D.

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25

Read, Paul William. "Functional characterization of highly purified human Rho/RhoGDI complexes expressed in Saccharomyces cerevisiae resulting in the development of a novel mammalian signal transduction tool /." 2000. http://wwwlib.umi.com/dissertations/fullcit/9975429.

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26

Köhler, Tim. "Regulation of Growth and Development by the Small GTPase Cdc42p and the Transcription Factor Tec1p in Saccharomyces cerevisiae." Doctoral thesis, 2003. http://hdl.handle.net/11858/00-1735-0000-0006-AE6F-C.

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